119 related articles for article (PubMed ID: 9887373)
1. Phylogenetic analysis of mitochondrial DNA in Japanese pedigrees of sensorineural hearing loss associated with the A1555G mutation.
Abe S; Usami S; Shinkawa H; Weston MD; Overbeck LD; Hoover DM; Kenyon JB; Horai S; Kimberling WJ
Eur J Hum Genet; 1998; 6(6):563-9. PubMed ID: 9887373
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. Two large French pedigrees with non syndromic sensorineural deafness and the mitochondrial DNA T7511C mutation: evidence for a modulatory factor.
Chapiro E; Feldmann D; Denoyelle F; Sternberg D; Jardel C; Eliot MM; Bouccara D; Weil D; Garabédian EN; Couderc R; Petit C; Marlin S
Eur J Hum Genet; 2002 Dec; 10(12):851-6. PubMed ID: 12461693
[TBL] [Abstract][Full Text] [Related]
4. [Mitochondrial DNA A1555G mutation of seven families with nonsyndromic hearing loss].
Ou QS; Cheng ZJ; Yang B; Jiang L; Chen J
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2009 Oct; 26(5):550-4. PubMed ID: 19806580
[TBL] [Abstract][Full Text] [Related]
5. Prevalence of the mitochondrial A 1555G mutation in Moroccan patients with non-syndromic hearing loss.
Nahili H; Charif M; Boulouiz R; Bounaceur S; Benrahma H; Abidi O; Chafik A; Rouba H; Kandil M; Barakat A
Int J Pediatr Otorhinolaryngol; 2010 Sep; 74(9):1071-4. PubMed ID: 20637512
[TBL] [Abstract][Full Text] [Related]
6. Whole mitochondrial genome screening in maternally inherited non-syndromic hearing impairment using a microarray resequencing mitochondrial DNA chip.
Lévêque M; Marlin S; Jonard L; Procaccio V; Reynier P; Amati-Bonneau P; Baulande S; Pierron D; Lacombe D; Duriez F; Francannet C; Mom T; Journel H; Catros H; Drouin-Garraud V; Obstoy MF; Dollfus H; Eliot MM; Faivre L; Duvillard C; Couderc R; Garabedian EN; Petit C; Feldmann D; Denoyelle F
Eur J Hum Genet; 2007 Nov; 15(11):1145-55. PubMed ID: 17637808
[TBL] [Abstract][Full Text] [Related]
7. Hearing loss due to the mitochondrial A1555G mutation in Italian families.
Casano RA; Bykhovskaya Y; Johnson DF; Hamon M; Torricelli F; Bigozzi M; Fischel-Ghodsian N
Am J Med Genet; 1998 Oct; 79(5):388-91. PubMed ID: 9779807
[TBL] [Abstract][Full Text] [Related]
8. Mitochondrial non-syndromic sensorineural hearing loss: a clinical, audiological and pathological study from Italy, and revision of the literature.
Berrettini S; Forli F; Passetti S; Rocchi A; Pollina L; Cecchetti D; Mancuso M; Siciliano G
Biosci Rep; 2008 Feb; 28(1):49-59. PubMed ID: 18215147
[TBL] [Abstract][Full Text] [Related]
9. [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]
10. [Audiological findings and mitochondrial DNA mutation in a large family with matrilineal sensorineural hearing loss].
Xing G; Bu X; Yan M; Lu L; Yang S
Zhonghua Er Bi Yan Hou Ke Za Zhi; 2000 Apr; 35(2):98-101. PubMed ID: 12768662
[TBL] [Abstract][Full Text] [Related]
11. New polymorphic mtDNA restriction site in the 12S rRNA gene detected in Tunisian patients with non-syndromic hearing loss.
Mkaouar-Rebai E; Tlili A; Masmoudi S; Charfeddine I; Fakhfakh F
Biochem Biophys Res Commun; 2008 May; 369(3):849-52. PubMed ID: 18325329
[TBL] [Abstract][Full Text] [Related]
12. Nonsyndromic sensorineural deafness associated with the A1555G mutation in the mitochondrial small subunit ribosomal RNA in a Balinese family.
Malik S; Sudoyo H; Sasmono T; Winata S; Arhya IN; Pramoonjago P; Sudana W; Marzuki S
J Hum Genet; 2003; 48(3):119-24. PubMed ID: 12624722
[TBL] [Abstract][Full Text] [Related]
13. Clinical evaluation and mitochondrial DNA sequence analysis in two Chinese families with aminoglycoside-induced and non-syndromic hearing loss.
Zhao L; Wang Q; Qian Y; Li R; Cao J; Hart LC; Zhai S; Han D; Young WY; Guan MX
Biochem Biophys Res Commun; 2005 Oct; 336(3):967-73. PubMed ID: 16168391
[TBL] [Abstract][Full Text] [Related]
14. Cochlear implantation in a patient with profound hearing loss with the A1555G mitochondrial DNA mutation and no history of aminoglycoside exposure.
Ulubil SA; Furze AD; Angeli SI
J Laryngol Otol; 2006 Mar; 120(3):230-2. PubMed ID: 16359140
[TBL] [Abstract][Full Text] [Related]
15. 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; Guan MX
Biochem Biophys Res Commun; 2005 Mar; 328(4):1244-51. PubMed ID: 15708009
[TBL] [Abstract][Full Text] [Related]
16. Deafness due to A1555G mitochondrial mutation without use of aminoglycoside.
Matsunaga T; Kumanomido H; Shiroma M; Ohtsuka A; Asamura K; Usami S
Laryngoscope; 2004 Jun; 114(6):1085-91. PubMed ID: 15179218
[TBL] [Abstract][Full Text] [Related]
17. Extremely low penetrance of deafness associated with the mitochondrial 12S rRNA T1095C mutation in three Chinese families.
Dai P; Yuan Y; Huang D; Qian Y; Liu X; Han D; Yuan H; Wang X; Young WY; Guan MX
Biochem Biophys Res Commun; 2006 Sep; 348(1):200-5. PubMed ID: 16875663
[TBL] [Abstract][Full Text] [Related]
18. [Screening for mitochondrial DNA mutation in two pedigrees with nonsyndromic inherited sensorineural hearing loss].
Li W; Han D; Yuan H; Wang Y; Cao J; Yang W; Jiang S
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2002 Feb; 19(1):64-7. PubMed ID: 11836692
[TBL] [Abstract][Full Text] [Related]
19. Distribution and frequencies of CDH23 mutations in Japanese patients with non-syndromic hearing loss.
Wagatsuma M; Kitoh R; Suzuki H; Fukuoka H; Takumi Y; Usami S
Clin Genet; 2007 Oct; 72(4):339-44. PubMed ID: 17850630
[TBL] [Abstract][Full Text] [Related]
20. Extremely low penetrance of deafness associated with the mitochondrial 12S rRNA mutation in 16 Chinese families: implication for early detection and prevention of deafness.
Dai P; Liu X; Han D; Qian Y; Huang D; Yuan H; Li W; Yu F; Zhang R; Lin H; He Y; Yu Y; Sun Q; Qin H; Li R; Zhang X; Kang D; Cao J; Young WY; Guan MX
Biochem Biophys Res Commun; 2006 Feb; 340(1):194-9. PubMed ID: 16375862
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]