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 *

123 related articles for article (PubMed ID: 36124184)

  • 1. 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]  

  • 2. 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]  

  • 3. [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]  

  • 4. 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]  

  • 5. A novel mutation of the RPGR gene in a Chinese X-linked retinitis pigmentosa family and possible involvement of X-chromosome inactivation.
    Wang Y; Lu L; Zhang D; Tan Y; Li D; He F; Jiao X; Yang M; Hejtmancik JF; Liu X
    Eye (Lond); 2021 Jun; 35(6):1688-1696. PubMed ID: 32839555
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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]  

  • 7. 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]  

  • 8. 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]  

  • 9. 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]  

  • 10. 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]  

  • 11. X-linked Retinitis Pigmentosa in Japan: Clinical and Genetic Findings in Male Patients and Female Carriers.
    Kurata K; Hosono K; Hayashi T; Mizobuchi K; Katagiri S; Miyamichi D; Nishina S; Sato M; Azuma N; Nakano T; Hotta Y
    Int J Mol Sci; 2019 Mar; 20(6):. PubMed ID: 30917587
    [TBL] [Abstract][Full Text] [Related]  

  • 12. A non-ancestral RPGR missense mutation in families with either recessive or semi-dominant X-linked retinitis pigmentosa.
    Banin E; Mizrahi-Meissonnier L; Neis R; Silverstein S; Magyar I; Abeliovich D; Roepman R; Berger W; Rosenberg T; Sharon D
    Am J Med Genet A; 2007 Jun; 143A(11):1150-8. PubMed ID: 17480003
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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]  

  • 14. Clinical and Electrophysiologic Characteristics of a Large Kindred with X-Linked Retinitis Pigmentosa Associated with the RPGR Locus.
    Tzu JH; Arguello T; Berrocal AM; Berrocal M; Weisman AD; Liu M; Hess D; Caputo M; Goldberg JL; Feuer WJ; Stone EM; Lam BL
    Ophthalmic Genet; 2015; 36(4):321-6. PubMed ID: 24555744
    [TBL] [Abstract][Full Text] [Related]  

  • 15. X-Chromosome Inactivation Is a Biomarker of Clinical Severity in Female Carriers of RPGR-Associated X-Linked Retinitis Pigmentosa.
    Fahim AT; Sullivan LS; Bowne SJ; Jones KD; Wheaton DKH; Khan NW; Heckenlively JR; Jayasundera KT; Branham KH; Andrews CA; Othman MI; Karoukis AJ; Birch DG; Daiger SP
    Ophthalmol Retina; 2020 May; 4(5):510-520. PubMed ID: 31953110
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Phenotypes in three Swedish families with X-linked retinitis pigmentosa caused by different mutations in the RPGR gene.
    Andréasson S; Ponjavic V; Abrahamson M; Ehinger B; Wu W; Fujita R; Buraczynska M; Swaroop A
    Am J Ophthalmol; 1997 Jul; 124(1):95-102. PubMed ID: 9222238
    [TBL] [Abstract][Full Text] [Related]  

  • 17. RP2 and RPGR mutations and clinical correlations in patients with X-linked retinitis pigmentosa.
    Sharon D; Sandberg MA; Rabe VW; Stillberger M; Dryja TP; Berson EL
    Am J Hum Genet; 2003 Nov; 73(5):1131-46. PubMed ID: 14564670
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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]  

  • 19. Clinical studies of X-linked retinitis pigmentosa in three Swedish families with newly identified mutations in the RP2 and RPGR-ORF15 genes.
    Andréasson S; Breuer DK; Eksandh L; Ponjavic V; Frennesson C; Hiriyanna S; Filippova E; Yashar BM; Swaroop A
    Ophthalmic Genet; 2003 Dec; 24(4):215-23. PubMed ID: 14566651
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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]  

    [Next]    [New Search]
    of 7.