(Q56786597)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22023169%20AND%20SRC:MED&resulttype=core&format=json

15 January 2020

title

Cleidocranial dysplasia: oral features and genetic analysis of 11 patients (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22023169%20AND%20SRC:MED&resulttype=core&format=json

15 January 2020

main subject

cleidocranial dysplasia

1 reference

1

1 reference

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15 January 2020

Luiz Alcino Gueiros

4

1 reference

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15 January 2020

Edgard Graner

8

1 reference

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15 January 2020

Pablo Agustin Vargas

10

1 reference

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15 January 2020

author name string

H Martelli-Júnior

5

1 reference

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15 January 2020

L M R Paranaíba

2

1 reference

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15 January 2020

A F Gouvêa

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22023169%20AND%20SRC:MED&resulttype=core&format=json

15 January 2020

J J Junior

6

1 reference

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15 January 2020

M A Lopes

7

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22023169%20AND%20SRC:MED&resulttype=core&format=json

15 January 2020

O P De Almeida

9

1 reference

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15 January 2020

R D Coletta

11

1 reference

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15 January 2020

publication date

24 October 2011

1 reference

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15 January 2020

1 reference

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15 January 2020

volume

18

1 reference

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15 January 2020

issue

2

1 reference

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15 January 2020

page(s)

184-190

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22023169%20AND%20SRC:MED&resulttype=core&format=json

A simple and cost-effective protocol for DNA isolation from buccal epithelial cells

15 January 2020

cites work

1 reference

https://api.crossref.org/works/10.1111%2FJ.1601-0825.2011.01862.X

Runx2 in normal tissues and cancer cells: A developing story.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1601-0825.2011.01862.X

Cleidocranial dysplasia with severe parietal bone dysplasia: C-terminal RUNX2 mutations

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1601-0825.2011.01862.X

The Drosophila segmentation gene runt encodes a novel nuclear regulatory protein that is also expressed in the developing nervous system

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1601-0825.2011.01862.X

Intrinsic transcriptional activation-inhibition domains of the polyomavirus enhancer binding protein 2/core binding factor alpha subunit revealed in the presence of the beta subunit

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1601-0825.2011.01862.X

Four novel RUNX2 mutations including a splice donor site result in the cleidocranial dysplasia phenotype.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1601-0825.2011.01862.X

Regulation of bone development and maintenance by Runx2.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1601-0825.2011.01862.X

Regulation of bone development and extracellular matrix protein genes by RUNX2.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1601-0825.2011.01862.X

PEBP2/PEA2 represents a family of transcription factors homologous to the products of the Drosophila runt gene and the human AML1 gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1601-0825.2011.01862.X

Mutations in the RUNX2 gene in patients with cleidocranial dysplasia

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1601-0825.2011.01862.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1601-0825.2011.01862.X

RUNX2 mutations in cleidocranial dysplasia patients.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1601-0825.2011.01862.X

Overlapping expression of Runx1(Cbfa2) and Runx2(Cbfa1) transcription factors supports cooperative induction of skeletal development

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1601-0825.2011.01862.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1601-0825.2011.01862.X

Correlation between genotype and supernumerary tooth formation in cleidocranial dysplasia

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1601-0825.2011.01862.X

Six novel mutations of the RUNX2 gene in Italian patients with cleidocranial dysplasia.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1601-0825.2011.01862.X

Delayed tooth eruption and suppressed osteoclast number in the eruption pathway of heterozygous Runx2/Cbfa1 knockout mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1601-0825.2011.01862.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1601-0825.2011.01862.X

Functional analysis of RUNX2 mutations in cleidocranial dysplasia: novel insights into genotype–phenotype correlations

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1601-0825.2011.01862.X

Mutational analysis of RUNX2 gene in Chinese patients with cleidocranial dysplasia.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1601-0825.2011.01862.X

10.1111/J.1601-0825.2011.01862.X

21 January 2018

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22023169%20AND%20SRC:MED&resulttype=core&format=json

15 January 2020

1 reference