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

Congenital Ichthyosis and Recurrent Eczema Associated with a Novel ALOXE3 Mutation.

Acta dermato-venereologica - 6 Apr 2017

Takeichi Takuya, Okuno Yusuke, Saito Chiyo, Kojima Daiei, Kono Michihiro, Morita Akimichi, Sugiura Kazumitsu, Akiyama Masashi

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 Biopsy
Share to DNA Mutational Analysis
Share to Eczema
Share to Ichthyosis, Lamellar

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Lipoxygenase

Share to Pruritus

Share to Recurrence

Source

Identifiers

PMID: 27868147
DOI: 10.2340/00015555-2549

Genes

ALOXE3

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

Congenital Ichthyosis and Recurrent Eczema Associated with a Novel ALOXE3 Mutation.PMID 27868147Read ↗

Meta-Analysis of Mutations in ALOX12B or ALOXE3 Identified in a Large Cohort of 224 Patients.Semantic proximity Read ↗

Molecular analysis of 250 patients with autosomal recessive congenital ichthyosis: evidence for mutation hotspots in ALOXE3 and allelic heterogeneity in ALOX12B.Semantic proximity Read ↗

Lamellar ichthyosis caused by a previously unreported homozygous ALOXE3 mutation in East Asia.Semantic proximity Read ↗

Mutations associated with a congenital form of ichthyosis (NCIE) inactivate the epidermal lipoxygenases 12-LOX and eLOX3Semantic proximity Read ↗

Variants in NIPAL4 and ALOXE3 cause autosomal recessive congenital ichthyosis in Pakistani families.Semantic proximity Read ↗

Novel mutations in the genes TGM1 and ALOXE3 underlying autosomal recessive congenital ichthyosis.Semantic proximity Read ↗

Spectrum of Autosomal Recessive Congenital Ichthyosis in Scandinavia: Clinical Characteristics and Novel and Recurrent Mutations in 132 Patients.Semantic proximity Read ↗

Inherited Nonsyndromic Ichthyoses: An Update on Pathophysiology, Diagnosis and Treatment.Semantic proximity Read ↗

Mutation spectrum and functional analysis of epidermis-type lipoxygenases in patients with autosomal recessive congenital ichthyosis.Semantic proximity Read ↗

Lamellar ichthyosis due to ALOX12B mutation.Semantic proximity Read ↗

Homozygous ALOXE3 Nonsense Variant Identified in a Patient with Non-Bullous Congenital Ichthyosiform Erythroderma Complicated by Superimposed Bullous Majocchi's Granuloma: The Consequences of Skin Barrier Dysfunction.Semantic proximity Read ↗

[New classification and genetic background of inherited ichthyoses].Semantic proximity Read ↗

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