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R T Swank

Showing results (81-90 of 98) with videos related to

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Recent Progress in Hormone Research|January 1, 1978
Genetic regulation of mammalian glucuronidaseR T Swank, K Paigen, R Davey, et al.
Proceedings of the National Academy of Sciences of the United States of America|December 24, 1996
A novel modifier gene for plasma von Willebrand factor level maps to distal mouse chromosome 11K L Mohlke, W C Nichols, R J Westrick, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|February 1, 1996
Molecular markers near the mouse brachymorphic (bm) gene, which affects connective tissues and bleeding timeM E Rusiniak, E P O'Brien, E K Novak, et al.
Molecular Genetics and Metabolism|September 10, 1999
Analyses of proteins involved in vesicular trafficking in platelets of mouse models of Hermansky Pudlak syndromeB Richards-Smith, E K Novak, E K Jang, et al.
Molecular Genetics and Metabolism|January 4, 2001
5'-UTR structural organization, transcript expression, and mutational analysis of the human Rab geranylgeranyl transferase alpha-subunit (RABGGTA) geneW Li, J C Detter, H J Weiss, et al.
Genome Research|June 1, 1996
An integrated genetic map of the pearl locus of mouse chromosome 13A B Seymour, B L Yanak, E P O'Brien, et al.
Genomics|November 15, 2001
The gene mutated in cocoa mice, carrying a defect of organelle biogenesis, is a homologue of the human Hermansky-Pudlak syndrome-3 geneT Suzuki, W Li, Q Zhang, et al.
Blood|June 1, 1994
von Willebrand disease in the RIIIS/J mouse is caused by a defect outside of the von Willebrand factor geneW C Nichols, K A Cooney, K L Mohlke, et al.
Blood|September 15, 1995
von Willebrand disease in the RIIIS/J mouse is caused by a defect outside of the von Willebrand factor geneW C Nichols, K A Cooney, K L Mohlke, et al.
Proceedings of the National Academy of Sciences of the United States of America|June 22, 2000
A mutation in Rab27a causes the vesicle transport defects observed in ashen miceS M Wilson, R Yip, D A Swing, et al.
Pageof 10

Showing results (81-90 of 98) with videos related to

Sort By:
Pageof 10
Recent Progress in Hormone Research|January 1, 1978
Genetic regulation of mammalian glucuronidaseR T Swank, K Paigen, R Davey, et al.
Proceedings of the National Academy of Sciences of the United States of America|December 24, 1996
A novel modifier gene for plasma von Willebrand factor level maps to distal mouse chromosome 11K L Mohlke, W C Nichols, R J Westrick, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|February 1, 1996
Molecular markers near the mouse brachymorphic (bm) gene, which affects connective tissues and bleeding timeM E Rusiniak, E P O'Brien, E K Novak, et al.
Molecular Genetics and Metabolism|September 10, 1999
Analyses of proteins involved in vesicular trafficking in platelets of mouse models of Hermansky Pudlak syndromeB Richards-Smith, E K Novak, E K Jang, et al.
Molecular Genetics and Metabolism|January 4, 2001
5'-UTR structural organization, transcript expression, and mutational analysis of the human Rab geranylgeranyl transferase alpha-subunit (RABGGTA) geneW Li, J C Detter, H J Weiss, et al.
Genome Research|June 1, 1996
An integrated genetic map of the pearl locus of mouse chromosome 13A B Seymour, B L Yanak, E P O'Brien, et al.
Genomics|November 15, 2001
The gene mutated in cocoa mice, carrying a defect of organelle biogenesis, is a homologue of the human Hermansky-Pudlak syndrome-3 geneT Suzuki, W Li, Q Zhang, et al.
Blood|June 1, 1994
von Willebrand disease in the RIIIS/J mouse is caused by a defect outside of the von Willebrand factor geneW C Nichols, K A Cooney, K L Mohlke, et al.
Blood|September 15, 1995
von Willebrand disease in the RIIIS/J mouse is caused by a defect outside of the von Willebrand factor geneW C Nichols, K A Cooney, K L Mohlke, et al.
Proceedings of the National Academy of Sciences of the United States of America|June 22, 2000
A mutation in Rab27a causes the vesicle transport defects observed in ashen miceS M Wilson, R Yip, D A Swing, et al.
Pageof 10