146 research outputs found
Canine Models of Inherited Musculoskeletal and Neurodegenerative Diseases
- Author
- Publication venue
- eScholarship@UMassChan
- Publication date
- 11/03/2020
- Field of study
Mouse models of human disease remain the bread and butter of modern biology and therapeutic discovery. Nonetheless, more often than not mouse models do not reproduce the pathophysiology of the human conditions they are designed to mimic. Naturally occurring large animal models have predominantly been found in companion animals or livestock because of their emotional or economic value to modern society and, unlike mice, often recapitulate the human disease state. In particular, numerous models have been discovered in dogs and have a fundamental role in bridging proof of concept studies in mice to human clinical trials. The present article is a review that highlights current canine models of human diseases, including Alzheimer\u27s disease, degenerative myelopathy, neuronal ceroid lipofuscinosis, globoid cell leukodystrophy, Duchenne muscular dystrophy, mucopolysaccharidosis, and fucosidosis. The goal of the review is to discuss canine and human neurodegenerative pathophysiologic similarities, introduce the animal models, and shed light on the ability of canine models to facilitate current and future treatment trials
Temperature and force dependence of nanoscale electron transport via the Cu protein Azurin
- Author
- Alessandrini A.
- Ambler R. P.
- Andolfi L.
- Andolfi L.
- Atsushi I.
- Bar G.
- Battistuzzi G.
- Benning M. M.
- Beratan D. N.
- Bizzarri A. R.
- Bonander N.
- Chi Q. J.
- Chi Q. J.
- Choi S. H.
- Das R.
- David Cahen
- Davis J. J.
- Davis J. J.
- Davis J. J.
- Engelkes V. B.
- Engeseth H. R.
- Farver O.
- Friis E. P.
- Gaigalas A. K.
- Good R. H. J.
- Gray H. B.
- Israel Pecht
- Jeuken L. J. C.
- Kuhle A.
- Lior Sepunaru
- Luo L.
- Marcus R. A.
- Marshall N. M.
- Maruccio G.
- Meier M.
- Mentovich E. D.
- Mordechai Sheves
- Nadav Amdursky
- Nar H.
- Palfey B. A.
- Rakshit T.
- Rakshit T.
- Regan J. J.
- Ron H.
- Ron I.
- Ron I.
- San Paulo A.
- Sepunaru L.
- Shen Y.
- Shepard W. E. B.
- Shinwari M. W.
- Sidney R. Cohen
- Skov L. K.
- Stamouli A.
- Tao N. J.
- Vandekamp M.
- Vilan A.
- Wenjie Li
- Wierzbinski E.
- Wold D. J.
- Xu D.
- Zaballa M.-E.
- Zhao J. W.
- Zhao J. W.
- Zhao J. W.
- Publication venue
- 'American Chemical Society (ACS)'
- Publication date
- 14/09/2012
- Field of study
The mechanisms of solid-state electron transport (ETp) via a monolayer of
immobilized Azurin (Az) was examined by conducting probe atomic force
microscopy (CP-AFM), both as function of temperature (248 - 373K) and of
applied tip force (6-12 nN). By varying both temperature and force in CP-AFM,
we find that the ETp mechanism can alter with a change in the force applied via
the tip to the proteins. As the applied force increases, ETp via Az changes
from temperature-independent to thermally activated at high temperatures. This
is in contrast to the Cu-depleted form of Az (apo-Az), where increasing the
applied force causes only small quantitative effects, that fit with a decrease
in electrode spacing. At low force ETp via holo-Az is temperature-independent
and thermally activated via apo-Az. This observation agrees with
macroscopic-scale measurements, thus confirming that the difference in ETp
dependence on temperature between holo- and apo-Az is an inherent one that may
reflect a difference in rigidity between the two forms. An important
implication of these results, which depend on CP-AFM measurements over a
significant temperature range, is that for ETp measurements on floppy systems,
such as proteins, the stress applied to the sample should be kept constant or,
at least controlled during measurement.Comment: 24 pages, 6 figures, plus Supporting Information with 4 pages and 2
figure
Immunization with apical membrane antigen 1 confers sterile infection-blocking immunity against Plasmodium sporozoite challenge in a rodent model
- Author
- Alessandro Sette
- Alexander
- Amante
- Anders
- Angela Trieu
- Apte
- Apte
- Armah
- Arnot
- Aurrecoechea
- Bai
- Beeson
- Biswas
- Bogdan
- Brake
- Bruder
- Bruder
- Bueno
- Burns
- Cardoso
- Carlton
- Cech
- Claser
- Coley
- Collins
- Cortes
- Cowman
- Crewther
- Czerkinsky
- Darrah
- Deans
- Denise L. Doolan
- Depinay
- Donnelly
- Doolan
- Doolan
- Doolan
- Douradinha
- Druilhe
- Dunachie
- Flanagan
- Giovannini
- Good
- Gray
- Hamid
- Hoffman
- Huaman
- J. H. Adams
- Jiang
- John Sidney
- Kaveh
- Kocken
- Lal
- Lamarque
- Langhorne
- Liew
- Lyke
- Malkin
- Mitchell
- Mullen
- Narum
- Narum
- Offeddu
- Olivieri
- Perlaza
- Pierce
- Pizarro
- Polhemus
- Randall
- Remarque
- Riglar
- Roederer
- Roestenberg
- Sagara
- Santos
- Schofield
- Sedegah
- Seder
- Silvie
- Simon H. Apte
- Sophie Schussek
- Spring
- Stowers
- Suhrbier
- Tarun
- Thera
- Thomas
- Thomas
- Trieu
- Tyler
- Vita
- Witney
- Xu
- Yu
- Zheng
- Zhou
- Publication venue
- 'American Society for Microbiology'
- Publication date
- 01/10/2013
- Field of study
Apical membrane antigen 1 (AMA-1) is a leading blood-stage malaria vaccine candidate. Consistent with a key role in erythrocytic invasion, AMA-1-specific antibodies have been implicated in AMA-1-induced protective immunity. AMA-1 is also expressed in sporozoites and in mature liver schizonts where it may be a target of protective cell-mediated immunity. Here, we demonstrate for the first time that immunization with AMA-1 can induce sterile infection-blocking immunity against Plasmodium sporozoite challenge in 80% of immunized mice. Significantly higher levels of gamma interferon (IFN-γ)/interleukin-2 (IL-2)/tumor necrosis factor (TNF) multifunctional T cells were noted in immunized mice than in control mice. We also report the first identification of minimal CD8 and CD4 T cell epitopes on Plasmodium yoelii AMA-1. These data establish AMA-1 as a target of both preerythrocytic- and erythrocytic-stage protective immune responses and validate vaccine approaches designed to induce both cellular and humoral immunity
Interaction Pattern of Arg 62 in the A-Pocket of Differentially Disease-Associated HLA-B27 Subtypes Suggests Distinct TCR Binding Modes
- Author
- A Ziegler
- AI Webb
- Alberto Cauli
- Alessandro Mathieu
- B Hess
- B Hess
- C Neumann-Haefelin
- Clive M. Gray
- D Narzi
- D Narzi
- D Rognan
- D Rognan
- DA Brewerton
- Daniele Narzi
- DE Koshland
- DM Gakamsky
- DR Madden
- DR Madden
- E Nurzia
- Elisa Nurzia
- F Paladini
- F Sieker
- F Sieker
- FE Tynan
- Fiorillo
- G Vriend
- GA Kaminski
- GB Stewart-Jones
- H Fabian
- H Rammensee
- HJC Berendsen
- J Sidney
- JA Lopez de Castro
- JB Reiser
- JD Reveille
- JD Wilson
- JM Brooks
- JW Yedwell
- L Kjer-Nielsen
- L Kjer-Nielsen
- L Schlosstein
- M Hulsmeyer
- M Hülsmeyer
- M Karplus
- M Ramos
- M Sathiamurthy
- MA Khan
- Maria Teresa Fiorillo
- MG Rudolph
- MT Fiorillo
- MT Fiorillo
- MT Fiorillo
- MT Fiorillo
- NJ Stam
- O Rotzschke
- OF Lange
- P Bowness
- P Bowness
- P Del Porto
- P Gomez
- Rainer A. Böckmann
- RC Hillig
- Rosa Sorrentino
- S Gonzalez-Roces
- SA Ellis
- Silvana Caristi
- SW Reid
- T Pöhlmann
- TA Darden
- U Omasits
- Valentina Tedeschi
- WF van Gunsteren
- WL Jorgensen
- XC Li
- Publication venue
- Public Library of Science
- Publication date
- 01/01/2012
- Field of study
The single amino acid replacement Asp116His distinguishes the two subtypes HLA-B*2705 and HLA-B*2709 which are, respectively, associated and non-associated with Ankylosing Spondylitis, an autoimmune chronic inflammatory disease. The reason for this differential association is so far poorly understood and might be related to subtype-specific HLA:peptide conformations as well as to subtype/peptide-dependent dynamical properties on the nanoscale. Here, we combine functional experiments with extensive molecular dynamics simulations to investigate the molecular dynamics and function of the conserved Arg62 of the α1-helix for both B27 subtypes in complex with the self-peptides pVIPR (RRKWRRWHL) and TIS (RRLPIFSRL), and the viral peptides pLMP2 (RRRWRRLTV) and NPflu (SRYWAIRTR). Simulations of HLA:peptide systems suggest that peptide-stabilizing interactions of the Arg62 residue observed in crystal structures are metastable for both B27 subtypes under physiological conditions, rendering this arginine solvent-exposed and, probably, a key residue for TCR interaction more than peptide-binding. This view is supported by functional experiments with conservative (R62K) and non-conservative (R62A) B*2705 and B*2709 mutants that showed an overall reduction in their capability to present peptides to CD8+ T cells. Moreover, major subtype-dependent differences in the peptide recognition suggest distinct TCR binding modes for the B*2705 versus the B*2709 subtype
Measurement of the W-boson mass in pp collisions at √s=7 TeV with the ATLAS detector
- Author
- A Salam
- A Sirlin
- A Valassi
- A. A. Affolder
- A. A. Alshehri
- A. A. E. Bannoura
- A. A. Elliot
- A. A. Grillo
- A. A. J. Lesage
- A. A. Komar
- A. A. Korol
- A. A. Maier
- A. A. Minaenko
- A. A. Nepomuceno
- A. A. O’Rourke
- A. A. Snesarev
- A. A. Solodkov
- A. A. Talyshev
- A. Aloisio
- A. Alonso
- A. Amorim
- A. Andreazza
- A. Angerami
- A. Annovi
- A. Antonov
- A. Arbuzov
- A. Artamonov
- A. Ashkenazi
- A. B. Fenyuk
- A. B. Kowalewska
- A. Baroncelli
- A. Basalaev
- A. Bassalat
- A. Beddall
- A. Bellerive
- A. Bethani
- A. Bingul
- A. Blue
- A. Bocci
- A. Borisov
- A. Boveia
- A. Brandt
- A. Bruni
- A. Buzatu
- A. C. Daniells
- A. C. König
- A. C. Martyniuk
- A. C. Schaffer
- A. C. Taylor
- A. Calandri
- A. Camplani
- A. Campoverde
- A. Castelli
- A. Catinaccio
- A. Cattai
- A. Cerri
- A. Cervelli
- A. Chafaq
- A. Chatterjee
- A. Chegwidden
- A. Cheplakov
- A. Chitan
- A. Chr. Dudder
- A. Ciocio
- A. Clark
- A. Coccaro
- A. Cortes-Gonzalez
- A. Cueto
- A. D. Pilkington
- A. Dattagupta
- A. De Benedetti
- A. De Maria
- A. De Salvo
- A. De Santo
- A. Dell’Acqua
- A. Demilly
- A. Dewhurst
- A. Di Ciaccio
- A. Di Girolamo
- A. Di Simone
- A. Dimitrievska
- A. Doria
- A. Dudarev
- A. Durglishvili
- A. E. Baas
- A. E. Barton
- A. E. Dumitriu
- A. E. Kiryunin
- A. E. Lionti
- A. Ereditato
- A. Ezhilov
- A. F. Saavedra
- A. F. Webb
- A. Farbin
- A. Farilla
- A. Favareto
- A. Ferrari
- A. Ferrer
- A. Filipčič
- A. Fischer
- A. Formica
- A. Forti
- A. G. Bogdanchikov
- A. G. Buckley
- A. G. Foster
- A. G. Goussiou
- A. G. Kharlamov
- A. G. Leister
- A. G. Myagkov
- A. Gabrielli
- A. Gabrielli
- A. Gascon Bravo
- A. Gaudiello
- A. Gershon
- A. Glazov
- A. Gomes
- A. Gongadze
- A. Gorišek
- A. Haas
- A. Hadef
- A. Hamilton
- A. Hasib
- A. Held
- A. Hoecker
- A. Hoummada
- A. Hrynevich
- A. I. Etienvre
