Results 281 to 290 of about 613,759 (317)
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Mitochondrial DNA in Telocytes
2017Telocyte (TC) is a new identified interstitial cell type with a small nuclear and one or several long and thin prolongations with enlargements on them. They were found in many mammals including humans, mouse, rats, dogs, and monkeys and play vital roles in many physiological and pathological conditions.
Dongli, Song +2 more
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MITOCHONDRIAL DNA AND HUMAN EVOLUTION
Annual Review of Genomics and Human Genetics, 2005▪ Abstract  Several unique properties of human mitochondrial DNA (mtDNA), including its high copy number, maternal inheritance, lack of recombination, and high mutation rate, have made it the molecule of choice for studies of human population history and evolution.
Pakendorf, Brigitte, Stoneking, Mark
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Paternal Inheritance of Mitochondrial DNA
New England Journal of Medicine, 2002This report describes a 28-year-old man with lifelong exercise intolerance. Evaluation revealed a mitochondrial myopathy due to a novel 2-bp mitochondrial DNA deletion in the ND2 gene, which codes for a subunit of enzyme complex I of the mitochondrial respiratory chain.
Marianne, Schwartz, John, Vissing
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Origin And Evolution Of Mitochondrial DNA
Annual Review of Cell and Developmental Biology, 1989Devant la diversite en taille, structure, organisation et mode d'expression du DNA mitochondrial, une mise a jour des dernieres hypotheses sur l'origine et l'evolution de ce genome est ...
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ASTENOZOOSPERMY AND MITOCHONDRIAL DNA
2006Male infertility, inability to fecundate the oocyte, is due to alterations of sperm characteristics (low number, low motility, altered morphology), to the quantity of semen or to the presence of alterations in the male genital line. 75% of infertile men deal with untreatable sub-fertility.
CARRA, Elena +2 more
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Cooperative sensing of mitochondrial DNA by ZBP1 and cGAS promotes cardiotoxicity
Cell, 2023Jingti Deng
exaly
Mitochondrial disease and mitochondrial DNA.
British journal of hospital medicine, 1991In the last decade there have been dramatic advances in the understanding of genetic, biochemical and clinical aspects of disorders of the mitochondrial respiratory chain. Neurological manifestations are prominent although involvement of other systems is increasingly recognized. This article reviews current understanding of mitochondrial disease and in
S R, Hammans, A E, Harding
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