333 related articles for article (PubMed ID: 7849699)
1. Deficiency of the human mitochondrial transcription factor h-mtTFA in infantile mitochondrial myopathy is associated with mtDNA depletion.
Poulton J; Morten K; Freeman-Emmerson C; Potter C; Sewry C; Dubowitz V; Kidd H; Stephenson J; Whitehouse W; Hansen FJ
Hum Mol Genet; 1994 Oct; 3(10):1763-9. PubMed ID: 7849699
[TBL] [Abstract][Full Text] [Related]
2. Low levels of mitochondrial transcription factor A in mitochondrial DNA depletion.
Larsson NG; Oldfors A; Holme E; Clayton DA
Biochem Biophys Res Commun; 1994 May; 200(3):1374-81. PubMed ID: 8185589
[TBL] [Abstract][Full Text] [Related]
3. Variation in mitochondrial DNA levels in muscle from normal controls. Is depletion of mtDNA in patients with mitochondrial myopathy a distinct clinical syndrome.
Poulton J; Sewry C; Potter CG; Bougeron T; Chretien D; Wijburg FA; Morten KJ; Brown G
J Inherit Metab Dis; 1995; 18(1):4-20. PubMed ID: 7623440
[TBL] [Abstract][Full Text] [Related]
4. Immunohistochemical detection of human mtDNA polymerase gamma and of human mitochondrial transcription factor A in cytochrome-c-oxidase-deficient oxyphil cells of hyperfunctional parathyroids.
Müller-Höcker J; Schäfer S; Copeland WC; Wiesner R; Seibel P
Virchows Arch; 1998 Dec; 433(6):529-36. PubMed ID: 9870686
[TBL] [Abstract][Full Text] [Related]
5. Modulation of mitochondrial transcription in response to mtDNA depletion and repletion in HeLa cells.
Seidel-Rogol BL; Shadel GS
Nucleic Acids Res; 2002 May; 30(9):1929-34. PubMed ID: 11972329
[TBL] [Abstract][Full Text] [Related]
6. Abnormal levels of human mitochondrial transcription factor A in skeletal muscle in mitochondrial encephalomyopathies.
Siciliano G; Mancuso M; Pasquali L; Manca ML; Tessa A; Iudice A
Neurol Sci; 2000; 21(5 Suppl):S985-7. PubMed ID: 11382203
[TBL] [Abstract][Full Text] [Related]
7. Down-regulation of mitochondrial transcription factor A during spermatogenesis in humans.
Larsson NG; Oldfors A; Garman JD; Barsh GS; Clayton DA
Hum Mol Genet; 1997 Feb; 6(2):185-91. PubMed ID: 9063738
[TBL] [Abstract][Full Text] [Related]
8. Human mitochondrial transcription factor A reduction and mitochondrial dysfunction in Hashimoto's hypothyroid myopathy.
Siciliano G; Monzani F; Manca ML; Tessa A; Caraccio N; Tozzi G; Piemonte F; Mancuso M; Santorelli FM; Ferrannini E; Murri L
Mol Med; 2002 Jun; 8(6):326-33. PubMed ID: 12428064
[TBL] [Abstract][Full Text] [Related]
9. Clinical heterogeneity associated with mitochondrial DNA depletion in muscle.
Campos Y; Martín MA; García-Silva T; del Hoyo P; Rubio JC; Castro-Gago M; García-Peñas J; Casas J; Cabello A; Ricoy JR; Arenas J
Neuromuscul Disord; 1998 Dec; 8(8):568-73. PubMed ID: 10093063
[TBL] [Abstract][Full Text] [Related]
10. MicroRNA-494 regulates mitochondrial biogenesis in skeletal muscle through mitochondrial transcription factor A and Forkhead box j3.
