BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

223 related articles for article (PubMed ID: 21423608)

  • 1. A mutation in synaptojanin 2 causes progressive hearing loss in the ENU-mutagenised mouse strain Mozart.
    Manji SS; Williams LH; Miller KA; Ooms LM; Bahlo M; Mitchell CA; Dahl HH
    PLoS One; 2011 Mar; 6(3):e17607. PubMed ID: 21423608
    [TBL] [Abstract][Full Text] [Related]  

  • 2. The BEACH protein LRBA is required for hair bundle maintenance in cochlear hair cells and for hearing.
    Vogl C; Butola T; Haag N; Hausrat TJ; Leitner MG; Moutschen M; Lefèbvre PP; Speckmann C; Garrett L; Becker L; Fuchs H; Hrabe de Angelis M; Nietzsche S; Kessels MM; Oliver D; Kneussel M; Kilimann MW; Strenzke N
    EMBO Rep; 2017 Nov; 18(11):2015-2029. PubMed ID: 28893864
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Melody, an ENU mutation in Caspase 3, alters the catalytic cysteine residue and causes sensorineural hearing loss in mice.
    Parker A; Hardisty-Hughes RE; Wisby L; Joyce S; Brown SD
    Mamm Genome; 2010 Dec; 21(11-12):565-76. PubMed ID: 21116635
    [TBL] [Abstract][Full Text] [Related]  

  • 4. A Novel ENU-Induced Mutation in Myo6 Causes Vestibular Dysfunction and Deafness.
    Wong EY; Xu CY; Brahmachary M; Xu PX
    PLoS One; 2016; 11(5):e0154984. PubMed ID: 27171474
    [TBL] [Abstract][Full Text] [Related]  

  • 5. MPZL2, Encoding the Epithelial Junctional Protein Myelin Protein Zero-like 2, Is Essential for Hearing in Man and Mouse.
    Wesdorp M; Murillo-Cuesta S; Peters T; Celaya AM; Oonk A; Schraders M; Oostrik J; Gomez-Rosas E; Beynon AJ; Hartel BP; Okkersen K; Koenen HJPM; Weeda J; Lelieveld S; Voermans NC; Joosten I; Hoyng CB; Lichtner P; Kunst HPM; Feenstra I; de Bruijn SE; ; Admiraal RJC; Yntema HG; van Wijk E; Del Castillo I; Serra P; Varela-Nieto I; Pennings RJE; Kremer H
    Am J Hum Genet; 2018 Jul; 103(1):74-88. PubMed ID: 29961571
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Hair Cell Loss, Spiral Ganglion Degeneration, and Progressive Sensorineural Hearing Loss in Mice with Targeted Deletion of Slc44a2/Ctl2.
    Kommareddi P; Nair T; Kakaraparthi BN; Galano MM; Miller D; Laczkovich I; Thomas T; Lu L; Rule K; Kabara L; Kanicki A; Hughes ED; Jones JM; Hoenerhoff M; Fisher SG; Altschuler RA; Dolan D; Kohrman DC; Saunders TL; Carey TE
    J Assoc Res Otolaryngol; 2015 Dec; 16(6):695-712. PubMed ID: 26463873
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Characterization of a novel ENU-generated myosin VI mutant mouse strain with congenital deafness and vestibular dysfunction.
    Williams LH; Miller KA; Dahl HH; Manji SS
    Hear Res; 2013 May; 299():53-62. PubMed ID: 23485424
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Generation and pathological characterization of a transgenic mouse model carrying a missense PJVK mutation.
    Cheng YF; Tsai YH; Huang CY; Lee YS; Chang PC; Lu YC; Hsu CJ; Wu CC
    Biochem Biophys Res Commun; 2020 Nov; 532(4):675-681. PubMed ID: 32917362
    [TBL] [Abstract][Full Text] [Related]  

