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R McInnes

Showing results (121-130 of 140) with videos related to

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American Journal of Medical Genetics|April 15, 1994
Barth syndrome: clinical observations and genetic linkage studiesJ Christodoulou, R R McInnes, V Jay, et al.
Plos One|March 8, 2013
Endothelin-2-mediated protection of mutant photoreceptors in inherited photoreceptor degenerationAlexa N Bramall, Michael J Szego, Laura R Pacione, et al.
Investigative Ophthalmology & Visual Science|November 6, 1998
Retinal degenerations with truncation mutations in the cone-rod homeobox (CRX) geneS G Jacobson, A V Cideciyan, Y Huang, et al.
Nature Genetics|May 10, 2000
Rom-1 is required for rod photoreceptor viability and the regulation of disk morphogenesisG Clarke, A F Goldberg, D Vidgen, et al.
Nature Genetics|April 16, 1998
De novo mutations in the CRX homeobox gene associated with Leber congenital amaurosisC L Freund, Q L Wang, S Chen, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 13, 2013
Neto2 is a KCC2 interacting protein required for neuronal Cl- regulation in hippocampal neuronsEvgueni A Ivakine, Brooke A Acton, Vivek Mahadevan, et al.
Human Molecular Genetics|July 2, 2004
Nuclear receptor NR2E3 gene mutations distort human retinal laminar architecture and cause an unusual degenerationSamuel G Jacobson, Alexander Sumaroka, Tomas S Aleman, et al.
Developmental Biology|September 27, 2005
The Iroquois homeobox gene, Irx5, is required for retinal cone bipolar cell developmentChi Wa Cheng, Robert L Chow, Mélanie Lebel, et al.
Eneuro|October 15, 2015
Disruption of Src Is Associated with Phenotypes Related to Williams-Beuren Syndrome and Altered Cellular Localization of TFII-ILaleh Sinai, Evgueni A Ivakine, Emily Lam, et al.
Stem Cells (Dayton, Ohio)|December 17, 2009
Maximizing functional photoreceptor differentiation from adult human retinal stem cellsTomoyuki Inoue, Brenda L K Coles, Kim Dorval, et al.
Pageof 14

Showing results (121-130 of 140) with videos related to

Sort By:
Pageof 14
American Journal of Medical Genetics|April 15, 1994
Barth syndrome: clinical observations and genetic linkage studiesJ Christodoulou, R R McInnes, V Jay, et al.
Plos One|March 8, 2013
Endothelin-2-mediated protection of mutant photoreceptors in inherited photoreceptor degenerationAlexa N Bramall, Michael J Szego, Laura R Pacione, et al.
Investigative Ophthalmology & Visual Science|November 6, 1998
Retinal degenerations with truncation mutations in the cone-rod homeobox (CRX) geneS G Jacobson, A V Cideciyan, Y Huang, et al.
Nature Genetics|May 10, 2000
Rom-1 is required for rod photoreceptor viability and the regulation of disk morphogenesisG Clarke, A F Goldberg, D Vidgen, et al.
Nature Genetics|April 16, 1998
De novo mutations in the CRX homeobox gene associated with Leber congenital amaurosisC L Freund, Q L Wang, S Chen, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 13, 2013
Neto2 is a KCC2 interacting protein required for neuronal Cl- regulation in hippocampal neuronsEvgueni A Ivakine, Brooke A Acton, Vivek Mahadevan, et al.
Human Molecular Genetics|July 2, 2004
Nuclear receptor NR2E3 gene mutations distort human retinal laminar architecture and cause an unusual degenerationSamuel G Jacobson, Alexander Sumaroka, Tomas S Aleman, et al.
Developmental Biology|September 27, 2005
The Iroquois homeobox gene, Irx5, is required for retinal cone bipolar cell developmentChi Wa Cheng, Robert L Chow, Mélanie Lebel, et al.
Eneuro|October 15, 2015
Disruption of Src Is Associated with Phenotypes Related to Williams-Beuren Syndrome and Altered Cellular Localization of TFII-ILaleh Sinai, Evgueni A Ivakine, Emily Lam, et al.
Stem Cells (Dayton, Ohio)|December 17, 2009
Maximizing functional photoreceptor differentiation from adult human retinal stem cellsTomoyuki Inoue, Brenda L K Coles, Kim Dorval, et al.
Pageof 14