Calpain mediates ischemic injury of the liver through modulation of apoptosis and necrosis.

No abstract is available for this paper.

• Publication year

  1999

• Venue

  Gastroenterology

• Publication date

  Unknown publication date

• Fields of study

  Biology, Medicine

• Identifiers
  DOI 10.1016/S0016-5085(99)70241-6PMID 9869615
• External record

  Open on Semantic Scholar

• Source metadata

  Semantic Scholar, PubMed

• No claims are published for this paper.

• No concepts are published for this paper.

• Hydrogen peroxide derived from hepatocytes induces sinusoidal endothelial cell apoptosis in perfused hypoxic rat liver.

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• L-selectin and ICAM-1 mediate reperfusion injury and neutrophil adhesion in the warm ischemic mouse liver.

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• Sinusoidal endothelial cell injury during hepatic preservation and reperfusion

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• Prevention of Apoptosis by Bcl-2: Release of Cytochrome c from Mitochondria Blocked

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• Enhanced liver calpain protease activity is a risk factor for dysfunction of human liver allografts.

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• The Release of Cytochrome c from Mitochondria: A Primary Site for Bcl-2 Regulation of Apoptosis

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  1997cited by this paper
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• Apoptosis in the failing human heart.

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• A Combinatorial Approach Defines Specificities of Members of the Caspase Family and Granzyme B

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• Mitochondrial permeability transition triggers lymphocyte apoptosis.

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• PKC inhibitors prevent endothelial dysfunction after myocardial ischemia-reperfusion in rats.

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• Calpain Inhibitor AK295 Protects Neurons From Focal Brain Ischemia: Effects of Postocdusion Intra-arterial Administration

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• Reperfusion injury induces apoptosis in rabbit cardiomyocytes.

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• pH-dependent nonlysosomal proteolysis contributes to lethal anoxic injury of rat hepatocytes.

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• Evidence that activation of platelet calpain is induced as a consequence of binding of adhesive ligand to the integrin, glycoprotein IIb-IIIa

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• Phagocyte recognition of cells undergoing apoptosis.

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• Cyclosporin and carnitine prevent the anoxic death of cultured hepatocytes by inhibiting the mitochondrial permeability transition.

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