Dr LIM Yaw Chyn

Current Appointment:
Assistant Professor to Departments of Pathology and Physiology

Education:

July 1988
Diploma in Medical laboratory Technology, National University of Malaysia, Kuala Lumpur, Malaysia
September 1992
M.Sc. with distinction in Biomedical Sciences, University of Bradford, Bradford, England
December 1995
Ph.D. in Biomedical Sciences, University of Bradford

Postdoctoral Training:

Dec 1995 - June 1996

Honorary Research Fellow in Biomedical Sciences, University of Bradford
Oct 1996 - June 2000
Research Fellow in Pathology (Vascular Research Division), Brigham and Women’s Hospital, Boston, USA
July 2000 - March 2003
Research Associate in Pathology, Brigham and Women’s Hospital

Previous Academic Appointments:

Dec 1995 - June 1996
Part-time Lecturer in Department of Biomedical Sciences, University of Bradford
October 1996 - June 2001
Research Fellow in Pathology, Harvard Medical School, Boston, USA

June 2001 - March 2003

Instructor in Pathology, Harvard Medical School

Research Interests:
The current focus of my laboratory is on the mechanisms underlying the interactions of tumor cells with the endothelium. One area of my research is to examine the functional integrity of adhesion molecules on lymphoma cells. Using immunostaining techniques and the in vitro parallel plate flow chamber system, I will correlate the levels of expression of various adhesion molecules on these neoplastic cells with their abilities to interact with endothelial adhesion molecules under defined flow conditions. In a parallel project, I am looking into the expression of sialylated carbohydrates on various tumor cell types, examining their potential function as selectin ligands and their role in tumor metastasis. A third area of my research interest is to identify and characterize functional heterogeneity between endothelial cells from different vascular beds. The study involves the development of reliable techniques to isolate and culture endothelial cells from different vascular beds/organs and to elucidate any physiological or functional differences, such as their adhesion molecules expression or chemokine production profiles in response to pro-inflammatory cytokines stimulation.