133 research outputs found
Molecular motors robustly drive active gels to a critically connected state
- Author
- A Clauset
- A Zemel
- AA Griffith
- Abhinav Sharma
- AC Martin
- AC Martin
- BS Gentry
- C Furusawa
- C Heussinger
- C Storm
- C Torres-Sosa
- C Weber
- CP Broedersz
- D Mizuno
- D Smith
- D Stauffer
- DS Courson
- E Evans
- E Weeks
- F Backouche
- F Jülicher
- FC MacKintosh
- FJ Nédélec
- Fred C. MacKintosh
- GH Koenderink
- GH Koenderink
- Gijsje H. Koenderink
- HP Zhang
- J Sedzinski
- J-F Joanny
- JD Halley
- José Alvarado
- L Corté
- L Haviv
- M Lenz
- M Sheinman
- M Sheinman
- M Soares e Silva
- M Van Hecke
- M Wyart
- Michael Sheinman
- MP Murrell
- O Chaudhuri
- OJN Bertrand
- PM Bendix
- R Ishikawa
- S Camalet
- S Köhler
- S Köhler
- S Wang
- S Wang
- SK Vogel
- SL Veatch
- SM Fielding
- T Mora
- T Sanchez
- T Vissers
- TB Liverpool
- U Schwarz
- US Schwarz
- W Bialek
- Publication venue
- 'Springer Science and Business Media LLC'
- Publication date
- 01/01/2013
- Field of study
Living systems often exhibit internal driving: active, molecular processes
drive nonequilibrium phenomena such as metabolism or migration. Active gels
constitute a fascinating class of internally driven matter, where molecular
motors exert localized stresses inside polymer networks. There is evidence that
network crosslinking is required to allow motors to induce macroscopic
contraction. Yet a quantitative understanding of how network connectivity
enables contraction is lacking. Here we show experimentally that myosin motors
contract crosslinked actin polymer networks to clusters with a scale-free size
distribution. This critical behavior occurs over an unexpectedly broad range of
crosslink concentrations. To understand this robustness, we develop a
quantitative model of contractile networks that takes into account network
restructuring: motors reduce connectivity by forcing crosslinks to unbind.
Paradoxically, to coordinate global contractions, motor activity should be low.
Otherwise, motors drive initially well-connected networks to a critical state
where ruptures form across the entire network.Comment: Main text: 21 pages, 5 figures. Supplementary Information: 13 pages,
8 figure
Utility of multispectral imaging for nuclear classification of routine clinical histopathology imagery
- Author
- A Neher
- B Weyn
- B Weyn
- B Weyn
- BS Manjunath
- C Angeletti
- CM Bishop
- David L Rimm
- DJ Zahniser
- F Schnorrenberg
- G van de Wouwer
- H Stark
- L Latson
- Laura E Boucheron
- LE Boucheron
- MA Brewer
- MA Roula
- MS Bartlett
- Neal R Harvey
- NH Anderson
- NR Harvey
- R Jaganath
- R Levenson
- RM Levenson
- RM Levenson
- S Theodoridis
- SM Gentry
- T Mairinger
- Zhiqiang Bi
- Publication venue
- BioMed Central
- Publication date
- 01/07/2007
- Field of study
<p>Abstract</p> <p>Background</p> <p>We present an analysis of the utility of multispectral versus standard RGB imagery for routine H&E stained histopathology images, in particular for pixel-level classification of nuclei. Our multispectral imagery has 29 spectral bands, spaced 10 nm within the visual range of 420–700 nm. It has been hypothesized that the additional spectral bands contain further information useful for classification as compared to the 3 standard bands of RGB imagery. We present analyses of our data designed to test this hypothesis.</p> <p>Results</p> <p>For classification using all available image bands, we find the best performance (equal tradeoff between detection rate and false alarm rate) is obtained from either the multispectral or our "ccd" RGB imagery, with an overall increase in performance of 0.79% compared to the next best performing image type. For classification using single image bands, the single best multispectral band (in the red portion of the spectrum) gave a performance increase of 0.57%, compared to performance of the single best RGB band (red). Additionally, red bands had the highest coefficients/preference in our classifiers. Principal components analysis of the multispectral imagery indicates only two significant image bands, which is not surprising given the presence of two stains.</p> <p>Conclusion</p> <p>Our results indicate that multispectral imagery for routine H&E stained histopathology provides minimal additional spectral information for a pixel-level nuclear classification task than would standard RGB imagery.</p
