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 *

314 related articles for article (PubMed ID: 31910043)

  • 41. Interaction of retinitis pigmentosa GTPase regulator (RPGR) with RAB8A GTPase: implications for cilia dysfunction and photoreceptor degeneration.
    Murga-Zamalloa CA; Atkins SJ; Peranen J; Swaroop A; Khanna H
    Hum Mol Genet; 2010 Sep; 19(18):3591-8. PubMed ID: 20631154
    [TBL] [Abstract][Full Text] [Related]  

  • 42. 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]  

  • 43. Inner retinal abnormalities in X-linked retinitis pigmentosa with RPGR mutations.
    Aleman TS; Cideciyan AV; Sumaroka A; Schwartz SB; Roman AJ; Windsor EA; Steinberg JD; Branham K; Othman M; Swaroop A; Jacobson SG
    Invest Ophthalmol Vis Sci; 2007 Oct; 48(10):4759-65. PubMed ID: 17898302
    [TBL] [Abstract][Full Text] [Related]  

  • 44. A single, abbreviated RPGR-ORF15 variant reconstitutes RPGR function in vivo.
    Hong DH; Pawlyk BS; Adamian M; Sandberg MA; Li T
    Invest Ophthalmol Vis Sci; 2005 Feb; 46(2):435-41. PubMed ID: 15671266
    [TBL] [Abstract][Full Text] [Related]  

  • 45. Gene replacement therapy rescues photoreceptor degeneration in a murine model of Leber congenital amaurosis lacking RPGRIP.
    Pawlyk BS; Smith AJ; Buch PK; Adamian M; Hong DH; Sandberg MA; Ali RR; Li T
    Invest Ophthalmol Vis Sci; 2005 Sep; 46(9):3039-45. PubMed ID: 16123399
    [TBL] [Abstract][Full Text] [Related]  

  • 46. 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]  

  • 47. 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]  

  • 48. Mid-stage intervention achieves similar efficacy as conventional early-stage treatment using gene therapy in a pre-clinical model of retinitis pigmentosa.
    Wert KJ; Sancho-Pelluz J; Tsang SH
    Hum Mol Genet; 2014 Jan; 23(2):514-23. PubMed ID: 24101599
    [TBL] [Abstract][Full Text] [Related]  

  • 49. A SYSTEMATIC LITERATURE REVIEW OF DISEASE PROGRESSION REPORTED IN RPGR -ASSOCIATED X-LINKED RETINITIS PIGMENTOSA.
    Lam BL; Scholl HPN; Doub D; Sperling M; Hashim M; Li N
    Retina; 2024 Jan; 44(1):1-9. PubMed ID: 37683184
    [TBL] [Abstract][Full Text] [Related]  

  • 50. 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]  

  • 51. 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]  

  • 52. Disease course of patients with X-linked retinitis pigmentosa due to RPGR gene mutations.
    Sandberg MA; Rosner B; Weigel-DiFranco C; Dryja TP; Berson EL
    Invest Ophthalmol Vis Sci; 2007 Mar; 48(3):1298-304. PubMed ID: 17325176
    [TBL] [Abstract][Full Text] [Related]  

  • 53. Two animal models of retinal degeneration are rescued by recombinant adeno-associated virus-mediated production of FGF-5 and FGF-18.
    Green ES; Rendahl KG; Zhou S; Ladner M; Coyne M; Srivastava R; Manning WC; Flannery JG
    Mol Ther; 2001 Apr; 3(4):507-15. PubMed ID: 11319911
    [TBL] [Abstract][Full Text] [Related]  

  • 54. Subretinal delivery of adeno-associated virus serotype 2 results in minimal immune responses that allow repeat vector administration in immunocompetent mice.
    Barker SE; Broderick CA; Robbie SJ; Duran Y; Natkunarajah M; Buch P; Balaggan KS; MacLaren RE; Bainbridge JW; Smith AJ; Ali RR
    J Gene Med; 2009 Jun; 11(6):486-97. PubMed ID: 19340848
    [TBL] [Abstract][Full Text] [Related]  

  • 55. 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]  

  • 56. 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]  

  • 57. Early-Onset X-Linked Retinitis Pigmentosa in a Heterozygous Female Harboring an Intronic Donor Splice Site Mutation in the Retinitis Pigmentosa GTPase Regulator Gene.
    Shifera AS; Kay CN
    Ophthalmic Genet; 2015; 36(3):251-6. PubMed ID: 24428633
    [TBL] [Abstract][Full Text] [Related]  

  • 58. 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]  

  • 59. 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]  

  • 60. Gene therapy in the rd6 mouse model of retinal degeneration.
    Dinculescu A; Min SH; Deng WT; Li Q; Hauswirth WW
    Adv Exp Med Biol; 2014; 801():711-8. PubMed ID: 24664762
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 16.