Retinal remodeling in human retinitis pigmentosa.
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B. Jones | C. Watt | R. Marc | M. Marmor | R. Pfeiffer | R E Marc | C B Watt | W. D. Ferrell | B W Jones | R L Pfeiffer | W D Ferrell | M Marmor | Rebecca L. Pfeiffer
[1] T. Wensel,et al. R9AP, a membrane anchor for the photoreceptor GTPase accelerating protein, RGS9-1 , 2002, Proceedings of the National Academy of Sciences of the United States of America.
[2] N. K. Dhingra,et al. Spontaneous oscillatory activity in rd1 mouse retina is transferred from ON pathway to OFF pathway via glycinergic synapse. , 2015, Journal of neurophysiology.
[3] Christine C. Boucard,et al. Changes in cortical grey matter density associated with long-standing retinal visual field defects , 2009, Brain : a journal of neurology.
[4] R. Marc,et al. Kainate activation of horizontal, bipolar, amacrine, and ganglion cells in the rabbit retina , 1999, The Journal of comparative neurology.
[5] Liang Xu,et al. Visual response properties of retinal ganglion cells in the royal college of surgeons dystrophic rat. , 2006, Investigative ophthalmology & visual science.
[6] R E Marc,et al. Pattern recognition of amino acid signatures in retinal neurons , 1995, The Journal of neuroscience : the official journal of the Society for Neuroscience.
[7] Günther Zeck,et al. Network Oscillations in Rod-Degenerated Mouse Retinas , 2011, The Journal of Neuroscience.
[8] E. Strettoi,et al. Modifications of retinal neurons in a mouse model of retinitis pigmentosa. , 2000, Proceedings of the National Academy of Sciences of the United States of America.
[9] S. Nelson,et al. Hebb and homeostasis in neuronal plasticity , 2000, Current Opinion in Neurobiology.
[10] Birgit Lorenz,et al. Mutations in RPE65 cause autosomal recessive childhood–onset severe retinal dystrophy , 1997, Nature Genetics.
[11] D. Oprian,et al. Heterozygous missense mutation in the rhodopsin gene as a cause of congenital stationary night blindness , 1993, Nature Genetics.
[12] B. Sagdullaev,et al. Disruption in dopaminergic innervation during photoreceptor degeneration , 2016, The Journal of comparative neurology.
[13] R. Marc. Retinal neurotransmitters, morphology, and color coding , 1982 .
[14] Angelika Braun,et al. Artificial vision with wirelessly powered subretinal electronic implant alpha-IMS , 2013, Proceedings of the Royal Society B: Biological Sciences.
[15] B. J. Klevering,et al. Autosomal-Recessive Retinitis Pigmentosa , 2010 .
[16] Gary J. Bennett,et al. Transsynaptic degeneration in the superficial dorsal horn after sciatic nerve injury: effects of a chronic constriction injury, transection, and strychnine , 1990, Pain.
[17] Janet Rossant,et al. Rom-1 is required for rod photoreceptor viability and the regulation of disk morphogenesis , 2000, Nature Genetics.
[18] J. S. Lauritzen,et al. Building retinal connectomes , 2012, Current Opinion in Neurobiology.
[19] B. Jones,et al. Retinoid receptors trigger neuritogenesis in retinal degenerations , 2012, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.
[20] J. M. Tamarit,et al. Long time remodeling during retinal degeneration evaluated by optical coherence tomography, immunocytochemistry and fundus autofluorescence. , 2016, Experimental eye research.
[21] T. Hain,et al. Early diagnosis of Usher syndrome in infants and children. , 1996, The American journal of otology.
[22] B. Jones,et al. Excitatory Self–signaling In Retinal Remodeling , 2004 .
[23] M. Lavail,et al. Mutation of the receptor tyrosine kinase gene Mertk in the retinal dystrophic RCS rat. , 2000, Human molecular genetics.
[24] P. Sieving,et al. Retinopathy induced in mice by targeted disruption of the rhodopsin gene , 1997, Nature Genetics.
[25] P. Sieving,et al. P23H rhodopsin transgenic rat: correlation of retinal function with histopathology. , 2000, Investigative ophthalmology & visual science.
[26] H. Wässle,et al. Voltage- and transmitter-gated currents in isolated rod bipolar cells of rat retina. , 1990, Journal of neurophysiology.
