Loud and clear evidence for gene silencing by epigenetic mechanisms in autism spectrum and related neurodevelopmental disorders

Clinical Genetics

Volumn 69, Issue 1, 2006, Pages 21-22

  Lopez Rangel, E ^a   Lewis, M E S ^a,b  

^a UNIVERSITY OF BRITISH COLUMBIA   (Canada)

^b The Autism Spectrum Disorders Canadian American Research Consortium (ASD CARC)   (Canada)

Author keywords

[No Author keywords available]

Indexed keywords

4 AMINOBUTYRIC ACID A RECEPTOR; BRAIN DERIVED NEUROTROPHIC FACTOR; CYCLIC AMP RESPONSIVE ELEMENT BINDING PROTEIN BINDING PROTEIN; GENOMIC DNA; HISTONE; HISTONE DEACETYLASE; METHYL CPG BINDING PROTEIN; METHYL CPG BINDING PROTEIN 1; METHYL CPG BINDING PROTEIN 2; METHYL CPG BINDING PROTEIN 3; METHYL CPG BINDING PROTEIN 4; RNA POLYMERASE; TRANSCRIPTION FACTOR; UBIQUITIN PROTEIN LIGASE E3; UNCLASSIFIED DRUG;

ARTICLE; AUTISM; CENTRAL NERVOUS SYSTEM DISEASE; CHROMOSOME 18Q; CHROMOSOME XQ; COGNITIVE DEVELOPMENT; DNA METHYLATION; DNA PROTEIN COMPLEX; DNA SEQUENCE; EPIGENETICS; GENE EXPRESSION REGULATION; GENE MUTATION; GENE REPRESSION; GENE SILENCING; GENETIC TRANSCRIPTION; HAPPY PUPPET SYNDROME; HUMAN; NERVOUS SYSTEM DEVELOPMENT; NONHUMAN; PATHOGENESIS; PRADER WILLI SYNDROME; PRIORITY JOURNAL; PROTEIN MODIFICATION; RETT SYNDROME;

ANGELMAN SYNDROME; AUTISTIC DISORDER; CHILD; CHILD DEVELOPMENT DISORDERS, PERVASIVE; EPIGENESIS, GENETIC; GENE SILENCING; HUMANS; METHYL-CPG-BINDING PROTEIN 2; MODELS, BIOLOGICAL; RETT SYNDROME;

EID: 33644856313     PISSN: 00099163     EISSN: 13990004     Source Type: Journal    
DOI: 10.1111/j.1399-0004.2006.00543a.x     Document Type: Article

References (0)