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R A Spritz

Showing results (41-50 of 98) with videos related to

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The Biochemical Journal|April 4, 2001
The molecular basis of oculocutaneous albinism type 1 (OCA1): sorting failure and degradation of mutant tyrosinases results in a lack of pigmentationK Toyofuku, I Wada, R A Spritz, et al.
American Journal of Human Genetics|June 1, 1995
Frequent intragenic deletion of the P gene in Tanzanian patients with type II oculocutaneous albinism (OCA2)R A Spritz, K Fukai, S A Holmes, et al.
Genomics|October 1, 1990
Human U1-70K ribonucleoprotein antigen gene: organization, nucleotide sequence, and mapping to locus 19q13.3R A Spritz, K Strunk, C S Surowy, et al.
Human Molecular Genetics|September 1, 1995
Linkage disequilibrium mapping of the gene for Hermansky-Pudlak syndrome to chromosome 10q23.1-q23.3K Fukai, J Oh, E Frenk, et al.
Oncogene|March 1, 1994
PTK1, a novel protein kinase required for proliferation of human melanocytesK Ezoe, S T Lee, K M Strunk, et al.
Gene Expression|May 1, 1991
A polymorphism of the human tyrosinase gene is associated with temperature-sensitive enzymatic activityR K Tripathi, L B Giebel, K M Strunk, et al.
Molecular and Cellular Biology|November 1, 1988
Loop I of U1 small nuclear RNA is the only essential RNA sequence for binding of specific U1 small nuclear ribonucleoprotein particle proteinsJ Hamm, V L van Santen, R A Spritz, et al.
The Journal of Clinical Investigation|March 1, 1991
A tyrosinase gene missense mutation in temperature-sensitive type I oculocutaneous albinism. A human homologue to the Siamese cat and the Himalayan mouseL B Giebel, R K Tripathi, R A King, et al.
Oncogene|November 1, 1992
Organization and nucleotide sequence of the human KIT (mast/stem cell growth factor receptor) proto-oncogeneL B Giebel, K M Strunk, S A Holmes, et al.
Cell|October 1, 1980
Complete nucleotide sequence of the human delta-globin geneR A Spritz, J K DeRiel, B G Forget, et al.
Pageof 10

Showing results (41-50 of 98) with videos related to

Sort By:
Pageof 10
The Biochemical Journal|April 4, 2001
The molecular basis of oculocutaneous albinism type 1 (OCA1): sorting failure and degradation of mutant tyrosinases results in a lack of pigmentationK Toyofuku, I Wada, R A Spritz, et al.
American Journal of Human Genetics|June 1, 1995
Frequent intragenic deletion of the P gene in Tanzanian patients with type II oculocutaneous albinism (OCA2)R A Spritz, K Fukai, S A Holmes, et al.
Genomics|October 1, 1990
Human U1-70K ribonucleoprotein antigen gene: organization, nucleotide sequence, and mapping to locus 19q13.3R A Spritz, K Strunk, C S Surowy, et al.
Human Molecular Genetics|September 1, 1995
Linkage disequilibrium mapping of the gene for Hermansky-Pudlak syndrome to chromosome 10q23.1-q23.3K Fukai, J Oh, E Frenk, et al.
Oncogene|March 1, 1994
PTK1, a novel protein kinase required for proliferation of human melanocytesK Ezoe, S T Lee, K M Strunk, et al.
Gene Expression|May 1, 1991
A polymorphism of the human tyrosinase gene is associated with temperature-sensitive enzymatic activityR K Tripathi, L B Giebel, K M Strunk, et al.
Molecular and Cellular Biology|November 1, 1988
Loop I of U1 small nuclear RNA is the only essential RNA sequence for binding of specific U1 small nuclear ribonucleoprotein particle proteinsJ Hamm, V L van Santen, R A Spritz, et al.
The Journal of Clinical Investigation|March 1, 1991
A tyrosinase gene missense mutation in temperature-sensitive type I oculocutaneous albinism. A human homologue to the Siamese cat and the Himalayan mouseL B Giebel, R K Tripathi, R A King, et al.
Oncogene|November 1, 1992
Organization and nucleotide sequence of the human KIT (mast/stem cell growth factor receptor) proto-oncogeneL B Giebel, K M Strunk, S A Holmes, et al.
Cell|October 1, 1980
Complete nucleotide sequence of the human delta-globin geneR A Spritz, J K DeRiel, B G Forget, et al.
Pageof 10