113 related articles for article (PubMed ID: 35417297)
21. Clinical applications of microperimetry in RPGR-related retinitis pigmentosa: a review.
Buckley TMW; Jolly JK; Josan AS; Wood LJ; Cehajic-Kapetanovic J; MacLaren RE
Acta Ophthalmol; 2021 Dec; 99(8):819-825. PubMed ID: 33783139
[TBL] [Abstract][Full Text] [Related]
22. Screening for mutations in RPGR and RP2 genes in Jordanian families with X-linked retinitis pigmentosa.
Haddad MF; Khabour OF; Abuzaideh KA; Shihadeh W
Genet Mol Res; 2016 Jun; 15(2):. PubMed ID: 27323122
[TBL] [Abstract][Full Text] [Related]
23. Clinical course of cone dystrophy caused by mutations in the RPGR gene.
Thiadens AA; Soerjoesing GG; Florijn RJ; Tjiam AG; den Hollander AI; van den Born LI; Riemslag FC; Bergen AA; Klaver CC
Graefes Arch Clin Exp Ophthalmol; 2011 Oct; 249(10):1527-35. PubMed ID: 21866333
[TBL] [Abstract][Full Text] [Related]
24. Novel mutations of RPGR in Chinese families with X-linked retinitis pigmentosa.
Zhang Z; Dai H; Wang L; Tao T; Xu J; Sun X; Yang L; Li G
BMC Ophthalmol; 2019 Nov; 19(1):240. PubMed ID: 31775781
[TBL] [Abstract][Full Text] [Related]
25. RPGR-Related X-Linked Retinitis Pigmentosa Carriers with a Severe "Male Pattern".
Salvetti AP; Nanda A; MacLaren RE
Ophthalmologica; 2021; 244(1):60-67. PubMed ID: 32434206
[TBL] [Abstract][Full Text] [Related]
26. Screening of a large cohort of leber congenital amaurosis and retinitis pigmentosa patients identifies novel LCA5 mutations and new genotype-phenotype correlations.
Mackay DS; Borman AD; Sui R; van den Born LI; Berson EL; Ocaka LA; Davidson AE; Heckenlively JR; Branham K; Ren H; Lopez I; Maria M; Azam M; Henkes A; Blokland E; Qamar R; Webster AR; Cremers FPM; Moore AT; Koenekoop RK; ; Andreasson S; de Baere E; Bennett J; Chader GJ; Berger W; Golovleva I; Greenberg J; den Hollander AI; Klaver CCW; Klevering BJ; Lorenz B; Preising MN; Ramsear R; Roberts L; Roepman R; Rohrschneider K; Wissinger B
Hum Mutat; 2013 Nov; 34(11):1537-1546. PubMed ID: 23946133
[TBL] [Abstract][Full Text] [Related]
27. Novel RPGR mutations with distinct retinitis pigmentosa phenotypes in French-Canadian families.
Koenekoop RK; Loyer M; Hand CK; Al Mahdi H; Dembinska O; Beneish R; Racine J; Rouleau GA
Am J Ophthalmol; 2003 Oct; 136(4):678-87. PubMed ID: 14516808
[TBL] [Abstract][Full Text] [Related]
28. Clinical features of a previously undescribed codon 216 (proline to serine) mutation in the peripherin/retinal degeneration slow gene in autosomal dominant retinitis pigmentosa.
Fishman GA; Stone E; Gilbert LD; Vandenburgh K; Sheffield VC; Heckenlively JR
Ophthalmology; 1994 Aug; 101(8):1409-21. PubMed ID: 8058286
[TBL] [Abstract][Full Text] [Related]
29. [Clinical findings in members of a Czech family with retinitis pigmentosa caused by the c.2426_2427delAG mutation in RPGR].
Kousal B; Skalická P; Diblík P; Kuthan P; Langrová H; Lišková P
Cesk Slov Oftalmol; 2013 Mar; 69(1):8-15. PubMed ID: 23822596
[TBL] [Abstract][Full Text] [Related]
30. Codon-Optimized RPGR Improves Stability and Efficacy of AAV8 Gene Therapy in Two Mouse Models of X-Linked Retinitis Pigmentosa.
Fischer MD; McClements ME; Martinez-Fernandez de la Camara C; Bellingrath JS; Dauletbekov D; Ramsden SC; Hickey DG; Barnard AR; MacLaren RE
Mol Ther; 2017 Aug; 25(8):1854-1865. PubMed ID: 28549772
[TBL] [Abstract][Full Text] [Related]
31.
