Disease-associated GPR56 mutations cause bilateral frontoparietal polymicrogyria via multiple mechanisms

Journal of Biological Chemistry

Volumn 286, Issue 16, 2011, Pages 14215-14225

  Chiang, Nien Yi ^a   Hsiao, Cheng Chih ^b   Huang, Yi Shu ^a   Chen, Hsin Yi ^b   Hsieh, I Ju ^a   Chang, Gin Wen ^b   Lin, Hsi Hsien ^b  

^a Graduate Institute of Biomedical Sciences   (Taiwan)

^b CHANG GUNG UNIVERSITY COLLEGE OF MEDICINE   (Taiwan)

Author keywords

[No Author keywords available]

Indexed keywords

BRAIN DEVELOPMENT; CELLULAR FUNCTION; ECTODOMAIN; EXTRACELLULAR LOOPS; EXTRACELLULAR REGION; G PROTEIN COUPLED RECEPTORS; LIPID RAFT; MOLECULAR MECHANISM; NOVEL PROTEINS; RECESSIVE DISORDER; SURFACE RECEPTORS; TRANSMEMBRANES; WILD TYPES;

REDUCTION;

GENE ENCODING;

G PROTEIN COUPLED RECEPTOR; G PROTEIN COUPLED RECEPTOR 56; UNCLASSIFIED DRUG;

ANIMAL CELL; ARTICLE; CONTROLLED STUDY; EMBRYO; FEMALE; FRONTAL LOBE; HUMAN; HUMAN CELL; LIPID RAFT; LOSS OF FUNCTION MUTATION; MICROGYRIA; NONHUMAN; NUCLEOTIDE SEQUENCE; PARIETAL LOBE; POINT MUTATION; PRIORITY JOURNAL; PROTEIN DEGRADATION; PROTEIN EXPRESSION; PROTEIN FUNCTION; PROTEIN LOCALIZATION; PROTEIN PROTEIN INTERACTION; WILD TYPE;

ANIMALS; CHO CELLS; CRICETINAE; CRICETULUS; GLYCOSAMINOGLYCANS; HUMANS; MALFORMATIONS OF CORTICAL DEVELOPMENT; MEMBRANE MICRODOMAINS; MICE; NERVOUS SYSTEM DISEASES; POINT MUTATION; PROTEIN BINDING; RECEPTORS, G-PROTEIN-COUPLED;

EID: 79954610847     PISSN: 00219258     EISSN: 1083351X     Source Type: Journal    
DOI: 10.1074/jbc.M110.183830     Document Type: Article

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