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For: Rocha MC, Rosa HS, Grady JP, Blakely EL, He L, Romain N, Haller RG, Newman J, McFarland R, Ng YS, Gorman GS, Schaefer AM, Tuppen HA, Taylor RW, Turnbull DM. Pathological mechanisms underlying single large-scale mitochondrial DNA deletions. Ann Neurol 2018;83:115-30. [PMID: 29283441 DOI: 10.1002/ana.25127] [Cited by in Crossref: 18] [Cited by in F6Publishing: 18] [Article Influence: 6.0] [Reference Citation Analysis]
Number Citing Articles
1 Warren C, McDonald D, Capaldi R, Deehan D, Taylor RW, Filby A, Turnbull DM, Lawless C, Vincent AE. Decoding mitochondrial heterogeneity in single muscle fibres by imaging mass cytometry. Sci Rep 2020;10:15336. [PMID: 32948797 DOI: 10.1038/s41598-020-70885-3] [Cited by in Crossref: 4] [Cited by in F6Publishing: 5] [Article Influence: 2.0] [Reference Citation Analysis]
2 Han B, Zhou T, Tu Y, Wang T, He Z, Li Y, Yuan J, Yang X, Sun H. Correlation between mitochondrial DNA 4977 bp deletion and presbycusis: A system review and meta-analysis. Medicine (Baltimore) 2019;98:e16302. [PMID: 31277167 DOI: 10.1097/MD.0000000000016302] [Cited by in Crossref: 1] [Article Influence: 0.3] [Reference Citation Analysis]
3 Jeppesen TD, Duno M, Vissing J. Mutation Load of Single, Large-Scale Deletions of mtDNA in Mitotic and Postmitotic Tissues. Front Genet 2020;11:547638. [PMID: 33133144 DOI: 10.3389/fgene.2020.547638] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.5] [Reference Citation Analysis]
4 Lawless C, Greaves L, Reeve AK, Turnbull DM, Vincent AE. The rise and rise of mitochondrial DNA mutations. Open Biol 2020;10:200061. [PMID: 32428418 DOI: 10.1098/rsob.200061] [Cited by in Crossref: 25] [Cited by in F6Publishing: 20] [Article Influence: 12.5] [Reference Citation Analysis]
5 Anteneová N, Kelifová S, Kolářová H, Vondráčková A, Tóthová I, Lišková P, Magner M, Zámečník J, Hansíková H, Zeman J, Tesařová M, Honzík T. The Phenotypic Spectrum of 47 Czech Patients with Single, Large-Scale Mitochondrial DNA Deletions. Brain Sci 2020;10:E766. [PMID: 33105723 DOI: 10.3390/brainsci10110766] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.5] [Reference Citation Analysis]
6 Tesarova M, Zeman J. Reply to Comment on: Sideroblastic anemia associated with multisystem mitochondrial disorders. Pediatr Blood Cancer 2019;66. [DOI: 10.1002/pbc.28007] [Cited by in Crossref: 3] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
7 Bury AG, Pyle A, Marcuccio F, Turnbull DM, Vincent AE, Hudson G, Actis P. A subcellular cookie cutter for spatial genomics in human tissue. Anal Bioanal Chem 2022. [PMID: 35233697 DOI: 10.1007/s00216-022-03944-5] [Reference Citation Analysis]
8 Finsterer J. Viability of diffusion tensor imaging for assessing retro-chiasmatic involvement in Kearns-Sayre syndrome remains elusive. Neuroradiology 2020;62:131-2. [PMID: 31807840 DOI: 10.1007/s00234-019-02325-7] [Reference Citation Analysis]
9 Vincent AE, Picard M. Multilevel heterogeneity of mitochondrial respiratory chain deficiency. J Pathol 2018;246:261-5. [PMID: 30058194 DOI: 10.1002/path.5146] [Cited by in Crossref: 4] [Cited by in F6Publishing: 3] [Article Influence: 1.0] [Reference Citation Analysis]
10 Smith F, Hopton S, Dallabona C, Gilberti M, Falkous G, Norwood F, Donnini C, Gorman GS, Clark B, Taylor RW, Kulasekararaj AG. Sideroblastic anemia with myopathy secondary to novel, pathogenic missense variants in the YARS2 gene. Haematologica 2018;103:e564-6. [PMID: 29976739 DOI: 10.3324/haematol.2018.194464] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 0.5] [Reference Citation Analysis]
