Thursday
October 29, 3:00pm
HSC 4E20

Colloquium announcement




Dan Goldowitz PhD 

Professor
Department of Medical Genetics
UBC
Scientific Director, NeuroDevNet NCE  
 
"New insights into the molecules and cells that make a cerebellum: transcriptomes and time courses and why the cerebellum is so cool"
Dear MiNDS students & faculty,

I am pleased to invite you to attend the MiNDS Colloquium TODAY, Thursday October 29th at 3:00 in HSC 4E20. Bring your coffee cup for coffee and cookies before the talk at 2:30.

Dr. Dan Goldowitz is a Professor in the Department of Medical Genetics and a Canada Research Chair Tier 1 as well as the interim Director of the Centre for Molecular Medicine and Therapeutics at UBC. Dr. Goldowitz received his PhD from the University of California at Irvine and completed his subsequent postdoctoral work at Harvard Children's Hospital in Boston, the Karolinska Institute in Stockholm, and the University of Utah School of Medicine in Salt Lake City. Dan Goldowitz is also the Scientific Director of NeuroDevNet. In this role he interacts with 200+ brain development researchers and professionals across Canada. 

Dr. Goldowitz's lab studies how genetic signals involved in the early development of the nervous system can cause neurodegenerative disease and brain disorders in children and adults. By understanding how the brain develops and is built, he will also be able understand how brain disorders develop. A major focus of his work is the application of molecular and bioinformatic technologies to study the entire gene regulatory network of the cerebellum, which is an area of the brain that is linked to autism, schizophrenia, mental retardation, and other brain disorders.

In his talk today, Dr. Goldowitz will speak about three sets of experiments that have emerged from the initial analyses of their time series data and will provide novel views on the molecular and cellular determinants of cerebellar progenitor populations. These will begin at 3 levels of analysis: 1) from the discovery of a previously unrecognized and striking cerebellar phenotype when Pax6 is deleted, 2) from the discovery of a new molecular player in early cerebellar development, Wls, and 3) from using the time series database to generate new hypotheses about molecular players in cerebellar development and to test these hypotheses with RNA-knockdown studies.
 
 
We look forward to seeing you at the talk tomorrow.
 
Regards
 
Sandra
 
---
on behalf of... 
Kathryn M Murphy PhD
Professor and Director MiNDS Graduate Program
Dept of Psychology Neuroscience & Behaviour
McMaster University
1280 Main St W 
Hamilton ON L8S 4K1