Wangding S; Colaiacovo S; Makar I; Saleh M
Ophthalmic Genet; 2022 Jun; 43(3):389-391. PubMed ID: 34957897
[TBL] [Abstract][Full Text] [Related]
32. High Symmetry of Visual Acuity and Visual Fields in RPGR-Linked Retinitis Pigmentosa.
Bellingrath JS; Ochakovski GA; Seitz IP; Kohl S; Zrenner E; Hanig N; Prokisch H; Weber BH; Downes SM; Ramsden S; MacLaren RE; Fischer MD
Invest Ophthalmol Vis Sci; 2017 Sep; 58(11):4457-4466. PubMed ID: 28863407
[TBL] [Abstract][Full Text] [Related]
33. Mutation analysis of the RPGR gene reveals novel mutations in south European patients with X-linked retinitis pigmentosa.
Miano MG; Testa F; Strazzullo M; Trujillo M; De Bernardo C; Grammatico B; Simonelli F; Mangino M; Torrente I; Ruberto G; Beneyto M; Antinolo G; Rinaldi E; Danesino C; Ventruto V; D'Urso M; Ayuso C; Baiget M; Ciccodicola A
Eur J Hum Genet; 1999 Sep; 7(6):687-94. PubMed ID: 10482958
[TBL] [Abstract][Full Text] [Related]
34. Identification of novel RPGR (retinitis pigmentosa GTPase regulator) mutations in a subset of X-linked retinitis pigmentosa families segregating with the RP3 locus.
Zito I; Thiselton DL; Gorin MB; Stout JT; Plant C; Bird AC; Bhattacharya SS; Hardcastle AJ
Hum Genet; 1999; 105(1-2):57-62. PubMed ID: 10480356
[TBL] [Abstract][Full Text] [Related]
35. Retinal phenotype of an X-linked pseudo-Usher syndrome in association with the G173R mutation in the RPGR gene.
Iannaccone A; Othman MI; Cantrell AD; Jennings BJ; Branham K; Swaroop A
Adv Exp Med Biol; 2008; 613():221-7. PubMed ID: 18188948
[No Abstract] [Full Text] [Related]
36. RPGR is mutated in patients with a complex X linked phenotype combining primary ciliary dyskinesia and retinitis pigmentosa.
Moore A; Escudier E; Roger G; Tamalet A; Pelosse B; Marlin S; Clément A; Geremek M; Delaisi B; Bridoux AM; Coste A; Witt M; Duriez B; Amselem S
J Med Genet; 2006 Apr; 43(4):326-33. PubMed ID: 16055928
[TBL] [Abstract][Full Text] [Related]
37. Somatic and gonadal mosaicism in X-linked retinitis pigmentosa.
Jin ZB; Gu F; Matsuda H; Yukawa N; Ma X; Nao-i N
Am J Med Genet A; 2007 Nov; 143A(21):2544-8. PubMed ID: 17935240
[TBL] [Abstract][Full Text] [Related]
38. Multiprotein complexes of Retinitis Pigmentosa GTPase regulator (RPGR), a ciliary protein mutated in X-linked Retinitis Pigmentosa (XLRP).
Murga-Zamalloa C; Swaroop A; Khanna H
Adv Exp Med Biol; 2010; 664():105-14. PubMed ID: 20238008
[TBL] [Abstract][Full Text] [Related]
39. Optimization of Retinal Gene Therapy for X-Linked Retinitis Pigmentosa Due to RPGR Mutations.
Beltran WA; Cideciyan AV; Boye SE; Ye GJ; Iwabe S; Dufour VL; Marinho LF; Swider M; Kosyk MS; Sha J; Boye SL; Peterson JJ; Witherspoon CD; Alexander JJ; Ying GS; Shearman MS; Chulay JD; Hauswirth WW; Gamlin PD; Jacobson SG; Aguirre GD
Mol Ther; 2017 Aug; 25(8):1866-1880. PubMed ID: 28566226
[TBL] [Abstract][Full Text] [Related]
40. The retinitis pigmentosa GTPase regulator interacting protein 1 (RPGRIP1) links RPGR to the nephronophthisis protein network.
Gerner M; Haribaskar R; Pütz M; Czerwitzki J; Walz G; Schäfer T
Kidney Int; 2010 May; 77(10):891-6. PubMed ID: 20200501
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
