208 research outputs found
TLR4 and NKT Cell Synergy in Immunotherapy against Visceral Leishmaniasis
- Author
- A Bendelac
- A Nieto
- A Satoskar
- AC Stanley
- AV Rachitskaya
- BR Lauwerys
- C-W Lee
- CN Baxeyanis
- D van der Wetering
- DJ Matthews
- DS O'Mahony
- E Muraille
- EK Ryu
- Eleanor M. Riley
- FF Tuon
- H Kanzler
- H Towbin
- HW Murray
- HW Murray
- I Okwor
- I Sada-Ovalle
- IF Hermans
- J Alexander
- J Alexander
- J Alexander
- J Liese
- J Mattner
- JF Flandin
- JM Doisne
- Joydeep Paul
- JU Baenziger
- K Anderson
- K Benlagha
- LE Rosas
- M Krummen
- M Taniguchi
- MD Howard
- ME Wilson
- MG Neeyea
- MG Netea
- MJ De Veer
- ML Mitchel
- MS Duthie
- MS Vincent
- MTM Roberts
- O Schulz
- P Kropf
- P Launois
- P Mukherjee
- P Tripathi
- R Medzhitov
- RW Leeden
- S Akira
- S Caielli
- S Dissanayake
- S Kar
- S Karmakar
- S Maruo
- S Sundar
- Siddhartha Kumar Bhaumik
- SK Bhaumik
- SK Bhaumik
- Subir Karmakar
- T De-Majumdar
- Tripti De
- U Schleicher
- Y Campos-Martin
- Publication venue
- Public Library of Science
- Publication date
- 01/01/2012
- Field of study
NKT cells play an important role in autoimmune diseases, tumor surveillance, and infectious diseases, providing in most cases protection against infection. NKT cells are reactive to CD1d presented glycolipid antigens. They can modulate immune responses by promoting the secretion of type 1, type 2, or immune regulatory cytokines. Pathogen-derived signals to dendritic cells mediated via Toll like Receptors (TLR) can be modulated by activated invariant Natural Killer T (iNKT) cells. The terminal β-(1–4)-galactose residues of glycans can modulate host responsiveness in a T helper type-1 direction via IFN-γ and TLRs. We have attempted to develop a defined immunotherapeutic, based on the cooperative action of a TLR ligand and iNKT cell using a mouse model of visceral leishmaniasis. We evaluated the anti-Leishmania immune responses and the protective efficacy of the β-(1–4)-galactose terminal NKT cell ligand glycosphingophospholipid (GSPL) antigen of L. donovani parasites. Our results suggest that TLR4 can function as an upstream sensor for GSPL and provoke intracellular inflammatory signaling necessary for parasite killing. Treatment with GSPL was able to induce a strong effective T cell response that contributed to effective control of acute parasite burden and led to undetectable parasite persistence in the infected animals. These studies for the first time demonstrate the interactions between a TLR ligand and iNKT cell activation in visceral leishmaniasis immunotherapeutic
Deducing the Temporal Order of Cofactor Function in Ligand-Regulated Gene Transcription: Theory and Experimental Verification
- Author
- Carson C. Chow
- Chunhua Guo
- CK Glass
- CL Newton
- D Szapary
- DA Gilchrist
- DH Price
- DM Lonard
- Edward J. Dougherty
- F Sauve
- FD Karim
- HM Reichardt
- I Rogatsky
- JD Chen
- JN Loeb
- JS Carroll
- KM Ong
- L Nagy
- L Xu
- L-N Song
- M Luo
- MG Rosenfeld
- Michael Schubert
- NJ Fuda
- NJ McKenna
- NJ Sarlis
- O Babur
- O Hakim
- OI Vivar
- P Ordentlich
- Q Wang
- R Metivier
- S Chooniedass-Kothari
- S John
- S John
- S Karmakar
- S Kaul
- S-M Huang
- S. Stoney Simons
- SC Wu
- SS Simons Jr
- T Kenakin
- W Chen
- Y He
- Y He
- Publication venue
- Public Library of Science
- Publication date
- 01/01/2012
- Field of study
