A Novel AXIN2 Missense Mutation Is Associated with Non-Syndromic Oligodontia (Q35787716)

10 August 2017

title

A Novel AXIN2 Missense Mutation Is Associated with Non-Syndromic Oligodontia (English)

1 reference

10 August 2017

Haochen Liu

1

1 reference

10 August 2017

Tingting Ding

series ordinal

2

1 reference

10 August 2017

Yuan Zhan

series ordinal

3

1 reference

10 August 2017

Hailan Feng

series ordinal

4

1 reference

10 August 2017

language of work or name

English

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publication date

25 September 2015

1 reference

10 August 2017

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10 August 2017

volume

10

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10 August 2017

issue

9

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10 August 2017

page(s)

e0138221

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Creative Commons Attribution 4.0 International

10 August 2017

copyright license

start time

25 September 2015

1 reference

April 2022 Public Data File from Crossref

copyright status

copyrighted

0 references

cites work

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Mutational analysis of AXIN2, MSX1, and PAX9 in two Mexican oligodontia families

27 July 2018

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Developmental disorders of the dentition: an update

27 July 2018

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

27 July 2018

1 reference

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Genetic background of nonsyndromic oligodontia: a systematic review and meta-analysis

27 July 2018

1 reference

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WNT10A missense mutation associated with a complete odonto-onycho-dermal dysplasia syndrome

27 July 2018

1 reference

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EDA gene mutations underlie non-syndromic oligodontia

27 July 2018

1 reference

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Protein structure prediction on the Web: a case study using the Phyre server

27 July 2018

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Genetic basis of tooth agenesis

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4583461

Axis inhibition protein 2 (AXIN2) polymorphisms and tooth agenesis

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4583461

Identification and functional analysis of two novel PAX9 mutations

27 July 2018

1 reference

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Novel EDA mutation resulting in X-linked non-syndromic hypodontia and the pattern of EDA-associated isolated tooth agenesis

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4583461

Axis inhibition protein 2 (AXIN2) polymorphisms may be a risk factor for selective tooth agenesis

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4583461

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27 July 2018

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

27 July 2018

1 reference

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The regulator of G protein signaling family

27 July 2018

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Mutation of PAX9 is associated with oligodontia

27 July 2018

1 reference

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Teeth. Where and how to make them.

27 July 2018

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Antagonistic interactions between FGF and BMP signaling pathways: a mechanism for positioning the sites of tooth formation

27 July 2018

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A human MSX1 homeodomain missense mutation causes selective tooth agenesis

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4583461

WNT10A mutations account for ¼ of population-based isolated oligodontia and show phenotypic correlations.

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4583461

Genetic basis of dental agenesis--molecular genetics patterning clinical dentistry

25 September 2018

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The ectodysplasin pathway: from diseases to adaptations

25 September 2018

1 reference

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WNT10A variants are associated with non-syndromic tooth agenesis in the general population

25 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4583461

Novel EDA p.Ile260Ser mutation linked to non-syndromic hypodontia

25 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4583461

Non-syndromic tooth agenesis associated with a nonsense mutation in ectodysplasin-A (EDA).

25 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4583461

Mutations in WNT10A are present in more than half of isolated hypodontia cases.

25 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4583461

Only four genes (EDA1, EDAR, EDARADD, and WNT10A) account for 90% of hypohidrotic/anhidrotic ectodermal dysplasia cases

25 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4583461

PAX9 polymorphisms and susceptibility to sporadic tooth agenesis: a case-control study in southeast China.

25 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4583461

Novel missense mutations in the AXIN2 gene associated with non-syndromic oligodontia

25 September 2018

1 reference

12 December 2020

A novel non-stop mutation in MSX1 causing autosomal dominant non-syndromic oligodontia

1 reference

12 December 2020

A novel missense mutation in MSX1 underlies autosomal recessive oligodontia with associated dental anomalies in Pakistani families

1 reference

12 December 2020

Schöpf-Schulz-Passarge syndrome resulting from a homozygous nonsense mutation in WNT10A

1 reference

12 December 2020

AXIN2-associated autosomal dominant ectodermal dysplasia and neoplastic syndrome

1 reference

12 December 2020

Isolated oligodontia associated with mutations in EDARADD, AXIN2, MSX1, and PAX9 genes

1 reference

12 December 2020

Schöpf-Schulz-Passarge syndrome resulting from a homozygous nonsense mutation, p.Cys107X, in WNT10A

1 reference

12 December 2020

Polymorphism in the Msx1 gene associated with hypodontia in a Brazilian family

1 reference

12 December 2020

10.1371/JOURNAL.PONE.0138221

Identifiers

DOI

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10 August 2017

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10 August 2017

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