BPG is committed to discovery and dissemination of knowledge
Cited by in F6Publishing
For: Spinazzola A, Zeviani M. Disorders from perturbations of nuclear-mitochondrial intergenomic cross-talk. J Intern Med 2009;265:174-92. [PMID: 19192035 DOI: 10.1111/j.1365-2796.2008.02059.x] [Cited by in Crossref: 48] [Cited by in F6Publishing: 39] [Article Influence: 3.7] [Reference Citation Analysis]
Number Citing Articles
1 Dong DW, Pereira F, Barrett SP, Kolesar JE, Cao K, Damas J, Yatsunyk LA, Johnson FB, Kaufman BA. Association of G-quadruplex forming sequences with human mtDNA deletion breakpoints. BMC Genomics 2014;15:677. [PMID: 25124333 DOI: 10.1186/1471-2164-15-677] [Cited by in Crossref: 70] [Cited by in F6Publishing: 58] [Article Influence: 8.8] [Reference Citation Analysis]
2 Jaberi E, Chitsazian F, Ali Shahidi G, Rohani M, Sina F, Safari I, Malakouti Nejad M, Houshmand M, Klotzle B, Elahi E. The novel mutation p.Asp251Asn in the β-subunit of succinate-CoA ligase causes encephalomyopathy and elevated succinylcarnitine. J Hum Genet 2013;58:526-30. [DOI: 10.1038/jhg.2013.45] [Cited by in Crossref: 19] [Cited by in F6Publishing: 17] [Article Influence: 2.1] [Reference Citation Analysis]
3 Spinazzola A. Mitochondrial DNA mutations and depletion in pediatric medicine. Seminars in Fetal and Neonatal Medicine 2011;16:190-6. [DOI: 10.1016/j.siny.2011.04.011] [Cited by in Crossref: 28] [Cited by in F6Publishing: 26] [Article Influence: 2.5] [Reference Citation Analysis]
4 Duchen MR, Szabadkai G. Roles of mitochondria in human disease. Essays Biochem 2010;47:115-37. [PMID: 20533904 DOI: 10.1042/bse0470115] [Cited by in Crossref: 113] [Cited by in F6Publishing: 95] [Article Influence: 9.4] [Reference Citation Analysis]
5 Dalla Rosa I, Cámara Y, Durigon R, Moss CF, Vidoni S, Akman G, Hunt L, Johnson MA, Grocott S, Wang L, Thorburn DR, Hirano M, Poulton J, Taylor RW, Elgar G, Martí R, Voshol P, Holt IJ, Spinazzola A. MPV17 Loss Causes Deoxynucleotide Insufficiency and Slow DNA Replication in Mitochondria. PLoS Genet 2016;12:e1005779. [PMID: 26760297 DOI: 10.1371/journal.pgen.1005779] [Cited by in Crossref: 44] [Cited by in F6Publishing: 38] [Article Influence: 7.3] [Reference Citation Analysis]
6 Bai RK, Chang J, Yeh KT, Lou MA, Lu JF, Tan DJ, Liu H, Wong LJ. Mitochondrial DNA content varies with pathological characteristics of breast cancer. J Oncol. 2011;2011:496189. [PMID: 22028711 DOI: 10.1155/2011/496189] [Cited by in Crossref: 27] [Cited by in F6Publishing: 31] [Article Influence: 2.5] [Reference Citation Analysis]
7 Hikmat O, Tzoulis C, Chong WK, Chentouf L, Klingenberg C, Fratter C, Carr LJ, Prabhakar P, Kumaraguru N, Gissen P, Cross JH, Jacques TS, Taanman J, Bindoff LA, Rahman S. The clinical spectrum and natural history of early-onset diseases due to DNA polymerase gamma mutations. Genet Med 2017;19:1217-25. [DOI: 10.1038/gim.2017.35] [Cited by in Crossref: 26] [Cited by in F6Publishing: 20] [Article Influence: 5.2] [Reference Citation Analysis]