Cofactors are intimately involved in steroid-regulated gene expression. Two critical questions are (1) the steps at which cofactors exert their biological activities and (2) the nature of that activity. Here we show that a new mathematical theory of steroid hormone action can be used to deduce the kinetic properties and reaction sequence position for the functioning of any two cofactors relative to a concentration limiting step (CLS) and to each other. The predictions of the theory, which can be applied using graphical methods similar to those of enzyme kinetics, are validated by obtaining internally consistent data for pair-wise analyses of three cofactors (TIF2, sSMRT, and NCoR) in U2OS cells. The analysis of TIF2 and sSMRT actions on GR-induction of an endogenous gene gave results identical to those with an exogenous reporter. Thus new tools to determine previously unobtainable information about the nature and position of cofactor action in any process displaying first-order Hill plot kinetics are now available
Autism Spectrum disorders (ASD) in South Asia: a systematic review
- Author
- A Kumar
- A Tareen
- Afzal Aftab
- AJ Baxter
- D Moher
- D Silberberg
- Developmental Disabilities Monitoring Network Surveillance Year and Principal Investigators
- DM Bassa
- EU Syed
- Golam Rabbani
- H Perera
- Helal Uddin Ahmed
- Imran Ahmed Chowdhury
- JG Williams
- JP Vandenbroucke
- KN Chowdhury
- L Wing
- M Al-Mendalawi
- M Elsabbagh
- M Juneja
- M M Jalal Uddin
- M Tomlinson
- Malabika Sarker
- MD Hossain
- MG Rabbani
- MM Rahman
- Mohammad Didar Hossain
- Mohd S Iqbal
- MSI Mullick
- N Imran
- N Imran
- N Mishra
- Nepal Government
- P Karmakar
- P Singhi
- Pran Gopal Datta
- Razin Iqbal Kabir
- S Chakraborty
- S Raina
- S Vakil
- SA Poovathinal
- Saima Wazed Hossain
- SM Ahmed
- SS Zaman
- TC Daley
- V Kalra
- Waziul Alam Chowdhury
- X Sun
- Publication venue
- 'Springer Science and Business Media LLC'
- Publication date
- Field of study
A Research Agenda for Helminth Diseases of Humans: Intervention for Control and Elimination
- Author
- A Alum
- A Diawara
- A Diawara
- A Garba
- A Garba
- A Gazzinelli
- A Lespine
- AA Da'dara
- AC Clements
- AC Clements
- AJ Wolstenholme
- AP Plaisier
- B Sripa
- B Sripa
- B Sripa
- Banchob Sripa
- BE Slatko
- BL Blagburn
- Boakye A. Boatin
- C Bourguinat
- C Bourguinat
- C Bourguinat
- C Bourguinat
- C Mackenzie
- CA Maxwell
- CF Curtis
- CF Curtis
- CF Curtis
- D Kerboeuf
- D Knox
- DB Lu
- DG Addiss
- DH Molyneux
- DJ Gray
- DJ Gray
- DJ Tisch
- DM Leathwick
- E Assana
- E Assana
- E Assana
- E Michael
- EA Ottesen
- EA Ottesen
- G Ahmad
- G Stepek
- G von Samson-Himmelstjerna
- GC Coles
- Guo-Jing Yang
- H Yuan
- HH Garcia
- HH Garcia
- HH Garcia
- HH Garcia
- HL Guyatt
- HL Smits
- HW Wu
- Héctor H. García
- I Fairweather
- IP Sunish
- J Keiser
- J Keiser
- J Keiser
- J Keiser
- J Utzinger
- J Utzinger
- J Utzinger
- J Vercruysse
- JA van Wyk
- James S. McCarthy
- JC Vieira
- JH Kolaczinski
- JKL Eng
- JM Bethony
- JM Hougard
- JS McCarthy
- JW Rudge
- JW Rudge
- K Ghosh
- KA Lindblade
- KD Ramaiah
- KD Ramaiah
- KD Ramaiah
- L Diawara
- L Tritten
- M Boussinesq
- M Kasný
- M Parker
- MA Rodríguez-Pérez
- MA Rodríguez-Pérez
- MA Rodríguez-Pérez
- María-Gloria Basáñez
- MD French
- ME Murdoch
- MG Basáñez
- MG Basáñez
- MJ Doenhoff
- ML Eberhard
- ML Eberhard
- ML Mottier
- MO Harhay
- MW Lightowlers
- MY Osei-Atweneboana
- NB Kabatereine
- P Olliaro
- P Steinmann
- PJ Hotez
- PJ Hotez
- PJ Hotez
- PJ Hotez
- PJ Martin
- PR Karmakar
- R Bergquist
- R Cobb
- R Ndyomugyenyi
- R Penzer
- RE Blanton
- RJ Dobson
- RM Lima
- RM Ramzy
- Roger K. Prichard
