283 related articles for article (PubMed ID: 24516401)
1. Mechanistically distinct mouse models for CRX-associated retinopathy.
Tran NM; Zhang A; Zhang X; Huecker JB; Hennig AK; Chen S
PLoS Genet; 2014 Feb; 10(2):e1004111. PubMed ID: 24516401
[TBL] [Abstract][Full Text] [Related]
2. Leber congenital amaurosis caused by a homozygous mutation (R90W) in the homeodomain of the retinal transcription factor CRX: direct evidence for the involvement of CRX in the development of photoreceptor function.
Swaroop A; Wang QL; Wu W; Cook J; Coats C; Xu S; Chen S; Zack DJ; Sieving PA
Hum Mol Genet; 1999 Feb; 8(2):299-305. PubMed ID: 9931337
[TBL] [Abstract][Full Text] [Related]
3. CrxRdy Cat: A Large Animal Model for CRX-Associated Leber Congenital Amaurosis.
Occelli LM; Tran NM; Narfström K; Chen S; Petersen-Jones SM
Invest Ophthalmol Vis Sci; 2016 Jul; 57(8):3780-92. PubMed ID: 27427859
[TBL] [Abstract][Full Text] [Related]
4. Mechanisms of blindness: animal models provide insight into distinct CRX-associated retinopathies.
Tran NM; Chen S
Dev Dyn; 2014 Oct; 243(10):1153-66. PubMed ID: 24888636
[TBL] [Abstract][Full Text] [Related]
5. Crx-L253X Mutation Produces Dominant Photoreceptor Defects in TVRM65 Mice.
Ruzycki PA; Linne CD; Hennig AK; Chen S
Invest Ophthalmol Vis Sci; 2017 Sep; 58(11):4644-4653. PubMed ID: 28903150
[TBL] [Abstract][Full Text] [Related]
6. OTX2 loss causes rod differentiation defect in CRX-associated congenital blindness.
Roger JE; Hiriyanna A; Gotoh N; Hao H; Cheng DF; Ratnapriya R; Kautzmann MA; Chang B; Swaroop A
J Clin Invest; 2014 Feb; 124(2):631-43. PubMed ID: 24382353
[TBL] [Abstract][Full Text] [Related]
7. Gene Therapy of Dominant CRX-Leber Congenital Amaurosis using Patient Stem Cell-Derived Retinal Organoids.
Kruczek K; Qu Z; Gentry J; Fadl BR; Gieser L; Hiriyanna S; Batz Z; Samant M; Samanta A; Chu CJ; Campello L; Brooks BP; Wu Z; Swaroop A
Stem Cell Reports; 2021 Feb; 16(2):252-263. PubMed ID: 33513359
[TBL] [Abstract][Full Text] [Related]
8. A range of clinical phenotypes associated with mutations in CRX, a photoreceptor transcription-factor gene.
Sohocki MM; Sullivan LS; Mintz-Hittner HA; Birch D; Heckenlively JR; Freund CL; McInnes RR; Daiger SP
Am J Hum Genet; 1998 Nov; 63(5):1307-15. PubMed ID: 9792858
[TBL] [Abstract][Full Text] [Related]
9. A complete, homozygous CRX deletion causing nullizygosity is a new genetic mechanism for Leber congenital amaurosis.
Ibrahim MT; Alarcon-Martinez T; Lopez I; Fajardo N; Chiang J; Koenekoop RK
Sci Rep; 2018 Mar; 8(1):5034. PubMed ID: 29568065
[TBL] [Abstract][Full Text] [Related]
10. De novo mutations in the cone-rod homeobox gene associated with leber congenital amaurosis in Chinese patients.
Zou X; Yao F; Liang X; Xu F; Li H; Sui R; Dong F
Ophthalmic Genet; 2015 Mar; 36(1):21-6. PubMed ID: 24001014
[TBL] [Abstract][Full Text] [Related]
11. Nuclear trafficking of photoreceptor protein crx: the targeting sequence and pathologic implications.
Fei Y; Hughes TE
Invest Ophthalmol Vis Sci; 2000 Sep; 41(10):2849-56. PubMed ID: 10967037
[TBL] [Abstract][Full Text] [Related]
12. Gene Augmentation for Autosomal Dominant CRX-Associated Retinopathies.
Sun C; Chen S
Adv Exp Med Biol; 2023; 1415():135-141. PubMed ID: 37440026
[TBL] [Abstract][Full Text] [Related]
13. Dominant Leber congenital amaurosis, cone-rod degeneration, and retinitis pigmentosa caused by mutant versions of the transcription factor CRX.
Rivolta C; Berson EL; Dryja TP
Hum Mutat; 2001 Dec; 18(6):488-98. PubMed ID: 11748842
[TBL] [Abstract][Full Text] [Related]
14. Electrophysiologic and phenotypic features of an autosomal cone-rod dystrophy caused by a novel CRX mutation.
Lines MA; Hébert M; McTaggart KE; Flynn SJ; Tennant MT; MacDonald IM
Ophthalmology; 2002 Oct; 109(10):1862-70. PubMed ID: 12359607
[TBL] [Abstract][Full Text] [Related]
15. Genotypic Profile and Clinical Characteristics of CRX-Associated Retinopathy in Koreans.
Kim DG; Joo K; Han J; Choi M; Kim SW; Park KH; Park SJ; Lee CS; Byeon SH; Woo SJ
Genes (Basel); 2023 May; 14(5):. PubMed ID: 37239417
[TBL] [Abstract][Full Text] [Related]
16. Pathogenicity discrimination and genetic test reference for CRX variants based on genotype-phenotype analysis.
Yi Z; Xiao X; Li S; Sun W; Zhang Q
Exp Eye Res; 2019 Dec; 189():107846. PubMed ID: 31626798
[TBL] [Abstract][Full Text] [Related]
17. Graded gene expression changes determine phenotype severity in mouse models of CRX-associated retinopathies.
Ruzycki PA; Tran NM; Kefalov VJ; Kolesnikov AV; Chen S
Genome Biol; 2015 Sep; 16(1):171. PubMed ID: 26324254
[TBL] [Abstract][Full Text] [Related]
18. Pathogenic variants in
Shepherdson JL; Friedman RZ; Zheng Y; Sun C; Oh IY; Granas DM; Cohen BA; Chen S; White MA
Genome Res; 2024 Mar; 34(2):243-255. PubMed ID: 38355306
[TBL] [Abstract][Full Text] [Related]
19. Two novel CRX mutant proteins causing autosomal dominant Leber congenital amaurosis interact differently with NRL.
Nichols LL; Alur RP; Boobalan E; Sergeev YV; Caruso RC; Stone EM; Swaroop A; Johnson MA; Brooks BP
Hum Mutat; 2010 Jun; 31(6):E1472-83. PubMed ID: 20513135
[TBL] [Abstract][Full Text] [Related]
20. Cat LCA-CRX Model, Homozygous for an Antimorphic Mutation Has a Unique Phenotype.
Occelli LM; Tran NM; Chen S; Petersen-Jones SM
Transl Vis Sci Technol; 2023 Jun; 12(6):15. PubMed ID: 37351895
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]