BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

148 related articles for article (PubMed ID: 20555336)

  • 81. Autosomal dominant retinitis pigmentosa (ADRP): a rhodopsin mutation in a Scottish family.
    Bell C; Converse CA; Collins MF; Esakowitz L; Kelly KF; Haites NE
    J Med Genet; 1992 Sep; 29(9):667-8. PubMed ID: 1404299
    [No Abstract]   [Full Text] [Related]  

  • 82. [Disease gene screening of known loci in a Chinese family with autosomal dominant retinitis pigmentosa].
    Liu W; Lu F; Qia LF; Sha ZQ; Liu XO; Ma S; Tang X; Chang JX; Yang ZL; Ye B
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2009 Feb; 26(1):70-3. PubMed ID: 19199256
    [TBL] [Abstract][Full Text] [Related]  

  • 83. Linkage between Rh blood group and autosomal dominant retinitis pigmentosa in ten Chinese families.
    Fei YJ; Blanton SH; Daiger SP; Luo CR
    Chin Med J (Engl); 1992 Jun; 105(6):486-9. PubMed ID: 1451549
    [TBL] [Abstract][Full Text] [Related]  

  • 84. Mutation analysis of
    Zhuang J; Zhang R; Zhou B; Cao Z; Zhou J; Chen X; Zhang N; Zhu Y; Yang J
    Ophthalmic Genet; 2024 Apr; 45(2):147-152. PubMed ID: 38284172
    [TBL] [Abstract][Full Text] [Related]  

  • 85. Exclusion of the involvement of all known retinitis pigmentosa loci in the disease present in a family of Irish origin provides evidence for a sixth autosomal dominant locus (RP8).
    Kumar-Singh R; Farrar GJ; Mansergh F; Kenna P; Bhattacharya S; Gal A; Humphries P
    Hum Mol Genet; 1993 Jul; 2(7):875-8. PubMed ID: 8364569
    [TBL] [Abstract][Full Text] [Related]  

  • 86. Knockout and Replacement Gene Surgery to Treat Rhodopsin-Mediated Autosomal Dominant Retinitis Pigmentosa.
    Sun X; Liang C; Chen Y; Cui T; Han J; Dai M; Zhang Y; Zhou Q; Li W
    Hum Gene Ther; 2024 Mar; 35(5-6):151-162. PubMed ID: 38368562
    [TBL] [Abstract][Full Text] [Related]  

  • 87. Molecular genetics of autosomal dominant retinitis pigmentosa (ADRP): a comprehensive study of 43 Italian families.
    Ziviello C; Simonelli F; Testa F; Anastasi M; Marzoli SB; Falsini B; Ghiglione D; Macaluso C; Manitto MP; Garrè C; Ciccodicola A; Rinaldi E; Banfi S
    J Med Genet; 2005 Jul; 42(7):e47. PubMed ID: 15994872
    [TBL] [Abstract][Full Text] [Related]  

  • 88. Linkage analysis of human chromosome 4: exclusion of autosomal dominant retinitis pigmentosa (ADRP) and detection of new linkage groups.
    Daiger SP; Humphries MM; Giesenschlag N; Sharp E; McWilliam P; Farrer J; Bradley D; Kenna P; McConnell DJ; Sparkes RS
    Cytogenet Cell Genet; 1989; 50(4):181-7. PubMed ID: 2572401
    [TBL] [Abstract][Full Text] [Related]  

  • 89. Identification of a novel RHO heterozygous nonsense mutation in a Chinese family with autosomal dominant retinitis pigmentosa.
    Liu W; Guo R; Hao H; Ji J
    BMC Ophthalmol; 2021 Oct; 21(1):360. PubMed ID: 34635090
    [TBL] [Abstract][Full Text] [Related]  

  • 90. Gene augmentation for adRP mutations in RHO.
    Lewin AS; Rossmiller B; Mao H
    Cold Spring Harb Perspect Med; 2014 Jul; 4(9):a017400. PubMed ID: 25037104
    [TBL] [Abstract][Full Text] [Related]  

