Gene interactions and pathways from curated databases and text-mining

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EPHB2 — ROCK1

Pathways - manually collected, often from reviews:

Text-mined interactions from Literome

Zhao et al., Mol Pharmacol 2006 : In summary, these results demonstrate that Src, Rho/ROCK , and an intact cytoskeleton contribute to overall ERK1/2 activation in SDF-1 stimulated cells and are indispensable for nuclear translocation of ERK1/2 and activation of transcription factors
Meriane et al., Stem Cells 2006 (MAP Kinase Signaling System) : Moreover, MMP- and ROCK dependent molecular events are implicated in the regulation of the S1P induced activation of ERK
Chapados et al., Circ Res 2006 (Disease Progression...) : Indeed, SMCs on denatured collagen possessed higher levels of RhoA activity than those on native collagen, and blocking RhoA or ROCK activities attenuated SMC spreading, ERK1/2 activity, and TN-C expression in SMCs on denatured collagen
Samarakoon et al., J Mol Cell Cardiol 2008 : Thus, two distinct pathways involving the EGFR/pp60(c-src)/MEK-ERK pathway and Rho/ROCK dependent SMAD2 activation are required for TGF-beta1 induced PAI-1 expression in VSMC
Mair et al., Br J Pharmacol 2008 (Anoxia...) : ROCK inhibition ablated increased pulmonary remodelling and hypertension observed in SERT+ mice, and ROCK1/2 protein levels were elevated in SERT+ PFs. ROCK inhibition also reduced 5-HT stimulated proliferation by suppressing MEK stimulated ERK phosphorylation
Khatiwala et al., J Bone Miner Res 2009 (MAP Kinase Signaling System) : Inhibition of RhoA and ROCK in MC3T3-E1 pre-osteoblasts cultured on substrates of varying compliance reduced ERK activity, whereas constitutively active RhoA enhanced it
Shih et al., J Bone Miner Res 2011 (Mechanotransduction, Cellular) : In addition, FAK affects osteogenic differentiation through ERK1/2, whereas ROCK regulates both FAK and ERK1/2
Chaturvedi et al., Am J Physiol Cell Physiol 2011 (MAP Kinase Signaling System...) : RhoA, ROCK inhibition, or RhoA, ROCK1 , ROCK2, mDia1, and FAK reduction by siRNA blocked deformation induced nuclear ERK phosphorylation without preventing ERK phosphorylation in the cytoplasmic protein fraction