P. O’Reilly

发表

SLK-mediated phosphorylation of paxillin is required for focal adhesion turnover and cell migration

L. Sabourin, K. Baron, Roshan K. Sriram, 2013, Oncogene.

The Ste20-like Kinase SLK Is Required for Cell Cycle Progression through G2*

C. Dissous, K. Cailliau, D. Franks, 2005, Journal of Biological Chemistry.

The Ste20-like kinase SLK is required for ErbB2-driven breast cancer cell motility

W. Muller, P. Siegel, K. Roovers, 2009, Oncogene.

The Ldb1 and Ldb2 transcriptional cofactors interact with the Ste20-like kinase SLK and regulate cell migration.

H. Westphal, R. Parks, L. Sabourin, 2009, Molecular biology of the cell.

Association of the Ste20-like Kinase (SLK) with the Microtubule

T. Flood, L. Sabourin, S. Wagner, 2002, The Journal of Biological Chemistry.

Distinct roles for Ste20-like kinase SLK in muscle function and regeneration

R. Kothary, L. Sabourin, C. Tsilfidis, 2013, Skeletal Muscle.

v-Src-dependent Down-regulation of the Ste20-like Kinase SLK by Casein Kinase II*

I. Gelman, L. Sabourin, Z. Chaar, 2006, Journal of Biological Chemistry.

Enediynyl peptides and iso-coumarinyl methyl sulfones as inhibitors of proprotein convertases PCSK8/SKI-1/S1P and PCSK4/PC4: Design, synthesis and biological evaluations.

A. Basak, A. Rajkumar, V. Trudeau, 2015, Bioorganic & medicinal chemistry letters.

LDL-R promoting activity of peptides derived from human PCSK9 catalytic domain (153-421): design, synthesis and biochemical evaluation.

A. Basak, Thomas A Lagace, Chunyu Lu, 2015, European journal of medicinal chemistry.