Floristic characterization of an Atlantic Rainforest remnant in Southern Sergipe: Crasto forest
- Author
- Adeline Brito Sales
- AMORIM AM
- AMORIM AMA
- AMORIM BS
- BARBOSA MR
- BARBOSA MRV
- CAMPOS G
- Carolyn Elinore Barnes Proença
- CLARKE KR
- CLARKE KR
- COSTA JBP
- DEAN W
- DOMĺNGUEZ LF
- FERRAZ EBN
- FIASCHI P
- FREYRE G
- GENTRY AH
- GENTRY AH
- GIULIETTI AM
- GORENSTEIN MR
- GWALI S
- HAMMER Ø
- HIETZ P
- Ilaíne Silveira Matos
- IVANAUSKAS NM
- JERUSALINSKY L
- LANDIM MF
- LANDIM MF
- LANDRUM LR
- LAURANCE WF
- LAURANCE WF
- LEITÃO FILHO HF
- LIMA HC
- LINARES-PALOMINO R
- MARQUES MCM
- MCVAUGH R
- MORI SA
- MUELLER-DOMBOIS D
- MURRAY-SMITH C
- MYERS N
- Myrna Friederichs Landim
- NASCIMENTO LM
- OLIVEIRA FILHO AT
- OLIVEIRA MA
- OLIVEIRA VB
- PEIXOTO GL
- PEREIRA MS
- PRATA APN
- PRATA APN
- PRIMACK RB
- PROENÇA CEB
- RANTA P
- REVEAL JL
- RIBEIRO MC
- RICHARDS PW
- RODAL MJN
- ROLIM SG
- SCHNITZER SA
- SILVA IA
- SOBRAL M
- STEHMANN JR
- TABARELLI M
- TABARELLI M
- TABARELLI M
- TABARELLI M
- TABARELLI M
- TOLIMIERI N
- VEIGA LM
- WEBB CO
- ZIPPARRO VB
- Publication venue
- 'FapUNIFESP (SciELO)'
- Publication date
- Field of study
Population Structure as Revealed by mtDNA and Microsatellites in Northern Fur Seals, Callorhinus ursinus, throughout Their Range
- Author
- AE York
- AJ Drummond
- AR Hoelzel
- AR Hoelzel
- AR Rogers
- AR Rogers
- BC Robertson
- Bobette R. Dickerson
- BS Weir
- BW Robson
- CA Mathee
- D Posada
- DW Coltman
- EC Pielou
- FG Chelnokov
- GA Antonelis
- J Allen P
- J Goodman S
- J Goudet
- J Goudet
- J Higdon
- J Rozas
- J Sambrook
- JD Baker
- JI Hoffman
- JI Hoffman
- JK Pritchard
- JT Sterling
- JW Bickham
- KA Call
- KW Kenyon
- KW Kenyon
- L Excoffier
- LP Wynen
- M Haberl
- M Raymond
- M Slatkin
- MA Lea
- MR Griben
- MW Bruford
- N Mantel
- Neil John Gemmell
- NJ Gemmell
- NJ Gemmell
- NN FitzSimmons
- Paul Bentzen
- RG Towell
- RG Trujillo
- RH Lander
- RL Gentry
- Rolf R. Ream
- RR Ream
- RR Ream
- RS Peterson
- RS Waples
- RW Slade
- S Goldsworthy
- Sacha N. Vignieri
- SW Guo
- TA Hall
- TK Zeppelin
- TR Loughlin
- Publication venue
- Public Library of Science
- Publication date
- 01/01/2009
- Field of study
Background: The northern fur seal (Callorhinus ursinus; NFS) is a widely distributed pinniped that has been shown to exhibit a high degree of philopatry to islands, breeding areas on an island, and even to specific segments of breeding areas. This level of philopatry could conceivably lead to highly genetically divergent populations. However, northern fur seals have the potential for dispersal across large distances and have experienced repeated rapid population expansions following glacial retreat and the more recent cessation of intensive harvest pressure. Methodology/Principal Findings: Using microsatellite and mitochondrial loci, we examined population structure in NFS throughout their range. We found only weak population genetic structure among breeding islands including significant FST and W ST values between eastern and western Pacific islands. Conclusions: We conclude that insufficient time since rapid population expansion events (both post glacial and following the cessation of intense harvest pressure) mixed with low levels of contemporary migration have resulted in an absence of genetic structure across the entire northern fur seal range
Analysis of Epitopes on Dengue Virus Envelope Protein Recognized by Monoclonal Antibodies and Polyclonal Human Sera by a High Throughput Assay
