RP1 is required for the correct stacking of outer segment discs.
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E. Pugh | E. Pierce | A. Lyubarsky | Qin Liu | J. Skalet
[1] C. Walsh,et al. The DCX-domain tandems of doublecortin and doublecortin-like kinase , 2003, Nature Structural Biology.
[2] K. Nave,et al. Genetic background determines phenotypic severity of the Plp rumpshaker mutation , 2003, Journal of neuroscience research.
[3] A. Godzik,et al. The retinitis pigmentosa GTPase regulator (RPGR)- interacting protein: Subserving RPGR function and participating in disk morphogenesis , 2003, Proceedings of the National Academy of Sciences of the United States of America.
[4] L. Ostrowski,et al. A Proteomic Analysis of Human Cilia , 2002, Molecular & Cellular Proteomics.
[5] Jiangang Gao,et al. Progressive photoreceptor degeneration, outer segment dysplasia, and rhodopsin mislocalization in mice with targeted disruption of the retinitis pigmentosa-1 (Rp1) gene , 2002, Proceedings of the National Academy of Sciences of the United States of America.
[6] S. Baker,et al. The intraflagellar transport protein, IFT88, is essential for vertebrate photoreceptor assembly and maintenance , 2002, The Journal of cell biology.
[7] E. Zrenner,et al. A novel mutation of the RP1 gene (Lys778ter) associated with autosomal dominant retinitis pigmentosa , 2002, The British journal of ophthalmology.
[8] J. Nathans,et al. A Photoreceptor-Specific Cadherin Is Essential for the Structural Integrity of the Outer Segment and for Photoreceptor Survival , 2001, Neuron.
[9] T. L. McGee,et al. Clinical features and mutations in patients with dominant retinitis pigmentosa-1 (RP1). , 2001, Investigative ophthalmology & visual science.
[10] A. Bird,et al. RP1 protein truncating mutations predominate at the RP1 adRP locus. , 2000, Investigative ophthalmology & visual science.
[11] C. Walsh,et al. Patient Mutations in Doublecortin Define a Repeated Tubulin-binding Domain* , 2000, The Journal of Biological Chemistry.
[12] Daniel Chui,et al. Genetic Evidence for Selective Transport of Opsin and Arrestin by Kinesin-II in Mammalian Photoreceptors , 2000, Cell.
[13] R G Weleber,et al. Disease expression of RP1 mutations causing autosomal dominant retinitis pigmentosa. , 2000, Investigative ophthalmology & visual science.
[14] R. D'Amato,et al. Genetic heterogeneity of angiogenesis in mice , 2000, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.
[15] M. Simon,et al. Mice Lacking G-Protein Receptor Kinase 1 Have Profoundly Slowed Recovery of Cone-Driven Retinal Responses , 2000, The Journal of Neuroscience.
[16] K. Frazer,et al. Photoreceptor localization of the KIF3A and KIF3B subunits of the heterotrimeric microtubule motor kinesin II in vertebrate retina. , 1999, Experimental eye research.
[17] M. Hims,et al. Mutations in the RP1 gene causing autosomal dominant retinitis pigmentosa. , 1999, Human molecular genetics.
[18] Scott L. Diamond,et al. Nuclear targeting peptide scaffolds for lipofection of nondividing mammalian cells , 1999, Nature Biotechnology.
[19] K. Steel,et al. Myosin VIIa Participates in Opsin Transport through The Photoreceptor Cilium , 1999, The Journal of Neuroscience.
[20] T. L. McGee,et al. Mutations in a gene encoding a new oxygen-regulated photoreceptor protein cause dominant retinitis pigmentosa , 1999, Nature Genetics.
[21] C. Walsh,et al. Doublecortin Is a Microtubule-Associated Protein and Is Expressed Widely by Migrating Neurons , 1999, Neuron.
[22] E. Pugh,et al. UV- and Midwave-Sensitive Cone-Driven Retinal Responses of the Mouse: A Possible Phenotype for Coexpression of Cone Photopigments , 1999, The Journal of Neuroscience.
[23] M. Bartolomei,et al. Deletion of the H19 differentially methylated domain results in loss of imprinted expression of H19 and Igf2. , 1998, Genes & development.
[24] L. Maquat,et al. Intron function in the nonsense-mediated decay of beta-globin mRNA: indications that pre-mRNA splicing in the nucleus can influence mRNA translation in the cytoplasm. , 1998, RNA.
[25] I. Scheffer,et al. doublecortin , a Brain-Specific Gene Mutated in Human X-Linked Lissencephaly and Double Cortex Syndrome, Encodes a Putative Signaling Protein , 1998, Cell.
[26] G. Travis,et al. The photoreceptor rim protein is an ABC transporter encoded by the gene for recessive Stargardt's disease (ABCR) , 1997, FEBS letters.
[27] B. Hogan,et al. The winged helix gene, Mf3, is required for normal development of the diencephalon and midbrain, postnatal growth and the milk-ejection reflex. , 1997, Development.
[28] E. Pugh,et al. Recovery phase of the murine rod photoresponse reconstructed from electroretinographic recordings , 1996, The Journal of neuroscience : the official journal of the Society for Neuroscience.
[29] D. Cooper,et al. Ectopic (illegitimate) transcription: new possibilities for the analysis and diagnosis of human genetic disease. , 1994, Annals of medicine.
