An update to the list of mouse mutants with neural tube closure defects and advances toward a complete genetic perspective of neural tube closure

Birth Defects Research Part A - Clinical and Molecular Teratology

Volumn 88, Issue 8, 2010, Pages 653-669

  Harris, Muriel J ^a   Juriloff, Diana M ^a  

^a UNIVERSITY OF BRITISH COLUMBIA   (Canada)

Author keywords

Craniorachischisis; Exencephaly; Mouse model; Neural tube defect; Spina bifida

Indexed keywords

INOSITOL; PROTEINASE ACTIVATED RECEPTOR;

ANENCEPHALUS; BIOCHEMICAL COMPOSITION; CELL FUNCTION; CHROMATIN; ENCEPHALOCELE; EPIGENETICS; EXENCEPHALY; FOLATE METABOLISM; GENE; GENE EXPRESSION; GENE FUNCTION; GENE MUTATION; GENETIC ASSOCIATION; GENETIC RISK; GESTATIONAL AGE; HUMAN; MATERNAL NUTRITION; MOUSE MUTANT; NEURAL TUBE DEFECT; NONHUMAN; PRIORITY JOURNAL; REVIEW; SPINA BIFIDA; VITAMIN SUPPLEMENTATION;

ANIMALS; CILIARY MOTILITY DISORDERS; DISEASE MODELS, ANIMAL; EPIGENOMICS; FEMALE; FOLIC ACID; HUMANS; INOSITOL; MALE; MICE; MICE, MUTANT STRAINS; MUTATION; NEURAL CREST; NEURAL TUBE DEFECTS; RECEPTORS, PROTEINASE-ACTIVATED;

EID: 77955649698     PISSN: 15420752     EISSN: 15420760     Source Type: Journal    
DOI: 10.1002/bdra.20676     Document Type: Review

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