Novel Mutation of the RUNX2 Gene in Patients with Cleidocranial Dysplasia.

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Novel Mutation of the RUNX2 Gene in Patients with Cleidocranial Dysplasia.

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2017 nî lūn-bûn

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2017年の論文

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2017年学术文章

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2017年学术文章

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2017年学术文章

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2017年学术文章

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2017年学术文章

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2017年学术文章

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2017年學術文章

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2017年學術文章

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Novel Mutation of the RUNX2 Gene in Patients with Cleidocranial Dysplasia.

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Novel Mutation of the RUNX2 Gene in Patients with Cleidocranial Dysplasia.

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Novel Mutation of the RUNX2 Gene in Patients with Cleidocranial Dysplasia.

@en

Novel Mutation of the RUNX2 Gene in Patients with Cleidocranial Dysplasia.

@nl

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Novel Mutation of the RUNX2 Gene in Patients with Cleidocranial Dysplasia.

@en

Novel Mutation of the RUNX2 Gene in Patients with Cleidocranial Dysplasia.

@nl

P1476

Novel Mutation of the RUNX2 Gene in Patients with Cleidocranial Dysplasia

@en

P2093

Anna Jaruga

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Ewa Hordyjewska

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Grzegorz Kandzierski

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P2860

Mutations involving the transcription factor CBFA1 cause cleidocranial dysplasia

AML1, AML2, and AML3, the human members of the runt domain gene-family: cDNA structure, expression, and chromosomal localization

Transcriptional repression by AML1 and LEF-1 is mediated by the TLE/Groucho corepressors

Immunoglobulin motif DNA recognition and heterodimerization of the PEBP2/CBF Runt domain

Structural analyses of DNA recognition by the AML1/Runx-1 Runt domain and its allosteric control by CBFbeta

Cbfa1, a candidate gene for cleidocranial dysplasia syndrome, is essential for osteoblast differentiation and bone development

Mutations in the RUNX2 gene in patients with cleidocranial dysplasia

Osf2/Cbfa1: a transcriptional activator of osteoblast differentiation

Targeted disruption of Cbfa1 results in a complete lack of bone formation owing to maturational arrest of osteoblasts

Novel complex disease allele mutations in cleidocranial dysplasia patients.

P304

253-260

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P31

scholarly article

P356

10.1159/000477307

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P433

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

P478

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P50

Przemko Tylzanowski

P577

2017-06-15T00:00:00Z

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P698

28878609

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P932

5582518

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