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 *

149 related articles for article (PubMed ID: 32821686)

  • 1. Myopia with X-linked retinitis pigmentosa results from a novel gross deletion of RPGR gene.
    Li HP; Yuan SQ; Wang XG; Sheng XL; Li XR
    Int J Ophthalmol; 2020; 13(8):1306-1311. PubMed ID: 32821686
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. 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]  

  • 4. 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]  

  • 5. Novel deletion of the RPGR gene in a Chinese family with X-linked retinitis pigmentosa.
    Zhao K; Wang L; Wang L; Wang L; Zhang Q; Wang Q
    Ophthalmic Genet; 2001 Sep; 22(3):187-94. PubMed ID: 11559860
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [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]  

  • 7. 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]  

  • 8. X-linked retinitis pigmentosa in two families with a missense mutation in the RPGR gene and putative change of glycine to valine at codon 60.
    Fishman GA; Grover S; Jacobson SG; Alexander KR; Derlacki DJ; Wu W; Buraczynska M; Swaroop A
    Ophthalmology; 1998 Dec; 105(12):2286-96. PubMed ID: 9855162
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Novel splice receptor-site mutation of RPGR in a Chinese family with X-linked retinitis pigmentosa.
    Wang J; Zhou C; Xiao Y; Liu H
    Medicine (Baltimore); 2018 Oct; 97(41):e12779. PubMed ID: 30313097
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Genetic analysis of Chinese families reveals a novel truncation allele of the retinitis pigmentosa GTPase regulator gene.
    Hu F; Zeng XY; Liu LL; Luo YL; Jiang YP; Wang H; Xie J; Hu CQ; Gan L; Huang L
    Int J Ophthalmol; 2014; 7(5):753-8. PubMed ID: 25349787
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. Three novel mutations of the RPGR gene exon ORF15 in three Japanese families with X-linked retinitis pigmentosa.
    Yokoyama A; Maruiwa F; Hayakawa M; Kanai A; Vervoort R; Wright AF; Yamada K; Niikawa N; Naōi N
    Am J Med Genet; 2001 Dec; 104(3):232-8. PubMed ID: 11754050
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Novel mutations of RPGR in Chinese retinitis pigmentosa patients and the genotype-phenotype correlation.
    Yang L; Yin X; Feng L; You D; Wu L; Chen N; Li A; Li G; Ma Z
    PLoS One; 2014; 9(1):e85752. PubMed ID: 24454928
    [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. 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]  

  • 16. Novel variants of RPGR in X-linked retinitis pigmentosa families and genotype-phenotype correlation.
    Parmeggiani F; Barbaro V; Migliorati A; Raffa P; Nespeca P; De Nadai K; Del Vecchio C; Palù G; Parolin C; Di Iorio E
    Eur J Ophthalmol; 2017 Mar; 27(2):240-248. PubMed ID: 27768226
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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]  

  • 18. A novel mutation of
    Sun HH; Zhao JC; Yang SL; Shi JD; Wei YS; Wang JC; Gu F; Chen L
    Int J Ophthalmol; 2022; 15(9):1423-1430. PubMed ID: 36124184
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Clinical characteristics of high myopia in female carriers of pathogenic
    Tran M; Kolesnikova M; Kim AH; Kowal T; Ning K; Mahajan VB; Tsang SH; Sun Y
    Ophthalmic Genet; 2023 Jun; 44(3):295-303. PubMed ID: 36017691
    [TBL] [Abstract][Full Text] [Related]  

  • 20. A novel missense mutation of RPGR identified from retinitis pigmentosa affects splicing of the ORF15 region and causes loss of transcript heterogeneity.
    Liu YS; Pan JQ; Wan JF; Ren CY; Xu ZH; Pan XB; Gao RN; Liu SQ; Zhang JL; Yao QH; Wang JH; Li EM; Rao JH; Hou P; Chen JH
    Biochem Biophys Res Commun; 2020 Oct; 531(2):172-179. PubMed ID: 32788070
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.