Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Romy T, Meier"'
Autor:
Romy T. Meier, Leendert Porcelijn, Suzanne Hofstede-van Egmond, Camila Caram-Deelder, Jonathan M. Coutinho, Yvonne M. C. Henskens, Marieke J. H. A. Kruip, An K. Stroobants, Jaap J. Zwaginga, C. Ellen van der Schoot, Masja de Haas, Rick Kapur
Publikováno v:
Antibodies, Vol 13, Iss 2, p 35 (2024)
Vaccine-induced thrombotic thrombocytopenia (VITT) is a rare but severe complication following COVID-19 vaccination, marked by thrombocytopenia and thrombosis. Analogous to heparin-induced thrombocytopenia (HIT), VITT shares similarities in anti-plat
Externí odkaz:
https://doaj.org/article/eae254c8916047379802a27df9b623a3
Autor:
Paul J. Lucassen, Eva F.G. Naninck, Aniko Korosi, Romy T. Meier, Eline M. van der Beek, Cato M H de Vos, Lidewij Schipper, Maralinde R. Abbink
Publikováno v:
Nutrients
Nutrients, Vol 12, Iss 2, p 570 (2020)
Nutrients, 12(2):570. MDPI AG
Nutrients, 12(2):570. Multidisciplinary Digital Publishing Institute (MDPI)
Volume 12
Issue 2
Nutrients, Vol 12, Iss 2, p 570 (2020)
Nutrients, 12(2):570. MDPI AG
Nutrients, 12(2):570. Multidisciplinary Digital Publishing Institute (MDPI)
Volume 12
Issue 2
Early life stress (ES) increases the risk to develop metabolic and brain disorders in adulthood. Breastfeeding (exclusivity and duration) is associated with improved metabolic and neurocognitive health outcomes, and the physical properties of the die
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0d24edc2940d6700c132b03ec4103bd4
https://doi.org/10.3390/nu12020570
https://doi.org/10.3390/nu12020570
Autor:
Menno H. Schut, Wilfred F. A. den Dunnen, Donna L. Smith, Eric Reits, Elly M. Hol, Gillian P. Bates, Willem Kamphuis, Willeke M. C. van Roon, Anna-Aster de Ruiter, Hendrikus Boddeke, Corien Grit, Anne H. P. Jansen, Nieske Brouwer, Romy T. Meier, Ilse C. op den Kelder, Maurik van Hal
Publikováno v:
Jansen, A H P, Van Hal, M, Op Den Kelder, I C, Meier, R T, De Ruiter, A, Schut, M H, Smith, D L, Grit, C, Brouwer, N, Kamphuis, W, Boddeke, H W G M, Den Dunnen, W F A, Van Roon, W M C, Bates, G P, Hol, E M & Reits, E A 2016, ' Frequency of nuclear mutant huntingtin inclusion formation in neurons and glia is cell-type-specific : Huntington Aggregation in Neurons and Glia ', Glia . https://doi.org/10.1002/glia.23050
Glia
Glia
Huntington's disease (HD) is an autosomal dominant inherited neurodegenerative disorder that is caused by a CAG expansion in the Huntingtin (HTT) gene, leading to HTT inclusion formation in the brain. The mutant huntingtin protein (mHTT) is ubiquitou
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8bd8a221357b45d0161481de6423ab55
https://kclpure.kcl.ac.uk/ws/files/56999913/Frequency_of_nuclear_mutant_JANSEN_Accepted_8Aug2016_GOLD_VoR.pdf
https://kclpure.kcl.ac.uk/ws/files/56999913/Frequency_of_nuclear_mutant_JANSEN_Accepted_8Aug2016_GOLD_VoR.pdf
Frequency of nuclear mutant huntingtin inclusion formation in neurons and glia is cell-type-specific
Autor:
Anne H P, Jansen, Maurik, van Hal, Ilse C, Op den Kelder, Romy T, Meier, Anna-Aster, de Ruiter, Menno H, Schut, Donna L, Smith, Corien, Grit, Nieske, Brouwer, Willem, Kamphuis, H W G M, Boddeke, Wilfred F A, den Dunnen, Willeke M C, van Roon, Gillian P, Bates, Elly M, Hol, Eric A, Reits
Publikováno v:
Glia
Huntington's disease (HD) is an autosomal dominant inherited neurodegenerative disorder that is caused by a CAG expansion in the Huntingtin (HTT) gene, leading to HTT inclusion formation in the brain. The mutant huntingtin protein (mHTT) is ubiquitou
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::30dfe1e8e85fdb908324c0e58dcaedec
https://pubmed.ncbi.nlm.nih.gov/27615381
https://pubmed.ncbi.nlm.nih.gov/27615381