GeorgeInanaMD

PubMed

• 70 citations
  RPE phagocytic function declines in age-related macular degeneration and is rescued by human umbilical tissue derived cells
  George Inana, Christopher Murat, Weijun An, Xiang Yao, Ian Ross Harris, Jing Cao> ;Journal of Translational Medicine. 2018 Mar 13
• 27 citations
  Human umbilical tissue-derived cells rescue retinal pigment epithelium dysfunction in retinal degeneration.
  Jing Cao, Christopher Murat, Weijun An, Xiang Yao, Lee John, Sandra Santulli-Marotto, Ian Ross Harris, George Inana> ;Stem Cells. 2016 Feb 1
• 128 citations
  UNC119 is required for G protein trafficking in sensory neurons
  Houbin Zhang, Ryan Constantine, Sergey M. Vorobiev, Yang Chen, Jayaraman Seetharaman, Yuanpeng J. Huang, Rong Xiao, Gaetano T. Montelione, Cecilia D. Gerstner, M. Wayn...> ;Nature Neuroscience. 2011 Jul 1
• 36 citations
  Targeted inactivation of synaptic HRG4 (UNC119) causes dysfunction in the distal photoreceptor and slow retinal degeneration, revealing a new function.
  Y. Ishiba, Tomomi Higashide, Naoki Mori, Akira Kobayashi, S. Kubota, M.J. McLaren, Hiromasa Satoh, Fulton Wong, George Inana> ;Experimental Eye Research. 2007 Mar 1
• 13 citations
  Truncation mutation in HRG4 (UNC119) leads to mitochondrial ANT-1-mediated photoreceptor synaptic and retinal degeneration by apoptosis.
  Naoki Mori, Y. Ishiba, S. Kubota, Akira Kobayashi, Tomomi Higashide, M.J. McLaren, George Inana> ;Investigative Ophthalmology & Visual Science. 2006 Apr 1
• 7 citations
  Truncation and mutagenesis analysis of the human X-arrestin gene promoter
  Takuro Fujimaki, Zhen Yong Huang, Hitoshi Kitagawa, Hitoshi Sakuma, Akira Murakami, Atsushi Kanai, M.J. McLaren, George Inana> ;Gene. 2004 Sep 15
• 43 citations
  Photoreceptor synaptic protein HRG4 (UNC119) interacts with ARL2 via a putative conserved domain.
  Akira Kobayashi, S. Kubota, Naoki Mori, M.J. McLaren, George Inana> ;FEBS Letters. 2003 Jan 16
• 16 citations
  Changes in retinal synaptic proteins in the transgenic model expressing a mutant HRG4 (UNC119).
  S. Kubota, Akira Kobayashi, Naoki Mori, Tomomi Higashide, M.J. McLaren, George Inana> ;Investigative Ophthalmology & Visual Science. 2002 Feb 1
• 96 citations
  HRG4 (UNC119) mutation found in cone-rod dystrophy causes retinal degeneration in a transgenic model.
  Akira Kobayashi, Tomomi Higashide, D. I. Hamasaki, S. Kubota, Hitoshi Sakuma, Weijun Weijun An, Takuro Fujimaki, M.J. McLaren, Richard G Weleber, George Inana> ;Investigative Ophthalmology & Visual Science. 2000 Oct 1
• 25 citations
  Characterization of the gene for HRG4 (UNC119), a novel photoreceptor synaptic protein homologous to unc-119.
  Tomomi Higashide, George Inana> ;Genomics. 1999 May 1
• 14 citations
  Genotype-phenotype correlation of a pyridoxine-responsive form of gyrate atrophy.
  Yukihiko Mashima, Richard G. Weleber, Nancy G. Kennaway, George Inana> ;Ophthalmic Genetics. 1999 Dec 1
• 21 citations
  Isolation and characterization of the human X-arrestin gene.
  Hitoshi Sakuma, Akira Murakami, Takuro Fujimaki, George Inana> ;Gene. 1998 Dec 11
• 42 citations
  Localization of HRG4, a photoreceptor protein homologous to Unc-119, in ribbon synapse
  Tomomi Higashide, M.J. McLaren, George Inana> ;Investigative Ophthalmology & Visual Science. 1998 Apr 1
• 87 citations
  Spectrum of Mutations in the RPGR Gene That Are Identified in 20% of Families with X-Linked Retinitis Pigmentosa
  M. Buraczynska, Weiping Wu, Ricardo Fujita, Kinga Buraczynska, Ellen Phelps, Sten Andréasson, Jean Bennett, David G. Birch, Gerald A. Fishman, Dennis R. Hoffman, Georg...> ;American Journal of Human Genetics. 1997 Dec 1
• 25 citations
  Inherited retinal degeneration: basic FGF induces phagocytic competence in cultured RPE cells from RCS rats
  M.J. McLaren, George Inana> ;FEBS Letters. 1997 Jul 21
• 6 citations
  Evaluation of the human gene encoding recoverin in patients with retinitis pigmentosa or an allied disease.
  A. H. Parminder, Akira Murakami, George Inana, Eliot L. Berson, Thaddeus P. Dryja> ;Investigative Ophthalmology & Visual Science. 1997 Mar 1
• 1 citations
  Genetic heterogeneity in Hispanic families with autosomal dominant juvenile glaucoma.
  Darrell WuDunn, Richard K. Parrish, George Inana> ;Ophthalmic Genetics. 1996 Sep 1
• 11 citations
  Analysis of basic fibroblast growth factor in rats with inherited retinal degeneration
  M.J. McLaren, W. An, Michael E. Brown, George Inana> ;FEBS Letters. 1996 May 27
• 39 citations
  Immunolocalization of X-arrestin in human cone photoreceptors
  Hitoshi Sakuma, George Inana, Akira Murakami, Tomomi Higashide, M.J. McLaren> ;FEBS Letters. 1996 Mar 11
• 8 citations
  Analysis of phosducin as a candidate gene for retinopathies
  Fumino Ara-iwata, Samuel G. Jacobson, J. Donald M. Gass, Yoshihiro Hotta, Keiko Fujiki, Mutsuko Hayakawa, George Inana> ;Ophthalmic Genetics. 1996 Mar 1
• 50 citations
  Cloning of the cDNA for a Novel Photoreceptor Protein (
  Tomomi Higashide, Akira Murakami, M.J. McLaren, George Inana> ;The Journal of Biological Chemistry. 1996 Jan 19
• 11 citations
  Heterogeneity and uniqueness of ornithine aminotransferase mutations found in Japanese gyrate atrophy patients
  Yukihiko Mashima, Takashi Shiono, Makoto Tamai, George Inana> ;Current Eye Research. 1996 Jul 1
• 27 citations
  A heterozygous putative null mutation in ROM1 without a mutation in peripherin/RDS in a family with retinitis pigmentosa
  Hitoshi Sakuma, George Inana, Akira Murakami, Toshihiro Yajima, Richard G. Weleber, William H. Murphey, J. Donald M. Gass, Yoshihiro Hotta, Mutsuko Hayakawa, Keiko Fuj...> ;Genomics. 1995 May 20
• 8 citations
  Rapid and efficient molecular analysis of gyrate atrophy using denaturing gradient gel electrophoresis.
  Yukihiko Mashima, T Shiono, G Inana> ;Investigative Ophthalmology & Visual Science. 1994 Mar 1
• 86 citations
  X-arrestin: a new retinal arrestin mapping to the X chromosome.
  Akira Murakami, Toshihiro Yajima, Hitoshi Sakuma, M.J. McLaren, George Inana> ;FEBS Letters. 1993 Nov 15
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