Absence of chloride intracellular channel 4 (CLIC4) predisposes to acute kidney injury but has minimal impact on recovery

BMC Nephrology

Volumn 15, Issue 1, 2014, Pages

  Edwards, John C ^a,b   Bruno, Jonathan ^a,b   Key, Phillip ^b   Cheng, Yao Wen ^a  

^a UNIVERSITY OF NORTH CAROLINA SCHOOL OF MEDICINE   (United States)

^b SAINT LOUIS UNIVERSITY SCHOOL OF MEDICINE   (United States)

Author keywords

Acute kidney injury; CLIC4; Glomerular endowment; Peritubular capillary network; Transforming growth factor

Indexed keywords

CHLORIDE CHANNEL; CHLORIDE INTRACELLULAR CHANNEL 4; FOLIC ACID; SMAD2 PROTEIN; SMAD3 PROTEIN; TRANSFORMING GROWTH FACTOR BETA; UNCLASSIFIED DRUG; CLIC4 PROTEIN, HUMAN;

ACUTE KIDNEY FAILURE; ANIMAL EXPERIMENT; ANIMAL MODEL; ARTICLE; CAPILLARY DENSITY; CONTROLLED STUDY; FEMALE; KIDNEY PROXIMAL TUBULE; KIDNEY SIZE; KIDNEY TUMOR; MALE; MOUSE; NONHUMAN; PROTEIN EXPRESSION; PROTEIN PHOSPHORYLATION; PROTEINURIA; UREA NITROGEN BLOOD LEVEL; WESTERN BLOTTING; ACUTE KIDNEY INJURY; ANIMAL; CONVALESCENCE; KIDNEY; KIDNEY TUBULE; KNOCKOUT MOUSE; METABOLISM; PATHOLOGY; PHYSIOLOGY;

ACUTE KIDNEY INJURY; ANIMALS; CHLORIDE CHANNELS; FEMALE; KIDNEY; KIDNEY TUBULES; MALE; MICE; MICE, KNOCKOUT; RECOVERY OF FUNCTION;

EID: 84899060917     PISSN: None     EISSN: 14712369     Source Type: Journal    
DOI: 10.1186/1471-2369-15-54     Document Type: Article

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