- A. I. Mincer
- A. J. Armbruster
- A. J. Barr
- A. J. Beddall
- A. J. Bevan
- A. J. Brennan
- A. J. Chuinard
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- A. J. Lankford
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- A. Juste Rozas
- A. K. Ciftci
- A. K. Duncan
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- A. Kaluza
- A. Kamenshchikov
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- A. Katre
- A. Khanov
- A. Khodinov
- A. Klimentov
- A. Knue
- A. Kobayashi
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- A. Kotwal
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- A. Krasznahorkay
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- A. L. Read
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- A. Lehan
- A. Liblong
- A. Limosani
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- A. M. Henriques Correia
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- A. Olariu
- A. Olszewski
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- A. Ouraou
- A. P. Colijn
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- A. Paramonov
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- A. R. Buzykaev
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- A. R. Stradling
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- A. Redelbach
- A. Reiss
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- A. Robichaud-Veronneau
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- A. Rodriguez Perez
- A. Romaniouk
- A. Rozanov
- A. Ruiz-Martinez
- A. Ruschke
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- A. S. Bell
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- A. S. Thompson
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- A. Salzburger
- A. Sanchez Pineda
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- A. Sbrizzi
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- A. Schwartzman
- A. Seiden
- A. Sfyrla
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- A. Vishwakarma
- A. W. J. Pin
- A. Warburton
- A. Washbrook
- A. White
- A. Wildauer
- A. Yamamoto
- A. Zaman
- A. Zemla
- A. Zhemchugov
- A. Zibell
- A. Zoccoli
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- B. Alvarez Gonzalez
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- B. Cole
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- B. D. Schoenrock
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- B. E. Cox
- B. E. Lindquist
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- B. G. Pope
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- B. H. Hooberman
- B. H. Smart
- B. Haney
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- B. J. Gallop
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- B. K. Gjelsten
- B. K. Wosiek
- B. Kaplan
- B. L. Clark
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- B. M. Flierl
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- B. M. Schachtner
- B. M. Waugh
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- B. Malaescu
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- B. Martin dit Latour
- B. Maček
- B. Meirose
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- B. Osculati
- B. P. Kerševan
- B. P. Nachman
- B. Pearson
- B. R. Mellado Garcia
- B. Ristić
- B. S. Acharya
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- B. Tong
- B. Trocmé
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- B. W. Allen
- B. Weinert
- B. Yabsley
- B. Zabinski
- B. Zhou
- C Balazs
- C. A. Chavez Barajas
- C. A. Johnson
- C. A. Lee
- C. A. Solans Sanchez
- C. Agheorghiesei
- C. Alexa
- C. Alpigiani
- C. Amelung
- C. Anastopoulos
- C. Antel
- C. B. Gwilliam
- C. B. Martin
- C. Becot
- C. Bernius
- C. Bertella
- C. Bertsche
- C. Betancourt
- C. Bini
- C. Bittrich
- C. Blocker
- C. Bock
- C. Bohm
- C. Bourdarios
- C. C. Chau
- C. C. Ohm
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- C. Clement
- C. D. Burgard
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- C. Eckardt
- C. Escobar
- C. F. Anders
- C. Farina
- C. Feng
- C. Ferretti
- C. Fischer
- C. Fukunaga
- C. G. Lester
- C. G. Zhu
- C. Gabaldon
- C. Galea
- C. García
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- C. Gay
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- C. Glasman
- C. Grefe
- C. Gumpert
- C. Gutschow
- C. Guyot
- C. Gwenlan
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- C. Haber
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- C. Helsens
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- C. J. E. Suster
- C. J. Potter
- C. J. Riegel
- C. J. S. Young
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- C. Kato
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- C. Lacasta
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- C. Leonidopoulos
- C. Leroy
- C. Li
- C. Luci
- C. Luedtke
- C. M. Buttar
- C. M. Delitzsch
- C. M. Hawkes
- C. M. Macdonald
- C. Maiani
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- C. Malone
- C. Meineck
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- C. Nellist
- C. O. Sander
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- C. P. Bee
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- C. P. Ward
- C. Padilla Aranda
- C. Peng
- C. Petridou
- C. R. Goudet
- C. R. Kilby
- C. Rangel-Smith
- C. Rembser
- C. Rizzi
- C. Roda
- C. S. Pollard
- C. S. Rogan
- C. Sandoval
- C. Santoni
- C. Sawyer
- C. Sbarra
- C. Schiavi
- C. Schillo
- C. Schmitt
- C. Serfon
- C. Stanescu
- C. T. Potter
- C. Troncon
- C. Unverdorben
- C. Valderanis
- C. Varni
- C. Vittori
- C. W. Black
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- C. Wang
- C. Wang
- C. Wanotayaroj
- C. Weiser
- C. Wiglesworth
- C. Willis
- C. Y. Lo
- C. Y. Shehu
- C. Young
- C. Zeitnitz
- C. Zhou
- C. Zimmermann
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- D. A. DeMarco
- D. A. Maximov
- D. A. Milstead
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- D. Barberis
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- D. Bogavac
- D. Bortoletto
- D. Boscherini
- D. Boumediene
- D. Britton
- D. Britzger
- D. Bruncko
- D. Bullock
- D. Büscher
- D. C. O’Neil
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- D. Cavalli
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- D. Costanzo
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- D. Denysiuk
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- D. I. Narrias Villar
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- T. Nooney
- T. Obermann
- T. Okuyama
- T. P. A. Åkesson
- T. P. Calvet
- T. Pauly
- T. R. Holmes
- T. R. V. Billoud
- T. R. Wyatt
- T. Ravenscroft
- T. Saito
- T. Scanlon
- T. Schwindt
- T. Sfiligoj
- T. Slavicek
- T. Sumida
- T. Sykora
- T. T. Tulbure
- T. Takeshita
- T. Tashiro
- T. Theveneaux-Pelzer
- T. Trefzger
- T. Varol
- T. Vazquez Schroeder
- T. Vickey
- T. Wang
- T. Wenaus
- T. Wengler
- T. Y. Ng
- T. Yamanaka
- T. Z. Kowalski
- T. Ženiš
- Th. D. Papadopoulou
- Torbjörn Sjöstrand
- Torbjörn Sjöstrand
- U Baur
- U. Blumenschein
- U. Bratzler
- U. De Sanctis
- U. Gul
- U. Klein
- U. Kruchonak
- U. Landgraf
- U. Mallik
- U. Parzefall
- U. Schnoor
- U. Schäfer
- U. Soldevila
- V. A. Bednyakov
- V. A. Kantserov
- V. A. Kramarenko
- V. A. Mitsou
- V. A. Schegelsky
- V. Andrei
- V. Araujo Ferraz
- V. B. Vinogradov
- V. Boisvert
- V. Bortolotto
- V. Büscher
- V. Canale
- V. Castillo Gimenez
- V. Cavaliere
- V. Cavasinni
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- V. Christodoulou
- V. Cindro
- V. Consorti
- V. Croft
- V. D. Peshekhonov
- V. Dao
- V. E. Ozcan
- V. Ellajosyula
- V. F. Kazanin
- V. Garonne
- V. Gratchev
- V. Hedberg
- V. Herget
- V. I. Martinez Outschoorn
- V. Ippolito
- V. Izzo
- V. J. Martin
- V. Jain
- V. Kartvelishvili
- V. Khovanskiy
- V. Kouskoura
- V. Kukhtin
- V. Kus
- V. Lyubushkin
- V. M. Cairo
- V. Morisbak
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- V. O. Tikhomirov
- V. O’Shea
- V. P. Maleev
- V. Pleskot
- V. Polychronakos
- V. R. Pascuzzi
- V. Radeka
- V. Radescu
- V. Rossetti
- V. S. Bobrovnikov
- V. S. Lang
- V. S. Martoiu
- V. Sanchez Martinez
- V. Scarfone
- V. Scharf
- V. Simak
- V. Smakhtin
- V. Solovyev
- V. Sorin
- V. Tsiskaridze
- V. Tsulaia
- V. Tudorache
- V. V. Kostyukhin
- V. V. Sulin
- V. Vacek
- V. Veeraraghavan
- V. Vercesi
- V. Vorobel
- V. Vrba
- V. Wallangen
- W-M. Yao
- W. A. Cribbs
- W. A. Leight
- W. B. Quayle
- W. Blum
- W. Buttinger
- W. C. Fisher
- W. D. Breaden Madden
- W. Dabrowski
- W. Davey
- W. F. Mader
- W. Fedorko
- W. Guan
- W. Guo
- W. H. Hopkins
- W. J. Dearnaley
- W. J. Fawcett
- W. J. Johnson
- W. J. Murray
- W. K. Balunas
- W. K. Brooks
- W. K. Di Clemente
- W. Kozanecki
- W. Lampl
- W. Lavrijsen
- W. Liebig
- W. Lukas
- W. Płaczek
- W. S. Chan
- W. Taylor
- W. Trischuk
- W. Van Den Wollenberg
- W. Vandelli
- W. Verkerke
- W. Wagner
- W. Walkowiak
- W. Wang
- W. Wang
- W. Wiedenmann
- X. Chen
- X. Hoad
- X. Ju
- X. Lei
- X. Li
- X. Lou
- X. Ruan
- X. Sun
- X. T. Meng
- X. Wu
- X. Zhang
- X. Zhao
- X. Zhuang
- Y. A. Kurochkin
- Y. Abulaiti
- Y. Amaral Coutinho
- Y. Arai
- Y. Benhammou
- Y. C. Yap
- Y. Chen
- Y. Cheng
- Y. Coadou
- Y. Du
- Y. Enari
- Y. F. Ryabov
- Y. Fang
- Y. Gao
- Y. Guo
- Y. H. Chiu
- Y. Hasegawa
- Y. Heng
- Y. Hernández Jiménez
- Y. Horii
- Y. Huang
- Y. Ikegami
- Y. Ilchenko
- Y. J. Lu
- Y. Jiang
- Y. K. Kim
- Y. Kataoka
- Y. Komori
- Y. Kulchitsky
- Y. L. Chan
- Y. L. Liu
- Y. Li
- Y. Liu
- Y. Ma
- Y. Makida
- Y. Minami
- Y. Minegishi
- Y. Ming
- Y. Nagasaka
- Y. Nakahama
- Y. Ninomiya
- Y. Noguchi
- Y. Okumura
- Y. Oren
- Y. P. Kulinich
- Y. Qin
- Y. Rodina
- Y. Rozen
- Y. S. Gao
- Y. Sakurai
- Y. Shen
- Y. Smirnov
- Y. Sugaya
- Y. Takubo
- Y. Tayalati
- Y. Tu
- Y. Unno
- Y. Wu
- Y. Yamaguchi
- Y. Yamazaki
- Y. Yang
- Y. Yasu
- Y. Zhang
- Y. Zhao
- Y. Zhu
- Yu. A. Tikhonov
- Z. Barnovska-Blenessy
- Z. D. Greenwood
- Z. Dolezal
- Z. H. Citron
- Z. Hubacek
- Z. J. Grout
- Z. Jiang
- Z. Liang
- Z. M. Karpova
- Z. Marshall
- Z. Rurikova
- Z. Xi
- Z. Yan
- Z. Yang
- Z. Zhang
- Z. Zhao
- Z. Zinonos
- Publication venue
- 'Springer Science and Business Media LLC'
- Publication date
- 18/12/2017
- Field of study
A measurement of the mass of the W boson is presented based on proton–proton collision data recorded in 2011 at a centre-of-mass energy of 7 TeV with the ATLAS detector at the LHC, and corresponding to 4.6 fb−1 of integrated luminosity. The selected data sample consists of 7.8×106 candidates in the W→μν channel and 5.9×106 candidates in the W→eν channel. The W-boson mass is obtained from template fits to the reconstructed distributions of the charged lepton transverse momentum and of the W boson transverse mass in the electron and muon decay channels, yielding
mW=80370±7 (stat.)±11(exp. syst.)
