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: 38014037)

  • 1. PCDH15 Dual-AAV Gene Therapy for Deafness and Blindness in Usher Syndrome Type 1F.
    Ivanchenko MV; Hathaway DM; Mulhall EM; Booth KT; Wang M; Peters CW; Klein AJ; Chen X; Li Y; György B; Corey DP
    bioRxiv; 2023 Nov; ():. PubMed ID: 38014037
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Mini-PCDH15 gene therapy rescues hearing in a mouse model of Usher syndrome type 1F.
    Ivanchenko MV; Hathaway DM; Klein AJ; Pan B; Strelkova O; De-la-Torre P; Wu X; Peters CW; Mulhall EM; Booth KT; Goldstein C; Brower J; Sotomayor M; Indzhykulian AA; Corey DP
    Nat Commun; 2023 Apr; 14(1):2400. PubMed ID: 37100771
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Dual AAV-based PCDH15 gene therapy achieves sustained rescue of visual function in a mouse model of Usher syndrome 1F.
    Riaz S; Sethna S; Duncan T; Naeem MA; Redmond TM; Riazuddin S; Riazuddin S; Carvalho LS; Ahmed ZM
    Mol Ther; 2023 Dec; 31(12):3490-3501. PubMed ID: 37864333
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Rescue of hearing by adenine base editing in a humanized mouse model of Usher syndrome type 1F.
    Peters CW; Hanlon KS; Ivanchenko MV; Zinn E; Linarte EF; Li Y; Levy JM; Liu DR; Kleinstiver BP; Indzhykulian AA; Corey DP
    Mol Ther; 2023 Aug; 31(8):2439-2453. PubMed ID: 37312453
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Case report: novel PCDH15 variant causes usher syndrome type 1F with congenital hearing loss and syndromic retinitis pigmentosa.
    Chen N; Lee H; Kim AH; Liu PK; Kang EY; Tseng YJ; Seo GH; Khang R; Liu L; Chen KJ; Wu WC; Hsiao MC; Wang NK
    BMC Ophthalmol; 2022 Nov; 22(1):441. PubMed ID: 36384460
    [TBL] [Abstract][Full Text] [Related]  

  • 6. PCDH15 is expressed in the neurosensory epithelium of the eye and ear and mutant alleles are responsible for both USH1F and DFNB23.
    Ahmed ZM; Riazuddin S; Ahmad J; Bernstein SL; Guo Y; Sabar MF; Sieving P; Riazuddin S; Griffith AJ; Friedman TB; Belyantseva IA; Wilcox ER
    Hum Mol Genet; 2003 Dec; 12(24):3215-23. PubMed ID: 14570705
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Ames Waltzer deaf mice have reduced electroretinogram amplitudes and complex alternative splicing of Pcdh15 transcripts.
    Haywood-Watson RJ; Ahmed ZM; Kjellstrom S; Bush RA; Takada Y; Hampton LL; Battey JF; Sieving PA; Friedman TB
    Invest Ophthalmol Vis Sci; 2006 Jul; 47(7):3074-84. PubMed ID: 16799054
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Mutations of the protocadherin gene PCDH15 cause Usher syndrome type 1F.
    Ahmed ZM; Riazuddin S; Bernstein SL; Ahmed Z; Khan S; Griffith AJ; Morell RJ; Friedman TB; Riazuddin S; Wilcox ER
    Am J Hum Genet; 2001 Jul; 69(1):25-34. PubMed ID: 11398101
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Proposed therapy, developed in a
    Sethna S; Zein WM; Riaz S; Giese AP; Schultz JM; Duncan T; Hufnagel RB; Brewer CC; Griffith AJ; Redmond TM; Riazuddin S; Friedman TB; Ahmed ZM
    Elife; 2021 Nov; 10():. PubMed ID: 34751129
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Mutations in the novel protocadherin PCDH15 cause Usher syndrome type 1F.
