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

A PCR-RFLP marker for the erythroid aminolevulinate synthase gene (ALAS2) on canine chromosome X.

Animal genetics - 1 Jun 1995

Boyer G, Nonneman D, Shibuya H, Stoy S J, O'Brien D, Johnson G S

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 5-Aminolevulinate Synthetase
Share to Chromosome Mapping
Share to DNA Primers
Share to Dogs

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Pedigree

Share to Polymerase Chain Reaction

Share to Polymorphism, Restriction Fragment Length

Share to X Chromosome

Source

Identifiers

PMID: 7793698
DOI: 10.1111/j.1365-2052.1995.tb03172.x

Genes

ALAS2

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 · 12 closest

A PCR-RFLP marker for the erythroid aminolevulinate synthase gene (ALAS2) on canine chromosome X.PMID 7793698Read ↗

Human δ-aminolevulinate synthase: Assignment of the housekeeping gene to 3p21 and the erythroid-specific gene to the X chromosomeSemantic proximity Read ↗

New mutation in erythroid-specific delta-aminolevulinate synthase as the cause of X-linked sideroblastic anemia responsive to pyridoxine.Semantic proximity Read ↗

A novel mutation, Ile289Thr, in the ALAS2 gene in a family with pyridoxine responsive sideroblastic anaemia.Semantic proximity Read ↗

A promoter mutation in the erythroid-specific 5-aminolevulinate synthase (ALAS2) gene causes X-linked sideroblastic anemia.Semantic proximity Read ↗

Sideroblastic anemia: molecular analysis of the ALAS2 gene in a series of 29 probands and functional studies of 10 missense mutationsSemantic proximity Read ↗

[A novel mutation of the ALAS2 gene in a family with X-linked sideroblastic anemia].Semantic proximity Read ↗

A new mutation of the ALAS2 gene in a large family with X-linked sideroblastic anemia.Semantic proximity Read ↗

Hereditary sideroblastic anaemia due to a mutation in exon 10 of the erythroid 5-aminolaevulinate synthase gene.Semantic proximity Read ↗

Molecular and functional analysis of the C-terminal region of human erythroid-specific 5-aminolevulinic synthase associated with X-linked dominant protoporphyria (XLDPP)Semantic proximity Read ↗

Identification and Characterization of a Conserved Erythroid-specific Enhancer Located in Intron 8 of the Human 5-Aminolevulinate Synthase 2 GeneSemantic proximity Read ↗

Molecular analysis of delta-aminolevulinic acid dehydratase (ALAD) gene polymorphism in a Turkish population.Semantic proximity Read ↗

X-linked sideroblastic anemia associated with a novel ALAS2 mutation and unfortunate skewed X-chromosome inactivation patterns.Semantic proximity Read ↗

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