±14(mod. syst.) MeV
=80370±19MeV,
where the first uncertainty is statistical, the second corresponds to the experimental systematic uncertainty, and the third to the physics-modelling systematic uncertainty. A measurement of the mass difference between the W+ and W−bosons yields mW+−mW−=−29±28 MeV
Genome-wide association study identifies six new loci influencing pulse pressure and mean arterial pressure.
- Author
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- Abecasis GR
- Abecasis Goncalo R.
- Absher D
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- Aherrahrou Z
- Ahmadi KR
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- Alizadeh Behrooz Z.
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- Wichmann HE
- Wichmann HE
- Wichmann HE
- Wichmann HE
- Wichmann H-Erich
- Wild P
- Wild PS
- Wild PS
- Wild SH
- Wild Sarah H.
- Wilde S
- Wilensky R
- Wilkinson IB
- Willemsen Gonneke
- Willenborg C
- Willerson JT
- Wilson JF
- Wilson James F.
- Winkelmann BR
- Winkler K
- Witteman JC
- Witteman JC
- Witteman JC
- Witteman JC
- Witteman Jacqueline C. M.
- Wright AF
- Wright BJ
- Wright Alan F.
- Yang Q
- Yang YA
- Yasmin
- Zaboli G
- Zeginigg Marion
- Zeller T
- Zeller T
- Zeller T
- Zemunik T
- Zerres K
- Zgaga L
- Zhang W
- Zhang Feng
- Zhang Weihua
- Zhao Jing Hua
- Ziegler A
- Ziegler A
- Ziegler A
- Ziegler A
- Ziegler A
- Ziegler A
- Zillikens MC
- Zitting Paavo
- Zweiker R
- Publication venue
- Nat Genet
- Publication date
- 01/01/2011
- Field of study
Numerous genetic loci have been associated with systolic blood pressure (SBP) and diastolic blood pressure (DBP) in Europeans. We now report genome-wide association studies of pulse pressure (PP) and mean arterial pressure (MAP). In discovery (N = 74,064) and follow-up studies (N = 48,607), we identified at genome-wide significance (P = 2.7 × 10(-8) to P = 2.3 × 10(-13)) four new PP loci (at 4q12 near CHIC2, 7q22.3 near PIK3CG, 8q24.12 in NOV and 11q24.3 near ADAMTS8), two new MAP loci (3p21.31 in MAP4 and 10q25.3 near ADRB1) and one locus associated with both of these traits (2q24.3 near FIGN) that has also recently been associated with SBP in east Asians. For three of the new PP loci, the estimated effect for SBP was opposite of that for DBP, in contrast to the majority of common SBP- and DBP-associated variants, which show concordant effects on both traits. These findings suggest new genetic pathways underlying blood pressure variation, some of which may differentially influence SBP and DBP
Participação nos lucros/resultados e criação de valor: um estudo exploratório
- Author
- ALLEN Everett T. Jr
- ARTHUR ANDERSEN.
- BASSO Leonardo F.C.
- BECKER Grace V.
- BELCHER Jr John G
- BERGER Lance A.
- BERGMAN Thomas J.
- BLACK Andrew
- DE LUCCA Márcia Martins Mendes
- DORNBUSCH R.
- EHRBAR Al.
- EIRANOVA Miguel D
- FRIEDLOB George T.
- GARRIDO Laercio M
- GOMES-MEJIA Luiz R.
- GONÇALVES Renato.
- GRAHAM-MOORE Brian
- GRAY Sidney
- GRAY Sidney J.
- HATTIANGADI Anita U
- ITTNER Christopher D.
- JOÃO Paulo S
- KANUNGO Rabindra N.
- KASSAI José Roberto
- KERLINGER Fred.
- KÖCHE José Carlos
- MARTIN John D.
- MARTINS Sergio S.
- MARTOCCHIO Joseph J
- MASTERNAK Robert.
- METZGER Bert L.
- MILKOVICH George T.
- NASCIMENTO A. M
- OLIVEIRA Silvio Luiz de
- PETERSON Pamela P.
- RAPPAPORT Alfred.
- RAY Russ
- ROSA Fernanda
- SANTOS Antonio Raimundo
- SCHUSTER Jay R.
- SHARPE William F
- SIMONSEN Mario Henrique
- STEWART G. Bennett III
- THOR Carl G.
- XAVIER Paulo R.
- YOUNG David S.
- ÁLVARES Antonio C T.
- Publication venue
- 'FapUNIFESP (SciELO)'
- Publication date
- Field of study
Large expert-curated database for benchmarking document similarity detection in biomedical literature search
- Author
- Aanei Carmen M.
- Abid Muhammad B.
- Abramowitz Matthew K.
- Abu-Zaid Ahmed
- Adamo Vincenzo
- Adeyemo Adebolajo A.
- Afnan Masoud
- Agarabi Cyrus
- Aggelidou Maria
- Ahmad Haroon
- Ahmad Rafi
- Aizat Wan M.
- Ajani Penelope A.
- Akinwumi Sayo A.
- Al-Farha Abd A.
- Al-Lawama Manar
- Al-Owaifeer Adi M.
- Al-Riyami Arwa Z.
- Alanio Alexandre
- Alaux Cedric
- Albery Gregory F.
- Albiol Joan
- Albrecht Dirk R.
- Albuquerque Lucia G.
- Alhowimel Ahmed
- Ali Junaid
- Alimba C.G.
- Allardyce Judith
- Almeida Gabriel M.F.
- Alonso-Caneiro David
- Alper Ozgul M.
- Alshehri Mansour
- Alsuhaibani Mohammed
- Alzghari Saeed K.
- Amer Said E.D.R.
- Amir Shimon
- Amiya Eisuke
- Ammerman Brooke A.
- Amorim Rogerio M.
- An Qianli
- Anazodo Udunna C.
- Andersen Stig U.
- Andersen Vibeke
- Angus Kathryn
- Anikin Andrey
- Aplin John D.
- Argyropoulos Christos
- Armitage Charles
- Asaduzzaman Muhammad
- Asady Hadi
- Ascher David B.
- Ashry Mohamed
- Asmann Yan W.
- Assaeed Abdulaziz M.
- Atack John M.
- Atanasov Atanas G.
- Atchison David A.
- Atkins Gerald J.
- Atlas Lauren
- Ato Dai
- Avery Simon V.
- Avillach Paul
- Azubuike Samuel O.
- Baade Peter D.
- Bach-Mortensen Anders
- Backman Lars
- Badie Christophe
- Bae Taeok
- Bagloee Saeed Asadi
- Bai Xiaoyong
- Baier Dirk
- Bail Kasia
- Baines Rebecca L.
- Baker Chris I.
- Bakkach Joaira
- Baldi Alfonso
- Ball Elizabeth
- Ballantyne Maghan
- Baltiansky Lior
- Ban Bo
- Bannon Ross
- Bansal Abhisheka
- Bar Ido
- Bardot Olivier
- Barnett Adrian G.
- Barraud Pierre
- Bartas Martin
- Basharat Zarrin
- Basner Mathias
- Bathelt Joe
- Batra Jyotsna
- Baumert Philipp
- Bazanova O.M.
- Beale Andrew
- Beck Charles R.
- Beck Jill
- Becker Daniel
- Beddoe Travis
- Belachew Kiflemariam Y.
- Bell Melanie L.
- Ben-Nafa Walid
- Benezeth Yannick
- Bengtsson-Palme Johan
- Benkeser David
- Berbesque Colette
- Berezikov Eugene
- Bergsland Niels
- Berners-Price Sue
- Bernhardt Peter
- Bernier Meghan L.
- Berrevoet Frederik
- Berry Edward
- Berthold Maximilian
- Bessa Theolis B.
- Beyene Tariku J.
- Bhardwaj Vivek
- Biedermann Peter H.W.
- Bijleveld Erik
- Billington Craig
- Binder Karin
- Birch John
- Bittner Florian
- Bitzer Michael
- Black Emma
- Blakely Randy D.
- Blanchard Adam M.
- Blancher Antoine
- Blanck Oliver
- Bland Nicholas S.
- Blankstein Ron
- Blaskovich Mark A.T.
- Bleackley Mark
- Blombach Fabian
- Blum Robert
- Boah Michael
- Boakye Dominic W.
- Bodagh Neil
- Boehme Karen A.
- Boelaert Marleen
- Bogdanos Dimitrios
- Bonatsos Vasileios
- Bonvin A.M.J.J.
- Boon Michele H.
- Borges Paulo
- Bosch Carles
- Bosch Oliver
- Bouboulis George
- Boudreau Shellie A.
- Bourgoin Thierry
- Bourke Emer
- Bouvard Daniel
- Boykin Laura M.
- Br\ufchl Albert
- Bradley Graeme
- Bradshaw William
- Bramoweth Adam D.
- Brand Thomas
- Braubach Oliver
- Braun Daniel
- Braun R. J.
- Brenneisen Peter
- Bridges Kristina M.
- Bromfield Elizabeth
- Brooks Anastasia
- Brown James A.L.
- Brown Joshua
- Brown Peter
- Browngardt Christopher
- Brownlie Jeremy
- Brox-Ponce Josue
- Brunetti Arturo
- Bukowy-Bieryllo Zuzanna
- Bul Kim C.M.
