Cortical dysplasia and skull defects in mice with a Foxc1 allele reveal the role of meningeal differentiation in regulating cortical development

Proceedings of the National Academy of Sciences of the United States of America

Volumn 104, Issue 35, 2007, Pages 14002-14007

  Zarbalis, Konstantinos ^a   Siegenthaler, Julie A ^a   Choe, Youngshik ^a   May, Scott R ^a,b   Peterson, Andrew S ^a,c   Pleasure, Samuel J ^a  

^a UNIVERSITY OF CALIFORNIA   (United States)

^b SALK INSTITUTE FOR BIOLOGICAL STUDIES   (United States)

^c GENENTECH INC   (United States)

Author keywords

Genetic screen; Meninges; Migration

Indexed keywords

LEUCINE; PHENYLALANINE; ETHYLNITROSOUREA; FORKHEAD TRANSCRIPTION FACTOR; FOXC1 PROTEIN, MOUSE; UNCLASSIFIED DRUG;

AGYRIA; ALLELE; AMINO ACID SUBSTITUTION; ANIMAL EXPERIMENT; ANIMAL MODEL; ANIMAL TISSUE; ARACHNOID; ARTICLE; BASEMENT MEMBRANE; BRAIN DEVELOPMENT; CELL MIGRATION; CONTROLLED STUDY; CORTICAL DYSPLASIA; DISEASE SEVERITY; DURA MATER; FOXC1 GENE; GENE; GENE FUNCTION; GENETIC SCREENING; HISTOLOGY; HITH GENE; MENINX; MISSENSE MUTATION; MOUSE; MUSCULAR DYSTROPHY; MUTAGENESIS; NONHUMAN; NUCLEOTIDE SEQUENCE; PIA MATER; PRIORITY JOURNAL; PROTEIN FUNCTION; SKULL DEFECT; AGING; ANIMAL; BRAIN CORTEX; CELL DIFFERENTIATION; CYTOLOGY; GENETICS; GROWTH, DEVELOPMENT AND AGING; NERVE CELL; PATHOLOGY; PHYSIOLOGY; POINT MUTATION;

MUS;

AGING; ANIMALS; CELL DIFFERENTIATION; CEREBRAL CORTEX; ETHYLNITROSOUREA; FORKHEAD TRANSCRIPTION FACTORS; MENINGES; MICE; NEURONS; POINT MUTATION;

EID: 35348924902     PISSN: 00278424     EISSN: None     Source Type: Journal    
DOI: 10.1073/pnas.0702618104     Document Type: Article

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