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

FGFR1 variants contributed to families with tooth agenesis.

Human genomics - 13 Oct 2023

Yao Siyue, Zhou Xi, Gu Min, Zhang Chengcheng, Bartsch Oliver, Vona Barbara, Fan Liwen, Ma Lan, Pan Yongchu

Abstract excerpt

BACKGROUND: Tooth agenesis is a common dental anomaly that can substantially affect both the ability to chew and the esthetic appearance of patients. This study aims to identify possible genetic factors that underlie various forms of tooth agenesis and to investigate the possible molecular mechanisms through which human dental pulp stem cells may play a role in this condition. RESULTS: Using whole-exome...

Read the complete abstract on PubMed

Topics

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

Share to Anodontia
Share to HEK293 Cells
Share to Mutation

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Mutation, Missense

Share to Receptor, Fibroblast Growth Factor, Type 1

Source

Open in PubMed Open full text

Identifiers

PMID: 37833774
DOI: 10.1186/s40246-023-00539-8
PMCID: PMC10576343

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 3 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

FGFR1 variants contributed to families with tooth agenesis.PMID 37833774Read ↗

Expanding the genetic spectrum of tooth agenesis using whole-exome sequencing.Semantic proximity Read ↗

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

Tooth agenesis: What do we know and is there a connection to cancer?Semantic proximity Read ↗

Whole-Exome Sequencing Identifies Novel Variants for Tooth Agenesis.Semantic proximity Read ↗

Interferon regulatory factor 6 (IRF6) and fibroblast growth factor receptor 1 (FGFR1) contribute to human tooth agenesis.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 ↗

Identification of novel candidate genes associated with non-syndromic tooth agenesis in Mongolian familiesSemantic proximity Read ↗

Dental agenesis: From molecular diagnosis to multidisciplinary managementSemantic proximity Read ↗

Ectrodactyly and Lethal Pulmonary Acinar Dysplasia Associated with Homozygous<i>FGFR2</i>Mutations Identified by Exome SequencingSemantic proximity Read ↗

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

Identification of a Novel FGFR2 Gene Mutation (c.514_515delinsCT, p.Ala172Leu) in a Chinese Neonate With Apert Syndrome: A Case Report.Semantic proximity Read ↗

A Novel LRP6 Mutation Highlights the Role of Wnt Signaling in Tooth Agenesis.Semantic proximity Read ↗

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