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Results: 1 to 20 of 140

1.

Large-scale screening of mitochondrial DNA mutations among Iranian patients with prelingual nonsyndromic hearing impairment.

Montazer Zohour M, Tabatabaiefar MA, Dehkordi FA, Farrokhi E, Akbari MT, Chaleshtori MH.

Genet Test Mol Biomarkers. 2012 Apr;16(4):271-8. doi: 10.1089/gtmb.2011.0176. Epub 2011 Nov 11.

PMID:
22077646
[PubMed - indexed for MEDLINE]
2.

[Prevalence of common genetic mutations and clinical characteristics analysis in patients at different ages with nonsyndromic hearing impairment].

Zhang CQ, Chen BB, Chen YY, Liu XJ, Zheng J, Gao JJ, Huang SY, Nan BY, Zhang YY, Yu X, Guan MX.

Yi Chuan. 2013 Mar;35(3):352-8. Chinese.

PMID:
23575541
[PubMed - indexed for MEDLINE]
3.

Absence of GJB2 gene mutations, the GJB6 deletion (GJB6-D13S1830) and four common mitochondrial mutations in nonsyndromic genetic hearing loss in a South African population.

Kabahuma RI, Ouyang X, Du LL, Yan D, Hutchin T, Ramsay M, Penn C, Liu XZ.

Int J Pediatr Otorhinolaryngol. 2011 May;75(5):611-7. doi: 10.1016/j.ijporl.2011.01.029. Epub 2011 Mar 9.

PMID:
21392827
[PubMed - indexed for MEDLINE]
4.

GJB2, SLC26A4 and mitochondrial DNA A1555G mutations in prelingual deafness in Northern Chinese subjects.

Guo YF, Liu XW, Guan J, Han MK, Wang DY, Zhao YL, Rao SQ, Wang QJ.

Acta Otolaryngol. 2008 Mar;128(3):297-303. doi: 10.1080/00016480701767382.

PMID:
18274916
[PubMed - indexed for MEDLINE]
5.

The A1555G mitochondrial DNA mutation in Greek patients with non-syndromic, sensorineural hearing loss.

Kokotas H, Grigoriadou M, Korres GS, Ferekidou E, Papadopoulou E, Neou P, Giannoulia-Karantana A, Kandiloros D, Korres S, Petersen MB.

Biochem Biophys Res Commun. 2009 Dec 18;390(3):755-7. doi: 10.1016/j.bbrc.2009.10.044. Epub 2009 Oct 14.

PMID:
19835846
[PubMed - indexed for MEDLINE]
6.

Low incidence of GJB2, GJB6 and mitochondrial DNA mutations in North Indian patients with non-syndromic hearing impairment.

Bhalla S, Sharma R, Khandelwal G, Panda NK, Khullar M.

Biochem Biophys Res Commun. 2009 Jul 31;385(3):445-8. doi: 10.1016/j.bbrc.2009.05.083. Epub 2009 May 22.

PMID:
19465004
[PubMed - indexed for MEDLINE]
7.

Mitochondrial DNA mutation screening in an ethnically diverse nonsyndromic deafness cohort.

Vivero RJ, Ouyang X, Yan D, Du L, Liu W, Angeli SI, Liu XZ.

Genet Test Mol Biomarkers. 2012 Sep;16(9):1146-8. doi: 10.1089/gtmb.2011.0365. Epub 2012 Aug 1.

PMID:
22853457
[PubMed - indexed for MEDLINE]
Free PMC Article
8.

[Study of mtDNA 12S rRNA A1555G, GJB2, GJB3 gene mutation in Uighur and Han people with hereditary nonsyndromic hearing loss in Xinjiang].

Li YH, Jiang H, Yang LJ, Xu HX, Li H, Li HW, Luo YH, Wang CW, Zou GH.

Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2010 Aug;45(8):645-51. Chinese.

PMID:
21055240
[PubMed - indexed for MEDLINE]
9.

Molecular epidemiological analysis of mitochondrial DNA12SrRNA A1555G, GJB2, and SLC26A4 mutations in sporadic outpatients with nonsyndromic sensorineural hearing loss in China.

Ji YB, Han DY, Lan L, Wang DY, Zong L, Zhao FF, Liu Q, Benedict-Alderfer C, Zheng QY, Wang QJ.

Acta Otolaryngol. 2011 Feb;131(2):124-9. doi: 10.3109/00016489.2010.483479. Epub 2010 Dec 16.

PMID:
21162657
[PubMed - indexed for MEDLINE]
Free PMC Article
10.