- S Brooker
- S Brooker
- S Chanteau
- S Lustigman
- S Lustigman
- S Lustigman
- S Riley
- S Touré
- S Wanji
- Sara Lustigman
- Simon Brooker
- ST Hong
- T Fürst
- T Huyse
- TG Geary
- TS Churcher
- TS Churcher
- U Duthaler
- V Dixit
- VA Hampshire
- W Zhang
- WJ Blackhall
- Y Hu
- Y Hu
- Y Zhang
- YH Liu
- Publication venue
- Public Library of Science
- Publication date
- 01/04/2012
- Field of study
Recognising the burden helminth infections impose on human populations, and particularly the poor, major intervention programmes have been launched to control onchocerciasis, lymphatic filariasis, soil-transmitted helminthiases, schistosomiasis, and cysticercosis. The Disease Reference Group on Helminth Infections (DRG4), established in 2009 by the Special Programme for Research and Training in Tropical Diseases (TDR), was given the mandate to review helminthiases research and identify research priorities and gaps. A summary of current helminth control initiatives is presented and available tools are described. Most of these programmes are highly dependent on mass drug administration (MDA) of anthelmintic drugs (donated or available at low cost) and require annual or biannual treatment of large numbers of at-risk populations, over prolonged periods of time. The continuation of prolonged MDA with a limited number of anthelmintics greatly increases the probability that drug resistance will develop, which would raise serious problems for continuation of control and the achievement of elimination. Most initiatives have focussed on a single type of helminth infection, but recognition of co-endemicity and polyparasitism is leading to more integration of control. An understanding of the implications of control integration for implementation, treatment coverage, combination of pharmaceuticals, and monitoring is needed. To achieve the goals of morbidity reduction or elimination of infection, novel tools need to be developed, including more efficacious drugs, vaccines, and/or antivectorial agents, new diagnostics for infection and assessment of drug efficacy, and markers for possible anthelmintic resistance. In addition, there is a need for the development of new formulations of some existing anthelmintics (e.g., paediatric formulations). To achieve ultimate elimination of helminth parasites, treatments for the above mentioned helminthiases, and for taeniasis and food-borne trematodiases, will need to be integrated with monitoring, education, sanitation, access to health services, and where appropriate, vector control or reduction of the parasite reservoir in alternative hosts. Based on an analysis of current knowledge gaps and identification of priorities, a research and development agenda for intervention tools considered necessary for control and elimination of human helminthiases is presented, and the challenges to be confronted are discussed
Regulation of immunity during visceral Leishmania infection
- Author
- A Caldas
- A Campos-Neto
- A Cope
- A Gallimore
- A Hammami
- A Maroof
- A Maroof
- A Nieto
- A Schietinger
- AC Ghose
- AC Stanley
- AC Stanley
- AJ Zajac
- AM Mangoud
- Anabela Cordeiro-da-Silva
- AP Freitas do Rosario
- B Galvao-Castro
- BM Owens
- BN Thomas
- BT Edelson
- BT Edelson
- C Trez De
- C Zaph
- CR Engwerda
- CR Engwerda
- CR Engwerda
- CR Engwerda
- CR Engwerda
- CR Engwerda
- D Jankovic
- D Nandan
- DA Vignali
- DL Sacks
- DR Faria
- E Cillari
- EJ Wherry
- EJ Wherry
- EM Carvalho
- F Chappuis
- F Real
- F Robert-Gangneux
- F Woelbing
