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J Nasir

Showing results (41-50 of 50) with videos related to

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Genomics|January 16, 1999
A yeast artificial chromosome-based physical map of the juvenile amyotrophic lateral sclerosis (ALS2) critical region on human chromosome 2q33-q34S Hadano, K Nichol, R R Brinkman, et al.
Cell|June 2, 1995
Targeted disruption of the Huntington's disease gene results in embryonic lethality and behavioral and morphological changes in heterozygotesJ Nasir, S B Floresco, J R O'Kusky, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|January 1, 1997
Localization of the cell death genes CPP32 and Mch-2 to human chromosome 4qJ Nasir, J L Theilmann, V Chopra, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|June 29, 1999
Genomic organization of the human caspase-9 gene on Chromosome 1p36. 1-p36.3S Hadano, J Nasir, K Nichol, et al.
Genomics|February 13, 2001
Cloning and characterization of three novel genes, ALS2CR1, ALS2CR2, and ALS2CR3, in the juvenile amyotrophic lateral sclerosis (ALS2) critical region at chromosome 2q33-q34: candidate genes for ALS2S Hadano, Y Yanagisawa, J Skaug, et al.
Human Molecular Genetics|February 1, 1996
Absence of disease phenotype and intergenerational stability of the CAG repeat in transgenic mice expressing the human Huntington disease transcriptY P Goldberg, M A Kalchman, M Metzler, et al.
Human Molecular Genetics|December 1, 1996
Human huntingtin derived from YAC transgenes compensates for loss of murine huntingtin by rescue of the embryonic lethal phenotypeJ G Hodgson, D J Smith, K McCutcheon, et al.
Neuron|July 13, 1999
A YAC mouse model for Huntington's disease with full-length mutant huntingtin, cytoplasmic toxicity, and selective striatal neurodegenerationJ G Hodgson, N Agopyan, C A Gutekunst, et al.
Nature Genetics|October 5, 2001
A gene encoding a putative GTPase regulator is mutated in familial amyotrophic lateral sclerosis 2S Hadano, C K Hand, H Osuga, et al.
Cell Death and Differentiation|April 14, 1999
Cell death attenuation by 'Usurpin', a mammalian DED-caspase homologue that precludes caspase-8 recruitment and activation by the CD-95 (Fas, APO-1) receptor complexD M Rasper, J P Vaillancourt, S Hadano, et al.
Pageof 5

Showing results (41-50 of 50) with videos related to

Sort By:
Pageof 5
You have reached the last page of results.This site can display upto 50 results.
Genomics|January 16, 1999
A yeast artificial chromosome-based physical map of the juvenile amyotrophic lateral sclerosis (ALS2) critical region on human chromosome 2q33-q34S Hadano, K Nichol, R R Brinkman, et al.
Cell|June 2, 1995
Targeted disruption of the Huntington's disease gene results in embryonic lethality and behavioral and morphological changes in heterozygotesJ Nasir, S B Floresco, J R O'Kusky, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|January 1, 1997
Localization of the cell death genes CPP32 and Mch-2 to human chromosome 4qJ Nasir, J L Theilmann, V Chopra, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|June 29, 1999
Genomic organization of the human caspase-9 gene on Chromosome 1p36. 1-p36.3S Hadano, J Nasir, K Nichol, et al.
Genomics|February 13, 2001
Cloning and characterization of three novel genes, ALS2CR1, ALS2CR2, and ALS2CR3, in the juvenile amyotrophic lateral sclerosis (ALS2) critical region at chromosome 2q33-q34: candidate genes for ALS2S Hadano, Y Yanagisawa, J Skaug, et al.
Human Molecular Genetics|February 1, 1996
Absence of disease phenotype and intergenerational stability of the CAG repeat in transgenic mice expressing the human Huntington disease transcriptY P Goldberg, M A Kalchman, M Metzler, et al.
Human Molecular Genetics|December 1, 1996
Human huntingtin derived from YAC transgenes compensates for loss of murine huntingtin by rescue of the embryonic lethal phenotypeJ G Hodgson, D J Smith, K McCutcheon, et al.
Neuron|July 13, 1999
A YAC mouse model for Huntington's disease with full-length mutant huntingtin, cytoplasmic toxicity, and selective striatal neurodegenerationJ G Hodgson, N Agopyan, C A Gutekunst, et al.
Nature Genetics|October 5, 2001
A gene encoding a putative GTPase regulator is mutated in familial amyotrophic lateral sclerosis 2S Hadano, C K Hand, H Osuga, et al.
Cell Death and Differentiation|April 14, 1999
Cell death attenuation by 'Usurpin', a mammalian DED-caspase homologue that precludes caspase-8 recruitment and activation by the CD-95 (Fas, APO-1) receptor complexD M Rasper, J P Vaillancourt, S Hadano, et al.
Pageof 5