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

Human enamel phenotype associated with amelogenesis imperfecta and a kallikrein-4 (g.2142G>A) proteinase mutation.

European journal of oral sciences - 1 May 2006

Wright J Tim, Daly Bill, Simmons Darrin, Hong Sung, Hart Suzanne P, Hart Tom C, Atsawasuwan Phimon, Yamauchi Mitsuo

Abstract excerpt

Kallikrein-4 is known to be highly expressed during the maturation stage of enamel formation and is thought to be critical for the final phase of crystallite growth. The purpose of this study was to evaluate the enamel phenotype in humans with a known KLK-4 mutation (g.2142G>A). Primary teeth fro...

Read the complete abstract on PubMed

Topics

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

Share to Amelogenesis Imperfecta
Share to Crystallization
Share to Crystallography

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Dental Enamel

Share to Dental Enamel Proteins

Share to Kallikreins

Share to Porosity

Share to Tooth, Deciduous

Source

Identifiers

PMID: 16674656
DOI: 10.1111/j.1600-0722.2006.00291.x

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-16674656-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 2 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Human enamel phenotype associated with amelogenesis imperfecta and a kallikrein-4 (g.2142G>A) proteinase mutation.PMID 16674656Read ↗

The genetics of amelogenesis imperfecta: a review of the literatureSemantic proximity Read ↗

Novel MMP20 and KLK4 Mutations in Amelogenesis Imperfecta.Semantic proximity Read ↗

The molecular basis of hereditary enamel defects in humans.Semantic proximity Read ↗

Mutation in kallikrein 4 causes autosomal recessive hypomaturation amelogenesis imperfectaSemantic proximity Read ↗

Human and mouse enamel phenotypes resulting from mutation or altered expression of AMEL, ENAM, MMP20 and KLK4.Semantic proximity Read ↗

The molecular etiologies and associated phenotypes of amelogenesis imperfecta.Semantic proximity Read ↗

Enamel Phenotypes: Genetic and Environmental Determinants.Semantic proximity Read ↗

Phenotype and enamel ultrastructure characteristics in patients with ENAM gene mutations g.13185-13186insAG and 8344delG.Semantic proximity Read ↗

[Phenotype analysis and the molecular mechanism of enamel hypoplasia].Semantic proximity Read ↗

Phenotypic variability in LAMA3-associated amelogenesis imperfecta.Semantic proximity Read ↗

Amelogenin p.M1T and p.W4S mutations underlying hypoplastic X-linked amelogenesis imperfecta.Semantic proximity Read ↗

Keratins as components of the enamel organic matrix.Semantic proximity Read ↗

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