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

Genetic study of non-syndromic tooth agenesis through the screening of paired box 9, msh homeobox 1, axin 2, and Wnt family member 10A genes: a case-series.

European journal of oral sciences - 1 Feb 2018

Haddaji Mastouri Marwa, De Coster Peter, Zaghabani Aicha, Jammali Frej, Raouahi Nabiha, Ben Salem Amina, Saad Ali, Coucke Paul, H'mida Ben Brahim Dorra

Abstract excerpt

Non-syndromic tooth agenesis (NSTA) is the most common developmental anomaly in humans. Several studies have been conducted on dental agenesis and numerous genes have been identified. However, the pathogenic mechanisms responsible for NSTA are not clearly understood. We studied a group of 28 patients with sporadic NSTA and nine patients with a family history of tooth agenesis. We focused on four genes - paired...

Read the complete abstract on PubMed

Topics

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

Share to Anodontia
Share to Axin Protein

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to MSX1 Transcription Factor

Share to Mutation, Missense

Share to PAX9 Transcription Factor

Share to Phenotype

Share to Polymorphism, Genetic

Share to Wnt Proteins

Source

Identifiers

PMID: 29114927
DOI: 10.1111/eos.12391

Genes

AXIN2
PAX9
MSX1

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Genetic study of non-syndromic tooth agenesis through the screening of paired box 9, msh homeobox 1, axin 2, and Wnt family member 10A genes: a case-series.PMID 29114927Read ↗

Mutation analysis by direct and whole exome sequencing in familial and sporadic tooth agenesis.Semantic proximity Read ↗

PAX9 gene mutations and tooth agenesis: A review.Semantic proximity Read ↗

Candidate gene analysis of tooth agenesis identifies novel mutations in six genes and suggests significant role for WNT and EDA signaling and allele combinations.Semantic proximity Read ↗

Functional analysis of a novel missense mutation in AXIN2 associated with non-syndromic tooth agenesis.Semantic proximity Read ↗

A screen of a large Czech cohort of oligodontia patients implicates a novel mutation in the PAX9 gene.Semantic proximity Read ↗

Mutational analysis of AXIN2, MSX1, and PAX9 in two Mexican oligodontia families.Semantic proximity Read ↗

Molecular basis of non-syndromic tooth agenesis: mutations of MSX1 and PAX9 reflect their role in patterning human dentition.Semantic proximity Read ↗

Identification of genetic risk factors for maxillary lateral incisor agenesis.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 ↗

Characterization of a novel mutation in PAX9 gene in a family with non-syndromic dental agenesis.Semantic proximity Read ↗

Genetic analysis: Wnt and other pathways in nonsyndromic 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 ↗

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