Showing 201 - 220 results of 1,674 for search '"retinitis pigmentosa"', query time: 0.14s Refine Results
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    Self-reported quality of life in patients with retinitis pigmentosa and maculopathy of Bothnia type by Marie SI Burstedt, Eva Mönestam

    Published 2010-03-01
    “…Marie SI Burstedt, Eva MönestamDepartment of Clinical Sciences/Ophthalmology, University of Umeå, SwedenPurpose: To assess vision-related quality-of-life subscales with objective measurements of visual function in patients affected with retinitis pigmentosa of Bothnia type (BD).Methods: Forty-nine patients answered the NEI-VFQ-25 questionnaire. …”
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    Retinitis pigmentosa-linked mutation in DHX38 modulates its splicing activity. by Mina Obuća, Zuzana Cvačková, Jan Kubovčiak, Michal Kolář, David Staněk

    Published 2022-01-01
    “…Retinitis pigmentosa (RP) is a hereditary disease affecting tens of thousands of people world-wide. …”
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  4. 204

    Novel mutations of RPGR in Chinese retinitis pigmentosa patients and the genotype-phenotype correlation. by Liping Yang, Xiaobei Yin, Lina Feng, Debo You, Lemeng Wu, Ningning Chen, Aijun Li, Genlin Li, Zhizhong Ma

    Published 2014-01-01
    “…X-linked Retinitis Pigmentosa (XLRP) accounts for 10-20% of all RP cases, and represents the most severe subtype of this disease. …”
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    Nonretinoid chaperones improve rhodopsin homeostasis in a mouse model of retinitis pigmentosa by Abhishek Vats, Yibo Xi, Bing Feng, Owen D. Clinger, Anthony J. St. Leger, Xujie Liu, Archisha Ghosh, Chase D. Dermond, Kira L. Lathrop, Gregory P. Tochtrop, Serge Picaud, Yuanyuan Chen

    Published 2022-05-01
    “…Rhodopsin-associated (RHO-associated) retinitis pigmentosa (RP) is a progressive retinal disease that currently has no cure. …”
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    A large animal model for CNGB1 autosomal recessive retinitis pigmentosa. by Paige A Winkler, Kari J Ekenstedt, Laurence M Occelli, Anton V Frattaroli, Joshua T Bartoe, Patrick J Venta, Simon M Petersen-Jones

    Published 2013-01-01
    “…Progressive retinal atrophy (PRA) is the canine equivalent of retinitis pigmentosa (RP). Similar to RP, PRA is a genetically heterogenous condition. …”
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    Unusual mode of dimerization of retinitis pigmentosa-associated F220C rhodopsin by George Khelashvili, Anoop Narayana Pillai, Joon Lee, Kalpana Pandey, Alexander M. Payne, Zarek Siegel, Michel A. Cuendet, Tylor R. Lewis, Vadim Y. Arshavsky, Johannes Broichhagen, Joshua Levitz, Anant K. Menon

    Published 2021-05-01
    “…We previously reported that the retinitis pigmentosa-linked F220C opsin mutant fails to dimerize in vitro, reconstituting as a monomer. …”
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    Sectoral activation of glia in an inducible mouse model of autosomal dominant retinitis pigmentosa by Michael T. Massengill, Neil F. Ash, Brianna M. Young, Cristhian J. Ildefonso, Alfred S. Lewin

    Published 2020-10-01
    “…Abstract Retinitis pigmentosa (RP) is a group of blinding disorders caused by diverse mutations, including in rhodopsin (RHO). …”
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