Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Identification of genetic variation in the human serotonin 1D beta receptor gene.

Biochemical and biophysical research communications - 15 Dec 1994

Nöthen M M, Erdmann J, Shimron-Abarbanell D, Propping P

Abstract excerpt

Disturbances of serotonergic pathways have been implicated in a wide variety of neuropsychiatric disorders such as depression, anxiety, migraine, and substance abuse. Genetic variation in genes coding for serotonin receptor proteins might well be involved in the genetic predisposition to these diseases and/or of pharmacogenetic relevance. Genomic samples from 46 unrelated healthy subjects were investigated by...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Alleles
Share to Amino Acid Sequence
Share to Base Sequence

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Share to Cloning, Molecular

Share to DNA Primers

Share to Genetic Variation

Share to Molecular Sequence Data

Share to Polymerase Chain Reaction

Source

Identifiers

PMID: 7802650
DOI: 10.1006/bbrc.1994.2792

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence. Graph snapshot: 2026-09-29.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Identification of genetic variation in the human serotonin 1D beta receptor gene.PMID 7802650Read ↗

Genetic diversity of the human serotonin receptor 1B (HTR1B) gene.Semantic proximity Read ↗

DNA variation and psychopharmacology of the human serotonin receptor 1B (HTR1B) gene.Semantic proximity Read ↗

Systematic screening for mutations in the promoter and the coding region of the 5-HT1A gene.Semantic proximity Read ↗

Two naturally occurring amino acid substitutions in the human 5-HT1A receptor: glycine 22 to serine 22 and isoleucine 28 to valine 28.Semantic proximity Read ↗

Mapping of the serotonin 5-HT1D beta autoreceptor gene on chromosome 6 and direct analysis for sequence variants.Semantic proximity Read ↗

Human 5-HT5A receptor gene: systematic screening for DNA sequence variation and linkage mapping on chromosome 7q34-q36 using a polymorphism in the 5' untranslated region.Semantic proximity Read ↗

A serotonin receptor gene (5HT1A) variant found in a Tourette's syndrome patient.Semantic proximity Read ↗

Novel mutations in the promoter and coding region of the human 5-HT1A receptor gene and association analysis in schizophrenia.Semantic proximity Read ↗

Genetic variation in human 5-HT receptors: potential pathogenetic and pharmacological role.Semantic proximity Read ↗

Systematic screening for mutations in the human serotonin-2A (5-HT2A) receptor gene: identification of two naturally occurring receptor variants and association analysis in schizophrenia.Semantic proximity Read ↗

A common C-1018G polymorphism in the human 5-HT1A receptor gene.Semantic proximity Read ↗

Serotonin2A receptor gene polymorphism in mood disorders.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.