نتایج جستجو برای: 26a

تعداد نتایج: 688  

2015
Sae-Won Lee Jimin Yang Su-Yeon Kim Han-Kyul Jeong Jaewon Lee Woo Jean Kim Eun Ju Lee Hyo-Soo Kim

The importance of epigenetic regulation for maintenance of embryonic stem cell (ESC) pluripotency or for initiation of differentiation is widely accepted. However, the molecular mechanisms are poorly understood. We recently reported that a hypoxic microenvironment induces ESC differentiation. In the present study, we found that hypoxia-responsive histone deacetylase 6 (HDAC6) performs an essent...

2017
Toshiyuki Fujiwara Nam-Jong Paik Thomas Platz

Department of Rehabilitation Medicine, Juntendo University Graduate School of Medicine, 2-1-1 Hongo, Bunkyo, Tokyo 113-8421, Japan Department of Rehabilitation Medicine, Seoul National University College of Medicine, Seoul National University Bundang Hospital, 173-82 Gumi-Ro, Bundang-Gu, Seongnam 13620, Republic of Korea BDH-Klinik Greifswald, Centre for Neurorehabilitation, Intensive Care, and...

Journal: :Experimental and Therapeutic Medicine 2018

Journal: :PloS one 2016
Xiao Lin Yu He Xue Hou Zhenming Zhang Rui Wang Qiong Wu

Active interactions between endothelial cells and smooth muscle cells (SMCs) are critical to maintaining the SMC phenotype. Exosomes play an important role in intercellular communication. However, little is known about the mechanisms that regulate endothelial cells and SMCs crosstalk. We aimed to determine the mechanisms underlying the regulation of the SMC phenotype by human umbilical vein end...

2014
Chenglin Jia Minqi Xiong Peiwei Wang Jingang Cui Xiaoye Du Qinbo Yang Wenjian Wang Yu Chen Teng Zhang

AIMS Atherosclerosis is the primary cause of cardiovascular diseases and stroke. The current study evaluated the interventional effects of a naturally occurring compound Notoginsenoside R1 (NR1) on atherosclerosis in ApoE-/- mice. METHODS AND RESULTS The atherosclerotic lesion was significantly alleviated by NR1 treatment and this attenuation was marked by reduction in lipid deposition, fibro...

2017
David J Sanz Jennifer A Hollywood Martina F Scallan Patrick T Harrison

Cystic Fibrosis is an autosomal recessive disorder caused by mutations in the CFTR gene. CRISPR mediated, template-dependent homology-directed gene editing has been used to correct the most common mutation, c.1521_1523delCTT / p.Phe508del (F508del) which affects ~70% of individuals, but the efficiency was relatively low. Here, we describe a high efficiency strategy for editing of three differen...

2015
Ana Virgínia Van Den Berg Leandro Magalhães Amanda Ferreira Vidal Aline Maria Pereira Ândrea Ribeiro-dos-Santos

Hodgkin Lymphoma (HL) is a neoplasia characterized by the restrict number of malignant cells present in the lymph node. Actual criteria in diagnostic standards don’t consider genetic and epigenetic alterations as risk factors in the development of this disease or in the response of the treatment. MicroRNAs (miRNAs) are important regulatory elements of genic expression that can be altered in the...

2012
Ling Lian Lujiang Qu Yanmei Chen Susan J. Lamont Ning Yang

Marek's disease is a lymphoproliferative neoplastic disease of the chicken, which poses a serious threat to poultry health. Marek's disease virus (MDV)-induced T-cell lymphoma is also an excellent biomedical model for neoplasia research. Recently, miRNAs have been demonstrated to play crucial roles in mediating neoplastic transformation. To investigate host miRNA expression profiles in the tumo...

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