[27] B. Jones,et al. Neural plasticity revealed by light-induced photoreceptor lesions. , 2006, Advances in experimental medicine and biology.
[28] C. Remé,et al. Light damage in the rat retina: glial fibrillary acidic protein accumulates in Müller cells in correlation with photoreceptor damage. , 1996, Ophthalmic research.
[29] J. Lupski,et al. A photoreceptor cell-specific ATP-binding transporter gene (ABCR) is mutated in recessive Starqardt macular dystrophy , 1997, Nature Genetics.
[30] B. Jones,et al. Retinal remodeling triggered by photoreceptor degenerations , 2003, The Journal of comparative neurology.
[31] A. J. Roman,et al. Improvement and decline in vision with gene therapy in childhood blindness. , 2015, The New England journal of medicine.
[32] W. Smith,et al. Dynamics of Arrestin-Rhodopsin Interactions , 2005, Journal of Biological Chemistry.
[33] Gautam B Awatramani,et al. An Intrinsic Neural Oscillator in the Degenerating Mouse Retina , 2011, The Journal of Neuroscience.
[34] Tanya M. Teslovich,et al. Comparative Genomics Identifies a Flagellar and Basal Body Proteome that Includes the BBS5 Human Disease Gene , 2004, Cell.
[35] K. Hokamp,et al. Gene expression changes during retinal development and rod specification , 2015, Molecular vision.
[36] M. Lavail,et al. Inherited retinal dystrophy in Mer knockout mice. , 2003, Advances in experimental medicine and biology.
[37] B. Jones,et al. Excitation mapping with the organic cation AGB2+ , 2005, Vision Research.
[38] B. Jones,et al. Neural remodeling in retinal degeneration , 2003, Progress in Retinal and Eye Research.
[39] G. A. Limb,et al. Chondroitin Sulfate Proteoglycans and Microglia Prevent Migration and Integration of Grafted Müller Stem Cells into Degenerating Retina , 2008, Stem cells.
[40] T. Wensel. Signal transducing membrane complexes of photoreceptor outer segments , 2008, Vision Research.
[41] T. Reh,et al. Adult donor rod photoreceptors integrate into the mature mouse retina. , 2011, Investigative ophthalmology & visual science.
[42] Martha E. Sommer,et al. Arrestin can act as a regulator of rhodopsin photochemistry , 2006, Vision Research.
[43] B. Sagdullaev,et al. Increased phosphorylation of Cx36 gap junctions in the AII amacrine cells of RD retina , 2015, Front. Cell. Neurosci..
[44] Zhixian Zhang,et al. Activation of RGS9-1GTPase Acceleration by Its Membrane Anchor, R9AP* , 2003, The Journal of Biological Chemistry.
[45] R. Marc,et al. Optogenetics for Retinal Disorders , 2014, Journal of ophthalmic & vision research.
[46] Krista I Kinard,et al. Neural reprogramming in retinal degeneration. , 2007, Investigative ophthalmology & visual science.
[47] R. Marc. Mapping glutamatergic drive in the vertebrate retina with a channel‐permeant organic cation , 1999, The Journal of comparative neurology.
[48] B. Jones,et al. Müller cell metabolic chaos during retinal degeneration. , 2016, Experimental eye research.
[49] B. Morquette,et al. The molecular basis of retinal ganglion cell death in glaucoma , 2012, Progress in Retinal and Eye Research.
[50] James R. Anderson,et al. Retinal remodeling in the Tg P347L rabbit, a large‐eye model of retinal degeneration , 2011, The Journal of comparative neurology.
[51] W. Berger,et al. Identification and functional characterization of a novel rhodopsin mutation associated with autosomal dominant CSNB. , 2008, Investigative ophthalmology & visual science.
[52] W. Baehr,et al. Naturally occurring animal models with outer retina phenotypes , 2009, Vision Research.
[53] R. Baldoni,et al. Aberrant activity in retinal degeneration impairs central visual processing and relies on Cx36-containing gap junctions. , 2016, Experimental eye research.
[54] I. Pinilla,et al. Cellular responses following retinal injuries and therapeutic approaches for neurodegenerative diseases , 2014, Progress in Retinal and Eye Research.
