Chromosome 15q11-13 abnormalities and other medical conditions in individuals with autism spectrum disorders
about
Mutation analysis of the NSD1 gene in patients with autism spectrum disorders and macrocephalyAbnormal behavior in a chromosome-engineered mouse model for human 15q11-13 duplication seen in autismMultiple rare variants in the etiology of autism spectrum disordersRapid birth-and-death evolution of imprinted snoRNAs in the Prader-Willi syndrome locus: implications for neural development in EuarchontogliresSNOntology: Myriads of novel snoRNAs or just a mirage?Annual Research Review: Transgenic mouse models of childhood-onset psychiatric disorders.Perinatal exposure to a noncoplanar polychlorinated biphenyl alters tonotopy, receptive fields, and plasticity in rat primary auditory cortexTransmission disequilibrium testing of the chromosome 15q11-q13 region in autismAnimal models of psychiatric disorders that reflect human copy number variation.A single-tube quantitative high-resolution melting curve method for parent-of-origin determination of 15q duplications.Increased CYFIP1 dosage alters cellular and dendritic morphology and dysregulates mTORThe neurobiology of mouse models syntenic to human chromosome 15q.Paternal sperm DNA methylation associated with early signs of autism risk in an autism-enriched cohortSignificant neuronal soma volume deficit in the limbic system in subjects with 15q11.2-q13 duplicationsRegulatory RNAs in brain function and disorders.Differences between the pattern of developmental abnormalities in autism associated with duplications 15q11.2-q13 and idiopathic autism.Identification of a distinct developmental and behavioral profile in children with Dup15q syndromeExpression of the Rho-GEF Pbl/ECT2 is regulated by the UBE3A E3 ubiquitin ligaseThe interstitial duplication 15q11.2-q13 syndrome includes autism, mild facial anomalies and a characteristic EEG signature.Medical conditions in autism spectrum disordersA neuropsychological assessment of frontal cognitive functions in Prader-Willi syndrome.The complex genetics in autism spectrum disorders.In vivo and in vitro disease modeling with CRISPR/Cas9.Repetitive behavior profiles: Consistency across autism spectrum disorder cohorts and divergence from Prader-Willi syndrome.Skeletal Site-specific Changes in Bone Mass in a Genetic Mouse Model for Human 15q11-13 Duplication Seen in Autism.The pathophysiology of restricted repetitive behavior.A complex chromosomal rearrangement involving chromosomes 2, 5, and X in autism spectrum disorder.The Emerging Field of Epitranscriptomics in Neurodevelopmental and Neuronal Disorders.
P2860
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P2860
Chromosome 15q11-13 abnormalities and other medical conditions in individuals with autism spectrum disorders
description
2004 nî lūn-bûn
@nan
2004 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած
@hyw
2004 թվականի սեպտեմբերին հրատարակված գիտական հոդված
@hy
2004年の論文
@ja
2004年論文
@yue
2004年論文
@zh-hant
2004年論文
@zh-hk
2004年論文
@zh-mo
2004年論文
@zh-tw
2004年论文
@wuu
name
Chromosome 15q11-13 abnormalit ...... with autism spectrum disorders
@ast
Chromosome 15q11-13 abnormalit ...... with autism spectrum disorders
@en
Chromosome 15q11-13 abnormalit ...... with autism spectrum disorders
@nl
type
label
Chromosome 15q11-13 abnormalit ...... with autism spectrum disorders
@ast
Chromosome 15q11-13 abnormalit ...... with autism spectrum disorders
@en
Chromosome 15q11-13 abnormalit ...... with autism spectrum disorders
@nl
prefLabel
Chromosome 15q11-13 abnormalit ...... with autism spectrum disorders
@ast
Chromosome 15q11-13 abnormalit ...... with autism spectrum disorders
@en
Chromosome 15q11-13 abnormalit ...... with autism spectrum disorders
@nl
P2093
P3181
P1433
P1476
Chromosome 15q11-13 abnormalit ...... with autism spectrum disorders
@en
P2093
Caroline E Browne
Emma Weisblatt
Joanne R Holmes
Josie Brown
Marijcke W M Veltman
N Simon Thomas
Nicholas R Dennis
Patrick F Bolton
Russell J Thompson
Sally Goodson
P3181
P356
10.1097/00041444-200409000-00002
P407
P577
2004-09-01T00:00:00Z