These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
111 related articles for article (PubMed ID: 38215527)
41. "Mitochondrial pathogenic mutations and metabolic alterations associated with COVID-19 disease severity". Kumari D; Singh Y; Singh S; Dogra V; Srivastava AK; Srivastava S; Garg I; Bargotya M; Hussain J; Ganju L; Varshney R J Med Virol; 2023 Feb; 95(2):e28553. PubMed ID: 36832542 [TBL] [Abstract][Full Text] [Related]
42. The genetic landscape of mitochondrial diseases in the next-generation sequencing era: a Portuguese cohort study. Nogueira C; Pereira C; Silva L; Laranjeira M; Lopes A; Neiva R; Rodrigues E; Campos T; Martins E; Bandeira A; Coelho M; Magalhães M; Damásio J; Gaspar A; Janeiro P; Gomes AL; Ferreira AC; Jacinto S; Vieira JP; Diogo L; Santos H; Mendonça C; Vilarinho L Front Cell Dev Biol; 2024; 12():1331351. PubMed ID: 38465286 [No Abstract] [Full Text] [Related]
43. Strategies for complete mitochondrial genome sequencing on Ion Torrent PGM™ platform in forensic sciences. Zhou Y; Guo F; Yu J; Liu F; Zhao J; Shen H; Zhao B; Jia F; Sun Z; Song H; Jiang X Forensic Sci Int Genet; 2016 May; 22():11-21. PubMed ID: 26809045 [TBL] [Abstract][Full Text] [Related]
44. Genetic Evidence for Elevated Pathogenicity of Mitochondrial DNA Heteroplasmy in Autism Spectrum Disorder. Wang Y; Picard M; Gu Z PLoS Genet; 2016 Oct; 12(10):e1006391. PubMed ID: 27792786 [TBL] [Abstract][Full Text] [Related]
45. Full mtDNA genome sequencing of Brazilian admixed populations: A forensic-focused evaluation of a MPS application as an alternative to Sanger sequencing methods. Avila E; Graebin P; Chemale G; Freitas J; Kahmann A; Alho CS Forensic Sci Int Genet; 2019 Sep; 42():154-164. PubMed ID: 31325893 [TBL] [Abstract][Full Text] [Related]
46. Clinical and bi-genomic DNA findings of patients suspected to have mitochondrial diseases. Gedikbasi A; Toksoy G; Karaca M; Gulec C; Balci MC; Gunes D; Gunes S; Aslanger AD; Unverengil G; Karaman B; Basaran S; Demirkol M; Gokcay GF; Uyguner ZO Front Genet; 2023; 14():1191159. PubMed ID: 37377599 [No Abstract] [Full Text] [Related]
47. Massive parallel sequencing of mitochondrial DNA genomes from mother-child pairs using the ion torrent personal genome machine (PGM). Ma K; Zhao X; Li H; Cao Y; Li W; Ouyang J; Xie L; Liu W Forensic Sci Int Genet; 2018 Jan; 32():88-93. PubMed ID: 29128545 [TBL] [Abstract][Full Text] [Related]
48. A strategy for a high enrichment of insect mitochondrial DNA for mitogenomic analysis. Yu X; Yang H; Liu J; Qi Y; Sun L; Tian X Gene; 2022 Jan; 808():145986. PubMed ID: 34600050 [TBL] [Abstract][Full Text] [Related]
49. Mitochondrial and nuclear disease panel (Mito-aND-Panel): Combined sequencing of mitochondrial and nuclear DNA by a cost-effective and sensitive NGS-based method. Abicht A; Scharf F; Kleinle S; Schön U; Holinski-Feder E; Horvath R; Benet-Pagès A; Diebold I Mol Genet Genomic Med; 2018 Nov; 6(6):1188-1198. PubMed ID: 30406974 [TBL] [Abstract][Full Text] [Related]
50. Comprehensive Mitochondrial Genome Analysis by Massively Parallel Sequencing. Palculict ME; Zhang VW; Wong LJ; Wang J Methods Mol Biol; 2016; 1351():3-17. PubMed ID: 26530670 [TBL] [Abstract][Full Text] [Related]
