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

No association between atopic dermatitis and the SLC9A3R1-NAT9 RUNX1 binding site polymorphism in Japanese patients.

Clinical and experimental dermatology - 1 Mar 2005

Hosomi N, Fukai K, Oiso N, Kato A, Fukui M, Ishii M

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 Adolescent
Share to Child
Share to Child, Preschool
Share to Dermatitis, Atopic

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Phosphoproteins

Share to Polymorphism, Restriction Fragment Length

Share to Sodium-Hydrogen Exchangers

Source

Identifiers

PMID: 15725257
DOI: 10.1111/j.1365-2230.2005.01720.x

Genes

NAT9
RUNX1

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

No association between atopic dermatitis and the SLC9A3R1-NAT9 RUNX1 binding site polymorphism in Japanese patients.PMID 15725257Read ↗

A putative RUNX1 binding site variant between SLC9A3R1 and NAT9 is associated with susceptibility to psoriasis.Semantic proximity Read ↗

Replication of genome-wide association studies on asthma and allergic diseases in Korean adult population.Semantic proximity Read ↗

AAT polymorphisms in intron 20 of NOS1 confer vulnerability to mite-induced allergic rhinitis in Chinese patients.Semantic proximity Read ↗

Correlation between polymorphisms of IL-18-607A/C and -137G/C and allergic rhinitis in Chinese population.Semantic proximity Read ↗

Correlation of KIF3A and OVOL1, but not ACTL9, with atopic dermatitis in Chinese pediatric patients.Semantic proximity Read ↗

Association of Cw11 in Japanese patients with psoriasis vulgaris.Semantic proximity Read ↗

Lack of association of CCR4 single nucleotide polymorphism with atopic dermatitis in Japanese patients.Semantic proximity Read ↗

Analysis of the relationship between the mutation site of the SLC39A4 gene and acrodermatitis enteropathica by reporting a rare Chinese twin: a case report and review of the literature.Semantic proximity Read ↗

Four phenotypes of atopic dermatitis in Japanese children: A general population birth cohort studySemantic proximity Read ↗

Genome-wide association study for atopy and allergic rhinitis in a Singapore Chinese population.Semantic proximity Read ↗

A rare variant in CYP27A1 and its association with atopic dermatitis with high serum total IgE.Semantic proximity Read ↗

[Association of single nucleotide polymorphisms of GATA3 with allergic rhinitis phenotypes in Chinese].Semantic proximity Read ↗

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