8 Felici R, Lapucci A, Cavone L, Pratesi S, Berlinguer-Palmini R, Chiarugi A. Pharmacological NAD-Boosting Strategies Improve Mitochondrial Homeostasis in Human Complex I-Mutant Fibroblasts. Mol Pharmacol 2015;87:965-71. [PMID: 25788480 DOI: 10.1124/mol.114.097204] [Cited by in Crossref: 23] [Cited by in F6Publishing: 20] [Article Influence: 3.3] [Reference Citation Analysis]
9 Larsson NG. Introduction: Euromit VII--summarizing 50 years of research on mitochondrial disease. J Intern Med 2009;265:170-3. [PMID: 19192034 DOI: 10.1111/j.1365-2796.2008.02064.x] [Reference Citation Analysis]
10 Venegas V, Halberg MC. Measurement of mitochondrial DNA copy number. Methods Mol Biol 2012;837:327-35. [PMID: 22215558 DOI: 10.1007/978-1-61779-504-6_22] [Cited by in Crossref: 77] [Cited by in F6Publishing: 67] [Article Influence: 7.7] [Reference Citation Analysis]
11 Wong LJ. Next generation molecular diagnosis of mitochondrial disorders. Mitochondrion 2013;13:379-87. [PMID: 23473862 DOI: 10.1016/j.mito.2013.02.001] [Cited by in Crossref: 52] [Cited by in F6Publishing: 37] [Article Influence: 5.8] [Reference Citation Analysis]
12 Gardner A, Boles RG. Beyond the serotonin hypothesis: mitochondria, inflammation and neurodegeneration in major depression and affective spectrum disorders. Prog Neuropsychopharmacol Biol Psychiatry 2011;35:730-43. [PMID: 20691744 DOI: 10.1016/j.pnpbp.2010.07.030] [Cited by in Crossref: 197] [Cited by in F6Publishing: 186] [Article Influence: 16.4] [Reference Citation Analysis]
13 Mineri R, Pavelka N, Fernandez-Vizarra E, Ricciardi-Castagnoli P, Zeviani M, Tiranti V. How do human cells react to the absence of mitochondrial DNA? PLoS One 2009;4:e5713. [PMID: 19492094 DOI: 10.1371/journal.pone.0005713] [Cited by in Crossref: 25] [Cited by in F6Publishing: 24] [Article Influence: 1.9] [Reference Citation Analysis]
14 Ghezzi D, Zeviani M. Mitochondrial Disorders: Nuclear Gene Mutations. eLS. Chichester: John Wiley & Sons, Ltd; 2001. [DOI: 10.1002/9780470015902.a0005540.pub2] [Cited by in Crossref: 3] [Cited by in F6Publishing: 1] [Article Influence: 0.3] [Reference Citation Analysis]
15 Lamperti C, Fang M, Invernizzi F, Liu X, Wang H, Zhang Q, Carrara F, Moroni I, Zeviani M, Zhang J, Ghezzi D. A novel homozygous mutation in SUCLA2 gene identified by exome sequencing. Mol Genet Metab 2012;107:403-8. [PMID: 23010432 DOI: 10.1016/j.ymgme.2012.08.020] [Cited by in Crossref: 30] [Cited by in F6Publishing: 31] [Article Influence: 3.0] [Reference Citation Analysis]
16 Saneto RP, Cohen BH, Copeland WC, Naviaux RK. Alpers-Huttenlocher syndrome. Pediatr Neurol 2013;48:167-78. [PMID: 23419467 DOI: 10.1016/j.pediatrneurol.2012.09.014] [Cited by in Crossref: 54] [Cited by in F6Publishing: 38] [Article Influence: 6.0] [Reference Citation Analysis]
17 Elachouri G, Vidoni S, Zanna C, Pattyn A, Boukhaddaoui H, Gaget K, Yu-Wai-Man P, Gasparre G, Sarzi E, Delettre C, Olichon A, Loiseau D, Reynier P, Chinnery PF, Rotig A, Carelli V, Hamel CP, Rugolo M, Lenaers G. OPA1 links human mitochondrial genome maintenance to mtDNA replication and distribution. Genome Res 2011;21:12-20. [PMID: 20974897 DOI: 10.1101/gr.108696.110] [Cited by in Crossref: 144] [Cited by in F6Publishing: 137] [Article Influence: 12.0] [Reference Citation Analysis]
