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R R McInnes

Showing results (41-50 of 74) with videos related to

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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.
Lancet (London, England)|March 7, 1981
Hyperornithinaemia and gyrate atrophy of the retina: improvement of vision during treatment with a low-arginine dietR R McInnes, S A Arshinoff, L Bell, et al.
Journal of Molecular Biology|June 3, 1994
Expression, purification, crystallization and preliminary X-ray analysis of human argininosuccinic acid lyaseM A Turner, A M Achyuthan, M S Hershfield, et al.
Neuron|June 1, 1992
Cloning of the cDNA for a novel photoreceptor membrane protein (rom-1) identifies a disk rim protein family implicated in human retinopathiesR A Bascom, S Manara, L Collins, et al.
Human Molecular Genetics|November 1, 1993
Polymorphisms and rare sequence variants at the ROM1 locusR A Bascom, L Liu, P Humphries, et al.
Proceedings of the National Academy of Sciences of the United States of America|June 28, 2001
Deficiency of rds/peripherin causes photoreceptor death in mouse models of digenic and dominant retinitis pigmentosaW Kedzierski, S Nusinowitz, D Birch, et al.
Investigative Ophthalmology & Visual Science|June 1, 1997
Pax-6, Prox 1, and Chx10 homeobox gene expression correlates with phenotypic fate of retinal precursor cellsT Belecky-Adams, S Tomarev, H S Li, et al.
Mechanisms of Development|December 4, 2001
Vsx1, a rapidly evolving paired-like homeobox gene expressed in cone bipolar cellsR L Chow, B Snow, J Novak, et al.
Genome Research|May 1, 1997
A differential hybridization scheme to identify photoreceptor-specific genesD A Swanson, C L Freund, J M Steel, et al.
Pediatrics|January 1, 1981
Metabolic abnormalities in the idiopathic Fanconi syndrome: studies of carbohydrate metabolism in two patientsR W Chesney, B S Kaplan, D Teitel, et al.
Pageof 8

Showing results (41-50 of 74) with videos related to

Sort By:
Pageof 8
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.
Lancet (London, England)|March 7, 1981
Hyperornithinaemia and gyrate atrophy of the retina: improvement of vision during treatment with a low-arginine dietR R McInnes, S A Arshinoff, L Bell, et al.
Journal of Molecular Biology|June 3, 1994
Expression, purification, crystallization and preliminary X-ray analysis of human argininosuccinic acid lyaseM A Turner, A M Achyuthan, M S Hershfield, et al.
Neuron|June 1, 1992
Cloning of the cDNA for a novel photoreceptor membrane protein (rom-1) identifies a disk rim protein family implicated in human retinopathiesR A Bascom, S Manara, L Collins, et al.
Human Molecular Genetics|November 1, 1993
Polymorphisms and rare sequence variants at the ROM1 locusR A Bascom, L Liu, P Humphries, et al.
Proceedings of the National Academy of Sciences of the United States of America|June 28, 2001
Deficiency of rds/peripherin causes photoreceptor death in mouse models of digenic and dominant retinitis pigmentosaW Kedzierski, S Nusinowitz, D Birch, et al.
Investigative Ophthalmology & Visual Science|June 1, 1997
Pax-6, Prox 1, and Chx10 homeobox gene expression correlates with phenotypic fate of retinal precursor cellsT Belecky-Adams, S Tomarev, H S Li, et al.
Mechanisms of Development|December 4, 2001
Vsx1, a rapidly evolving paired-like homeobox gene expressed in cone bipolar cellsR L Chow, B Snow, J Novak, et al.
Genome Research|May 1, 1997
A differential hybridization scheme to identify photoreceptor-specific genesD A Swanson, C L Freund, J M Steel, et al.
Pediatrics|January 1, 1981
Metabolic abnormalities in the idiopathic Fanconi syndrome: studies of carbohydrate metabolism in two patientsR W Chesney, B S Kaplan, D Teitel, et al.
Pageof 8