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dihydrolipoamide

 
National Institutes of Health

Papers overview

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Review
2019
Review
2019
ABSTRACT Mitophagy is a vital form of autophagy for selective removal of dysfunctional or redundant mitochondria. Accumulating… Expand
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Highly Cited
2007
Highly Cited
2007
ABSTRACT To add new insight to our previous work on the molecular epidemiology of Bordetella pertussis in Argentina, the prn and… Expand
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Highly Cited
2005
Highly Cited
2005
Pyruvate dehydrogenase deficiency is a major cause of primary lactic acidosis and neurological dysfunction in infancy and early… Expand
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Highly Cited
1997
Highly Cited
1997
The term congenital lactic acidosis (CLA) refers to a group of inborn errors of mitochondrial metabolism variably characterised… Expand
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Review
1990
Review
1990
  • M. Patel, T. Roche
  • FASEB journal : official publication of the…
  • 1990
  • Corpus ID: 8112416
In most organisms, the pyruvate dehydrogenase complex catalyzes the pivotal irreversible reaction that leads to the consumption… Expand
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Highly Cited
1989
Highly Cited
1989
Antimitochondrial autoantibodies are characteristically present in sera of patients with primary biliary cirrhosis. The… Expand
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Highly Cited
1989
Highly Cited
1989
The availability of recombinant mitochondrial autoantigens may permit the experimental study of the pathophysiology of primary… Expand
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Highly Cited
1988
Highly Cited
1988
Autoantibodies against mitochondria occur in the sera of patients with primary biliary cirrhosis (PBC) with characteristic… Expand
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Highly Cited
1988
Highly Cited
1988
Autoantibodies to mitochondrial antigens are characteristic of the autoimmune liver disease primary biliary cirrhosis (PBC), but… Expand
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Highly Cited
1988
Highly Cited
1988
Primary biliary cirrhosis is a chronic, destructive autoimmune liver disease of humans. Patient sera are characterized by a high… Expand
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