11 Saldaña-Martínez A, Muñoz ML, Pérez-Ramírez G, Montiel-Sosa JF, Montoya J, Emperador S, Ruiz-Pesini E, Cuevas-Covarrubias S, López-Valdez J, Ramírez RG. Whole sequence of the mitochondrial DNA genome of Kearns Sayre Syndrome patients: Identification of deletions and variants. Gene 2019;688:171-81. [PMID: 30528267 DOI: 10.1016/j.gene.2018.11.085] [Cited by in Crossref: 7] [Cited by in F6Publishing: 4] [Article Influence: 1.8] [Reference Citation Analysis]
12 Zhu Y, You J, Xu C, Gu X. Associations of mitochondrial DNA 3777-4679 region mutations with maternally inherited essential hypertensive subjects in China. BMC Med Genet 2020;21:105. [PMID: 32414374 DOI: 10.1186/s12881-020-01045-7] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 1.5] [Reference Citation Analysis]
13 Oliveira MT, Pontes CB, Ciesielski GL. Roles of the mitochondrial replisome in mitochondrial DNA deletion formation. Genet Mol Biol 2020;43:e20190069. [PMID: 32141473 DOI: 10.1590/1678-4685-GMB-2019-0069] [Cited by in Crossref: 4] [Cited by in F6Publishing: 3] [Article Influence: 2.0] [Reference Citation Analysis]
14 Frazier AE, Vincent AE, Turnbull DM, Thorburn DR, Taylor RW. Assessment of mitochondrial respiratory chain enzymes in cells and tissues. Methods Cell Biol 2020;155:121-56. [PMID: 32183956 DOI: 10.1016/bs.mcb.2019.11.007] [Cited by in Crossref: 7] [Cited by in F6Publishing: 5] [Article Influence: 2.3] [Reference Citation Analysis]
15 Bris C, Goudenège D, Desquiret-Dumas V, Gueguen N, Bannwarth S, Gaignard P, Rucheton B, Trimouille A, Allouche S, Rouzier C, Saadi S, Jardel C, Slama A, Barth M, Verny C, Spinazzi M, Cassereau J, Colin E, Armelle M, Pereon Y, Martin-Negrier ML, Paquis-Flucklinger V, Letournel F, Lenaers G, Bonneau D, Reynier P, Amati-Bonneau P, Procaccio V. Improved detection of mitochondrial DNA instability in mitochondrial genome maintenance disorders. Genet Med 2021;23:1769-78. [PMID: 34040194 DOI: 10.1038/s41436-021-01206-w] [Reference Citation Analysis]
16 Bury AG, Robertson FM, Pyle A, Payne BAI, Hudson G. The Isolation and Deep Sequencing of Mitochondrial DNA. Methods Mol Biol 2021;2277:433-47. [PMID: 34080167 DOI: 10.1007/978-1-0716-1270-5_27] [Reference Citation Analysis]
17 Ostojic SM, Ratgeber L, Olah A, Betlehem J, Pongras A. What do over-trained athletes and patients with neurodegenerative diseases have in common? Mitochondrial dysfunction. Exp Biol Med (Maywood) 2021;246:1241-3. [PMID: 33554650 DOI: 10.1177/1535370221990619] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
18 La Morgia C, Maresca A, Caporali L, Valentino ML, Carelli V. Mitochondrial diseases in adults. J Intern Med 2020;287:592-608. [DOI: 10.1111/joim.13064] [Cited by in Crossref: 8] [Cited by in F6Publishing: 10] [Article Influence: 4.0] [Reference Citation Analysis]
19 Chen C, Vincent AE, Blain AP, Smith AL, Turnbull DM, Reeve AK. Investigation of mitochondrial biogenesis defects in single substantia nigra neurons using post-mortem human tissues. Neurobiology of Disease 2020;134:104631. [DOI: 10.1016/j.nbd.2019.104631] [Cited by in Crossref: 16] [Cited by in F6Publishing: 15] [Article Influence: 8.0] [Reference Citation Analysis]
20 Lehmann D, Tuppen HAL, Campbell GE, Alston CL, Lawless C, Rosa HS, Rocha MC, Reeve AK, Nicholls TJ, Deschauer M, Zierz S, Taylor RW, Turnbull DM, Vincent AE. Understanding mitochondrial DNA maintenance disorders at the single muscle fibre level. Nucleic Acids Res 2019;47:7430-43. [PMID: 31147703 DOI: 10.1093/nar/gkz472] [Cited by in Crossref: 7] [Cited by in F6Publishing: 5] [Article Influence: 2.3] [Reference Citation Analysis]