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Bart De Strooper

From Wikipedia, the free encyclopedia

Bart De Strooper is a Belgian molecular biologist and professor at Vlaams Instituut voor Biotechnologie and KU Leuven (Leuven, Belgium) and the UK Dementia Research Institute and University College London, UK. De Strooper's research seeks to translate genetic data into the identification and treatment of neurodegenerative diseases and treatments. interest are the secretases, proteases which cleave the amyloid precursor protein (APP), resulting in amyloid peptides.

Career

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De Strooper obtained an MD at the KU Leuven in 1985 and a PhD in 1992. He would go on to complete his postdoc at the European Molecular Biology Laboratory (EMBL) in Heidelberg Germany under Dr. Carlos Dotti.[1] De Strooper returned to his alma mater in 1999, joining the VIB Center for the Biology of Disease, now known as the VIB-KU Leuven Center for Brain & Disease Research. Along with continued advancement in neurodegenerative diseases, De Strooper became the center's Departmental Director in 2007, leading over 250 neuroscience researchers.[2] He would also serve as a Professor of Neurodegenerative Diseases at University College London.[1]  

In December 2016 he became the director of the UK Dementia Research Institute (DRI) at University College London.[3] Under De Strooper's leadership, the DRI "established seven major research centres, recruited over 60 Principal Investigators, and built a community of 800-plus researches".[4] De Strooper voluntarily stepped down from the role in November 2022, citing a desire to focus on dementia and translational neuroscience at the UCL Queen Square Institute of Neurology. He continues to collaborate with the Academy of Medical Sciences fellowship, to which he was elected to in 2020.

Awards

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Together with Christian Haass, De Strooper received the Potamkin Prize in 2002.[5] The following year he was the recipient of the 2003 Alois Alzheimer Award of the Deutscher Gesellschaft für Gerontopsychiatrie und psychotherapie and the 2005 Joseph Maisin Prize for fundamental biomedical sciences.He received the 2008 Metlife Foundation Award for Medical Research in Alzheimer's Disease along with Robert Vassar and Philip C. Wong[6]

He shared the 2018 Brain Prize with John Hardy, Christian Haass and Michel Goedert.[7] The same year Expertscape, a research ranking publisher, recognized Dr. Strooper as one of the top experts in the world in Alzheimer's disease.[8] In the same year, De Strooper was awarded the prestigious Commander of the Order of Leopold I, a national honorary orders of Knightood.

References

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  1. ^ "Bart De Strooper". Cure Alzheimer's Fund. Retrieved 7 November 2023.
  2. ^ "Bart De Strooper". Crick. 15 September 2023. Retrieved 7 November 2023.
  3. ^ "Director announced to lead landmark UK Dementia Research Institute". Alzheimer's society. 14 December 2016. Retrieved 14 December 2016.
  4. ^ "Comment: Professor Bart De Strooper steps down as Director of the UK Dementia Research Institute". www.dementiasplatform.uk. Retrieved 7 November 2023.
  5. ^ American Academy of Neurology. "2002 Potamkin prize recognizes the ground-breaking work of Alzheimer's disease researchers in Germany, Belgium".
  6. ^ "MetLife Foundation Awards for Medical Research in Alzheimer's Disease" (PDF). Archived from the original (PDF) on 13 October 2018.
  7. ^ "Home - Lundbeckfonden - The Brain Prize". www.thebrainprize.org. Retrieved 29 July 2018.
  8. ^ "Expertscape: Alzheimer Disease, November 2018". expertscape.com. November 2018. Retrieved 15 November 2018.
  • De Strooper, B.; Saftig, P.; Craessaerts, K.; Vanderstichele, H.; Guhde, G.; Annaert, W.; von Figura, K.; Van Leuven, F. (1998). "Deficiency of presenilin-1 inhibits the normal cleavage of amyloid precursor protein". Nature. 391 (6665): 387–90. doi:10.1038/34910. PMID 9450754. S2CID 4397720.
  • De Strooper, B.; Kopan, R.; Annaert, W.; Cupers, P.; Saftig, P.; Craessaerts, K.; Mumm, J. S.; Schroeter, E. H.; Schrijvers, V.; Wolfe, M. S.; Ray, W. J.; Goate, A. (1999). "A presenilin-1-dependent gamma-secretase-like protease mediates release of Notch intracellular domain". Nature. 398 (6727): 518–22. doi:10.1038/19083. PMID 10206645. S2CID 4346474.

Sources

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