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J Justice

Showing results (221-230 of 299) with videos related to

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Molecular Endocrinology (Baltimore, Md.)|December 31, 2004
A novel mouse model of hypogonadotrophic hypogonadism: N-ethyl-N-nitrosourea-induced gonadotropin-releasing hormone receptor gene mutationAndrew J Pask, Haruhiko Kanasaki, Ursula B Kaiser, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|March 6, 2009
The ataxia3 mutation in the N-terminal cytoplasmic domain of sodium channel Na(v)1.6 disrupts intracellular traffickingLisa M Sharkey, Xiaoyang Cheng, Valerie Drews, et al.
Genes & Development|January 1, 1989
A new family of mouse homeo box-containing genes: molecular structure, chromosomal location, and developmental expression of Hox-7.1R E Hill, P F Jones, A R Rees, et al.
Nature Communications|August 3, 2019
Identification of a neurocircuit underlying regulation of feeding by stress-related emotional responsesYuanzhong Xu, Yungang Lu, Ryan M Cassidy, et al.
Genomics|August 1, 1992
A molecular genetic linkage map of mouse chromosome 18 reveals extensive linkage conservation with human chromosomes 5 and 18M J Justice, D J Gilbert, K W Kinzler, et al.
Plos One|April 28, 2017
Alpha-1 antitrypsin supplementation improves alveolar macrophages efferocytosis and phagocytosis following cigarette smoke exposureKarina A Serban, Daniela N Petrusca, Andrew Mikosz, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|December 22, 1999
A comparative transcript map and candidates for mutant phenotypes in the Tyrp1 (brown) deletion complex homologous to human 9p21-23E H Simpson, R Suffolk, J A Bell, et al.
Developmental Cell|March 20, 2004
A twist code determines the onset of osteoblast differentiationPeter Bialek, Britt Kern, Xiangli Yang, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|June 1, 1996
Location of the 9257 and ataxia mutations on mouse chromosome 18A J Griffith, G L Radice, D L Burgess, et al.
Plos One|December 5, 2013
A point mutation in the gene for asparagine-linked glycosylation 10B (Alg10b) causes nonsyndromic hearing impairment in mice (Mus musculus)Frank J Probst, Rebecca R Corrigan, Daniela Del Gaudio, et al.
Pageof 30

Showing results (221-230 of 299) with videos related to

Sort By:
Pageof 30
Molecular Endocrinology (Baltimore, Md.)|December 31, 2004
A novel mouse model of hypogonadotrophic hypogonadism: N-ethyl-N-nitrosourea-induced gonadotropin-releasing hormone receptor gene mutationAndrew J Pask, Haruhiko Kanasaki, Ursula B Kaiser, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|March 6, 2009
The ataxia3 mutation in the N-terminal cytoplasmic domain of sodium channel Na(v)1.6 disrupts intracellular traffickingLisa M Sharkey, Xiaoyang Cheng, Valerie Drews, et al.
Genes & Development|January 1, 1989
A new family of mouse homeo box-containing genes: molecular structure, chromosomal location, and developmental expression of Hox-7.1R E Hill, P F Jones, A R Rees, et al.
Nature Communications|August 3, 2019
Identification of a neurocircuit underlying regulation of feeding by stress-related emotional responsesYuanzhong Xu, Yungang Lu, Ryan M Cassidy, et al.
Genomics|August 1, 1992
A molecular genetic linkage map of mouse chromosome 18 reveals extensive linkage conservation with human chromosomes 5 and 18M J Justice, D J Gilbert, K W Kinzler, et al.
Plos One|April 28, 2017
Alpha-1 antitrypsin supplementation improves alveolar macrophages efferocytosis and phagocytosis following cigarette smoke exposureKarina A Serban, Daniela N Petrusca, Andrew Mikosz, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|December 22, 1999
A comparative transcript map and candidates for mutant phenotypes in the Tyrp1 (brown) deletion complex homologous to human 9p21-23E H Simpson, R Suffolk, J A Bell, et al.
Developmental Cell|March 20, 2004
A twist code determines the onset of osteoblast differentiationPeter Bialek, Britt Kern, Xiangli Yang, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|June 1, 1996
Location of the 9257 and ataxia mutations on mouse chromosome 18A J Griffith, G L Radice, D L Burgess, et al.
Plos One|December 5, 2013
A point mutation in the gene for asparagine-linked glycosylation 10B (Alg10b) causes nonsyndromic hearing impairment in mice (Mus musculus)Frank J Probst, Rebecca R Corrigan, Daniela Del Gaudio, et al.
Pageof 30