檢索結果 - Andrew Keniry
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A Comprehensive Survey of Single Nucleotide Polymorphisms (SNPs) across <i>Mycobacterium bovis</i> Strains and <i>M. bovis</i> BCG Vaccine Strains Refines the Genealogy and Defines... 由 M. Carmen Garcia Pelayo, Swapna Uplekar, Andrew Keniry, Pablo Mendoza Lopez, Thierry Garnier, Javier Nuñez Garcia, Laura Boschiroli, Xiangmei Zhou, Julian Parkhill, Noel H. Smith, R. Glyn Hewinson, Stewart T. Cole, Stephen V. Gordon
出版 2009Artigo -
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Suv39h-catalyzed H3K9me3 is critical for euchromatic genome organization and the maintenance of gene transcription 由 Christine R. Keenan, Hannah D. Coughlan, Nadia Iannarella, Andrés Tapia del Fierro, Andrew Keniry, Timothy M. Johanson, Wing Fuk Chan, Alexandra L. Garnham, Lachlan Whitehead, Marnie E. Blewitt, Gordon K. Smyth, Rhys S. Allan
出版 2024Artigo -
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Jarid2 regulates hematopoietic stem cell function by acting with polycomb repressive complex 2 由 Sarah Kinkel, Roman Galeev, Christoffer Flensburg, Andrew Keniry, Kelsey Breslin, Omer Gilan, Stanley Chun-Wei Lee, Joy Liu, Kelan Chen, Linden J. Gearing, Darcy Moore, Warren S. Alexander, Mark A. Dawson, Ian J. Majewski, Alicia Oshlack, Jonas Larsson, Marnie E. Blewitt
出版 2015Artigo -
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Genetic and environmental factors determining clinical outcomes and cost of warfarin therapy: a prospective study 由 Andrea Jorgensen, Sameh Alzubiedi, Jieying Eunice Zhang, Andrew Keniry, Anita Hanson, Dyfrig Hughes, Diane Van Eker, Lisa Stevens, Karen Hawkins, Cheng‐Hong Toh, Farhad Kamali, Ann K. Daly, David Fitzmaurice, Alison J. Coffey, Paula Williamson, Brian Kevin Park, Panos Deloukas, Munir Pirmohamed
出版 2009Artigo -
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Smchd1 Targeting to the Inactive X Is Dependent on the Xist-HnrnpK-PRC1 Pathway 由 Natasha Jansz, Tatyana B. Nesterova, Andrew Keniry, Megan Iminitoff, Peter F. Hickey, Greta Pintacuda, Osamu Masui, Simon Kobelke, Niall D. Geoghegan, Kelsey Breslin, Tracy A. Willson, Kelly L. Rogers, Graham F. Kay, Archa H. Fox, Haruhiko Koseki, Neil Brockdorff, James M. Murphy, Marnie E. Blewitt
出版 2018Artigo -
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Setdb1-mediated H3K9 methylation is enriched on the inactive X and plays a role in its epigenetic silencing 由 Andrew Keniry, Linden J. Gearing, Natasha Jansz, Joy Liu, Aliaksei Z. Holik, Peter F. Hickey, Sarah Kinkel, Darcy Moore, Kelsey Breslin, Kelan Chen, Ruijie Liu, Catherine Phillips, Miha Pakusch, Christine Biben, Julie M. Sheridan, Benjamin T. Kile, Catherine Carmichael, Matthew E. Ritchie, Douglas J. Hilton, Marnie E. Blewitt
出版 2016Artigo -
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IL23R Variation Determines Susceptibility But Not Disease Phenotype in Inflammatory Bowel Disease 由 Mark Tremelling, Fraser Cummings, Sheila Fisher, John Mansfield, Rhian Gwilliam, Andrew Keniry, Elaine R. Nimmo, Hazel E. Drummond, Clive M. Onnie, Natalie J. Prescott, Jeremy Sanderson, Francesca Bredin, Carlo Berzuini, Alastair Forbes, Cathryn M. Lewis, Lon R. Cardon, Panos Deloukas, Derek P. Jewell, Christopher G. Mathew, Miles Parkes, Jack Satsangi
出版 2007Artigo -
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Genome-wide binding and mechanistic analyses of Smchd1-mediated epigenetic regulation 由 Kelan Chen, Jiang Hu, Darcy Moore, Ruijie Liu, Sarah A. Kessans, Kelsey Breslin, Isabelle S. Lucet, Andrew Keniry, Huei San Leong, Clare L. Parish, Douglas J. Hilton, Richard J.L.F. Lemmers, Silvère M. van der Maarel, Peter E. Czabotar, Renwick C. J. Dobson, Matthew E. Ritchie, Graham F. Kay, James M. Murphy, Marnie E. Blewitt
出版 2015Artigo -
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Unique properties of a subset of human pluripotent stem cells with high capacity for self-renewal 由 Kevin X. Lau, Elizabeth A. Mason, Joshua Kie, David P. De Souza, Joachim Kloehn, Dedreia Tull, Malcolm J. McConville, Andrew Keniry, Tamara Beck, Marnie E. Blewitt, Matthew E. Ritchie, Shalin H. Naik, Daniela Amann‐Zalcenstein, Othmar Korn, Shian Su, Irene Gallego Romero, Catrina Spruce, Christopher L. Baker, Tracy C. McGarr, Christine A. Wells, Martín F. Pera