- Author
- Alan L. Rothman
- AP Goncalvez
- B Kaufmann
- B Shrestha
- BD Lindenbach
- BS Davis
- CH Calisher
- Chih-Hsuan Lu
- Chih-Yun Lai
- CY Lai
- DJ Gubler
- DR Burton
- DS Burke
- E Konishi
- EA Henchal
- F Megret
- FX Heinz
- GD Gromowski
- GD Gromowski
- GE Nybakken
- Gwong-Jen Chang
- Han-Chung Wu
- Hong-En Lin
- HP Hu
- I Ferlenghi
- I-Ju Liu
- IM Yu
- J Schalich
- J Zlatkovic
- JA Roberson
- JD Brien
- Jih-Jin Tsai
- JM Mackenzie
- JM Murray
- JT Roehrig
- Jyh-Hsiung Huang
- K Stadler
- K Stiasny
- M Beltramello
- M Thali
- M Throsby
- Mei-Ying Liao
- MK Gentry
- MR Vogt
- MS Diamond
- O Lisova
- O Makarova
- P Keelapang
- Pi-Chun Li
- R Muzumder
- RJ Kuhn
- S Sukupolvi-Petty
- S Sukupolvi-Petty
- S Welsch
- SB Halstead
- SB Halstead
- SM Lok
- SS Chiou
- SS Whitehead
- T Oliphant
- TC Pierson
- VB Randolph
- W Dejnirattisai
- WD Crill
- WD Crill
- WD Crill
- Wei-Kung Wang
- Wen-Yang Tsai
- WM Wahala
- Y Modis
- Y Modis
- YC Chen
- Yi-Chieh Wu
- Publication venue
- Public Library of Science
- Publication date
- 01/01/2012
- Field of study
Dengue virus is the leading cause of arboviral diseases worldwide. The envelope protein is the major target of neutralizing antibodies and vaccine development. While previous studies have reported several epitopes on envelope protein, the possibility of interdomain epitopes and the relationship of epitopes to neutralizing potency remain unexplored. We developed a high throughput dot blot assay by using 67 alanine mutants of surface-exposed envelope residues as a systematic approach to identify epitopes recognized by mouse monoclonal antibodies and polyclonal human sera. Our results suggested the presence of interdomain epitopes more frequent than previously appreciated. Compared with monoclonal antibodies generated by traditional protocol, the potent neutralizing monoclonal antibodies generated by a new protocol showed several unique features of their epitopes. Moreover, the predominant epitopes of antibodies against envelope protein in polyclonal sera can be identified by this assay. These findings have implications for future development of epitope-specific diagnostics and epitope-based dengue vaccine, and add to our understanding of humoral immune responses to dengue virus at the epitope level
Genetic Determinants of Lipid Traits in Diverse Populations from the Population Architecture using Genomics and Epidemiology (PAGE) Study
- Author
- A Adeyemo
- Barbara Cochran
- Barbara V. Howard
- BE Himes
- BS Weir
- C Sabatti
- C Wallace
- CA Hodgkinson
- Cara L. Carty
- Charles B. Eaton
- Charles Kooperberg
- Christopher A. Haiman
- Christopher S. Carlson
- CJ Willer
- CJ Willer
- D Ge
- DA Nielsen
- Dana C. Crawford
- Dave Duggan
- DB Hancock
- DE Adkins
- DM Waterworth
- Elisa T. Lee
- EN Smith
- ET Lee
- Fredrick R. Schumacher
- G Genovese
- Garnet Anderson
- GD Friedman
- GL Anderson
- Greg Gibson
- HH Goring
- HJ Edenberg
- IM Heid
- J Hallmayer
- J Shi
- J Wu
- Jean W. MacCluer
- Jeff Haessler
- JM Norris
- José L. Ambite
- JS Kooner
- K Bozaoglu
- K Nakayama
- K Pelak
- Karen C. Johnson
- Kari E. North
- KE North
- Kira Taylor
- Kristin Brown-Gentry
- LA Hindorff
- LA Hindorff
- Laurence N. Kolonel
- LJ Bierut
- LN Kolonel
- Logan Dumitrescu
- Loïc Le Marchand
- LP Fried
- Lucia A. Hindorff
- Lyle G. Best
- Lynne R. Wilkens
- M Bostrom
- MD Mailman
- ME Keebler
- ME Keebler
- MG Hayes
- Mh Chang
- Miguel Quibrera
- MS Sandhu
- Myriam Fornage
- N Ahituv
- N Palmer
- NA Rosenberg
- Nora Franceschini
- P Sebastiani
- PA Kanetsky
- Petra Bůžková
- PJ Talmud
- PM Ridker
- PMA Sleiman
- R Burkhardt
- R Gupta
- R Saxena
- RA Mathias
- Ralph V. Shohet
- RC Deo
- Richard B. Devereux
- S Kariuki
- S Kathiresan
- S Kathiresan
- S Pendergrass
- S Zollner
- SA Pendergrass
- Sandra Laston
- Sarah A. Pendergrass
- SFC Vaessen
- Shelley A. Cole
- SJ Kang
- Steven Buyske
- T Matise
- T Matise
