Genetic Analysis of Disheveled 2 and Disheveled 3 in Human Neural Tube Defects

Journal of Molecular Neuroscience

Volumn 49, Issue 3, 2013, Pages 582-588

  De Marco, Patrizia ^a   Merello, Elisa ^a   Consales, Alessandro ^a   Piatelli, Gianluca ^a   Cama, Armando ^a   Kibar, Zoha ^b   Capra, Valeria ^a  

^a G GASLINI INSTITUTE   (Italy)

^b UNIVERSITY OF MONTREAL   (Canada)

Author keywords

Disheveled (Dvl); Mouse models; Neural tube defects (NTDs); Planar cell polarity (PCP) pathway

Indexed keywords

DISHEVELLED 2; DISHEVELLED 3; GENOMIC DNA; PHOSPHOPROTEIN; UNCLASSIFIED DRUG; CADHERIN; CARRIER PROTEIN; CELSR1 CADHERIN, HUMAN; DISHEVELLED PROTEINS; MEMBRANE PROTEIN; SIGNAL PEPTIDE; SIGNAL TRANSDUCING ADAPTOR PROTEIN; VANGL1 PROTEIN, HUMAN; VANGL2 PROTEIN, HUMAN;

AGENESIS; ANIMAL EXPERIMENT; ANIMAL MODEL; ARTICLE; CELL POLARITY; CONTROLLED STUDY; EXON; FAMILY HISTORY; GENE INACTIVATION; GENE INSERTION; GENE INTERACTION; GENETIC ANALYSIS; GENOTYPE; HUMAN; HUMAN CELL; MAJOR CLINICAL STUDY; MISSENSE MUTATION; MOUSE; NEURAL TUBE DEFECT; NEURULATION; NONHUMAN; NUCLEOTIDE SEQUENCE; ORTHOLOGY; RISK FACTOR; SPINAL DYSRAPHISM; STOP CODON; WNT SIGNALING PATHWAY; AMINO ACID SUBSTITUTION; CHEMISTRY; DNA SEQUENCE; ETHNIC GROUP; FEMALE; GENE EXPRESSION REGULATION; GENETICS; MALE; PHYSIOLOGY; POINT MUTATION; SIGNAL TRANSDUCTION;

ANIMALIA;

ADAPTOR PROTEINS, SIGNAL TRANSDUCING; AMINO ACID SUBSTITUTION; CADHERINS; CARRIER PROTEINS; CELL POLARITY; CODON, NONSENSE; ETHNIC GROUPS; EXONS; FEMALE; GENOTYPE; HUMANS; INTRACELLULAR SIGNALING PEPTIDES AND PROTEINS; MALE; MEMBRANE PROTEINS; MUTAGENESIS, INSERTIONAL; MUTATION, MISSENSE; NEURAL TUBE DEFECTS; PHOSPHOPROTEINS; POINT MUTATION; SEQUENCE ANALYSIS, DNA; SIGNAL TRANSDUCTION; WNT SIGNALING PATHWAY;

MLCS; MLOWN;

EID: 84880330899     PISSN: 08958696     EISSN: 15591166     Source Type: Journal    
DOI: 10.1007/s12031-012-9871-9     Document Type: Article

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