Ngā hua rapu - Michael Cheeseman
- E whakaatu ana i te 1 - 20 hua o te 20
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Otitis media in the Tgif knockout mouse implicates TGFβ signalling in chronic middle ear inflammatory disease mā Hilda Tateossian, Susan Morse, Andrew Parker, Philomena Mburu, Nick Warr, Abraham Acevedo‐Arozena, Michael Cheeseman, Sara Wells, Steve D. M. Brown
I whakaputaina 2013Artigo -
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Minor Abnormalities of Testis Development in Mice Lacking the Gene Encoding the MAPK Signalling Component, MAP3K1 mā Nick Warr, Debora Bogani, Pam Siggers, Rachel Brixey, Hilda Tateossian, Asha Dopplapudi, Sara Wells, Michael Cheeseman, Ying Xia, Harry Ostrer, Andy Greenfield
I whakaputaina 2011Artigo -
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Oxr1 Is Essential for Protection against Oxidative Stress-Induced Neurodegeneration mā Peter L. Oliver, Mattéa J. Finelli, Benjamin Edwards, Emmanuelle Bitoun, Darcy L. Butts, Esther B. E. Becker, Michael Cheeseman, Benjamin Davies, Kay E. Davies
I whakaputaina 2011Artigo -
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A mutation in the F-box gene, Fbxo11, causes otitis media in the Jeff mouse mā Rachel E. Hardisty-Hughes, Hilda Tateossian, Susan Morse, M. Rosario Romero, Alice Middleton, Zuzanna Tymowska‐Lalanne, A. Jackie Hunter, Michael Cheeseman, Steve D. M. Brown
I whakaputaina 2006Artigo -
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Haploinsufficiency of the murine Col3a1 locus causes aortic dissection: a novel model of the vascular type of Ehlers–Danlos syndrome mā Lee B. Smith, Patrick W. F. Hadoke, Emma Dyer, Martin A. Denvir, David G. Brownstein, Eileen Miller, Nancy A. Nelson, Sara Wells, Michael Cheeseman, Andy Greenfield
I whakaputaina 2010Artigo -
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Multiple endocrine neoplasia type 1 knockout mice develop parathyroid, pancreatic, pituitary and adrenal tumours with hypercalcaemia, hypophosphataemia and hypercorticosteronaemia mā Brian Harding, Manuel C. Lemos, Adam J. Reed, Gerard Walls, Jeshmi Jeyabalan, Michael R. Bowl, Hilda Tateossian, Nicky Sullivan, Tertius Hough, William D. Fraser, Olaf Ansorge, Michael Cheeseman, Rajesh V. Thakker
I whakaputaina 2009Artigo -
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Loss of Mitogen-Activated Protein Kinase Kinase Kinase 4 (MAP3K4) Reveals a Requirement for MAPK Signalling in Mouse Sex Determination mā Debora Bogani, Pam Siggers, Rachel Brixey, Nick Warr, Sarah Beddow, Jessica K. Edwards, Debbie Williams, Dagmar Wilhelm, Peter Koopman, Richard A. Flavell, Hongbo Chi, Harry Ostrer, Sara Wells, Michael Cheeseman, Andy Greenfield
I whakaputaina 2009Artigo -
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Static respiratory cilia associated with mutations in Dnahc11/DNAH11: A mouse model of PCD mā Jane S. Lucas, Elizabeth Adam, Patricia Goggin, Claire L. Jackson, Nicola Powles‐Glover, Saloni H Patel, James Humphreys, Martin Fray, Emilie Falconnet, Jean‐Louis Blouin, Michael Cheeseman, Lucia Bartoloni, Dominic P. Norris, Peter M. Lackie
I whakaputaina 2011Artigo -
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Panel 4: Recent Advances in Otitis Media in Molecular Biology, Biochemistry, Genetics, and Animal Models mā Jiandong Li, Ann Hermansson, Allen F. Ryan, Lauren O. Bakaletz, Steve D. M. Brown, Michael Cheeseman, Steven K. Juhn, Timothy T. K. Jung, David Lim, Jae Hyang Lim, Jizhen Lin, Sung‐Kyun Moon, J. Christopher Post
