المؤلفون: Deng Pan, Xiao Zhang, Kangxin Jin, Zi-Bing Jin

المصدر: Stem Cell Research & Therapy, Vol 14, Iss 1, Pp 1-16 (2023)

مصطلحات موضوعية: CRX, Haploinsufficiency, Photoreceptor, Human, Retinal organoids, Development, Medicine (General), R5-920, Biochemistry, QD415-436

وصف الملف: electronic resource

Relation: https://doaj.org/toc/1757-6512

URL الوصول: https://doaj.org/article/17b6c0f08abc40a3a5f426287f6775eb

المؤلفون: Pan, Deng^{Aff1, IDs13287023035903_cor1}, Zhang, Xiao, Jin, Kangxin, Jin, Zi-Bing^{Aff1, IDs13287023035903_cor4}

المصدر: Stem Cell Research & Therapy. 14(1)

المؤلفون: Yiqiao Zheng, Shiming Chen

المصدر: Frontiers in Cellular Neuroscience, Vol 18 (2024)

مصطلحات موضوعية: CRX, homeodomain, gene regulation, molecular genetics, inherited retinopathy, dominant diseases, Neurosciences. Biological psychiatry. Neuropsychiatry, RC321-571

وصف الملف: electronic resource

Relation: https://www.frontiersin.org/articles/10.3389/fncel.2024.1347436/full; https://doaj.org/toc/1662-5102

URL الوصول: https://doaj.org/article/e81898d3bbfc47ad88cbf3ec96275caf

المؤلفون: Sun, Chi^Aff13, Chen, Shiming^{Aff13, Aff14}

المساهمون: Crusio, Wim E., Series Editor^Aff1, Dong, Haidong, Series Editor^Aff2, Radeke, Heinfried H., Series Editor^Aff3, Rezaei, Nima, Series Editor^Aff4, Steinlein, Ortrud, Series Editor^Aff5, Xiao, Junjie, Series Editor^Aff6, Ash, John D., editor^Aff7, Pierce, Eric, editor^Aff8, Anderson, Robert E., editor^Aff9, Bowes Rickman, Catherine, editor^Aff10, Hollyfield, Joe G., editor^Aff11, Grimm, Christian, editor^Aff12

المصدر: Retinal Degenerative Diseases XIX : Mechanisms and Experimental Therapy. 1415:135-141

المؤلفون: Chirco, Kathleen R, Chew, Shereen, Moore, Anthony T, Duncan, Jacque L, Lamba, Deepak A

المصدر: Stem Cell Reports. 16(11)

مصطلحات موضوعية: Neurosciences, Neurodegenerative, Pediatric, Eye Disease and Disorders of Vision, Genetics, Eye, Good Health and Well Being, Alleles, Base Sequence, Cell Line, Gene Editing, Gene Expression Profiling, Genes, Dominant, Genetic Predisposition to Disease, Homeodomain Proteins, Humans, Induced Pluripotent Stem Cells, Leber Congenital Amaurosis, Microscopy, Electron, Transmission, Models, Biological, Mutation, Organoids, Phenotype, Polymorphism, Single Nucleotide, RNA-Seq, Retina, Trans-Activators, CRISPR/Cas9, CRX, LCA7, Leber congenital amaurosis, allelic knockdown, gene editing, photoreceptors cells, retinal organoid, scRNA-seq, Biochemistry and Cell Biology, Clinical Sciences

وصف الملف: application/pdf

URL الوصول: https://escholarship.org/uc/item/37t711p3

المؤلفون: Marco Piergentili, Vito Spagnuolo, Vittoria Murro, Dario Pasquale Mucciolo, Dario Giorgio, Ilaria Passerini, Elisabetta Pelo, Fabrizio Giansanti, Gianni Virgili, Andrea Sodi

المصدر: Medicina, Vol 60, Iss 5, p 797 (2024)

مصطلحات موضوعية: CRX gene, late-onset retinal dystrophy, pericentral retinitis pigmentosa, sector retinitis pigmentosa, genotype, Medicine (General), R5-920

وصف الملف: electronic resource

Relation: https://www.mdpi.com/1648-9144/60/5/797; https://doaj.org/toc/1010-660X; https://doaj.org/toc/1648-9144

URL الوصول: https://doaj.org/article/aaba84c752f247698c8be8da66b9d452

المؤلفون: Yiqiao Zheng, Chi Sun, Xiaodong Zhang, Philip A Ruzycki, Shiming Chen

المصدر: eLife, Vol 12 (2023)

مصطلحات موضوعية: homeodomain, transcription factor, DNA-binding specificity, CRX disease mutations, inherited retinal diseases, photoreceptor development, Medicine, Science, Biology (General), QH301-705.5

وصف الملف: electronic resource

Relation: https://elifesciences.org/articles/87147; https://doaj.org/toc/2050-084X

URL الوصول: https://doaj.org/article/6fb6d80a3f3c4ac6a89bbf37b214b857

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المؤلفون: Audo, Isabelle^{Aff1, Aff2}, Meunier, Isabelle^{Aff3, Aff4}, Sahel, José-Alain^{Aff1, Aff2, Aff5, Aff6, Aff7, Aff8}, Huckfeldt, Rachel, Section editor^Aff9

المساهمون: Albert, Daniel M., editor^Aff101, Miller, Joan W., editor^Aff102, Azar, Dimitri T., editor^Aff103, Young, Lucy H., editor^Aff104

المصدر: Albert and Jakobiec's Principles and Practice of Ophthalmology. :3967-3995

المؤلفون: Yu Fujinami-Yokokawa, Lizhu Yang, Kwangsic Joo, Kazushige Tsunoda, Xiao Liu, Mineo Kondo, Seong Joon Ahn, Hui Li, Kyu Hyung Park, Hisateru Tachimori, Hiroaki Miyata, Se Joon Woo, Ruifang Sui, Kaoru Fujinami

المصدر: Genes, Vol 14, Iss 10, p 1869 (2023)

مصطلحات موضوعية: occult macular dystrophy, miyake disease, RP1L1, CRX, GUCY2D, non-RP1L1, Genetics, QH426-470

وصف الملف: electronic resource

Relation: https://www.mdpi.com/2073-4425/14/10/1869; https://doaj.org/toc/2073-4425

URL الوصول: https://doaj.org/article/2707648afb6048ccae72254dc7f7a76a