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R A Spritz

Showing results (51-60 of 98) with videos related to

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Gene|June 15, 1990
The human RD protein is closely related to nuclear RNA-binding proteins and has been highly conservedC S Surowy, G Hoganson, J Gosink, et al.
Cytogenetics and Cell Genetics|January 1, 1979
Gene dosage effect: intraband mapping of human soluble glutamic oxaloacetic transaminaseR A Spritz, B S Emanuel, C J Chern, et al.
The Journal of Investigative Dermatology|June 1, 1997
Organization and nucleotide sequence of the human Hermansky-Pudlak syndrome (HPS) geneT Bailin, J Oh, G H Feng, et al.
Human Molecular Genetics|February 3, 2000
The Hermansky-Pudlak syndrome (HPS) protein is part of a high molecular weight complex involved in biogenesis of early melanosomesJ Oh, Z X Liu, G H Feng, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 1, 1985
Nucleotide sequence, evolution, and expression of the fetal globin gene of the spider monkey Ateles geoffroyiL B Giebel, V L van Santen, J L Slightom, et al.
The Journal of Biological Chemistry|November 25, 1992
Mutational mapping of the catalytic activities of human tyrosinaseR K Tripathi, V J Hearing, K Urabe, et al.
American Journal of Medical Genetics|December 26, 2001
Duplication of 15q11.2-q14, including the P gene, in a woman with generalized skin hyperpigmentationK Akahoshi, K Fukai, A Kato, et al.
American Journal of Human Genetics|November 1, 1992
Mutations of the KIT (mast/stem cell growth factor receptor) proto-oncogene account for a continuous range of phenotypes in human piebaldismR A Spritz, S A Holmes, R Ramesar, et al.
Nucleic Acids Research|December 21, 1981
Two cloned beta thalassemia genes are associated with amber mutations at codon 39R Pergolizzi, R A Spritz, S Spence, et al.
Molecular and Cellular Biology|October 1, 1989
Direct, sequence-specific binding of the human U1-70K ribonucleoprotein antigen protein to loop I of U1 small nuclear RNAC S Surowy, V L van Santen, S M Scheib-Wixted, et al.
Pageof 10

Showing results (51-60 of 98) with videos related to

Sort By:
Pageof 10
Gene|June 15, 1990
The human RD protein is closely related to nuclear RNA-binding proteins and has been highly conservedC S Surowy, G Hoganson, J Gosink, et al.
Cytogenetics and Cell Genetics|January 1, 1979
Gene dosage effect: intraband mapping of human soluble glutamic oxaloacetic transaminaseR A Spritz, B S Emanuel, C J Chern, et al.
The Journal of Investigative Dermatology|June 1, 1997
Organization and nucleotide sequence of the human Hermansky-Pudlak syndrome (HPS) geneT Bailin, J Oh, G H Feng, et al.
Human Molecular Genetics|February 3, 2000
The Hermansky-Pudlak syndrome (HPS) protein is part of a high molecular weight complex involved in biogenesis of early melanosomesJ Oh, Z X Liu, G H Feng, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 1, 1985
Nucleotide sequence, evolution, and expression of the fetal globin gene of the spider monkey Ateles geoffroyiL B Giebel, V L van Santen, J L Slightom, et al.
The Journal of Biological Chemistry|November 25, 1992
Mutational mapping of the catalytic activities of human tyrosinaseR K Tripathi, V J Hearing, K Urabe, et al.
American Journal of Medical Genetics|December 26, 2001
Duplication of 15q11.2-q14, including the P gene, in a woman with generalized skin hyperpigmentationK Akahoshi, K Fukai, A Kato, et al.
American Journal of Human Genetics|November 1, 1992
Mutations of the KIT (mast/stem cell growth factor receptor) proto-oncogene account for a continuous range of phenotypes in human piebaldismR A Spritz, S A Holmes, R Ramesar, et al.
Nucleic Acids Research|December 21, 1981
Two cloned beta thalassemia genes are associated with amber mutations at codon 39R Pergolizzi, R A Spritz, S Spence, et al.
Molecular and Cellular Biology|October 1, 1989
Direct, sequence-specific binding of the human U1-70K ribonucleoprotein antigen protein to loop I of U1 small nuclear RNAC S Surowy, V L van Santen, S M Scheib-Wixted, et al.
Pageof 10