  • 91. Rhodopsin mutations in Chinese patients with retinitis pigmentosa.
    Chan WM; Yeung KY; Pang CP; Baum L; Lau TC; Kwok AK; Lam DS
    Br J Ophthalmol; 2001 Sep; 85(9):1046-8. PubMed ID: 11520753
    [TBL] [Abstract][Full Text] [Related]  

  • 92. Identification of an IMPDH1 mutation in autosomal dominant retinitis pigmentosa (RP10) revealed following comparative microarray analysis of transcripts derived from retinas of wild-type and Rho(-/-) mice.
    Kennan A; Aherne A; Palfi A; Humphries M; McKee A; Stitt A; Simpson DA; Demtroder K; Orntoft T; Ayuso C; Kenna PF; Farrar GJ; Humphries P
    Hum Mol Genet; 2002 Mar; 11(5):547-57. PubMed ID: 11875049
    [TBL] [Abstract][Full Text] [Related]  

  • 93. CRISPR DNA Base Editing Strategies for Treating Retinitis Pigmentosa Caused by Mutations in
    Kaukonen M; McClements ME; MacLaren RE
    Genes (Basel); 2022 Jul; 13(8):. PubMed ID: 35893064
    [TBL] [Abstract][Full Text] [Related]  

  • 94. Low frequency of rhodopsin mutations in South African patients with autosomal dominant retinitis pigmentosa.
    Roberts L; Ramesar R; Greenberg J
    Clin Genet; 2000 Jul; 58(1):77-8. PubMed ID: 10945667
    [No Abstract]   [Full Text] [Related]  

  • 95. [Autosomal dominant hereditary retinopathia pigmentosa with genetic heterogeneity].
    Orth U; Samanns C; Gusseck H; Niemeyer G; Ludwig M; Meitinger T; Schinzel A; Schwinger E; Gal A
    Fortschr Ophthalmol; 1991; 88(5):455-9. PubMed ID: 1757031
    [TBL] [Abstract][Full Text] [Related]  

  • 96. CRISPR genome surgery in a novel humanized model for autosomal dominant retinitis pigmentosa.
    Wu WH; Tsai YT; Huang IW; Cheng CH; Hsu CW; Cui X; Ryu J; Quinn PMJ; Caruso SM; Lin CS; Tsang SH
    Mol Ther; 2022 Apr; 30(4):1407-1420. PubMed ID: 35150888
    [TBL] [Abstract][Full Text] [Related]  

  • 97. Autosomal dominant retinitis pigmentosa: exclusion of a gene from extensive regions of chromosomes 6, 13, 20, and 21.
    Farrar GJ; McWilliam P; Sharp EM; Kenna P; Bradley DG; Humphries MM; McConnell DJ; Humphries P
    Genomics; 1989 Oct; 5(3):612-8. PubMed ID: 2613243
    [TBL] [Abstract][Full Text] [Related]  

  • 98. Current therapeutic strategies for P23H RHO-linked RP.
    Nguyen AT; Campbell M; Kiang AS; Humphries MM; Humphries P
    Adv Exp Med Biol; 2014; 801():471-6. PubMed ID: 24664733
    [TBL] [Abstract][Full Text] [Related]  

  • 99. Light in retinitis pigmentosa.
    Kennan A; Aherne A; Humphries P
    Trends Genet; 2005 Feb; 21(2):103-10. PubMed ID: 15661356
    [TBL] [Abstract][Full Text] [Related]  

  • 100. Mutations in TOPORS: a rare cause of autosomal dominant retinitis pigmentosa in continental Europe?
    Schob C; Orth U; Gal A; Kindler S; Chakarova CF; Bhattacharya SS; RĂ¼ther K
    Ophthalmic Genet; 2009 Jun; 30(2):96-8. PubMed ID: 19373681
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 8.