Yamamoto H; Morino K; Nishio Y; Ugi S; Yoshizaki T; Kashiwagi A; Maegawa H
Am J Physiol Endocrinol Metab; 2012 Dec; 303(12):E1419-27. PubMed ID: 23047984
[TBL] [Abstract][Full Text] [Related]
11. Mitochondrial DNA depletion in a patient with long survival.
Vu TH; Tanji K; Valsamis H; DiMauro S; Bonilla E
Neurology; 1998 Oct; 51(4):1190-3. PubMed ID: 9781557
[TBL] [Abstract][Full Text] [Related]
12. Apoptosis in mitochondrial myopathies is linked to mitochondrial proliferation.
Auré K; Fayet G; Leroy JP; Lacène E; Romero NB; Lombès A
Brain; 2006 May; 129(Pt 5):1249-59. PubMed ID: 16537564
[TBL] [Abstract][Full Text] [Related]
13. Failed upregulation of TFAM protein and mitochondrial DNA in oxidatively deficient fibers of chronic obstructive pulmonary disease locomotor muscle.
Konokhova Y; Spendiff S; Jagoe RT; Aare S; Kapchinsky S; MacMillan NJ; Rozakis P; Picard M; Aubertin-Leheudre M; Pion CH; Bourbeau J; Hepple RT; Taivassalo T
Skelet Muscle; 2016; 6():10. PubMed ID: 26893822
[TBL] [Abstract][Full Text] [Related]
14. Mitochondrial transcription factor A regulates BCL2L1 gene expression and is a prognostic factor in serous ovarian cancer.
Kurita T; Izumi H; Kagami S; Kawagoe T; Toki N; Matsuura Y; Hachisuga T; Kohno K
Cancer Sci; 2012 Feb; 103(2):239-444. PubMed ID: 22098591
[TBL] [Abstract][Full Text] [Related]
15. Mitochondrial DNA copy number threshold in mtDNA depletion myopathy.
Durham SE; Bonilla E; Samuels DC; DiMauro S; Chinnery PF
Neurology; 2005 Aug; 65(3):453-5. PubMed ID: 16087914
[TBL] [Abstract][Full Text] [Related]
16. Mitochondrial myopathy induces a starvation-like response.
Tyynismaa H; Carroll CJ; Raimundo N; Ahola-Erkkilä S; Wenz T; Ruhanen H; Guse K; Hemminki A; Peltola-Mjøsund KE; Tulkki V; Oresic M; Moraes CT; Pietiläinen K; Hovatta I; Suomalainen A
Hum Mol Genet; 2010 Oct; 19(20):3948-58. PubMed ID: 20656789
[TBL] [Abstract][Full Text] [Related]
17. Cytochrome c oxidase deficiency in the muscle of patients with zidovudine myopathy is segmental and affects both mitochondrial DNA- and nuclear DNA-encoded subunits.
Yerroum M; Pham-Dang C; Authier FJ; Monnet I; Gherardi R; Chariot P
Acta Neuropathol; 2000 Jul; 100(1):82-6. PubMed ID: 10912924
[TBL] [Abstract][Full Text] [Related]
18. Mitochondrial transcription factor A (mtTFA) and diabetes.
Choi YS; Kim S; Pak YK
Diabetes Res Clin Pract; 2001 Dec; 54 Suppl 2():S3-9. PubMed ID: 11733104
[TBL] [Abstract][Full Text] [Related]
19. Increased mitochondrial DNA copy-number in CEM cells resistant to delayed toxicity of 2',3'-dideoxycytidine.
Bjerke M; Franco M; Johansson M; Balzarini J; Karlsson A
Biochem Pharmacol; 2008 Mar; 75(6):1313-21. PubMed ID: 18206854
[TBL] [Abstract][Full Text] [Related]
20. Mitochondrial DNA depletion in single fibers in a patient with novel TK2 mutations.
Roos S; Lindgren U; Ehrstedt C; Moslemi AR; Oldfors A
Neuromuscul Disord; 2014 Aug; 24(8):713-20. PubMed ID: 24953930
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
