Defects in processing and trafficking of the AE1 Cl-/HCO 3- exchanger associated with inherited distal renal tubular acidosis

Clinical and Experimental Nephrology

Volumn 8, Issue 1, 2004, Pages 1-11

  Shayakul, Chairat ^a   Alper, Seth L ^b  

^a MAHIDOL UNIVERSITY   (Thailand)

^b HARVARD MEDICAL SCHOOL   (United States)

Author keywords

Biogenesis; Chloride bicarbonate exchange; dRTA; Endoplasmic reticulum; Intercalated cell; Ovalocytosis; Spherocytosis

Indexed keywords

ADENOSINE TRIPHOSPHATASE; AMINO ACID DERIVATIVE; BICARBONATE; CHLORIDE; MEMBRANE PROTEIN; POLYPEPTIDE;

AMINO TERMINAL SEQUENCE; AUTOSOMAL RECESSIVE INHERITANCE; CARBOXY TERMINAL SEQUENCE; CELL POLARITY; DIABETES MELLITUS; EPITHELIUM CELL; ERYTHROID CELL; FAMILIAL DISEASE; FIBROSIS; GENE MUTATION; HEREDITARY HEMOLYTIC ANEMIA; HEREDITARY SPHEROCYTOSIS; HUMAN; HYPOKALEMIA; IMMUNOLOGICAL PROCEDURES; ISCHEMIA; KIDNEY CALCIFICATION; KIDNEY DISTAL TUBULE; KIDNEY EPITHELIUM; KIDNEY TUBULE ACIDOSIS; MUSCLE WEAKNESS; PATHOGENESIS; PROTEIN DOMAIN; PROTEIN EXPRESSION; PROTEIN SYNTHESIS; REVIEW; SYSTEMIC LUPUS ERYTHEMATOSUS;

ACIDOSIS, RENAL TUBULAR; AMINO ACID SEQUENCE; ANIMALS; ANION EXCHANGE PROTEIN 1, ERYTHROCYTE; CELL MEMBRANE; GENES, DOMINANT; HUMANS; MEMBRANE PROTEINS; MOLECULAR SEQUENCE DATA; MUTATION; PROTEIN STRUCTURE, TERTIARY; PROTEIN TRANSPORT; SPHEROCYTOSIS, HEREDITARY;

EID: 1942486244     PISSN: 13421751     EISSN: None     Source Type: Journal    
DOI: 10.1007/s10157-003-0271-x     Document Type: Review

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