104 related articles for article (PubMed ID: 16671096)
21. Tandem duplication/triplication correlated with poly-cytosine stretch variation in human mitochondrial DNA D-loop region.
Hung WY; Lin JC; Lee LM; Wu CW; Tseng LM; Yin PH; Chi CW; Lee HC
Mutagenesis; 2008 Mar; 23(2):137-42. PubMed ID: 18252697
[TBL] [Abstract][Full Text] [Related]
22. Mitochondrial DNA restriction map and cytochrome c oxidase subunits I and II sequence divergence of corn stalk borer Sesamia nonagrioides (Lepidoptera: Noctuidae).
Kourti A
Biochem Genet; 2006 Oct; 44(7-8):321-32. PubMed ID: 16977511
[TBL] [Abstract][Full Text] [Related]
23. mtDNA mutations increase tumorigenicity in prostate cancer.
Petros JA; Baumann AK; Ruiz-Pesini E; Amin MB; Sun CQ; Hall J; Lim S; Issa MM; Flanders WD; Hosseini SH; Marshall FF; Wallace DC
Proc Natl Acad Sci U S A; 2005 Jan; 102(3):719-24. PubMed ID: 15647368
[TBL] [Abstract][Full Text] [Related]
24. Association of myopathy with large-scale mitochondrial DNA duplications and deletions: which is pathogenic?
Manfredi G; Vu T; Bonilla E; Schon EA; DiMauro S; Arnaudo E; Zhang L; Rowland LP; Hirano M
Ann Neurol; 1997 Aug; 42(2):180-8. PubMed ID: 9266727
[TBL] [Abstract][Full Text] [Related]
25. Mitochondrial DNA variation is associated with measurable differences in life-history traits and mitochondrial metabolism in Drosophila simulans.
Ballard JW; Melvin RG; Katewa SD; Maas K
Evolution; 2007 Jul; 61(7):1735-47. PubMed ID: 17598752
[TBL] [Abstract][Full Text] [Related]
26. The effects of ethidium bromide induced loss of mitochondrial DNA on mitochondrial phenotype and ultrastructure in a human leukemia T-cell line (MOLT-4 cells).
Armand R; Channon JY; Kintner J; White KA; Miselis KA; Perez RP; Lewis LD
Toxicol Appl Pharmacol; 2004 Apr; 196(1):68-79. PubMed ID: 15050409
[TBL] [Abstract][Full Text] [Related]
27. Novel single base pair COX III subunit deletion of mitochondrial DNA associated with rhabdomyolysis.
Marotta R; Chin J; Kirby DM; Chiotis M; Cook M; Collins SJ
J Clin Neurosci; 2011 Feb; 18(2):290-2. PubMed ID: 21163656
[TBL] [Abstract][Full Text] [Related]
28. 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]
29. Mitochondrial DNA alterations in colorectal cancer cell lines.
Chihara N; Amo T; Tokunaga A; Yuzuriha R; Wolf AM; Asoh S; Suzuki H; Uchida E; Ohta S
J Nippon Med Sch; 2011; 78(1):13-21. PubMed ID: 21389643
[TBL] [Abstract][Full Text] [Related]
30. MtDNA mutations associated with sideroblastic anaemia cause a defect of mitochondrial cytochrome c oxidase.
Bröker S; Meunier B; Rich P; Gattermann N; Hofhaus G
Eur J Biochem; 1998 Nov; 258(1):132-8. PubMed ID: 9851701
[TBL] [Abstract][Full Text] [Related]
31. Role of ectopically expressed mtDNA encoded cytochrome c oxidase subunit I (MT-COI) in tumorigenesis.
Singh RK; Saini SK; Prakasam G; Kalairasan P; Bamezai RNK
Mitochondrion; 2019 Nov; 49():56-65. PubMed ID: 31299394
[TBL] [Abstract][Full Text] [Related]
32. A pathogenic 15-base pair deletion in mitochondrial DNA-encoded cytochrome c oxidase subunit III results in the absence of functional cytochrome c oxidase.
Hoffbuhr KC; Davidson E; Filiano BA; Davidson M; Kennaway NG; King MP
J Biol Chem; 2000 May; 275(18):13994-4003. PubMed ID: 10788526
[TBL] [Abstract][Full Text] [Related]
33. Suppression of a mitochondrial tRNA gene mutation phenotype associated with changes in the nuclear background.
Hao H; Morrison LE; Moraes CT
Hum Mol Genet; 1999 Jun; 8(6):1117-24. PubMed ID: 10332045
[TBL] [Abstract][Full Text] [Related]
34. Mitochondrial D-loop and cytochrome oxidase C subunit I polymorphisms among the breast cancer patients of Mizoram, Northeast India.
Ghatak S; Lallawmzuali D; Lalmawia ; Sapkota R; Zothanpuia ; Pautu JL; Muthukumaran RB; Senthil Kumar N
Curr Genet; 2014 Aug; 60(3):201-12. PubMed ID: 24719079
[TBL] [Abstract][Full Text] [Related]
35. The pattern of natural selection in somatic cancer mutations of human mtDNA.
Stafford P; Chen-Quin EB
J Hum Genet; 2010 Sep; 55(9):605-12. PubMed ID: 20613764
[TBL] [Abstract][Full Text] [Related]
36. Quaternary protein modeling to predict the function of DNA variation found in human mitochondrial cytochrome c oxidase.
Horan MP; Rumbley JN; Melvin RG; Le Couteur DG; Ballard JW
J Hum Genet; 2013 Mar; 58(3):127-34. PubMed ID: 23303385
[TBL] [Abstract][Full Text] [Related]
37. Recurrent myoglobinuria due to a nonsense mutation in the COX I gene of mitochondrial DNA.
Karadimas CL; Greenstein P; Sue CM; Joseph JT; Tanji K; Haller RG; Taivassalo T; Davidson MM; Shanske S; Bonilla E; DiMauro S
Neurology; 2000 Sep; 55(5):644-9. PubMed ID: 10980727
[TBL] [Abstract][Full Text] [Related]
38. Two point mutations in mitochondrial DNA of cytochrome c oxidase coexist with normal mtDNA in a patient with Alzheimer's disease.
Qiu X; Chen Y; Zhou M
Brain Res; 2001 Mar; 893(1-2):261-3. PubMed ID: 11223014
[TBL] [Abstract][Full Text] [Related]
39. Mitochondria and tumors: a new perspective.
Chintha R; Kaipa PR; Sekhar N; Hasan Q
Indian J Cancer; 2013; 50(3):206-13. PubMed ID: 24061460
[TBL] [Abstract][Full Text] [Related]
40. A novel sporadic mutation in cytochrome c oxidase subunit II as a cause of rhabdomyolysis.
McFarland R; Taylor RW; Chinnery PF; Howell N; Turnbull DM
Neuromuscul Disord; 2004 Feb; 14(2):162-6. PubMed ID: 14733964
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
