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

GREM2 nucleotide variants and the risk of tooth agenesis.

Oral diseases - 1 May 2018

Mostowska A, Biedziak B, Zadurska M, Bogdanowicz A, Olszewska A, Cieślińska K, Firlej E, Jagodziński P P

Abstract excerpt

OBJECTIVE: The etiology of tooth agenesis (TA) is multifactorial and still not fully understood. The aim of the study was to test whether variants of GREM2, encoding a bone morphogenetic protein (BMP) antagonist, are associated with the risk of this common dental anomaly in a Polish population. SUBJECTS AND METHODS: Direct sequencing of the GREM2 coding sequence including exon/intron boundaries was performed in...

Read the complete abstract on PubMed

Topics

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

Share to Anodontia
Share to Cytokines
Share to DNA Mutational Analysis

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Gene Frequency

Share to Intercellular Signaling Peptides and Proteins

Share to Mutation

Share to Phenotype

Share to Young Adult

Source

Identifiers

PMID: 28992378
DOI: 10.1111/odi.12793

Genes

GREM2

Variants

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026. Manifest publication-graph-cohort-2026-09-06.1.

Source receipt: pubmed, retrieved 6 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

GREM2 nucleotide variants and the risk of tooth agenesis.PMID 28992378Read ↗

Genetic Variants of BMP2 and Their Association with the Risk of Non-Syndromic Tooth Agenesis.Semantic proximity Read ↗

Nucleotide variants of genes encoding components of the Wnt signalling pathway and the risk of non-syndromic tooth agenesis.Semantic proximity Read ↗

Dental agenesis: genetic and clinical perspectives.Semantic proximity Read ↗

Genotypic and phenotypic correlations in tooth agenesis: insights from WNT10A and EDA mutations in syndromic and non-syndromic forms.Semantic proximity Read ↗

GREMLIN 2 Mutations and Dental Anomalies.Semantic proximity Read ↗

Analyses of oligodontia phenotypes and genetic etiologies.Semantic proximity Read ↗

WNT10A coding variants and maxillary lateral incisor agenesis with associated dental anomalies.Semantic proximity Read ↗

BMPR2 Variants Underlie Nonsyndromic Oligodontia.Semantic proximity Read ↗

Targeted next-generation sequencing (NGS) analysis of mutations in nonsyndromic tooth agenesis candidate genes : Analysis of a Turkish cohort.Semantic proximity Read ↗

A novel WNT10A mutation causes non-syndromic hypodontia in an Egyptian family.Semantic proximity Read ↗

Genetic variations in MMP9 and MMP13 contribute to tooth agenesis in a Brazilian population.Semantic proximity Read ↗

The genetic basis of hypodontia in dental development.Semantic proximity Read ↗

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