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 *

392 related articles for article (PubMed ID: 30782832)

  • 1. Dual AAV-mediated gene therapy restores hearing in a DFNB9 mouse model.
    Akil O; Dyka F; Calvet C; Emptoz A; Lahlou G; Nouaille S; Boutet de Monvel J; Hardelin JP; Hauswirth WW; Avan P; Petit C; Safieddine S; Lustig LR
    Proc Natl Acad Sci U S A; 2019 Mar; 116(10):4496-4501. PubMed ID: 30782832
    [TBL] [Abstract][Full Text] [Related]  

  • 2. A dual-AAV approach restores fast exocytosis and partially rescues auditory function in deaf otoferlin knock-out mice.
    Al-Moyed H; Cepeda AP; Jung S; Moser T; Kügler S; Reisinger E
    EMBO Mol Med; 2019 Jan; 11(1):. PubMed ID: 30509897
    [TBL] [Abstract][Full Text] [Related]  

  • 3. AAV-Mediated Gene Therapy Restores Hearing in Patients with DFNB9 Deafness.
    Qi J; Tan F; Zhang L; Lu L; Zhang S; Zhai Y; Lu Y; Qian X; Dong W; Zhou Y; Zhang Z; Yang X; Jiang L; Yu C; Liu J; Chen T; Wu L; Tan C; Sun S; Song H; Shu Y; Xu L; Gao X; Li H; Chai R
    Adv Sci (Weinh); 2024 Mar; 11(11):e2306788. PubMed ID: 38189623
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Overloaded Adeno-Associated Virus as a Novel Gene Therapeutic Tool for Otoferlin-Related Deafness.
    Rankovic V; Vogl C; Dörje NM; Bahader I; Duque-Afonso CJ; Thirumalai A; Weber T; Kusch K; Strenzke N; Moser T
    Front Mol Neurosci; 2020; 13():600051. PubMed ID: 33488357
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Dual and triple AAV delivery of large therapeutic gene sequences into the inner ear.
    Akil O
    Hear Res; 2020 Sep; 394():107912. PubMed ID: 32067799
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Substitutions in the conserved C2C domain of otoferlin cause DFNB9, a form of nonsyndromic autosomal recessive deafness.
    Mirghomizadeh F; Pfister M; Apaydin F; Petit C; Kupka S; Pusch CM; Zenner HP; Blin N
    Neurobiol Dis; 2002 Jul; 10(2):157-64. PubMed ID: 12127154
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Dual-AAV delivery of large gene sequences to the inner ear.
    Reisinger E
    Hear Res; 2020 Sep; 394():107857. PubMed ID: 31810595
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Identities and frequencies of mutations of the otoferlin gene (OTOF) causing DFNB9 deafness in Pakistan.
    Choi BY; Ahmed ZM; Riazuddin S; Bhinder MA; Shahzad M; Husnain T; Riazuddin S; Griffith AJ; Friedman TB
    Clin Genet; 2009 Mar; 75(3):237-43. PubMed ID: 19250381
    [TBL] [Abstract][Full Text] [Related]  

  • 9. A missense mutation in the conserved C2B domain of otoferlin causes deafness in a new mouse model of DFNB9.
    Longo-Guess C; Gagnon LH; Bergstrom DE; Johnson KR
    Hear Res; 2007 Dec; 234(1-2):21-8. PubMed ID: 17967520
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Tmc gene therapy restores auditory function in deaf mice.
    Askew C; Rochat C; Pan B; Asai Y; Ahmed H; Child E; Schneider BL; Aebischer P; Holt JR
    Sci Transl Med; 2015 Jul; 7(295):295ra108. PubMed ID: 26157030
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Single and Dual Vector Gene Therapy with AAV9-PHP.B Rescues Hearing in Tmc1 Mutant Mice.
    Wu J; Solanes P; Nist-Lund C; Spataro S; Shubina-Oleinik O; Marcovich I; Goldberg H; Schneider BL; Holt JR
    Mol Ther; 2021 Mar; 29(3):973-988. PubMed ID: 33212302
    [TBL] [Abstract][Full Text] [Related]  

