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C T McMurray

Showing results (41-50 of 49) with videos related to

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Journal of Neuroimmunology|April 1, 2000
Genetic variation in the B7-1 gene in patients with multiple sclerosisB G Weinshenker, D D Hebrink, C Klein, et al.
American Journal of Human Genetics|April 1, 1997
Different mechanisms underlie DNA instability in Huntington disease and colorectal cancerG M Goellner, D Tester, S Thibodeau, et al.
American Journal of Medical Genetics|April 18, 1997
Gly(247)-->Asp proenkephalin A mutation is rare in schizophrenia populationsM J Mikesell, Y D Barron, V L Nimgaonkar, et al.
Neurology|May 5, 1999
Genetic variants in the tumor necrosis factor receptor 1 gene in patients with MSB G Weinshenker, D Hebrink, D M Wingerchuk, et al.
Human Molecular Genetics|October 1, 1995
Increased instability of intermediate alleles in families with sporadic Huntington disease compared to similar sized intermediate alleles in the general populationY P Goldberg, C T McMurray, J Zeisler, et al.
Molecular Cell|January 15, 2000
Inhibition of FEN-1 processing by DNA secondary structure at trinucleotide repeatsC Spiro, R Pelletier, M L Rolfsmeier, et al.
Neurology|March 10, 2004
Association of APOE polymorphisms with disease severity in MS is limited to womenO H Kantarci, D D Hebrink, S J Achenbach, et al.
Molecular Cell|July 14, 1998
GAA instability in Friedreich's Ataxia shares a common, DNA-directed and intraallelic mechanism with other trinucleotide diseasesA M Gacy, G M Goellner, C Spiro, et al.
Genes and Immunity|January 28, 2005
IFNG polymorphisms are associated with gender differences in susceptibility to multiple sclerosisO H Kantarci, A Goris, D D Hebrink, et al.
Pageof 5

Showing results (41-50 of 49) with videos related to

Sort By:
Pageof 5
You have reached the last page of results.This site can display upto 49 results.
Journal of Neuroimmunology|April 1, 2000
Genetic variation in the B7-1 gene in patients with multiple sclerosisB G Weinshenker, D D Hebrink, C Klein, et al.
American Journal of Human Genetics|April 1, 1997
Different mechanisms underlie DNA instability in Huntington disease and colorectal cancerG M Goellner, D Tester, S Thibodeau, et al.
American Journal of Medical Genetics|April 18, 1997
Gly(247)-->Asp proenkephalin A mutation is rare in schizophrenia populationsM J Mikesell, Y D Barron, V L Nimgaonkar, et al.
Neurology|May 5, 1999
Genetic variants in the tumor necrosis factor receptor 1 gene in patients with MSB G Weinshenker, D Hebrink, D M Wingerchuk, et al.
Human Molecular Genetics|October 1, 1995
Increased instability of intermediate alleles in families with sporadic Huntington disease compared to similar sized intermediate alleles in the general populationY P Goldberg, C T McMurray, J Zeisler, et al.
Molecular Cell|January 15, 2000
Inhibition of FEN-1 processing by DNA secondary structure at trinucleotide repeatsC Spiro, R Pelletier, M L Rolfsmeier, et al.
Neurology|March 10, 2004
Association of APOE polymorphisms with disease severity in MS is limited to womenO H Kantarci, D D Hebrink, S J Achenbach, et al.
Molecular Cell|July 14, 1998
GAA instability in Friedreich's Ataxia shares a common, DNA-directed and intraallelic mechanism with other trinucleotide diseasesA M Gacy, G M Goellner, C Spiro, et al.
Genes and Immunity|January 28, 2005
IFNG polymorphisms are associated with gender differences in susceptibility to multiple sclerosisO H Kantarci, A Goris, D D Hebrink, et al.
Pageof 5