
Royal Holloway, University of London, UKLRRK2: function and dysfunction
28—30 March 2012
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A Biochemical Society Focused Meeting Mutations in the multidomain enzyme LRRK2 are the most common genetic cause of Parkinson’s disease, but despite intensive investigation we still know very little about the normal function of this protein or how mutations lead to disease. Topics
Reviews by the speakers, based on their presentations at this major international meeting, will be published exclusively in Biochemical Society Transactions (Volume 40, part 5).
Abstract deadline: 1 February 2012. Abstract submission is now available. Earlybird registration deadline: 27 February 2012.
Not a member of the Biochemical Society? Join today and save up to £100 on your registration fee. Oral communication slots are available at this meeting. All attendees, particularly researchers in the early stages of their career, are invited to submit a poster abstract for consideration as an oral communication. Student Bursaries are available for this meeting.
'Eureka Moments: making proteins, making a difference'. As part of our centenary celebrations, a number of the Society’s Honorary Members have been asked to talk about the important moments in their careers and the future of the discipline. The third to be released is that of Greg Winter who spoke to Michael Neuberger and Brian Hartley about the important moments in his career and the future of the discipline. Watch the interview now! |
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