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Items: 1 to 20 of 231

1.

Evidence that specific mtDNA point mutations may not accumulate in skeletal muscle during normal human aging.

Pallotti F, Chen X, Bonilla E, Schon EA.

Am J Hum Genet. 1996 Sep;59(3):591-602.

2.

Differential occurrence of mutations in mitochondrial DNA of human skeletal muscle during aging.

Zhang C, Liu VW, Addessi CL, Sheffield DA, Linnane AW, Nagley P.

Hum Mutat. 1998;11(5):360-71. Erratum in: Hum Mutat 1998;12(1):69.

PMID:
9600454
3.

Oxidative phosphorylation dysfunction does not increase the rate of accumulation of age-related mtDNA deletions in skeletal muscle.

Tengan CH, Gabbai AA, Shanske S, Zeviani M, Moraes CT.

Mutat Res. 1997 Sep 5;379(1):1-11.

PMID:
9330617
4.

Lack of age-related increase of mitochondrial DNA amount in brain, skeletal muscle and human heart.

Frahm T, Mohamed SA, Bruse P, Gemünd C, Oehmichen M, Meissner C.

Mech Ageing Dev. 2005 Nov;126(11):1192-200.

PMID:
16099018
5.
6.

MtDNA mutations in aging and apoptosis.

Chomyn A, Attardi G.

Biochem Biophys Res Commun. 2003 May 9;304(3):519-29. Review.

PMID:
12729587
7.

Concerted action of two novel tRNA mtDNA point mutations in chronic progressive external ophthalmoplegia.

Kornblum C, Zsurka G, Wiesner RJ, Schröder R, Kunz WS.

Biosci Rep. 2008 Apr;28(2):89-96. doi: 10.1042/BSR20080004.

PMID:
18384291
8.

Age-related mitochondrial genotypic and phenotypic alterations in human skeletal muscle.

Pesce V, Cormio A, Fracasso F, Vecchiet J, Felzani G, Lezza AM, Cantatore P, Gadaleta MN.

Free Radic Biol Med. 2001 Jun 1;30(11):1223-33.

PMID:
11368920
9.

Accumulation of the common mitochondrial DNA deletion induced by ionizing radiation.

Prithivirajsingh S, Story MD, Bergh SA, Geara FB, Ang KK, Ismail SM, Stevens CW, Buchholz TA, Brock WA.

FEBS Lett. 2004 Jul 30;571(1-3):227-32.

10.

Point mutations of the mtDNA control region in normal and neurodegenerative human brains.

Chinnery PF, Taylor GA, Howell N, Brown DT, Parsons TJ, Turnbull DM.

Am J Hum Genet. 2001 Feb;68(2):529-32. Epub 2000 Dec 21.

11.

Mitochondrial DNA damage in lymphocytes: a role in immunosenescence?

Ross OA, Hyland P, Curran MD, McIlhatton BP, Wikby A, Johansson B, Tompa A, Pawelec G, Barnett CR, Middleton D, Barnett YA.

Exp Gerontol. 2002 Jan-Mar;37(2-3):329-40.

PMID:
11772520
12.

Quantitative PCR analysis of mitochondrial DNA content in patients with mitochondrial disease.

Bai RK, Perng CL, Hsu CH, Wong LJ.

Ann N Y Acad Sci. 2004 Apr;1011:304-9.

PMID:
15126306
13.

Age-dependent 6kb deletion in human liver mitochondrial DNA.

Yen TC, Pang CY, Hsieh RH, Su CH, King KL, Wei YH.

Biochem Int. 1992 Mar;26(3):457-68.

PMID:
1627156
14.

Mutations in the cardiac mitochondrial DNA control region associated with cardiomyopathy and aging.

Marín-García J, Zoubenko O, Goldenthal MJ.

J Card Fail. 2002 Apr;8(2):93-100.

PMID:
12016633
16.

Defects of the respiratory chain in the normal human liver and in cirrhosis during aging.

Müller-Höcker J, Aust D, Rohrbach H, Napiwotzky J, Reith A, Link TA, Seibel P, Hölzel D, Kadenbach B.

Hepatology. 1997 Sep;26(3):709-19.

PMID:
9303502
17.

Mitochondrial DNA mutations as a fundamental mechanism in physiological declines associated with aging.

Pak JW, Herbst A, Bua E, Gokey N, McKenzie D, Aiken JM.

Aging Cell. 2003 Feb;2(1):1-7.

PMID:
12882328
18.

[Mitochondrial DNA mutation analysis in 97 Chinese patients with mitochondrial cephalomyopathy].

Wang ZX, Luan XH, Zhang Y, Yang YL, Qi Y, Bu DF, Yuan Y.

Zhonghua Yi Xue Za Zhi. 2008 Dec 16;88(46):3254-6. Chinese.

PMID:
19159548
19.

Accumulation of deletions in MtDNA during tissue aging: analysis by long PCR.

Reynier P, Malthiery Y.

Biochem Biophys Res Commun. 1995 Dec 5;217(1):59-67.

PMID:
8526940
20.

Role of mitochondrial DNA mutations in human aging: implications for the central nervous system and muscle.

Brierley EJ, Johnson MA, Lightowlers RN, James OF, Turnbull DM.

Ann Neurol. 1998 Feb;43(2):217-23.

PMID:
9485063

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