نتایج جستجو برای: nanog

تعداد نتایج: 2396  

Journal: :The Journal of Cell Biology 2009
Xin Zhang Irina Neganova Stefan Przyborski Chunbo Yang Michael Cooke Stuart P. Atkinson George Anyfantis Stefan Fenyk W. Nicol Keith Stacey F. Hoare Owen Hughes Tom Strachan Miodrag Stojkovic Philip W. Hinds Lyle Armstrong Majlinda Lako

In this study, we show that NANOG, a master transcription factor, regulates S-phase entry in human embryonic stem cells (hESCs) via transcriptional regulation of cell cycle regulatory components. Chromatin immunoprecipitation combined with reporter-based transfection assays show that the C-terminal region of NANOG binds to the regulatory regions of CDK6 and CDC25A genes under normal physiologic...

2013
WEN JI ZHENG JIANG

The aim of the present study was to employ RNA interference (RNAi) technology to construct and select shRNA-Nanog recombinant plasmids for the inhibition of Nanog gene expression and transfer these plasmids into the human gastric cancer cell line, SGC-7901, as well as to detect the expression of Nanog and the effects on the proliferation, migration, invasion, cell cycle and apoptosis of SGC-790...

Journal: :The EMBO journal 2010
Marie Zbinden Arnaud Duquet Aiala Lorente-Trigos Sandra-Nadia Ngwabyt Isabel Borges Ariel Ruiz i Altaba

A cohort of genes associated with embryonic stem (ES) cell behaviour, including NANOG, are expressed in a number of human cancers. They form an ES-like signature we first described in glioblastoma multiforme (GBM), a highly invasive and incurable brain tumour. We have also shown that HEDGEHOG-GLI (HH-GLI) signalling is required for GBM growth, stem cell expansion and the expression of this (ES)...

Journal: :Molecular medicine reports 2012
Haitao Zhou Shiyan Chen Wei Wang Zhiqiang Wang Xiuli Wu Zhijian Zhang

Nanog is an essential transcription factor maintaining the self-renewal and pluripotency of embryonic stem cells, which binds to nuclear factor-κB (NF-κB) proteins, inhibits their transcriptional activity and represses their pro-differentiation activity. The persistent and excessive activation of microglial cells, as primary immune cells in the ce...

Journal: :Cell 2005
Laurie A. Boyer Tong Ihn Lee Megan F. Cole Sarah E. Johnstone Stuart S. Levine Jacob P. Zucker Matthew G. Guenther Roshan M. Kumar Heather L. Murray Richard G. Jenner David K. Gifford Douglas A. Melton Rudolf Jaenisch Richard A. Young

The transcription factors OCT4, SOX2, and NANOG have essential roles in early development and are required for the propagation of undifferentiated embryonic stem (ES) cells in culture. To gain insights into transcriptional regulation of human ES cells, we have identified OCT4, SOX2, and NANOG target genes using genome-scale location analysis. We found, surprisingly, that OCT4, SOX2, and NANOG c...

2015
Xin Yin Bo-Heng Zhang Su-Su Zheng Dong-Mei Gao Shuang-Jian Qiu Wei-Zhong Wu Zheng-Gang Ren

BACKGROUND Oct4 and Nanog are key regulatory genes that maintain the pluripotency and self-renewal properties of embryonic stem cells. We previously reported that the two stemness markers were tightly associated with cancer progression and poor outcomes of hepatocellular carcinoma. In this study, we demonstrate that coexpression of Oct4/Nanog modulates activation of signal transducer and activa...

2011
Ade Kallas Martin Pook Martti Maimets Külli Zimmermann Toivo Maimets

Nocodazole is a known destabiliser of microtubule dynamics and arrests cell-cycle at the G2/M phase. In the context of the human embryonic stem cell (hESC) it is important to understand how this arrest influences the pluripotency of cells. Here we report for the first time the changes in the expression of transcription markers Nanog and Oct4 as well as SSEA-3 and SSEA-4 in human embryonic cells...

Journal: :Journal of molecular cell biology 2013
Yizhuo Zhou Shanshan Li Qiongping Huang Lele Xie Xueliang Zhu

Nanog, Sox2, and Oct4 are key transcription factors critical for the pluripotency and self-renewal of embryonic stem (ES) cells. Their downregulations lead to differentiation, accompanied with changes in cell motility. Whether these factors impact cell motility directly, however, is not clear. Here we addressed this question by initially assessing their effect in non-stem cells. We found that t...

Journal: :Cellular physiology and biochemistry : international journal of experimental cellular physiology, biochemistry, and pharmacology 2015
Zhi-kun Guo Kang Guo Huanhuan Luo Ling-min Mu Qiong Li Yu-qiao Chang

OBJECTIVES To investigate the expression dynamic of nanog gene in the development of rat myocardial tissues. METHODS SD rats were studied at 5 time points before and after birth. The techniques of immunohistochemistry, immunofluorescence, western blotting and RT-PCR were used to investigate the expression of nanog gene in the rat myocardial tissues at different embryonic (E) and postnatal (P)...

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