- Bull James A.
- Bullen Benjamin
- Burt Austin
- Burton Kathryn J.
- Bush Stephen J.
- Butkowski Eugene G.
- Butler Lisa M.
- Byrareddy Siddappa N.
- Byrne Hugh J.
- Cabantous Stephanie
- Cai Yufeng
- Calabr\uf2 Giovanna E.
- Calatayud Sara
- Callahan Tiffany J.
- Campana Luca G.
- Campbell Matthew
- Candal Eva
- Canham Colin D.
- Cao Bing
- Cao Zanxia
- Cao Zehong
- Cardoso Pedro
- Carlson Kimberly
- Carninci Piero
- Carroll Grace
- Carter Dee
- Carvajal Richard
- Cascella Marco
- Casillas S\uf2nia
- Castelvetro Valter
- Caswell Patrick T.
- Catry Thibault
- Cavalli Giacomo
- Cernava Tomislav
- Cerovsky Vaclav
- Ch\ue1vez-Fumagalli Miguel A.
- Chacko George
- Chagoyen Monica
- Chakraborty Sayan
- Chalmers Kelsey
- Chan Sherwin S.
- Chandrasekaran Arun R.
- Chang Shun C.
- Chang Wei
- Chao Fengqing
- Chao Jie
- Charrier Elisabeth E.
- Chatterjee Pranab
- Chatzitheochari Stella
- Che Zhengping
- Chen Andrew T.Y.
- Chen Branson
- Chen Chang-Er
- Chen Chang-Shi
- Chen Dong F.
- Chen Haimin
- Chen Hao
- Chen He
- Chen Huaming
- Chen Hui
- Chen Jui-Tung
- Chen Liming
- Chen Xiaoyin
- Chen Xin
- Chen Yi-Chun
- Chen Yinglong
- Chen Youning
- Chen Yu-Chih
- Chen Zhao
- Cheng Changxiu
- Cheng Jianlin
- Cheng Shuiqin
- Chenguang [NO FIRST NAME IN SCOPUS]
- Cheung Johnny T.K.
- Chhatriwalla Adnan K.
- Chikowe Ibrahim
- Chinapaw Mai
- Chinopoulos Christos
- Cho William C.S.
- Choi Jane R.
- Choi Youngrok
- Chong Lillian
- Chowdhury Debashish
- Chowdhury Mohiuddin A.K.
- Christensen Martin R.
- Christoffersen Tore
- Chuang Trees-Juen
- Chung Hee-Jung
- Chwalibog Andre
- Ciresi A.
- Cobine Paul A.
- Cockcroft Shamshad
- Coelho Luis P.
- Colella Vito
- Collevatti Rosane G.
- Comel Jo\ue3o C.
- Conesa Ana
- Conway Aaron
- Cook Penny A.
- Cooke Robert S.C.
- Cooper David N.
- Cooper Jeffrey
- Coqueret Olivier
- Corea Enoka M.
- Cornejo Diego A.V.
- Cosacak Mehmet I.
- Cosse Cyril
- Costa Antonio
- Costa Bruno M.
- Costa Elisio
- Costa Vincent D.
- Cottini Marzia
- Coupland Carol
- Covington Natalie V.
- Crawford Stephanie Y.
- Cruz Aparecido D.
- Cu\uedv P\ue1raic O.
- Cuenda Ana
- Cui Huijuan
- Cui Qiang
- Cui Yanru
- Culver David C.
- Cunningham Catriona
- Cuypers Maarten
- Cyr Normand
- D\u27Angiulli Amedeo
- Dahms Tanya E.S.
- Dai Zhanwu
- Daigle France
- Dalgleish Raymond
- Dalrymple Brian P.
- Danchin Antoine
- Danielsen H\ue5vard E.
- Dao Myriam
- Darras S\ue9bastien
- Dauga Delphine
- Daulatabad Swapna V.
- Davidson Sean M.
- Day David A.
- de Keersmaecker Kim
- de Leeuw Frank-Erik
- de Maio Nicola
- Dean Lorraine T.
- Debrabant Birgit
- Degirmenci Volkan
- Del Tredici Andria L.
- Delahay Robin M.
- Delarocque Julien
- Demaison Luc
- Deng Zaian
- Denzel Martin S.
- Deschodt Mieke
- Devkota Hari P.
- Devkota Kiran
- Devos Lucie
- Devriendt Koenraad
- Dhar Aurup R.
- Dhariwal Raman
- Dhaval [NO FIRST NAME IN SCOPUS]
- Diao Jiajie
- Ding Jiandong
- Ding Ke-Feng
- Dings Ruud P.M.
- Diodato Daria
- Diouf Barthelemy
- Dixon Ray
- Dlamini S.V.
- Doan Lisa V.
- Dogan Yunus
- Domingues Helena S.
- Dong Kexian
- Dong X.C.
- Dong Zheng
- Donner Claudio F.
- Dono Marcos
- Doxey Andrew C.
- Dressick Walter
- Drevon Christian A.
- Dreyer Niklas
- Duan Huiling
- Ducho Christian
- Ducommun Bernard
- Dudley Kevin J.
- Duffey Maelle
- Dufies Maeva
- Duijf Pascal H.G.
- Dumaz Nicolas
- Dutt Avik
- Dwarakanath Bilikere S.
- Ebell Mark H.
- Echeverr\ueda Natalia
- Ecke Thorsten
- Eckweiler Denitsa
- Eerola Tuomas
- Effiong Andem
- Egea Luis G.
- Ehret Felix
- Eisenhardt Steffen
- Eixarch Elisenda
- Ekstrand Chelsea
- El-Adawy Hosny
- El-Esawi Mohamed A.
- El-Said Mohammed
- Elewa Yaser H.A.
- Elkum Naser
- Emmrich Julius V.
- Engel Michael S.
- Engel Nadja
- Epp Trevor
- Erickson Timothy B.
- Esfahlani Shabnam S.
- Eskelinen Eeva-Liisa
- Eskew Evan A.
- Esnakula Ashwini K.
- Eustace Alex J.
- Evangelou Evangelos
- Fairhead Michael
- Falk Sebastian
- Fallah Mazyar
- Falter-Wagner Christine M.
- Fan Dongsheng
- Fan Xiao
- Farber Debora B.
- Fardet Tanguy
- Farhoudi Ramin
- Faruk Mohammed
- Faville Marty J.
- Faye Martin
- Feghali Karine A.
- Feifei Shi
- Fejzo Marlena S.
- Feleke Berhanu E.
- Ferguson Trevor S.
- Fernandez-Fernandez Beatriz
- Fernandez-Triana Jose
- Festa Fernanda
- Feteira Antonio
- Feurer Thomas
- Feyerabend Frank
- Fierz Walter
- Filipp Fabian
- Flegel Willy A.
- Fleres Francesco
- Flood-Page Patrick
- Florio Tullio
- Foley Kieran G.
- Forano Evelyne
- Forsayeth John
- Foster Emma J.
- Foster Stephen
- Founou Luria L.
- Fox Simon A.
- Franks Steven J.
- Freitas Angela
- Frentiu Francesca D.
- Friebe Michael
- Frilander Mikko J.
- Fu Fan
- Fu Xinmiao
- Fujita Satoshi
- Furer Tzvi
- Furuta Saori
- Fuss Johannes
- Gabrielsen Mads
- Gadelkareem Rabea A.
- Gajda Maksymilian
- Galea Ian
- Galimov Evgeny
- Galluzzi Luca
- Gani Federica
- Ganpule Arvind P.
- Gao Jianzhao
- Gao Tian
- Gao Yibo
- Garc\ueda-Alix Antonio
- Garcia-Rivera Enid J.
- Garip Gulcan
- Gatchell Michael
- Gaullier Guillaume
- Gazdar Adi
- Gebremedhin [NO FIRST NAME IN SCOPUS]
- Gedye Kristene
- Gelfer Yael
- Gemmill Alison
- George Ronald B.
- Ghelardi Emilia
- Ghosh Sayantan
- Gianchecchi Elena
- Giganti Francesco
- Gill Martin R.
- Gilliham Matthew
- Giordano Maurizio
- Giunta Cecilia
- Gladue Douglas P.
- Gleason Joshua M.
- Gleeson Paul A.
- Gloyn Liz
- Gnasso Agostino
- Goarant Cyrille
- Gobet Ang\ue9lique
- Goggs Robert
- Gong Haipeng
- Gonz\ue1lezlez-Prendes Rayner
- Goodin Amie
- Goodyear Carl S.
- Gora Diop
- Gough Michael J.
- Gouil Quentin
- Govender Pragashnie
- Govinden Usha
- Goyal Ravinder
- Gr\ue9bert Th\ue9ophile
- Gr\ufcneberg Patrick
- Grabowski Piotr
- Graham Emily B.
- Graham Kathryn E.
- Grande-P\ue9rez Ana
- Graves Patricia M.
- Greene Garrett
- Greenwald Noah F.
- Greidanus Harm
- Greiff Victor
- Grey James
- Grice Darren
- Gridneva Zoya
- Grimm Dominik G.
- Groen Ewout J.N.
- Grothe Michel J.
- Gruber Jens
- Grunau Christoph
- Grundle D.S.
- Grybos Malgorzata
- Guerra-Mora Jos\ue9 R.
- Guerrero Fabricio
- Guignard L\ue9o
- Guisado J.L.
- Gumede Nicksy
- Gumulya Yosephine
- Guo Chengying
- Guo Xinyi
- Guo Yabin
- Gupta Himanshu
- Gurevich Vsevolod V.
- Gurney-Champion Oliver J.
- Gusev Oleg
- Guti\ue9rrez-Sacrist\ue1n Alba
- H\ufcttner Felix J.
- Habes Mohamad
- Hacker Elke
- Hackshaw Allan
- Haenssgen Marco J.
- Hage Steffen R.
- Hagen Guy
- Hahn Steven
- Hall Adam
- Hall Richard
- Haller Dagmar M.
- Hammerschmidt Sven
- Han Hyemin
- Han Jianwei
- Han Qian
- Han Renzhi
- Handfield Martin
- Hanson Jack
- Haore Gbaguidi
- Hapuarachchi Hapuarachchige C.
- Harder Timm
- Hardingham Jennifer E.
- Harper Paul
- Harrison Pille
- Hartmann Marcus D.
- Harvey David J.
- Hasler David
- Haston Scott
- He Shuonan
- Heck Michelle
- Heers Marcel
- Heffler Enrico
- Heijne Marloes
- Heinemann Stephanie
- Heinrich Michael
- Helanter\ue4 Heikki
- Herbelet Sandrine
- Hew Khe F.
- Higginbottom Daniel B.
- Higuchi Yohei
- Hilaire Cynthia St.
- Hilton Rachel
- Hiroi Noboru
- Hobbs Emma
- Hodzic Enisa
- Hoenner Xavier
- Hogg William E.
- Hogrebe Alexander
- Hojsgaard Diego
- Holgate Joan Y.
- Hone Andrew
- Hongoh Yuichi
- Honjo Ken
- Horbar Jeffrey
- Hori Hikaru
- Hu Guoku
- Hu Pingzhao
- Huang Ancheng
- Huang Guangqun
- Huang Zhengping
- Huber Heinz P.
