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R McInnes

Showing results (81-90 of 140) with videos related to

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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.
Human Mutation|August 31, 2006
Deletion hotspot in the argininosuccinate lyase gene: association with topoisomerase II and DNA polymerase alpha sitesJohn Christodoulou, Hugh J Craig, David C Walker, et al.
Development (Cambridge, England)|December 4, 2004
Chx10 repression of Mitf is required for the maintenance of mammalian neuroretinal identityD Jonathan Horsford, Minh-Thanh T Nguyen, Grant C Sellar, 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.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|July 8, 2011
Neto1 is an auxiliary subunit of native synaptic kainate receptorsMan Tang, Kenneth A Pelkey, David Ng, et al.
The American Journal of Pathology|October 1, 1991
Renal disease in carrier female dogs with X-linked hereditary nephritis. Implications for female patients with this diseaseR Baumal, P Thorner, V E Valli, 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 14

Showing results (81-90 of 140) with videos related to

Sort By:
Pageof 14
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.
Human Mutation|August 31, 2006
Deletion hotspot in the argininosuccinate lyase gene: association with topoisomerase II and DNA polymerase alpha sitesJohn Christodoulou, Hugh J Craig, David C Walker, et al.
Development (Cambridge, England)|December 4, 2004
Chx10 repression of Mitf is required for the maintenance of mammalian neuroretinal identityD Jonathan Horsford, Minh-Thanh T Nguyen, Grant C Sellar, 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.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|July 8, 2011
Neto1 is an auxiliary subunit of native synaptic kainate receptorsMan Tang, Kenneth A Pelkey, David Ng, et al.
The American Journal of Pathology|October 1, 1991
Renal disease in carrier female dogs with X-linked hereditary nephritis. Implications for female patients with this diseaseR Baumal, P Thorner, V E Valli, 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 14