[55] Francois Tremblay,et al. Mutation of the calcium channel gene Cacna1f disrupts calcium signaling, synaptic transmission and cellular organization in mouse retina. , 2005, Human molecular genetics.
[56] Vittorio Porciatti,et al. Morphological and Functional Abnormalities in the Inner Retina of the rd/rd Mouse , 2002, The Journal of Neuroscience.
[57] J. Sebag,et al. Apoptotic photoreceptor cell death after traumatic retinal detachment in humans. , 1996, Archives of ophthalmology.
[58] A. Fulton,et al. Mutations in the RPE65 gene in patients with autosomal recessive retinitis pigmentosa or leber congenital amaurosis. , 1998, Proceedings of the National Academy of Sciences of the United States of America.
[59] K Rohrschneider,et al. Autosomal recessive retinitis pigmentosa and cone-rod dystrophy caused by splice site mutations in the Stargardt's disease gene ABCR. , 1998, Human molecular genetics.
[60] Wei He,et al. Slowed recovery of rod photoresponse in mice lacking the GTPase accelerating protein RGS9-1 , 2000, Nature.
[61] L. V. Johnson,et al. Age-related macular degeneration and the extracellular matrix. , 2004, The New England journal of medicine.
[62] A. Milam,et al. Histopathology of the human retina in retinitis pigmentosa. , 1998, Progress in retinal and eye research.
[63] Radha Ayyagari,et al. Loss of functional ELOVL4 depletes very long-chain fatty acids (≥C28) and the unique ω-O-acylceramides in skin leading to neonatal death , 2007 .
[64] E J Chichilnisky,et al. Changes in physiological properties of rat ganglion cells during retinal degeneration. , 2011, Journal of neurophysiology.
[65] F. Rieke,et al. Essential role of Ca2+-binding protein 4, a Cav1.4 channel regulator, in photoreceptor synaptic function , 2004, Nature Neuroscience.
[66] Margaret Fahnestock,et al. Kindling and status epilepticus models of epilepsy: rewiring the brain , 2004, Progress in Neurobiology.
[67] B. Jones,et al. Extreme retinal remodeling triggered by light damage: implications for age related macular degeneration , 2008, Molecular vision.
[68] Zy Li,et al. Rod photoreceptor neurite sprouting in retinitis pigmentosa , 1995, The Journal of neuroscience : the official journal of the Society for Neuroscience.
[69] T. Dryja,et al. Mutation spectrum of the gene encoding the beta subunit of rod phosphodiesterase among patients with autosomal recessive retinitis pigmentosa. , 1995, Proceedings of the National Academy of Sciences of the United States of America.
[70] Botond Roska,et al. Gene therapy for blindness. , 2013, Annual review of neuroscience.
[71] J. Morrison,et al. Differential Subcellular Regulation of NMDAR1 Protein and mRNA in Dendrites of Dentate Gyrus Granule Cells after Perforant Path Transection , 1997, The Journal of Neuroscience.
[72] J. S. Lauritzen,et al. The AII amacrine cell connectome: a dense network hub , 2014, Front. Neural Circuits.
[73] Xiaoming Jin,et al. Epilepsy following cortical injury: Cellular and molecular mechanisms as targets for potential prophylaxis , 2009, Epilepsia.
[74] B. Sagdullaev,et al. Aberrant synaptic input to retinal ganglion cells varies with morphology in a mouse model of retinal degeneration , 2014, The Journal of comparative neurology.
[75] Felice A. Dunn. Photoreceptor Ablation Initiates the Immediate Loss of Glutamate Receptors in Postsynaptic Bipolar Cells in Retina , 2015, The Journal of Neuroscience.
[76] C. Morgans,et al. Rod bipolar cells and horizontal cells form displaced synaptic contacts with rods in the outer nuclear layer of the nob2 retina , 2007, The Journal of comparative neurology.
[77] Stanislao Rizzo,et al. The Argus II Retinal Prosthesis: 12-month outcomes from a single-study center. , 2014, American journal of ophthalmology.
[78] B. Jones,et al. Retinal Remodeling: Circuitry Revisions Triggered by Photoreceptor Degeneration , 2006 .
[79] Kenneth R Alexander,et al. Night blindness and abnormal cone electroretinogram ON responses in patients with mutations in the GRM6 gene encoding mGluR6. , 2005, Proceedings of the National Academy of Sciences of the United States of America.
