Zobrazeno 1 - 10
of 1 653
pro vyhledávání: '"Vervliet A"'
Autor:
K. Ahuja, M. Vandenabeele, F. Nami, E. Lefevere, J. Van hoecke, S. Bergmans, M. Claes, T. Vervliet, K. Neyrinck, T. Burg, D. De Herdt, P. Bhaskar, Y. Zhu, Z. J. Looser, J. Loncke, W. Gsell, M. Plaas, P. Agostinis, J. V. Swinnen, L. Van Den Bosch, G. Bultynck, A. S. Saab, E. Wolfs, Y. C. Chai, U. Himmelreich, C. Verfaillie, L. Moons, L. De Groef
Publikováno v:
Acta Neuropathologica Communications, Vol 12, Iss 1, Pp 1-23 (2024)
Abstract Wolfram syndrome (WS) is a rare childhood disease characterized by diabetes mellitus, diabetes insipidus, blindness, deafness, neurodegeneration and eventually early death, due to autosomal recessive mutations in the WFS1 (and WFS2) gene. Wh
Externí odkaz:
https://doaj.org/article/1fc5ac8a195045e784ceddeab1da8565
Autor:
Mailis Liiv, Annika Vaarmann, Dzhamilja Safiulina, Vinay Choubey, Ruby Gupta, Malle Kuum, Lucia Janickova, Zuzana Hodurova, Michal Cagalinec, Akbar Zeb, Miriam A. Hickey, Yi-Long Huang, Nana Gogichaishvili, Merle Mandel, Mario Plaas, Eero Vasar, Jens Loncke, Tim Vervliet, Ting-Fen Tsai, Geert Bultynck, Vladimir Veksler, Allen Kaasik
Publikováno v:
Nature Communications, Vol 15, Iss 1, Pp 1-18 (2024)
Abstract Wolfram syndrome is a rare genetic disease caused by mutations in the WFS1 or CISD2 gene. A primary defect in Wolfram syndrome involves poor ER Ca2+ handling, but how this disturbance leads to the disease is not known. The current study, per
Externí odkaz:
https://doaj.org/article/7119060b6c6844ed9cd995417943a2ed
Autor:
Loncke, Jens, de Ridder, Ian, Kale, Justin, Wagner, Larry, Kaasik, Allen, Parys, Jan B., Kerkhofs, Martijn, Andrews, David W., Yule, David, Vervliet, Tim, Bultynck, Geert
Publikováno v:
In BBA - Molecular Cell Research January 2025 1872(1)
Publikováno v:
In Behaviour Research and Therapy July 2024 178
Autor:
Dalile, Boushra, Fuchs, Annalena, La Torre, Danique, Vervliet, Bram, Van Oudenhove, Lukas, Verbeke, Kristin
Publikováno v:
In Progress in Neuropsychopharmacology & Biological Psychiatry 20 April 2024 131
Publikováno v:
In Journal of Mood and Anxiety Disorders March 2024 5
Autor:
Susan Simorgh, Seyed Ahmad Mousavi, San Kit To, Vincent Pasque, Keimpe Wierda, Tim Vervliet, Meghdad Yeganeh, Paria Pooyan, Yoke Chin Chai, Catherine Verfaillie, Hossein Baharvand
Publikováno v:
EXCLI Journal : Experimental and Clinical Sciences, Vol 22, Pp 1055-1076 (2023)
Human cerebral organoids (COs) are self-organizing three-dimensional (3D) neural structures that provide a human-specific platform to study the cellular and molecular processes that underlie different neurological events. The first step of CO generat
Externí odkaz:
https://doaj.org/article/6912e5eb3a054960b29aa13708ffd2f2
The proposed article aims at offering a comprehensive tutorial for the computational aspects of structured matrix and tensor factorization. Unlike existing tutorials that mainly focus on {\it algorithmic procedures} for a small set of problems, e.g.,
Externí odkaz:
http://arxiv.org/abs/2006.08183
Autor:
Van Eyndhoven, Simon, Dupont, Patrick, Tousseyn, Simon, Vervliet, Nico, Van Paesschen, Wim, Van Huffel, Sabine, Hunyadi, Borbála
EEG-correlated fMRI analysis is widely used to detect regional blood oxygen level dependent fluctuations that are significantly synchronized to interictal epileptic discharges, which can provide evidence for localizing the ictal onset zone. However,
Externí odkaz:
http://arxiv.org/abs/2004.14185
Publikováno v:
28th European Signal Processing Conference (EUSIPCO), 2021, pp. 1020-1024
The decomposition of tensors into simple rank-1 terms is key in a variety of applications in signal processing, data analysis and machine learning. While this canonical polyadic decomposition (CPD) is unique under mild conditions, including prior kno
Externí odkaz:
http://arxiv.org/abs/2003.03502