202 related articles for article (PubMed ID: 36292680)
1. Mitochondrial tRNAGln 4394C>T Mutation May Contribute to the Clinical Expression of 1555A>G-Induced Deafness.
Ding Y; Teng Y; Guo Q; Leng J
Genes (Basel); 2022 Oct; 13(10):. PubMed ID: 36292680
[TBL] [Abstract][Full Text] [Related]
2. Mitochondrial haplotypes may modulate the phenotypic manifestation of the deafness-associated 12S rRNA 1555A>G mutation.
Lu J; Qian Y; Li Z; Yang A; Zhu Y; Li R; Yang L; Tang X; Chen B; Ding Y; Li Y; You J; Zheng J; Tao Z; Zhao F; Wang J; Sun D; Zhao J; Meng Y; Guan MX
Mitochondrion; 2010 Jan; 10(1):69-81. PubMed ID: 19818876
[TBL] [Abstract][Full Text] [Related]
3. Contribution of the tRNA
Meng F; He Z; Tang X; Zheng J; Jin X; Zhu Y; Ren X; Zhou M; Wang M; Gong S; Mo JQ; Shu Q; Guan MX
J Biol Chem; 2018 Mar; 293(9):3321-3334. PubMed ID: 29348176
[TBL] [Abstract][Full Text] [Related]
4. A six-generation Chinese family in haplogroup B4C1C exhibits high penetrance of 1555A > G-induced hearing Loss.
Bai Y; Wang Z; Dai W; Li Q; Chen G; Cong N; Guan M; Li H
BMC Med Genet; 2010 Sep; 11():129. PubMed ID: 20822538
[TBL] [Abstract][Full Text] [Related]
5. Allele-specific PCR for detecting the deafness-associated mitochondrial 12S rRNA mutations.
Ding Y; Xia BH; Liu Q; Li MY; Huang SX; Zhuo GC
Gene; 2016 Oct; 591(1):148-152. PubMed ID: 27397648
[TBL] [Abstract][Full Text] [Related]
6. Unique penetrance of hearing loss in a five-generation Chinese family with the mitochondrial 12S rRNA 1555A > G mutation.
Men M; Jiang L; Wang H; Liu Y; Hu Z; He C; Feng Y
Acta Otolaryngol; 2011 Sep; 131(9):970-5. PubMed ID: 21504270
[TBL] [Abstract][Full Text] [Related]
7. Genetic correction of TRMU allele restored the mitochondrial dysfunction-induced deficiencies in iPSCs-derived hair cells of hearing-impaired patients.
Chen C; Guan MX
Hum Mol Genet; 2022 Sep; 31(18):3068-3082. PubMed ID: 35467742
[TBL] [Abstract][Full Text] [Related]
8. 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]
9. Audio profiles in mitochondrial deafness m.1555A>G and m.3243A>G show distinct differences.
Iwanicka-Pronicka K; Pollak A; Skórka A; Lechowicz U; Korniszewski L; Westfal P; Skarżyński H; Płoski R
Med Sci Monit; 2015 Mar; 21():694-700. PubMed ID: 25744662
[TBL] [Abstract][Full Text] [Related]
10. Normal hearing in a child with the m.1555A>G mutation despite repeated exposure to aminoglycosides. Has the penetrance of this pharmacogenetic interaction been overestimated?
Al-Malky G; Suri R; Sirimanna T; Dawson SJ
Int J Pediatr Otorhinolaryngol; 2014 Jun; 78(6):969-73. PubMed ID: 24703164
[TBL] [Abstract][Full Text] [Related]
11. The Mitochondrial tRNAHis G12192A Mutation May Modulate the Clinical Expression of Deafness-Associated tRNAThr G15927A Mutation in a Chinese Pedigree.
