(Q51921714)

17 April 2018

title

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

1 reference

17 April 2018

author name string

Alexandre R Vieira

1

1 reference

17 April 2018

Adriana Modesto

2

1 reference

17 April 2018

Raquel Meira

3

1 reference

17 April 2018

Anna Renata Schneider Barbosa

4

1 reference

17 April 2018

Andrew C Lidral

5

1 reference

17 April 2018

Jeffrey C Murray

6

1 reference

17 April 2018

language of work or name

English

0 references

publication date

1 March 2007

1 reference

17 April 2018

American Journal of Medical Genetics

published in

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17 April 2018

volume

143A

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17 April 2018

issue

6

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17 April 2018

page(s)

538-545

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17 April 2018

Interferon regulatory factor-6: a gene predisposing to isolated cleft lip with or without cleft palate in the Belgian population

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2570343

Variation in IRF6 contributes to nonsyndromic cleft lip and palate

22 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2570343

Significant association between IRF6 820G->A and non-syndromic cleft lip with or without cleft palate in the Thai population

22 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2570343

Mutations that cause osteoglophonic dysplasia define novel roles for FGFR1 in bone elongation

22 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2570343

Strong evidence of linkage disequilibrium between polymorphisms at the IRF6 locus and nonsyndromic cleft lip with or without cleft palate, in an Italian population

22 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2570343

Interferon regulatory factor 6 (IRF6) gene variants and the risk of isolated cleft lip or palate

22 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2570343

Mutations in AXIN2 cause familial tooth agenesis and predispose to colorectal cancer

22 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2570343

Family-based tests for associating haplotypes with general phenotype data: application to asthma genetics

22 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2570343

Genetic association studies of cleft lip and/or palate with hypodontia outside the cleft region

22 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2570343

Oral clefts and syndromic forms of tooth agenesis as models for genetics of isolated tooth agenesis

22 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2570343

Mutations in IRF6 cause Van der Woude and popliteal pterygium syndromes

22 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2570343

The role of MSX1 in human tooth agenesis

22 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2570343

MSX1 mutation is associated with orofacial clefting and tooth agenesis in humans

22 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2570343

FGFR1 is fused to the centrosome-associated protein CEP110 in the 8p12 stem cell myeloproliferative disorder with t(8;9)(p12;q33)

22 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2570343

Splicing mutations of 54-bp exons in the COL11A1 gene cause Marshall syndrome, but other mutations cause overlapping Marshall/Stickler phenotypes

22 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2570343

An allele of COL9A2 associated with intervertebral disc disease

22 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2570343

A common mutation in the fibroblast growth factor receptor 1 gene in Pfeiffer syndrome

22 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2570343

Associations of some variables to tooth formation in children with isolated cleft palate.

22 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2570343

Symmetry and combinations of hypodontia in non-cleft and cleft palate children

22 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2570343

Stop codon in the procollagen II gene (COL2A1) in a family with the Stickler syndrome (arthro-ophthalmopathy)

22 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2570343

Congenital absence of teeth: a review with emphasis on inheritance patterns

22 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2570343

Hypodontia: Prevalence amongst Jewish populations of different origin

22 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2570343

MSX1, PAX9, and TGFA contribute to tooth agenesis in humans.

22 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2570343

Loss-of-function mutations in FGFR1 cause autosomal dominant Kallmann syndrome.

13 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2570343

The family based association test method: strategies for studying general genotype--phenotype associations.

13 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2570343

Anomalies in number of teeth in patients with lip and/or palate clefts

13 August 2018

1 reference

12 December 2020

Frequency of tooth agenesis in CLP patients with eruption of all four third molars

1 reference

12 December 2020

Numeric anomalies of teeth in concomitant hypodontia and hyperdontia

1 reference

12 December 2020

Dental anomalies in patients with familial and sporadic cleft lip and palate

1 reference

12 December 2020

Dental Abnormalities, Bone Graft Quality, and Periodontal Conditions in Patients With Unilateral Cleft Lip and Palate at Different Phases of Orthodontic Treatment

1 reference

12 December 2020

GOLD--graphical overview of linkage disequilibrium

1 reference

12 December 2020

Abnormalities of the maxillary incisors in children with cleft lip and palate

1 reference

12 December 2020

Dental abnormalities and ectopic eruption in patients with isolated cleft palate

1 reference

12 December 2020

Identifiers

DOI

10.1002/AJMG.A.31620

1 reference

17 April 2018

PMCID

2570343

1 reference

17 April 2018

PubMed ID

17318851

1 reference

17 April 2018