Novel MSX1 frameshift causes autosomal-dominant oligodontia (Q36453481)

14 August 2017

Novel MSX1 frameshift causes autosomal-dominant oligodontia (English)

1 reference

14 August 2017

J-W Kim

1

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14 August 2017

J P Simmer

series ordinal

2

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14 August 2017

B P-J Lin

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3

1 reference

14 August 2017

J C-C Hu

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4

1 reference

14 August 2017

language of work or name

English

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publication date

1 March 2006

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Journal of Dental Research

14 August 2017

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14 August 2017

85

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14 August 2017

3

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14 August 2017

267-271

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Studies on Pax9-Msx1 protein interactions

14 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2238638

Novel mutation of the initiation codon of PAX9 causes oligodontia

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2238638

MSX1 cooperates with histone H1b for inhibition of transcription and myogenesis

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2238638

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

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2238638

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

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2238638

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

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2238638

Molecular basis of non-syndromic tooth agenesis: mutations of MSX1 and PAX9 reflect their role in patterning human dentition

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2238638

Complete sequencing shows a role for MSX1 in non-syndromic cleft lip and palate

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2238638

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

30 September 2017

2 references

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2238638

30 September 2017

https://api.crossref.org/works/10.1177%2F154405910608500312

The role of MSX1 in human tooth agenesis

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2238638

Haploinsufficiency of PAX9 is associated with autosomal dominant hypodontia

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2238638

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

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2238638

Msx homeobox genes inhibit differentiation through upregulation of cyclin D1.

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2238638

A nonsense mutation in MSX1 causes Witkop syndrome

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2238638

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

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2238638

Mutation of PAX9 is associated with oligodontia

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2238638

Msx1 antagonizes the myogenic activity of Pax3 in migrating limb muscle precursors.

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2238638

Transcriptional autorepression of Msx1 gene is mediated by interactions of Msx1 protein with a multi-protein transcriptional complex containing TATA-binding protein, Sp1 and cAMP-response-element-binding protein-binding protein (CBP/p300)

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2238638

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

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2238638

Protein complex formation between Msx1 and Lhx2 homeoproteins is incompatible with DNA binding activity

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2238638

Heterodimerization of Msx and Dlx homeoproteins results in functional antagonism

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2238638

Msx1 controls inductive signaling in mammalian tooth morphogenesis

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2238638

A human MSX1 homeodomain missense mutation causes selective tooth agenesis

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2238638

Msx1 deficient mice exhibit cleft palate and abnormalities of craniofacial and tooth development

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2238638

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

28 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2238638

Epidemiological significance of Hoffmeister's "Genetically determined predisposition to disturbed development of the dentition".

21 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2238638

A novel mutation in human PAX9 causes molar oligodontia

21 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2238638

MSX1 gene is deleted in Wolf-Hirschhorn syndrome patients with oligodontia

21 September 2018

1 reference

12 December 2020

A novelMSX1 mutation in hypodontia

1 reference

12 December 2020

Agenesis of third molars in young Czech population

1 reference

12 December 2020

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

1 reference

12 December 2020

10.1177/154405910608500312

Identifiers

DOI

1 reference

14 August 2017

1 reference

14 August 2017

PubMed publication ID

16498076

1 reference