The effects of neurological disorder-related codon variations of ABCA13 on the function of the ABC protein

Bioscience, Biotechnology and Biochemistry

Volumn 76, Issue 12, 2012, Pages 2289-2293

  Tomioka, Maiko ^a   Toda, Yoshinobu ^b   Kurisu, Junko ^a   Kimura, Yasuhisa ^c   Kengaku, Mineko ^a   Ueda, Kazumitsu ^a,c  

^a KYOTO UNIVERSITY   (Japan)

^b TENRI HEALTH CARE UNIVERSITY   (Japan)

^c KYOTO UNIVERSITY   (Japan)

Author keywords

ABC protein; ATP binding cassette protein A13 (ABCA13); Neurological disorders; Neurons; Single nucleotide polymorphisms (SNPs)

Indexed keywords

APOLIPOPROTEIN A-I (APOA-I); ATP-BINDING CASSETTE; CEREBRAL CORTEX; CHOLESTEROL EFFLUX; NEUROLOGICAL DISORDERS; PHYSIOLOGICAL FUNCTIONS; SINGLE NUCLEOTIDE POLYMORPHISMS;

NEUROLOGY; NEURONS; NUCLEOTIDES;

PROTEINS;

ABC TRANSPORTER; ABCA13 PROTEIN, MOUSE; APOLIPOPROTEIN A1; CHOLESTEROL; NUCLEOTIDE;

AMINO ACID SEQUENCE; ANIMAL; ARTICLE; CELL MEMBRANE; CELL STRAIN HEK293; CHEMICAL STRUCTURE; CHEMISTRY; CODON; GENE EXPRESSION REGULATION; GENETICS; HUMAN; METABOLISM; MOLECULAR GENETICS; MOUSE; MUTATION; NEUROLOGIC DISEASE; PROTEIN TERTIARY STRUCTURE; SINGLE NUCLEOTIDE POLYMORPHISM;

AMINO ACID SEQUENCE; ANIMALS; APOLIPOPROTEIN A-I; ATP-BINDING CASSETTE TRANSPORTERS; CELL MEMBRANE; CHOLESTEROL; CODON; GENE EXPRESSION REGULATION; HEK293 CELLS; HUMANS; MICE; MODELS, MOLECULAR; MOLECULAR SEQUENCE DATA; MUTATION; NERVOUS SYSTEM DISEASES; NUCLEOTIDES; POLYMORPHISM, SINGLE NUCLEOTIDE; PROTEIN STRUCTURE, TERTIARY;

EID: 84871632788     PISSN: 09168451     EISSN: 13476947     Source Type: Journal    
DOI: 10.1271/bbb.120563     Document Type: Article

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