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Donna M Martin

Showing results (21-30 of 104) with videos related to

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Molecular and Cellular Neurosciences|January 22, 2008
Cre fate mapping reveals lineage specific defects in neuronal migration with loss of Pitx2 function in the developing mouse hypothalamus and subthalamic nucleusJennifer M Skidmore, John D Cramer, James F Martin, et al.
Genes|November 17, 2015
Super Enhancers in Cancers, Complex Disease, and Developmental DisordersAdrienne R Niederriter, Arushi Varshney, Stephen C J Parker, et al.
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.
American Journal of Medical Genetics. Part A|November 23, 2015
Atypical phenotypes associated with pathogenic CHD7 variants and a proposal for broadening CHARGE syndrome clinical diagnostic criteriaCaitlin L Hale, Adrienne N Niederriter, Glenn E Green, 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.
Social Cognitive and Affective Neuroscience|March 26, 2013
Serotonin transporter genotype impacts amygdala habituation in youth with autism spectrum disordersJillian Lee Wiggins, Johnna R Swartz, Donna M Martin, et al.
Genesis (New York, N.Y. : 2000)|September 8, 2011
A novel TaulacZ allele reveals a requirement for Pitx2 in formation of the mammillothalamic tractJennifer M Skidmore, Mindy R Waite, Gonzalo Alvarez-Bolado, et al.
American Journal of Medical Genetics. Part A|January 13, 2016
12th International CHARGE syndrome conference proceedingsDonna M Martin, Nancy Salem-Hartshorne, Timothy S Hartshorne, et al.
American Journal of Medical Genetics. Part A|December 28, 2002
Interrupted aortic arch in a child with trisomy 5q31.1q35.1 due to a maternal (20;5) balanced insertionDonna M Martin, Margaret H Mindell, Christine A Kwierant, et al.
Neuroscience Letters|June 13, 2013
C-terminals in the mouse branchiomotor nuclei originate from the magnocellular reticular formationToshiyasu Matsui, Yu Hongo, Yoshinori Haizuka, et al.
Pageof 11

Showing results (21-30 of 104) with videos related to

Sort By:
Pageof 11
Molecular and Cellular Neurosciences|January 22, 2008
Cre fate mapping reveals lineage specific defects in neuronal migration with loss of Pitx2 function in the developing mouse hypothalamus and subthalamic nucleusJennifer M Skidmore, John D Cramer, James F Martin, et al.
Genes|November 17, 2015
Super Enhancers in Cancers, Complex Disease, and Developmental DisordersAdrienne R Niederriter, Arushi Varshney, Stephen C J Parker, et al.
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.
American Journal of Medical Genetics. Part A|November 23, 2015
Atypical phenotypes associated with pathogenic CHD7 variants and a proposal for broadening CHARGE syndrome clinical diagnostic criteriaCaitlin L Hale, Adrienne N Niederriter, Glenn E Green, 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.
Social Cognitive and Affective Neuroscience|March 26, 2013
Serotonin transporter genotype impacts amygdala habituation in youth with autism spectrum disordersJillian Lee Wiggins, Johnna R Swartz, Donna M Martin, et al.
Genesis (New York, N.Y. : 2000)|September 8, 2011
A novel TaulacZ allele reveals a requirement for Pitx2 in formation of the mammillothalamic tractJennifer M Skidmore, Mindy R Waite, Gonzalo Alvarez-Bolado, et al.
American Journal of Medical Genetics. Part A|January 13, 2016
12th International CHARGE syndrome conference proceedingsDonna M Martin, Nancy Salem-Hartshorne, Timothy S Hartshorne, et al.
American Journal of Medical Genetics. Part A|December 28, 2002
Interrupted aortic arch in a child with trisomy 5q31.1q35.1 due to a maternal (20;5) balanced insertionDonna M Martin, Margaret H Mindell, Christine A Kwierant, et al.
Neuroscience Letters|June 13, 2013
C-terminals in the mouse branchiomotor nuclei originate from the magnocellular reticular formationToshiyasu Matsui, Yu Hongo, Yoshinori Haizuka, et al.
Pageof 11