Zobrazeno 1 - 10
of 60
pro vyhledávání: '"Helen Stevens"'
Autor:
Vincent Plagnol, Joanna M M Howson, Deborah J Smyth, Neil Walker, Jason P Hafler, Chris Wallace, Helen Stevens, Laura Jackson, Matthew J Simmonds, Type 1 Diabetes Genetics Consortium, Polly J Bingley, Stephen C Gough, John A Todd
Publikováno v:
PLoS Genetics, Vol 7, Iss 8, p e1002216 (2011)
The genetic basis of autoantibody production is largely unknown outside of associations located in the major histocompatibility complex (MHC) human leukocyte antigen (HLA) region. The aim of this study is the discovery of new genetic associations wit
Externí odkaz:
https://doaj.org/article/476544fd02664068abcb4c5a0a51170c
Autor:
Vincent Plagnol, Elif Uz, Chris Wallace, Helen Stevens, David Clayton, Tayfun Ozcelik, John A Todd
Publikováno v:
PLoS ONE, Vol 3, Iss 8, p e2966 (2008)
Lymphoblastoid cell lines (LCL) are being actively and extensively used to examine the expression of specific genes and genome-wide expression profiles, including allele specific expression assays. However, it has recently been shown that approximate
Externí odkaz:
https://doaj.org/article/eb2ec1a3a1f24a98a4e28eee1433ebfe
Autor:
Thomas W. Westerling Iii, David M. Goodman, Holly B. Laws, Rebecca Drill, Jack Beinashowitz, Helen Stevens, Shelby Ortega, Robert Drinkwater
Publikováno v:
Psychoanalytic Psychology. 36:73-81
Autor:
Chapy Venkatesan, Bahareh Aslani-Amoli, Steve J Motew, Sarah Stanmyre, J. Stephen Jones, Andrei Racila, Maria Stepanova, Stephanie Garofalo, Lynn H. Gerber, Erin Hodson, Zobair M. Younossi, Michael Homeyer, Andrej Kolacevski, David J. Allen, Linda Henry, Helen Stevens, John Paul Verderese, Brian Lam
Publikováno v:
Clinical Infectious Diseases: An Official Publication of the Infectious Diseases Society of America
Background Neutralizing monoclonal antibody (NmAb) treatments have received Emergency Use Authorization to treat patients with mild or moderate COVID-19 infection. To date, no real- world data on the efficacy of NmAbs have been reported from clinical
Autor:
M. Zarowiecki, A. Devereau, S.M. Wood, J. M. Boissiere, G. Elgar, Cara Forster, Liesbeth Keldermans, A. Sieghart, Allyn McConkie-Rosell, Augusto Rendon, S. R. Thompson, D. Polychronopoulos, Alexandre Arkader, Julien Thevenon, D. Kasperaviciute, Alma Kuechler, Bryan L. Krock, Dominique Martin-Coignard, Damian Smedley, T. Rahim, Barbara Mikat, Amber Begtrup, Priya Prasad, Lindsay B. Henderson, A. Stuckey, Mathilde Nizon, Tim Hubbard, I. U. S. Leong, M. Bleda, L. Lahnstein, C. E. H. Craig, Bertrand Isidor, Sarah Leigh, Joanne Mason, L. Moutsianas, T. Fowler, A. Siddiq, J. Pullinger, Marco Angelozzi, J. Ambrose, S. A. Watters, Saadet Mercimek-Andrews, K. Lawson, Claudia A. L. Ruivenkamp, Ian D. Krantz, J. E. Holman, Solveig Heide, Christel Depienne, Elizabeth T. DeChene, L. C. Daugherty, Alvaro Serrano Russi, Arianna Tucci, Mark J. Caulfield, Marie T. McDonald, Boris Keren, A. C. Need, Damara Ortiz, Nicola Foulds, William Spooner, Dara Tolchin, Eduardo Calpena, C. R. Boustred, Abdul Haseeb, Rudolf Gorazd, Charles Coutton, Alona Sosinsky, D. Perez-Gil, Sarah Stewart, J. M. Hackett, Giada Melistaccio, Andrew O.M. Wilkie, Radka Stoeva, Cédric Le Caignec, Pauline Le Tanno, Benjamin Cogné, Martina Mueller, Naghmeh Dorrani, Pedro Furió-Tarí, Gijs W. E. Santen, Hermann-Josef Lüdecke, Jessica P. Yeager, Julian A. Martinez-Agosto, Damien Haye, Kieran B. Pechter, Mohnish Suri, Livija Medne, M. J. Welland, Patrick Reed, K. Savage, G. C. Chan, Anne C.H. Tsai, F. Maleady-Crowe, A. de Burca, Ellen M. McDonagh, T. Rogers, F. Boardman-Pretty, Emily Lancaster, Katherine R. Smith, Christopher A. Odhams, Véronique Lefebvre, M. Ryten, Olivier Pichon, D. Halai, Aleš Maver, Christine Patch, R. E. Foulger, Frédéric Bilan, Helen Stevens, Hilde Van Esch, Eleanor Williams, Brigitte Gilbert-Dussardier, C. Tregidgo, K. Witkowska, F. J. Lopez, Gwenaël Le Guyader, Richard H Scott, M. Kayikci, Ellen Thomas, E. Walsh
