Four novelRUNX2 mutations including a splice donor site result in the cleidocranial dysplasia phenotype-Reference-Cited by-同舟云学术

Four novelRUNX2 mutations including a splice donor site result in the cleidocranial dysplasia phenotype

Published:2006 Issue:1 Volume:207 Page:114-122
ISSN:0021-9541
Container-title:Journal of Cellular Physiology
language:en
Short-container-title:J. Cell. Physiol.

Author:

Kim Hyo-Jin,Nam Soon-Hyeun,Kim Hyun-Jung,Park Hyo-Sang,Ryoo Hyun-Mo,Kim Shin-Yoon,Cho Tae-Joon,Kim Seung-Gon,Bae Suk-Chul,Kim In-San,Stein Janet L.,van Wijnen Andre J.,Stein Gary S.,Lian Jane B.,Choi Je-Yong

Publisher

Wiley

Subject

Cell Biology,Clinical Biochemistry,Physiology

Reference38 articles.

1. Runt homology domain proteins in osteoblast differentiation: AML3/CBFA1 is a major component of a bone-specific complex

2. Subnuclear targeting of Runx/Cbfa/AML factors is essential for tissue-specific differentiation during embryonic development

3. Transcriptional regulation of chondrocyte maturation: Potential involvement of transcription factors in OA pathogenesis

4. Genetic control of cell differentiation in the skeleton

5. Osf2/Cbfa1: A Transcriptional Activator of Osteoblast Differentiation

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