- FO Novais
- G Arango Duque
- G Matlashewski
- GD Victora
- GR Cooper
- H Aslan
- HT Jin
- HT Jin
- HW Murray
- HW Murray
- HW Murray
- HW Murray
- HW Murray
- HW Murray
- HW Murray
- HW Murray
- HW Murray
- I Muller
- I Muller
- I Vouldoukis
- J Alvar
- J Chavas
- J Griensven van
- J Lehmann
- J Zhu
- JE Dalton
- JG Cyster
- JJ Stern
- JL Amprey
- JP Gigley
- JS Cervia
- JS Yi
- JW Moore
- Jérôme Estaquier
- K Ghosh
- KE Squires
- KJ Esch
- KN Gibson-Corley
- KN Gibson-Corley
- L Beattie
- L Beattie
- L Beattie
- LE Rosas
- LE Rosas
- LE Smith
- LU Buxbaum
- M Ato
- M Barral-Netto
- M Guilliams
- M Olivier
- M Resende
- M Saraiva
- M Svensson
- M Svensson
- MA Nolte
- MC Cumont
- MC Tumang
- ME Wilson
- ME Wilson
- MG Pitta
- Mireille Laforge
- MJ McElrath
- ML Murphy
- ML Murphy
- MM Kane
- MS Nascimento
- N Rolao
- N Santarem
- NA Ansari
- NA Gomes
- ND Glennie
- OP Singh
- OP Singh
- P Gallo
- P Kaye
- P Tsagozis
- P Tsagozis
- P Yurdakul
- PA Kager
- PM Gorak
- PM Kaye
- PT Bunn
- R Badaro
- R Bankoti
- R Kumar
- R Phillips
- R Polley
- R Polley
- R Polley
- R Porrozzi
- RD Pearson
- RE Mebius
- Ricardo Silvestre
- RJ Faleiro
- RT Kenney
- S Bhattacharyya
- S Crotty
- S Gautam
- S Gautam
- S Honore
- S Ito
- S Karmakar
- S Kaur
- S Lopez Kostka
- S Nakayamada
- S Nylen
- S Nylen
- S Oghumu
- S Santos Cda
- S Stager
- S Stager
- SA Costa Lima
- SA Miles
- SC Smelt
- SC Smelt
- SE Cotterell
- SL Colpitts
- SM Kaech
- T Joshi
- V Diniz-Atayde
- V Leclercq
- V Peruhype-Magalhaes
- V Rodrigues
- Vasco Rodrigues
- VL Matta da
- W Ouyang
- WE Agu
- WG Shreffler
- Y Belkaid
- Publication venue
- 'Springer Science and Business Media LLC'
- Publication date
- 01/01/2016
- Field of study
Unicellular eukaryotes of the genus Leishmania are collectively responsible for a heterogeneous group of diseases known as leishmaniasis. The visceral form of leishmaniasis, caused by L. donovani or L. infantum, is a devastating condition, claiming 20,000 to 40,000 lives annually, with particular incidence in some of the poorest regions of the world. Immunity to Leishmania depends on the development of protective type I immune responses capable of activating infected phagocytes to kill intracellular amastigotes. However, despite the induction of protective responses, disease progresses due to a multitude of factors that impede an optimal response. These include the action of suppressive cytokines, exhaustion of specific T cells, loss of lymphoid tissue architecture and a defective humoral response. We will review how these responses are orchestrated during the course of infection, including both early and chronic stages, focusing on the spleen and the liver, which are the main target organs of visceral Leishmania in the host. A comprehensive understanding of the immune events that occur during visceral Leishmania infection is crucial for the implementation of immunotherapeutic approaches that complement the current anti-Leishmania chemotherapy and the development of effective vaccines to prevent disease.The research leading to these results has received funding from the European Community’s Seventh Framework Programme under grant agreement No.602773 (Project KINDRED). VR is supported by a post-doctoral fellowship granted by the KINDReD consortium. RS thanks the Foundation for Science and Technology (FCT) for an Investigator Grant (IF/00021/2014). This work was supported by grants to JE from ANR (LEISH-APO, France), Partenariat Hubert Curien (PHC) (program Volubilis, MA/11/262). JE acknowledges the support of the Canada Research Chair Program
