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Dive into the research topics where Martin Vervaart is active. These topic labels come from the works of this person. Together they form a unique fingerprint.
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Research output
- 5 Article
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A conserved complex lipid signature marks human muscle aging and responds to short-term exercise
Janssens, G. E., Molenaars, M., Herzog, K., Grevendonk, L., Remie, C. M. E., Vervaart, M. A. T., Elfrink, H. L., Wever, E. J. M., Schomakers, B. V., Denis, S. W., Waterham, H. R., Pras-Raves, M. L., van Weeghel, M., van Kampen, A. H. C., Tammaro, A., Butter, L. M., van der Rijt, S., Florquin, S., Jongejan, A. & Moerland, P. D. & 4 others, , May 2024, In: Nature Aging. 4, 5, p. 681-693 13 p.Research output: Contribution to journal › Article › Academic › peer-review
Open AccessFile77 Downloads (Pure) -
Discovery of novel diagnostic biomarkers for Sjögren-Larsson syndrome by untargeted lipidomics
Vaz, F. M., Staps, P., van Klinken, J. B., van Lenthe, H., Vervaart, M., Wanders, R. J. A., Pras-Raves, M. L., van Weeghel, M., Salomons, G. S., Ferdinandusse, S., Wevers, R. A. & Willemsen, M. A. A. P., 1 Mar 2024, In: BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR AND CELL BIOLOGY OF LIPIDS. 1869, 2, p. 159447 159447.Research output: Contribution to journal › Article › Academic › peer-review
Open AccessFile30 Downloads (Pure) -
An improved functional assay in blood spot to diagnose Barth syndrome using the monolysocardiolipin/cardiolipin ratio
Vaz, F. M., van Lenthe, H., Vervaart, M. A. T., Stet, F. S., Klinkspoor, J. H., Vernon, H. J., Goorden, S. M. I., Houtkooper, R. H., Kulik, W. & Wanders, R. J. A., Jan 2022, In: Journal of inherited metabolic disease. 45, 1, p. 29-37 9 p.Research output: Contribution to journal › Article › Academic › peer-review
Open AccessFile31 Downloads (Pure) -
Metabolomics and lipidomics in Caenorhabditis elegans using a single-sample preparation
Molenaars, M., Schomakers, B. V., Elfrink, H. L., Gao, A. W., Vervaart, M. A. T., Pras-Raves, M. L., Luyf, A. C., Smith, R. L., Sterken, M. G., Kammenga, J. E., van Kampen, A. H. C., Janssens, G. E., Vaz, F. M., van Weeghel, M. & Houtkooper, R. H., 1 Apr 2021, In: Disease models & mechanisms. 14, 4, dmm.047746.Research output: Contribution to journal › Article › Academic › peer-review
Open Access -
Mutations in PCYT2 disrupt etherlipid biosynthesis and cause a complex hereditary spastic paraplegia
Deciphering Developmental Disorders Study, 1 Nov 2019, In: Brain. 142, 11, p. 3382-3397 16 p.Research output: Contribution to journal › Article › Academic › peer-review
Open AccessFile32 Downloads (Pure)