Gene deletion mutants reveal a role for semaphorin receptors of the plexin-B family in mechanisms underlying corticogenesis

Molecular and Cellular Biology

Volumn 30, Issue 3, 2010, Pages 764-780

  Hirschberg, A ^a   Deng, S ^a   Korostylev, A ^a   Paldy, E ^a   Costa, M R ^b   Worzfeld, T ^a   Vodrazka, P ^a   Wizenmann, A ^b   Gotz M ^b   Offermanns, S ^a   Kuner, R ^a  

^a UNIVERSITY OF HEIDELBERG   (Germany)

^b INSTITUTE OF EPIDEMIOLOGY   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

4 AMINOBUTYRIC ACID RECEPTOR; PLEXIN; PLEXIN B1; PLEXIN B2; PROTEIN RECEPTOR; SEMAPHORIN; SEMAPHORIN 4D; SEMAPHORIN RECEPTOR; UNCLASSIFIED DRUG;

ANIMAL CELL; ANIMAL EXPERIMENT; ANIMAL MODEL; ANIMAL TISSUE; ARTICLE; BRAIN CORTEX; BRAIN DEVELOPMENT; BRAIN NERVE CELL; CELL DIFFERENTIATION; CELL MATURATION; CELL MIGRATION; CONTROLLED STUDY; EMBRYO; EX VIVO STUDY; FEMALE; FOREBRAIN; GENE DELETION; GENE EXPRESSION PROFILING; IN VIVO STUDY; INTERNEURON; MOUSE; NEOCORTEX; NONHUMAN; PRIORITY JOURNAL; PROTEIN DEFICIENCY; PROTEIN FUNCTION; PROTEIN PROTEIN INTERACTION; PROTOPLASMATIC ASTROCYTE; SIGNAL TRANSDUCTION;

ANIMALS; CELL MOVEMENT; GENE EXPRESSION REGULATION, DEVELOPMENTAL; MICE; MICE, KNOCKOUT; MUTATION; NEOCORTEX; NERVE TISSUE PROTEINS; NEURONS; RECEPTORS, CELL SURFACE; SEMAPHORINS; SEQUENCE DELETION;

MURINAE; MUS;

EID: 75149162590     PISSN: 02707306     EISSN: None     Source Type: Journal    
DOI: 10.1128/MCB.01458-09     Document Type: Article

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