Lissencephaly associated mutations suggest a requirement for the PAFAH1B heterotrimeric complex in brain development

Mechanisms of Development

Volumn 92, Issue 2, 2000, Pages 263-271

  Sweeney, Kimberley J ^a   Clark, Gary D ^b   Prokscha, Alexander ^a   Dobyns, William B ^c   Eichele, Gregor ^a  

^a MAX PLANCK INSTITUTE FOR BIOPHYSICAL CHEMISTRY   (Germany)

^b BAYLOR COLLEGE OF MEDICINE   (United States)

^c UNIVERSITY OF CHICAGO   (United States)

Author keywords

Propeller structure; 29 kDa; 30 kDa; Brain development; Cortical malformation; Heterotrimeric complex; LIS1; Lissencephaly; Miller Dieker syndrome; Mutation; Neuronal migration; PAFAH1B; PAFAH1B1; PAFAH1B2; PAFAH1B3; Platelet activating factor; WD40 repeat protein; Yeast two hybrid

Indexed keywords

1 ALKYL 2 ACETYLGLYCEROPHOSPHOCHOLINE ESTERASE; MUTANT PROTEIN; PROTEIN SUBUNIT;

AGYRIA; ARTICLE; BRAIN DEVELOPMENT; CELL MIGRATION; COMPLEX FORMATION; CONTROLLED STUDY; GENE MUTATION; HUMAN; MILLER DIEKER SYNDROME; NONHUMAN; PRIORITY JOURNAL; PROTEIN ASSEMBLY; PROTEIN PROTEIN INTERACTION;

1-ALKYL-2-ACETYLGLYCEROPHOSPHOCHOLINE ESTERASE; BRAIN; DIMERIZATION; GLUTATHIONE TRANSFERASE; HUMANS; MICROTUBULE-ASSOCIATED PROTEINS; MUTAGENESIS, SITE-DIRECTED; MUTATION; PHOSPHOLIPASES A; RECOMBINANT PROTEINS; REPETITIVE SEQUENCES, AMINO ACID; TWO-HYBRID SYSTEM TECHNIQUES;

ACRONICTA LEPORINA;

EID: 0034176845     PISSN: 09254773     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0925-4773(00)00242-2     Document Type: Article

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