نتایج جستجو برای: runx2 gene

تعداد نتایج: 1142462  

2012
Nyam-Osor Chimge Sanjeev K. Baniwal Jingqin Luo Simon Coetzee Omar Khalid Benjamin P. Berman Debu Tripathy Matthew J. Ellis Baruch Frenkel

Purpose: To assess the clinical significance of the interaction between estrogen and Runx2 signaling, previously shown in vitro. ExperimentalDesign:MCF7/Rx2 breast cancer cells were treatedwith estradiol and/or doxycycline to induce Runx2, and global gene expression was profiled to define genes regulated by estradiol, Runx2, or both. Anchorage-independent growthwas assessed by soft-agar colony ...

Journal: :Genetics and molecular research : GMR 2010
G X Wang R P Sun F L Song

Cleidocranial dysplasia (CCD) is an autosomal-dominant heritable skeletal disease caused by heterozygous mutations in the RUNX2 gene. We studied a Chinese family that included three affected individuals with CCD phenotypes; the clinical features of patients with CCD include delayed closure of fontanelles, frontal bossing, dysplasia of clavicles, late tooth eruption, and other skeletal anomalies...

2011
Xinli Zhang Kang Ting Catherine M Bessette Cymbeline T Culiat Sang Jin Sung Haofu Lee Feng Chen Jia Shen James J Wang Shun'ichi Kuroda Chia Soo

Mesenchymal stem cell commitment to an osteoprogenitor lineage requires the activity of Runx2, a molecule implicated in the etiopathology of multiple congenital craniofacial anomalies. Through promoter analyses, we have recently identified a new direct transcriptional target of Runx2, Nell-1, a craniosynostosis (CS)-associated molecule with potent osteogenic properties. This study investigated ...

Journal: :Biomaterials 2011
Jai-Sun Lee Jong-Min Lee Gun-Il Im

In the present study, we tested the hypothesis that electroporation-mediated transfer of Runx2, Osterix, or both genes enhances the in vitro and in vivo osteogenesis from adipose stem cells (ASCs). ASCs were transfected with Runx2, Osterix, or both genes using electroporation, and further cultured in monolayer or in PLGA scaffold under osteogenic medium for 14 days, then analyzed for in vitro o...

2017
Xianli Zhang Yang Liu Xiaozhe Wang Xiangyu Sun Chenying Zhang Shuguo Zheng

Cleidocranial dysplasia (CCD) is an autosomal dominant inheritable skeletal disorder characterized by cranial dysplasia, clavicle hypoplasia and dental abnormalities. This disease is mainly caused by heterozygous mutations in RUNX2, a gene that encodes an osteoblast-specific transcription factor. In the present study, mutational analyses of RUNX2 gene were performed on four unrelated Chinese pa...

2015
Effat Farrokhi Keihan Ghatreh Samani Morteza Hashemzadeh Mohammad Amin Tabatabaiefar

BACKGROUND Vascular calcification is an important stage in atherosclerosis. During this stage, vascular smooth muscle cells (VSMC) synthesize many osteogenic factors such as osteonectin (encoded by SPARC). Oxidative stress plays a critical role in atherosclerosis progression, and its accumulation in the vascular wall stimulates the development of atherosclerosis and vascular calcification. The ...

Journal: :The Journal of biological chemistry 2000
T L McCarthy C Ji Y Chen K K Kim M Imagawa Y Ito M Centrella

Transcription factor CCAAT/enhancer-binding protein delta (C/EBPdelta) is normally associated with acute-phase gene expression. However, it is expressed constitutively in primary osteoblast cultures where it increases insulin-like growth factor I synthesis in a cAMP-dependent way. Here we show that the 3' proximal region of the C/EBPdelta gene promoter contains a binding sequence for Runt domai...

2015
Daniel W. Young Anthony N. Imbalzano Jeffrey A. Nickerson Arthur B. Pardee Jane B. Lian Jitesh Pratap Amjad Javed Brian Wiener Yasuyuki Ohkawa Andre J. van Wijnen Gary S. Stein Janet L. Stein Sayyed K. Zaidi Xiaoqing Yang Mario Galindo Sayyed K Zaidi Jean Underwood Jeffrey Nickerson Sheldon Penman

The Runx family of transcription factors performs an essential role in animal development by controllng gene expression programs that mediate cell proliferation growth and differentiation. The work described in this thesis is concerned with understanding mechanisms by which Runx proteins support this program of gene expression within the architectural context of the mammalian cell nucleus. Mult...

Journal: :Journal of cellular biochemistry 2011
Tae-Geon Kwon Xiang Zhao Qian Yang Yan Li Chunxi Ge Guisheng Zhao Renny T Franceschi

Angiogenesis and bone formation are intimately related processes. Hypoxia during early bone development stabilizes hypoxia-inducible factor-1α (HIF-1α) and increases angiogenic signals including vascular endothelial growth factor (VEGF). Furthermore, stabilization of HIF-1α by genetic or chemical means stimulates bone formation. On the other hand, deficiency of Runx2, a key osteogenic transcrip...

Journal: :Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research 2012
Yan Li Chunxi Ge Jason P Long Dana L Begun Jose A Rodriguez Steven A Goldstein Renny T Franceschi

Bone can adapt its structure in response to mechanical stimuli. At the cellular level, this involves changes in chromatin organization, gene expression, and differentiation, but the underlying mechanisms are poorly understood. Here we report on the involvement of RUNX2, a bone-related transcription factor, in this process. Fluid flow shear stress loading of preosteoblasts stimulated translocati...

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