51. Mitochondrial DNA analysis in primary congenital glaucoma. Tanwar M; Dada T; Sihota R; Dada R Mol Vis; 2010 Mar; 16():518-33. PubMed ID: 20361014 [TBL] [Abstract][Full Text] [Related]
52. Performance evaluation of a mitogenome capture and Illumina sequencing protocol using non-probative, case-type skeletal samples: Implications for the use of a positive control in a next-generation sequencing procedure. Marshall C; Sturk-Andreaggi K; Daniels-Higginbotham J; Oliver RS; Barritt-Ross S; McMahon TP Forensic Sci Int Genet; 2017 Nov; 31():198-206. PubMed ID: 29101892 [TBL] [Abstract][Full Text] [Related]
53. Profiling of mitochondrial heteroplasmy in single human oocytes by next-generation sequencing. Russo V; Ancora M; Gatta V; Orsini M; Prencipe G; Peserico A; Colosimo A; El Khatib M; Mauro A; Di Berardino C; Scialabba S; Tiboni GM; Marcacci M; Cammà C; Barboni B Mol Reprod Dev; 2022 Dec; 89(12):646-654. PubMed ID: 36444830 [TBL] [Abstract][Full Text] [Related]
54. Detection of mitochondrial DNA variants at low level heteroplasmy in pediatric CNS and extra-CNS solid tumors with three different enrichment methods. Kaneva K; Merkurjev D; Ostrow D; Ryutov A; Triska P; Stachelek K; Cobrinik D; Biegel JA; Gai X Mitochondrion; 2020 Mar; 51():97-103. PubMed ID: 31972374 [TBL] [Abstract][Full Text] [Related]
55. Identifying Somatic Mitochondrial DNA Mutations. An J; Min KI; Ju YS Methods Mol Biol; 2022; 2493():153-165. PubMed ID: 35751814 [TBL] [Abstract][Full Text] [Related]
56. MitoRS, a method for high throughput, sensitive, and accurate detection of mitochondrial DNA heteroplasmy. Marquis J; Lefebvre G; Kourmpetis YAI; Kassam M; Ronga F; De Marchi U; Wiederkehr A; Descombes P BMC Genomics; 2017 Apr; 18(1):326. PubMed ID: 28441938 [TBL] [Abstract][Full Text] [Related]
57. MITO-FIND: A study in 390 patients to determine a diagnostic strategy for mitochondrial disease. Kerr M; Hume S; Omar F; Koo D; Barnes H; Khan M; Aman S; Wei XC; Alfuhaid H; McDonald R; McDonald L; Newell C; Sparkes R; Hittel D; Khan A Mol Genet Metab; 2020; 131(1-2):66-82. PubMed ID: 32980267 [TBL] [Abstract][Full Text] [Related]
58. Spectrum of mitochondrial genomic variation in parathyroid neoplasms. Hu Y; Zhang X; Wang O; Xing X; Cui M; Wang M; Song C; Liao Q Endocrine; 2021 Dec; 74(3):690-697. PubMed ID: 34296389 [TBL] [Abstract][Full Text] [Related]
59. Origins and functional consequences of somatic mitochondrial DNA mutations in human cancer. Ju YS; Alexandrov LB; Gerstung M; Martincorena I; Nik-Zainal S; Ramakrishna M; Davies HR; Papaemmanuil E; Gundem G; Shlien A; Bolli N; Behjati S; Tarpey PS; Nangalia J; Massie CE; Butler AP; Teague JW; Vassiliou GS; Green AR; Du MQ; Unnikrishnan A; Pimanda JE; Teh BT; Munshi N; Greaves M; Vyas P; El-Naggar AK; Santarius T; Collins VP; Grundy R; Taylor JA; Hayes DN; Malkin D; ; ; ; Foster CS; Warren AY; Whitaker HC; Brewer D; Eeles R; Cooper C; Neal D; Visakorpi T; Isaacs WB; Bova GS; Flanagan AM; Futreal PA; Lynch AG; Chinnery PF; McDermott U; Stratton MR; Campbell PJ Elife; 2014 Oct; 3():. PubMed ID: 25271376 [TBL] [Abstract][Full Text] [Related]