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Pigment Cell Research|May 23, 2007
A mouse model of Waardenburg syndrome type IV resulting from an ENU-induced mutation in endothelin 3Ivana Matera, Jody L Cockroft, Jennifer L Moran, et al.
Frontiers in Molecular Neuroscience|August 8, 2022
The Transcription Factor Pou3f1 Sheds Light on the Development and Molecular Diversity of Glutamatergic Cerebellar Nuclear Neurons in the MouseJoshua Po Han Wu, Joanna Yeung, Maryam Rahimi-Balaei, et al.
Behavior Genetics|June 7, 2008
Genetic mapping of vocalization to a series of increasing acute footshocks using B6.A consomic and B6.D2 congenic mouse strainsDouglas B Matthews, Elissa J Chesler, Melloni N Cook, et al.
Biochemical and Biophysical Research Communications|August 10, 2010
Foxn3 is essential for craniofacial development in mice and a putative candidate involved in human congenital craniofacial defectsGeorge Samaan, Danielle Yugo, Sangeetha Rajagopalan, et al.
Cerebellum (London, England)|December 6, 2013
Glutamate dysfunction associated with developmental cerebellar damage: relevance to autism spectrum disordersEric McKimm, Beau Corkill, Dan Goldowitz, et al.
Frontiers in Genetics|March 3, 2020
Neonatal Alcohol Exposure in Mice Induces Select Differentiation- and Apoptosis-Related Chromatin Changes Both Independent of and Dependent on SexSamantha L Schaffner, Alexandre A Lussier, Jessica A Baker, et al.
Human Molecular Genetics|April 13, 2007
An integrative genomics strategy for systematic characterization of genetic loci modulating phenotypesLei Bao, Jeremy L Peirce, Mi Zhou, et al.
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