A novel, complex RUNX2 gene mutation causes cleidocranial dysplasia

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Syringic acid, a phenolic acid, promotes osteoblast differentiation by stimulation of Runx2 expression and targeting of Smad7 by miR-21 in mouse mesenchymal stem cells.

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A novel, complex RUNX2 gene mutation causes cleidocranial dysplasia

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A novel, complex RUNX2 gene mutation causes cleidocranial dysplasia

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A novel, complex RUNX2 gene mutation causes cleidocranial dysplasia

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label

A novel, complex RUNX2 gene mutation causes cleidocranial dysplasia

@ast

A novel, complex RUNX2 gene mutation causes cleidocranial dysplasia

@en

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A novel, complex RUNX2 gene mutation causes cleidocranial dysplasia

@ast

A novel, complex RUNX2 gene mutation causes cleidocranial dysplasia

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P1476

A novel, complex RUNX2 gene mutation causes cleidocranial dysplasia

@en

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Cuixian Liu

http://www.w3.org/2001/XMLSchema#string

Fu Xiong

http://www.w3.org/2001/XMLSchema#string

Jiajing Chen

http://www.w3.org/2001/XMLSchema#string

Qiuyue Chen

http://www.w3.org/2001/XMLSchema#string

Wen'an Xu

http://www.w3.org/2001/XMLSchema#string

P2860

Mutations involving the transcription factor CBFA1 cause cleidocranial dysplasia

I-TASSER: a unified platform for automated protein structure and function prediction

DNA recognition by the RUNX1 transcription factor is mediated by an allosteric transition in the RUNT domain and by DNA bending

Osf2/Cbfa1: a transcriptional activator of osteoblast differentiation

Role of the RUNX2 p.R225Q mutation in cleidocranial dysplasia: a rare presentation and an analysis of the RUNX2 protein structure.

The I-TASSER Suite: protein structure and function prediction.

Disease mutations in RUNX1 and RUNX2 create nonfunctional, dominant-negative, or hypomorphic alleles.

Tissue-specific calibration of extracellular matrix material properties by transforming growth factor-β and Runx2 in bone is required for hearing

A novel RUNX2 missense mutation predicted to disrupt DNA binding causes cleidocranial dysplasia in a large Chinese family with hyperplastic nails.

Cbfβ deletion in mice recapitulates cleidocranial dysplasia and reveals multiple functions of Cbfβ required for skeletal development.

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s12881-017-0375-x

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scholarly article

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10.1186/S12881-017-0375-X

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Buling Wu

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2017-02-07T00:00:00Z

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A novel, complex RUNX2 gene mutation causes cleidocranial dysplasia

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P2860

P2860

A novel, complex RUNX2 gene mutation causes cleidocranial dysplasia

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P1433

P1476

P2093

P2860

P2888

P304

P31

P356

P433

P478

P50

P577

P6179

P698

P932

P356

P1433

P1476

P2093

P2860

P2888

P304

P31

P356

P433

P478

P50

P577

P6179

P698

P932