نتایج جستجو برای: mitochondrial deletions

تعداد نتایج: 150658  

Journal: :Journal of clinical pathology 1998
S S Papiha H Rathod I Briceno J Pooley H K Datta

BACKGROUND It has been suggested that the accumulation of damage to mitochondrial DNA is a major cause of age related, degenerative disease. Aging is known to cause bone loss leading to a fall in bone mineral density and disruption of bone microarchitecture. However, despite the evidence of age related bone loss, no attempt has been made to detect specific deletions of mitochondrial DNA in the ...

Journal: :Brain : a journal of neurology 2012
Dario Ronchi Caterina Garone Andreina Bordoni Purificacion Gutierrez Rios Sarah E Calvo Michela Ripolone Michela Ranieri Mafalda Rizzuti Luisa Villa Francesca Magri Stefania Corti Nereo Bresolin Vamsi K Mootha Maurizio Moggio Salvatore DiMauro Giacomo P Comi Monica Sciacco

The molecular diagnosis of mitochondrial disorders still remains elusive in a large proportion of patients, but advances in next generation sequencing are significantly improving our chances to detect mutations even in sporadic patients. Syndromes associated with mitochondrial DNA multiple deletions are caused by different molecular defects resulting in a wide spectrum of predominantly adult-on...

Journal: :Trends in genetics : TIG 2010
Xinhong Guo Konstantin Yu Popadin Natalya Markuzon Yuriy L Orlov Yevgenya Kraytsberg Kim J Krishnan Gábor Zsurka Douglas M Turnbull Wolfram S Kunz Konstantin Khrapko

Perfect direct repeats and, in particular, the prominent 13 bp repeat, are thought to cause mitochondrial DNA (mtDNA) deletions, which have been associated with the aging process. Accordingly, individuals lacking the 13 bp repeat are highly prevalent among centenarians and overall number of perfect repeats in mammalian mitochondrial genomes negatively correlates with species' longevity. However...

Journal: :Genetics 2012
Lidza Kalifa Daniel F Quintana Laura K Schiraldi Naina Phadnis Garry L Coles Rey A Sia Elaine A Sia

Mitochondrial DNA (mtDNA) deletions are associated with sporadic and inherited diseases and age-associated neurodegenerative disorders. Approximately 85% of mtDNA deletions identified in humans are flanked by short directly repeated sequences; however, mechanisms by which these deletions arise are unknown. A limitation in deciphering these mechanisms is the essential nature of the mitochondrial...

Journal: :genetics in the 3rd millennium 0
حسن حسنی کومله hassan hassani kumleh national institute for genetic engineering and biotechnology, tehran, iran غلام حسین ریاضی gholam hossein riazi national institute for genetic engineering and biotechnology, tehran, iran مسعود هوشمند massoud houshmand national institute for genetic engineering and biotechnology, tehran, iran محمد حسین صنعتی mohammad hossein sanati national institute for genetic engineering and biotechnology, tehran, iran کوروش قره گوزلو kourosh gharagozli national institute for genetic engineering and biotechnology, tehran, iran مهدی شفا شریعت پناه mehdi shafa shariat panahi national institute for genetic engineering and biotechnology, tehran, iran

multiple sclerosis (ms) is a demyelinating disease of the central nervous system characterized by morphological hallmarks of inflammation, demyelination and axonal loss. to date, little attention has been paid to the contribution of mitochondrial respiratory chain enzyme activities to ms. in this study, kinetic analysis of mitochondrial respiratory chain complex i enzyme (measured as nadh ferri...

2016
Karolina A. Rygiel Helen A. Tuppen John P. Grady Amy Vincent Emma L. Blakely Amy K. Reeve Robert W. Taylor Martin Picard James Miller Doug M. Turnbull

Mitochondrial DNA (mtDNA) rearrangements are an important cause of mitochondrial disease and age related mitochondrial dysfunction in tissues including brain and skeletal muscle. It is known that different mtDNA deletions accumulate in single cells, but the detailed nature of these rearrangements is still unknown. To evaluate this we used a complementary set of sensitive assays to explore the m...

2013
Graham R Campbell Amy K Reeve Iryna Ziabreva Richard Reynolds Doug M Turnbull Don J Mahad

BACKGROUND Mitochondrial dysfunction is an established feature of multiple sclerosis (MS). We recently described high levels of mitochondrial DNA (mtDNA) deletions within respiratory enzyme-deficient (lacking mitochondrial respiratory chain complex IV with intact complex II) neurons and choroid plexus epithelial cells in progressive MS. OBJECTIVES The objective of this paper is to determine w...

Journal: :Molecular biology and evolution 1994
N Saitou S Ueda

Insertions and deletions are responsible for gaps in aligned nucleotide sequences, but they have been usually ignored when the number of nucleotide substitutions was estimated. We compared six sets of nuclear and mitochondrial noncoding DNA sequences of primates and obtained the estimates of the evolutionary rate of insertion and deletion. The maximum-parsimony principle was applied to locate i...

Journal: :Human molecular genetics 2004
Yutaka Nishigaki Ramon Marti Michio Hirano

Mitochondrial neurogastrointestinal encephalomyopathy (MNGIE) is an autosomal recessive multisystem disorder associated with depletion, multiple deletions and site-specific point mutations of mitochondrial DNA (mtDNA). MNGIE is caused by loss-of-function mutations in the gene encoding thymidine phosphorylase (TP; endothelial cell growth factor 1). Deficiency of TP leads to dramatically elevated...

نمودار تعداد نتایج جستجو در هر سال

با کلیک روی نمودار نتایج را به سال انتشار فیلتر کنید