Parameterization of a coarse-grained model of cholesterol with point-dipole electrostatics
- Author
- A Filippov
- A Filippov
- A Grossfield
- A Kessel
- A-L Kuo
- AI Jewett
- AM Smondyrev
- AM Smondyrev
- C Arnarez
- C Cecchi
- C Díaz-Tejada
- C Gliss
- C Hofsäß
- C Laing
- C Rosetti
- CJ Dickson
- D Hakobyan
- D Marsh
- D Papahadjopoulos
- D Reith
- D Scherfeld
- D Tang
- DA Brown
- DG Ackerman
- DH Jong de
- DJ Price
- E Darve
- E Falck
- E Falck
- E London
- E London
- E Sackmann
- F Liu
- F Meyer de
- F Ogushi
- FJM Meyer de
- G Khelashvili
- G Lindblom
- G Lindblom
- G Orädd
- G Szabo
- G Voronoï
- GA Khelashvili
- GW Stockton
- H Flyvbjerg
- H Khandelia
- H Scott
- H Shen
- H. Khandelia
- HA Scheidt
- HJ Berendsen
- HJ Pownall
- J Comer
- J Henin
- J Huang
- J Huang
- J Hénin
- J Nagle
- J Owicki
- J Taylor
- J Uusitalo
- J Virtanen
- J-M Frédérick
- JB Klauda
- JB Lim
- JC Lawrence
- JC Phillips
- JD Perlmutter
- JH Ipsen
- JJ Uusitalo
- JJ Uusitalo
- JR Silvius
- K Hadley
- K Hadley
- K Simons
- K Tanaka
- K Tu
- L Darré
- L Miao
- L Zhuang
- L. G. Dias
- M Alwarawrah
- M Ferraro
- M Grunze
- M Ndao
- M Orsi
- M Orsi
- M Orsi
- M Orsi
- M Pasenkiewicz-Gierula
- M Zuckermann
- M. Orsi
- MC Pitman
- MD Daily
- MG Taylor
- ML Berkowitz
- ML Frazier
- MP Allen
- MR Vist
- N Gershfeld
- N Kahya
- N Kučerka
- NM Hooper
- O Berger
- O Edholm
- P Chong
- P Jedlovszky
- P Siani
- P Wydro
- P. Siani
- PF Almeida
- PF Almeida
- PF Renshaw
- PJ Somerharju
- PS Schmalhorst
- Q Ma
- Q Waheed
- R Guixà-González
- R Long
- R Murari
- RF Almeida De
- RS Davis
- S Chiu
- S Chiu
- S Genheden
- S Genheden
- S Genheden
- S Genheden
- S Genheden
- S Izvekov
- S Izvekov
- S Jo
- S Jo
- S Karmakar
- S Miyamoto
- S Nawaz
- S Plimpton
- SA Pandit
- SJ Marrink
- SJ Marrink
- SL Duncan
- T Darden
- T Murtola
- T Murtola
- T Murtola
- T Róg
- T Róg
- TC Moore
- TM Ferreira
- TP McMullen
- U Essmann
- VV Chaban
- W Humphrey
- W Kleemann
- W Vaz
- W-C Hung
- WD Bennett
- WG Wood
- WL Dunn
- X Wang
- Y Wang
- Y Zhang
- Y Zhang
- Z Cournia
- Publication venue
- 'Springer Science and Business Media LLC'
- Publication date
- 01/01/2018
- Field of study
© 2018, Springer Nature Switzerland AG. We present a new coarse-grained (CG) model of cholesterol (CHOL) for the electrostatic-based ELBA force field. A distinguishing feature of our CHOL model is that the electrostatics is modeled by an explicit point dipole which interacts through an ideal vacuum permittivity. The CHOL model parameters were optimized in a systematic fashion, reproducing the electrostatic and nonpolar partitioning free energies of CHOL in lipid/water mixtures predicted by full-detailed atomistic molecular dynamics simulations. The CHOL model has been validated by comparison to structural, dynamic and thermodynamic properties with experimental and atomistic simulation reference data. The simulation of binary DPPC/cholesterol mixtures covering the relevant biological content of CHOL in mammalian membranes is shown to correctly predict the main lipid behavior as observed experimentally
Search for strongly interacting massive particles generating trackless jets in proton-proton collisions at s = 13 TeV
- Author
- Aarrestad TK
- Aarup Petersen H
- Abbaneo D
- Abbiendi G
- Abbrescia M
- Abdullin S
- Abercrombie D
- Acharya H
- Acosta D
- Acosta JG
- Adam W
- Adams E
- Adams MR
- Adams T
- Adloff C
- Adzic P
- Agapitos A
- Agarwal G