Audiological and genetic features of the mtDNA mutations.

Liu XZ, Angeli S, Ouyang XM, Liu W, Ke XM, Liu YH, Liu SX, Du LL, Deng XW, Yuan H, Yan D.

Acta Otolaryngol. 2008 Jul;128(7):732-8. doi: 10.1080/00016480701719011.

PMID:
18568513
[PubMed - indexed for MEDLINE]
11.

[Detecting of mtDNA mutations at position A3243G and G3316A in patients with type 2 diabetes mellitus in Wenzhou].

Zhao J, Ji JZ, Wang DW, Zhang J, Wu HJ, Lu JX.

Yi Chuan. 2006 Oct;28(10):1206-12. Chinese.

PMID:
17035175
[PubMed - indexed for MEDLINE]
12.

Prevalence of GJB2 mutations in prelingual deafness in the Greek population.

Pampanos A, Economides J, Iliadou V, Neou P, Leotsakos P, Voyiatzis N, Eleftheriades N, Tsakanikos M, Antoniadi T, Hatzaki A, Konstantopoulou I, Yannoukakos D, Gronskov K, Brondum-Nielsen K, Grigoriadou M, Gyftodimou J, Iliades T, Skevas A, Petersen MB.

Int J Pediatr Otorhinolaryngol. 2002 Sep 2;65(2):101-8.

PMID:
12176179
[PubMed - indexed for MEDLINE]
13.

GJB2 mutation spectrum in 209 hearing impaired individuals of predominantly Caribbean Hispanic and African descent.

Shan J, Chobot-Rodd J, Castellanos R, Babcock M, Shanske A, Parikh SR, Morrow BE, Samanich J.

Int J Pediatr Otorhinolaryngol. 2010 Jun;74(6):611-8. doi: 10.1016/j.ijporl.2010.03.004. Epub 2010 Apr 9.

PMID:
20381175
[PubMed - indexed for MEDLINE]
14.

Extremely low penetrance of hearing loss in four Chinese families with the mitochondrial 12S rRNA A1555G mutation.

Young WY, Zhao L, Qian Y, Wang Q, Li N, Greinwald JH Jr, Guan MX.

Biochem Biophys Res Commun. 2005 Mar 25;328(4):1244-51.

PMID:
15708009
[PubMed - indexed for MEDLINE]
15.

Spectrum of GJB2 (Cx26) gene mutations in Iranian Azeri patients with nonsyndromic autosomal recessive hearing loss.

Davarnia B, Babanejad M, Fattahi Z, Nikzat N, Bazazzadegan N, Pirzade A, Farajollahi R, Nishimura C, Jalalvand K, Arzhangi S, Kahrizi K, Smith RJ, Najmabadi H.

Int J Pediatr Otorhinolaryngol. 2012 Feb;76(2):268-71. doi: 10.1016/j.ijporl.2011.11.019. Epub 2011 Dec 14.

PMID:
22172221
[PubMed - indexed for MEDLINE]
16.

Prevalence of mitochondrial DNA mutations in childhood/congenital onset non-syndromal sensorineural hearing impairment.

Hutchin TP, Thompson KR, Parker M, Newton V, Bitner-Glindzicz M, Mueller RF.

J Med Genet. 2001 Apr;38(4):229-31.

PMID:
11283203
[PubMed - indexed for MEDLINE]
Free PMC Article
17.

Mitochondrial haplotype and phenotype of 13 Chinese families may suggest multi-original evolution of mitochondrial C1494T mutation.

Zhu Y, Li Q, Chen Z, Kun Y, Liu L, Liu X, Yuan H, Zhai S, Han D, Dai P.

Mitochondrion. 2009 Nov;9(6):418-28. doi: 10.1016/j.mito.2009.07.006. Epub 2009 Aug 12.

PMID:
19682603
[PubMed - indexed for MEDLINE]
18.

Mutations in GJB2, GJB6, and mitochondrial DNA are rare in African American and Caribbean Hispanic individuals with hearing impairment.

Samanich J, Lowes C, Burk R, Shanske S, Lu J, Shanske A, Morrow BE.

Am J Med Genet A. 2007 Apr 15;143A(8):830-8.

PMID:
17357124
[PubMed - indexed for MEDLINE]
19.

[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;22(2):125-8. Chinese.

PMID:
15793769
[PubMed - indexed for MEDLINE]
20.

[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;82(6):397-401. German.

PMID:
12851846
[PubMed - indexed for MEDLINE]

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