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

[Expression of the partial protein encoded by mutated COL4A5 gene and analysis of the structure by circular dichroism].

Beijing da xue xue bao. Yi xue ban = Journal of Peking University. Health sciences - 1 Apr 2004

Wang Yun-feng, Ding Jie, Bu Ding-fang, Wang Fang

Abstract excerpt

OBJECTIVE: To analyze the protein structure encoded by COL4A5 gene with a missense mutation and to discuss the effect of gene mutation on basic structure and predicted secondary structure of the encoded protein. METHODS: A fragment of cDNA with a g.3246G T mutation resulting in p.G1015V from an X...

Read the complete abstract on PubMed

Topics

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

Share to Circular Dichroism
Share to Collagen Type IV
Share to Nephritis, Hereditary

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Protein Folding

Share to Protein Structure, Secondary

Share to Recombinant Proteins

Share to Reverse Transcriptase Polymerase Chain Reaction

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

Source

Identifiers

PMID: 15100740

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 1 Sept 2026. Prepared record publication-15100740-2026-09-01.1. Manifest publication-graph-cohort-2026-09-01.1.

Source receipt: PubMed via Helena Literature Corpus, retrieved 1 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

[Expression of the partial protein encoded by mutated COL4A5 gene and analysis of the structure by circular dichroism].PMID 15100740Read ↗

[Proteins structure changes of COL4A5 gene point mutations and structure-phenotype relations in Alport syndrome].Semantic proximity Read ↗

Effect of glycine substitutions on alpha5(IV) chain structure and structure-phenotype correlations in Alport syndrome.Semantic proximity Read ↗

Molecular dynamics and minigene assay of new splicing variant c.4298-20T>A of COL4A5 gene that cause Alport syndromeSemantic proximity Read ↗

Molecular dynamics and minigene assay of a splicing COL4A5 gene variant causing Alport syndromeSemantic proximity Read ↗

[Thin basement membrane nephropathy: a mutation in COL4A5 gene].Semantic proximity Read ↗

A novel COL4A5 splicing mutation causes alport syndrome in a Chinese family.Semantic proximity Read ↗

[Identification of a novel variant of COL4A5 gene in a pedigree affected with Alport syndrome].Semantic proximity Read ↗

[COL4A5 genotypes and clinical characteristics of children with Alport syndrome].Semantic proximity Read ↗

[Analysis of two Chinese pedigrees affected with Alport syndrome due to novel variants of COL4A5 gene].Semantic proximity Read ↗

Three exonic variants in the COL4A5 gene alter RNA splicing in a minigene assay.Semantic proximity Read ↗

The COL4A5 gene in Japanese Alport syndrome patients: spectrum of mutations of all exons. The Japanese Alport Network.Semantic proximity Read ↗

[Genetic and clinical analysis of a pedigree affected with X-linked dominant Alport syndrome due to a novel variant of COL4A5 gene].Semantic proximity Read ↗

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