[30] A. Matus,et al. A novel strategy for the immunological tagging of cDNA constructs. , 1993, Gene.
[31] T. Lamb,et al. Amplification and kinetics of the activation steps in phototransduction. , 1993, Biochimica et biophysica acta.
[32] M. Chaitin,et al. Immunogold localization of myosin in the photoreceptor cilium. , 1992, Investigative ophthalmology & visual science.
[33] Donald J. Zack,et al. A locus control region adjacent to the human red and green visual pigment genes , 1992, Neuron.
[34] R. Molday,et al. Cloning of the CDNA for a novel photoreceptor membrane protein (rom-1) identifies a disk rim protein family implicated in human retinopathies , 1992, Neuron.
[35] E N Pugh,et al. A quantitative account of the activation steps involved in phototransduction in amphibian photoreceptors. , 1992, The Journal of physiology.
[36] S. Daiger,et al. Linkage mapping of autosomal dominant retinitis pigmentosa (RP1) to the pericentric region of human chromosome 8. , 1991, Genomics.
[37] David S. Williams,et al. Organization of actin filaments and immunocolocalization of alpha‐actinin in the connecting cilium of rat photoreceptors , 1989, The Journal of comparative neurology.
[38] R. Fariss,et al. Disruption of microfilament organization and deregulation of disk membrane morphogenesis by cytochalasin D in rod and cone photoreceptors , 1988, The Journal of comparative neurology.
[39] M. Kaplan,et al. Lengths of immunolabeled ciliary microtubules in frog photoreceptor outer segments. , 1987, Experimental eye research.
[40] G K Lewis,et al. Isolation of monoclonal antibodies specific for human c-myc proto-oncogene product , 1985, Molecular and cellular biology.
[41] D. Papermaster,et al. Actin in the photoreceptor connecting cilium: immunocytochemical localization to the site of outer segment disk formation , 1984, The Journal of cell biology.
[42] Don H. Anderson,et al. Disc morphogenesis in vertebrate photoreceptors , 1980, Vision Research.
[43] H. Towbin,et al. Electrophoretic transfer of proteins from polyacrylamide gels to nitrocellulose sheets: procedure and some applications. , 1979, Proceedings of the National Academy of Sciences of the United States of America.
[44] S. Fisher,et al. The photoreceptors and pigment epithelium of the adult Xenopus retina: morphology and outer segment renewal , 1978, Proceedings of the Royal Society of London. Series B. Biological Sciences.
[45] D. Anderson,et al. Mammalian cones: disc shedding, phagocytosis, and renewal. , 1978, Investigative ophthalmology & visual science.
[46] M. Spence,et al. Probable genetic linkage between autosomal dominant retinitis pigmentosa (RP) and amylase (AMY2): evidence of an RP locus on chromosome 1. , 1977, American journal of human genetics.
[47] U. K. Laemmli,et al. Cleavage of Structural Proteins during the Assembly of the Head of Bacteriophage T4 , 1970, Nature.
[48] W. A. Hagins,et al. Dark current and photocurrent in retinal rods. , 1970, Biophysical journal.
[49] R. W. Young,et al. Passage of newly formed protein through the connecting cilium of retina rods in the frog. , 1968, Journal of ultrastructure research.
[50] R. W. Young. THE RENEWAL OF PHOTORECEPTOR CELL OUTER SEGMENTS , 1967, The Journal of cell biology.
[51] S. Nilsson. RECEPTOR CELL OUTER SEGMENT DEVELOPMENT AND ULTRASTRUCTURE OF THE DISK MEMBRANES IN THE RETINA OF THE TADPOLE (RANA PIPIENS). , 1964, Journal of ultrastructure research.
[52] D. Klein,et al. Immunocytochemical demonstration of retinal S-antigen in the pineal organ of four mammalian species , 2004, Cell and Tissue Research.
[53] A. Milam,et al. Identification and subcellular localization of the RP1 protein in human and mouse photoreceptors. , 2002, Investigative ophthalmology & visual science.
[54] A. Goldberg,et al. Photoreceptor renewal: a role for peripherin/rds. , 2002, International review of cytology.
[55] Katrina Spilsbury,et al. Addition of a c-myc epitope tag within the VEGF protein does not affect in vitro biological activity. , 2001, Biochemistry and cell biology = Biochimie et biologie cellulaire.
[56] E. Pugh,et al. The Origin of the Major Rod- and Cone-Driven Components of the Rodent Electroretinogram and the Effect of Age and Light-Rearing History on the Magnitude of These Components , 1998 .
[57] T. Williams,et al. Photostasis and Related Phenomena , 1998, Springer US.
[58] U. Wolfrum. Centrin in the photoreceptor cells of mammalian retinae. , 1995, Cell motility and the cytoskeleton.
[59] Alexandra L. Joyner,et al. Gene targeting: a practical approach. , 1993 .
[60] J. Besharse,et al. Transmembrane assemblage of the photoreceptor connecting cilium and motile cilium transition zone contain a common immunologic epitope. , 1990, Cell motility and the cytoskeleton.
[61] L. Molday,et al. Peripherin. A rim-specific membrane protein of rod outer segment discs. , 1987, Investigative ophthalmology & visual science.