18 Khan S, Raghuram GV, Pathak N, Jain SK, Chandra DH, Mishra PK. Impairment of mitochondrial-nuclear cross talk in neutrophils of patients with type 2 diabetes mellitus. Indian J Clin Biochem 2014;29:38-44. [PMID: 24478547 DOI: 10.1007/s12291-013-0321-4] [Cited by in Crossref: 4] [Cited by in F6Publishing: 5] [Article Influence: 0.4] [Reference Citation Analysis]
19 Douglas GV, Wiszniewska J, Lipson MH, Witt DR, McDowell T, Sifry-Platt M, Hirano M, Craigen WJ, Wong LJ. Detection of uniparental isodisomy in autosomal recessive mitochondrial DNA depletion syndrome by high-density SNP array analysis. J Hum Genet 2011;56:834-9. [PMID: 22011815 DOI: 10.1038/jhg.2011.112] [Cited by in Crossref: 15] [Cited by in F6Publishing: 13] [Article Influence: 1.4] [Reference Citation Analysis]
20 Smits P, Mattijssen S, Morava E, van den Brand M, van den Brandt F, Wijburg F, Pruijn G, Smeitink J, Nijtmans L, Rodenburg R, van den Heuvel L. Functional consequences of mitochondrial tRNA Trp and tRNA Arg mutations causing combined OXPHOS defects. Eur J Hum Genet 2010;18:324-9. [PMID: 19809478 DOI: 10.1038/ejhg.2009.169] [Cited by in Crossref: 27] [Cited by in F6Publishing: 25] [Article Influence: 2.1] [Reference Citation Analysis]
21 Hikmat O, Naess K, Engvall M, Klingenberg C, Rasmussen M, Tallaksen CME, Samsonsen C, Brodtkorb E, Ostergaard E, de Coo R, Pias-Peleteiro L, Isohanni P, Uusimaa J, Darin N, Rahman S, Bindoff LA. The impact of gender, puberty, and pregnancy in patients with POLG disease. Ann Clin Transl Neurol 2020;7:2019-25. [PMID: 32949115 DOI: 10.1002/acn3.51199] [Cited by in Crossref: 1] [Cited by in F6Publishing: 2] [Article Influence: 0.5] [Reference Citation Analysis]
22 Venegas V, Wang J, Dimmock D, Wong LJ. Real-time quantitative PCR analysis of mitochondrial DNA content. Curr Protoc Hum Genet 2011;Chapter 19:Unit 19.7.. [PMID: 21234878 DOI: 10.1002/0471142905.hg1907s68] [Cited by in Crossref: 53] [Cited by in F6Publishing: 59] [Article Influence: 4.8] [Reference Citation Analysis]
23 Rio M, Lebre A, Rötig A, Munnich A. Approccio diagnostico delle citopatie mitocondriali del bambino. EMC - Neurologia 2014;14:1-8. [DOI: 10.1016/s1634-7072(14)66665-4] [Reference Citation Analysis]
24 Money KM, Olah Z, Korade Z, Garbett KA, Shelton RC, Mirnics K. An altered peripheral IL6 response in major depressive disorder. Neurobiol Dis 2016;89:46-54. [PMID: 26804030 DOI: 10.1016/j.nbd.2016.01.015] [Cited by in Crossref: 15] [Cited by in F6Publishing: 14] [Article Influence: 2.5] [Reference Citation Analysis]
25 Scaglia F. Nuclear Gene Defects in Mitochondrial Disorders. In: Wong, Ph.d. LC, editor. Mitochondrial Disorders. Totowa: Humana Press; 2012. pp. 17-34. [DOI: 10.1007/978-1-61779-504-6_2] [Cited by in Crossref: 8] [Cited by in F6Publishing: 8] [Article Influence: 0.7] [Reference Citation Analysis]
26 Tavares MV, Santos MJ, Domingues AP, Pratas J, Mendes C, Simões M, Moura P, Diogo L, Grazina M. Antenatal manifestations of mitochondrial disorders. J Inherit Metab Dis 2013;36:805-11. [DOI: 10.1007/s10545-012-9567-x] [Cited by in Crossref: 9] [Cited by in F6Publishing: 7] [Article Influence: 1.0] [Reference Citation Analysis]