- Teri A. Manolio
- TI Pollin
- TM Teslovich
- W Gauderman
- WJ Gauderman
- WT Friedewald
- Y Hiura
- YS Aulchenko
- YY Teo
- Publication venue
- Public Library of Science
- Publication date
- 01/01/2011
- Field of study
For the past five years, genome-wide association studies (GWAS) have identified hundreds of common variants associated with human diseases and traits, including high-density lipoprotein cholesterol (HDL-C), low-density lipoprotein cholesterol (LDL-C), and triglyceride (TG) levels. Approximately 95 loci associated with lipid levels have been identified primarily among populations of European ancestry. The Population Architecture using Genomics and Epidemiology (PAGE) study was established in 2008 to characterize GWAS–identified variants in diverse population-based studies. We genotyped 49 GWAS–identified SNPs associated with one or more lipid traits in at least two PAGE studies and across six racial/ethnic groups. We performed a meta-analysis testing for SNP associations with fasting HDL-C, LDL-C, and ln(TG) levels in self-identified European American (∼20,000), African American (∼9,000), American Indian (∼6,000), Mexican American/Hispanic (∼2,500), Japanese/East Asian (∼690), and Pacific Islander/Native Hawaiian (∼175) adults, regardless of lipid-lowering medication use. We replicated 55 of 60 (92%) SNP associations tested in European Americans at p<0.05. Despite sufficient power, we were unable to replicate ABCA1 rs4149268 and rs1883025, CETP rs1864163, and TTC39B rs471364 previously associated with HDL-C and MAFB rs6102059 previously associated with LDL-C. Based on significance (p<0.05) and consistent direction of effect, a majority of replicated genotype-phentoype associations for HDL-C, LDL-C, and ln(TG) in European Americans generalized to African Americans (48%, 61%, and 57%), American Indians (45%, 64%, and 77%), and Mexican Americans/Hispanics (57%, 56%, and 86%). Overall, 16 associations generalized across all three populations. For the associations that did not generalize, differences in effect sizes, allele frequencies, and linkage disequilibrium offer clues to the next generation of association studies for these traits
Behavioral genetics and taste
- Author
- A Hajnal
- AA Bachmanov
- AA Bachmanov
- AA Bachmanov
- AA Bachmanov
- AA Bachmanov
- AA Bachmanov
- AA Bachmanov
- AA Bachmanov
- AA Bachmanov
- AA Bachmanov
- AA Bachmanov
- AA Bachmanov
- AA Bachmanov
- AA Bachmanov
- AA Bachmanov
- AA Bachmanov
- AA Bachmanov
- AA Bachmanov
- AA Bachmanov
- AA Bachmanov
- AB Kampov-Polevoy
- AB Kampov-Polevoy
- AB Kampov-Polevoy
- AB Kampov-Polevoy
- AB Kampov-Polevoy
- AC Spector
- AC Spector
- AD Salbe
- AF Blakeslee
- AH McDaniel
- AI Spielman
- AJ Drewnowski
- AL Fox
- AL Fox
- AL Huang
- Alexander A Bachmanov
- AS Levine
- B Bufe
- BA Gosnell
- BA McMillen
- BG Green
- BK Formaker
- BK Formaker
- BK Smith
- BM Reddy
- BS Kotlus
- C Conte
- C Conte
- C Kuhn
- CD Dotson
- CG Capeless
- CG Capeless
- CH Lemon
- CL Hubell
- CP Richter
- D Denton
- D Drayna
- D Drayna
- DA Blizard
- DA Blizard
- DA Blizard
- DA Blizard
- DA Rodgers
- DA Rodgers
- DA Rodgers
- DB Harder
- DB Harder
- DB Harder
- DB Harder
- DG Mook
- DH Overstreet
- DH Overstreet
- DP Atchley
- DR Reed
- DR Reed
- DR Reed
- DR Reed
- DS Cannon
- E Adler
- E Sainz
- E Terenina-Rigaldie
- E Terenina-Rigaldie
- EE Midkiff
- EE Midkiff
- EE Midkiff
- EX Freed
- FA Caputo
- G Hellekant
- G Nelson
- G Nelson
- G Whitney
- G Whitney
- G Whitney
- GA Falciglia
- GE McClearn
- GJ Lawrence
- GK Beauchamp
- GK Beauchamp
- GK Beauchamp
- GQ Zhao
- GT Wong
- H Harris
- H Harris
- H Looy
- H Looy
- H Matsunami
- H Xu
- HJ Grill
- I Le Roy
- I Ramirez
- IE Lush
- IE Lush
- IE Lush
- IE Lush
- IE Lush
- IE Lush
- IE Lush
- IE Lush
- IL Bernstein
- J Brand
- J Chandrashekar
- J Chandrashekar
- J Liao
- J-X Guinard
- JA Desor
- JC Molina
- JC Smith
- JD Boughter Jr
- JD Boughter Jr
- JF Gent
