The role of the neutral amino acid transporter B0AT1 (SLC6A19) in hartnup disorder and protein nutrition

IUBMB Life

Volumn 61, Issue 6, 2009, Pages 591-599

  Bröer, Stefan ^a  

^a AUSTRALIAN NATIONAL UNIVERSITY   (Australia)

Author keywords

Aminoaciduria; Angiotensin converting enzyme; Epithelial cells

Indexed keywords

AMINO ACID TRANSPORTER; ANGIOTENSIN CONVERTING ENZYME 2; PROTEIN SLCA19; UNCLASSIFIED DRUG; DIPEPTIDYL CARBOXYPEPTIDASE; MEMBRANE PROTEIN; SLC6A19 PROTEIN, HUMAN; TMEM27 PROTEIN, MOUSE;

GENE EXPRESSION; GENE IDENTIFICATION; GENE INTERACTION; GENE MUTATION; GENETIC ANALYSIS; HARTNUP DISEASE; HUMAN; KIDNEY CLEARANCE; MULTIGENE FAMILY; NONHUMAN; PROTEIN INTAKE; REVIEW; AMINO ACID SEQUENCE; ANIMAL; GENETICS; MOUSE; PATHOPHYSIOLOGY; PHYSIOLOGY;

AMINO ACID SEQUENCE; AMINO ACID TRANSPORT SYSTEMS, NEUTRAL; ANIMALS; HARTNUP DISEASE; HUMANS; MEMBRANE GLYCOPROTEINS; MICE; PEPTIDYL-DIPEPTIDASE A;

EID: 69449090536     PISSN: 15216543     EISSN: 15216551     Source Type: Journal    
DOI: 10.1002/iub.210     Document Type: Review

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