Ding Y; Teng YS; Zhuo GC; Xia BH; Leng JH
Curr Mol Med; 2019; 19(2):136-146. PubMed ID: 30854964
[TBL] [Abstract][Full Text] [Related]
12. Mitochondrial m.1584A 12S m62A rRNA methylation in families with m.1555A>G associated hearing loss.
O'Sullivan M; Rutland P; Lucas D; Ashton E; Hendricks S; Rahman S; Bitner-Glindzicz M
Hum Mol Genet; 2015 Feb; 24(4):1036-44. PubMed ID: 25305075
[TBL] [Abstract][Full Text] [Related]
13. Mitochondrial ND5 T12338C, tRNA(Cys) T5802C, and tRNA(Thr) G15927A variants may have a modifying role in the phenotypic manifestation of deafness-associated 12S rRNA A1555G mutation in three Han Chinese pedigrees.
Chen B; Sun D; Yang L; Zhang C; Yang A; Zhu Y; Zhao J; Chen Y; Guan M; Wang X; Li R; Tang X; Wang J; Tao Z; Lu J; Guan MX
Am J Med Genet A; 2008 May; 146A(10):1248-58. PubMed ID: 18386806
[TBL] [Abstract][Full Text] [Related]
14. Mitochondrial 12S rRNA variants in 1642 Han Chinese pediatric subjects with aminoglycoside-induced and nonsyndromic hearing loss.
Lu J; Li Z; Zhu Y; Yang A; Li R; Zheng J; Cai Q; Peng G; Zheng W; Tang X; Chen B; Chen J; Liao Z; Yang L; Li Y; You J; Ding Y; Yu H; Wang J; Sun D; Zhao J; Xue L; Wang J; Guan MX
Mitochondrion; 2010 Jun; 10(4):380-90. PubMed ID: 20100600
[TBL] [Abstract][Full Text] [Related]
15. [Modification factors associated with maternally inherited non-syndromic hearing loss].
Hong WJ; Zheng BJ; Qian JF; Wu H; Jin H; Zhu YT
Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi; 2017 Jun; 52(6):472-477. PubMed ID: 28635225
[TBL] [Abstract][Full Text] [Related]
16. Frequency of mitochondrial m.1555A > G mutation in Syrian patients with non-syndromic hearing impairment.
Kaheel H; Breß A; Hassan MA; Shah AA; Amin M; Bakhit YHY; Kniper M
BMC Ear Nose Throat Disord; 2018; 18():7. PubMed ID: 29942192
[TBL] [Abstract][Full Text] [Related]
17. [Mitochondrial DNA mutations in matrilineal nonsyndromic deafness pedigrees of southwest China].
Zhang N; Qiao X; Wang L; Liang C
Hua Xi Yi Ke Da Xue Xue Bao; 2001 Dec; 32(4):596-8, 626. PubMed ID: 12528560
[TBL] [Abstract][Full Text] [Related]
18. Mitochondrial mutation m.1555A>G as a risk factor for failed newborn hearing screening in a large cohort of preterm infants.
Göpel W; Berkowski S; Preuss M; Ziegler A; Küster H; Felderhoff-Müser U; Gortner L; Mögel M; Härtel C; Herting E;
BMC Pediatr; 2014 Aug; 14():210. PubMed ID: 25155176
[TBL] [Abstract][Full Text] [Related]
19. Novel nucleotide changes in mutational analysis of mitochondrial 12SrRNA gene in patients with nonsyndromic and aminoglycoside-induced hearing loss.
Dowlati MA; Derakhshandeh-Peykar P; Houshmand M; Farhadi M; Shojaei A; Fallah M; Mohammadi E; Tajdini A; Arastoo S; Tavakkoly-Bazzaz J
Mol Biol Rep; 2013 Mar; 40(3):2689-95. PubMed ID: 23242658
[TBL] [Abstract][Full Text] [Related]
20. Complete mitochondrial genome analysis and clinical documentation of a five-generational Indian family with mitochondrial 1555A>G mutation and postlingual hearing loss.
Subathra M; Selvakumari M; Ramesh A; Ramakrishnan R; Karan KR; Kaur M; Manikandan M; Srikumari Srisailapathy CR
Ann Hum Genet; 2014 May; 78(3):217-34. PubMed ID: 24660976
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]