  • 9. ROR1 is essential for proper innervation of auditory hair cells and hearing in humans and mice.
    Diaz-Horta O; Abad C; Sennaroglu L; Foster J; DeSmidt A; Bademci G; Tokgoz-Yilmaz S; Duman D; Cengiz FB; Grati M; Fitoz S; Liu XZ; Farooq A; Imtiaz F; Currall BB; Morton CC; Nishita M; Minami Y; Lu Z; Walz K; Tekin M
    Proc Natl Acad Sci U S A; 2016 May; 113(21):5993-8. PubMed ID: 27162350
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Exocyst Complex Member EXOC5 Is Required for Survival of Hair Cells and Spiral Ganglion Neurons and Maintenance of Hearing.
    Lee B; Baek JI; Min H; Bae SH; Moon K; Kim MA; Kim YR; Fogelgren B; Lipschutz JH; Lee KY; Bok J; Kim UK
    Mol Neurobiol; 2018 Aug; 55(8):6518-6532. PubMed ID: 29327200
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Severe vestibular and auditory impairment in three alleles of Ames waltzer (av) mice.
    Raphael Y; Kobayashi KN; Dootz GA; Beyer LA; Dolan DF; Burmeister M
    Hear Res; 2001 Jan; 151(1-2):237-249. PubMed ID: 11124469
    [TBL] [Abstract][Full Text] [Related]  

  • 12. The novel mouse mutation Oblivion inactivates the PMCA2 pump and causes progressive hearing loss.
    Spiden SL; Bortolozzi M; Di Leva F; de Angelis MH; Fuchs H; Lim D; Ortolano S; Ingham NJ; Brini M; Carafoli E; Mammano F; Steel KP
    PLoS Genet; 2008 Oct; 4(10):e1000238. PubMed ID: 18974863
    [TBL] [Abstract][Full Text] [Related]  

  • 13. An ENU-induced mutation of Cdh23 causes congenital hearing loss, but no vestibular dysfunction, in mice.
    Manji SS; Miller KA; Williams LH; Andreasen L; Siboe M; Rose E; Bahlo M; Kuiper M; Dahl HH
    Am J Pathol; 2011 Aug; 179(2):903-14. PubMed ID: 21689626
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Mutations in LOXHD1, an evolutionarily conserved stereociliary protein, disrupt hair cell function in mice and cause progressive hearing loss in humans.
    Grillet N; Schwander M; Hildebrand MS; Sczaniecka A; Kolatkar A; Velasco J; Webster JA; Kahrizi K; Najmabadi H; Kimberling WJ; Stephan D; Bahlo M; Wiltshire T; Tarantino LM; Kuhn P; Smith RJ; Müller U
    Am J Hum Genet; 2009 Sep; 85(3):328-37. PubMed ID: 19732867
    [TBL] [Abstract][Full Text] [Related]  

  • 15. CTCF is required for maintenance of auditory hair cells and hearing function in the mouse cochlea.
    Ma JH; Kim HP; Bok J; Shin JO
    Biochem Biophys Res Commun; 2018 Sep; 503(4):2646-2652. PubMed ID: 30107916
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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]  

  • 17. Analysis of the mouse mutant Cloth-ears shows a role for the voltage-gated sodium channel Scn8a in peripheral neural hearing loss.
    Mackenzie FE; Parker A; Parkinson NJ; Oliver PL; Brooker D; Underhill P; Lukashkina VA; Lukashkin AN; Holmes C; Brown SD
    Genes Brain Behav; 2009 Oct; 8(7):699-713. PubMed ID: 19737145
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Mutations of the mouse ELMO domain containing 1 gene (Elmod1) link small GTPase signaling to actin cytoskeleton dynamics in hair cell stereocilia.
    Johnson KR; Longo-Guess CM; Gagnon LH
    PLoS One; 2012; 7(4):e36074. PubMed ID: 22558334
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Tailchaser (Tlc): a new mouse mutation affecting hair bundle differentiation and hair cell survival.
    Kiernan AE; Zalzman M; Fuchs H; Hrabe de Angelis M; Balling R; Steel KP; Avraham KB
    J Neurocytol; 1999; 28(10-11):969-85. PubMed ID: 10900098
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Sphingosine 1-phosphate (S1P) signaling is required for maintenance of hair cells mainly via activation of S1P2.
    Herr DR; Grillet N; Schwander M; Rivera R; Müller U; Chun J
    J Neurosci; 2007 Feb; 27(6):1474-8. PubMed ID: 17287522
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 12.