[80] B. Jones,et al. Retinal remodelling , 2005, Clinical & experimental optometry.
[81] G. Acland,et al. Intravitreal injection of ciliary neurotrophic factor (CNTF) causes peripheral remodeling and does not prevent photoreceptor loss in canine RPGR mutant retina. , 2007, Experimental eye research.
[82] Paul S. Bernstein,et al. Mutation of the Stargardt Disease Gene (ABCR) in Age-Related Macular Degeneration , 1997 .
[83] M. Iadarola,et al. Chronic tooth pulp inflammation causes transient and persistent expression of Fos in dynorphin-rich regions of rat brainstem , 2000, Brain Research.
[84] R. Marc,et al. A molecular phenotype atlas of the zebrafish retina , 2001, Journal of neurocytology.
[85] W. Smith,et al. Dynamics of Arrestin-Rhodopsin Interactions , 2006, Journal of Biological Chemistry.
[86] B. Jones,et al. Retinal remodeling during retinal degeneration. , 2005, Experimental eye research.
[87] Antonio Oliviero,et al. Spinal Cord Injury Immediately Changes the State of the Brain , 2010, The Journal of Neuroscience.
[88] B. Jones,et al. Effect of shape and coating of a subretinal prosthesis on its integration with the retina. , 2009, Experimental eye research.
[89] Peter Davies,et al. Dendritic changes in Alzheimer's disease and factors that may underlie these changes , 1998, Progress in Neurobiology.
[90] V. Sheffield,et al. Bardet-Biedl syndrome genes are important in retrograde intracellular trafficking and Kupffer's vesicle cilia function. , 2006, Human molecular genetics.
[91] R. Marc,et al. Amino acid signatures in the normal cat retina. , 1998, Investigative ophthalmology & visual science.
[92] L. Peichl,et al. Kainic acid induces sprouting of retinal neurons. , 1984, Science.
[93] R. Sullivan,et al. Neuronal migration and glial remodeling in degenerating retinas of aged rats and in nonneovascular AMD. , 2003, Investigative ophthalmology & visual science.
[94] Akimichi Kaneko,et al. l-Glutamate-induced responses in OFF-type bipolar cells of the cat retina , 1995, Vision Research.
[95] Robert E Marc,et al. Molecular Phenotyping of Retinal Ganglion Cells , 2002, The Journal of Neuroscience.
[96] R. Marc,et al. Amino Acid Signatures in the Primate Retina , 1996, The Journal of Neuroscience.
[97] B. Jones,et al. Computational molecular phenotyping of retinal sheet transplants to rats with retinal degeneration , 2012, The European journal of neuroscience.
[98] S. Stasheff,et al. Emergence of sustained spontaneous hyperactivity and temporary preservation of OFF responses in ganglion cells of the retinal degeneration (rd1) mouse. , 2008, Journal of neurophysiology.
[99] A. J. Roman,et al. Inner retinal abnormalities in X-linked retinitis pigmentosa with RPGR mutations. , 2007, Investigative ophthalmology & visual science.
[100] P. Detwiler,et al. Network Oscillations Drive Correlated Spiking of ON and OFF Ganglion Cells in the rd1 Mouse Model of Retinal Degeneration , 2014, PloS one.
[101] G. Parmigiani,et al. Identification of gene expression changes associated with the progression of retinal degeneration in the rd1 mouse. , 2004, Investigative ophthalmology & visual science.
[102] W. Smith,et al. Dynamics of Arrestin-Rhodopsin Interactions , 2007, Journal of Biological Chemistry.
[103] Joan W. Miller,et al. Etanercept, a Widely Used Inhibitor of Tumor Necrosis Factor-α (TNF- α), Prevents Retinal Ganglion Cell Loss in a Rat Model of Glaucoma , 2012, PloS one.
[104] W. Baehr,et al. Mutant rhodopsin transgene expression on a null background. , 2001, Investigative ophthalmology & visual science.
[105] Weng Tao,et al. Ciliary neurotrophic factor (CNTF) for human retinal degeneration: phase I trial of CNTF delivered by encapsulated cell intraocular implants. , 2006, Proceedings of the National Academy of Sciences of the United States of America.
[106] S K Fisher,et al. Neurite outgrowth from bipolar and horizontal cells after experimental retinal detachment. , 1998, Investigative ophthalmology & visual science.
