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Donna M Martin

Showing results (41-50 of 104) with videos related to

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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.
Journal of Cell Science|February 25, 2005
PITX2, beta-catenin and LEF-1 interact to synergistically regulate the LEF-1 promoterUsha Vadlamudi, Herbert M Espinoza, Mrudula Ganga, et al.
American Journal of Medical Genetics. Part A|February 7, 2016
Duplication 2p25 in a child with clinical features of CHARGE syndromeEthan D Sperry, Jane L Schuette, Conny M A van Ravenswaaij-Arts, et al.
Molecular and Cellular Neurosciences|September 20, 2011
Distinct populations of GABAergic neurons in mouse rhombomere 1 express but do not require the homeodomain transcription factor PITX2Mindy R Waite, Kaia Skaggs, Parisa Kaviany, et al.
Experimental Eye Research|November 7, 2022
Chromatin remodeler Chd7 regulates photoreceptor development and outer segment lengthLaura A Krueger, Jessica D Bills, Zun Yi Lim, 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.
American Journal of Medical Genetics. Part A|July 31, 2008
Branchiootorenal syndrome and oculoauriculovertebral spectrum features associated with duplication of SIX1, SIX6, and OTX2 resulting from a complex chromosomal rearrangementZhishuo Ou, Donna M Martin, Jirair K Bedoyan, et al.
Molecular and Cellular Neurosciences|November 14, 2012
Pleiotropic and isoform-specific functions for Pitx2 in superior colliculus and hypothalamic neuronal developmentMindy R Waite, Jennifer M Skidmore, Joseph A Micucci, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|March 6, 2007
Loss of Chd7 function in gene-trapped reporter mice is embryonic lethal and associated with severe defects in multiple developing tissuesElizabeth A Hurd, Patrice L Capers, Marsha N Blauwkamp, et al.
American Journal of Medical Genetics. Part A|May 27, 2010
Duplication 16p11.2 in a child with infantile seizure disorderJirair K Bedoyan, Ravinesh A Kumar, Jyotsna Sudi, et al.
Pageof 11

Showing results (41-50 of 104) with videos related to

Sort By:
Pageof 11
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.
Journal of Cell Science|February 25, 2005
PITX2, beta-catenin and LEF-1 interact to synergistically regulate the LEF-1 promoterUsha Vadlamudi, Herbert M Espinoza, Mrudula Ganga, et al.
American Journal of Medical Genetics. Part A|February 7, 2016
Duplication 2p25 in a child with clinical features of CHARGE syndromeEthan D Sperry, Jane L Schuette, Conny M A van Ravenswaaij-Arts, et al.
Molecular and Cellular Neurosciences|September 20, 2011
Distinct populations of GABAergic neurons in mouse rhombomere 1 express but do not require the homeodomain transcription factor PITX2Mindy R Waite, Kaia Skaggs, Parisa Kaviany, et al.
Experimental Eye Research|November 7, 2022
Chromatin remodeler Chd7 regulates photoreceptor development and outer segment lengthLaura A Krueger, Jessica D Bills, Zun Yi Lim, 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.
American Journal of Medical Genetics. Part A|July 31, 2008
Branchiootorenal syndrome and oculoauriculovertebral spectrum features associated with duplication of SIX1, SIX6, and OTX2 resulting from a complex chromosomal rearrangementZhishuo Ou, Donna M Martin, Jirair K Bedoyan, et al.
Molecular and Cellular Neurosciences|November 14, 2012
Pleiotropic and isoform-specific functions for Pitx2 in superior colliculus and hypothalamic neuronal developmentMindy R Waite, Jennifer M Skidmore, Joseph A Micucci, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|March 6, 2007
Loss of Chd7 function in gene-trapped reporter mice is embryonic lethal and associated with severe defects in multiple developing tissuesElizabeth A Hurd, Patrice L Capers, Marsha N Blauwkamp, et al.
American Journal of Medical Genetics. Part A|May 27, 2010
Duplication 16p11.2 in a child with infantile seizure disorderJirair K Bedoyan, Ravinesh A Kumar, Jyotsna Sudi, et al.
Pageof 11