27 Hikmat O, Vederhus BJ, Benestad MR, Engeset IME, Klingenberg C, Rasmussen M, Tallaksen CM, Brodtkorb E, Elgen IB, Bindoff LA. Mental health and health related quality of life in mitochondrial POLG disease. Mitochondrion 2020;55:95-9. [PMID: 32976988 DOI: 10.1016/j.mito.2020.09.005] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.5] [Reference Citation Analysis]
28 Wang W, Shen P, Thiyagarajan S, Lin S, Palm C, Horvath R, Klopstock T, Cutler D, Pique L, Schrijver I, Davis RW, Mindrinos M, Speed TP, Scharfe C. Identification of rare DNA variants in mitochondrial disorders with improved array-based sequencing. Nucleic Acids Res. 2011;39:44-58. [PMID: 20843780 DOI: 10.1093/nar/gkq750] [Cited by in Crossref: 17] [Cited by in F6Publishing: 14] [Article Influence: 1.4] [Reference Citation Analysis]
29 Rivera H, Merinero B, Martinez-Pardo M, Arroyo I, Ruiz-Sala P, Bornstein B, Serra-Suhe C, Gallardo E, Marti R, Moran MJ, Ugalde C, Perez-Jurado LA, Andreu AL, Garesse R, Ugarte M, Arenas J, Martin MA. Marked mitochondrial DNA depletion associated with a novel SUCLG1 gene mutation resulting in lethal neonatal acidosis, multi-organ failure, and interrupted aortic arch. Mitochondrion 2010;10:362-8. [PMID: 20227526 DOI: 10.1016/j.mito.2010.03.003] [Cited by in Crossref: 26] [Cited by in F6Publishing: 22] [Article Influence: 2.2] [Reference Citation Analysis]
30 Wong LJ. Molecular genetics of mitochondrial disorders. Dev Disabil Res Rev 2010;16:154-62. [PMID: 20818730 DOI: 10.1002/ddrr.104] [Cited by in Crossref: 50] [Cited by in F6Publishing: 41] [Article Influence: 4.5] [Reference Citation Analysis]
31 Posada IJ, Gallardo ME, Domínguez C, Rivera H, Cabello A, Arenas J, Martín MA, Garesse R, Bornstein B. Depleción del ácido desoxirribonucleico mitocondrial y mutaciones de POLG en un paciente con neuropatía sensorial atáxica, disartria y oftalmoplejía. Medicina Clínica 2010;135:452-5. [DOI: 10.1016/j.medcli.2010.03.031] [Cited by in Crossref: 5] [Cited by in F6Publishing: 6] [Article Influence: 0.4] [Reference Citation Analysis]
32 Saneto RP, Naviaux RK. Polymerase gamma disease through the ages. Dev Disabil Res Revs 2010;16:163-74. [DOI: 10.1002/ddrr.105] [Cited by in Crossref: 55] [Cited by in F6Publishing: 46] [Article Influence: 4.6] [Reference Citation Analysis]
33 Kasote DM, Hegde MV, Katyare SS. Mitochondrial dysfunction in psychiatric and neurological diseases: cause(s), consequence(s), and implications of antioxidant therapy. Biofactors 2013;39:392-406. [PMID: 23460132 DOI: 10.1002/biof.1093] [Cited by in Crossref: 32] [Cited by in F6Publishing: 26] [Article Influence: 3.6] [Reference Citation Analysis]
34 Wong LC. Biochemical and Molecular Methods for the Study of Mitochondrial Disorders. In: Wong LC, editor. Mitochondrial Disorders Caused by Nuclear Genes. New York: Springer; 2013. pp. 27-45. [DOI: 10.1007/978-1-4614-3722-2_2] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.1] [Reference Citation Analysis]
