نتایج جستجو برای: tbx3

تعداد نتایج: 280  

Journal: :Circulation research 2009
Elizabeth M McNally Eric C Svensson

A vexing problem for clinicians in the management of children and adults with congenital heart disease is the management of the accompanying arrhythmias. In the recent decade, the mutational spectrum associated with human congenital heart disease has begun to come into focus.1 The number of distinct genes implicated in human congenital heart disease is considerable, and a large portion of mutat...

Journal: :European urology 2012
Raju Kandimalla Angela A G van Tilborg Lucie C Kompier Dominique J P M Stumpel Ronald W Stam Chris H Bangma Ellen C Zwarthoff

BACKGROUND DNA methylation markers could serve as useful biomarkers, both as markers for progression and for urine-based diagnostic assays. OBJECTIVE Identify bladder cancer (BCa)-specific methylated DNA sequences for predicting pTa-specific progression and detecting BCa in voided urine. DESIGN, SETTING, AND PARTICIPANTS Genome-wide methylation analysis was performed on 44 bladder tumours u...

Journal: :PLoS ONE 2007
Inês Ribeiro Yasuhiko Kawakami Dirk Büscher Ángel Raya Joaquín Rodríguez-León Masanobu Morita Concepción Rodríguez Esteban Juan Carlos Izpisúa Belmonte

BACKGROUND The heart forms from a linear tube that is subject to complex remodeling during embryonic development. Hallmarks of this remodeling are the looping of the heart tube and the regionalization into chamber and non-chamber myocardium. Cardiomyocytes in the future chamber myocardium acquire different cellular and physiological characteristics through activation of a chamber-specific genet...

2013
Jun Wang Yan Bai Hong Li Stephanie B. Greene Elzbieta Klysik Wei Yu Robert J. Schwartz Trevor J. Williams James F. Martin

Among the most common human congenital anomalies, cleft lip and palate (CL/P) affects up to 1 in 700 live births. MicroRNA (miR)s are small, non-coding RNAs that repress gene expression post-transcriptionally. The miR-17-92 cluster encodes six miRs that have been implicated in human cancers and heart development. We discovered that miR-17-92 mutant embryos had severe craniofacial phenotypes, in...

Journal: :Human molecular genetics 2015
Xiangfeng Lu Laiyuan Wang Xu Lin Jianfeng Huang C Charles Gu Meian He Hongbing Shen Jiang He Jingwen Zhu Huaixing Li James E Hixson Tangchun Wu Juncheng Dai Ling Lu Chong Shen Shufeng Chen Lin He Zengnan Mo Yongchen Hao Xingbo Mo Xueli Yang Jianxin Li Jie Cao Jichun Chen Zhongjie Fan Ying Li Liancheng Zhao Hongfan Li Fanghong Lu Cailiang Yao Lin Yu Lihua Xu Jianjun Mu Xianping Wu Ying Deng Dongsheng Hu Weidong Zhang Xu Ji Dongshuang Guo Zhirong Guo Zhengyuan Zhou Zili Yang Renping Wang Jun Yang Xiaoyang Zhou Weili Yan Ningling Sun Pingjin Gao Dongfeng Gu

Hypertension is a common disorder and the leading risk factor for cardiovascular disease and premature deaths worldwide. Genome-wide association studies (GWASs) in the European population have identified multiple chromosomal regions associated with blood pressure, and the identified loci altogether explain only a small fraction of the variance for blood pressure. The differences in environmenta...

2011
Tomoki Yano Yuji Yamazaki Makoto Adachi Katsuya Okawa Philippe Fort Masami Uji Shoichiro Tsukita Sachiko Tsukita

The spatiotemporal regulation of E-cadherin expression is important during body plan development and carcinogenesis. We found that Tara (Trio-associated repeat on actin) is enriched in cadherin-based adherens junctions (AJs), and its knockdown in MDCK cells (Tara-KD cells) significantly decreases the expression of E-cadherin. Tara-KD activates Rac1 through the Trio RhoGEF, which binds to E-cadh...

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