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R R McInnes

Showing results (31-40 of 74) with videos related to

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The Journal of Biological Chemistry|September 17, 1998
Association of the TLX-2 homeodomain and 14-3-3eta signaling proteinsS J Tang, T C Suen, R R McInnes, et al.
Genomics|September 15, 1994
The retinal outer segment membrane protein-1 gene (Rom1) maps to the proximal end of mouse chromosome 19B A Taylor, S J Phillips, R A Bascom, et al.
Kidney International|September 1, 1978
Renal handling of phosphate in vivo and in vitro by the X-linked hypophosphatemic male mouse: evidence for a defect in the brush border membraneH S Tenenhouse, C R Scriver, R R McInnes, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 26, 1994
Canine X chromosome-linked hereditary nephritis: a genetic model for human X-linked hereditary nephritis resulting from a single base mutation in the gene encoding the alpha 5 chain of collagen type IVK Zheng, P S Thorner, P Marrano, et al.
Molecular and Cellular Biology|May 1, 1986
Molecular cloning of cDNA for rat argininosuccinate lyase and its expression in rat hepatoma cell linesM A Lambert, L R Simard, P N Ray, et al.
Proceedings of the National Academy of Sciences of the United States of America|December 1, 1990
Molecular analysis of human argininosuccinate lyase: mutant characterization and alternative splicing of the coding regionD C Walker, D A McCloskey, L R Simard, et al.
Human Molecular Genetics|April 1, 1996
A ubiquitin C-terminal hydrolase gene on the proximal short arm of the X chromosome: implications for X-linked retinal disordersD A Swanson, C L Freund, L Ploder, et al.
Pediatrics|September 1, 1982
Use of tetrahydropterins in the treatment of hyperphenylalaninemia due to defective synthesis of tetrahydrobiopterin: evidence that peripherally administered tetrahydropterins enter the brainS Kaufman, G Kapatos, R R McInnes, et al.
Human Molecular Genetics|October 1, 1995
Mutation analysis of the ROM1 gene in retinitis pigmentosaR A Bascom, L Liu, J R Heckenlively, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 1, 1991
Photoreceptor peripherin is the normal product of the gene responsible for retinal degeneration in the rds mouseG Connell, R Bascom, L Molday, et al.
Pageof 8

Showing results (31-40 of 74) with videos related to

Sort By:
Pageof 8
The Journal of Biological Chemistry|September 17, 1998
Association of the TLX-2 homeodomain and 14-3-3eta signaling proteinsS J Tang, T C Suen, R R McInnes, et al.
Genomics|September 15, 1994
The retinal outer segment membrane protein-1 gene (Rom1) maps to the proximal end of mouse chromosome 19B A Taylor, S J Phillips, R A Bascom, et al.
Kidney International|September 1, 1978
Renal handling of phosphate in vivo and in vitro by the X-linked hypophosphatemic male mouse: evidence for a defect in the brush border membraneH S Tenenhouse, C R Scriver, R R McInnes, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 26, 1994
Canine X chromosome-linked hereditary nephritis: a genetic model for human X-linked hereditary nephritis resulting from a single base mutation in the gene encoding the alpha 5 chain of collagen type IVK Zheng, P S Thorner, P Marrano, et al.
Molecular and Cellular Biology|May 1, 1986
Molecular cloning of cDNA for rat argininosuccinate lyase and its expression in rat hepatoma cell linesM A Lambert, L R Simard, P N Ray, et al.
Proceedings of the National Academy of Sciences of the United States of America|December 1, 1990
Molecular analysis of human argininosuccinate lyase: mutant characterization and alternative splicing of the coding regionD C Walker, D A McCloskey, L R Simard, et al.
Human Molecular Genetics|April 1, 1996
A ubiquitin C-terminal hydrolase gene on the proximal short arm of the X chromosome: implications for X-linked retinal disordersD A Swanson, C L Freund, L Ploder, et al.
Pediatrics|September 1, 1982
Use of tetrahydropterins in the treatment of hyperphenylalaninemia due to defective synthesis of tetrahydrobiopterin: evidence that peripherally administered tetrahydropterins enter the brainS Kaufman, G Kapatos, R R McInnes, et al.
Human Molecular Genetics|October 1, 1995
Mutation analysis of the ROM1 gene in retinitis pigmentosaR A Bascom, L Liu, J R Heckenlively, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 1, 1991
Photoreceptor peripherin is the normal product of the gene responsible for retinal degeneration in the rds mouseG Connell, R Bascom, L Molday, et al.
Pageof 8