Jia F, Wang F, Li S, Cui Y, Yu Y
BMC Med Genomics. 2025; 18(1):11.
PMID: 39810209
PMC: 11734420.
DOI: 10.1186/s12920-024-02067-3.
Sun X, Bulekova K, Yang J, Lai M, Pitsillides A, Liu X
Mitochondrion. 2024; 79:101954.
PMID: 39245194
PMC: 11568909.
DOI: 10.1016/j.mito.2024.101954.
Sun X, Bulekova K, Yang J, Lai M, Pitsillides A, Liu X
medRxiv. 2024; .
PMID: 38260412
PMC: 10802757.
DOI: 10.1101/2024.01.12.24301233.
Zhang T, Su R, Xiang W, Wang W
Ir J Med Sci. 2023; 193(2):937-943.
PMID: 37561388
DOI: 10.1007/s11845-023-03484-6.
Vila-Sanjurjo A, Mallo N, Elson J, Smith P, Blakely E, Taylor R
Front Physiol. 2023; 14():1163496.
PMID: 37362424
PMC: 10285412.
DOI: 10.3389/fphys.2023.1163496.
Assessment of Amikacin- and Capreomycin-Related Adverse Drug Reactions in Patients with Multidrug-Resistant Tuberculosis and Exploring the Role of Genetic Factors.
Freimane L, Barkane L, Kivrane A, Sadovska D, Ulanova V, Ranka R
J Pers Med. 2023; 13(4).
PMID: 37108985
PMC: 10145258.
DOI: 10.3390/jpm13040599.
Heterologous Inferential Analysis (HIA) and Other Emerging Concepts: In Understanding Mitochondrial Variation In Pathogenesis: There is no More Low-Hanging Fruit.
Vila-Sanjurjo A, Smith P, Elson J
Methods Mol Biol. 2021; 2277:203-245.
PMID: 34080154
DOI: 10.1007/978-1-0716-1270-5_14.
Human Mitoribosome Biogenesis and Its Emerging Links to Disease.
Lopez Sanchez M, Kruger A, Shiriaev D, Liu Y, Rorbach J
Int J Mol Sci. 2021; 22(8).
PMID: 33917098
PMC: 8067846.
DOI: 10.3390/ijms22083827.
[Current status of newborn deafness gene screeningin parts of China].
Wen C, Huang L, Xie S, Zhao X, Yu Y, Cheng X
Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2020; 34(11):972-977.
PMID: 33254312
PMC: 10133122.
DOI: 10.13201/j.issn.2096-7993.2020.11.003.
Whole-Genome Resequencing of Twenty Individuals Provides a Brand-New Variant Dataset for .
Bi C, Lu N, Han T, Huang Z, Chen J, He C
Biomed Res Int. 2020; 2020:3697342.
PMID: 32090082
PMC: 7008246.
DOI: 10.1155/2020/3697342.
The prevalence of mitochondrial mutations associated with aminoglycoside-induced deafness in ethnic Latvian population: the appraisal of the evidence.
Igumnova V, Veidemane L, Viksna A, capligina V, Zole E, Ranka R
J Hum Genet. 2018; 64(3):199-206.
PMID: 30523288
DOI: 10.1038/s10038-018-0544-6.
Analysis of mitochondrial A1555G mutation in infants with hearing impairment.
Wu L, Li R, Chen J, Chen Y, Yang M, Wu Q
Exp Ther Med. 2018; 15(6):5307-5313.
PMID: 29805548
PMC: 5958681.
DOI: 10.3892/etm.2018.6078.
Contribution of the tRNA 4317A→G mutation to the phenotypic manifestation of the deafness-associated mitochondrial 12S rRNA 1555A→G mutation.
Meng F, He Z, Tang X, Zheng J, Jin X, Zhu Y
J Biol Chem. 2018; 293(9):3321-3334.
PMID: 29348176
PMC: 5836119.
DOI: 10.1074/jbc.RA117.000530.
Simultaneous multi‑gene mutation screening using SNPscan in patients from ethnic minorities with nonsyndromic hearing‑impairment in Northwest China.
Duan S, Ma J, Yang X, Guo Y
Mol Med Rep. 2017; 16(5):6722-6728.
PMID: 28901477
PMC: 5865789.
DOI: 10.3892/mmr.2017.7431.
PharmGKB summary: very important pharmacogene information for MT-RNR1.
Barbarino J, McGregor T, Altman R, Klein T
Pharmacogenet Genomics. 2016; 26(12):558-567.
PMID: 27654872
PMC: 5083147.
DOI: 10.1097/FPC.0000000000000247.
Mutation Analysis of the Common Deafness Genes in Patients with Nonsyndromic Hearing Loss in Linyi by SNPscan Assay.
Zhang F, Xiao Y, Xu L, Zhang X, Zhang G, Li J
Biomed Res Int. 2016; 2016:1302914.
PMID: 27247933
PMC: 4876198.
DOI: 10.1155/2016/1302914.
Prevalence of mitochondrial DNA mutations in sporadic patients with nonsyndromic sensorineural hearing loss.
Jiang H, Chen J, Li Y, Lin P, He J, Yang B
Braz J Otorhinolaryngol. 2016; 82(4):391-6.
PMID: 26873147
PMC: 9449052.
DOI: 10.1016/j.bjorl.2015.06.006.
Mutation Spectrum of Common Deafness-Causing Genes in Patients with Non-Syndromic Deafness in the Xiamen Area, China.
Jiang Y, Huang S, Deng T, Wu L, Chen J, Kang D
PLoS One. 2015; 10(8):e0135088.
PMID: 26252218
PMC: 4529078.
DOI: 10.1371/journal.pone.0135088.
A meta-analysis and systematic review of the prevalence of mitochondrially encoded 12S RNA in the general population: Is there a role for screening neonates requiring aminoglycosides?.
Ibekwe T, Bhimrao S, Westerberg B, Kozak F
Afr J Paediatr Surg. 2015; 12(2):105-13.
PMID: 26168747
PMC: 4955414.
DOI: 10.4103/0189-6725.160342.
GJB2 Mutation Spectrum and Genotype-Phenotype Correlation in 1067 Han Chinese Subjects with Non-Syndromic Hearing Loss.
Zheng J, Ying Z, Cai Z, Sun D, He Z, Gao Y
PLoS One. 2015; 10(6):e0128691.
PMID: 26043044
PMC: 4456361.
DOI: 10.1371/journal.pone.0128691.