EMT/MET and Adult Neoplasms, Embryonic Re-Expression,  Pathogenesis, Progression, and Therapy:

http://www.aacr.org/home/scientists/meetings--workshops/special-conferences/emt-and-cancer-progression-and-treatment.aspx


"EMT and Cancer Progression and Treatment".

February 28 - March 2, 2010
Westin Arlington Gateway Hotel
Arlington, Virginia

VIEW PROGRAM

CHAIRPERSONS:
John S. Condeelis, Albert Einstein College of Medicine, Bronx, NY
David M. Epstein, OSI Pharmaceuticals, Inc., Farmingdale, NY
Robert A. Weinberg, Whitehead Institute for Biomedical Research, Cambridge, MA

Underwriting Supporter

Early registration deadline:
Monday, November 30

Abstract submission and
award application deadline:
Monday, December 14
 

Epithelial to mesenchymal transition (EMT) is a physiological transcriptional reprogramming event used in normal organ development, and is characterized by the combined loss of epithelial cell junctions and cell polarity, and the gain of a mesenchymal phenotype. This reprogramming event allows for organ development through de-differentiation of normal epithelial cells, their migration through an extracellular matrix, and finally re-differentiation, homotypic adhesion and organ growth. EMT and mesenchymal to epithelial transition (MET) processes are now recognized in cancer progression. Understanding EMT/MET at the molecular level promises new insights into mechanisms of progression, detection of metastases, and therapeutic intervention. This conference is dedicated to these goals.

http://www.embryomas.net/



Further Topics in:  Euchromatin,  active DNA, and  RNA  ribo-regulators:

Links to Current Research in Euchromatin:
Links to Euchromatin Activator RNA Reviews:
Links to Euchromatin Activator RNA Research:
Links to Ultrastructural Probes of DNase I-Sensitive Sites:
Links to RNA as a Therapeutic Agent:
Links to Hodgkin Lymphoma Immuno-Pathology:
Links to Activated T-Lymphocyte Immunotherapy:
Links to Medical Systems Biology:
Links to Selective Gene Transcription:
Links to RNA-Induced Epigenetics:
Links to RNA-Induced Embryogenesis:
Links to RNA and Biological Causality:
Links to Reprogramming and Neoplasia:

A Brief History of Activator RNA:

"Ultrastructural Probes of Active DNA Sites, and the RNA Activators of DNA".
(PowerPoint Presentation).


Top of Page - Euchromatin NetworkEuchromatin ResearchResearch in Quantitative Radiology


For Further Information and Feedback:

Jeannette A. Hovsepian, M.D.
E-mail: frensasc@ix.netcom.com
Phone:  +1 650 367 6483



euchromatin: "the most active portion of the genome within the cell nucleus".
embryoma:  "adult neoplasm expressing one or more embryo-exclusive genes".