MELAS gene

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

Topic mentions per year

Topic mentions per year

1987-2017
01219872017

Papers overview

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Review
2014
Review
2014
BACKGROUND The pathophysiology of hypertension in patients with mitochondrial diseases is different from that of the general… (More)
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2013
2013
Mitochondrial DNA (mtDNA) content is thought to remain stable over the preimplantation period of human embryogenesis that is… (More)
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2011
2011
Mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episodes (MELAS) is a mitochondrial disease most usually caused… (More)
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2008
2008
We find explicitly the Bellman function for the dyadic maximal operator on L as the solution of a Bellman PDE of Monge–Ampère… (More)
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2002
2002
BACKGROUND Most pathogenic human mitochondrial DNA (mtDNA) mutations are heteroplasmic (i.e., mutant and wild-type mtDNA coexist… (More)
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2001
2001
The effect of zooprophylaxis on malaria transmission has not been studied on the African continent despite that the World Health… (More)
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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… (More)
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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… (More)
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1988
1988
Two patients are reported with mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes in whom CT… (More)
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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… (More)
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