(Q51973628)

English

Diversity of supernumerary tooth formation in siblings with cleidocranial dysplasia having identical mutation in RUNX2 : possible involvement of non-genetic or epigenetic regulation.

scientific article published in November 2007

In more languages

default for all languages

No label defined

No description defined

Statements

scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

19 April 2018

http://europepmc.org/abstract/MED/17973689

Diversity of supernumerary tooth formation in siblings with cleidocranial dysplasia having identical mutation in RUNX2 : possible involvement of non-genetic or epigenetic regulation. (English)

1 reference

Europe PubMed Central

PubMed publication ID

19 April 2018

http://europepmc.org/abstract/MED/17973689

1 reference

based on heuristic

inferred from title

cleidocranial dysplasia

1 reference

based on heuristic

inferred from title

author name string

Suda N

1

1 reference

Europe PubMed Central

PubMed publication ID

19 April 2018

http://europepmc.org/abstract/MED/17973689

Hamada T

2

1 reference

Europe PubMed Central

PubMed publication ID

19 April 2018

http://europepmc.org/abstract/MED/17973689

Hattori M

3

1 reference

Europe PubMed Central

PubMed publication ID

19 April 2018

http://europepmc.org/abstract/MED/17973689

Torii C

4

1 reference

Europe PubMed Central

PubMed publication ID

19 April 2018

http://europepmc.org/abstract/MED/17973689

Kosaki K

5

1 reference

Europe PubMed Central

PubMed publication ID

19 April 2018

http://europepmc.org/abstract/MED/17973689

Moriyama K

6

1 reference

Europe PubMed Central

PubMed publication ID

19 April 2018

http://europepmc.org/abstract/MED/17973689

publication date

1 November 2007

1 reference

Europe PubMed Central

PubMed publication ID

19 April 2018

http://europepmc.org/abstract/MED/17973689

Orthodontics & Craniofacial Research

1 reference

Europe PubMed Central

PubMed publication ID

19 April 2018

http://europepmc.org/abstract/MED/17973689

10

1 reference

Europe PubMed Central

PubMed publication ID

19 April 2018

http://europepmc.org/abstract/MED/17973689

4

1 reference

Europe PubMed Central

PubMed publication ID

19 April 2018

http://europepmc.org/abstract/MED/17973689

222-225

1 reference

Europe PubMed Central

PubMed publication ID

19 April 2018

http://europepmc.org/abstract/MED/17973689

Functional analysis of RUNX2 mutations in Japanese patients with cleidocranial dysplasia demonstrates novel genotype-phenotype correlations

1 reference

https://api.crossref.org/works/10.1111%2FJ.1601-6343.2007.00404.X

21 January 2018

Mutations involving the transcription factor CBFA1 cause cleidocranial dysplasia

1 reference

https://api.crossref.org/works/10.1111%2FJ.1601-6343.2007.00404.X

21 January 2018

The Runt domain identifies a new family of heteromeric transcriptional regulators.

1 reference

https://api.crossref.org/works/10.1111%2FJ.1601-6343.2007.00404.X

21 January 2018

Mutation analysis of core binding factor A1 in patients with cleidocranial dysplasia

1 reference

https://api.crossref.org/works/10.1111%2FJ.1601-6343.2007.00404.X

21 January 2018

Mutations in the RUNX2 gene in patients with cleidocranial dysplasia

1 reference

https://api.crossref.org/works/10.1111%2FJ.1601-6343.2007.00404.X

21 January 2018

DHPLC in clinical molecular diagnostic services

1 reference

https://api.crossref.org/works/10.1111%2FJ.1601-6343.2007.00404.X

21 January 2018

Comprehensive screening of CREB-binding protein gene mutations among patients with Rubinstein-Taybi syndrome using denaturing high-performance liquid chromatography.

1 reference

https://api.crossref.org/works/10.1111%2FJ.1601-6343.2007.00404.X

21 January 2018

The genetic basis of tooth development and dental defects.

1 reference

https://api.crossref.org/works/10.1111%2FJ.1601-6343.2007.00404.X

21 January 2018

Epigenetic regulation of gene expression: how the genome integrates intrinsic and environmental signals

1 reference

https://api.crossref.org/works/10.1111%2FJ.1601-6343.2007.00404.X

21 January 2018

Missense mutations abolishing DNA binding of the osteoblast-specific transcription factor OSF2/CBFA1 in cleidocranial dysplasia.

1 reference

https://api.crossref.org/works/10.1111%2FJ.1601-6343.2007.00404.X

21 January 2018

Identifiers

10.1111/J.1601-6343.2007.00404.X

1 reference

Europe PubMed Central

PubMed publication ID

19 April 2018

http://europepmc.org/abstract/MED/17973689

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

19 April 2018

http://europepmc.org/abstract/MED/17973689

Sitelinks

Wikipedia(0 entries)

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(0 entries)

Retrieved from "https://www.wikidata.org/w/index.php?title=Q51973628&oldid=2077314682"