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

No causative DLL4 mutations in periodic catatonia patients from 15q15 linked families.

Schizophrenia research - 1 Jun 2005

McKeane D P, Meyer J, Dobrin S E, Melmed K M, Ekawardhani S, Tracy N A, Lesch K P, Stephan D A

Abstract excerpt

Two well-supported theories of schizophrenia pathogenesis are the neurotransmitter theory and the neurodevelopmental theory, suggesting, respectively, that dysregulation of neurotransmitter signaling and abnormal brain development are causative in this disease. The strongest evidence of neurotransmitter involvement are suggestions of abnormal dopamine signaling in the prefrontal cortex and one of the strongest...

Read the complete abstract on PubMed

Topics

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

Share to Blood Proteins
Share to Calcium-Binding Proteins

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Chromosomes, Human, Pair 15

Share to Germany

Share to Intercellular Signaling Peptides and Proteins

Share to Prefrontal Cortex

Share to Receptor, Notch4

Share to Receptors, Notch

Source

Identifiers

PMID: 15820317
DOI: 10.1016/j.schres.2004.07.017

Genes

DLL4
NOTCH4

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

No causative DLL4 mutations in periodic catatonia patients from 15q15 linked families.PMID 15820317Read ↗

Mutation analysis of the zinc transporter gene SLC30A4 reveals no association with periodic catatonia on chromosome 15q15.Semantic proximity Read ↗

Splitting schizophrenia: periodic catatonia-susceptibility locus on chromosome 15q15.Semantic proximity Read ↗

The chromosome 15q14 locus for bipolar disorder and schizophrenia: is C15orf53 a major candidate gene?Semantic proximity Read ↗

Shared susceptibility region on chromosome 15 between autism and catatonia.Semantic proximity Read ↗

No missense mutation of WKL1 in a subgroup of probands with schizophrenia.Semantic proximity Read ↗

Evaluation of conserved and ultra-conserved non-genic sequences in chromosome 15q15-linked periodic catatonia.Semantic proximity Read ↗

Investigation of Rare Single-Nucleotide PCDH15 Variants in Schizophrenia and Autism Spectrum Disorders.Semantic proximity Read ↗

The role of Pannexin gene variants in schizophrenia: systematic analysis of phenotypes.Semantic proximity Read ↗

MLC1 polymorphisms are specifically associated with periodic catatonia, a subgroup of chronic schizophrenia.Semantic proximity Read ↗

Evaluation of multiple putative risk alleles within the 15q13.3 region for genetic generalized epilepsy.Semantic proximity Read ↗

Systematic mutation analysis of KIAA0767 and KIAA1646 in chromosome 22q-linked periodic catatonia.Semantic proximity Read ↗

Is the WKL1 gene associated with schizophrenia?Semantic proximity Read ↗

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