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

[Transport mechanism of glycoproteins by ERGIC-53 and the disease caused by defect in a gene coding ERGIC-53].

Tanpakushitsu kakusan koso. Protein, nucleic acid, enzyme - 1 Sept 2008

Yamamoto Kazuo

Abstract excerpt

No abstract is available from the source.

Read the complete abstract on PubMed

Topics

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

Share to Endoplasmic Reticulum
Share to Factor V Deficiency
Share to Glycoproteins
Share to Hemophilia A

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Lectins

Share to Mannose-Binding Lectins

Share to Protein Folding

Share to Vesicular Transport Proteins

Source

Identifiers

PMID: 21089350

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 8 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 8 closest

[Transport mechanism of glycoproteins by ERGIC-53 and the disease caused by defect in a gene coding ERGIC-53].PMID 21089350Read ↗

ERGIC-53 and traffic in the secretory pathwaySemantic proximity Read ↗

Sequence-function correlations and dynamics of ERG isoforms. ERG8 is the black sheep of the family.Semantic proximity Read ↗

Mistargeting of the lectin ERGIC-53 to the endoplasmic reticulum of HeLa cells impairs the secretion of a lysosomal enzyme.Semantic proximity Read ↗

[Abnormal connection of mutant PS1 to glycosphingolipids metabolism].Semantic proximity Read ↗

ERGIC-53 is a functional mannose-selective and calcium-dependent human homologue of leguminous lectins.Semantic proximity Read ↗

Molecular characterization of the ERGIC-53 gene in two Japanese patients with combined factor V-factor VIII deficiency.Semantic proximity Read ↗

Oligomerization and interacellular localization of the glycoprotein receptor ERGIC-53 is independent of disulfide bonds.Semantic proximity Read ↗

[Diseases and gene defects].Semantic proximity Read ↗

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