- JI Glendinning
- JI Glendinning
- JI Glendinning
- JK Belknap
- JK Belknap
- JK Belknap
- JL Fuller
- JL Fuller
- JL Hansen
- JM Olson
- John D Boughter
- JP Montmayeur
- JT Fitzsimons
- K Hoshishima
- K Hoshishima
- K Lu
- K Scott
- K Scott
- KL Mueller
- KS Curtis
- KS Gannon
- LH Snyder
- LM Bartoshuk
- LM Bartoshuk
- LM Bartoshuk
- LR Intranuovo
- LS Greene
- M Behrens
- M Inoue
- M Inoue
- M Inoue
- M Inoue
- M Kitagawa
- M Max
- M Nachman
- M Nachman
- MA Austin
- MA Enoch
- MA Hoon
- MD Basson
- MD Stockton
- ME Dinehart
- ME Frank
- ME Frank
- ME Yamamoto
- MG Tordoff
- ML Pelchat
- MM Minear
- N Chaudhari
- N Sako
- N Shigemura
- N Shigemura
- N Soranzo
- NE Rowland
- NK Dess
- NK Dess
- O Lugaz
- O Pucilowski
- P Mombaerts
- P Shi
- PM Conneally
- PM Di Lorenzo
- R Di Nicolantonio
- R DiNicolantonio
- R DiNicolantonio
- RB Stewart
- RB Stewart
- RD Mattes
- RP Warren
- RT Gentry
- S Damak
- S Eylam
- S Eylam
- S Eylam
- S Manita
- S Marella
- SA Lanier
- SA Simon
- SB Harrap
- SI Sollars
- SI Sollars
- SI Sollars
- SJ St John
- SN Clarke
- SR George
- SR Lewis
- ST DiCarlo
- SW Kiefer
- SW Kiefer
- SW Kiefer
- T Foroud
- TA Gilbertson
- TA Richter
- TJ Phillips
- TM Nelson
- TM Nelson
- TR Scott
- TW Klein
- UK Kim
- UK Kim
- VB Duffy
- WE Pelz
- X Li
- X Li
- X Li
- X Li
- X Li
- X Wang
- Y Go
- Y Go
- Y Ishimaru
- Y Maruyama
- Y Nie
- Y Ninomiya
- Y Ninomiya
- Y Ninomiya
- Y Ninomiya
- Y Ninomiya
- Y Ninomiya
- Y Ninomiya
- Y Ninomiya
- Y Ninomiya
- YA Blednov
- YK Cho
- Publication venue
- BioMed Central
- Publication date
- 01/01/2007
- Field of study
This review focuses on behavioral genetic studies of sweet, umami, bitter and salt taste responses in mammals. Studies involving mouse inbred strain comparisons and genetic analyses, and their impact on elucidation of taste receptors and transduction mechanisms are discussed. Finally, the effect of genetic variation in taste responsiveness on complex traits such as drug intake is considered. Recent advances in development of genomic resources make behavioral genetics a powerful approach for understanding mechanisms of taste
Measurement and interpretation of same-sign W boson pair production in association with two jets in pp collisions at s = 13 TeV with the ATLAS detector
- Author
- Aad G
- Abbott B
- Abeling K
- Abicht NJ
- Abidi SH
- Aboulhorma A
- Abramowicz H
- Abreu H
- Abulaiti Y
- Abusleme Hoffman AC
- Acharya BS
- Adam Bourdarios C
- Adamczyk L
- Adamek L
- Addepalli SV
- Addison MJ
- Adelman J
- Adiguzel A
- Adye T
- Affolder AA
- Afik Y
- Agaras MN
- Agarwala J
- Aggarwal A
- Agheorghiesei C
- Ahmad A
- Ahmadov F
- Ahmed WS
- Ahuja S
- Ai X
- Aielli G
- Aikot A
- Ait Tamlihat M
- Aitbenchikh B
- Aizenberg I
- Akbiyik M
- Akimov AV
- Akiyama D
- Akolkar NN
- Al Khoury K
- Alberghi GL
- Albert J
- Albicocco P
- Albouy GL
- Alderweireldt S
- Aleksa M
- Aleksandrov IN
- Alexa C
- Alexopoulos T
- Alfonsi F
- Algren M
- Alhroob M
- Ali B
- Ali HMJ
- Ali S
- Alibocus SW
- Aliev M
- Alimonti G
- Alkakhi W
- Allaire C
- Allbrooke BMM
- Allen JF
- Allendes Flores CA
- Allport PP
- Aloisio A
- Alonso F
- Alpigiani C
- Alvarez Estevez M
- Alvarez Fernandez A
- Alves Cardoso M
- Alviggi MG
- Aly M
- Amaral Coutinho Y
- Ambler A
- Amelung C
- Amerl M
- Ames CG
- Amidei D
- Amor Dos Santos SP
- Amos KR
- Ananiev V
- Anastopoulos C
- Andeen T
- Anders JK
- Andrean SY
- Andreazza A
- Angelidakis S
- Angerami A
- Anisenkov AV
- Annovi A
- Antel C
- Anthony MT
- Antipov E
- Antonelli M
- Anulli F
- Aoki M
- Aoki T
- Aparisi Pozo JA
- Aparo MA
- Aperio Bella L
- Appelt C
- Apyan A
- Aranzabal N
- Arcangeletti C
- Arce ATH
- Arena E
- Arguin J-F
- Argyropoulos S
- Arling J-H
- Arnaez O
- Arnold H
- Artoni G
- Asada H
- Asai K
- Asai S
- Asbah NA
- Assamagan K
- Astalos R
- Atashi S
- Atkin RJ
- Atkinson M
- Atmani H
- Atmasiddha PA
- Augsten K
- Auricchio S
- Auriol AD
- Austrup VA
- Avolio G
- Axiotis K
