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

Molecular abnormality of a unique Japanese glucose-6-phosphate dehydrogenase variant (G6PD Kobe) with a greatly increased affinity for galactose-6-phosphate.

American journal of hematology - 1 Feb 1994

Hirono A, Nakayama S, Fujii H, Miwa S

Abstract excerpt

Systematic molecular analysis of a Japanese class 1 glucose-6-phosphate dehydrogenase (G6PD) variant (G6PD Kobe) cDNA revealed a unique nucleotide substitution (1318 C to T) in exon 11, which predicts a substitution of leucine for phenylalanine at residue 440. This substitution is located in a region surrounding the putative structural NADP-binding domain. The markedly abnormal kinetics of glucose-6-phosphate...

Read the complete abstract on PubMed

Topics

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

Share to Base Sequence
Share to Genetic Variation

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Share to Glucosephosphate Dehydrogenase

Share to Molecular Sequence Data

Source

Identifiers

PMID: 8141125
DOI: 10.1002/ajh.2830450217

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. Graph snapshot: 2026-09-29.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Molecular abnormality of a unique Japanese glucose-6-phosphate dehydrogenase variant (G6PD Kobe) with a greatly increased affinity for galactose-6-phosphate.PMID 8141125Read ↗

Molecular abnormality of G6PD Konan and G6PD Ube, the most common glucose-6-phosphate dehydrogenase variants in Japan.Semantic proximity Read ↗

Molecular analysis of eight biochemically unique glucose-6-phosphate dehydrogenase variants found in Japan.Semantic proximity Read ↗

Glucose-6-phosphate dehydrogenase deficiency: a historical perspectiveSemantic proximity Read ↗

G6PD Nara: a new class 1 glucose-6-phosphate dehydrogenase variant with an eight amino acid deletion.Semantic proximity Read ↗

Glucose-6-Phosphate Dehydrogenase: Update and Analysis of New Mutations around the World.Semantic proximity Read ↗

Identification of a case of glucose-6-phosphate dehydrogenase deficiency with G6PD Mediterranean-Middle East subtype in China.Semantic proximity Read ↗

Human glucose-6-phosphate dehydrogenase: structure and function of normal and variant enzymes.Semantic proximity Read ↗

Study of glucose-6-phosphate dehydrogenase: history and molecular biology.Semantic proximity Read ↗

Gene symbol: G6PD. Disease: Glucose-6-phosphate dehydrogenase deficiency.Semantic proximity Read ↗

The genetics of glucose-6-phosphate dehydrogenase deficiency.Semantic proximity Read ↗

Glucose-6-phosphate dehydrogenase--from oxidative stress to cellular functions and degenerative diseases.Semantic proximity Read ↗

Evaluation of Three Mutations in Codon 385 of Glucose-6-Phosphate Dehydrogenase via Biochemical and In Silico Analysis.Semantic proximity Read ↗

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