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4. Cochlear alterations in deaf and unaffected subjects carrying the deafness-associated A1555G mutation in the mitochondrial 12S rRNA gene. Bravo O; Ballana E; Estivill X Biochem Biophys Res Commun; 2006 Jun; 344(2):511-6. PubMed ID: 16631122 [TBL] [Abstract][Full Text] [Related]
5. Prevalence and clinical features of the mitochondrial m.1555A>G mutation in Taiwanese patients with idiopathic sensorineural hearing loss and association of haplogroup F with low penetrance in three families. Wu CC; Chiu YH; Chen PJ; Hsu CJ Ear Hear; 2007 Jun; 28(3):332-42. PubMed ID: 17485982 [TBL] [Abstract][Full Text] [Related]
6. Phenotypic characterization of hereditary hearing impairment linked to DFNA25. Thirlwall AS; Brown DJ; McMillan PM; Barker SE; Lesperance MM Arch Otolaryngol Head Neck Surg; 2003 Aug; 129(8):830-5. PubMed ID: 12925340 [TBL] [Abstract][Full Text] [Related]
7. Familial auditory neuropathy. Wang Q; Gu R; Han D; Yang W Laryngoscope; 2003 Sep; 113(9):1623-9. PubMed ID: 12972945 [TBL] [Abstract][Full Text] [Related]
8. [Analysis of mitochondrial 12S rRNA and tRNA(Ser(UCN)) genes in patients with nonsyndromic sensorineural hearing loss from various regions of Russia]. Dzhemileva LU; Posukh OL; Tazetdinov AM; Barashkov NA; Zhuravskiĭ SG; Ponidelko SN; Markova TG; Tadinova VN; Fedorova SA; Maksimova NR; Khusnutdinova EK Genetika; 2009 Jul; 45(7):982-91. PubMed ID: 19705751 [TBL] [Abstract][Full Text] [Related]
14. [Progress in genetic testing and prevention of hereditary hearing disorders]. Markova TG; Poliakov AV Vestn Otorinolaringol; 2007; (4):7-10. PubMed ID: 17828104 [TBL] [Abstract][Full Text] [Related]
15. Function and expression pattern of nonsyndromic deafness genes. Hilgert N; Smith RJ; Van Camp G Curr Mol Med; 2009 Jun; 9(5):546-64. PubMed ID: 19601806 [TBL] [Abstract][Full Text] [Related]
16. A novel SLC26A4 (PDS) deafness mutation retained in the endoplasmic reticulum. Brownstein ZN; Dror AA; Gilony D; Migirov L; Hirschberg K; Avraham KB Arch Otolaryngol Head Neck Surg; 2008 Apr; 134(4):403-7. PubMed ID: 18427006 [TBL] [Abstract][Full Text] [Related]
17. Acoustic overstimulation facilitates the expression of glutamate-cysteine ligase catalytic subunit probably through enhanced DNA binding of activator protein-1 and/or NF-kappaB in the murine cochlea. Nagashima R; Sugiyama C; Yoneyama M; Kuramoto N; Kawada K; Ogita K Neurochem Int; 2007; 51(2-4):209-15. PubMed ID: 17559975 [TBL] [Abstract][Full Text] [Related]
18. Nonsyndromic hereditary hearing loss. Li XC; Friedman RA Otolaryngol Clin North Am; 2002 Apr; 35(2):275-85. PubMed ID: 12391618 [TBL] [Abstract][Full Text] [Related]
19. Genes encoding mitochondrial respiratory chain components are profoundly down-regulated with aging in the cochlea of DBA/2J mice. Someya S; Yamasoba T; Prolla TA; Tanokura M Brain Res; 2007 Nov; 1182():26-33. PubMed ID: 17964557 [TBL] [Abstract][Full Text] [Related]
20. Mutations in the COCH gene are a frequent cause of autosomal dominant progressive cochleo-vestibular dysfunction, but not of Meniere's disease. Usami S; Takahashi K; Yuge I; Ohtsuka A; Namba A; Abe S; Fransen E; Patthy L; Otting G; Van Camp G Eur J Hum Genet; 2003 Oct; 11(10):744-8. PubMed ID: 14512963 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]