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D Goldowitz

Showing results (71-80 of 81) with videos related to

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The Journal of Comparative Neurology|March 5, 1998
Novel receptor protein tyrosine phosphatase (RPTPrho) and acidic fibroblast growth factor (FGF-1) transcripts delineate a rostrocaudal boundary in the granule cell layer of the murine cerebellar cortexP E McAndrew, A Frostholm, J E Evans, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|November 14, 1997
Cerebellar disorganization characteristic of reeler in scrambler mutant mice despite presence of reelinD Goldowitz, R C Cushing, E Laywell, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|August 1, 1995
Mapping the Bst mutation on mouse chromosome 16: a model for human optic atrophyD S Rice, R W Williams, P Ward-Bailey, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|July 1, 1987
A highly abundant transcript in adult murine cerebellar granule cells contains repetitive sequences homologous to L1H Schaal, D Goldowitz, U A Heinlein, et al.
Neurobiology of Disease|November 26, 2008
CAG repeat lengths > or =335 attenuate the phenotype in the R6/2 Huntington's disease transgenic mouseI Dragatsis, D Goldowitz, N Del Mar, et al.
Nature|October 24, 1997
Scrambler and yotari disrupt the disabled gene and produce a reeler-like phenotype in miceM Sheldon, D S Rice, G D'Arcangelo, et al.
Neurobiology of Disease|July 2, 2005
Increased calbindin-D28k immunoreactivity in striatal projection neurons of R6/2 Huntington's disease transgenic miceZ Sun, H B Wang, Y P Deng, et al.
Genomics|October 28, 2008
Next generation tools for high-throughput promoter and expression analysis employing single-copy knock-ins at the Hprt1 locusG S Yang, K G Banks, R J Bonaguro, et al.
Genes, Brain, and Behavior|December 5, 2009
High-throughput behavioral phenotyping in the expanded panel of BXD recombinant inbred strainsV M Philip, S Duvvuru, B Gomero, et al.
Clinical Genetics|January 6, 2011
19p13.2 microduplication causes a Sotos syndrome-like phenotype and alters gene expressionA M Lehman, C du Souich, D Chai, et al.
Pageof 9

Showing results (71-80 of 81) with videos related to

Sort By:
Pageof 9
The Journal of Comparative Neurology|March 5, 1998
Novel receptor protein tyrosine phosphatase (RPTPrho) and acidic fibroblast growth factor (FGF-1) transcripts delineate a rostrocaudal boundary in the granule cell layer of the murine cerebellar cortexP E McAndrew, A Frostholm, J E Evans, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|November 14, 1997
Cerebellar disorganization characteristic of reeler in scrambler mutant mice despite presence of reelinD Goldowitz, R C Cushing, E Laywell, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|August 1, 1995
Mapping the Bst mutation on mouse chromosome 16: a model for human optic atrophyD S Rice, R W Williams, P Ward-Bailey, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|July 1, 1987
A highly abundant transcript in adult murine cerebellar granule cells contains repetitive sequences homologous to L1H Schaal, D Goldowitz, U A Heinlein, et al.
Neurobiology of Disease|November 26, 2008
CAG repeat lengths > or =335 attenuate the phenotype in the R6/2 Huntington's disease transgenic mouseI Dragatsis, D Goldowitz, N Del Mar, et al.
Nature|October 24, 1997
Scrambler and yotari disrupt the disabled gene and produce a reeler-like phenotype in miceM Sheldon, D S Rice, G D'Arcangelo, et al.
Neurobiology of Disease|July 2, 2005
Increased calbindin-D28k immunoreactivity in striatal projection neurons of R6/2 Huntington's disease transgenic miceZ Sun, H B Wang, Y P Deng, et al.
Genomics|October 28, 2008
Next generation tools for high-throughput promoter and expression analysis employing single-copy knock-ins at the Hprt1 locusG S Yang, K G Banks, R J Bonaguro, et al.
Genes, Brain, and Behavior|December 5, 2009
High-throughput behavioral phenotyping in the expanded panel of BXD recombinant inbred strainsV M Philip, S Duvvuru, B Gomero, et al.
Clinical Genetics|January 6, 2011
19p13.2 microduplication causes a Sotos syndrome-like phenotype and alters gene expressionA M Lehman, C du Souich, D Chai, et al.
Pageof 9