BEGIN:VCALENDAR
VERSION:2.0
PRODID:-//Bordeaux Neurocampus - ECPv4.9.10//NONSGML v1.0//EN
CALSCALE:GREGORIAN
METHOD:PUBLISH
X-WR-CALNAME:Bordeaux Neurocampus
X-ORIGINAL-URL:https://www.bordeaux-neurocampus.fr/en/
X-WR-CALDESC:Events for Bordeaux Neurocampus
BEGIN:VTIMEZONE
TZID:Europe/Paris
BEGIN:DAYLIGHT
TZOFFSETFROM:+0100
TZOFFSETTO:+0200
TZNAME:CEST
DTSTART:20230326T010000
END:DAYLIGHT
BEGIN:STANDARD
TZOFFSETFROM:+0200
TZOFFSETTO:+0100
TZNAME:CET
DTSTART:20231029T010000
END:STANDARD
END:VTIMEZONE
BEGIN:VEVENT
DTSTART;TZID=Europe/Paris:20230622T090000
DTEND;TZID=Europe/Paris:20230622T090000
DTSTAMP:20260422T222450
CREATED:20230614T211846Z
LAST-MODIFIED:20230615T151219Z
UID:160456-1687424400-1687424400@www.bordeaux-neurocampus.fr
SUMMARY:Seminar - Wiebke Moebius
DESCRIPTION:Venue : CGFB \n\nWiebke Moebius\nhttps://www.uni-goettingen.de/en/535756.html \nTitle\nWhat we learned about myelin biology by volume EM \nAbstract\nBy using mouse genetics we investigate the cell biology and functions of the myelinating glia cells in the central as well as in the peripheral nervous system. By electron microscopy\, one astonishing feature of myelin is the appearance as a solid and rather non-dynamic structure. Also\, myelin proteins are known to turn over very slowly. To address this question we apply inducible knock-out strategies in the adult mouse\, we can observe spatial and temporal changes in the myelin ultrastructure. To understand these and other myelin-related structural processes better\, we developed protocols in electron microscopy to visualize structural features in normal and diseased state. With the help of a focused ion beam-scanning electron microscopy (FIB-SEM) we are able to add the third dimension to the ultrastructural analysis which is indispensable for the understanding of complex tissues or local connectivity. \n
URL:https://www.bordeaux-neurocampus.fr/en/event/seminar-wiebke-moebius/
CATEGORIES:Cajal Lectures,For scientists,home-event
END:VEVENT
END:VCALENDAR