Zobrazeno 1 - 10
of 34
pro vyhledávání: '"Mia L. Pras‐Raves"'
Autor:
Yorrick R.J. Jaspers, Sven W. Meyer, Mia L. Pras-Raves, Inge M.E. Dijkstra, Eric J.M. Wever, Adrie D. Dane, Jan-Bert van Klinken, Gajja S. Salomons, Riekelt H. Houtkooper, Marc Engelen, Stephan Kemp, Michel Van Weeghel, Frédéric M. Vaz
Publikováno v:
Journal of Lipid Research, Vol 65, Iss 6, Pp 100567- (2024)
Lipids play pivotal roles in an extensive range of metabolic and physiological processes. In recent years, the convergence of trapped ion mobility spectrometry and MS has enabled 4D-lipidomics, a highly promising technology for comprehensive lipid an
Externí odkaz:
https://doaj.org/article/deec6247e3684b2caada44c6c89b50f6
Autor:
Anke P. Willems, Maria van der Ham, Birgit G. M. Schiebergen-Bronkhorst, Mirjam van Aalderen, Martina M. J. de Barse, Fini E. De Gruyter, Ilja N. van Hoek, Mia L. Pras-Raves, Monique G. M. de Sain-van der Velden, Hubertus C. M. T. Prinsen, Nanda M. Verhoeven-Duif, Judith J. M. Jans
Publikováno v:
Frontiers in Molecular Biosciences, Vol 10 (2023)
Background: Early diagnosis of inherited metabolic diseases (IMDs) is important because treatment may lead to reduced mortality and improved prognosis. Due to their diversity, it is a challenge to diagnose IMDs in time, effecting an emerging need for
Externí odkaz:
https://doaj.org/article/89486e7f1dfe48a3b0c77bddceeb9e23
Autor:
Ntsiki M. Held, M. Renate Buijink, Hyung L. Elfrink, Sander Kooijman, Georges E. Janssens, Angela C. M. Luyf, Mia L. Pras-Raves, Frédéric M. Vaz, Stephan Michel, Riekelt H. Houtkooper, Michel van Weeghel
Publikováno v:
Scientific Reports, Vol 11, Iss 1, Pp 1-13 (2021)
Abstract Lipid metabolism is under the control of the circadian system and circadian dysregulation has been linked to obesity and dyslipidemia. These factors and outcomes have also been associated to, or affected by, the process of aging. Here, we in
Externí odkaz:
https://doaj.org/article/9c02010f9abc4c868131db2f81cf7e9b
Adaptations of the 3T3-L1 adipocyte lipidome to defective ether lipid catabolism upon Agmo knockdown
Autor:
Sabrina Sailer, Katharina Lackner, Mia L. Pras-Raves, Eric J.M. Wever, Jan B. van Klinken, Adriaan D. Dane, Stephan Geley, Jakob Koch, Georg Golderer, Gabriele Werner-Felmayer, Markus A. Keller, Werner Zwerschke, Frédéric M. Vaz, Ernst R. Werner, Katrin Watschinger
Publikováno v:
Journal of Lipid Research, Vol 63, Iss 6, Pp 100222- (2022)
Little is known about the physiological role of alkylglycerol monooxygenase (AGMO), the only enzyme capable of cleaving the 1-O-alkyl ether bond of ether lipids. Expression and enzymatic activity of this enzyme can be detected in a variety of tissues
Externí odkaz:
https://doaj.org/article/2dea3320485f4a99830874c9c9ea55f9
Autor:
Arwen W. Gao, Iliana A. Chatzispyrou, Rashmi Kamble, Yasmine J. Liu, Katharina Herzog, Reuben L. Smith, Henk van Lenthe, Martin A. T. Vervaart, Arno van Cruchten, Angela C. Luyf, Antoine van Kampen, Mia L. Pras-Raves, Frédéric M. Vaz, Riekelt H. Houtkooper
Publikováno v:
Scientific Reports, Vol 7, Iss 1, Pp 1-14 (2017)
Abstract Abnormal nutrient metabolism is a hallmark of aging, and the underlying genetic and nutritional framework is rapidly being uncovered, particularly using C. elegans as a model. However, the direct metabolic consequences of perturbations in li
Externí odkaz:
https://doaj.org/article/f244d9a20b94447d85bf084d64d7035a
Autor:
Katharina Herzog, Mia L. Pras-Raves, Martin A.T. Vervaart, Angela C.M. Luyf, Antoine H.C. van Kampen, Ronald J.A. Wanders, Hans R. Waterham, Frédéric M. Vaz
Publikováno v:
Journal of Lipid Research, Vol 57, Iss 8, Pp 1447-1454 (2016)
Peroxisomes are subcellular organelles involved in various metabolic processes, including fatty acid and phospholipid homeostasis. The Zellweger spectrum disorders (ZSDs) represent a group of diseases caused by a defect in the biogenesis of peroxisom
Externí odkaz:
https://doaj.org/article/2d4807b1c2e04208b2bf2500b4f686da
Autor:
Hanneke A. Haijes, Marcel Willemsen, Maria Van der Ham, Johan Gerrits, Mia L. Pras-Raves, Hubertus C. M. T. Prinsen, Peter M. Van Hasselt, Monique G. M. De Sain-van der Velden, Nanda M. Verhoeven-Duif, Judith J. M. Jans
Publikováno v:
Metabolites, Vol 9, Iss 1, p 12 (2019)
In metabolic diagnostics, there is an emerging need for a comprehensive test to acquire a complete view of metabolite status. Here, we describe a non-quantitative direct-infusion high-resolution mass spectrometry (DI-HRMS) based metabolomics method a
Externí odkaz:
https://doaj.org/article/f11723bf334b4ab69cbe6cb8e48d9633
Autor:
Paul Goede, Rob C. I. Wüst, Bauke V. Schomakers, Simone Denis, Frédéric M. Vaz, Mia L. Pras‐Raves, Michel Weeghel, Chun‐Xia Yi, Andries Kalsbeek, Riekelt H. Houtkooper
Publikováno v:
FASEB Journal, 36(2):e22133, 1-17. FASEB
FASEB journal, 36(2):e22133. FASEB
de Goede, P, Wüst, R C I, Schomakers, B V, Denis, S, Vaz, F M, Pras-Raves, M L, van Weeghel, M, Yi, C-X, Kalsbeek, A & Houtkooper, R H 2022, ' Time-restricted feeding during the inactive phase abolishes the daily rhythm in mitochondrial respiration in rat skeletal muscle ', FASEB Journal, vol. 36, no. 2, e22133, pp. 1-17 . https://doi.org/10.1096/fj.202100707R
de Goede, P, Wüst, R C I, Schomakers, B V, Denis, S, Vaz, F M, Pras-Raves, M L, van Weeghel, M, Yi, C-X, Kalsbeek, A & Houtkooper, R H 2022, ' Time-restricted feeding during the inactive phase abolishes the daily rhythm in mitochondrial respiration in rat skeletal muscle ', FASEB Journal, vol. 36, no. 2, e22133 . https://doi.org/10.1096/fj.202100707R
FASEB Journal, 36(2):e22133. FASEB
FASEB journal, 36(2):e22133. FASEB
de Goede, P, Wüst, R C I, Schomakers, B V, Denis, S, Vaz, F M, Pras-Raves, M L, van Weeghel, M, Yi, C-X, Kalsbeek, A & Houtkooper, R H 2022, ' Time-restricted feeding during the inactive phase abolishes the daily rhythm in mitochondrial respiration in rat skeletal muscle ', FASEB Journal, vol. 36, no. 2, e22133, pp. 1-17 . https://doi.org/10.1096/fj.202100707R
de Goede, P, Wüst, R C I, Schomakers, B V, Denis, S, Vaz, F M, Pras-Raves, M L, van Weeghel, M, Yi, C-X, Kalsbeek, A & Houtkooper, R H 2022, ' Time-restricted feeding during the inactive phase abolishes the daily rhythm in mitochondrial respiration in rat skeletal muscle ', FASEB Journal, vol. 36, no. 2, e22133 . https://doi.org/10.1096/fj.202100707R
FASEB Journal, 36(2):e22133. FASEB
Shift-workers show an increased incidence of type 2 diabetes mellitus (T2DM). A possible mechanism is the disruption of the circadian timing of glucose homeostasis. Skeletal muscle mitochondrial function is modulated by the molecular clock. We used t
Autor:
Merel E. Hermans, Michel van Weeghel, Frédéric M. Vaz, Sacha Ferdinandusse, Carla E. M. Hollak, Hidde H. Huidekoper, Mirian C. H. Janssen, André B. P. van Kuilenburg, Mia L. Pras‐Raves, Mirjam M. C. Wamelink, Ronald J. A. Wanders, Mendy M. Welsink‐Karssies, Annet M. Bosch
