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Molecular and Cellular Neurosciences
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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 nucleus
Jennifer M Skidmore, John D Cramer, James F Martin, et al.
Genes
|
November 17, 2015
Super Enhancers in Cancers, Complex Disease, and Developmental Disorders
Adrienne 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 mice
Elizabeth 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 criteria
Caitlin 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 ear
Elizabeth 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 disorders
Jillian 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 tract
Jennifer 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 proceedings
Donna 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 insertion
Donna 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 formation
Toshiyasu Matsui, Yu Hongo, Yoshinori Haizuka, et al.
Page
of 11
Search research articles
Search
Showing results (21-30 of 104) with videos related to
Sort By:
Page
of 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 nucleus
Jennifer M Skidmore, John D Cramer, James F Martin, et al.
Genes
|
November 17, 2015
Super Enhancers in Cancers, Complex Disease, and Developmental Disorders
Adrienne 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 mice
Elizabeth 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 criteria
Caitlin 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 ear
Elizabeth 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 disorders
Jillian 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 tract
Jennifer 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 proceedings
Donna 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 insertion
Donna 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 formation
Toshiyasu Matsui, Yu Hongo, Yoshinori Haizuka, et al.
Page
of 11