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The malate-aspartate shuttle is important for de novo serine biosynthesis.
Cell Rep. 2023 Sep 26;42(9):113043. doi: 10.1016/j.celrep.2023.113043. Epub 2023 Aug 30.
Cell Rep. 2023.
PMID: 37647199
Free article.
PPARγ lipodystrophy mutants reveal intermolecular interactions required for enhancer activation.
Madsen MS, Broekema MF, Madsen MR, Koppen A, Borgman A, Gräwe C, Thomsen EGK, Westland D, Kranendonk MEG, Koerkamp MG, Hamers N, Bonvin AMJJ, Pittol JMR, Natarajan KN, Kersten S, Holstege FCP, Monajemi H, van Mil SWC, Vermeulen M, Kragelund BB, Cassiman D, Mandrup S, Kalkhoven E.
Madsen MS, et al. Among authors: westland d.
Nat Commun. 2022 Nov 19;13(1):7090. doi: 10.1038/s41467-022-34766-9.
Nat Commun. 2022.
PMID: 36402763
Free PMC article.
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Phosphoproteomic Analysis of FLCN Inactivation Highlights Differential Kinase Pathways and Regulatory TFEB Phosphoserines.
Glykofridis IE, Henneman AA, Balk JA, Goeij-de Haas R, Westland D, Piersma SR, Knol JC, Pham TV, Boekhout M, Zwartkruis FJT, Wolthuis RMF, Jimenez CR.
Glykofridis IE, et al. Among authors: westland d.
Mol Cell Proteomics. 2022 Sep;21(9):100263. doi: 10.1016/j.mcpro.2022.100263. Epub 2022 Jul 19.
Mol Cell Proteomics. 2022.
PMID: 35863698
Free PMC article.
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Recurrent exon-deleting activating mutations in AHR act as drivers of urinary tract cancer.
Vlaar JM, Borgman A, Kalkhoven E, Westland D, Besselink N, Shale C, Faltas BM, Priestley P, Kuijk E, Cuppen E.
Vlaar JM, et al. Among authors: westland d.
Sci Rep. 2022 Jun 16;12(1):10081. doi: 10.1038/s41598-022-14256-0.
Sci Rep. 2022.
PMID: 35710704
Free PMC article.
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Loss of FLCN-FNIP1/2 induces a non-canonical interferon response in human renal tubular epithelial cells.
Glykofridis IE, Knol JC, Balk JA, Westland D, Pham TV, Piersma SR, Lougheed SM, Derakhshan S, Veen P, Rooimans MA, van Mil SE, Böttger F, Poddighe PJ, van de Beek I, Drost J, Zwartkruis FJ, de Menezes RX, Meijers-Heijboer HE, Houweling AC, Jimenez CR, Wolthuis RM.
Glykofridis IE, et al. Among authors: westland d.
Elife. 2021 Jan 18;10:e61630. doi: 10.7554/eLife.61630.
Elife. 2021.
PMID: 33459596
Free PMC article.
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MDH1 deficiency is a metabolic disorder of the malate-aspartate shuttle associated with early onset severe encephalopathy.
Broeks MH, Shamseldin HE, Alhashem A, Hashem M, Abdulwahab F, Alshedi T, Alobaid I, Zwartkruis F, Westland D, Fuchs S, Verhoeven-Duif NM, Jans JJM, Alkuraya FS.
Broeks MH, et al. Among authors: westland d.
Hum Genet. 2019 Dec;138(11-12):1247-1257. doi: 10.1007/s00439-019-02063-z. Epub 2019 Sep 19.
Hum Genet. 2019.
PMID: 31538237
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