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George Inana

Research Profile

Chemicals & Drugs

Disorders

Anatomy

Procedures

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Nucleic Acid Hybridization

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Houbin Zhang; Yang Chen; Ryan Constantine; M Wayne Davis; Cecilia D Gerstner; Christopher P Hill; Yuanpeng Janet Huang; George Inana; Erik M Jorgensen; Gaetano T Montelione; Jayaraman Seetharaman; Liang Tong; Sergey Vorobiev; Frank G Whitby; Rong Xiao; Wolfgang Baehr
UNC119 is required for G protein trafficking in sensory neurons.
Yasutsugu Ishiba; Tomomi Higashide; Naoki Mori; Akira Kobayashi; Shinya Kubota; Margaret J McLaren; Hiromasa Satoh; Fulton Wong; George Inana
Targeted inactivation of synaptic HRG4 (UNC119) causes dysfunction in the distal photoreceptor and slow retinal degeneration, revealing a new function.
Naoki Mori; Yasutsugu Ishiba; Shinya Kubota; Akira Kobayashi; Tomomi Higashide; Margaret J McLaren; George Inana
Truncation mutation in HRG4 (UNC119) leads to mitochondrial ANT-1-mediated photoreceptor synaptic and retinal degeneration by apoptosis.

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All Publications

2011: Houbin Zhang; Yang Chen; Ryan Constantine; M Wayne Davis; Cecilia D Gerstner; Christopher P Hill; Yuanpeng Janet Huang; George Inana; Erik M Jorgensen; Gaetano T Montelione; Jayaraman Seetharaman; Liang Tong; Sergey Vorobiev; Frank G Whitby; Rong Xiao; Wolfgang Baehr
UNC119 is required for G protein trafficking in sensory neurons.
Nature neuroscience 2011;14(7):874-80.
2007: Yasutsugu Ishiba; Tomomi Higashide; Naoki Mori; Akira Kobayashi; Shinya Kubota; Margaret J McLaren; Hiromasa Satoh; Fulton Wong; George Inana
Targeted inactivation of synaptic HRG4 (UNC119) causes dysfunction in the distal photoreceptor and slow retinal degeneration, revealing a new function.
Experimental eye research 2007;84(3):473-85.
2006: Naoki Mori; Yasutsugu Ishiba; Shinya Kubota; Akira Kobayashi; Tomomi Higashide; Margaret J McLaren; George Inana
Truncation mutation in HRG4 (UNC119) leads to mitochondrial ANT-1-mediated photoreceptor synaptic and retinal degeneration by apoptosis.
Investigative ophthalmology & visual science 2006;47(4):1281-92.
2004: Takuro Fujimaki; Zhen-Yong Huang; Hitoshi Kitagawa; Hitoshi Sakuma; Akira Murakami; Atsushi Kanai; Margaret J McLaren; George Inana
Truncation and mutagenesis analysis of the human X-arrestin gene promoter.
Gene 2004;339():139-47.
2003: Akira Kobayashi; Shinya Kubota; Naoki Mori; Margaret J McLaren; George Inana
Photoreceptor synaptic protein HRG4 (UNC119) interacts with ARL2 via a putative conserved domain.
FEBS letters 2003;534(1-3):26-32.
2002: Eriko Fujiwara; Hui Qiu; Mu Liu; Byron Lam; Jean-Marie Parel; George Inana; Duco Hamasaki
Reliability and significance of measurements of a-wave latency in rats.
Japanese journal of ophthalmology 2002;46(4):419-25.
2002: Shinya Kubota; Akira Kobayashi; Naoki Mori; Tomomi Higashide; Margaret J McLaren; George Inana
Changes in retinal synaptic proteins in the transgenic model expressing a mutant HRG4 (UNC119).
Investigative ophthalmology & visual science 2002;43(2):308-13.
2000: Akira Kobayashi; Tomomi Higashide; Duco Hamasaki; Shinya Kubota; H Sakuma; W An; T Fujimaki; Margaret J McLaren; Richard G Weleber; George Inana
HRG4 (UNC119) mutation found in cone-rod dystrophy causes retinal degeneration in a transgenic model.
Investigative ophthalmology & visual science 2000;41(11):3268-77.