35 Lapucci A, Pittelli M, Rapizzi E, Felici R, Moroni F, Chiarugi A. Poly(ADP-ribose) polymerase-1 is a nuclear epigenetic regulator of mitochondrial DNA repair and transcription. Mol Pharmacol. 2011;79:932-940. [PMID: 21441600 DOI: 10.1124/mol.110.070110] [Cited by in Crossref: 50] [Cited by in F6Publishing: 49] [Article Influence: 4.5] [Reference Citation Analysis]
36 Rinaldi T, Dallabona C, Ferrero I, Frontali L, Bolotin-Fukuhara M. Mitochondrial diseases and the role of the yeast models. FEMS Yeast Res 2010;10:1006-22. [PMID: 20946356 DOI: 10.1111/j.1567-1364.2010.00685.x] [Cited by in Crossref: 30] [Cited by in F6Publishing: 28] [Article Influence: 2.5] [Reference Citation Analysis]
37 Schaller A, Desetty R, Hahn D, Jackson CB, Nuoffer JM, Gallati S, Levinger L. Impairment of mitochondrial tRNAIle processing by a novel mutation associated with chronic progressive external ophthalmoplegia. Mitochondrion 2011;11:488-96. [PMID: 21292040 DOI: 10.1016/j.mito.2011.01.005] [Cited by in Crossref: 15] [Cited by in F6Publishing: 13] [Article Influence: 1.4] [Reference Citation Analysis]
38 Kalko SG, Paco S, Jou C, Rodríguez MA, Meznaric M, Rogac M, Jekovec-Vrhovsek M, Sciacco M, Moggio M, Fagiolari G, De Paepe B, De Meirleir L, Ferrer I, Roig-Quilis M, Munell F, Montoya J, López-Gallardo E, Ruiz-Pesini E, Artuch R, Montero R, Torner F, Nascimento A, Ortez C, Colomer J, Jimenez-Mallebrera C. Transcriptomic profiling of TK2 deficient human skeletal muscle suggests a role for the p53 signalling pathway and identifies growth and differentiation factor-15 as a potential novel biomarker for mitochondrial myopathies. BMC Genomics 2014;15:91. [PMID: 24484525 DOI: 10.1186/1471-2164-15-91] [Cited by in Crossref: 64] [Cited by in F6Publishing: 63] [Article Influence: 8.0] [Reference Citation Analysis]
39 Schon EA, DiMauro S, Hirano M, Gilkerson RW. Therapeutic prospects for mitochondrial disease. Trends Mol Med 2010;16:268-76. [PMID: 20556877 DOI: 10.1016/j.molmed.2010.04.007] [Cited by in Crossref: 75] [Cited by in F6Publishing: 65] [Article Influence: 6.3] [Reference Citation Analysis]
40 Hikmat O, Eichele T, Tzoulis C, Bindoff LA. Understanding the Epilepsy in POLG Related Disease. Int J Mol Sci 2017;18:E1845. [PMID: 28837072 DOI: 10.3390/ijms18091845] [Cited by in Crossref: 19] [Cited by in F6Publishing: 16] [Article Influence: 3.8] [Reference Citation Analysis]
41 Zabalza R, Nurminen A, Kaguni LS, Garesse R, Gallardo ME, Bornstein B. Co-occurrence of four nucleotide changes associated with an adult mitochondrial ataxia phenotype. BMC Res Notes 2014;7:883. [PMID: 25488682 DOI: 10.1186/1756-0500-7-883] [Cited by in Crossref: 4] [Cited by in F6Publishing: 3] [Article Influence: 0.5] [Reference Citation Analysis]
42 Jha R, Patel H, Dubey R, Goswami JN, Bhagwat C, Saini L, K Manokaran R, John BM, Kovilapu UB, Mohimen A, Saxena A, Sondhi V. Clinical and molecular spectrum associated with Polymerase-γ related disorders. J Child Neurol 2022;:8830738211067065. [PMID: 34986040 DOI: 10.1177/08830738211067065] [Reference Citation Analysis]