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Genome-wide screens for in vivo Tinman binding sites identify cardiac enhancers with diverse functional architectures.

机译：用于体内Tinman结合位点的全基因组筛选鉴定具有多种功能结构的心脏增强剂。

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Hong Jin; Robert Stojnic; Boris Adryan; Anil Ozdemir; Angelike Stathopoulos; Manfred Frasch;
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1. Genome-Wide Screens for In Vivo Tinman Binding Sites Identify Cardiac Enhancers with Diverse Functional Architectures [J] . Hong Jin, Robert Stojnic, Boris Adryan, PLoS Genetics . 2013,第1期

机译：体内 Tinman结合位点的全基因组筛选可识别具有多种功能结构的心脏增强剂
2. Cardiac enhancer activity of the homeobox gene tinman depends on CREB consensus binding sites in Drosophila. [J] . Venkatesh TV, Park M, Ocorr K, Genesis: the journal of genetics and development . 2000,第1期

机译：同源盒基因tinman的心脏增强活性取决于果蝇中的CREB共有结合位点。
3. A Genome-Wide Screen for β-Catenin Binding Sites Identifies a Downstream Enhancer Element That Controls c-Myc Gene Expression [J] . Gregory S. Yochum, Ryan Cleland, Richard H. Goodman Molecular and Cellular Biology . 2008,第24期

机译：β-连环蛋白结合位点的全基因组筛选确定了控制c-Myc基因表达的下游增强子元件
4. Study of the Binding Capacity of Heparin Functionalized Magnetic Microparticles for Cardiac Lipoprotein Lipase and their Preliminary Evaluation Ex Vivo in Rat Hearts [C] . Veronika Schmitt, Brian Rodrigues, Urs O. Hafeli, International Conference on the Scientific and Clinical Applications of Magnetic Carriers . 2010

机译：肝素官能化磁性微粒对心脏脂蛋白脂肪酶的结合能力及其在大鼠心中的初步评价
5. A Genome-Wide RNAi Screen Identifies CDC-42 and GDI-1 as In Vivo Regulators of Invadopodia [D] . Lohmer, Lauren Renee Lilley 2015

机译：全基因组的RNAi筛选确定CDC-42和GDI-1为Invadopodia的体内调节剂。
6. Genome-Wide Screens for In Vivo Tinman Binding Sites Identify Cardiac Enhancers with Diverse Functional Architectures [O] . Hong Jin, Robert Stojnic, Boris Adryan, 2013

机译：体内Tinman结合位点的全基因组筛选可识别具有多种功能架构的心脏增强剂
7. Genome-Wide Screens for In Vivo Tinman Binding Sites Identify Cardiac Enhancers with Diverse Functional Architectures [O] . Jin Hong, Stojnic Robert, Adryan Boris, 2013

机译：体内Tinman结合位点的全基因组筛选可识别具有多种功能架构的心脏增强剂

Genome-wide screens for in vivo Tinman binding sites identify cardiac enhancers with diverse functional architectures.

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