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MELAS gene

Known as: MELAS, mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episodes 
 
National Institutes of Health

Papers overview

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2017
2017
The cell penetrating peptide, Pep-1, has been shown to facilitate cellular uptake of foreign mitochondria but further research is… Expand
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2015
2015
Abstract MELAS syndrome is a mitochondrial disorder that is caused mainly by the m.3243A > G mutation in mitochondrial DNA. Here… Expand
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Highly Cited
2013
Highly Cited
2013
Mitochondrial DNA (mtDNA) content is thought to remain stable over the preimplantation period of human embryogenesis that is… Expand
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Highly Cited
2011
Highly Cited
2011
Mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episodes (MELAS) is a mitochondrial disease most usually caused… Expand
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Highly Cited
2008
Highly Cited
2008
Abstract We find explicitly the Bellman function for the dyadic maximal operator on L p as the solution of a Bellman partial… Expand
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2002
2002
BACKGROUND Most pathogenic human mitochondrial DNA (mtDNA) mutations are heteroplasmic (i.e., mutant and wild-type mtDNA coexist… Expand
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1999
1999
In this article An. melas infestation rate for P. falciparum is compared to the rate of An. gambiae in the coastal and lagoon… Expand
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1995
1995
INTRODUCTION MELAS is most often due to an mentally transmitted A-G transition mutation of mitochondrial DNA (mtDNA) at position… Expand
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1988
1988
Two patients are reported with mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes in whom CT… Expand
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1987
1987
Polytene chromosome studies on the member species of the Anopheles gambiae complex in The Gambia and surrounding areas in Senegal… Expand
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