- Aggleton R
- Agram J-L
- Aguilar-Benitez M
- Ahmad A
- Ahmad M
- Ahmed A
- Ahuja S
- Aime C
- Akchurin N
- Akgun B
- Akpinar A
- Albajar C
- Albergo S
- Albert A
- Albrow M
- Alcaraz Maestre J
- Aldaya Martin M
- Aldá Júnior WL
- Aleksandrov A
- Alexander J
- Alhusseini M
- Alimena J
- Alison J
- Allen B
- Almond J
- Alvarez Gonzalez B
- Alverson G
- Alves GA
- Aly R
- Alyari M
- Amapane N
- Amendola C
- Amin N
- Amram O
- Amsler C
- Anagnostou G
- Andrea J
- Andreev V
- Andreev Y
- Andrews MB
- Androsov K
- Antchev G
- Antunovic Z
- Apanasevich L
- Apollinari G
- Appelt E
- Apresyan A
- Apyan A
- Araujo M
- Arcaro D
- Arcidiacono R
- Arenton MW
- Argiro S
- Arneodo M
- Aruta C
- Asavapibhop B
- Asawatangtrakuldee C
- Asenov P
- Asghar MI
- Asilar E
- Askew A
- Asmuss P
- Aspell P
- Atakisi IO
- Atanassov I
- Ather MW
- Attikis A
- Auffray E
- Aushev T
- Auzinger G
- Avati V
- Avery P
- Avila C
- Awais A
- Awan MIM
- Ayala E
- Ayala G
- Aydogmus Sen F
- Azarkin M
- Azhgirey I
- Aziz T
- Azzi P
- Azzurri P
- Baarmand MM
- Babaev A
- Babounikau I
- Bacchetta N
- Bachiller I
- Bachtis M
- Backhaus M
- Baden A
- Baechler J
- Baginyan A
- Bagliesi G
- Bahinipati S
- Baillon P
- Bainbridge R
- Bakas G
- Bakhshiansohi H
- Bakirci MN
- Baldenegro Barrera C
- Ball AH
- Ban Y
- Band R
- Bandyopadhyay H
- Banerjee S
- Banerjee S
- Bansal S
- Barbagli G
- Barberis E
- Bargassa P
- Baringer P
- Barnes VE
- Barney D
- Baron O
- Barrio Luna M
- Bartek R
- Bartosik N
- Bartók M
- Bastos D
- Battilana C
- Baty A
- Bauer G
- Bauerdick LAT
- Baxter S
- Bayshev I
- Bean A
- Beauceron S
- Beaudette F
- Becerril Gonzalez H
- Bechtel J
- Bedoya CF
- Beghin D
- Behera PK
- Behera SC
- Behnke O
- Bein S
- Belchior Batista Das Chagas E
- Belforte S
- Bell KW
- Bellan R
- Belloni A
- Bellora A
- Belyaev A
- Belyaev A
- Benaglia A
- Benato L
- Bencze G
- Bendavid J
- Benecke A
- Benelli G
- Beni N
- Benitez JF
- Benussi L
- Berardi V
- Berenguer Antequera J
- Beretvas A
- Bergauer T
- Berger P
- Berger T
- Beri SB
- Bermúdez Martínez A
- Bernardes CA
- Bernet C
- Berretti M
- Berry D
- Berryhill J
- Bertacchi V
- Besancon M
- Beschi A
- Bhal E
- Bhardwaj A
- Bharti M
- Bhat MA
- Bhat PC
- Bhatnagar V
- Bhattacharya R
- Bhattacharya S
- Bhattacharya S
- Bhattacharya S
- Bheesette S
- Bhowmik D
- Bhowmik S
- Bhyun JH
- Bi R
- Bialkowska H
- Bianchini L
- Bianco M
- Bianco S
- Biasini M
- Biino C
- Bilei GM
- Bilin B
- Bin Anuar AA
- Bisello D
- Black K
- Blekman F
- Blinov V
- Bloch D
- Bloch P
- Bloom K
- Bluj M
- Blumenfeld B
- Boccali T
- Bocci A
- Bodek A
- Boimska B
- Boletti A
- Bologna S
- Bols ES
- Bonacorsi D
- Bonanomi M
- Bonham B
- Bonomally S
- Boos E
- Boran F
- Borchsh V
- Borg J
- Borgonovi L
- Bornheim A
- Borras K
- Bortignon P
- Bose T
- Bossini E
- Botta C
- Botta V
- Bottigli U
- Boudoul G
- Bouhali O
- Bourgatte G
- Bourilkov D
- Bozzo M
- Bragagnolo A
- Braghieri A
- Braibant-Giacomelli S
- Brainerd C
- Brandao Malbouisson H
- Brandt S
- Branson JG
- Breedon R
- Breeze S
- Brew C
- Brigljevic V
- Brinkerhoff A
- Brivio F
- Brochero Cifuentes JA
- Brom J-M
- Brondolin E
- Brooke JJ
- Brown RM
- Brunner D
- Bruno G
- Brzhechko D
- Brücken E
- Bucci R
- Buccilli A
- Buchanan J
- Buchmuller O
- Buchot Perraguin A
- Bueghly J
- Bundock A
- Bunkowski K
- Buontempo S
- Burkett K
- Burkhardt H
- Burkle B
- Burt K
- Bury F
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- Butler PH
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- Bylinkin A
