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

Analysis of N- and O-linked protein glycosylation in children with Prader-Willi syndrome.

Journal of intellectual disability research : JIDR - 1 Oct 2010

Munce T, Heussler H S, Bowling F G

Abstract excerpt

BACKGROUND: Current genotype-phenotype correlations in Prader-Willi syndrome (PWS) are struggling to give an explanation of the diversity in phenotype and there is a need to move towards a molecular understanding of PWS. A range of functions related to glycoproteins are involved in the pathophysiology of PWS and it may be that abnormal glycosylation is contributing to the biological phenotype. The objective of...

Read the complete abstract on PubMed

Topics

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

Share to Apolipoprotein C-III
Share to Glycoproteins
Share to Glycosylation

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Isoelectric Focusing

Share to N-Acetylneuraminic Acid

Share to Prader-Willi Syndrome

Share to Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization

Share to Transferrin

Source

Identifiers

PMID: 20825553
DOI: 10.1111/j.1365-2788.2010.01323.x

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.

Research trail→

Click a neighbor to travelStep 1 · 11 closest

Analysis of N- and O-linked protein glycosylation in children with Prader-Willi syndrome.PMID 20825553Read ↗

Congenital disorder of glycosylation type Id: clinical phenotype, molecular analysis, prenatal diagnosis, and glycosylation of fetal proteins.Semantic proximity Read ↗

Apolipoprotein C-III O-glycoform profiling of 500 serum samples by matrix-assisted laser desorption/ionization mass spectrometry for diagnosis of congenital disorders of glycosylation.Semantic proximity Read ↗

Screening for "prelysosomal disorders": carbohydrate-deficient glycoprotein syndromes.Semantic proximity Read ↗

Transferrin mutations at the glycosylation site complicate diagnosis of congenital disorders of glycosylation type I.Semantic proximity Read ↗

Glycosylation and behavioral symptoms in neurological disordersSemantic proximity Read ↗

The restricted nature of protein glycosylation in the mammalian brainSemantic proximity Read ↗

The novel transferrin E592A variant impairs the diagnostics of congenital disorders of glycosylation.Semantic proximity Read ↗

Human Plasma Glycome in Attention-Deficit Hyperactivity Disorder and Autism Spectrum DisordersSemantic proximity Read ↗

The carbohydrate deficient glycoprotein syndrome in three Japanese children.Semantic proximity Read ↗

Population studies of Vitamin D Binding Protein microheterogeneity by mass spectrometry lead to characterization of its genotype-dependent O-glycosylation patterns.Semantic proximity Read ↗

Microheterogeneity of some serum glycoproteins in neurodegenerative diseases.Semantic proximity Read ↗

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