Publikováno v:
Hermans, M E, van Weeghel, M, Vaz, F M, Ferdinandusse, S, Hollak, C E M, Huidekoper, H H, Janssen, M C H, van Kuilenburg, A B P, Pras-Raves, M L, Wamelink, M M C, Wanders, R J A, Welsink-Karssies, M M & Bosch, A M 2022, ' Multi-omics in classical galactosemia : Evidence for the involvement of multiple metabolic pathways ', Journal of Inherited Metabolic Disease, vol. 45, no. 6, pp. 1094-1105 . https://doi.org/10.1002/jimd.12548
Journal of inherited metabolic disease, 45(6), 1094-1105. Springer Netherlands
Journal of Inherited Metabolic Disease, 45(6), 1094-1105. Springer Netherlands
Journal of Inherited Metabolic Disease, 45, 1094-1105
Journal of Inherited Metabolic Disease, 45, 6, pp. 1094-1105
Journal of inherited metabolic disease, 45(6), 1094-1105. Springer Netherlands
Journal of Inherited Metabolic Disease, 45(6), 1094-1105. Springer Netherlands
Journal of Inherited Metabolic Disease, 45, 1094-1105
Journal of Inherited Metabolic Disease, 45, 6, pp. 1094-1105
Contains fulltext : 286854.pdf (Publisher’s version ) (Open Access) Classical galactosemia (CG) is one of the more frequent inborn errors of metabolism affecting approximately 1:40.000 people. Despite a life-saving galactose-restricted diet, patien
Autor:
Martin Lammens, Gert Van Goethem, Michèl A.A.P. Willemsen, Bram Heijs, Marjolein Breur, Martin Giera, Mia L. Pras-Raves, Pippa Staps, Marianna Bugiani, Ron A. Wevers, Marinette van der Graaf, Annemieke Groen, William B. Rizzo, Frédéric M. Vaz, Antoine H. C. van Kampen, Sacha Ferdinandusse
Publikováno v:
Journal of Inherited Metabolic Disease
Staps, P, Rizzo, W B, Vaz, F M, Bugiani, M, Giera, M, Heijs, B, van Kampen, A H C, Pras-Raves, M L, Breur, M, Groen, A, Ferdinandusse, S, van der Graaf, M, Van Goethem, G, Lammens, M, Wevers, R A & Willemsen, M A A P 2020, ' Disturbed brain ether lipid metabolism and histology in Sjögren-Larsson syndrome ', Journal of Inherited Metabolic Disease, vol. 43, no. 6, pp. 1265-1278 . https://doi.org/10.1002/jimd.12275
Journal of inherited metabolic disease
Journal of Inherited Metabolic Disease, 43(6), 1265-1278. Springer Netherlands
Journal of Inherited Metabolic Disease, 43(6), 1265-1278. WILEY
Journal of Inherited Metabolic Disease, 43, 6, pp. 1265-1278
Journal of Inherited Metabolic Disease, 43, 1265-1278
Journal of inherited metabolic disease, 43(6), 1265-1278. Springer Netherlands
Staps, P, Rizzo, W B, Vaz, F M, Bugiani, M, Giera, M, Heijs, B, van Kampen, A H C, Pras-Raves, M L, Breur, M, Groen, A, Ferdinandusse, S, van der Graaf, M, Van Goethem, G, Lammens, M, Wevers, R A & Willemsen, M A A P 2020, ' Disturbed brain ether lipid metabolism and histology in Sjögren-Larsson syndrome ', Journal of Inherited Metabolic Disease, vol. 43, no. 6, pp. 1265-1278 . https://doi.org/10.1002/jimd.12275
Journal of inherited metabolic disease
Journal of Inherited Metabolic Disease, 43(6), 1265-1278. Springer Netherlands
Journal of Inherited Metabolic Disease, 43(6), 1265-1278. WILEY
Journal of Inherited Metabolic Disease, 43, 6, pp. 1265-1278
Journal of Inherited Metabolic Disease, 43, 1265-1278
Journal of inherited metabolic disease, 43(6), 1265-1278. Springer Netherlands
Contains fulltext : 229584.pdf (Publisher’s version ) (Open Access) Sjögren-Larsson syndrome (SLS) is a rare neurometabolic syndrome caused by deficient fatty aldehyde dehydrogenase. Patients exhibit intellectual disability, spastic paraplegia, an