  • 12. AAV1-hOTOF gene therapy for autosomal recessive deafness 9: a single-arm trial.
    Lv J; Wang H; Cheng X; Chen Y; Wang D; Zhang L; Cao Q; Tang H; Hu S; Gao K; Xun M; Wang J; Wang Z; Zhu B; Cui C; Gao Z; Guo L; Yu S; Jiang L; Yin Y; Zhang J; Chen B; Wang W; Chai R; Chen ZY; Li H; Shu Y
    Lancet; 2024 May; 403(10441):2317-2325. PubMed ID: 38280389
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Bilateral gene therapy in children with autosomal recessive deafness 9: single-arm trial results.
    Wang H; Chen Y; Lv J; Cheng X; Cao Q; Wang D; Zhang L; Zhu B; Shen M; Xu C; Xun M; Wang Z; Tang H; Hu S; Cui C; Jiang L; Yin Y; Guo L; Zhou Y; Han L; Gao Z; Zhang J; Yu S; Gao K; Wang J; Chen B; Wang W; Chen ZY; Li H; Shu Y
    Nat Med; 2024 Jul; 30(7):1898-1904. PubMed ID: 38839897
    [TBL] [Abstract][Full Text] [Related]  

  • 14. OTOF encodes multiple long and short isoforms: genetic evidence that the long ones underlie recessive deafness DFNB9.
    Yasunaga S; Grati M; Chardenoux S; Smith TN; Friedman TB; Lalwani AK; Wilcox ER; Petit C
    Am J Hum Genet; 2000 Sep; 67(3):591-600. PubMed ID: 10903124
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Recovery kinetics of dual AAV-mediated human otoferlin expression.
    Sellon JB; So KS; D'Arcangelo A; Cancelarich S; Drummond MC; Slade PG; Pan N; Gibson TM; Yang T; Burns JC; Palermo AT; Becker L
    Front Mol Neurosci; 2024; 17():1376128. PubMed ID: 38952419
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Targeted Allele Suppression Prevents Progressive Hearing Loss in the Mature Murine Model of Human TMC1 Deafness.
    Yoshimura H; Shibata SB; Ranum PT; Moteki H; Smith RJH
    Mol Ther; 2019 Mar; 27(3):681-690. PubMed ID: 30686588
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Perinatal Gjb2 gene transfer rescues hearing in a mouse model of hereditary deafness.
    Iizuka T; Kamiya K; Gotoh S; Sugitani Y; Suzuki M; Noda T; Minowa O; Ikeda K
    Hum Mol Genet; 2015 Jul; 24(13):3651-61. PubMed ID: 25801282
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Hearing restoration by gene replacement therapy for a multisite-expressed gene in a mouse model of human DFNB111 deafness.
    Jiang L; Hu SW; Wang Z; Zhou Y; Tang H; Chen Y; Wang D; Fan X; Han L; Li H; Shi D; He Y; Shu Y
    Am J Hum Genet; 2024 Oct; 111(10):2253-2264. PubMed ID: 39241775
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [Local administration of an AAV-TMPRSS3 vector in aged Tmprss3 mutant mice with progressive deafness restores hearing].
    Richard ÉM; Delprat B
    Med Sci (Paris); 2024 May; 40(5):402-404. PubMed ID: 38819271
    [No Abstract]   [Full Text] [Related]  

  • 20. A mutation in OTOF, encoding otoferlin, a FER-1-like protein, causes DFNB9, a nonsyndromic form of deafness.
    Yasunaga S; Grati M; Cohen-Salmon M; El-Amraoui A; Mustapha M; Salem N; El-Zir E; Loiselet J; Petit C
    Nat Genet; 1999 Apr; 21(4):363-9. PubMed ID: 10192385
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 20.