Neutral amino acid transport in epithelial cells and its malfunction in Hartnup disorder

Biochemical Society Transactions

Volumn 33, Issue 1, 2005, Pages 233-236

  Broer S ^a   Cavanaugh, J A ^b   Rasko, J E J ^c  

^a AUSTRALIAN NATIONAL UNIVERSITY   (Australia)

^b CANBERRA HOSPITAL   (Australia)

^c ROYAL PRINCE ALFRED HOSPITAL   (Australia)

Author keywords

Amino acid transport; Hartnup disorder; SLC6A19; System B0; System NBB

Indexed keywords

AMINO ACID TRANSPORTER; CARRIER PROTEIN; CHLORIDE ION; PROTEIN BOAT1; PROTEIN SLC6A19; SODIUM ION; UNCLASSIFIED DRUG;

ALLELE; AMINO ACID TRANSPORT; AUSTRALIA; AUTOSOMAL RECESSIVE DISORDER; CEREBELLAR ATAXIA; CHROMOSOME 5P; CLINICAL FEATURE; CONFERENCE PAPER; ELECTROPHYSIOLOGY; EPITHELIUM CELL; FAMILY; GENE IDENTIFICATION; GENE LOCUS; GENE MAPPING; HARTNUP DISEASE; HOMOZYGOSITY; HUMAN; IN SITU HYBRIDIZATION; IN VITRO STUDY; INTESTINE CELL; JAPAN; KIDNEY CELL; NEUROLOGIC DISEASE; PEDIGREE; PELLAGRA; PHOTOSENSITIVITY DISORDER; PRIORITY JOURNAL; PROTEIN DIET; PROTEIN EXPRESSION; RASH; SKIN; WILD TYPE;

AMINO ACID SEQUENCE; AMINO ACIDS; ANIMALS; BIOLOGICAL TRANSPORT; EPITHELIAL CELLS; GASTROINTESTINAL TRACT; HARTNUP DISEASE; HUMANS; KIDNEY; MICE; MOLECULAR SEQUENCE DATA;

EID: 14644386887     PISSN: 03005127     EISSN: None     Source Type: Journal    
DOI: 10.1042/BST0330233     Document Type: Conference Paper

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