出版 2020Artigo -
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Genetic determinants of ulcerative colitis include the ECM1 locus and five loci implicated in Crohn's disease 由 Sheila Fisher, Mark Tremelling, Carl A. Anderson, Rhian Gwilliam, Suzannah Bumpstead, Natalie J. Prescott, Elaine R. Nimmo, Dunecan Massey, Carlo Berzuini, C. Mark Johnson, Jeffrey C. Barrett, Fraser Cummings, Hazel E. Drummond, Charlie W. Lees, Clive M. Onnie, Catherine Hanson, Katarzyna Błaszczyk, Michael Inouye, Philip Ewels, Rathi Ravindrarajah, Andrew Keniry, Sarah Hunt, Martyn Carter, Nick Watkins, Willem H. Ouwehand, Cathryn M. Lewis, Lon R. Cardon, Alan Lobo, Alastair Forbes, Jeremy Sanderson, Derek P. Jewell, John Mansfield, Panos Deloukas, Christopher G. Mathew, Miles Parkes, Jack Satsangi
出版 2008Artigo -
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Repeated Replication and a Prospective Meta-Analysis of the Association Between Chromosome 9p21.3 and Coronary Artery Disease 由 Heribert Schunkert, Anika Götz, Peter S. Braund, Ralph McGinnis, David‐Alexandre Trégouët, Massimo Mangino, Patrick Linsel‐Nitschke, François Cambien, Christian Hengstenberg, Klaus Stark, Stefan Blankenberg, Laurence Tiret, Pierre Ducimetière, Andrew Keniry, Mohammed J. R. Ghori, Stefan Schreiber, Nour Eddine El Mokhtari, Alistair S. Hall, Richard J. Dixon, Alison H. Goodall, Henrike Liptau, Helen Perlstein Pollard, Dániel Schwarz, Ludwig A. Hothorn, H.‐Erich Wichmann, Inke R. König, Marcus Fischer, Christa Meisinger, Willem H. Ouwehand, Panos Deloukas, John R. Thompson, Jeanette Erdmann, Andreas Ziegler, Nilesh J. Samani
出版 2008Revisão -
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Common variants near MC4R are associated with fat mass, weight and risk of obesity 由 Ruth J. F. Loos, Cecilia M. Lindgren, Shengxu Li, Eleanor Wheeler, Jing Hua Zhao, Inga Prokopenko, Michael Inouye, Rachel M. Freathy, Antony Attwood, J. Beckmann, Sonja I Berndt, Sven Bergmann, Amanda J. Bennett, Sheila Bingham, Murielle Bochud, Matthew A. Brown, Stéphane Cauchi, John Connell, Cyrus Cooper, George Davey Smith, Ian N.M. Day, Christian Dina, Subhajyoti De, Emmanouil T. Dermitzakis, Alex S. F. Doney, Katherine S. Elliott, Paul Elliott, David M. Evans, I. Sadaf Farooqi, Philippe Froguel, Jilur Ghori, Christopher J. Groves, Rhian Gwilliam, David Hadley, Alistair S. Hall, Andrew T. Hattersley, Johannes Hebebrand, Iris M. Heid, Blanca Herrera, Anke Hinney, Sarah Hunt, Marjo‐Riitta Järvelin, Toby Johnson, Jennifer D M Jolley, Fredrik Karpe, Andrew Keniry, Kay-Tee Khaw, Robert Luben, Massimo Mangino, Jonathan Marchini, Wendy L. McArdle, Ralph McGinnis, Stephen Eyre, Patricia B. Munroe, Andrew D Morris, Andy Ness, Matthew Neville, Alexandra C. Nica, Ken K. Ong, Stephen O’Rahilly, Katharine R. Owen, Colin N. A. Palmer, Konstantinos A. Papadakis, Simon Potter, Anneli Pouta, Lu Qi, Joshua C. Randall, Nigel W. Rayner, Susan M. Ring, Manjinder S. Sandhu, André Scherag, Matthew Sims, Kijoung Song, Nicole Soranzo, Elizabeth K. Speliotes, Holly Syddall, Sarah A. Teichmann, Nicholas J. Timpson, Jonathan H. Tobias, Manuela Uda, Carla Ivane Ganz Vogel, Chris Wallace, Dawn Waterworth, Michael N. Weedon, Cristen J. Willer, Vicki Wraight, Xin Yuan, Eleftheria Zeggini, Joel N. Hirschhorn, David P. Strachan, Willem H. Ouwehand, Mark J. Caulfield, Nilesh J. Samani, Timothy M. Frayling, Péter Vollenweider, Gérard Waeber, Vincent Mooser, Panos Deloukas, Mark I. McCarthy, Nicholas J. Wareham
出版 2008Artigo
相關主題
Biology
Gene
Genetics
Cell biology
Genotype
Medicine
Epigenetics
Internal medicine
Single-nucleotide polymorphism
Chromatin
DNA methylation
Gene expression
Genome-wide association study
Allele
Computational biology
Gene silencing
Odds ratio
SNP
Bisulfite sequencing
Confidence interval
Crohn's disease
DNA sequencing
Disease
Embryonic stem cell
Genetic association
Haplotype
Immunology
Inflammatory bowel disease
Locus (genetics)
Methylation