BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

110 related articles for article (PubMed ID: 23850727)

  • 1. Biallelic nonsense mutations in the otogelin-like gene (OTOGL) in a child affected by mild to moderate hearing impairment.
    Bonnet C; Louha M; Loundon N; Michalski N; Verpy E; Smagghe L; Hardelin JP; Rouillon I; Jonard L; Couderc R; Gherbi S; Garabedian EN; Denoyelle F; Petit C; Marlin S
    Gene; 2013 Sep; 527(2):537-40. PubMed ID: 23850727
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Otogelin, otogelin-like, and stereocilin form links connecting outer hair cell stereocilia to each other and the tectorial membrane.
    Avan P; Le Gal S; Michel V; Dupont T; Hardelin JP; Petit C; Verpy E
    Proc Natl Acad Sci U S A; 2019 Dec; 116(51):25948-25957. PubMed ID: 31776257
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Similar phenotypes caused by mutations in OTOG and OTOGL.
    Oonk AM; Leijendeckers JM; Huygen PL; Schraders M; del Campo M; del Castillo I; Tekin M; Feenstra I; Beynon AJ; Kunst HP; Snik AF; Kremer H; Admiraal RJ; Pennings RJ
    Ear Hear; 2014; 35(3):e84-91. PubMed ID: 24378291
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Mutations in OTOGL, encoding the inner ear protein otogelin-like, cause moderate sensorineural hearing loss.
    Yariz KO; Duman D; Zazo Seco C; Dallman J; Huang M; Peters TA; Sirmaci A; Lu N; Schraders M; Skromne I; Oostrik J; Diaz-Horta O; Young JI; Tokgoz-Yilmaz S; Konukseven O; Shahin H; Hetterschijt L; Kanaan M; Oonk AM; Edwards YJ; Li H; Atalay S; Blanton S; Desmidt AA; Liu XZ; Pennings RJ; Lu Z; Chen ZY; Kremer H; Tekin M
    Am J Hum Genet; 2012 Nov; 91(5):872-82. PubMed ID: 23122586
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Otoacoustic emissions and brainstem evoked potentials in compound carriers of connexin 26 mutations.
    Engel-Yeger B; Zaaroura S; Zlotogora J; Shalev S; Hujeirat Y; Carrasquillo M; Saleh B; Pratt H
    Hear Res; 2003 Jan; 175(1-2):140-51. PubMed ID: 12527132
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [Phenotype and genotype analysis of recessive hereditary moderate sensorineural hearing loss caused by new mutations in OTOGL gene].
    Feng ML; Huang SS; Tang FZ; Zhang X; Li XH; Qiu SW; Yuan YY
    Zhonghua Yi Xue Za Zhi; 2021 Jan; 101(2):115-121. PubMed ID: 33455126
    [No Abstract]   [Full Text] [Related]  

  • 7. Mutations of the gene encoding otogelin are a cause of autosomal-recessive nonsyndromic moderate hearing impairment.
    Schraders M; Ruiz-Palmero L; Kalay E; Oostrik J; del Castillo FJ; Sezgin O; Beynon AJ; Strom TM; Pennings RJ; Zazo Seco C; Oonk AM; Kunst HP; Domínguez-Ruiz M; García-Arumi AM; del Campo M; Villamar M; Hoefsloot LH; Moreno F; Admiraal RJ; del Castillo I; Kremer H
    Am J Hum Genet; 2012 Nov; 91(5):883-9. PubMed ID: 23122587
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Targeted disruption of otog results in deafness and severe imbalance.
    Simmler MC; Cohen-Salmon M; El-Amraoui A; Guillaud L; Benichou JC; Petit C; Panthier JJ
    Nat Genet; 2000 Feb; 24(2):139-43. PubMed ID: 10655058
    [TBL] [Abstract][Full Text] [Related]  

