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Mark A. Durham
Mark A. Durham
University of Michigan
Biology
CHARGE syndrome
Genetics
Gene
Neural stem cell
4
Papers
97
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CHD7 and retinoic acid signaling cooperate to regulate neural stem cell and inner ear development in mouse models of CHARGE syndrome
2014
Human Molecular Genetics
Joseph A. Micucci
Wanda S. Layman
Elizabeth A. Hurd
Ethan D. Sperry
Sophia F. Frank
Mark A. Durham
Donald L. Swiderski
Jennifer M. Skidmore
Peter C. Scacheri
Yehoash Raphael
Donna M. Martin
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Citations (46)
The chromatin remodeling protein CHD7, mutated in CHARGE syndrome, is necessary for proper craniofacial and tracheal development
2014
Developmental Dynamics
Ethan D. Sperry
Elizabeth A. Hurd
Mark A. Durham
Elyse N. Reamer
Adam B. Stein
Donna M. Martin
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Citations (30)
Macrocerebellum, epilepsy, intellectual disability, and gut malrotation in a child with a 16q24.1-q24.2 contiguous gene deletion
2014
American Journal of Medical Genetics Part A
Andrea H. Seeley
Mark A. Durham
Mark Micale
Jeffrey Wesolowski
Bradley R. Foerster
Donna M. Martin
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Citations (6)
Disruption of RAB40AL function leads to Martin–Probst syndrome, a rare X-linked multisystem neurodevelopmental human disorder
2012
Journal of Medical Genetics
Jirair K. Bedoyan
Valerie M. Schaibley
Weiping Peng
Yongsheng Bai
Kajari Mondal
Amol C. Shetty
Mark A. Durham
Joseph A. Micucci
Arti Dhiraaj
Jennifer M. Skidmore
Julie B Kaplan
Cindy Skinner
Charles E. Schwartz
Anthony Antonellis
Michael E. Zwick
James D. Cavalcoli
Jun Li
Donna M. Martin
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Citations (15)
1