I whakaputaina 2013Revisão -
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KATNAL1 Regulation of Sertoli Cell Microtubule Dynamics Is Essential for Spermiogenesis and Male Fertility mā Lee B. Smith, Laura Milne, Nancy A. Nelson, Sharon L. Eddie, Pamela Brown, Nina Atanassova, Moira K. O’Bryan, Liza O’Donnell, Danielle Rhodes, Sara Wells, Diane Napper, Patrick M. Nolan, Zuzanna Lalanne, Michael Cheeseman, Josephine Peters
I whakaputaina 2012Artigo -
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HIF–VEGF Pathways Are Critical for Chronic Otitis Media in Junbo and Jeff Mouse Mutants mā Michael Cheeseman, Hayley E. Tyrer, Debbie Williams, Tertius Hough, Paras Pathak, Maria R. Romero, Helen Hilton, Sulzhan Bali, Andrew Parker, Lucie Vizor, Thomas Purnell, Kate Vowell, Sara Wells, Mahmood F. Bhutta, Paul Potter, Steve D. M. Brown
I whakaputaina 2011Artigo -
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Mutation at the Evi1 Locus in Junbo Mice Causes Susceptibility to Otitis Media mā Nick Parkinson, Rachel E. Hardisty-Hughes, Hilda Tateossian, Hsun-Tien Tsai, Debra Brooker, Sue Morse, Zuzanna Lalane, Francesca E. Mackenzie, Martin Fray, Pete Glenister, Anne-Marie Woodward, Sian Polley, Ivana Barbaric, Neil Dear, Tertius Hough, A. Jackie Hunter, Michael Cheeseman, Steve D. M. Brown
I whakaputaina 2006Artigo -
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A Mutation in the Mitochondrial Fission Gene Dnm1l Leads to Cardiomyopathy mā Houman Ashrafian, Louise Docherty, Vincenzo Leo, Christopher Towlson, Monica Neilan, Violetta Steeples, Craig A. Lygate, Tertius Hough, Stuart Townsend, Debbie Williams, Sara Wells, Dominic P. Norris, Sarah Glyn-Jones, John M. Land, Ivana Barbaric, Zuzanne Lalanne, Paul Denny, Dorota Szumska, Shoumo Bhattacharya, Julian L. Griffin, Iain P. Hargreaves, Narcís Fernández‐Fuentes, Michael Cheeseman, Hugh Watkins, T. Neil Dear
I whakaputaina 2010Artigo -
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Pleiotropic Impacts of Macrophage and Microglial Deficiency on Development in Rats with Targeted Mutation of the <i>Csf1r</i> Locus mā Clare Pridans, Anna Raper, Gemma M. Davis, Joana Alves, Kristin A. Sauter, Lucas Lefèvre, Tim Regan, Stephen Meek, Linda Sutherland, Alison J. Thomson, Sara Clohisey, Stephen J. Bush, Rocío Rojo, Zofia M. Lisowski, Robert Wallace, Kathleen Grabert, Kyle R. Upton, Yi Ting Tsai, Deborah Brown, Lee B. Smith, Kim Summers, Neil A. Mabbott, Pedro Piccardo, Michael Cheeseman, Tom Burdon, David Hume
I whakaputaina 2018Artigo -
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A genome-wide association scan implicates DCHS2, RUNX2, GLI3, PAX1 and EDAR in human facial variation mā Kaustubh Adhikari, Macarena Fuentes‐Guajardo, Mirsha Quinto‐Sánchez, Javier Mendoza‐Revilla, Juan Camilo Chacón-Duque, Víctor Acuña-Alonzo, Claudia Jaramillo, William Arias, Rodrigo Barquera, Gastón Macín Pérez, Jorge Gómez‐Valdés, Hugo Villamil‐Ramírez, Tábita Hünemeier, Virgínia Ramallo, Caio César Silva de Cerqueira, Malena Hurtado, Valeria Villegas, Vanessa Granja, Carla Gallo, Giovanni Poletti, Lavínia Schüler‐Faccini, Francisco M. Salzano, María Cátira Bortolini, Samuel Canizales‐Quinteros, Michael Cheeseman, Javier Rosique Gracia, Gabriel Bedoya, Francisco Rothhammer, Denis J. Headon, Rolando González‐José, David J. Balding, Andrés Ruiz‐Linares