  • 9. A novel early truncation mutation in OTOG causes prelingual mild hearing loss without vestibular dysfunction.
    Yu S; Choi HJ; Lee JS; Lee HJ; Rim JH; Choi JY; Gee HY; Jung J
    Eur J Med Genet; 2019 Jan; 62(1):81-84. PubMed ID: 29800624
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Audiological and electrocochleography findings in hearing-impaired children with connexin 26 mutations and otoacoustic emissions.
    Santarelli R; Cama E; Scimemi P; Dal Monte E; Genovese E; Arslan E
    Eur Arch Otorhinolaryngol; 2008 Jan; 265(1):43-51. PubMed ID: 17701047
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Deterioration in Distortion Product Otoacoustic Emissions in Auditory Neuropathy Patients With Distinct Clinical and Genetic Backgrounds.
    Kitao K; Mutai H; Namba K; Morimoto N; Nakano A; Arimoto Y; Sugiuchi T; Masuda S; Okamoto Y; Morita N; Sakamoto H; Shintani T; Fukuda S; Kaga K; Matsunaga T
    Ear Hear; 2019; 40(1):184-191. PubMed ID: 29688962
    [TBL] [Abstract][Full Text] [Related]  

  • 12. The OTOGL p.Arg925* Variant is Associated with Moderate Hearing Loss in a Syrian Nonconsanguineous Family.
    Barake R; Abou-Rizk S; Nemer G; Bassim M
    Genet Test Mol Biomarkers; 2017 Jul; 21(7):445-449. PubMed ID: 28426234
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Auditory neuropathy in patients carrying mutations in the otoferlin gene (OTOF).
    Rodríguez-Ballesteros M; del Castillo FJ; Martín Y; Moreno-Pelayo MA; Morera C; Prieto F; Marco J; Morant A; Gallo-Terán J; Morales-Angulo C; Navas C; Trinidad G; Tapia MC; Moreno F; del Castillo I
    Hum Mutat; 2003 Dec; 22(6):451-6. PubMed ID: 14635104
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Molecular study of patients with auditory neuropathy.
    Carvalho GM; Ramos PZ; Castilho AM; Guimarães AC; Sartorato EL
    Mol Med Rep; 2016 Jul; 14(1):481-90. PubMed ID: 27177047
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Differential effects of salicylate, quinine, and furosemide on Guinea pig inner and outer hair cell function revealed by the input-output relation of the auditory brainstem response.
    Pienkowski M; Ulfendahl M
    J Am Acad Audiol; 2011 Feb; 22(2):104-12. PubMed ID: 21463565
    [TBL] [Abstract][Full Text] [Related]  

  • 16. A new Otogelin ENU mouse model for autosomal-recessive nonsyndromic moderate hearing impairment.
    El Hakam Kamareddin C; Magnol L; Blanquet V
    Springerplus; 2015; 4():730. PubMed ID: 26636018
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Identification of neonatal hearing impairment: evaluation of transient evoked otoacoustic emission, distortion product otoacoustic emission, and auditory brain stem response test performance.
    Norton SJ; Gorga MP; Widen JE; Folsom RC; Sininger Y; Cone-Wesson B; Vohr BR; Mascher K; Fletcher K
    Ear Hear; 2000 Oct; 21(5):508-28. PubMed ID: 11059707
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [Effect of inner ear hearing loss on delayed otoacoustic emissions (TEOAE) and distortion products (DPOAE)].
    Hoth S
    Laryngorhinootologie; 1996 Dec; 75(12):709-18. PubMed ID: 9081275
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Audiological evaluation of affected members from a Dutch DFNA8/12 (TECTA) family.
    Plantinga RF; Cremers CW; Huygen PL; Kunst HP; Bosman AJ
    J Assoc Res Otolaryngol; 2007 Mar; 8(1):1-7. PubMed ID: 17136632
    [TBL] [Abstract][Full Text] [Related]  

  • 20. GJB2-associated hearing loss undetected by hearing screening of newborns.
    Minami SB; Mutai H; Nakano A; Arimoto Y; Taiji H; Morimoto N; Sakata H; Adachi N; Masuda S; Sakamoto H; Yoshida H; Tanaka F; Morita N; Sugiuchi T; Kaga K; Matsunaga T
    Gene; 2013 Dec; 532(1):41-5. PubMed ID: 24013081
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.