[107] Noam Y. Harel,et al. Can regenerating axons recapitulate developmental guidance during recovery from spinal cord injury? , 2006, Nature Reviews Neuroscience.
[108] J. Heckenlively,et al. The nob2 mouse, a null mutation in Cacna1f: Anatomical and functional abnormalities in the outer retina and their consequences on ganglion cell visual responses , 2006, Visual Neuroscience.
[109] D. Pow,et al. Direct immunocytochemical evidence for the transfer of glutamine from glial cells to neurons: Use of specific antibodies directed against thed-stereoisomers of glutamate and glutamine , 1996, Neuroscience.
[110] F. Riemslag,et al. Mutations in GRM6 cause autosomal recessive congenital stationary night blindness with a distinctive scotopic 15-Hz flicker electroretinogram. , 2005, Investigative ophthalmology & visual science.
[111] Fumitaka Osakada,et al. Detection of localized retinal malfunction in retinal degeneration model using a multielectrode array system , 2009, Journal of neuroscience research.
[112] M. Yamashita,et al. Responses of rod bipolar cells isolated from the rat retina to the glutamate agonist 2-amino-4-phosphonobutyric acid (APB) , 1991, The Journal of neuroscience : the official journal of the Society for Neuroscience.
[113] L. Molday,et al. ABCR expression in foveal cone photoreceptors and its role in Stargardt macular dystrophy , 2000, Nature Genetics.
[114] B. Jones,et al. Retinal remodeling in inherited photoreceptor degenerations , 2003, Molecular Neurobiology.
[115] A. Milam,et al. Abnormalities in rod photoreceptors, amacrine cells, and horizontal cells in human retinas with retinitis pigmentosa. , 2000, American journal of ophthalmology.
[116] B. Jones,et al. Retinal remodeling , 2012, Japanese Journal of Ophthalmology.
[117] M. McCall,et al. Immunohistochemical analysis of the outer plexiform layer in the nob mouse shows no abnormalities , 2003, Visual Neuroscience.
[118] M. Slaughter,et al. 2-amino-4-phosphonobutyric acid: a new pharmacological tool for retina research. , 1981, Science.
[119] G. A. Limb,et al. Human Müller stem cell (MIO-M1) transplantation in a rat model of glaucoma: survival, differentiation, and integration. , 2008, Investigative ophthalmology & visual science.
[120] Malcolm M. Slaughter,et al. Bipolar cells in the mudpuppy retina use an excitatory amino acid neurotransmitter , 1983, Nature.
[121] B. Boycott,et al. Functional architecture of the mammalian retina. , 1991, Physiological reviews.
[122] R. Allikmets. Simple and complex ABCR: genetic predisposition to retinal disease. , 2000, American journal of human genetics.
[123] E. Strettoi,et al. Remodeling of second-order neurons in the retina of rd/rd mutant mice , 2003, Vision Research.
[124] M. Sandberg,et al. Recessive mutations in the gene encoding the β–subunit of rod phosphodiesterase in patients with retinitis pigmentosa , 1993, Nature Genetics.
[125] N. Cuenca,et al. Regressive and reactive changes in the connectivity patterns of rod and cone pathways of P23H transgenic rat retina , 2004, Neuroscience.
[126] J. S. Lauritzen,et al. Rapid glutamate receptor 2 trafficking during retinal degeneration , 2012, Molecular Neurodegeneration.
[127] T. Aleman,et al. Long-term protection of retinal structure but not function using RAAV.CNTF in animal models of retinitis pigmentosa. , 2001, Molecular therapy : the journal of the American Society of Gene Therapy.
[128] M. Kalloniatis,et al. Neurochemical architecture of the normal and degenerating rat retina , 1996, The Journal of comparative neurology.
[129] D. Mastronarde,et al. A Computational Framework for Ultrastructural Mapping of Neural Circuitry , 2009, PLoS biology.
[130] S. Haverkamp,et al. Characterization of neurite outgrowth and ectopic synaptogenesis in response to photoreceptor dysfunction , 2012, Cellular and Molecular Life Sciences.
[131] T. Wensel,et al. Characterization of R9AP, a membrane anchor for the photoreceptor GTPase-accelerating protein, RGS9-1. , 2004, Methods in enzymology.