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

MSX1 and orofacial clefting with and without tooth agenesis.

Journal of dental research - 1 Jun 2006

Modesto A, Moreno L M, Krahn K, King S, Lidral A C

Abstract excerpt

MSX1 has been considered a strong candidate for orofacial clefting, based on mouse expression studies and knockout models, as well as association and linkage studies in humans. MSX1 mutations are also causal for hereditary tooth agenesis. We tested the hypothesis that individuals with orofacial c...

Read the complete abstract on PubMed

Topics

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

Share to Anodontia
Share to Cleft Lip
Share to Cleft Palate

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Cytosine

Share to Guanine

Share to MSX1 Transcription Factor

Share to Regulatory Elements, Transcriptional

Share to Thymine

Source

Open in PubMed Open full text

Identifiers

PMID: 16723652
DOI: 10.1177/154405910608500612
PMCID: PMC2241923

Genes

MSX1

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-16723652-2026-09-02.2. 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

MSX1 and orofacial clefting with and without tooth agenesis.PMID 16723652Read ↗

MSX1 mutation is associated with orofacial clefting and tooth agenesis in humans.Semantic proximity Read ↗

Complete sequencing shows a role for MSX1 in non-syndromic cleft lip and palate.Semantic proximity Read ↗

Novel nonsense mutation in MSX1 causes tooth agenesis with cleft lip in a Chinese family.Semantic proximity Read ↗

A novel MSX1 intronic mutation associated with autosomal dominant non-syndromic oligodontia in a large Chinese family pedigree.Semantic proximity Read ↗

Orodental malformations associated with human MSX1 sequence variants.Semantic proximity Read ↗

Association between MSX1 SNPs and nonsyndromic cleft lip with or without cleft palate in the Korean population.Semantic proximity Read ↗

The role of MSX1 in tooth agenesis in Iranians.Semantic proximity Read ↗

A human MSX1 homeodomain missense mutation causes selective tooth agenesis.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 ↗

MSH homeobox 1 polymorphisms and the risk of non-syndromic orofacial clefts: a meta-analysis.Semantic proximity Read ↗

MSX1 gene polymorphisms in non-syndromic cleft lip and/or palate.Semantic proximity Read ↗

MSX1 mutations and associated disease phenotypes: genotype-phenotype relations.Semantic proximity Read ↗

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