526 related articles for article (PubMed ID: 16301523)
21. Analysis of multiple mitochondrial DNA deletions in inclusion body myositis.
Moslemi AR; Lindberg C; Oldfors A
Hum Mutat; 1997; 10(5):381-6. PubMed ID: 9375854
[TBL] [Abstract][Full Text] [Related]
22. Mitochondrial DNA deletion mutations in patients with neuropsychiatric symptoms.
Kato M; Nakamura M; Ichiba M; Tomiyasu A; Shimo H; Higuchi I; Ueno S; Sano A
Neurosci Res; 2011 Apr; 69(4):331-6. PubMed ID: 21185889
[TBL] [Abstract][Full Text] [Related]
23. Autosomal disorders of mitochondrial DNA maintenance.
Van Goethem G
Acta Neurol Belg; 2006 Jun; 106(2):66-72. PubMed ID: 16898256
[TBL] [Abstract][Full Text] [Related]
24. Mitochondrial DNA mutations and oxidative damage in aging and diseases: an emerging paradigm of gerontology and medicine.
Wei YH
Proc Natl Sci Counc Repub China B; 1998 Apr; 22(2):55-67. PubMed ID: 9615468
[TBL] [Abstract][Full Text] [Related]
25. Investigation on mtDNA deletions and twinkle gene mutation (G1423C) in Iranian patients with chronic progressive external opthalmoplagia.
Houshmand M; Panahi MS; Hosseini BN; Dorraj GH; Tabassi AR
Neurol India; 2006 Jun; 54(2):182-5. PubMed ID: 16804265
[TBL] [Abstract][Full Text] [Related]
26. Two novel mutations in PEO1 (twinkle) gene associated with chronic external ophthalmoplegia.
Ronchi D; Fassone E; Bordoni A; Sciacco M; Lucchini V; Di Fonzo A; Rizzuti M; Colombo I; Napoli L; Ciscato P; Moggio M; Cosi A; Collotta M; Corti S; Bresolin N; Comi GP
J Neurol Sci; 2011 Sep; 308(1-2):173-6. PubMed ID: 21689831
[TBL] [Abstract][Full Text] [Related]
27. Infantile-onset spinocerebellar ataxia and mitochondrial recessive ataxia syndrome are associated with neuronal complex I defect and mtDNA depletion.
Hakonen AH; Goffart S; Marjavaara S; Paetau A; Cooper H; Mattila K; Lampinen M; Sajantila A; Lönnqvist T; Spelbrink JN; Suomalainen A
Hum Mol Genet; 2008 Dec; 17(23):3822-35. PubMed ID: 18775955
[TBL] [Abstract][Full Text] [Related]
28. Animal models for mitochondrial disease.
Wallace DC
Methods Mol Biol; 2002; 197():3-54. PubMed ID: 12013805
[TBL] [Abstract][Full Text] [Related]
29. Multiple mitochondrial DNA deletions in a patient with mitochondrial myopathy and cardiomyopathy but no ophthalmoplegia.
Takei Y; Ikeda S; Yanagisawa N; Takahashi W; Sekiguchi M; Hayashi T
Muscle Nerve; 1995 Nov; 18(11):1321-5. PubMed ID: 7565930
[TBL] [Abstract][Full Text] [Related]
30. Structure-function defects of the twinkle amino-terminal region in progressive external ophthalmoplegia.
Holmlund T; Farge G; Pande V; Korhonen J; Nilsson L; Falkenberg M
Biochim Biophys Acta; 2009 Feb; 1792(2):132-9. PubMed ID: 19084593
[TBL] [Abstract][Full Text] [Related]
31. Multiple deletions of mitochondrial DNA in several tissues of a patient with severe retarded depression and familial progressive external ophthalmoplegia.
Suomalainen A; Majander A; Haltia M; Somer H; Lönnqvist J; Savontaus ML; Peltonen L
J Clin Invest; 1992 Jul; 90(1):61-6. PubMed ID: 1634620
[TBL] [Abstract][Full Text] [Related]
32. TWINKLE is an essential mitochondrial helicase required for synthesis of nascent D-loop strands and complete mtDNA replication.
Milenkovic D; Matic S; Kühl I; Ruzzenente B; Freyer C; Jemt E; Park CB; Falkenberg M; Larsson NG
Hum Mol Genet; 2013 May; 22(10):1983-93. PubMed ID: 23393161
[TBL] [Abstract][Full Text] [Related]
33. Recessive Twinkle mutations in early onset encephalopathy with mtDNA depletion.
Hakonen AH; Isohanni P; Paetau A; Herva R; Suomalainen A; Lönnqvist T
Brain; 2007 Nov; 130(Pt 11):3032-40. PubMed ID: 17921179
[TBL] [Abstract][Full Text] [Related]
34. Clonal expansion of mitochondrial DNA with multiple deletions in autosomal dominant progressive external ophthalmoplegia.
Moslemi AR; Melberg A; Holme E; Oldfors A
Ann Neurol; 1996 Nov; 40(5):707-13. PubMed ID: 8957011
[TBL] [Abstract][Full Text] [Related]
35. [Molecular biology of mitochondrial DNA and mutations in mitochondrial cytopathy].
Ito T
Nihon Rinsho; 1993 Jun; 51(6):1425-8. PubMed ID: 8320824
[TBL] [Abstract][Full Text] [Related]
36. Somatic mtDNA mutations cause aging phenotypes without affecting reactive oxygen species production.
Trifunovic A; Hansson A; Wredenberg A; Rovio AT; Dufour E; Khvorostov I; Spelbrink JN; Wibom R; Jacobs HT; Larsson NG
Proc Natl Acad Sci U S A; 2005 Dec; 102(50):17993-8. PubMed ID: 16332961
[TBL] [Abstract][Full Text] [Related]
37. Twinkle and POLG defects enhance age-dependent accumulation of mutations in the control region of mtDNA.
Wanrooij S; Luoma P; van Goethem G; van Broeckhoven C; Suomalainen A; Spelbrink JN
Nucleic Acids Res; 2004; 32(10):3053-64. PubMed ID: 15181170
[TBL] [Abstract][Full Text] [Related]
38. Random point mutations with major effects on protein-coding genes are the driving force behind premature aging in mtDNA mutator mice.
Edgar D; Shabalina I; Camara Y; Wredenberg A; Calvaruso MA; Nijtmans L; Nedergaard J; Cannon B; Larsson NG; Trifunovic A
Cell Metab; 2009 Aug; 10(2):131-8. PubMed ID: 19656491
[TBL] [Abstract][Full Text] [Related]
39. Mice with only rat mtDNA are required as models of mitochondrial diseases.
Yamaoka M; Mikami T; Ono T; Nakada K; Hayashi JI
Biochem Biophys Res Commun; 2001 Apr; 282(3):707-11. PubMed ID: 11401519
[TBL] [Abstract][Full Text] [Related]
40. Novel mutation in C10orf2 associated with multiple mtDNA deletions, chronic progressive external ophthalmoplegia and premature aging.
Paramasivam A; Meena AK; Pedaparthi L; Jyothi V; Uppin MS; Jabeen SA; Sundaram C; Thangaraj K
Mitochondrion; 2016 Jan; 26():81-5. PubMed ID: 26689116
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]