Autism and multiple exostoses associated with an X;8 translocation occurring within the GRPR gene and 3' to the SDC2 gene.
about
Autism-like socio-communicative deficits and stereotypies in mice lacking heparan sulfateChromosomal basis of X chromosome inactivation: identification of a multigene domain in Xp11.21-p11.22 that escapes X inactivationThe role of heparan sulfate deficiency in autistic phenotype: potential involvement of Slit/Robo/srGAPs-mediated dendritic spine formationThe Involvement of Neuron-Specific Factors in Dendritic Spinogenesis: Molecular Regulation and Association with Neurological DisordersImprinting, the X-chromosome, and the male brain: explaining sex differences in the liability to autismBTBR T+tf/J mice: autism-relevant behaviors and reduced fractone-associated heparan sulfateIdentification of novel genes associated with fracture healing in osteoporosis induced by Krm2 overexpression or Lrp5 deficiency.Sex-specific expression of gastrin-releasing peptide receptor: relationship to smoking history and risk of lung cancer.Bombesin-like peptides: studies on food intake and social behaviour with receptor knock-out mice.The role of rare structural variants in the genetics of autism spectrum disorders.Identification of mutations in TRAPPC9, which encodes the NIK- and IKK-beta-binding protein, in nonsyndromic autosomal-recessive mental retardationDisease susceptibility genes for autism.A cryptic deletion of 2q35 including part of the PAX3 gene detected by breakpoint mapping in a child with autism and a de novo 2;8 translocationThe complex nature of constitutional de novo apparently balanced translocations in patients presenting with abnormal phenotypesMolecular genetics of autism spectrum disorder.Gastrin-releasing peptide receptor expression in non-cancerous bronchial epithelia is associated with lung cancer: a case-control study.Cytogenetics and gene discovery in psychiatric disorders.Cell surface heparan sulfate proteoglycan syndecan-2 induces the maturation of dendritic spines in rat hippocampal neurons.Genome-wide association study of posttraumatic stress disorder in a cohort of Iraq-Afghanistan era veteransGastrin-releasing peptide receptors in the central nervous system: role in brain function and as a drug target.Elevated gastrin-releasing peptide receptor mRNA expression in buccal mucosa: association with head and neck squamous cell carcinoma.Clinical Outcomes and Counselling Issues regarding Partial Trisomy of Terminal Xp in a Child with Developmental Delay.Mosaic partial pericentromeric trisomy 8 and maternal uniparental disomy in a male patient with autism spectrum disorder.Self administration of oxycodone by adolescent and adult mice affects striatal neurotransmitter receptor gene expression.NPR-9 regulates the innate immune response in Caenorhabditis elegans by antagonizing the activity of AIB interneurons.Exclusion of the gastrin-releasing peptide receptor (GRPR) locus as a candidate gene for Rett syndrome.Heparan sulfate deficiency in autistic postmortem brain tissue from the subventricular zone of the lateral ventricles.Analysis of the gastrin-releasing peptide receptor gene in Italian patients with autism spectrum disorders.Gender- and smoking-related bladder cancer risk.Augmented Responses to Ozone in Obese Mice Require IL-17A and Gastrin-releasing Peptide.Rescue of social behavior impairment by clozapine and alterations in the expression of neuronal receptors in a rat model of neurodevelopmental impairment induced by GRPR blockade.Autism and the X chromosome: no linkage to microsatellite loci detected using the affected sibling pair method.Two patients with balanced translocations and autistic disorder: CSMD3 as a candidate gene for autism found in their common 8q23 breakpoint area.Disruption of chromodomain helicase DNA binding protein 2 (CHD2) causes scoliosis.
P2860
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P2860
Autism and multiple exostoses associated with an X;8 translocation occurring within the GRPR gene and 3' to the SDC2 gene.
description
1997 nî lūn-bûn
@nan
1997 թուականի Օգոստոսին հրատարակուած գիտական յօդուած
@hyw
1997 թվականի օգոստոսին հրատարակված գիտական հոդված
@hy
1997年の論文
@ja
1997年論文
@yue
1997年論文
@zh-hant
1997年論文
@zh-hk
1997年論文
@zh-mo
1997年論文
@zh-tw
1997年论文
@wuu
name
Autism and multiple exostoses ...... gene and 3' to the SDC2 gene.
@ast
Autism and multiple exostoses ...... gene and 3' to the SDC2 gene.
@en
Autism and multiple exostoses ...... gene and 3' to the SDC2 gene.
@nl
type
label
Autism and multiple exostoses ...... gene and 3' to the SDC2 gene.
@ast
Autism and multiple exostoses ...... gene and 3' to the SDC2 gene.
@en
Autism and multiple exostoses ...... gene and 3' to the SDC2 gene.
@nl
prefLabel
Autism and multiple exostoses ...... gene and 3' to the SDC2 gene.
@ast
Autism and multiple exostoses ...... gene and 3' to the SDC2 gene.
@en
Autism and multiple exostoses ...... gene and 3' to the SDC2 gene.
@nl
P2093
P356
P1476
Autism and multiple exostoses ...... gene and 3' to the SDC2 gene.
@en
P2093
Ishikawa-Brush Y
Willard HF
P304
P356
10.1093/HMG/6.8.1241
P577
1997-08-01T00:00:00Z