- Huber Michael
- Hueso Luis E.
- Huirne Judith
- Hulse-Kemp Amanda M.
- Hunter Kylie E.
- Hurt Lisa
- Idborg Helena
- Ide Kazuki
- Ijzerman Adriaan P.
- Ikeo Kazuho
- Ikonomopoulou Maria P.
- Ingley Evan
- Iskander-Rizk Sophinese
- Iyer Lavanya M.
- J\ue9gousse Clara
- Jahan Yasmin
- Jakeman Philip M.
- James Ameh S.
- Janga Sarath C.
- Janzen Thijs
- Jayaraman Jayakumar
- Jean-Quartier Claire
- Jeltsch Albert
- Jensen Arne
- Jeon Sang-Min
- Jesus Carlos
- Jeurissen Patrick
- Jia Hong
- Jia Husen
- Jia Shuqin
- Jia Yangyang
- Jian Gao
- Jiang Fan
- Jiang Jianping
- Jiang Xingyu
- Jibb Lindsay A.
- Jin Yi
- Jo Daehyun
- Joel Emmanuel
- Joffroy Bastian
- Johnson Andrew M.
- Johnson Daniel M.
- Johnston Marie
- Jongen Stefan
- Jonscher Karen R.
- Jorens Philippe G.
- Jorgensen Jens O.L.
- Josse Claire
- Joubert Johan W.
- Jung Sin-Ho
- Junior Antonio M.
- Jurman Giuseppe
- Jutzeler Catherine
- Kabra Dhiraj
- Kahan Thomas
- Kaiser Stefan
- Kalatzis Panagiotis
- Kamagata Koji
- Kamboj Sunjeev K.
- Kambondo George
- Kamiya Haruyuki
- Kane Nolan C.
- Kang Yong-Kook
- Kanj Souha S.
- Karamanos Yannis
- Karim Masud
- Karmakar Chandan
- Karnati Priyanka
- Karp Natasha A.
- Karsay Kathrin
- Kasian Olga
- Kauppila Joonas H.
- Kaur Harsheen
- Kaya Cihan
- Kaye Linda K.
- Ke An
- Keitel Anne
- Kelly Daniel
- Kelly Ryan
- Kelly Sarah
- Kelly Shona
- Kempe Andreas
- Kenna Ralph
- Kennedy Jonathan
- Keown Jeremy R.
- Kersten Birgit
- Khalaf Roy A.
- Khalid Javaria M.
- Khan Murad M.
- Khatlani T.
- Kheir Fayez
- Khider Tarig
- Khoo Chin M.
- Khwaja Nyil
- Kichatova V.S.
- Kickert Rob
- Kidibule Peter E.
- Kieselmann Jennifer P.
- Kievit Rogier A.
- Kijanka Gregor S.
- Kim Hyeon J.
- Kim Yong-Min
- King Sarah R.B.
- Kinyanjui Timothy
- Kiraǧ N\ufckhet
- Kish J.K.
- Kitazawa Takeshi
- Kiyani Musa
- Klein Reinhild
- Klempnauer Karl-Heinz
- Kleppe Andreas
- Klump Hannes
- Kluz Tomasz
- Knox Paul
- Kobayashi Tatsuya
- Kobold Sebastian
- Koch Karl-Wilhelm
- Kohanbash Gary
- Kohls Gregor
- Kohonen-Corish Maija R.J.
- Koleva-Kolarova Rositsa G.
- Kong Xiangpeng
- Konkle-Parker Deborah
- Korpela Kalevi M.
- Kosanic Sasha
- Kostrikis Leondios G.
- Koutoukidis Dimitrios A.
- Kovesi Tom
- Kraiczy Peter
- Kramer Paul
- Kraschnewski Jennifer L.
- Kratz Harald
- Krause G\ufcnter
- Krebsbach Paul H.
- Kristensen S\uf8ren R.
- Kristiansson Erik
- Kueberuwa Gray
- Kugler Jan-Michael
- Kulkarni Ameya
- Kumar Addanki P.
- Kumar Dilip
- Kumar Gyanendra
- Kumar Narendra
- Kumar Nitin
- Kumari Prerna
- Kunimatsu Akira
- Kurdak Hatice
- Kurgan Lukasz
- Kurniawan Nicholas A.
- Kwon Young D.
- Labutin Dmitry
- Lachat Carl
- Lacy-Colson Jon
- Lagisz Malgorzata
- Lai Hei M.
- Laky Brenda
- Lalaouna David
- Lamberts Aniek
- Lammerding Jan
- Lange Matthias
- Lanza Giuseppe
- Larrosa Mar
- Laslett Andrew L.
- Latif Asam
- Lau Colleen L.
- Lauschke Volker M.
- Laverman Gozewijn D.
- Lazo-Langner Alejandro
- Le Thuc D.
- Leclair Elizabeth E.
- Leclercq Guy
- Lee Kyung-Woo
- Lee Ming-Yih
- Lee Moon-Soo
- Lee Senhong
- Leem Jung W.
- Leightley Daniel
- Leite Andreia
- Lercher Lukas
- Lewis James S.
- Li Bingling
- Li Genyuan
- Li Jian
- Li Jiansheng
- Li Jiuyong
- Li Maoteng
- Li Qingchun
- Li Tangliang
- Li Ying
- Li Yongzhe
- Li You
- Li Zhixiu
- Liang Dai
- Liang Huakang
- Liang Shide
- Liao Wei-Ting
- Liao Zheng-Yin
- Lidbury Brett A.
- Lieb Klaus
- Liehr Thomas
- Liew Alan W.C.
- Lim Chinten J.
- Lim Renly
- Lim Yau Y.
- Lima Luiz R.A.
- Lin Jessica
- Lin Li
- Lin Michael Z.
- Lindsey Merry L.
- Line Paul-Dag
- Ling Tong
- Linn Sabrina N.
- Litfin Thomas
- Liu Dengcai
- Liu Enwu
- Liu Fang
- Liu Fengbin
- Liu Haiyan
- Liu Hongde
- Liu Siqi
- Liu Xiaodong
- Liu Yu-Peng
- Liu Yuchen
- Liu Zhonghua
- Liusuo Wang
- Lizer J.
- Lloyd Vett K.
- Lo Te-Wen
- Lobreglio Giambattista
- Locci Emanuela
- Loft Nikolai D.
- Loidl Josef
- Lopez-Escamez Jose A.
- Lopez-Ruiz Francisco J.
- Lorenzen Johan
- Lorkowski Stefan
- Lovell Nigel H.
- Lowies Cher
- Lu Cheng
- Lu Hua
- Lu Jin-Jian
- Lu Qiang
- Lu Wei
- Lu Yao
- Lu Zhiyong
- Luengo Gustavo S.
- Lum Fok M.
- Lund Bjarte A.
- Lundh Lars-Gunnar
- Luo Hang
- Lussier Alexandre A.
- Luu Andreas M.
- Lygirou Vasiliki
- Lynch Iseult
- Lysy Philippe A.
- Lyu Ran
- Ma Chuang
- Ma Lan
- Ma Liping
- Ma Lisong
- Ma Ruiyan
- Ma Wujun
- Mabb Angela
- Machhi Jatin
- Mack Heather G.
- Mackey David A.
- Macleod Angus
- Macwan Isaac
- Madala Hanumantha R.
- Madani Nima
- Mahato Ajay K.
- Mahavadi Poornima
- Mahdavi S.R.
- Maher Pamela
- Maher Toby
- Mai Zhi-Ming
- Maibach Edward W.
- Maity Sankar N.
- Majeed Haroon
- Major Rupert W.
- Makowiecki Kalina
- Malgrange Brigitte
- Mali Samira
- Mallinson Daniel J.
- Mallis Panagiotis
- Mamoulakis Charalampos
- Mangoni Arduino A.
- Manke Thomas
- Manstead Antony S.R.
- Mantalaris Athanasios
- Mao Wenzhi
- Marchbank Kevin J.
- Margelyte Ruta
- Maria Caracausi
- Marinello Francesco
- Markonis Y.
- Marsal Jan
- Marschalek Rolf
- Marschall H. U.
- Marsili Luca
- Mart\uedn Carmen S.
- Martin Adam
- Martin Francis L.
- Martinez-Raga Jose
- Martinez-Salas Encarnacion
- Martinez-Sobrido Luis
- Martis Elvis
- Marvin-Dowle Katie
- Marzocchi Ugo
- Mason Leanda D.
- Mather Diane E.
- Mathieu Daniel
- Matsui Yoichi
- Mavoa Suzanne
- Maza Elie
- McCrum Christopher
- McCutcheon James E.
- McGarrigle Christine A.
- McKay Gareth J.
- McMillan Brian
- McMillan Nigel
- McWilliams Lorna
- Meads Catherine
- Medina Loreta
- Megersa Moa
- Mendes Caetano S.M.
- Menichetti Julia
- Mercieca-Bebber Rebecca
- Meresh Edwin
- Merideth Ben
- Merino-Plaza Maria J.
- Merlaen Britt
- Merrick B. Alex
- Meseko Clement
- Messina Rossella
- Metzger Dennis W.
- Meule Adrian
- Meunier Frederic A.
- Michaelis Martin
- Micheau Olivier
- Middelveen Marianne
- Miele Adriana E.
- Mier Pablo
- Mihara Hisaaki
- Miller Jack J.
- Min Rogier
- Minde David-Paul M.
- Minges Alexander
- Mintz Eric M.
- Miotla Pawel
- Mishra Anand K.
- Mishra Eleanor
- Mishra Virendra R.
- Mitchell Kate M.
- Mizukami Takuo
- Moal Iain
- Moalic Yann
- Mohapatra D.P.
- Mohebbi Alireza
- Molari Massimiliano
- Molleman Lucas
- Mondal Saiful R.
- Montagutelli Xavier
- Monteiro Antonia
- Montes Matthieu
- Moore Matthew D.
- Moores Carly
- Moran John V.
- Morcillo Esteban
- Morozov Sergey Y.
- Morrice Nicola
- Mort Matthew
- Moskalensky Alexander E.
- Moss W.N.
- Mota Jorge
- Moultos Othonas A.
- Moyer Robert
- Mozaheb Zahra
- Muhammad Junaid
- Mukherjee Maheswari
- Murai Noriyuki
- Murphy Denis J.
- Murphy Susan K.
- Murray Shauna A.
- Musinguzi Conrad
- Muth Thilo
- Muyaya Ley
- Naganawa Shinji
- Nagler Katja
- Nakayama Kazuhiko
- Nammi Srinivas
- Nandakumar Kutty S.
- Nandhakumar Amar
- Nanou Afroditi
- Naqash Amreen
- Narayan Edward
- Nasios Grigorios
- Natoli Roman M.
- Navaratnarajah [NO FIRST NAME IN SCOPUS]
- Navarin Nicol\uf2
- Negera Edessa
- Neumann Philipp-Alexander
- Ng Grace
- Ng Sheryl H.X.
- Nguyen Frederique
- Nguyen Joe T.
- Nguyen Thi T.H.
- Ni Duan
- Nicol Christine
- Nicoletti Rosario
- Nida [NO FIRST NAME IN SCOPUS]
- Nie Jiyun
- Nie Yingjiu
- Niehof Monika
- Niemeyer Frank
- Nilsen Erlend B.
- Nilsson Henrik
- Nixon Brett
- Nobile Clarissa J.