1999: Y G Mashima; Richard G Weleber; Nancy G Kennaway; George Inana
Genotype-phenotype correlation of a pyridoxine-responsive form of gyrate atrophy.
Ophthalmic genetics 1999;20(4):219-24.
1999: Tomomi Higashide; George Inana
Characterization of the gene for HRG4 (UNC119), a novel photoreceptor synaptic protein homologous to unc-119.
Genomics 1999;57(3):446-50.
1998: H Sakuma; A Murakami; T Fujimaki; George Inana
Isolation and characterization of the human X-arrestin gene.
Gene 1998;224(1-2):87-95.
1998: Tomomi Higashide; Margaret J McLaren; George Inana
Localization of HRG4, a photoreceptor protein homologous to Unc-119, in ribbon synapse.
Investigative ophthalmology & visual science 1998;39(5):690-8.
1997: Monika Buraczynska; W Wu; Ricardo Fujita; Kinga Buraczynska; E Phelps; Sten Andréasson; J Bennett; David G Birch; Gerald A Fishman; Dennis R Hoffman; George Inana; Samuel G Jacobson; Maria A Musarella; Paul Sieving; Anand Swaroop
Spectrum of mutations in the RPGR gene that are identified in 20% of families with X-linked retinitis pigmentosa.
American journal of human genetics 1997;61(6):1287-92.
1997: Margaret J McLaren; George Inana
Inherited retinal degeneration: basic FGF induces phagocytic competence in cultured RPE cells from RCS rats.
FEBS letters 1997;412(1):21-9.
1997: A H Parminder; A Murakami; George Inana; Eliot L Berson; Thaddeus P Dryja
Evaluation of the human gene encoding recoverin in patients with retinitis pigmentosa or an allied disease.
Investigative ophthalmology & visual science 1997;38(3):704-9.
1997: S K Gupta; Christine A B Jollimore; M J McLaren; George Inana; Melanie E M Kelly
Mammalian retinal pigment epithelial cells in vitro respond to the neurokines ciliary neurotrophic factor and leukemia inhibitory factor.
Biochemistry and cell biology = Biochimie et biologie cellulaire 1997;75(2):119-25.
1996: D WuDunn; Richard K Parrish; George Inana
Genetic heterogeneity in Hispanic families with autosomal dominant juvenile glaucoma.
Ophthalmic genetics 1996;17(3):87-94.
1996: Y Mashima; T Shiono; M Tamai; George Inana
Heterogeneity and uniqueness of ornithine aminotransferase mutations found in Japanese gyrate atrophy patients.
Current eye research 1996;15(7):792-6.
1996: Margaret J McLaren; W An; M E Brown; George Inana
Analysis of basic fibroblast growth factor in rats with inherited retinal degeneration.
FEBS letters 1996;387(1):63-70.
1996: H Sakuma; George Inana; A Murakami; Tomomi Higashide; Margaret J McLaren
Immunolocalization of X-arrestin in human cone photoreceptors.
FEBS letters 1996;382(1-2):105-10.
1996: F Ara-Iwata; S G Jacobson; J D Gass; Y Hotta; K Fujiki; M Hayakawa; George Inana
Analysis of phosducin as a candidate gene for retinopathies.
Ophthalmic genetics 1996;17(1):3-14.
1996: Tomomi Higashide; A Murakami; Margaret J McLaren; George Inana
Cloning of the cDNA for a novel photoreceptor protein.
The Journal of biological chemistry 1996;271(3):1797-804.
1995: H Sakuma; George Inana; A Murakami; T Yajima; Richard G Weleber; W H Murphey; J D Gass; Y Hotta; M Hayakawa; K Fujiki
A heterozygous putative null mutation in ROM1 without a mutation in peripherin/RDS in a family with retinitis pigmentosa.
Genomics 1995;27(2):384-6.
1994: Y Mashima; T Shiono; George Inana
Rapid and efficient molecular analysis of gyrate atrophy using denaturing gradient gel electrophoresis.
Investigative ophthalmology & visual science 1994;35(3):1065-70.
1993: A Murakami; T Yajima; H Sakuma; Margaret J McLaren; George Inana
