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

The molecular basis of hereditary enamel defects in humans.

Journal of dental research - 1 Jan 2015

Wright J T, Carrion I A, Morris C

Abstract excerpt

The formation of human enamel is highly regulated at the molecular level and involves thousands of genes. Requisites for development of this highly mineralized tissue include cell differentiation; production of a unique extracellular matrix; processing of the extracellular matrix; altering of cell function during different stages of enamel formation; cell movement and attachment; regulation of ion and protein...

Read the complete abstract on PubMed

Topics

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

Share to Amelogenesis
Share to Bone and Dental Protein Studies
Share to Databases, Genetic

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

Share to dental development and anomalies

Share to Dental Enamel

Share to Dental Enamel Hypoplasia

Share to Dental Enamel Proteins

Share to Phenotype

Source

Open in PubMed Open full text

Identifiers

PMID: 25389004
DOI: 10.1177/0022034514556708
PMCID: PMC4270810

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

The molecular basis of hereditary enamel defects in humans.PMID 25389004Read ↗

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

Molecular-based phenotype variations in amelogenesis imperfecta.Semantic proximity Read ↗

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

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

Amelogenesis Imperfecta; Genes, Proteins, and PathwaysSemantic proximity Read ↗

Enamel formation and amelogenesis imperfecta.Semantic proximity Read ↗

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

DENTAL ENAMEL FORMATION AND IMPLICATIONS FOR ORAL HEALTH AND DISEASE.Semantic proximity Read ↗

WDR72 Mutations Associated with Amelogenesis Imperfecta and AcidosisSemantic proximity Read ↗

Epigenetics in developmental defects of enamel: A scoping reviewSemantic proximity Read ↗

E<scp>namelin and</scp> A<scp>utosomal-dominant</scp> A<scp>melogenesis</scp> I<scp>mperfecta</scp>Semantic proximity Read ↗

Mutations in the beta propeller WDR72 cause autosomal-recessive hypomaturation amelogenesis imperfecta.Semantic proximity Read ↗

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