- Azuelos G
- Babal D
- Bachacou H
- Bachas K
- Bachiu A
- Backman F
- Badea A
- Bagnaia P
- Bahmani M
- Bailey AJ
- Bailey VR
- Baines JT
- Baines L
- Bakalis C
- Baker OK
- Bakos E
- Bakshi Gupta D
- Balakrishnan V
- Balasubramanian R
- Baldin EM
- Balek P
- Ballabene E
- Balli F
- Baltes LM
- Balunas WK
- Balz J
- Banas E
- Bandieramonte M
- Bandyopadhyay A
- Bansal S
- Barak L
- Barakat M
- Barberio EL
- Barberis D
- Barbero M
- Barel MZ
- Barends KN
- Barillari T
- Barisits M-S
- Barklow T
- Baron Moreno DA
- Baron P
- Baroncelli A
- Barone G
- Barr AJ
- Barr JD
- Barranco Navarro L
- Barreiro Guimarães da Costa J
- Barreiro F
- Barron U
- Barros Teixeira MG
- Barsov S
- Bartels F
- Bartoldus R
- Barton AE
- Bartos P
- Basan A
- Baselga M
- Bassalat A
- Basso MJ
- Basson CR
- Bates RL
- Batlamous S
- Batley JR
- Batool B
- Battaglia M
- Battulga D
- Bauce M
- Bauer M
- Bauer P
- Bazzano Hurrell LT
- Beacham JB
- Beau T
- Beauchemin PH
- Becherer F
- Bechtle P
- Beck HP
- Becker K
- Becot C
- Beddall AJ
- Bednyakov VA
- Bee CP
- Beemster LJ
- Beermann TA
- Begalli M
- Begel M
- Behera A
- Behr JK
- Beirer JF
- Beisiegel F
- Belfkir M
- Bella G
- Bellagamba L
- Bellerive A
- Bellos P
- Beloborodov K
- Belyaev NL
- Benchekroun D
- Bendebba F
- Benhammou Y
- Benoit M
- Bensinger JR
- Bentvelsen S
- Beresford L
- Beretta M
- Bergeaas Kuutmann E
- Berger N
- Bergmann B
- Beringer J
- Bernardi G
- Bernius C
- Bernlochner FU
- Bernon F
- Berry T
- Berta P
- Berthold A
- Bertram IA
- Bethke S
- Betti A
- Bevan AJ
- Bhamjee M
- Bhatta S
- Bhattacharya DS
- Bhattarai P
- Bhopatkar VS
- Bi R
- Bianchi RM
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- Zhemchugov A
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- Zhulanov V
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- Åkesson TPA
- Öncel ÖO
- Ženiš T
- Živković L
- Publication venue
- Springer Nature
- Publication date
- 01/04/2024
- Field of study
This paper presents the measurement of fducial and diferential cross sections for both the inclusive and electroweak production of a same-sign W-boson pair in association with two jets (W±W±jj) using 139 fb−1 of proton-proton collision data recorded at a centre-of-mass energy of √s = 13 TeV by the ATLAS detector at the Large Hadron Collider. The analysis is performed by selecting two same-charge leptons, electron or muon, and at least two jets with large invariant mass and a large rapidity diference. The measured fducial cross sections for electroweak and inclusive W±W±jj production are 2.92 ± 0.22 (stat.) ± 0.19 (syst.)fb and 3.38±0.22 (stat.)±0.19 (syst.)fb, respectively, in agreement with Standard Model predictions. The measurements are used to constrain anomalous quartic gauge couplings by extracting 95% confdence level intervals on dimension-8 operators. A search for doubly charged Higgs bosons H±± that are produced in vector-boson fusion processes and decay into a same-sign W boson pair is performed. The largest deviation from the Standard Model occurs for an H±± mass near 450 GeV, with a global signifcance of 2.5 standard deviations
Combination of searches for heavy spin-1 resonances using 139 fb−1 of proton-proton collision data at s = 13 TeV with the ATLAS detector
- Author
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- Zhemchugov A
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- Zwalinski L
- Åkesson TPA
- Öncel ÖO
- Ženiš T
- Živković L
- Publication venue
- Springer Nature
- Publication date
- 19/04/2024
- Field of study
A combination of searches for new heavy spin-1 resonances decaying into different pairings of W, Z, or Higgs bosons, as well as directly into leptons or quarks, is presented. The data sample used corresponds to 139 fb−1 of proton-proton collisions at
= 13 TeV collected during 2015–2018 with the ATLAS detector at the CERN Large Hadron Collider. Analyses selecting quark pairs (qq, bb,
