Protein kinase G oxidation is a major cause of injury during sepsis

Proceedings of the National Academy of Sciences of the United States of America

Volumn 110, Issue 24, 2013, Pages 9909-9913

  Rudyk, Olena ^a   Phinikaridou, Alkystis ^a   Prysyazhna, Oleksandra ^a   Burgoyne, Joseph R ^a   Botnar, René M ^a   Eaton, Philip ^a  

^a ST THOMAS HOSPITAL   (United Kingdom)

Author keywords

Cardiovascular function; Endotoxin; Redox

Indexed keywords

CYCLIC GMP DEPENDENT PROTEIN KINASE; CYCLIC GMP DEPENDENT PROTEIN KINASE 1;

ANIMAL EXPERIMENT; ANIMAL MODEL; ARTICLE; BLOOD VESSEL PERMEABILITY; CONTROLLED STUDY; ENZYME ACTIVATION; ENZYME METABOLISM; HEART OUTPUT; INJURY; MOUSE; NONHUMAN; OXIDATIVE STRESS; PRIORITY JOURNAL; SEPSIS; VASODILATATION;

CARDIOVASCULAR FUNCTION; ENDOTOXIN; REDOX;

AMINO ACID SUBSTITUTION; ANIMALS; CYCLIC GMP-DEPENDENT PROTEIN KINASE TYPE I; ENZYME ACTIVATION; HYPOTENSION; IMMUNOBLOTTING; L-LACTATE DEHYDROGENASE; MICE; MICE, INBRED C57BL; MICE, TRANSGENIC; MULTIPLE ORGAN FAILURE; OXIDATION-REDUCTION; SEPSIS;

MUS;

EID: 84878990819     PISSN: 00278424     EISSN: 10916490     Source Type: Journal    
DOI: 10.1073/pnas.1301026110     Document Type: Article

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