نتایج جستجو برای: suz12

تعداد نتایج: 245  

Journal: :The Journal of biological chemistry 2007
Robert F Gillespie Lorraine J Gudas

The retinoic acid receptor (RAR) alpha, beta(2), and gamma isotypes each regulate specific subsets of target genes in F9 teratocarcinoma stem cells. We used chromatin immunoprecipitation assays to monitor the association of RARgamma, retinoic X receptor (RXR) alpha, and coregulators with the RARbeta(2), Hoxa1, and Cyp26A1 retinoic acid response elements (RAREs) in F9 wild type and RARalpha, -be...

2016
Nan Xie Cheng Wang Zehang Zhuang Jinson Hou Xiqiang Liu Yue Wu Haichao Liu Hongzhang Huang

We aimed to determine the specific miRNA profile of tumor budding cells and investigate the potential role of miR-320a in invasion and metastasis of tongue squamous cell carcinoma (TSCC). We collected tumor budding cells and paired central tumor samples from five TSCC specimens with laser capture microdissection and examined the specimens using a miRNA microarray. The specific miRNA signature o...

Journal: :Reproduction 2008
Pablo J Ross Neli P Ragina Ramon M Rodriguez Amy E Iager Kannika Siripattarapravat Nestor Lopez-Corrales Jose B Cibelli

Trimethylation of histone H3 at lysine 27 (H3K27me3) is established by polycomb group genes and is associated with stable and heritable gene silencing. The aim of this study was to characterize the expression of polycomb genes and the dynamics of H3K27me3 during bovine oocyte maturation and preimplantation development. Oocytes and in vitro-produced embryos were collected at different stages of ...

Journal: :Disease models & mechanisms 2009
Xavier Miró Xunlei Zhou Susann Boretius Thomas Michaelis Christian Kubisch Gonzalo Alvarez-Bolado Peter Gruss

Polycomb proteins are epigenetic regulators of gene expression. Human central nervous system (CNS) malformations are congenital defects of the brain and spinal cord. One example of a human CNS malformation is Chiari malformation (CM), which presents as abnormal brainstem growth and cerebellar herniation, sometimes accompanied by spina bifida and cortical defects; it can occur in families. Clini...

Journal: :PLoS Genetics 2008
Anders M. Lindroth Yoon Jung Park Chelsea M. McLean Gregoriy A. Dokshin Jenna M. Persson Herry Herman Diego Pasini Xavier Miró Mary E. Donohoe Jeannie T. Lee Kristian Helin Paul D. Soloway

At the imprinted Rasgrf1 locus in mouse, a cis-acting sequence controls DNA methylation at a differentially methylated domain (DMD). While characterizing epigenetic marks over the DMD, we observed that DNA and H3K27 trimethylation are mutually exclusive, with DNA and H3K27 methylation limited to the paternal and maternal sequences, respectively. The mutual exclusion arises because one mark prev...

2011
He Zhang Beibei Niu Ji-Fan Hu Shengfang Ge Haibo Wang Tao Li Jianqun Ling Brandon N. Steelman Guanxiang Qian Andrew R. Hoffman

Monoallelic expression of IGF2 is regulated by CCCTC binding factor (CTCF) binding to the imprinting control region (ICR) on the maternal allele, with subsequent formation of an intrachromosomal loop to the promoter region. The N-terminal domain of CTCF interacts with SUZ12, part of the polycomb repressive complex-2 (PRC2), to silence the maternal allele. We synthesized decoy CTCF proteins, fus...

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