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 *

180 related articles for article (PubMed ID: 16648588)

  • 1. 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]  

  • 2. A QTL on Chr 5 modifies hearing loss associated with the fascin-2 variant of DBA/2J mice.
    Johnson KR; Longo-Guess CM; Gagnon LH
    Mamm Genome; 2015 Aug; 26(7-8):338-47. PubMed ID: 26092689
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. Identification of three novel hearing loss mouse strains with mutations in the Tmc1 gene.
    Manji SS; Miller KA; Williams LH; Dahl HH
    Am J Pathol; 2012 Apr; 180(4):1560-9. PubMed ID: 22330676
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Mutation of the TBCE gene causes disturbance of microtubules in the auditory nerve and cochlear outer hair cell degeneration accompanied by progressive hearing loss in the pmn/pmn mouse.
    Rak K; Frenz S; Radeloff A; Groh J; Jablonka S; Martini R; Hagen R; Mlynski R
    Exp Neurol; 2013 Dec; 250():333-40. PubMed ID: 24120439
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Polygenic inheritance of sensorineural hearing loss (Snhl2, -3, and -4) and organ of Corti patterning defect in the ALR/LtJ mouse strain.
    Latoche JR; Neely HR; Noben-Trauth K
    Hear Res; 2011 May; 275(1-2):150-9. PubMed ID: 21185929
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. CD1 hearing-impaired mice. II. Group latencies and optimal f2/f1 ratios of distortion product otoacoustic emissions, and scanning electron microscopy.
    Le Calvez S; Guilhaume A; Romand R; Aran JM; Avan P
    Hear Res; 1998 Jun; 120(1-2):51-61. PubMed ID: 9667430
    [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. 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]  

  • 11. Tmc2 expression partially restores auditory function in a mouse model of DFNB7/B11 deafness caused by loss of Tmc1 function.
    Nakanishi H; Kurima K; Pan B; Wangemann P; Fitzgerald TS; Géléoc GS; Holt JR; Griffith AJ
    Sci Rep; 2018 Aug; 8(1):12125. PubMed ID: 30108230
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Beethoven, a mouse model for dominant, progressive hearing loss DFNA36.
    Vreugde S; Erven A; Kros CJ; Marcotti W; Fuchs H; Kurima K; Wilcox ER; Friedman TB; Griffith AJ; Balling R; Hrabé De Angelis M; Avraham KB; Steel KP
    Nat Genet; 2002 Mar; 30(3):257-8. PubMed ID: 11850623
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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]  

  • 14. Sensory transduction is required for normal development and maturation of cochlear inner hair cell synapses.
    Lee J; Kawai K; Holt JR; Géléoc GS
    Elife; 2021 Nov; 10():. PubMed ID: 34734805
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Quantitative genetics of age-related retinal degeneration: a second F1 intercross between the A/J and C57BL/6 strains.
    Danciger M; Yang H; Ralston R; Liu Y; Matthes MT; Peirce J; Lavail MM
    Mol Vis; 2007 Jan; 13():79-85. PubMed ID: 17277741
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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]  

  • 17. The goya mouse mutant reveals distinct newly identified roles for MAP3K1 in the development and survival of cochlear sensory hair cells.
    Parker A; Cross SH; Jackson IJ; Hardisty-Hughes R; Morse S; Nicholson G; Coghill E; Bowl MR; Brown SD
    Dis Model Mech; 2015 Dec; 8(12):1555-68. PubMed ID: 26542706
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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]  

  • 19. 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]  

  • 20. Phenotype and genetics of progressive sensorineural hearing loss (Snhl1) in the LXS set of recombinant inbred strains of mice.
    Noben-Trauth K; Latoche JR; Neely HR; Bennett B
    PLoS One; 2010 Jul; 5(7):e11459. PubMed ID: 20628639
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.