These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

192 related articles for article (PubMed ID: 35794468)

  • 1. Identification of RPGR ORF15 mutation for X-linked retinitis pigmentosa in a large Chinese family and in vitro correction with prime editor.
    Lv X; Zheng Z; Zhi X; Zhou Y; Lv J; Zhou Y; Wu B; Liu S; Shi W; Song Z; Xu J; Qu J; Xu D; Gu F
    Gene Ther; 2023 Feb; 30(1-2):160-166. PubMed ID: 35794468
    [TBL] [Abstract][Full Text] [Related]  

  • 2. A novel de novo frameshift mutation of RPGR ORF15 is associated with X-linked retinitis pigmentosa in a Chinese family.
    Chang W; Ding Q; Tang Z; Liu P; Jiang F; Ke T; Ren X; Wang Z; Liu J; Wang QK; Liu M
    Mol Vis; 2007 Aug; 13():1548-54. PubMed ID: 17893654
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Identification of a novel RPGR exon ORF15 mutation in a family with X-linked retinitis pigmentosa.
    Jin ZB; Gu F; Ma X; Nao-i N
    Arch Ophthalmol; 2007 Oct; 125(10):1407-12. PubMed ID: 17923551
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Novel RPGR-ORF15 mutations in X-linked retinitis pigmentosa patients.
    Gan DK; He CL; Shu HR; Hoffman MR; Jin ZB
    Neurosci Lett; 2011 Aug; 500(1):16-9. PubMed ID: 21683121
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Mutations in the X-linked retinitis pigmentosa genes RPGR and RP2 found in 8.5% of families with a provisional diagnosis of autosomal dominant retinitis pigmentosa.
    Churchill JD; Bowne SJ; Sullivan LS; Lewis RA; Wheaton DK; Birch DG; Branham KE; Heckenlively JR; Daiger SP
    Invest Ophthalmol Vis Sci; 2013 Feb; 54(2):1411-6. PubMed ID: 23372056
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Prevalence of
    Vinikoor-Imler LC; Simpson C; Narayanan D; Abbasi S; Lally C
    Ophthalmic Genet; 2022 Oct; 43(5):581-588. PubMed ID: 36004681
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Identification of novel mutations in X-linked retinitis pigmentosa families and implications for diagnostic testing.
    Neidhardt J; Glaus E; Lorenz B; Netzer C; Li Y; Schambeck M; Wittmer M; Feil S; Kirschner-Schwabe R; Rosenberg T; Cremers FP; Bergen AA; Barthelmes D; Baraki H; Schmid F; Tanner G; Fleischhauer J; Orth U; Becker C; Wegscheider E; Nürnberg G; Nürnberg P; Bolz HJ; Gal A; Berger W
    Mol Vis; 2008 Jun; 14():1081-93. PubMed ID: 18552978
    [TBL] [Abstract][Full Text] [Related]  

  • 8. X-linked retinitis pigmentosa: RPGR mutations in most families with definite X linkage and clustering of mutations in a short sequence stretch of exon ORF15.
    Bader I; Brandau O; Achatz H; Apfelstedt-Sylla E; Hergersberg M; Lorenz B; Wissinger B; Wittwer B; Rudolph G; Meindl A; Meitinger T
    Invest Ophthalmol Vis Sci; 2003 Apr; 44(4):1458-63. PubMed ID: 12657579
    [TBL] [Abstract][Full Text] [Related]  

  • 9. The first reported case of a deletion of the entire RPGR gene in a family with X-linked retinitis pigmentosa.
    Mihailovic N; Schimpf-Linzenbold S; Sattler I; Eter N; Heiduschka P
    Ophthalmic Genet; 2022 Oct; 43(5):679-684. PubMed ID: 35652150
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Mutations in RPGR and RP2 of Chinese patients with X-linked retinitis pigmentosa.
    Ji Y; Wang J; Xiao X; Li S; Guo X; Zhang Q
    Curr Eye Res; 2010 Jan; 35(1):73-9. PubMed ID: 20021257
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Homozygous females for a X-linked RPGR-ORF15 mutation in an Iranian family with retinitis pigmentosa.
    Beigi F; Del Pozo-Valero M; Martin-Merida I; Manaviat MR; Ayuso C; Ghasemi N
    Exp Eye Res; 2021 Oct; 211():108714. PubMed ID: 34390733
    [TBL] [Abstract][Full Text] [Related]  

  • 12. [Novel RPGR gene mutation in a Chinese family with X-linked recessive retinitis pigmentosa].
    Li ZL; Zhuang WJ; Zhao W; Zhang XF; Wang J; Meng RH; Rong WN; Sheng XL
    Zhonghua Yan Ke Za Zhi; 2011 Jun; 47(6):516-20. PubMed ID: 21914266
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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]  

  • 14. A novel missense variant c.G644A (p.G215E) of the RPGR gene in a Chinese family causes X-linked retinitis pigmentosa.
    Fu J; Cheng J; Zhou Q; Wei C; Chen H; Lv H; Fu J
    Biosci Rep; 2019 Oct; 39(10):. PubMed ID: 31652454
    [TBL] [Abstract][Full Text] [Related]  

  • 15. A novel RPGR gene mutation in a Chinese family with X-linked dominant retinitis pigmentosa.
    Li Y; Dong B; Hu AL; Cui TT; Zheng YY
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2005 Aug; 22(4):396-8. PubMed ID: 16086276
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [ORF15 exon of the RPGR gene in retinitis pigmentosa – technically difficult, diagnostically important].
    Ołdak M; Ruszkowska E; Siwiec S; Pollak A; Stawiński P; Szulborski K; Szaflik JP
    Klin Oczna; 2016; 118(2):139-43. PubMed ID: 29912501
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Phenotypic high myopia in X-linked retinitis pigmentosa secondary to a novel mutation in the RPGR gene.
    Sanchez Tocino H; Diez Montero C; Villanueva Gómez A; Lobo Valentin R; Montero-Moreno JA
    Ophthalmic Genet; 2019 Apr; 40(2):170-176. PubMed ID: 31033374
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Mutational analysis of RPGR and RP2 genes in Japanese patients with retinitis pigmentosa: identification of four mutations.
    Jin ZB; Liu XQ; Hayakawa M; Murakami A; Nao-i N
    Mol Vis; 2006 Oct; 12():1167-74. PubMed ID: 17093403
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Identification of novel X-linked gain-of-function RPGR-ORF15 mutation in Italian family with retinitis pigmentosa and pathologic myopia.
    Parmeggiani F; Barbaro V; De Nadai K; Lavezzo E; Toppo S; Chizzolini M; Palù G; Parolin C; Di Iorio E
    Sci Rep; 2016 Dec; 6():39179. PubMed ID: 27995965
    [TBL] [Abstract][Full Text] [Related]  

  • 20. A novel mutation in retinitis pigmentosa GTPase regulator gene with a distinctive retinitis pigmentosa phenotype in a Chinese family.
    Sheng X; Li Z; Zhang X; Wang J; Ren H; Sun Y; Meng R; Rong W; Zhuang W
    Mol Vis; 2010 Aug; 16():1620-8. PubMed ID: 20806050
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.