- Nolan Fiona
- Nolet Philippe
- Nord\ue9n Rickard
- Nordberg Ana
- Norris Adam D.
- Notcovich Shirli
- Nowicki Jessica P.
- Nwaiwu Ogueri
- O\u27Mahony Margaret
- O\u27Toole Ronan
- Obeidat Monther
- Ogami Koichi
- Oh Deog-Hwan
- Ohgami Robert S.
- Ohlsson Sophie
- Ohst Barnabas
- Ohtomo Toshihiko
- Olatunbosun Oluremi
- Oldenmenger Wendy H.
- Ollivier Quinn R.
- Olofsson Per
- Olova Nelly
- Olszewski Pawel
- Olumayede Emmanuel
- Onzima Robert
- Orme Mark W.
- Ortiz Alberto
- Osses Dani\uebl F.
- Oster Henrik
- Ostrikov Kostya
- Otto Siegmar
- Ou Jianhong
- Outeiro Tiago F.
- Ouyang Songying
- Owais Mohammed
- Pace-Asciak Pia
- Paganoni Sabrina
- Page Andrew
- Pallebage-Gamarallage Menuka
- Palm Christoph
- Palma Jose-Alberto
- Pan Chih-Long
- Pan Zihang
- Panthee Suresh
- Panwar Ajay
- Paradies Yin
- Parchi Piero
- Park Caroline
- Park Charny
- Park Dong I.
- Park Seyoung
- Parsons Jerod R.
- Parsons Michael H.
- Parsons Nick
- Pascal Pigny
- Paterson Russell
- Patil Chandrashekhar D.
- Patterson Chris
- Paul Elisabeth
- Pearce Simon P.
- Pearson James A.
- Peckham Michelle
- Pedemonte Nicoletta
- Pedro Sansoa A.
- Peifer Mark
- Pelkonen Tuula
- Pelleri Maria C.
- Pellizzon Michael A.
- Penagos-Tabaree Felipe
- Peng Xiangda
- Peng Yousong
- Perco Paul
- Pereira Joana L.
- Peres Marco A.
- Perry Samuel R.
- Peter Jessica
- Peterson Brent M.
- Petrelli M.
- Pezzuolo Andrea
- Pheko Mpho
- Pianosi Paolo T.
- Pichugin Alexander
- Pinto Carlos J.C.
- Pinto Ines M.
- Pinto Karina A.
- Pinzi Valentina
- Piotrowski Marcin
- Piovesan Allison
- Plantinga Arnoud
- Plevris John N.
- Pluess Michael
- Podolsky Illya M.
- Pollesello Piero
- Polz Martin
- Ponti Giovanna
- Popoola Segun I.
- Porcelli Piero
- Portilla Maribel
- Portillo M.C.
- Pourret Olivier
- Pozdnyakov Ilya
- Prajapati Anilkumar S.
- Pranata Raymond
- Prescott Julie
- Pridans Clare
- Prieto Daniel
- Prince Martin
- Pritchard Antonia L.
- Psaroulaki Anna
- Pujala Ravi K.
- Pulia Michael
- Pulido-Arjona Leonardo
- Pullan Wayne
- Pusch Stefan
- Qi Dongchen
- Qi Peng-Fei
- Qi Xingshun
- Qian Siyu
- Qin Lei
- Quinn Gwendolyn P.
- Quinn Terence J.
- Rafe Ali
- Rafiq Muhammad
- Raghava Gajendra P.S.
- Rahimi Farid
- Rahman Proton
- Rahman Shaifur
- Rai Nayanjot K.
- Raikou Vaia D.
- Raman Ayush
- Ramula Satu
- Ranft Andreas
- Raote Ishier
- Rappsilber Juri
- Rassaf Tienush
- Raucher-Ch\ue9n\ue9 [NO FIRST NAME IN SCOPUS]
- Rawski Rafal
- Ray Asit
- Raza Ali
- Razak Lubna A.
- Rebl Henrike
- Reddan Tristan
- Refai Osama
- Refardt Julie
- Regan Tim
- Rehfeldt Florian
- Reiling Jan H.
- Remacle Claire
- Reschke Cristina R.
- Rezaei Mohsen
- Rhodes Johanna
- Ricciardi Walter
- Richa Tambi
- Richardson Mark F.
- Riddick Eric W.
- Riess Olaf
- Ritter Uwe
- Riva Giuseppe
- Roach Neil W.
- Roberts David D.
- Roberts Nicola J.
- Robinson K.R.
- Robles Guillermo
- Rodrigues Tiago
- Rodriguez Cesar
- Roislien Jo
- Roobol Monique J.
- Ross Kehinde
- Ross Stephanie A.
- Rossoni Luca
- Rotge Jean-Yves
- Rouet Romain
- Rovas Alexandros
- Rowe Alexandra
- Rowe Anna D.
- Rudolf Kevin
- Ruepp Andreas
- Rusch Peter
- Rust Petra
- S\uf6relius Karl
- Saad Sonia
- Sabnis Sandeep C.
- Sack George H.
- Sacks Frank M.
- Sadoine Margaux L.
- Safaei Soroush
- Saggar Manish
- Saito Yu
- Salama Mohamed F.
- Saleh Sherif
- Sallmon Hannes
- Sampson Christopher
- Santos Manuela
- Saudemont Aurore
- Sava Gianni
- Schmidt Axel
- Schmutz Axel
- Schneeberger Pierre H.H.
- Schrading Simone
- Schramm Alexander
- Schreiber Martin
- Schuele Birgitt
- Schuler Sidney
- Schulte Leon N.
- Schuon Robert A.
- Schurr Roey
- Schwotzer Daniela
- Schymkowitz Joost
- Sczyrba Alexander
- Searles Stephen
- Sebastian Agata
- Seib Kate L.
- Selinski Jennifer
- Seltmann Stefanie
- Senghore Thomas
- Seow Esmond
- Sepanski Robert
- Sergeant Kjell
- Sha Feng
- Shabalin Ivan G.
- Shahid Shaouli
- Shalchyan Vahid
- Shalev Nir
- Shang Jin-Long
- Sharma Neeraj
- Sharma Saurab
- Sheehan Barry
- Shen Jun
- Shi Chunhu
- Shi Han-Ping
- Shimada Tomohiro
- Shin Jeon-Soo
- Shirvalkar Prasad
- Shiryayev Oleg
- Shohayeb Belal
- Shortt Colette
- Siebers Robert
- Sillanp\ue4\ue4 Elina
- Silveyra Patricia
- Singer Josef
- Singh Jugpreet
- Singh Mandeep
- Singh Manisha
- Skinner Debra
- Small Ian
- Smeets Paul A.M.
- Smith Simon S.
- Smith Taylor
- Smout Michael J.
- So Po-Wah
- Soares Ant\uf3nio
- Solano Francisco
- Solomon-Moore Emma
- Sommerlad Andrew
- Sonenshine Daniel E.
- Song Chunjiao
- Song Haijun
- Song Jiangning
- Song Lijuan
- Soraggi Samuele
- Sorzano Carlos O.
- Southall Tony
- Speakman John R.
- Spearman Paul
- Srinivasan Mandyam V.
- Srivastava Kshitij
- Srivastava Rupesh K.
- Stabile Laura P.
- Staege Martin S.
- Stanley Ryan
- Stasiak A.
- Steadman Kathryn J.
- Steckhan Nico
- Stein Nils
- Stella Alessandro
- Stephens Andrew W.
- Stevanovic Dejan
- Stewart Christopher J.
- Stewart Douglas I.
- Stine Keith
- Storlazzi Curt
- Stoynova Nataliya V.
- Strehlow Jan
- Strobl Frederic
- Strzalka Wojciech
- Suarez Oscar M.
- Subhash Santhilal
- Subissi Lorenzo
- Subramaniapillai Mehala
- Sukocheva Olga
- Sultana Taranum
- Sumant Anirudha V.
- Summers Mathew J.
- Sun Gang
- Sun Jim
- Sun Xianbao
- Sundar Raghav
- Supriyanto Irwan
- Surve Chinmay R.
- Suzuki Tomo
- Swali Ritu
- Sydes Matthew
- Syme Caitlin
- Szabo Attila
- Szymanski Wiktor
- Tacon Paul
- Taherzadeh Ghazaleh
- Tahir Nur D.M.
- Tai Chan N.P.
- Takeuchi Hisashi
- Tamaian Radu
- Tan Aik-Choon
- Tan Cher M.
- Tan Ene-Choo
- Tan Kok H.
- Tanadini-Lang S.
- Tanaka Kozo
- Tang Fei
- Tang Haixu
- Tang Jun
- Tang Young
- Tanino Y.
- Tantawy Marwa
- Tao Wanyin
- Targett-Adams Paul
- Tayebi Mourad
- Tayyem Reema
- Tebbe Christoph C.
- Telfer Evelyn E.
- Tellechea Juan I.
- Tempel Wolfram
- Tennakoon Sumudu
- Teodorczyk-Injeyan Julita A.
- Terrier Olivier
- Teseo Serafino
- Testa Jean
- Testoni Ines
- Theron G.
- Thijs Gert
- Thomas Lisa-Marie
- Thorne Sally
- Thrift Amanda G.
- Tian Chang F.
- Tian Yu-Shi
- Tian Zhiqi
- Tiffon Celine
- Tingting Qian
- Tinnefeld Philip
- Tjahjono Daryono H.
- Toelzer Christine
- Tofani Marco
- Tolle Fabrice
- Tomov Nikola
- Tong Xin
- Torga Gonzalo
- Toth Ervin
- Tovar Miguel
- Tr\uf6der Simon E.
- Tran Linh
- Tressoldi Patrizio
- Tripathi Sushil
- Tsapas Apostolos
- Tsirigotis Konstantinos
- Tuladhar Anil M.
- Turak Ayse
- Tuttle Lisa M.
- Tuttle Neil
- Tzotzos George
- Uchendu Florence
- Udo Edet E.
- Uhle Florian
- Ukubuiwe Azubuike C.
- Ung Carolina O.L.
- Utsumi Toshiaki
- Uversky Vladimir N.
- Vaidyanathan Subramanian
- Vaillant Michel
- Valenti Anna
- Valgepea Kaspar
- Valsesia Armand
- van de Mortel Thea
- van den Bos Wouter
- van Dessel Pieter
- van Meerten Tom
- van Nieuwerburgh Filip
- van Raaij Mark J.
- van Ruitenbeek Jan
- Vandenbroucke Roosmarijn E.
- Vanneste Sven
- Vatanparast Hamid
- Vavvas Demetrios G.
- Veiga Feliciano H.
- Vendrell Marc
- Verheijen Geert P.
- Verloh Niklas
- Verlot Pierre
- Vesk Peter A.
- Veys Ralf
- Vickers Paul
- Vickstrom Casey
- Victor Victor M.
- Vidal Arnau
- Villemur Richard
- Villet Martin H.
- Vindin Howard
- Vitriol Veronica
- Viveiros Miguel
- Vohl Marie-Claude
- Voolstra Christian R.
- Vorholt Julia A.
- Voskarides Konstantinos
- Voutchkova Denitza D.
- Vuillemin Anne
- Wakelin Steven
- Waldron Levi
- Walker Mirella
- Walsh Laurence J.
- Wang Amanda Y.