Publikováno v:
American Journal of Human Genetics, 106(6), 830-845. CELL PRESS
Am J Hum Genet
Am J Hum Genet
SOX6 belongs to a family of 20 SRY-related HMG-box-containing (SOX) genes that encode transcription factors controlling cell fate and differentiation in many developmental and adult processes. For SOX6, these processes include, but are not limited to
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::25e4b2005e77addcf2aa011f8a987ba7
https://www.sciencedirect.com/science/article/pii/S0002929720301245?via=ihub
https://www.sciencedirect.com/science/article/pii/S0002929720301245?via=ihub
Autor:
Ed Oakley, David Levitt, Christine Brabyn, David Thomas, Libby Haskell, Franz E Babl, Meredith L Borland, Elizabeth Cotterell, Kam Sinn, Jocelyn Neutze, Janine Spencer, David Stuart Armstrong, Stuart R Dalziel, Paul A Bauert, Lydia Garside, Sharon O'Brien, Andreas Schibler, Helen Stevens, Michael Zhang, Nicola McKay
Publikováno v:
Journal of Paediatrics and Child Health. 55:42-53
AIM: Bronchiolitis is the most common lower respiratory tract disorder in infants aged less than 12 months, and research has demonstrated that there is substantial variation in practice patterns despite treatment being well defined. In order to align
Autor:
Sharon, O'Brien, Meredith L, Borland, Elizabeth, Cotterell, David, Armstrong, Franz, Babl, Paul, Bauert, Christine, Brabyn, Lydia, Garside, Libby, Haskell, David, Levitt, Nicola, McKay, Jocelyn, Neutze, Andreas, Schibler, Kam, Sinn, Janine, Spencer, Helen, Stevens, David, Thomas, Michael, Zhang, Ed, Oakley, Stuart R, Dalziel
Publikováno v:
Journal of paediatrics and child health. 55(1)
Bronchiolitis is the most common lower respiratory tract disorder in infants aged less than 12 months, and research has demonstrated that there is substantial variation in practice patterns despite treatment being well defined. In order to align and
Autor:
Kara Hunter, Sarah L Caddy, Marcin L. Pekalski, Jia Lu, Neil Walker, Ian Goodfellow, Deborah J. Smyth, Ben Challis, Linda S. Wicker, Ricardo C. Ferreira, Antony J. Cutler, John A. Todd, Helen Stevens, João J. Oliveira, Jane Kennet, Frank Waldron-Lynch
Publikováno v:
Wellcome Open Research
Background: The infection of a participant with norovirus during the adaptive study of interleukin-2 dose on regulatory T cells in type 1 diabetes (DILT1D) allowed a detailed insight into the cellular and cytokine immune responses to this prevalent g
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a98ccae176cb89cd87e82d6eec071fd3
https://www.repository.cam.ac.uk/handle/1810/265111
https://www.repository.cam.ac.uk/handle/1810/265111
Publikováno v:
Early human development. 108
Publikováno v:
Diabetic Medicine
Aims Owing to strong linkage disequilibrium between markers, pinpointing disease associations within genetic regions is difficult in European ancestral populations, most notably the very strong association of the HLA-DRB1*03-DQA1*05:01-DQB1*02:01 hap