Handzic N, Pecar D, Durgut S, Salihefendic L, Konjhodzic R
Acta Inform Med. 2025; 32(3-4):221-224.
PMID: 40061003
PMC: 11889429.
DOI: 10.5455/aim.2024.32.221-224.
Bond S, King E, Walker S, Yang C, Liu Y, Liu K
Nat Commun. 2025; 16(1):2338.
PMID: 40057508
PMC: 11890779.
DOI: 10.1038/s41467-025-57299-3.
Haarkotter C, Roca-Rada X, Saiz M, Vinueza-Espinosa D, Galvez X, Medina-Lozano M
Genes (Basel). 2025; 16(1).
PMID: 39858570
PMC: 11764906.
DOI: 10.3390/genes16010023.
Huang A, Xue H, Xie T, Xiang L, Chen Z, Ma A
J Transl Med. 2025; 23(1):70.
PMID: 39815317
PMC: 11734335.
DOI: 10.1186/s12967-025-06077-2.
Cabrera-Alarcon J, Cruz R, Rosa-Moreno M, Latorre-Pellicer A, de Almeida S, Riancho J
Commun Biol. 2025; 8(1):33.
PMID: 39789223
PMC: 11718132.
DOI: 10.1038/s42003-024-07314-y.
The Association of Mitochondrial tRNA G5783A Mutation with Major Depressive Disorder in Two Han Chinese Families.
Jing P, Yu H, Sun W, Liang M, Xia T, Yang H
Neuropsychiatr Dis Treat. 2025; 21():15-24.
PMID: 39776895
PMC: 11705967.
DOI: 10.2147/NDT.S465744.
Ethnogenetic analysis reveals the Bronze Age genetic affiliation of Yashkuns with West Eurasians.
Khan M, Zahid T, Sabar M, Masood T, Ali Q, Han S
Sci Rep. 2024; 14(1):31414.
PMID: 39733090
PMC: 11682329.
DOI: 10.1038/s41598-024-83136-6.
Deafness-associated mitochondrial 12S rRNA mutation reshapes mitochondrial and cellular homeostasis.
He Y, Tang Z, Zhu G, Cai L, Chen C, Guan M
J Biol Chem. 2024; 301(2):108124.
PMID: 39716492
PMC: 11791119.
DOI: 10.1016/j.jbc.2024.108124.
Family relations of Moche elite burials on the North Coast of Peru (~500 CE): Analyses of the Señora de Cao and relatives.
Quilter J, Harkins K, Fanco Jordan R, Marsh E, Prieto G, Verano J
Proc Natl Acad Sci U S A. 2024; 122(1):e2416321121.
PMID: 39715432
PMC: 11725780.
DOI: 10.1073/pnas.2416321121.
Ancient genomes reveal a deep history of Treponema pallidum in the Americas.
Barquera R, Sitter T, Kirkpatrick C, Ramirez D, Kocher A, Spyrou M
Nature. 2024; .
PMID: 39694065
DOI: 10.1038/s41586-024-08515-5.
An easy-to-use pipeline to analyze amplicon-based Next Generation Sequencing results of human mitochondrial DNA from degraded samples.
Cuesta-Aguirre D, Malgosa A, Santos C
PLoS One. 2024; 19(11):e0311115.
PMID: 39570888
PMC: 11581256.
DOI: 10.1371/journal.pone.0311115.
Major depressive disorder is associated with mitochondrial T14502C mutation in two Han Chinese families.
Jing P, Yu H, Wu T, Yu B, Liang M, Xia T
World J Psychiatry. 2024; 14(11):1746-1754.
PMID: 39564165
PMC: 11572673.
DOI: 10.5498/wjp.v14.i11.1746.
Mutation of CRYAB encoding a conserved mitochondrial chaperone and antiapoptotic protein causes hereditary optic atrophy.
Wang C, Zhang L, Nie Z, Liang M, Liu H, Yi Q
JCI Insight. 2024; 10(1.
PMID: 39561005
PMC: 11721302.
DOI: 10.1172/jci.insight.182209.
The quality and detection limits of mitochondrial heteroplasmy by long read nanopore sequencing.
Slapnik B, Sket R, crepinsek K, Tesovnik T, Jenko Bizjan B, Kovac J
Sci Rep. 2024; 14(1):26778.
PMID: 39501054
PMC: 11538439.
DOI: 10.1038/s41598-024-78270-0.
African-Colombian woman with preeclampsia and high-risk APOL1 genotype: A case report.
Duran C, Gutierrez-Medina J, Trivino Arias J, Sandoval-Calle L, Barbosa M, Useche E
Medicine (Baltimore). 2024; 103(44):e40284.
PMID: 39496047
PMC: 11537606.
DOI: 10.1097/MD.0000000000040284.
Massively parallel sequencing of mitochondrial genome in primary open angle glaucoma identifies somatically acquired mitochondrial mutations in ocular tissue.
Vallabh N, Lane B, Simpson D, Fuchs M, Choudhary A, Criddle D
Sci Rep. 2024; 14(1):26324.
PMID: 39487142
PMC: 11530638.
DOI: 10.1038/s41598-024-72684-6.
Changes in Gene, Telomere Length, and Mitochondrial DNA in Benign Prostatic Hyperplasia Patients.
Zole E, Baumanis E, Freimane L, Dale R, Leise A, Lietuvietis V
Biomedicines. 2024; 12(10).
PMID: 39457663
PMC: 11505421.
DOI: 10.3390/biomedicines12102349.
SAFARI: Pangenome Alignment of Ancient DNA Using Purine/Pyrimidine Encodings.
Rubin J, van Waaij J, Kraft L, Siren J, Sackett P, Renaud G
bioRxiv. 2024; .
PMID: 39415996
PMC: 11482861.
DOI: 10.1101/2024.08.12.607489.
Identification of sequence polymorphism in the D-loop region of mitochondrial DNA as a risk factor for breast cancer.
Nie Q, Zhang W, Lin S, Huang M, Li Y, Qiu Y
Cancer Sci. 2024; 115(12):4064-4073.
PMID: 39401980
PMC: 11611757.
DOI: 10.1111/cas.16353.
Low Genetic Impact of the Roman Occupation of Britain in Rural Communities.
Scheib C, Hui R, Rose A, DAtanasio E, Inskip S, Dittmar J
Mol Biol Evol. 2024; 41(9).
PMID: 39268685
PMC: 11393495.
DOI: 10.1093/molbev/msae168.