- Bylsma B
- Cabrera A
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- Capeans Garrido M
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- Carrillo Moreno S
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- Castaneda Hernandez A
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- Cheng T
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- Chernyavskaya N
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- Cipriani M
- Ciriolo V
- Cirkovic P
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- Cittolin S
- Ciulli V
- Civinini C
- Claes DR
- Clare R
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- Clerbaux B
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- Connor P
- Consuegra Rodríguez S
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- Cranshaw DJ
- Creanza D
- Cremonesi M
- Cristella L
- Csanád M
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- Darwish MR
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- De Boer W
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- De Iorio A
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- De La Cruz-Burelo E
- De Lentdecker G
- De Leo K
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- De Trocóniz JF
- De Wit A
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- Deelen N
- Defranchis MM
- Deile M
- Dejardin M
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- Del Re D
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- Delannoy AG
- Delcourt M
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- Dell'Orso R
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- Demina R
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- Denegri D
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- Dermenev A
- Dev N
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- Dezoort G
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- Di Maria R
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- Diamantopoulou M
- Diaz D
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- Dutta D
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- Ecklund KM
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- Elvira VD
- Eminizer M
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- Errico F
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- Eusebi R
- Evangelou I
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- Ivanchenko V
- Ivanov A
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- Özçelik Ö
- Široký J
- Publication venue
- 'Springer Science and Business Media LLC'
- Publication date
- 01/01/2022
- Field of study
A search for dark matter in the form of strongly interacting massive particles (SIMPs) using the CMS detector at the LHC is presented. The SIMPs would be produced in pairs that manifest themselves as pairs of jets without tracks. The energy fraction of jets carried by charged particles is used as a key discriminator to suppress efficiently the large multijet background, and the remaining background is estimated directly from data. The search is performed using proton-proton collision data corresponding to an integrated luminosity of 16.1 fb - 1 , collected with the CMS detector in 2016. No significant excess of events is observed above the expected background. For the simplified dark matter model under consideration, SIMPs with masses up to 100 GeV are excluded and further sensitivity is explored towards higher masses
Guidelines for the use and interpretation of assays for monitoring autophagy (4th edition)1.