I whakaputaina 2016Artigo -
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A genome-wide association study identifies multiple loci for variation in human ear morphology mā Kaustubh Adhikari, Guillermo Reales, Andrew J. Smith, Esra Konka, Jutta Palmen, Mirsha Quinto‐Sánchez, Víctor Acuña-Alonzo, Claudia Jaramillo, William Arias, Macarena Fuentes‐Guajardo, María Gabriela Pizarro Inostroza, Rodrigo Barquera, Gastón Macín Pérez, Jorge Gómez‐Valdés, Hugo Villamil‐Ramírez, Tábita Hünemeier, Virgínia Ramallo, Caio César Silva de Cerqueira, Malena Hurtado, Valeria Villegas, Vanessa Granja, Carla Gallo, Giovanni Poletti, Lavínia Schüler‐Faccini, Francisco M. Salzano, María Cátira Bortolini, Samuel Canizales‐Quinteros, Francisco Rothhammer, Gabriel Bedoya, Rosario Calderón, Javier Rosique Gracia, Michael Cheeseman, Mahmood F. Bhutta, Steve E. Humphries, Rolando González‐José, Denis J. Headon, David J. Balding, Andrés Ruiz‐Linares
I whakaputaina 2015Artigo -
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Limb development genes underlie variation in human fingerprint patterns mā Jinxi Li, James D. Glover, Haiguo Zhang, Meifang Peng, Jingze Tan, Chandana Basu Mallick, Dan Hou, Yajun Yang, Sijie Wu, Yu Liu, Qianqian Peng, Shijie Zheng, Edie I. Crosse, Alexander Medvinsky, Richard A. Anderson, Helen Brown, Ziyu Yuan, Shen Zhou, Yanqing Xu, John P. Kemp, Yvonne Ho, Danuta Z. Loesch, Lizhong Wang, Yingxiang Li, Senwei Tang, Xiaoli Wu, Robin Walters, Kuang Lin, Ruogu Meng, Jun Lv, Jonathan M. Chernus, Katherine Neiswanger, Eleanor Feingold, David M. Evans, Sarah E. Medland, Nicholas G. Martin, Seth M. Weinberg, Mary L. Marazita, Gang Chen, Zhengming Chen, Yong Zhou, Michael Cheeseman, Lan Wang, Jin Li, Denis J. Headon, Sijia Wang
I whakaputaina 2022Artigo -
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Novel gene function revealed by mouse mutagenesis screens for models of age-related disease mā Paul Potter, Michael R. Bowl, Prashanthini Jeyarajan, Laura Wisby, Andrew Blease, Michelle Goldsworthy, Michelle M. Simon, Simon Greenaway, Vincent Michel, Alun R. Barnard, Carlos Aguilar, Thomas Agnew, Gareth Banks, Andrew Blake, Lauren Chessum, Joanne Dorning, Sara Falcone, Laurence Goosey, Shelley Harris, A. Haynes, Ines Heise, Rosie Hillier, Tertius Hough, Angela Hoslin, Marie Hutchison, Ruairidh King, Saumya Kumar, Heena V. Lad, Gemma Law, Robert E. MacLaren, Susan Morse, T. NICOL, Andrew Parker, Karen Pickford, Siddharth Sethi, Becky Starbuck, Femke Stelma, Michael Cheeseman, Sally H. Cross, F. Foster, Ian J. Jackson, Stuart N. Peirson, Rajesh V. Thakker, Tonia L. Vincent, Cheryl L. Scudamore, Sara Wells, A. Amraoui, Christine Petit, Abraham Acevedo‐Arozena, Patrick M. Nolan, Roger Cox, Ann‐Marie Mallon, Steve D.M. Brown
I whakaputaina 2016Artigo
Ngā utauta rapu:
Ngā marau whai pānga
Biology
Gene
Genetics
Medicine
Endocrinology
Cell biology
Internal medicine
Otitis
Pathology
Anatomy
Immunology
Mutation
Phenotype
Disease
Middle ear
Mutant
Biochemistry
Calcium
Cancer research
Computational biology
Evolutionary biology
Genome
Genome-wide association study
Genotype
Inflammation
Inner ear
Kinase
Lung
Missense mutation
Neuroscience