Myocardin and ternary complex factors compete for SRF to control smooth muscle gene expression
By Zhigao Wang, Da-Zhi Wang, D. Hockemeyer, John R. McAnally, Alfred Nordheim, E. Olson. Nature, 2004
600 citations recorded by the source corpus.
Subfields: Cardiology and Cardiovascular Medicine, Molecular Biology
View Paper: https://www.semanticscholar.org/paper/b841b44b1e1116523b8efdffc229524ef33beae1
How researchers see this paper
The researchers whose trusted networks rank it highest, strongest advocate first. Every researcher gets a different order.
In Cardiology and Cardiovascular Medicine
In Molecular Biology
- E. Olson
- J. Richardson
- R. Bassel-Duby
- E. Small
- X. Qi
- Matthew J. Potthoff
- L. Sutherland
- David P. Bartel
Citations in the corpus
- MicroRNAs miR-143 and miR-145 modulate cytoskeletal dynamics and responsiveness of smooth muscle cells to injury. (2009, background): “The results of this study reveal that SRF controls the expression of miR-143 and miR-145 in SMCs, and these miRNAs, in turn, feed back to control the expression and function of multiple components of the cytoskeleton and the SRF regulatory network (Fig. 7). In response to injury, differentiated SMCs”
- Linking actin dynamics and gene transcription to drive cellular motile functions (2010, unknown): “MRTFs and TCFs display mutually exclusive interactions with SR”
- MEF2: a central regulator of diverse developmental programs (2007, background): “IHH produced by prehypertrophic chondrocytes induces the expression of PTHrP, which regulates the rate at which chondrocytes undergo hypertrophy (Karaplis et al., 1994; Lanske et al., 1996; St-Jacques et al., 1999; Vortkamp et al., 1996; Weir et al., 1996).”