- Wang Fang
- Wang Fuan
- Wang Horng-Dar
- Wang Jinhui
- Wang Jiucun
- Wang Jun
- Wang Qing
- Wang Teng
- Wang Xiaomin
- Wang Yun
- Wang Zhenxing
- Watanabe Yoichi
- Watari Ricky
- Waugh Jason
- Webb S.A.
- Webster Rebecca
- Webster Ruth
- Wei Junnian
- Wei Pan
- Weigert Andreas
- Weinstock Christof
- Welter Danielle
- Wen Jet-Chau
- Werner Gijsbert D.A.
- Werten Sebastiaan
- Westermair Anna L.
- Wham Carol
- White Ethan P.
- Wibowo David
- Widera Darius
- Wiener Jan
- Wilharm Gottfried
- Wilkinson Simon
- Williams Brendan A.
- Williams Richard
- Willmann Raffaella
- Wilson Alex
- Wilson Coralie
- Wingenbach Tanja S.H.
- Winslade Matthew
- Wirth Brunhilde
- Wojan Timothy R.
- Woldesemayat Adugna A.
- Wolff Mathieu
- Wong Alvin
- Wong Bryan M.
- Workman Alan D.
- Wu Dalei
- Wu Tzu-Wei
- Wu Yi-Rui
- Wuerbel Hanno
- Wyart [NO FIRST NAME IN SCOPUS]
- Xavier Rose M.
- Xia Wenfeng
- Xiang Tingxiu
- Xiao Han
- Xiao Shumin
- Xiao Xiangshu
- Xie Li-Xin
- Xiong Peng
- Xu Beisi
- Xu Dong
- Xu Haotian
- Xu J.W.
- Xu Jialin
- Xu Jianping
- Xu Juan
- Xu Jun
- Xu Shicai
- Xu Shilin
- Xu Taosheng
- Xu Ziyue
- Xue Bin
- Xue Yu
- Yadollahpour Ali
- Yalcin Suayib
- Yamato Masayuki
- Yan Hong
- Yang Chongjun
- Yang Dongdong
- Yang En-Cheng
- Yang Hui
- Yang Long
- Yang Mingjun
- Yang Shiqi
- Yang Sunny Y.
- Yang Wei
- Yang Yongliang
- Yankilevich Patricio
- Yao Ruifeng
- Yao Wen
- Yassine Abdul-Amir
- Ye Yuzhen
- Ye Zhi-Qiang
- Yeung Andy W.K.
- Yin Cong-Cong
- Yin Qinan
- Yli-Kauhaluoma Jari
- Yoneyama Hiroshi
- Yoon Jihoon G.
- You Yuyi
- Yousefzadeh Abbas
- Yu Chenglong
- Yu Ying
- Yu Yongbo
- Yuan Christina M.
- Yuan Guo-Cheng
- Yuh Chiou-Hwa
- Zabetakis Ioannis
- Zaccolo Manuela
- Zaitsu Masayoshi
- Zare Asma
- Zaritsky Arno
- Zaucha Jan
- Zeineb Zian
- Zeng Chen
- Zeng Erliang
- Zeng Zhen
- Zevnik Branko
- Zhan Jian
- Zhan Xiao-Yong
- Zhang Chengrong
- Zhang Chi
- Zhang Chongxing
- Zhang Gong
- Zhang Haowen
- Zhang Jilei
- Zhang Junpeng
- Zhang Kai
- Zhang Li
- Zhang Linxing
- Zhang Rongqiang
- Zhang Tongchuan
- Zhang Tuo
- Zhang Wei
- Zhang Weijia
- Zhang Xianglilan
- Zhang Xiaolei
- Zhang Yao
- Zhang Yi
- Zhang Yingkai
- Zhang Yusen
- Zhang Zhe
- Zhang Zhiyong
- Zhang Zhong-Yin
- Zhang Zhongheng
- Zhao Guoyan
- Zhao Haochen
- Zhao Jing
- Zhao Xin
- Zhao Yuan
- Zheng Shan
- Zhou Bailing
- Zhou Jianyu
- Zhou Kai
- Zhou Min
- Zhou Xiaofan
- Zhou Xiaoyan
- Zhou Yaoqi
- Zhu Dongjie
- Zhu Shu
- Zhu Zhenxing
- Ziegler Andreas
- Zinke Katharina
- Zuberbier Torsten
- Zuckerman Hannah
- Publication venue
- Publication date
- 01/01/2019
- Field of study
Document recommendation systems for locating relevant literature have mostly relied on methods developed a decade ago. This is largely due to the lack of a large offline gold-standard benchmark of relevant documents that cover a variety of research fields such that newly developed literature search techniques can be compared, improved and translated into practice. To overcome this bottleneck, we have established the RElevant LIterature SearcH consortium consisting of more than 1500 scientists from 84 countries, who have collectively annotated the relevance of over 180 000 PubMed-listed articles with regard to their respective seed (input) article/s. The majority of annotations were contributed by highly experienced, original authors of the seed articles. The collected data cover 76% of all unique PubMed Medical Subject Headings descriptors. No systematic biases were observed across different experience levels, research fields or time spent on annotations. More importantly, annotations of the same document pairs contributed by different scientists were highly concordant. We further show that the three representative baseline methods used to generate recommended articles for evaluation (Okapi Best Matching 25, Term Frequency-Inverse Document Frequency and PubMed Related Articles) had similar overall performances. Additionally, we found that these methods each tend to produce distinct collections of recommended articles, suggesting that a hybrid method may be required to completely capture all relevant articles. The established database server located at https://relishdb.ict.griffith.edu.au is freely available for the downloading of annotation data and the blind testing of new methods. We expect that this benchmark will be useful for stimulating the development of new powerful techniques for title and title/abstract-based search engines for relevant articles in biomedical research.Peer reviewe
Finishing the euchromatic sequence of the human genome
- Author
- . Haifeng
- . Magner
- . Yin
- Abbott Scott
- Abbott-Ozersky Amanda
- Abdellah Zahra
- Abouelleil Amr
- Abrajano Anne
- Adachi Tamami
- Adam Catherine
- Adams Charles Q.
- Adamson Aaron
- Adekoya Emmanuel
- Adio-Oduola Babajide
- Aerts Andrea
- Aggarwal Arun
- Ahmadi Alireza
- Ahmed Shahana
- Aimable Matthew
- Ainscough Rachael
- Ait-Zahra Mostafa
- Aizu Tomoyuki
- Alcivare Dana
- Alegria Michelle
- Ali Alla
- Ali Johar
- Allegria-hartmann Michelle
- Alleman Jennifer
- Allen Carlana C.
- Allen Heather
- Allen Nicole R.
- Allen Susan
- Allen Thaddeus
- Almeida Jeff
- Almond Claire
- Alsbrooks Stephen L.
- Altherr Michael R.
- Amaratunge Harshinie C.
- Ambler Andrew
- Ambrose Karen
- Ambrose Kerrie
- Amemiya Chris
- Amico-Keller Gina
- Amin Amita G.
- Anderson Mechele
- Anderson Scott
- Anderson Scott
- Andora Janice
- Andredesz Carol
- Andrew Robert
- Andrews Dan
- Andrews Daniel
- Andrews Neil
- Andrews Stephanie
- Andriese Tim
- Anthouard Véronique
- Antonarakis Stylianos E.
- Anyalebechi Vivian
- Aoki Norie
- Apostolou Sinoula
- Apweiler Eva
- Arachchi Harindra
- Arai Rie
- Arbery Hazel
- Arcaina Marlon
- Arcaina Terisita
- Archer Beth
- Arellano Andre
- Arellano-Jones Perry
- Armbruster Jeff
- Armstrong Jon
- Arredondo Dilrukshi P.
- Arredondo Heather Hope
- Artiguenave François
- Asakawa Shuichi
- Asakawa Teruyo
- Ash Gareth
- Ashcroft Kevin
- Ashurst Jennifer
- Ashwell Robert
- Ashworth Linda K.
- Aslanidis Cara
- Asomugha Chinwe O.
- Asuncion Lawreen
- Atkin Deborah
- Atkinson Andrea
- Atkinson Barry
- Attix Cristina
- Attwood John
- Aubin Keith
- Auger Katherine
- Austin Shannon Michelle
- Avila Aaron
- Avis Terry
- Ayele Mulu
- Babayan Primo
- Babbage Anne
- Babbage Sarah
- Bach Phil
- Bachatsang Pasang
- Bacon Joanne
- Badri Hummy
- Baertsch Robert
- Bagguley Claire
- Bailey Jonathan
- Bajorek Eva
- Baker Andrew
- Baker Dan
- Baker M.
- Baker Richard
- Bakis Michele
- Baldwin Jennifer
- Banda Michael
- Banerjee Ruby
- Bao Jingyue
- Bao Qiyu
- Bao Weidong
- Bao Weidong
- Baptiste Pertrice
- Barbaria Joseph A.
- Barbe Valérie
- Bardill Simon
- Barker Daniel
- Barker Darren
- Barker Gary
- Barlow Karen
- Baron Laurent
- Barrett Anika
- Bartlett Rebecca
- Basham Victoria
- Bashman David
- Basu Suba
- Bateman Alex
- Bates Karen
- Battles John
- Batzer Mark
- Baumgart Cornelia
- Baumohl Jason
- Baynes Caroline
- Bayul Tashi
- Beall Keith
- Beard Lisa
- Beard Susan
- Beare David
- Beasley Alastair
- Beasley Helen
- Beasley Oliver
- Beaucham Leslie
- Beaudet Arthur
- Beck Alfred
- Beck Stephen
- Becker Michael
- Bell Emma
- Bell George I.
- Bellard Terell M.
- Bellerby Damian
- Bellerby Tristram
- Belter Edward A., Jr.
- Bemrose Richard
- Benard Michael Anthony
- BenKahla Alia
- Benke J
- Benner William
- Bennett James
- Bensasson Douda
- Bentley Andrew
- Bentley Dan
- Bentley David
- Berardinis Véronique de
- Bercovitz John
- Berghoff Amy
- Bergmann Anne
- Berkowicz Nicolas
- Berks Mary
- Berks Michael
- Bethel Graeme
- Beugelsdijk Tony J.
- Bhakta Rita
- Bhuchar Venita
- Bi Shihua
- Bian Xuemeng
- Bieri Tamberlyn
- Bimage Kesha E.
- Bird Christine
- Birditt Brian
- Birney Ewan
- Birney Ewan
- Birren Bruce
- Bissell Helen
- Biswalo Kaneza
- Bituin Aleksandr
- Black Stacey
- Blackburne-Maze Suzanne
- Blair Jessica Anne
- Blakey Sarah
- Blanks Tia
- Blasiar Darin
- Blazej Robert
- Blitshsteyn Berta
- Blomstrom David B.
- Bloom Scott
- Bloom Toby
- Blumer Heather
- Blye Jason
- Blyth Peter R.
- Blöcker Helmut
- Boatright Elizabeth
- Boehm John
- Boen Juanan
- Boguslavskiy Leonid
- Bolton Christel
- Bolund Lars
- Bondoc Marnel
- Bonfield James
- Bonnett Ralph
- Bonnin David
- Border Richard
- Borowsky Mark
- Borzym Katja
- Boukhgalter Boris
- Bowen Eric
- Bradley Amanda
- Bradshaw-Cordum Holly
- Brady Nicola
- Brandriff Brigitte F.
