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Page 1
The shifting lipidomic landscape of blood monocytes and neutrophils during pneumonia.
Schuurman AR, Chouchane O, Butler JM, Peters-Sengers H, Joosten S, Brands X, Haak BW, Otto NA, Uhel F, Klarenbeek A, van Linge CC, van Kampen A, Pras-Raves M, van Weeghel M, van Eijk M, Ferraz MJ, Faber DR, de Vos A, Scicluna BP, Vaz FM, Wiersinga WJ, van der Poll T. Schuurman AR, et al. Among authors: van kampen a. JCI Insight. 2024 Feb 22;9(4):e164400. doi: 10.1172/jci.insight.164400. JCI Insight. 2024. PMID: 38385743 Free PMC article.
Principles and practice of lipidomics.
Vaz FM, Pras-Raves M, Bootsma AH, van Kampen AH. Vaz FM, et al. J Inherit Metab Dis. 2015 Jan;38(1):41-52. doi: 10.1007/s10545-014-9792-6. Epub 2014 Nov 20. J Inherit Metab Dis. 2015. PMID: 25409862 Review.
Cardiolipin or MTCH2 can serve as tBID receptors during apoptosis.
Raemy E, Montessuit S, Pierredon S, van Kampen AH, Vaz FM, Martinou JC. Raemy E, et al. Among authors: van kampen ah. Cell Death Differ. 2016 Jul;23(7):1165-74. doi: 10.1038/cdd.2015.166. Epub 2016 Jan 22. Cell Death Differ. 2016. PMID: 26794447 Free PMC article.
Defining functional classes of Barth syndrome mutation in humans.
Lu YW, Galbraith L, Herndon JD, Lu YL, Pras-Raves M, Vervaart M, Van Kampen A, Luyf A, Koehler CM, McCaffery JM, Gottlieb E, Vaz FM, Claypool SM. Lu YW, et al. Among authors: van kampen a. Hum Mol Genet. 2016 May 1;25(9):1754-70. doi: 10.1093/hmg/ddw046. Epub 2016 Feb 16. Hum Mol Genet. 2016. PMID: 26908608 Free PMC article.
A sensitive mass spectrometry platform identifies metabolic changes of life history traits in C. elegans.
Gao AW, Chatzispyrou IA, Kamble R, Liu YJ, Herzog K, Smith RL, van Lenthe H, Vervaart MAT, van Cruchten A, Luyf AC, van Kampen A, Pras-Raves ML, Vaz FM, Houtkooper RH. Gao AW, et al. Among authors: van lenthe h, van cruchten a, van kampen a. Sci Rep. 2017 May 25;7(1):2408. doi: 10.1038/s41598-017-02539-w. Sci Rep. 2017. PMID: 28546536 Free PMC article.
Plasma lipidomics as a diagnostic tool for peroxisomal disorders.
Herzog K, Pras-Raves ML, Ferdinandusse S, Vervaart MAT, Luyf ACM, van Kampen AHC, Wanders RJA, Waterham HR, Vaz FM. Herzog K, et al. Among authors: van kampen ahc. J Inherit Metab Dis. 2018 May;41(3):489-498. doi: 10.1007/s10545-017-0114-7. Epub 2017 Dec 5. J Inherit Metab Dis. 2018. PMID: 29209936 Free PMC article.
Mutations in PCYT2 disrupt etherlipid biosynthesis and cause a complex hereditary spastic paraplegia.
Vaz FM, McDermott JH, Alders M, Wortmann SB, Kölker S, Pras-Raves ML, Vervaart MAT, van Lenthe H, Luyf ACM, Elfrink HL, Metcalfe K, Cuvertino S, Clayton PE, Yarwood R, Lowe MP, Lovell S, Rogers RC; Deciphering Developmental Disorders Study; van Kampen AHC, Ruiter JPN, Wanders RJA, Ferdinandusse S, van Weeghel M, Engelen M, Banka S. Vaz FM, et al. Among authors: van weeghel m, van lenthe h, van kampen ahc. Brain. 2019 Nov 1;142(11):3382-3397. doi: 10.1093/brain/awz291. Brain. 2019. PMID: 31637422 Free PMC article.
Disturbed brain ether lipid metabolism and histology in Sjögren-Larsson syndrome.
Staps P, Rizzo WB, Vaz FM, Bugiani M, Giera M, Heijs B, van Kampen AHC, Pras-Raves ML, Breur M, Groen A, Ferdinandusse S, van der Graaf M, Van Goethem G, Lammens M, Wevers RA, Willemsen MAAP. Staps P, et al. Among authors: van goethem g, van kampen ahc, van der graaf m. J Inherit Metab Dis. 2020 Nov;43(6):1265-1278. doi: 10.1002/jimd.12275. Epub 2020 Jul 9. J Inherit Metab Dis. 2020. PMID: 32557630 Free PMC article.
322 results