نتایج جستجو برای: sox9

تعداد نتایج: 2137  

Journal: :Developmental cell 2012
Peter Dy Weihuan Wang Pallavi Bhattaram Qiuqing Wang Lai Wang R Tracy Ballock Véronique Lefebvre

The transcription factor Sox9 is necessary for early chondrogenesis, but its subsequent roles in the cartilage growth plate, a highly specialized structure that drives skeletal growth and endochondral ossification, remain unclear. Using a doxycycline-inducible Cre transgene and Sox9 conditional null alleles in the mouse, we show that Sox9 is required to maintain chondrocyte columnar proliferati...

2007
Hongyun Wang Nicole C. McKnight Tao Zhang Michael L. Lu Steven P. Balk Xin Yuan

SOX9 is a member of the SOX [Sry-related high-mobility group (HMG) box] family of HMG DNA-binding domain transcription factors and is required for the development and differentiation of multiple cell lineages. This report shows that basal epithelial cells express SOX9 in normal prostate, with no detectable expression in luminal epithelial cells. In contrast, SOX9 is expressed in primary prostat...

Journal: :The Journal of heredity 2005
A K Hett C Pitra I Jenneckens A Ludwig

The Sox9 gene of Acipenser sturio, one of the most primitive vertebrates, was analyzed. No sex-specific differences were observed. Sturgeon Sox9 consists of three exons and two introns with completely conserved exon-intron boundaries showing high levels of homology to other vertebrate Sox9 sequences, especially in the N-terminus region containing the HMG box. We found strong evidence for negati...

2013
Elise Martin Xavier Caubit Rannar Airik Christine Vola Ahmed Fatmi Andreas Kispert Laurent Fasano

Smooth muscle cells are of key importance for the proper functioning of different visceral organs including those of the urogenital system. In the mouse ureter, the two transcriptional regulators TSHZ3 and SOX9 are independently required for initiation of smooth muscle differentiation from uncommitted mesenchymal precursor cells. However, it has remained unclear whether TSHZ3 and SOX9 act indep...

2015
Baojin Yao Qiuqing Wang Chia-Feng Liu Pallavi Bhattaram Wei Li Timothy J. Mead James F. Crish Véronique Lefebvre

Two decades after the discovery that heterozygous mutations within and around SOX9 cause campomelic dysplasia, a generalized skeleton malformation syndrome, it is well established that SOX9 is a master transcription factor in chondrocytes. In contrast, the mechanisms whereby translocations in the --350/-50-kb region 5' of SOX9 cause severe disease and whereby SOX9 expression is specified in cho...

2017
Nitzan Gonen Alexander Quinn Helen C O'Neill Peter Koopman Robin Lovell-Badge

During mouse sex determination, transient expression of the Y-linked gene Sry up-regulates its direct target gene Sox9, via a 3.2 kb testis specific enhancer of Sox9 (TES), which includes a core 1.4 kb element, TESCO. SOX9 activity leads to differentiation of Sertoli cells, rather than granulosa cells from the bipotential supporting cell precursor lineage. Here, we present functional analysis o...

Journal: :The Journal of clinical investigation 2013
Changmeng Cai Hongyun Wang Housheng Hansen He Sen Chen Lingfeng He Fen Ma Lorelei Mucci Qianben Wang Christopher Fiore Adam G Sowalsky Massimo Loda X Shirley Liu Myles Brown Steven P Balk Xin Yuan

Fusion of the androgen receptor-regulated (AR-regulated) TMPRSS2 gene with ERG in prostate cancer (PCa) causes androgen-stimulated overexpression of ERG, an ETS transcription factor, but critical downstream effectors of ERG-mediating PCa development remain to be established. Expression of the SOX9 transcription factor correlated with TMPRSS2:ERG fusion in 3 independent PCa cohorts, and ERG-depe...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 2000
S Murakami M Kan W L McKeehan B de Crombrugghe

Recent experiments have established that Sox9 is required for chondrocyte differentiation. Here, we show that fibroblast growth factors (FGFs) markedly enhance Sox9 expression in mouse primary chondrocytes as well as in C3H10T1/2 cells that express low levels of Sox9. FGFs also strongly increase the activity of a Sox9-dependent chondrocyte-specific enhancer in the gene for collagen type II. Tra...

2017
Michael D Hall Caroline A Murray Michael J Valdez Alan O Perantoni

To date, mutations within the coding region and translocations around the SOX9 gene both constitute the majority of genetic lesions underpinning human campomelic dysplasia (CD). While pathological coding-region mutations typically result in a non-functional SOX9 protein, little is known about what mechanism(s) controls normal SOX9 expression, and subsequently, which signaling pathways may be in...

Journal: :The international journal of biochemistry & cell biology 2010
Takayuki Furumatsu Chisa Shukunami Michiyo Amemiya-Kudo Hitoshi Shimano Toshifumi Ozaki

During musculoskeletal development, Sry-type HMG box 9 (Sox9) has a crucial role in mesenchymal condensation and chondrogenesis. On the other hand, a tissue-specific basic helix-loop-helix (bHLH) transcription factor Scleraxis (Scx) regulates the differentiation of tendon and ligament progenitors. Whereas these two transcription factors cooperatively participate in the determination of cellular...

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