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R McInnes

Showing results (61-70 of 140) with videos related to

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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.
The Journal of Pediatrics|February 1, 1991
Combined transient and peripheral defects in tetrahydrobiopterin synthesisJ Allanson, R McInnes, L Bradley, et al.
Kidney International|March 1, 1989
Abnormalities in the NC1 domain of collagen type IV in GBM in canine hereditary nephritisP Thorner, R Baumal, V E Valli, et al.
Celestial Mechanics and Dynamical Astronomy|November 13, 2020
Orbit period modulation for relative motion using continuous low thrust in the two-body and restricted three-body problemsC S Arnot, C R McInnes, R J McKay, 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.
Annual Review of Neuroscience|October 7, 2003
Progress toward understanding the genetic and biochemical mechanisms of inherited photoreceptor degenerationsLaura R Pacione, Michael J Szego, Sakae Ikeda, 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.
Genomics|April 1, 1993
Identification of the mutation in murine histidinemia (his) and genetic mapping of the murine histidase locus (Hal) on chromosome 10R G Taylor, D Grieco, G A Clarke, et al.
Pageof 14

Showing results (61-70 of 140) with videos related to

Sort By:
Pageof 14
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.
The Journal of Pediatrics|February 1, 1991
Combined transient and peripheral defects in tetrahydrobiopterin synthesisJ Allanson, R McInnes, L Bradley, et al.
Kidney International|March 1, 1989
Abnormalities in the NC1 domain of collagen type IV in GBM in canine hereditary nephritisP Thorner, R Baumal, V E Valli, et al.
Celestial Mechanics and Dynamical Astronomy|November 13, 2020
Orbit period modulation for relative motion using continuous low thrust in the two-body and restricted three-body problemsC S Arnot, C R McInnes, R J McKay, 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.
Annual Review of Neuroscience|October 7, 2003
Progress toward understanding the genetic and biochemical mechanisms of inherited photoreceptor degenerationsLaura R Pacione, Michael J Szego, Sakae Ikeda, 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.
Genomics|April 1, 1993
Identification of the mutation in murine histidinemia (his) and genetic mapping of the murine histidase locus (Hal) on chromosome 10R G Taylor, D Grieco, G A Clarke, et al.
Pageof 14