, and tb) or third-generation leptons (τν and ττ) are included in this kind of combination for the first time. A simplified model predicting a spin-1 heavy vector-boson triplet is used. Cross-section limits are set at the 95% confidence level and are compared with predictions for the benchmark model. These limits are also expressed in terms of constraints on couplings of the heavy vector-boson triplet to quarks, leptons, and the Higgs boson. The complementarity of the various analyses increases the sensitivity to new physics, and the resulting constraints are stronger than those from any individual analysis considered. The data exclude a heavy vector-boson triplet with mass below 5.8 TeV in a weakly coupled scenario, below 4.4 TeV in a strongly coupled scenario, and up to 1.5 TeV in the case of production via vector-boson fusion
Evaluation of appendicitis risk prediction models in adults with suspected appendicitis
- Author
- Abbas Sh
- Abbas Sh
- Abbassi Oa
- Abbott T
- Abdelgadir Am
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- García-Gutierrez C
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- Redondo E
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- Reese G
- Regina G
- Rehman S
- Rehman S
- Rekhraj S
- Ren Kz
- Renshaw S
- Renshaw S
- Renzi Cr
- Resende Fm
- Rezacova M
- Rezvani S
- Riaz W
- Riba-Combatti L
- Ribaudo M
- Ribeiro B
- Rich Je
- Richardson Td
- Ridaura N
- Riera E
- Rigby S
- Rigney B
- Rinkoff S
- Ripoli Mc
- Robb Hd
- Robertson C
- Robinson A
- Robinson A
- Robinson D
- Robinson D
- Rocha R
- Rodger V
- Rodicio-Miravalles Jl
- Rodriguez L
- Rodriguez-Lopez M
- Rodriguez-Lopez M
- Rodriguez-Lopez M
- Rodríguez Ec
- Rojo Ja
- Roldán-Ortiz S
- Rolph R
- Romano J
- Romano R
- Romario Uf
- Romoli L
- Roncero Ls
- Ronda Rn
- Roomi S
- Rosa Mj
- Rosat A
- Roscio F
- Roscio F
- Roscio F
- Rossi C
- Rossi D
- Rossi Gm
- Roth N
- Rothnie K
- Roxburgh C
- Roy C
- Ruano A
- Rubbini M
- Rudland I
- Ruffolo C
- Rufo E
- Ruggiu Gv
- Ruiz-Marín M
- Ruiz-Marín M
- Rupani S
- Rupasinghe Sn
- Rupasinghe Sn
- Rutherford Dg
- Ruzvidzo F
- Ruzzenente A
- Saad M
- Saad M
- Saavedra-Chacón M
- Saba A
- Sabia D
- Sacco R
- Sacks R
- Sadek S
- Saghir N
- Sagnotta A
- Sagnotta A
- Saha A
- Sahay Sj
- Sahnan K
- Sahnan K
- Sainz B
- Sainz B
- Sajid Ms
- Salama Y
- Salamone G
- Salamone G
- Salamone G
- Salamone G
- Salandini Mc
- Salem A
- Salim S
- Salva Ab
- Salvador H
- Samartin C
- Sammarco G
- Sammarco G
- Samuel M
- Sana S
- Sanchez Er
- Sanchez Er
- Sanchez L
- Sanchez-Garcia S
- Sanchez-Guillen L
- Sanchez-Guillen L
- Sanchez-Martinez A
- Sancho-Muriel J
- Sandu L
- Sanna S
- Santamaria C
- Santamaría Pc
- Santarrufina-Martínez S
- Santos Sc
- Santurro L
- Sanz-Navarro S
- Sarmah P
- Sarmah P
- Sarmah P
- Sarveswaran J
- Sasia D
- Sasia D
- Saunders S
- Savill A
- Savino G
- Savino G
- Savioli F
- Scabini S
- Scabini S
- Scabini S
- Scandroglio Is
- Scanlon K
- Scatizzi M
- Scialandrone G
- Scricciolo M
- Sebastian Jf
- Sebastián-Tomás Jc
- Seddon Tc
- Segalini E
- Segura-Sampedro Jj
- Sena G
- Sena-Ruiz F
- Seneviratne N
- Sepe C
- Serventi F
- Serventi F
- Seth M
- Setshwaelo T
- Sezen E
- Sgardelis P
- Sgrò A
- Sgrò A
- Sgrò A
- Shah J
- Shah K
- Shah Sm
- Shah Sm
- Shaikh Ia
- Shakoor Z
- Shanmuganathan V
- Shanmugarajah K
- Sharma A
- Sharma A
- Sharma P
- Sharp Ol
- Sharp Ol
- Shaw Av
- Shepherd Ja
- Sherif Ma
- Shet S
- Shetty Vd
- Shingler G
- Shiwani Mh
- Shrestha D
- Shurlock J
- Sian T
- Siaw O
- Siddique K
- Siddiqui Mn
- Siddiqui Za
- Sierra-Grañón Je
- Siggens Kl
- Sihra N
- Silva A
- Silva I
- Silvestri V
- Simioni A
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- Simmonds L
- Simo V
- Simoes J
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- Singh J
- Singh P
- Singh S
- Singhal T
- Singhal T
- Sivaloganathan P
- Skalamera I
- Skerritt C
- Slezak I
- Smallcombe N
- Smart Cj
- Smart Cj
- Smart Nj
- Smart Nj
- Smoker H
- Soares A. S.
