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R A Spritz

Showing results (31-40 of 98) with videos related to

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Oncogene|December 1, 1993
A survey of protein tyrosine kinase mRNAs expressed in normal human melanocytesS T Lee, K M Strunk, R A Spritz
Genomics|March 1, 1991
Organization and nucleotide sequences of the human tyrosinase gene and a truncated tyrosinase-related segmentL B Giebel, K M Strunk, R A Spritz
Biochimica Et Biophysica Acta|January 4, 1979
I-cell disease: intracellular desialylation of lysosomal enzymes using an influenza virus vectorR A Spritz, P M Coates, F S Lief
American Journal of Human Genetics|February 1, 1992
Dominant negative and loss of function mutations of the c-kit (mast/stem cell growth factor receptor) proto-oncogene in human piebaldismR A Spritz, L B Giebel, S A Holmes
Journal of Medical Genetics|July 1, 1991
A nonsense mutation in the tyrosinase gene of Afghan patients with tyrosinase negative (type IA) oculocutaneous albinismL B Giebel, M A Musarella, R A Spritz
The Journal of Investigative Dermatology|July 1, 1993
Novel mutations of the KIT (mast/stem cell growth factor receptor) proto-oncogene in human piebaldismR A Spritz, S A Holmes, P Itin, et al.
American Journal of Human Genetics|August 1, 1986
Normal dosage of the insulin and insulin-like growth factor II genes in patients with the Beckwith-Wiedemann syndromeR A Spritz, D Mager, R M Pauli, et al.
The Journal of Investigative Dermatology|August 1, 1997
Mutational analysis of copper binding by human tyrosinaseR A Spritz, L Ho, M Furumura, et al.
The EMBO Journal|August 1, 1985
The two intervening sequences of human beta- and gamma-globin pre-mRNAs are excised in a preferred temporal order in vitroK M Lang, V L van Santen, R A Spritz
Human Molecular Genetics|May 1, 1997
Mouse pale ear (ep) is homologous to human Hermansky-Pudlak syndrome and contains a rare 'AT-AC' intronG H Feng, T Bailin, J Oh, et al.
Pageof 10

Showing results (31-40 of 98) with videos related to

Sort By:
Pageof 10
Oncogene|December 1, 1993
A survey of protein tyrosine kinase mRNAs expressed in normal human melanocytesS T Lee, K M Strunk, R A Spritz
Genomics|March 1, 1991
Organization and nucleotide sequences of the human tyrosinase gene and a truncated tyrosinase-related segmentL B Giebel, K M Strunk, R A Spritz
Biochimica Et Biophysica Acta|January 4, 1979
I-cell disease: intracellular desialylation of lysosomal enzymes using an influenza virus vectorR A Spritz, P M Coates, F S Lief
American Journal of Human Genetics|February 1, 1992
Dominant negative and loss of function mutations of the c-kit (mast/stem cell growth factor receptor) proto-oncogene in human piebaldismR A Spritz, L B Giebel, S A Holmes
Journal of Medical Genetics|July 1, 1991
A nonsense mutation in the tyrosinase gene of Afghan patients with tyrosinase negative (type IA) oculocutaneous albinismL B Giebel, M A Musarella, R A Spritz
The Journal of Investigative Dermatology|July 1, 1993
Novel mutations of the KIT (mast/stem cell growth factor receptor) proto-oncogene in human piebaldismR A Spritz, S A Holmes, P Itin, et al.
American Journal of Human Genetics|August 1, 1986
Normal dosage of the insulin and insulin-like growth factor II genes in patients with the Beckwith-Wiedemann syndromeR A Spritz, D Mager, R M Pauli, et al.
The Journal of Investigative Dermatology|August 1, 1997
Mutational analysis of copper binding by human tyrosinaseR A Spritz, L Ho, M Furumura, et al.
The EMBO Journal|August 1, 1985
The two intervening sequences of human beta- and gamma-globin pre-mRNAs are excised in a preferred temporal order in vitroK M Lang, V L van Santen, R A Spritz
Human Molecular Genetics|May 1, 1997
Mouse pale ear (ep) is homologous to human Hermansky-Pudlak syndrome and contains a rare 'AT-AC' intronG H Feng, T Bailin, J Oh, et al.
Pageof 10