- Brannon Wade
- Branscomb Elbert
- Bray Jason
- Bray-Allen Sarah
- Brettin Thomas
- Bridgeman Anne
- Bridgers Michael
- Brimhall Angela K.
- Brokstein Peter
- Brook Jonathan
- Brooking Shane
- Brottier Philippe
- Brown Andrew
- Brown Clive
- Brown Jacqui
- Brown Margaret
- Brown Mary
- Brown Mary J.
- Brown Michael
- Brown Nancy C.
- Bruce David D.
- Bruce Robert
- Bruno William J.
- Bruskiewich Richard
- Bryant Jackie
- Bryant Jennifer E.
- Bryant Nathaniel P.
- Brüls Thomas
- Buatsi Delali
- Buck David
- Buckingham Judith M.
- Buckle Veronica
- Buczek Donald
- Budd Claire
- Buhay Christian J.
- Bulbul Kerem
- Buller Sarah
- Bunker Nathan
- Burberry Jill
- Burch Paula Ellen
- Burford Deborah
- Burgess Joanne
- Burgin Matt
- Burkett Carrie E.
- Burkhart-Schultz Karolyn
- Burrell Kevin L.
- Burrill Wayne
- Burrows Christine
- Burton Christine
- Burton John
- Butcher Phil
- Butler Adam
- Butler Jon
- Butler Paul
- Caenepeel Sean
- Cahill Patrick
- Cai Tianjing
- Cai Zhen
- Cairns Murray
- Calderon Eliana
- Callen David F.
- Camarata Jody
- Camire David
- Camm Nick
- Campbell Christopher
- Campbell Connie S.
- Campbell Evelyn W.
- Campbell Mary I.
- Campbell Mary L.
- Campo Kevin
- Canning Bruno
- Cao Ting
- Cao Yuzhu
- Caoile Chenier
- Cardenas Faviola
- Cardenas Lolo
- Cardenas Veronica
- Carder Carol
- Carder Paul
- Carpenter Kelly
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- Zhou Yang
- Zhou Yi
- Zhu Bingying
- Zhu Bofeng
- Zhu Fenghua
- Zhu Genfeng
- Zhu Genfeng
- Zhu Miao
- Zhu Ning
- Zhu Yongge
- Zhu Zhen
- Zhuang Shitao
- Zierten Deborah
- Zimmer Andrew
- Zody Michael C.
- Zollo Massimo
- Zorrilla Sara E.
- Zuo Lin
- Publication venue
- LSU Digital Commons
- Publication date
- 21/10/2004
- Field of study
The sequence of the human genome encodes the genetic instructions for human physiology, as well as rich information about human evolution. In 2001, the International Human Genome Sequencing Consortium reported a draft sequence of the euchromatic portion of the human genome. Since then, the international collaboration has worked to convert this draft into a genome sequence with high accuracy and nearly complete coverage. Here, we report the result of this finishing process. The current genome sequence (Build 35) contains 2.85 billion nucleotides interrupted by only 341 gaps. It covers ∼99% of the euchromatic genome and is accurate to an error rate of ∼1 event per 100,000 bases. Many of the remaining euchromatic gaps are associated with segmental duplications and will require focused work with new methods. The near-complete sequence, the first for a vertebrate, greatly improves the precision of biological analyses of the human genome including studies of gene number, birth and death. Notably, the human enome seems to encode only 20,000-25,000 protein-coding genes. The genome sequence reported here should serve as a firm foundation for biomedical research in the decades ahead
31st Annual Meeting and Associated Programs of the Society for Immunotherapy of Cancer (SITC 2016) : part two
- Author
- Abassi Yama
- Abelin Jennifer G
- Abolhalaj Milad
- Abraham Tara S
- Adam Ammar
- Adams David
- Adams Homer
- Adams Sarah F
- Adamus Tomasz
- Addepalli Murali
- Addepalli Murali
- Adjei Alex A
- Agapova Larissa
- Agarwala Sanjiv
- Ager Casey
- Aggarwal Charu
- Agnello Giulia
- Agudo Judith
- Aguilar Ethan G
- Aguilera Todd
- Ahamadi Malidi
- Ahn Yong-Oon
- Ahrens Eric T
- Aizer Ayal
- Ajina Reham
- Akerley Wallace
- Al-Muftah Mariam
- Albershardt Tina C
- Albershardt Tina C
- Albrekt Ann-Sofie
- Alekar Shilpa
- Alemany Ramon
- Alemany Ramon
- Alexander Brian
- Allbritton Omaira
- Allen Clint T
- Alley Evan W
- Allison James
- Allison James
- Allison James
- Alston Tesha
- Alt Jürgen
- Alters Susan
- Amatulli Michael
- Anand Snjezana
- Anand Snjezana
- Anand Snjezana
- Anderson Clark
- Anderson Mark
- Andersson Bengt
- Andre Pascale
- Andtbacka Robert H I
- Andtbacka Robert H I
- Angiuoli Sam
- Ansari Tameem
- Anthony Scott
- Antonarakis Emmanuel S
- Antonia Scott J
- Anwar Firoz
- Aquino-Michaels Keston
- Archer Jacob F
- Arina Ainhoa
- Armand Philippe
- Armenta Paul
- Armet Caroline M
- Arnoux Thomas
- Ascarateil Stephane
- Askmyr David
- Atkins Michael
- Atkins Michael B
- Atkinson Victoria
- Au Katrina
- Autio Karen A
- Awad Mark
- Bagarazzi Mark
- Bai Dina
- Baia Gilson
- Baird Jason
- Bajaj Anshika
- Balatoni Timea
- Balboni Tracy
- Balch Leslie
- Bang Andrew
- Bao Riyue
- Bao Yangyi
- Bao Yangyi
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- Barberi Theresa
- Barker Christopher A
- Barnea Eytan
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- Bartkowiak Todd
- Bartlett David
- Bartlett David
- Bartlett David
- Bartlett David
- Barton Sunjay M
- Barve Minal
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- Bauer Todd W
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- Brockstedt Dirk G
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- Dhupkar Pooja
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- DiCostanzo AriCeli
- Diede Scott J
- Dietz Allan B
- Dillhoff Mary
- Dillon Patrick
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- Ding Yueyun
- Doberstein Stephen K
- Dobkin Julie
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- Donahue Renee
- Dorsey Frank C
- Dovedi Simon
- Downs-Canner Stephanie
- Drake Charles
- Drake Charles G
- Drake Charles G
- Driessens Gregory
- Driscoll Kyla
- Druker Brian J
- Dubensky Thomas W
- Dubensky Thomas W
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- Edwards Robert P
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- Engelhard Victor H
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- Ferris Robert L
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- Fesenkova Valentyna
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- Fong Lawrence
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- Formenti Silvia C
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- Gajewski Thomas F
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- Gajewski Thomas F
- Gajewski Thomas F
- Gajewski Thomas F
- Gajewski Thomas F
- Galeassi Nadejda
- Gamble Alicia
- Gamble Alicia
- Gameiro Sofia
- Gameiro Sofia R
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- Gardner Kellie
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- Gartrell Robyn
- Gartrell Robyn
- Gasmi Billel
- Gastineau Dennis A
- Gaughan Elizabeth
- Gauthier Audrey
- Gauthier Kelsey S
- Geissler Michael
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- Gladstone Douglas
- Glickman Laura H
- Gnad-Vogt Ulrike
- Godwin John
- Gomes Bruno
- Gong Jian
- Gong Jian
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- Gooding William
- Gooding William
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- Gray Michael
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- Grenga Italia
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- Griesinger Frank
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- Grossenbacher Steven K
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- Guerriero Jennifer
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- Guiducci Cristina
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- Guo Zeng-qing
- Gupta Ravi
- Gupta Sachin
- Gupta Sumati
- Gustafson Michael P
- Gutierrez Andres A
- Guttridge Denis
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- Hailemichael Yared
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- Hall Gerald
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- Hamdy Freddie
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- Hardwick James
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- Hellmann Matthew D
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- Hendrickx Wouter
- Hendrickx Wouter
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- Heo Dae S
- Herbert Garth S
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- Herranz Mireia U
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- Zeng Xue
- Zha Yuanyuan
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- Zhang Jing
- Zhang Ping
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- Zhang Winter
- Zhang Yanping
- Zhao Fei
- Zhao Leyna
- Zhao Xingli
- Zheng Lianxing
- Zheng Wenxin
- Zheng Xianxian
- Zheng Yi
- Zhong Hong
- Zhou Li
- Zhou Xiangjun
- Zippelius Alfred
- Zloza Andrew
- Zloza Andrew
- Zloza Andrew
- Zloza Andrew
- Zloza Andrew
- Zou Jun
- Zuba-Surma Ewa
- Zubkova Olga
- Zureikat Amer
- Publication venue
- 'Springer Science and Business Media LLC'
- Publication date
- 01/01/2016
- Field of study
Background
The immunological escape of tumors represents one of the main ob- stacles to the treatment of malignancies. The blockade of PD-1 or CTLA-4 receptors represented a milestone in the history of immunotherapy. However, immune checkpoint inhibitors seem to be effective in specific cohorts of patients. It has been proposed that their efficacy relies on the presence of an immunological response. Thus, we hypothesized that disruption of the PD-L1/PD-1 axis would synergize with our oncolytic vaccine platform PeptiCRAd.
Methods
We used murine B16OVA in vivo tumor models and flow cytometry analysis to investigate the immunological background.
Results
First, we found that high-burden B16OVA tumors were refractory to combination immunotherapy. However, with a more aggressive schedule, tumors with a lower burden were more susceptible to the combination of PeptiCRAd and PD-L1 blockade. The therapy signifi- cantly increased the median survival of mice (Fig. 7). Interestingly, the reduced growth of contralaterally injected B16F10 cells sug- gested the presence of a long lasting immunological memory also against non-targeted antigens. Concerning the functional state of tumor infiltrating lymphocytes (TILs), we found that all the immune therapies would enhance the percentage of activated (PD-1pos TIM- 3neg) T lymphocytes and reduce the amount of exhausted (PD-1pos TIM-3pos) cells compared to placebo. As expected, we found that PeptiCRAd monotherapy could increase the number of antigen spe- cific CD8+ T cells compared to other treatments. However, only the combination with PD-L1 blockade could significantly increase the ra- tio between activated and exhausted pentamer positive cells (p= 0.0058), suggesting that by disrupting the PD-1/PD-L1 axis we could decrease the amount of dysfunctional antigen specific T cells. We ob- served that the anatomical location deeply influenced the state of CD4+ and CD8+ T lymphocytes. In fact, TIM-3 expression was in- creased by 2 fold on TILs compared to splenic and lymphoid T cells. In the CD8+ compartment, the expression of PD-1 on the surface seemed to be restricted to the tumor micro-environment, while CD4 + T cells had a high expression of PD-1 also in lymphoid organs. Interestingly, we found that the levels of PD-1 were significantly higher on CD8+ T cells than on CD4+ T cells into the tumor micro- environment (p < 0.0001).
Conclusions
In conclusion, we demonstrated that the efficacy of immune check- point inhibitors might be strongly enhanced by their combination with cancer vaccines. PeptiCRAd was able to increase the number of antigen-specific T cells and PD-L1 blockade prevented their exhaus- tion, resulting in long-lasting immunological memory and increased median survival
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