SCT, secretin, 6343

N. diseases: 230; N. variants: 0
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0004352
Disease: Autistic Disorder
Autistic Disorder
0.330 Therapeutic disease CTD_human After administration of secretin, the Autism Diagnostic Interview-Revised (ADI-R) score improved in 7 of the 12 children. 16168596 2006
CUI: C0004352
Disease: Autistic Disorder
Autistic Disorder
0.330 GeneticVariation disease BEFREE We did not find evidence of a relationship between human secretin gene mutation and autism. 16225821 2005
CUI: C0004352
Disease: Autistic Disorder
Autistic Disorder
0.330 Therapeutic disease CTD_human These findings suggest that secretin promotes the metabolism of serotonin and dopamine in the central nervous system, which may contribute to improvement in clinical symptoms of autism. 15272612 2004
CUI: C0004352
Disease: Autistic Disorder
Autistic Disorder
0.330 Therapeutic disease CTD_human Since autism is hypothesized to be a hypoglutamatergic disorder we investigated the in vivo effects of secretin on extracellular amino acids in the rat brain. 15206007 2004
CUI: C0004352
Disease: Autistic Disorder
Autistic Disorder
0.330 Therapeutic disease CTD_human Recent observations that the deficits in social reciprocity skills seen in young (3-4-year-old) autistic children are improved after secretin infusions suggest an additional influence on neuronal activity.We show here that i.v. administration of secretin in rats induces Fos protein expression in the neurons of the central amygdala as well as the area postrema, bed nucleus of the stria terminalis, external lateral parabrachial nucleus and supraoptic nucleus. 12732234 2003
CUI: C0004352
Disease: Autistic Disorder
Autistic Disorder
0.330 GeneticVariation disease BEFREE The human secretin gene: fine structure in 11p15.5 and sequence variation in patients with autism. 12160732 2002
CUI: C0004352
Disease: Autistic Disorder
Autistic Disorder
0.330 GeneticVariation disease LHGDN While the secretin gene (SCT) was not found to be mutated in the majority of autistic patients, rare heterozygous sequence variants were identified in three patients. 12160732 2002
CUI: C0004352
Disease: Autistic Disorder
Autistic Disorder
0.330 Biomarker disease BEFREE The study of the transcriptional control of human secretin and its receptor should shed light on the pathological developments of pancreatic cancer and autism in the future. 10437774 1999