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.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

196 related items for PubMed ID: 23575541

  • 21. GJB2 and mitochondrial A1555G gene mutations in nonsyndromic profound hearing loss and carrier frequencies in healthy individuals.
    Baysal E, Bayazit YA, Ceylaner S, Alatas N, Donmez B, Ceylaner G, San I, Korkmaz B, Yilmaz A, Menevse A, Altunyay S, Gunduz B, Goksu N, Arslan A, Ekmekci A.
    J Genet; 2008 Apr; 87(1):53-7. PubMed ID: 18560174
    [Abstract] [Full Text] [Related]

  • 22.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 23.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 24. Maternally inherited aminoglycoside-induced and nonsyndromic hearing loss is associated with the 12S rRNA C1494T mutation in three Han Chinese pedigrees.
    Chen J, Yang L, Yang A, Zhu Y, Zhao J, Sun D, Tao Z, Tang X, Wang J, Wang X, Tsushima A, Lan J, Li W, Wu F, Yuan Q, Ji J, Feng J, Wu C, Liao Z, Li Z, Greinwald JH, Lu J, Guan MX.
    Gene; 2007 Oct 15; 401(1-2):4-11. PubMed ID: 17698299
    [Abstract] [Full Text] [Related]

  • 25. Familial progressive sensorineural deafness is mainly due to the mtDNA A1555G mutation and is enhanced by treatment of aminoglycosides.
    Estivill X, Govea N, Barceló E, Badenas C, Romero E, Moral L, Scozzri R, D'Urbano L, Zeviani M, Torroni A.
    Am J Hum Genet; 1998 Jan 15; 62(1):27-35. PubMed ID: 9490575
    [Abstract] [Full Text] [Related]

  • 26.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 27. Prevalence of mutations in GJB2, SLC26A4, and mtDNA in children with severe or profound sensorineural hearing loss in southwestern China.
    Qing J, Zhou Y, Lai R, Hu P, Ding Y, Wu W, Xiao Z, Ho PT, Liu Y, Liu J, Du L, Yan D, Goldstein BJ, Liu X, Xie D.
    Genet Test Mol Biomarkers; 2015 Jan 15; 19(1):52-8. PubMed ID: 25493717
    [Abstract] [Full Text] [Related]

  • 28. Discrimination of A1555G and C1494T point mutations in the mitochondrial 12S rRNA gene by on/off switch.
    Guo ZF, Guo WS, Xiao L, Gao GQ, Lan F, Lu XG, Li K, Liao DF.
    Appl Biochem Biotechnol; 2012 Jan 15; 166(1):234-42. PubMed ID: 22068689
    [Abstract] [Full Text] [Related]

  • 29.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 30.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 31.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 32. Additional clinical manifestations in children with sensorineural hearing loss and biallelic GJB2 mutations: who should be offered GJB2 testing?
    Kenna MA, Rehm HL, Robson CD, Frangulov A, McCallum J, Yaeger D, Krantz ID.
    Am J Med Genet A; 2007 Jul 15; 143A(14):1560-6. PubMed ID: 17455295
    [Abstract] [Full Text] [Related]

  • 33.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 34. [Mutations analysis in a pedigree with maternally inherited sensorineural hearing loss].
    Xu C, Zhang H, Zhang Y, Zhao S, Geng X, Shan Y, Shan X.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2005 Apr 15; 22(2):125-8. PubMed ID: 15793769
    [Abstract] [Full Text] [Related]

  • 35. Prevalence of Mutations in Deafness-Causing Genes in Cochlear Implanted Patients with Profound Nonsyndromic Sensorineural Hearing Loss in Shandong Province, China.
    Luo J, Bai X, Zhang F, Xiao Y, Gu L, Han Y, Fan Z, Li J, Xu L, Wang H.
    Ann Hum Genet; 2017 Nov 15; 81(6):258-266. PubMed ID: 28786104
    [Abstract] [Full Text] [Related]

  • 36.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 37. GJB2 and GJB6 screening in Tunisian patients with autosomal recessive deafness.
    Trabelsi M, Bahri W, Habibi M, Zainine R, Maazoul F, Ghazi B, Chaabouni H, Mrad R.
    Int J Pediatr Otorhinolaryngol; 2013 May 15; 77(5):714-6. PubMed ID: 23434199
    [Abstract] [Full Text] [Related]

  • 38.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 39. GJB2 (Cx26) gene mutations in Chinese patients with congenital sensorineural deafness and a report of one novel mutation.
    Xiao ZA, Xie DH.
    Chin Med J (Engl); 2004 Dec 15; 117(12):1797-801. PubMed ID: 15603707
    [Abstract] [Full Text] [Related]

  • 40. [Non-invasive screening for GJB2 mutations in buccal smears for the diagnosis of inherited hearing impairment].
    Schade G, Kothe C, Ruge G, Hess M, Meyer CG.
    Laryngorhinootologie; 2003 Jun 15; 82(6):397-401. PubMed ID: 12851846
    [Abstract] [Full Text] [Related]

    Page: [Previous] [Next] [New Search]
    of 10.