检索结果 - Cheryl Y. Gregory‐Evans
- Showing 1 - 18 results of 18
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NLRP3 inflammasome activation drives bystander cone photoreceptor cell death in a P23H rhodopsin model of retinal degeneration 由 Ishaq A. Viringipurampeer, Andrew Metcalfe, Emran Bashar, Olena Sivak, Anat Yanai, Zeinabsadat Mohammadi, Orson L. Moritz, Cheryl Y. Gregory‐Evans, Kevin Gregory‐Evans
出版 2016Artigo -
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SNP genome scanning localizes oto-dental syndrome to chromosome 11q13 and microdeletions at this locus implicate FGF3 in dental and inner-ear disease and FADD in ocular coloboma 由 Cheryl Y. Gregory‐Evans, Mariya Moosajee, Matt Hodges, Donna S. Mackay, Laurence Gamé, Neil Vargesson, Agnès Bloch‐Zupan, Franz Rüschendorf, Lourdes Santos‐Pinto, G Wackens, Kevin Gregory‐Evans
出版 2007Artigo -
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Mutations in LRP5 or FZD4 Underlie the Common Familial Exudative Vitreoretinopathy Locus on Chromosome 11q 由 Carmel Toomes, H.M. Bottomley, Richard M. Jackson, Katherine V. Towns, Sheila Scott, David A. Mackey, Jamie E. Craig, Li Jiang, Zhenglin Yang, Richard C. Trembath, Geoffrey Woodruff, Cheryl Y. Gregory‐Evans, Kevin Gregory-Evans, Michael Parker, Graeme Black, Louise Downey, Kang Zhang, Chris F. Inglehearn
出版 2004Artigo -
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Cone-Rod Dystrophy Due to Mutations in a Novel Photoreceptor-Specific Homeobox Gene () Essential for Maintenance of the Photoreceptor 由 Carol L. Freund, Cheryl Y. Gregory‐Evans, Takahisa Furukawa, Myrto Papaioannou, Jens Looser, Lynda Ploder, James Bellingham, David Ng, Jo-Anne Herbrick, Alessandra M.V. Duncan, Stephen W. Scherer, Lap-Chee Tsui, Aphrodite Loutradis-Anagnostou, Samuel G. Jacobson, Constance L. Cepko, Shomi S. Bhattacharya, Roderick R. McInnes
出版 1997Artigo -
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Discovery and characterization of small molecules targeting the DNA-binding ETS domain of ERG in prostate cancer 由 Miriam Butler, Mani Roshan‐Moniri, Michael Hsing, Desmond Lau, Ari Kim, Paul Yen, Marta Mroczek, Mannan Nouri, Scott Lien, Peter Axerio-Cilies, Kush Dalal, Clement Yau, Fariba Ghaidi, Yubin Guo, Takeshi Yamazaki, Sam Lawn, Martin Gleave, Cheryl Y. Gregory‐Evans, Lawrence P. McIntosh, Michael Cox, Paul S. Rennie, Artem Cherkasov
出版 2017Artigo -
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Loss-of-function mutations in<i>KIF14</i>cause severe microcephaly and kidney development defects in humans and zebrafish 由 Madeline Louise Reilly, Marijn Stokman, Virginie Magry, Marc Jeanpierre, Marine Alves, Mohammadjavad Paydar, Jacqueline R. Hellinga, Marion Delous, Daniel Pouly, Marion Failler, Jéléna Martinovic, Laurence Lœuillet, Brigitte Leroy, Julia Tantau, J. Roume, Cheryl Y. Gregory‐Evans, Xianghong Shan, Isabel Filges, John S. Allingham, Benjamin H. Kwok, Sophie Saunier, Rachel H. Giles, Alexandre Benmerah
出版 2018Artigo -
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Neuropilin-1 is upregulated in the adaptive response of prostate tumors to androgen-targeted therapies and is prognostic of metastatic progression and patient mortality 由 Brian Wan-Chi Tse, Marianna Volpert, Ellca Ratther, Nataly Stylianou, Mannan Nouri, K McGowan, Melanie Lehman, Stephen J. McPherson, Mani Roshan‐Moniri, Miriam Butler, Josselin Caradec, Cheryl Y. Gregory‐Evans, Jacqui McGovern, Rajdeep Das, Mandeep Takhar, Nicholas Erho, Mohamed Alshalafa, Elai Davicioni, Edward M. Schaeffer, Robert B. Jenkins, Ashley E. Ross, R. Jeffrey Karnes, Robert B. Den, Ladan Fazli, Philip A. Gregory, Martin Gleave, Elizabeth D. Williams, Paul S. Rennie, Ralph Buttyan, Jennifer H. Gunter, Luke A. Selth, Pamela J. Russell, Colleen C. Nelson, Brett G. Hollier
出版 2017Artigo
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