Search Results - Michael Cheeseman

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  1. 1
    Understanding the aetiology and resolution of chronic otitis media from animal and human studies

    Understanding the aetiology and resolution of chronic otitis media from animal and human studies by Mahmood F. Bhutta, Ruth B. Thornton, Lea‐Ann S. Kirkham, Joseph E. Kerschner, Michael Cheeseman

    Published 2017
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  2. 2
    Activating calcium-sensing receptor mutation in the mouse is associated with cataracts and ectopic calcification

    Activating calcium-sensing receptor mutation in the mouse is associated with cataracts and ectopic calcification by Tertius Hough, Debora Bogani, Michael Cheeseman, Jack Favor, M. Andrew Nesbit, Rajesh V. Thakker, Mary F. Lyon

    Published 2004
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  3. 3
    Otitis media in the Tgif knockout mouse implicates TGFβ signalling in chronic middle ear inflammatory disease

    Otitis media in the Tgif knockout mouse implicates TGFβ signalling in chronic middle ear inflammatory disease by Hilda Tateossian, Susan Morse, Andrew Parker, Philomena Mburu, Nick Warr, Abraham Acevedo‐Arozena, Michael Cheeseman, Sara Wells, Steve D. M. Brown

    Published 2013
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  4. 4
    Minor Abnormalities of Testis Development in Mice Lacking the Gene Encoding the MAPK Signalling Component, MAP3K1

    Minor Abnormalities of Testis Development in Mice Lacking the Gene Encoding the MAPK Signalling Component, MAP3K1 by Nick Warr, Debora Bogani, Pam Siggers, Rachel Brixey, Hilda Tateossian, Asha Dopplapudi, Sara Wells, Michael Cheeseman, Ying Xia, Harry Ostrer, Andy Greenfield

    Published 2011
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  5. 5
    Oxr1 Is Essential for Protection against Oxidative Stress-Induced Neurodegeneration

    Oxr1 Is Essential for Protection against Oxidative Stress-Induced Neurodegeneration by Peter L. Oliver, Mattéa J. Finelli, Benjamin Edwards, Emmanuelle Bitoun, Darcy L. Butts, Esther B. E. Becker, Michael Cheeseman, Benjamin Davies, Kay E. Davies

    Published 2011
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  6. 6
    A mutation in the F-box gene, Fbxo11, causes otitis media in the Jeff mouse

    A mutation in the F-box gene, Fbxo11, causes otitis media in the Jeff mouse by 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

    Published 2006
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  7. 7
    Haploinsufficiency of the murine Col3a1 locus causes aortic dissection: a novel model of the vascular type of Ehlers–Danlos syndrome

    Haploinsufficiency of the murine Col3a1 locus causes aortic dissection: a novel model of the vascular type of Ehlers–Danlos syndrome by 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

    Published 2010
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  8. 8
    Multiple endocrine neoplasia type 1 knockout mice develop parathyroid, pancreatic, pituitary and adrenal tumours with hypercalcaemia, hypophosphataemia and hypercorticosteronaemia

    Multiple endocrine neoplasia type 1 knockout mice develop parathyroid, pancreatic, pituitary and adrenal tumours with hypercalcaemia, hypophosphataemia and hypercorticosteronaemia by 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

    Published 2009
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  9. 9
    Loss of Mitogen-Activated Protein Kinase Kinase Kinase 4 (MAP3K4) Reveals a Requirement for MAPK Signalling in Mouse Sex Determination

    Loss of Mitogen-Activated Protein Kinase Kinase Kinase 4 (MAP3K4) Reveals a Requirement for MAPK Signalling in Mouse Sex Determination by 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

    Published 2009
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  10. 10
    Static respiratory cilia associated with mutations in Dnahc11/DNAH11: A mouse model of PCD

    Static respiratory cilia associated with mutations in Dnahc11/DNAH11: A mouse model of PCD by 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

    Published 2011
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  11. 11
    Panel 4: Recent Advances in Otitis Media in Molecular Biology, Biochemistry, Genetics, and Animal Models

    Panel 4: Recent Advances in Otitis Media in Molecular Biology, Biochemistry, Genetics, and Animal Models by 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

    Published 2013
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  12. 12
    KATNAL1 Regulation of Sertoli Cell Microtubule Dynamics Is Essential for Spermiogenesis and Male Fertility

    KATNAL1 Regulation of Sertoli Cell Microtubule Dynamics Is Essential for Spermiogenesis and Male Fertility by 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

    Published 2012
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  13. 13
    HIF–VEGF Pathways Are Critical for Chronic Otitis Media in Junbo and Jeff Mouse Mutants

    HIF–VEGF Pathways Are Critical for Chronic Otitis Media in Junbo and Jeff Mouse Mutants by 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

    Published 2011
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  14. 14
    Mutation at the Evi1 Locus in Junbo Mice Causes Susceptibility to Otitis Media

    Mutation at the Evi1 Locus in Junbo Mice Causes Susceptibility to Otitis Media by 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

    Published 2006
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  15. 15
    A Mutation in the Mitochondrial Fission Gene Dnm1l Leads to Cardiomyopathy

    A Mutation in the Mitochondrial Fission Gene Dnm1l Leads to Cardiomyopathy by 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

    Published 2010
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  16. 16
    Pleiotropic Impacts of Macrophage and Microglial Deficiency on Development in Rats with Targeted Mutation of the <i>Csf1r</i> Locus

    Pleiotropic Impacts of Macrophage and Microglial Deficiency on Development in Rats with Targeted Mutation of the <i>Csf1r</i> Locus by 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

    Published 2018
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  17. 17
    A genome-wide association scan implicates DCHS2, RUNX2, GLI3, PAX1 and EDAR in human facial variation

    A genome-wide association scan implicates DCHS2, RUNX2, GLI3, PAX1 and EDAR in human facial variation by 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

    Published 2016
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  18. 18
    A genome-wide association study identifies multiple loci for variation in human ear morphology

    A genome-wide association study identifies multiple loci for variation in human ear morphology by 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

    Published 2015
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  19. 19
    Limb development genes underlie variation in human fingerprint patterns

    Limb development genes underlie variation in human fingerprint patterns by 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

    Published 2022
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  20. 20
    Novel gene function revealed by mouse mutagenesis screens for models of age-related disease

    Novel gene function revealed by mouse mutagenesis screens for models of age-related disease by 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

    Published 2016
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