Search Results - Shepherd, Rebecca 

Triiodothyronine (T3) Induces Limited Transcriptional and DNA Methylation Reprogramming in Human Monocytes by Shepherd, Rebecca, Kim, Bowon, Saffery, Richard, Novakovic, Boris

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G-CSF and AMD3100 mobilize monocytes into the blood that stimulate angiogenesis in vivo through a paracrine mechanism by Capoccia, Benjamin J., Shepherd, Rebecca M., Link, Daniel C.

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Sexual Dimorphism in Innate Immunity: The Role of Sex Hormones and Epigenetics by Shepherd, Rebecca, Cheung, Ada S., Pang, Ken, Saffery, Richard, Novakovic, Boris

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“Lessons from Rare Forms of Osteoarthritis” by Shepherd, Rebecca F., Kerns, Jemma G., Ranganath, Lakshminarayan R., Gallagher, James A., Taylor, Adam M.

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Angiogenic cells can be rapidly mobilized and efficiently harvested from the blood following treatment with AMD3100 by Shepherd, Rebecca M., Capoccia, Benjamin J., Devine, Steven M., DiPersio, John, Trinkaus, Kathryn M., Ingram, David, Link, Daniel C.

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A Potential Role for Epigenetically Mediated Trained Immunity in Food Allergy by Imran, Samira, Neeland, Melanie R., Shepherd, Rebecca, Messina, Nicole, Perrett, Kirsten P., Netea, Mihai G., Curtis, Nigel, Saffery, Richard, Novakovic, Boris

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Development of the Fearless, Tearless Transition model of care for adolescents with an intellectual disability and/or autism spectrum disorder with mental health comorbidities by Culnane, Evelyn, Loftus, Hayley, Efron, Daryl, Williams, Katrina, Di Iorio, Nikki, Shepherd, Rebecca, Marraffa, Catherine, Lubitz, Lionel, Antolovich, Giuliana, Prakash, Chidambaram

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Gender-affirming hormone therapy induces specific DNA methylation changes in blood by Shepherd, Rebecca, Bretherton, Ingrid, Pang, Ken, Mansell, Toby, Czajko, Anna, Kim, Bowon, Vlahos, Amanda, Zajac, Jeffrey D., Saffery, Richard, Cheung, Ada, Novakovic, Boris

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Project Score database: a resource for investigating cancer cell dependencies and prioritizing therapeutic targets by Dwane, Lisa, Behan, Fiona M, Gonçalves, Emanuel, Lightfoot, Howard, Yang, Wanjuan, van der Meer, Dieudonne, Shepherd, Rebecca, Pignatelli, Miguel, Iorio, Francesco, Garnett, Mathew J

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An IL-7-dependent rebound in thymic T cell output contributes to the bone loss induced by estrogen deficiency by Ryan, Michaela Robbie, Shepherd, Rebecca, Leavey, Jennifer K., Gao, Yuhao, Grassi, Francesco, Schnell, Frederick J., Qian, Wei-Ping, Kersh, Gilbert J., Weitzmann, M. Neale, Pacifici, Roberto

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Transcriptomic Remodelling of Fetal Endothelial Cells During Establishment of Inflammatory Memory by Weiss, Elisa, Vlahos, Amanda, Kim, Bowon, Wijegunasekara, Sachintha, Shanmuganathan, Dhanya, Aitken, Thomas, Joo, Ji-Hoon E., Imran, Samira, Shepherd, Rebecca, Craig, Jeffrey M., Green, Mark, Hiden, Ursula, Novakovic, Boris, Saffery, Richard

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COSMIC: mining complete cancer genomes in the Catalogue of Somatic Mutations in Cancer by Forbes, Simon A., Bindal, Nidhi, Bamford, Sally, Cole, Charlotte, Kok, Chai Yin, Beare, David, Jia, Mingming, Shepherd, Rebecca, Leung, Kenric, Menzies, Andrew, Teague, Jon W., Campbell, Peter J., Stratton, Michael R., Futreal, P. Andrew

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The mutational signature profile of known and suspected human carcinogens in mice by Riva, Laura, Pandiri, Arun R., Li, Yun Rose, Droop, Alastair, Hewinson, James, Quail, Michael A., Iyer, Vivek, Shepherd, Rebecca, Herbert, Ronald A., Campbell, Peter J., Sills, Robert C., Alexandrov, Ludmil B., Balmain, Allan, Adams, David J.

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Unsupervised correction of gene-independent cell responses to CRISPR-Cas9 targeting by Iorio, Francesco, Behan, Fiona M., Gonçalves, Emanuel, Bhosle, Shriram G., Chen, Elisabeth, Shepherd, Rebecca, Beaver, Charlotte, Ansari, Rizwan, Pooley, Rachel, Wilkinson, Piers, Harper, Sarah, Butler, Adam P., Stronach, Euan A., Saez-Rodriguez, Julio, Yusa, Kosuke, Garnett, Mathew J.