    Alagramam KN; Yuan H; Kuehn MH; Murcia CL; Wayne S; Srisailpathy CR; Lowry RB; Knaus R; Van Laer L; Bernier FP; Schwartz S; Lee C; Morton CC; Mullins RF; Ramesh A; Van Camp G; Hageman GS; Woychik RP; Smith RJ
    Hum Mol Genet; 2001 Aug; 10(16):1709-18. PubMed ID: 11487575
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Assessment of retinal structure and function in Ames waltzer mice.
    Ball SL; Bardenstein D; Alagramam KN
    Invest Ophthalmol Vis Sci; 2003 Sep; 44(9):3986-92. PubMed ID: 12939319
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Photoreceptor expression of the Usher syndrome type 1 protein protocadherin 15 (USH1F) and its interaction with the scaffold protein harmonin (USH1C).
    Reiners J; Märker T; Jürgens K; Reidel B; Wolfrum U
    Mol Vis; 2005 May; 11():347-55. PubMed ID: 15928608
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Gene structure and mutant alleles of PCDH15: nonsyndromic deafness DFNB23 and type 1 Usher syndrome.
    Ahmed ZM; Riazuddin S; Aye S; Ali RA; Venselaar H; Anwar S; Belyantseva PP; Qasim M; Riazuddin S; Friedman TB
    Hum Genet; 2008 Oct; 124(3):215-23. PubMed ID: 18719945
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Elasticity and Thermal Stability are Key Determinants of Hearing Rescue by Mini-Protocadherin-15 Proteins.
    Pedro De-la-Torre ; Wen H; Brower J; Martínez-Pérez K; Narui Y; Yeh F; Hale E; Ivanchenko MV; Corey DP; Sotomayor M; Indzhykulian AA
    bioRxiv; 2024 Jun; ():. PubMed ID: 38948700
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Characterization of the Kyoto circling (KCI) rat carrying a spontaneous nonsense mutation in the protocadherin 15 (Pcdh15) gene.
    Naoi K; Kuramoto T; Kuwamura Y; Gohma H; Kuwamura M; Serikawa T
    Exp Anim; 2009 Jan; 58(1):1-10. PubMed ID: 19151506
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Profound, prelingual nonsyndromic deafness maps to chromosome 10q21 and is caused by a novel missense mutation in the Usher syndrome type IF gene PCDH15.
    Doucette L; Merner ND; Cooke S; Ives E; Galutira D; Walsh V; Walsh T; MacLaren L; Cater T; Fernandez B; Green JS; Wilcox ER; Shotland LI; Li XC; Lee M; King MC; Young TL
    Eur J Hum Genet; 2009 May; 17(5):554-64. PubMed ID: 19107147
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Characterization of Usher syndrome type I gene mutations in an Usher syndrome patient population.
    Ouyang XM; Yan D; Du LL; Hejtmancik JF; Jacobson SG; Nance WE; Li AR; Angeli S; Kaiser M; Newton V; Brown SD; Balkany T; Liu XZ
    Hum Genet; 2005 Mar; 116(4):292-9. PubMed ID: 15660226
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Mutation screening of the PCDH15 gene in Spanish patients with Usher syndrome type I.
    Jaijo T; Oshima A; Aller E; Carney C; Usami S; Millán JM; Kimberling WJ
    Mol Vis; 2012; 18():1719-26. PubMed ID: 22815625
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Truncating variants in the majority of the cytoplasmic domain of PCDH15 are unlikely to cause Usher syndrome 1F.
    Perreault-Micale C; Frieden A; Kennedy CJ; Neitzel D; Sullivan J; Faulkner N; Hallam S; Greger V
    J Mol Diagn; 2014 Nov; 16(6):673-8. PubMed ID: 25307757
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Large genomic rearrangements within the PCDH15 gene are a significant cause of USH1F syndrome.
    Le Guédard S; Faugère V; Malcolm S; Claustres M; Roux AF
    Mol Vis; 2007 Jan; 13():102-7. PubMed ID: 17277737
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.