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Elizabeth A Hurd

Showing results (1-10 of 17) with videos related to

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Infection and Immunity|June 24, 2004
Increased susceptibility of secretor factor gene Fut2-null mice to experimental vaginal candidiasisElizabeth A Hurd, Steven E Domino
Glycobiology|October 25, 2003
LacZ expression in Fut2-LacZ reporter mice reveals estrogen-regulated endocervical glandular expression during estrous cycle, hormone replacement, and pregnancySteven E Domino, Elizabeth A Hurd
Tumour Biology : the Journal of the International Society for Oncodevelopmental Biology and Medicine|February 1, 2007
Cell surface fucosylation does not affect development of colon tumors in mice with germline Smad3 mutationSteven E Domino, David M Karnak, Elizabeth A Hurd
Human Molecular Genetics|May 21, 2011
Reproductive dysfunction and decreased GnRH neurogenesis in a mouse model of CHARGE syndromeWanda S Layman, Elizabeth A Hurd, Donna M Martin
Investigative Ophthalmology & Visual Science|December 17, 2015
Mouse Models for the Dissection of CHD7 Functions in Eye Development and the Molecular Basis for Ocular Defects in CHARGE SyndromePhilip J Gage, Elizabeth A Hurd, Donna M Martin
Mechanisms of Development|June 19, 2012
Delayed fusion and altered gene expression contribute to semicircular canal defects in Chd7 deficient miceElizabeth A Hurd, Joseph A Micucci, Elyse N Reamer, et al.
Glycobiology|June 17, 2005
Gastrointestinal mucins of Fut2-null mice lack terminal fucosylation without affecting colonization by Candida albicansElizabeth A Hurd, Jessica M Holmén, Gunnar C Hansson, et al.
Development (Cambridge, England)|August 26, 2010
The ATP-dependent chromatin remodeling enzyme CHD7 regulates pro-neural gene expression and neurogenesis in the inner earElizabeth A Hurd, Heather K Poucher, Katherine Cheng, et al.
The Journal of Comparative Neurology|August 21, 2007
Defects in vestibular sensory epithelia and innervation in mice with loss of Chd7 function: implications for human CHARGE syndromeMeredith E Adams, Elizabeth A Hurd, Lisa A Beyer, et al.
Developmental Dynamics : an Official Publication of the American Association of Anatomists|July 1, 2014
The chromatin remodeling protein CHD7, mutated in CHARGE syndrome, is necessary for proper craniofacial and tracheal developmentEthan D Sperry, Elizabeth A Hurd, Mark A Durham, et al.
Pageof 2

Showing results (1-10 of 17) with videos related to

Sort By:
Pageof 2
Infection and Immunity|June 24, 2004
Increased susceptibility of secretor factor gene Fut2-null mice to experimental vaginal candidiasisElizabeth A Hurd, Steven E Domino
Glycobiology|October 25, 2003
LacZ expression in Fut2-LacZ reporter mice reveals estrogen-regulated endocervical glandular expression during estrous cycle, hormone replacement, and pregnancySteven E Domino, Elizabeth A Hurd
Tumour Biology : the Journal of the International Society for Oncodevelopmental Biology and Medicine|February 1, 2007
Cell surface fucosylation does not affect development of colon tumors in mice with germline Smad3 mutationSteven E Domino, David M Karnak, Elizabeth A Hurd
Human Molecular Genetics|May 21, 2011
Reproductive dysfunction and decreased GnRH neurogenesis in a mouse model of CHARGE syndromeWanda S Layman, Elizabeth A Hurd, Donna M Martin
Investigative Ophthalmology & Visual Science|December 17, 2015
Mouse Models for the Dissection of CHD7 Functions in Eye Development and the Molecular Basis for Ocular Defects in CHARGE SyndromePhilip J Gage, Elizabeth A Hurd, Donna M Martin
Mechanisms of Development|June 19, 2012
Delayed fusion and altered gene expression contribute to semicircular canal defects in Chd7 deficient miceElizabeth A Hurd, Joseph A Micucci, Elyse N Reamer, et al.
Glycobiology|June 17, 2005
Gastrointestinal mucins of Fut2-null mice lack terminal fucosylation without affecting colonization by Candida albicansElizabeth A Hurd, Jessica M Holmén, Gunnar C Hansson, et al.
Development (Cambridge, England)|August 26, 2010
The ATP-dependent chromatin remodeling enzyme CHD7 regulates pro-neural gene expression and neurogenesis in the inner earElizabeth A Hurd, Heather K Poucher, Katherine Cheng, et al.
The Journal of Comparative Neurology|August 21, 2007
Defects in vestibular sensory epithelia and innervation in mice with loss of Chd7 function: implications for human CHARGE syndromeMeredith E Adams, Elizabeth A Hurd, Lisa A Beyer, et al.
Developmental Dynamics : an Official Publication of the American Association of Anatomists|July 1, 2014
The chromatin remodeling protein CHD7, mutated in CHARGE syndrome, is necessary for proper craniofacial and tracheal developmentEthan D Sperry, Elizabeth A Hurd, Mark A Durham, et al.
Pageof 2