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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 cortex
P 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 reelin
D 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 atrophy
D 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 L1
H 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 mouse
I 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 mice
M 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 mice
Z 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 locus
G 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 strains
V 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 expression
A M Lehman, C du Souich, D Chai, et al.
Page
of 9
Search research articles
Search
Showing results (71-80 of 81) with videos related to
Sort By:
Page
of 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 cortex
P 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 reelin
D 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 atrophy
D 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 L1
H 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 mouse
I 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 mice
M 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 mice
Z 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 locus
G 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 strains
V 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 expression
A M Lehman, C du Souich, D Chai, et al.
Page
of 9