X-arrestin: a new retinal arrestin mapping to the X chromosome.
FEBS letters 1993;334(2):203-9.
1993: Margaret J McLaren; George Inana; C Y Li
Double fluorescent vital assay of phagocytosis by cultured retinal pigment epithelial cells.
Investigative ophthalmology & visual science 1993;34(2):317-26.
1993: Margaret J McLaren; T Sasabe; C Y Li; M E Brown; George Inana
Spontaneously arising immortal cell line of rat retinal pigmented epithelial cells.
Experimental cell research 1993;204(2):311-20.
1993: J B Bateman; T L Kojis; R M Cantor; C Heinzmann; J T Ngo; M Anne Spence; George Inana; J D Kivlin; D Curtis; RS Sparkes
Linkage analysis of Norrie disease with an X-chromosomal ornithine aminotransferase locus.
Transactions of the American Ophthalmological Society 1993;91():299-307; discussion 307-8.
1992: Samuel G Jacobson; A J Roman; Artur Vahe Cideciyan; M G Robey; Takeshi Iwata; George Inana
X-linked retinitis pigmentosa: functional phenotype of an RP2 genotype.
Investigative ophthalmology & visual science 1992;33(13):3481-92.
1992: Y Mashima; Richard G Weleber; N G Kennaway; George Inana
A single-base change at a splice acceptor site in the ornithine aminotransferase gene causes abnormal RNA splicing in gyrate atrophy.
Human genetics 1992;90(3):305-7.
1992: A Murakami; T Yajima; George Inana
Isolation of human retinal genes: recoverin cDNA and gene.
Biochemical and biophysical research communications 1992;187(1):234-44.
1992: Y Mashima; A Murakami; Richard G Weleber; N G Kennaway; L Clarke; T Shiono; George Inana
Nonsense-codon mutations of the ornithine aminotransferase gene with decreased levels of mutant mRNA in gyrate atrophy.
American journal of human genetics 1992;51(1):81-91.
1992: Y Akaki; Y Hotta; Y Mashima; A Murakami; N G Kennaway; Richard G Weleber; George Inana
A deletion in the ornithine aminotransferase gene in gyrate atrophy.
The Journal of biological chemistry 1992;267(18):12950-4.
1992: Y Hotta; George Inana
Expression of human ornithine aminotransferase (OAT) in OAT-deficient Chinese hamster ovary cells and fibroblasts of gyrate atrophy patient.
Japanese journal of ophthalmology 1992;36(1):28-32.
1991: T Sasabe; George Inana
Mechanism of suppression of malignancy in hybrids between Y79 retinoblastoma and NIH3T3 cells.
Investigative ophthalmology & visual science 1991;32(7):2011-9.
1991: George Inana; Y Hotta; C Zintz; C Chambers; N G Kennaway; Richard G Weleber; A Nakajima; T Shiono
Molecular basis of ornithine aminotransferase defect in gyrate atrophy.
Progress in clinical and biological research 1991;362():191-219.
1990: C B Zintz; George Inana
Analysis of the human ornithine aminotransferase gene family.
Experimental eye research 1990;50(6):759-70.
1990: Narendra Tuteja; Michael Danciger; I Klisak; Renu Tuteja; George Inana; T Mohandas; RS Sparkes; Debora B Farber
Isolation and characterization of cDNA encoding the gamma-subunit of cGMP phosphodiesterase in human retina.
Gene 1990;88(2):227-32.
1990: J T Ngo; J B Bateman; M Anne Spence; V Cortessis; RS Sparkes; J D Kivlin; T Mohandas; George Inana
Ornithine aminotransferase (OAT): recombination between an X-linked OAT sequence (7.5 kb) and the Norrie disease locus.
Genomics 1990;6(1):123-8.
1989: George Inana; C Chambers; Y Hotta; L Inouye; D Filpula; S Pulford; T Shiono
Point mutation affecting processing of the ornithine aminotransferase precursor protein in gyrate atrophy.
The Journal of biological chemistry 1989;264(29):17432-6.
1989: Y Hotta; George Inana
Gene transfer and expression of human ornithine aminotransferase.
