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Regulation of human microglial gene expression and function via RNAase-H active antisense oligonucleotides in vivo in Alzheimer's disease.
Vandermeulen L, Geric I, Fumagalli L, Kreir M, Lu A, Nonneman A, Premereur J, Wolfs L, Policarpo R, Fattorelli N, De Bondt A, Van Den Wyngaert I, Asselbergh B, Fiers M, De Strooper B, d'Ydewalle C, Mancuso R. Vandermeulen L, et al. Among authors: d ydewalle c. Mol Neurodegener. 2024 Apr 24;19(1):37. doi: 10.1186/s13024-024-00725-9. Mol Neurodegener. 2024. PMID: 38654375 Free PMC article.
Missing lnc(RNAs) in Alzheimer's Disease?
Policarpo R, d'Ydewalle C. Policarpo R, et al. Among authors: d ydewalle c. Genes (Basel). 2021 Dec 23;13(1):39. doi: 10.3390/genes13010039. Genes (Basel). 2021. PMID: 35052379 Free PMC article. Review.
From Junk to Function: LncRNAs in CNS Health and Disease.
Policarpo R, Sierksma A, De Strooper B, d'Ydewalle C. Policarpo R, et al. Among authors: d ydewalle c. Front Mol Neurosci. 2021 Jul 19;14:714768. doi: 10.3389/fnmol.2021.714768. eCollection 2021. Front Mol Neurosci. 2021. PMID: 34349622 Free PMC article. Review.
Age-dependent SMN expression in disease-relevant tissue and implications for SMA treatment.
Ramos DM, d'Ydewalle C, Gabbeta V, Dakka A, Klein SK, Norris DA, Matson J, Taylor SJ, Zaworski PG, Prior TW, Snyder PJ, Valdivia D, Hatem CL, Waters I, Gupte N, Swoboda KJ, Rigo F, Bennett CF, Naryshkin N, Paushkin S, Crawford TO, Sumner CJ. Ramos DM, et al. Among authors: d ydewalle c. J Clin Invest. 2019 Nov 1;129(11):4817-4831. doi: 10.1172/JCI124120. J Clin Invest. 2019. PMID: 31589162 Free PMC article. Clinical Trial.
HDAC6 is a therapeutic target in mutant GARS-induced Charcot-Marie-Tooth disease.
Benoy V, Van Helleputte L, Prior R, d'Ydewalle C, Haeck W, Geens N, Scheveneels W, Schevenels B, Cader MZ, Talbot K, Kozikowski AP, Vanden Berghe P, Van Damme P, Robberecht W, Van Den Bosch L. Benoy V, et al. Among authors: d ydewalle c. Brain. 2018 Mar 1;141(3):673-687. doi: 10.1093/brain/awx375. Brain. 2018. PMID: 29415205 Free PMC article.
A dominant mutation in FBXO38 causes distal spinal muscular atrophy with calf predominance.
Sumner CJ, d'Ydewalle C, Wooley J, Fawcett KA, Hernandez D, Gardiner AR, Kalmar B, Baloh RH, Gonzalez M, Züchner S, Stanescu HC, Kleta R, Mankodi A, Cornblath DR, Boylan KB, Reilly MM, Greensmith L, Singleton AB, Harms MB, Rossor AM, Houlden H. Sumner CJ, et al. Among authors: d ydewalle c. Am J Hum Genet. 2013 Nov 7;93(5):976-83. doi: 10.1016/j.ajhg.2013.10.006. Epub 2013 Oct 24. Am J Hum Genet. 2013. PMID: 24207122 Free PMC article.
Charcot-Marie-Tooth disease: emerging mechanisms and therapies.
d'Ydewalle C, Benoy V, Van Den Bosch L. d'Ydewalle C, et al. Int J Biochem Cell Biol. 2012 Aug;44(8):1299-304. doi: 10.1016/j.biocel.2012.04.020. Epub 2012 Apr 30. Int J Biochem Cell Biol. 2012. PMID: 22575637 Review.
15 results