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Data mining using the Catalogue of Somatic Mutations in Cancer BioMart by Shepherd, Rebecca, Forbes, Simon A., Beare, David, Bamford, S., Cole, Charlotte G., Ward, Sari, Bindal, Nidhi, Gunasekaran, Prasad, Jia, Mingming, Kok, Chai Yin, Leung, Kenric, Menzies, Andrew, Butler, Adam P., Teague, Jon W., Campbell, Peter J., Stratton, Michael R., Futreal, P. Andrew

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Agreement between two large pan-cancer CRISPR-Cas9 gene dependency data sets by Dempster, Joshua M., Pacini, Clare, Pantel, Sasha, Behan, Fiona M., Green, Thomas, Krill-Burger, John, Beaver, Charlotte M., Younger, Scott T., Zhivich, Victor, Najgebauer, Hanna, Allen, Felicity, Gonçalves, Emanuel, Shepherd, Rebecca, Doench, John G., Yusa, Kosuke, Vazquez, Francisca, Parts, Leopold, Boehm, Jesse S., Golub, Todd R., Hahn, William C., Root, David E., Garnett, Mathew J., Tsherniak, Aviad, Iorio, Francesco

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Mutational signatures of ionizing radiation in second malignancies by Behjati, Sam, Gundem, Gunes, Wedge, David C., Roberts, Nicola D., Tarpey, Patrick S., Cooke, Susanna L., Van Loo, Peter, Alexandrov, Ludmil B., Ramakrishna, Manasa, Davies, Helen, Nik-Zainal, Serena, Hardy, Claire, Latimer, Calli, Raine, Keiran M., Stebbings, Lucy, Menzies, Andy, Jones, David, Shepherd, Rebecca, Butler, Adam P., Teague, Jon W., Jorgensen, Mette, Khatri, Bhavisha, Pillay, Nischalan, Shlien, Adam, Futreal, P. Andrew, Badie, Christophe, McDermott, Ultan, Bova, G. Steven, Richardson, Andrea L., Flanagan, Adrienne M., Stratton, Michael R., Campbell, Peter J.

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Mutations in ZDHHC9, Which Encodes a Palmitoyltransferase of NRAS and HRAS, Cause X-Linked Mental Retardation Associated with a Marfanoid Habitus by Raymond, F. Lucy, Tarpey, Patrick S., Edkins, Sarah, Tofts, Calli, O’Meara, Sarah, Teague, Jon, Butler, Adam, Stevens, Claire, Barthorpe, Syd, Buck, Gemma, Cole, Jennifer, Dicks, Ed, Gray, Kristian, Halliday, Kelly, Hills, Katy, Hinton, Jonathon, Jones, David, Menzies, Andrew, Perry, Janet, Raine, Keiran, Shepherd, Rebecca, Small, Alexandra, Varian, Jennifer, Widaa, Sara, Mallya, Uma, Moon, Jenny, Luo, Ying, Shaw, Marie, Boyle, Jackie, Kerr, Bronwyn, Turner, Gillian, Quarrell, Oliver, Cole, Trevor, Easton, Douglas F., Wooster, Richard, Bobrow, Martin, Schwartz, Charles E., Gecz, Jozef, Stratton, Michael R., Futreal, P. Andrew

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Mutations in the BRWD3 Gene Cause X-Linked Mental Retardation Associated with Macrocephaly by Field, Michael , Tarpey, Patrick S. , Smith, Raffaella , Edkins, Sarah , O’Meara, Sarah , Stevens, Claire , Tofts, Calli , Teague, Jon , Butler, Adam , Dicks, Ed , Barthorpe, Syd , Buck, Gemma , Cole, Jennifer , Gray, Kristian , Halliday, Kelly , Hills, Katy , Jenkinson, Andrew , Jones, David , Menzies, Andrew , Mironenko, Tatiana , Perry, Janet , Raine, Keiran , Richardson, David , Shepherd, Rebecca , Small, Alexandra , Varian, Jennifer , West, Sofie , Widaa, Sara , Mallya, Uma , Wooster, Richard , Moon, Jenny , Luo, Ying , Hughes, Helen , Shaw, Marie , Friend, Kathryn L. , Corbett, Mark , Turner, Gillian , Partington, Michael , Mulley, John , Bobrow, Martin , Schwartz, Charles , Stevenson, Roger , Gecz, Jozef , Stratton, Michael R. , Andrew Futreal, P. , Lucy Raymond, F. 

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Mutation analysis of 24 known cancer genes in the NCI-60 cell line set by Ikediobi, Ogechi N., Davies, Helen, Bignell, Graham, Edkins, Sarah, Stevens, Claire, O’Meara, Sarah, Santarius, Thomas, Avis, Tim, Barthorpe, Syd, Brackenbury, Lisa, Buck, Gemma, Butler, Adam, Clements, Jody, Cole, Jennifer, Dicks, Ed, Forbes, Simon, Gray, Kristian, Halliday, Kelly, Harrison, Rachel, Hills, Katy, Hinton, Jonathan, Hunter, Chris, Jenkinson, Andy, Jones, David, Kosmidou, Vivienne, Lugg, Richard, Menzies, Andrew, Mironenko, Tatiana, Parker, Adrian, Perry, Janet, Raine, Keiran, Richardson, David, Shepherd, Rebecca, Small, Alex, Smith, Raffaella, Solomon, Helen, Stephens, Philip, Teague, Jon, Tofts, Calli, Varian, Jennifer, Webb, Tony, West, Sofie, Widaa, Sara, Yates, Andy, Reinhold, William, Weinstein, John N., Stratton, Michael R., Futreal, P. Andrew, Wooster, Richard

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