Identification and functional analysis of two novel PAX9 mutations (Q33666378)

28 July 2017

title

Identification and functional analysis of two novel PAX9 mutations (English)

1 reference

28 July 2017

Ying Wang

1

1 reference

28 July 2017

Hua Wu

2

1 reference

28 July 2017

Jingfeng Wu

3

1 reference

28 July 2017

Hongshan Zhao

4

1 reference

28 July 2017

Xiaoxia Zhang

5

1 reference

28 July 2017

Gabriele Mues

6

1 reference

28 July 2017

Rena N D'Souza

7

1 reference

28 July 2017

Hailan Feng

8

1 reference

28 July 2017

Hitesh Kapadia

9

1 reference

28 July 2017

language of work or name

1 reference

14 August 2008

1 reference

28 July 2017

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28 July 2017

volume

189

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28 July 2017

issue

1-4

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28 July 2017

page(s)

80-87

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Exclusion of coding region mutations in MSX1, PAX9 and AXIN2 in eight patients with severe oligodontia phenotype

28 July 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2824186

Novel mutation of the initiation codon of PAX9 causes oligodontia

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2824186

A novel missense mutation in the paired domain of PAX9 causes non-syndromic oligodontia

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2824186

Novel identification of a four-base-pair deletion mutation in PITX2 in a Rieger syndrome family

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2824186

Functional analysis of a mutation in PAX9 associated with familial tooth agenesis in humans

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2824186

A missense mutation in PAX9 in a family with distinct phenotype of oligodontia

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2824186

Novel mutation in the paired box sequence of PAX9 gene in a sporadic form of oligodontia

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2824186

Epithelial-mesenchymal signalling regulating tooth morphogenesis

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2824186

Haploinsufficiency of PAX9 is associated with autosomal dominant hypodontia

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2824186

Identification of a nonsense mutation in the PAX9 gene in molar oligodontia

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2824186

A nonsense mutation in MSX1 causes Witkop syndrome

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2824186

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

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2824186

Mutation of PAX9 is associated with oligodontia

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2824186

Pax9-deficient mice lack pharyngeal pouch derivatives and teeth and exhibit craniofacial and limb abnormalities.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2824186

Identification of a novel mutation in the PAX9 gene in a family affected by oligodontia and other dental anomalies.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2824186

Genes affecting tooth morphogenesis.

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2824186

The genetic basis of tooth development and dental defects.

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2824186

Functional consequences of interactions between Pax9 and Msx1 genes in normal and abnormal tooth development.

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2824186

Molecular characterization of a novel PAX9 missense mutation causing posterior tooth agenesis

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2824186

Reduction of Pax9 gene dosage in an allelic series of mouse mutants causes hypodontia and oligodontia.

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2824186

[Novel mutations of PAX9 gene in Chinese patients with oligodontia].

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2824186

A novel mutation in human PAX9 causes molar oligodontia

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2824186

Novel missense mutations and a 288-bp exonic insertion in PAX9 in families with autosomal dominant hypodontia

30 October 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/18701815

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

A novel mutation in PAX9 causes familial form of molar oligodontia

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/18701815

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1159/000151448

1 reference

28 July 2017

1 reference

28 July 2017

1 reference