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

Absence of association between two HECTD2 polymorphisms and sporadic Creutzfeldt-Jakob disease.

Dementia and geriatric cognitive disorders - 1 Jan 2011

Jeong Byung-Hoon, Lee Kyung-Hee, Lee Yun-Jung, Yun Jisuk, Park Young-Jae, Cho Han-Jeong, Kim Young-Hoon, Cho Young-Sook, Choi Eun-Kyoung, Carp Richard I, Kim Yong-Sun

Abstract excerpt

BACKGROUND: HECT (homologous to E6-AP carboxyl terminus) E3 ubiquitin ligases are fundamental components of the eukaryotic ubiquitin-proteasome system and are involved in the pathogenesis of several human diseases, including polyglutamine diseases. HECTD2, an E3 ubiquitin ligase, has been linked...

Read the complete abstract on PubMed

Topics

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

Share to Creutzfeldt-Jakob Syndrome
Share to DNA
Share to Gene Frequency

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Haplotypes

Share to Polymorphism, Genetic

Share to Republic of Korea

Share to Reverse Transcriptase Polymerase Chain Reaction

Share to Ubiquitin-Protein Ligases

Source

Identifiers

PMID: 21335971
DOI: 10.1159/000324133

Genes

HECTD2

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026. Prepared record publication-21335971-2026-09-04.2. Manifest publication-graph-cohort-2026-09-04.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 4 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Absence of association between two HECTD2 polymorphisms and sporadic Creutzfeldt-Jakob disease.PMID 21335971Read ↗

HECTD2 is associated with susceptibility to mouse and human prion disease.Semantic proximity Read ↗

Lack of association between 14-3-3 beta gene (YWHAB) polymorphisms and sporadic Creutzfeldt-Jakob disease (CJD).Semantic proximity Read ↗

Genetic association of a cathepsin D polymorphism and sporadic Creutzfeldt-Jakob disease.Semantic proximity Read ↗

Genome wide association studies and prion disease.Semantic proximity Read ↗

RARB and STMN2 polymorphisms are not associated with sporadic Creutzfeldt-Jakob disease (CJD) in the Korean population.Semantic proximity Read ↗

PRNP 1368 polymorphism is not associated with sporadic Creutzfeldt-Jakob disease in the Korean population.Semantic proximity Read ↗

Variants of PLCXD3 are not associated with variant or sporadic Creutzfeldt-Jakob disease in a large international study.Semantic proximity Read ↗

A polymorphism in the YWHAH gene encoding 14-3-3 eta that is not associated with sporadic Creutzfeldt-Jakob disease (CJD).Semantic proximity Read ↗

Polymorphisms at codons 56 and 174 of the prion-like protein gene (PRND) are not associated with sporadic Creutzfeldt-Jakob disease.Semantic proximity Read ↗

The first report of RPSA polymorphisms, also called 37/67 kDa LRP/LR gene, in sporadic Creutzfeldt-Jakob disease (CJD).Semantic proximity Read ↗

Cathepsin D (C224T) polymorphism in sporadic and genetic Creutzfeldt-Jakob disease.Semantic proximity Read ↗

APOE gene polymorphisms and susceptibility to Creutzfeldt-Jakob disease.Semantic proximity Read ↗

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