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Conformational changes opening and closing the CFTR chloride channel — UCL Neuroscience Society
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Conformational changes opening and closing the CFTR chloride channel

  • UCL H. O. Schild LT, Medical Science Building Gower Street London, England, WC1E 6BT United Kingdom (map)

Dr. Linsdell's lab is carrying out research to understand the structure and function of CFTR, the chloride channel that is mutated in cystic fibrosis. They are using electrophysiological recording techniques to study the detailed function of normal and mutant forms of the protein.

Host: Dr Paola Vergani

Source:: http://medicine.dal.ca/departments/department-sites/physiology/our-people/our-faculty/paul-linsdell.html
Earlier Event: November 4
Roles of spastic paraplegia gene products in organisation of axonal endoplasmic reticulum
Later Event: November 9
Mental Health Question Time - Dementia: care or cure

The committee hopes to see you soon!

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The committee hopes to see you soon! ⋆