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- Abdel-Aziz AK
- Abdelfatah S
- Abdellatif M
- Abdoli A
- Abel S
- Abeliovich H
- Abildgaard MH
- Abudu YP
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- Agostinis P
- Agrewala JN
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- Aguilar PV
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- Ahmed ZM
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- Akoumianaki T
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- Zimmermann CM
- Ziviani E
- Zoladek T
- Zong W-X
- Zorov DB
- Zorzano A
- Zou W
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- Zuryn S
- Zwerschke W
- Álvarez ÉMC
- Ávalos Y
- Önal G
- Üstün S
- Čolić M
- Đokić J
- Žerovnik E
- Publication venue
- 'Informa UK Limited'
- Publication date
- 01/01/2021
- Field of study
In 2008, we published the first set of guidelines for standardizing research in autophagy. Since then, this topic has received increasing attention, and many scientists have entered the field. Our knowledge base and relevant new technologies have also been expanding. Thus, it is important to formulate on a regular basis updated guidelines for monitoring autophagy in different organisms. Despite numerous reviews, there continues to be confusion regarding acceptable methods to evaluate autophagy, especially in multicellular eukaryotes. Here, we present a set of guidelines for investigators to select and interpret methods to examine autophagy and related processes, and for reviewers to provide realistic and reasonable critiques of reports that are focused on these processes. These guidelines are not meant to be a dogmatic set of rules, because the appropriateness of any assay largely depends on the question being asked and the system being used. Moreover, no individual assay is perfect for every situation, calling for the use of multiple techniques to properly monitor autophagy in each experimental setting. Finally, several core components of the autophagy machinery have been implicated in distinct autophagic processes (canonical and noncanonical autophagy), implying that genetic approaches to block autophagy should rely on targeting two or more autophagy-related genes that ideally participate in distinct steps of the pathway. Along similar lines, because multiple proteins involved in autophagy also regulate other cellular pathways including apoptosis, not all of them can be used as a specific marker for bona fide autophagic responses. Here, we critically discuss current methods of assessing autophagy and the information they can, or cannot, provide. Our ultimate goal is to encourage intellectual and technical innovation in the field
Evidence for Top Quark Production in Nucleus-Nucleus Collisions
- Author
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- Aarup Petersen H
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- Abbiendi G
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- Zuolo D
- Zygala L
- Álvarez Fernández A
- Özçelik Ö
- Publication venue
- Publication date
- 01/01/2019
- Field of study
Peer reviewe
Search for dark matter produced in association with a Higgs boson decaying to a pair of bottom quarks in proton-proton collisions at root s=13TeV
- Author
- Aarrestad TK
- Abbaneo D
- Abbiendi G
- Abbrescia M
- Abdullah WATW
- Abdullin S
- Abercrombie D
- Acharya H
- Acosta D
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- Wisecarver A
- Wissing C
- Wittich P
- Wolf M
- Wolf R
- Wolfe E
- Wong K
- Wong WY
- Wood D
- Woodard A
- Wozniak KA
- Wozniewski S
- Wright D
- Wu Z
- Wuchterl S
- Wulz C-E
- Wuyckens S
- Wyslouch B
- Würthwein F
- Xia F
- Xiao J
- Xiao M
- Xiao R
- Xie S
- Xie W
- Yagil A
- Yalvac M
- Yan F
- Yang UK
- Yang YC
- Yao Y
- Yarar H
- Yates BR
- Yazgan E
- Yetkin EA
- Yi K
- Yohay R
- Yoo HD
- Yoo J
- Yoon I
- You Z
- Yu D
- Yu GB
- Yu I
- Yu SS
- Yuan L
- Yuan S
- Yumiceva F
- Yusli MN
- Yzquierdo AP-C
- Zabi A
- Zacharopoulou A
- Zahid S
- Zaleski S
- Zalewski P
- Zanetti M
- Zarubin A
- Zarucki M
- Zecchinelli AG
- Zenaiev O
- Zeuner WD
- Zghiche A
- Zhang F
- Zhang H
- Zhang J
- Zhang S
- Zhang W
- Zhang Y
- Zhang Z
- Zhao J
- Zhizhin I
- Zhokin A
- Zhu DH
- Zhu RY
- Ziemons T
- Zientek M
- Zlebcik R
- Zobec J
- Zoi I
- Zolkapli Z
- Zorbakir IS
- Zorbilmez C
- Zotto P
- Zou D
- Zucchetta A
- Zumerle G
- Zuo X
- Zuolo D
- Zygala L
- Álvarez CR
- Özçelik Ö
- Publication venue
- Publication date
- 01/01/2018
- Field of study
A search for dark matter produced in association with a Higgs boson decaying to a pair of bottom quarks is performed in proton-proton collisions at a center-of-mass energy of 13 TeV collected with the CMS detector at the LHC. The analyzed data sample corresponds to an integrated luminosity of 35.9 fb(-1). The signal is characterized by a large missing transverse momentum recoiling against a bottom quark-antiquark system that has a large Lorentz boost. The number of events observed in the data is consistent with the standard model background prediction. Results are interpreted in terms of limits both on parameters of the type-2 two-Higgs doublet model extended by an additional light pseudoscalar boson a (2HDM+a) and on parameters of a baryonic Z simplified model. The 2HDM+a model is tested experimentally for the first time. For the baryonic Z model, the presented results constitute the most stringent constraints to date.Peer reviewe
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