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

Novel cleft susceptibility genes in chromosome 6q.

Journal of dental research - 1 Sept 2010

Letra A, Menezes R, Fonseca R F, Govil M, McHenry T, Murphy M J, Hennebold J D, Granjeiro J M, Castilla E E, Orioli I M, Martin R, Marazita M L, Bjork B C, Vieira A R

Abstract excerpt

Cleft lip/palate is a defect of craniofacial development. In previous reports, chromosome 6q has been suggested as a candidate region for cleft lip/palate. A multipoint posterior probability of linkage analysis of multiplex families from the Philippines attributed an 88% probability of harboring...

Read the complete abstract on PubMed

Topics

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

Share to Chi-Square Distribution
Share to Chromosomes, Human, Pair 6
Share to Cleft Lip

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Cleft Palate

Share to Databases, Genetic

Share to Monomeric Clathrin Assembly Proteins

Share to Serine Endopeptidases

Share to Serine Proteases

Source

Open in PubMed Open full text

Identifiers

PMID: 20511563
DOI: 10.1177/0022034510370004
PMCID: PMC2924960

Genes

PRSS35
SNAP91

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-20511563-2026-09-02.2. 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 · 8 closest

Novel cleft susceptibility genes in chromosome 6q.PMID 20511563Read ↗

Expression and mutation analyses implicate ARHGAP29 as the etiologic gene for the cleft lip with or without cleft palate locus identified by genome-wide association on chromosome 1p22.Semantic proximity Read ↗

Meta-analysis Reveals Genome-Wide Significance at 15q13 for Nonsyndromic Clefting of Both the Lip and the Palate, and Functional Analyses Implicate GREM1 As a Plausible Causative Gene.Semantic proximity Read ↗

IRF6 rs2235375 single nucleotide polymorphism is associated with isolated non-syndromic cleft palate but not with cleft lip with or without palate in South Indian population.Semantic proximity Read ↗

Fine Mapping of 6q23.1 Identifies TULP4 as Contributing to Clefts.Semantic proximity Read ↗

[Association of non-syndromic cleft lip and cleft palate with microsatellite markers located in 6p].Semantic proximity Read ↗

A mutation in mouse Pak1ip1 causes orofacial clefting while human PAK1IP1 maps to 6p24 translocation breaking points associated with orofacial clefting.Semantic proximity Read ↗

Novel genetic linkage of rat Sp6 mutation to Amelogenesis imperfecta.Semantic proximity Read ↗

Exploration of Genetic Variants of Non-syndromic Cleft Lip with or without Palate and Underlying Mechanisms.Semantic proximity Read ↗

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