- Soares As
- Soares As
- Soares As
- Soares As
- Soares As
- Soh B
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- Soliani P
- Solinas L
- Sooriyamoorthy T
- Soria-Aledo V
- Soria-Aledo V
- Soriano Jt
- Sorrentino L
- Sousa Hs
- Souter J
- Sparta C
- Spaziani A
- Speake D
- Speake D
- Springate El
- Sreedharan L
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- Staderini F
- Stecca T
- Stella M
- Stephens Gf
- Stephens Gf
- Stevenson R
- Stewart Dj
- Stoica I
- Storey R
- Stoyanov Ti
- Strachan E
- Strange Ja
- Stubbs Bm
- Stupalkowska W
- Stupalkowska W
- Suarez-Cabrera A
- Suero Ca
- Sultana A
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- Sunter H
- Surg Pt
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- Suárez-Sánchez A
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- Symons N
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- Szucs A
- Szucs A
- Sánchez-Cifuentes A
- Sánchez-Fuentes Mn
- Sánchez-Rubio M
- Tabain V
- Taglietti L
- Tague Le
- Tahir W
- Tailor K
- Tallon-Aguilar L
- Tallon-Aguilar L
- Tamayo-López Mj
- Tamborska A
- Tamini N
- Tamini N
- Tamini N
- Tan Cy
- Tan Cy
- Tan E
- Tan Hl
- Tan S
- Tang Am
- Tapiolas I
- Tarazi M
- Tatulli F
- Tay Yh
- Tayeh S
- Taylor M
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- Taylor Ns
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- Tezas S
- Thaha Ma
- Thakral N
- Thakur D
- Thava B
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- Thaventhiran Aj
- Theodoropoulou K
- Thomas At
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- Vallve-Bernal M
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- Vigorita V
- Vijay V
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- Viviani E
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- Vulcano I
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- Yang P
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- Yeung K
- Yoganathan S
- Yoong S
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- Zelazek M
- Zerpa C
- Zhang Ay
- Zhou S
- Zorrilla L
- Zuin M
- Zurleni Tz
- Publication venue
- 'Wiley'
- Publication date
- 01/01/2019
- Field of study
Background
Appendicitis is the most common general surgical emergency worldwide, but its diagnosis remains challenging. The aim of this study was to determine whether existing risk prediction models can reliably identify patients presenting to hospital in the UK with acute right iliac fossa (RIF) pain who are at low risk of appendicitis.
Methods
A systematic search was completed to identify all existing appendicitis risk prediction models. Models were validated using UK data from an international prospective cohort study that captured consecutive patients aged 16–45 years presenting to hospital with acute RIF in March to June 2017. The main outcome was best achievable model specificity (proportion of patients who did not have appendicitis correctly classified as low risk) whilst maintaining a failure rate below 5 per cent (proportion of patients identified as low risk who actually had appendicitis).
Results
Some 5345 patients across 154 UK hospitals were identified, of which two‐thirds (3613 of 5345, 67·6 per cent) were women. Women were more than twice as likely to undergo surgery with removal of a histologically normal appendix (272 of 964, 28·2 per cent) than men (120 of 993, 12·1 per cent) (relative risk 2·33, 95 per cent c.i. 1·92 to 2·84; P < 0·001). Of 15 validated risk prediction models, the Adult Appendicitis Score performed best (cut‐off score 8 or less, specificity 63·1 per cent, failure rate 3·7 per cent). The Appendicitis Inflammatory Response Score performed best for men (cut‐off score 2 or less, specificity 24·7 per cent, failure rate 2·4 per cent).
Conclusion
Women in the UK had a disproportionate risk of admission without surgical intervention and had high rates of normal appendicectomy. Risk prediction models to support shared decision‐making by identifying adults in the UK at low risk of appendicitis were identified
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