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 *

197 related articles for article (PubMed ID: 35283480)

  • 1. Preventing autosomal-dominant hearing loss in Bth mice with CRISPR/CasRx-based RNA editing.
    Zheng Z; Li G; Cui C; Wang F; Wang X; Xu Z; Guo H; Chen Y; Tang H; Wang D; Huang M; Chen ZY; Huang X; Li H; Li GL; Hu X; Shu Y
    Signal Transduct Target Ther; 2022 Mar; 7(1):79. PubMed ID: 35283480
    [TBL] [Abstract][Full Text] [Related]  

  • 2. A novel DFNA36 mutation in TMC1 orthologous to the Beethoven (Bth) mouse associated with autosomal dominant hearing loss in a Chinese family.
    Zhao Y; Wang D; Zong L; Zhao F; Guan L; Zhang P; Shi W; Lan L; Wang H; Li Q; Han B; Yang L; Jin X; Wang J; Wang J; Wang Q
    PLoS One; 2014; 9(5):e97064. PubMed ID: 24827932
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Treatment of autosomal dominant hearing loss by in vivo delivery of genome editing agents.
    Gao X; Tao Y; Lamas V; Huang M; Yeh WH; Pan B; Hu YJ; Hu JH; Thompson DB; Shu Y; Li Y; Wang H; Yang S; Xu Q; Polley DB; Liberman MC; Kong WJ; Holt JR; Chen ZY; Liu DR
    Nature; 2018 Jan; 553(7687):217-221. PubMed ID: 29258297
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Tmc1 Point Mutation Affects Ca2+ Sensitivity and Block by Dihydrostreptomycin of the Mechanoelectrical Transducer Current of Mouse Outer Hair Cells.
    Corns LF; Johnson SL; Kros CJ; Marcotti W
    J Neurosci; 2016 Jan; 36(2):336-49. PubMed ID: 26758827
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Optimized AAV Vectors for TMC1 Gene Therapy in a Humanized Mouse Model of DFNB7/11.
    Marcovich I; Baer NK; Shubina-Oleinik O; Eclov R; Beard CW; Holt JR
    Biomolecules; 2022 Jun; 12(7):. PubMed ID: 35883470
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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]  

  • 7. Specific knockdown of
    Guo Y; Han L; Han S; Tang H; Wang S; Cui C; Chen B; Li H; Shu Y
    Mol Ther Nucleic Acids; 2022 Jun; 28():643-655. PubMed ID: 35615000
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Allele-specific gene editing prevents deafness in a model of dominant progressive hearing loss.
    György B; Nist-Lund C; Pan B; Asai Y; Karavitaki KD; Kleinstiver BP; Garcia SP; Zaborowski MP; Solanes P; Spataro S; Schneider BL; Joung JK; Géléoc GSG; Holt JR; Corey DP
    Nat Med; 2019 Jul; 25(7):1123-1130. PubMed ID: 31270503
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [Advances in hereditary hearing loss caused by TMC1 mutations].
    Wu K; Wang H; Wang Q
    Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi; 2016 Mar; 51(3):224-9. PubMed ID: 27033582
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Multiple quantitative trait loci modify cochlear hair cell degeneration in the Beethoven (Tmc1Bth) mouse model of progressive hearing loss DFNA36.
    Noguchi Y; Kurima K; Makishima T; de Angelis MH; Fuchs H; Frolenkov G; Kitamura K; Griffith AJ
    Genetics; 2006 Aug; 173(4):2111-9. PubMed ID: 16648588
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Mutations of TMC1 cause deafness by disrupting mechanoelectrical transduction.
    Nakanishi H; Kurima K; Kawashima Y; Griffith AJ
    Auris Nasus Larynx; 2014 Oct; 41(5):399-408. PubMed ID: 24933710
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Prevalence and clinical features of autosomal dominant and recessive TMC1-associated hearing loss.
    Nishio SY; Usami SI
    Hum Genet; 2022 Apr; 141(3-4):929-937. PubMed ID: 34523024
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Novel autosomal dominant TMC1 variants linked to hearing loss: insight into protein-lipid interactions.
    Cho SH; Yun Y; Lee DH; Cha JH; Lee SM; Lee J; Suh MH; Lee JH; Oh SH; Park MK; Lee SY
    BMC Med Genomics; 2023 Dec; 16(1):320. PubMed ID: 38066485
    [TBL] [Abstract][Full Text] [Related]  

  • 14. CRISPR-CasRx knock-in mice for RNA degradation.
    Li J; Zhu D; Hu S; Nie Y
    Sci China Life Sci; 2022 Nov; 65(11):2248-2256. PubMed ID: 35412223
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Gene editing in a Myo6 semi-dominant mouse model rescues auditory function.
    Xue Y; Hu X; Wang D; Li D; Li Y; Wang F; Huang M; Gu X; Xu Z; Zhou J; Wang J; Chai R; Shen J; Chen ZY; Li GL; Yang H; Li H; Zuo E; Shu Y
    Mol Ther; 2022 Jan; 30(1):105-118. PubMed ID: 34174443
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Tmc1 is necessary for normal functional maturation and survival of inner and outer hair cells in the mouse cochlea.
    Marcotti W; Erven A; Johnson SL; Steel KP; Kros CJ
    J Physiol; 2006 Aug; 574(Pt 3):677-98. PubMed ID: 16627570
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Methods for
    Chuang YF; Wang PY; Kumar S; Lama S; Lin FL; Liu GS
    Front Cell Dev Biol; 2021; 9():667879. PubMed ID: 34178991
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Mutation analysis of TMC1 identifies four new mutations and suggests an additional deafness gene at loci DFNA36 and DFNB7/11.
    Hilgert N; Alasti F; Dieltjens N; Pawlik B; Wollnik B; Uyguner O; Delmaghani S; Weil D; Petit C; Danis E; Yang T; Pandelia E; Petersen MB; Goossens D; Favero JD; Sanati MH; Smith RJ; Van Camp G
    Clin Genet; 2008 Sep; 74(3):223-32. PubMed ID: 18616530
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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]  

  • 20. In vivo base editing restores sensory transduction and transiently improves auditory function in a mouse model of recessive deafness.
    Yeh WH; Shubina-Oleinik O; Levy JM; Pan B; Newby GA; Wornow M; Burt R; Chen JC; Holt JR; Liu DR
    Sci Transl Med; 2020 Jun; 12(546):. PubMed ID: 32493795
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.