Investigative ophthalmology & visual science 1989;30(6):1024-31.
1989: J T Ngo; J B Bateman; V Cortessis; RS Sparkes; T Mohandas; George Inana; M Anne Spence
Norrie disease: linkage analysis using a 4.2-kb RFLP detected by a human ornithine aminotransferase cDNA probe.
Genomics 1989;4(4):539-45.
1989: Y Hotta; N G Kennaway; Richard G Weleber; George Inana
Inheritance of ornithine aminotransferase gene, mRNA, and enzyme defect in a family with gyrate atrophy of the choroid and retina.
American journal of human genetics 1989;44(3):353-7.
1989: George Inana; Y Hotta; C Zintz; A Nakajima; T Shiono; N G Kennaway; Richard G Weleber
Molecular genetics of ornithine aminotransferase defect in gyrate atrophy.
Progress in clinical and biological research 1989;314():99-111.
1988: M Nakamura; Paul Russell; Deborah A Carper; George Inana; J H Kinoshita
Alteration of a developmentally regulated, heat-stable polypeptide in the lens of the Philly mouse. Implications for cataract formation.
The Journal of biological chemistry 1988;263(35):19218-21.
1988: George Inana; Y Hotta; C Zintz; K Takki; Richard G Weleber; N G Kennaway; K Nakayasu; A Nakajima; T Shiono
Expression defect of ornithine aminotransferase gene in gyrate atrophy.
Investigative ophthalmology & visual science 1988;29(7):1001-5.
1988: S Totsuka; George Inana
[Growth characteristics of hybrids between retinoblastoma and non-malignant cell].
Nippon Ganka Gakkai zasshi 1988;92(5):870-5.
1988: S Totsuka; P Matsumura; George Inana
[Molecular biological study of retinoblastoma hybrids between retinoblastoma and non-malignant cell].
Nippon Ganka Gakkai zasshi 1988;92(5):828-36.
1988: George Inana; I Inoue; S Totsuka; C Zintz; Y Hotta; T Shiono; K Nakayasu; A Nakajima; T Ohura; E Kominami
[Molecular genetics of gyrate atrophy].
Tanpakushitsu kakusan koso. Protein, nucleic acid, enzyme 1988;33(5):518-22.
1987: D J Barrett; J B Bateman; RS Sparkes; T Mohandas; I Klisak; George Inana
Chromosomal localization of human ornithine aminotransferase gene sequences to 10q26 and Xp11.2.
Investigative ophthalmology & visual science 1987;28(7):1037-42.
1987: George Inana; S Totsuka; C Zintz; Y Hotta; T Shiono; T Ohura; E Kominami; N Katunuma
Molecular genetics of gyrate atrophy.
Progress in clinical and biological research 1987;247():163-72.
1986: George Inana; S Totsuka; M Redmond; T Dougherty; J Nagle; T Shiono; T Ohura; E Kominami; N Katunuma
Molecular cloning of human ornithine aminotransferase mRNA.
Proceedings of the National Academy of Sciences of the United States of America 1986;83(5):1203-7.
1985: A T Garber; C Winkler; T Shinohara; C R King; George Inana; J Piatigorsky; R J Gold
Selective loss of a family of gene transcripts in a hereditary murine cataract.
Science (New York, N.Y.) 1985;227(4682):74-7.
1984: Joram Piatigorsky; John M Nickerson; C R King; George Inana; J F Hejtmancik; J W Hawkins; Teresa Borras; T Shinohara; Graeme Wistow; B Norman
Crystallin genes: templates for lens transparency.
Ciba Foundation symposium 1984;106():191-207.
1983: George Inana; J Piatigorsky; B Norman; Christine Slingsby; T Blundell
Gene and protein structure of a beta-crystallin polypeptide in murine lens: relationship of exons and structural motifs.
Nature 1983;302(5906):310-5.
1982: George Inana; T Shinohara; J V Maizel; J Piatigorsky
Evolution and diversity of the crystallins. Nucleotide sequence of a beta-crystallin mRNA from the mouse lens.
The Journal of biological chemistry 1982;257(15):9064-71.