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NRF2 Shortage in Human Skin Fibroblasts Dysregulates Matrisome Gene Expression and Affects Collagen Fibrillogenesis.
Salamito M, Gillet B, Syx D, Vaganay E, Malbouyres M, Cerutti C, Tissot N, Exbrayat-Héritier C, Perez P, Jones C, Hughes S, Malfait F, Haydont V, Jäger S, Ruggiero F. Salamito M, et al. Among authors: malfait f. J Invest Dermatol. 2023 Mar;143(3):386-397.e12. doi: 10.1016/j.jid.2022.07.034. Epub 2022 Sep 20. J Invest Dermatol. 2023. PMID: 38487918 Free article.
Classic Ehlers-Danlos Syndrome.
Malfait F, Symoens S, Syx D. Malfait F, et al. 2007 May 29 [updated 2024 Feb 1]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2024. 2007 May 29 [updated 2024 Feb 1]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2024. PMID: 20301422 Free Books & Documents. Review.
Flemish network on rare connective tissue diseases (CTD): patient pathways in systemic sclerosis. First steps taken.
Piette Y, Van den Bossche F, Aerts J, Aerts N, Ajeganova S, Badot V, Berghen N, Blockmans D, Brusselle G, Caeyers N, De Decker M, De Haes P, De Cock C, De Keyser F, De Langhe E, Delcroix M, De Nutte H, De Pauw M, Depicker A, De Sutter A, De Sutter J, Du Four T, Frank C, Goubau J, Guiot J, Gutermuth J, Heeman L, Houssiau F, Hennes I, Lenaerts J, Lintermans A, Loeys B, Luyten H, Maeyaert B, Malfait F, Moeyersoons A, Mostmans Y, Nijs J, Poppe B, Polfliet K, Ruttens D, Sabato V, Schoeters E, Slabbynck H, Stuer A, Tamirou F, Thevissen K, Van Kersschaever G, Vanneuville B, Van Offel J, Vanthuyne M, Van Wabeke J, Verbist C, Vos I, Westhovens R, Wuyts W, Yserbyt J, Smith V. Piette Y, et al. Among authors: malfait f. Acta Clin Belg. 2024 Feb;79(1):26-33. doi: 10.1080/17843286.2023.2280737. Epub 2024 Jan 2. Acta Clin Belg. 2024. PMID: 38108332 Free article.
Syntaxin 18 Defects in Human and Zebrafish Unravel Key Roles in Early Cartilage and Bone Development.
Guillemyn B, De Saffel H, Bek JW, Tapaneeyaphan P, De Clercq A, Jarayseh T, Debaenst S, Willaert A, De Rycke R, Byers PH, Rosseel T, Coucke P, Blaumeiser B, Syx D, Malfait F, Symoens S. Guillemyn B, et al. Among authors: malfait f. J Bone Miner Res. 2023 Nov;38(11):1718-1730. doi: 10.1002/jbmr.4914. Epub 2023 Sep 30. J Bone Miner Res. 2023. PMID: 37718532 Free article.
Analysis of matrisome expression patterns in murine and human dorsal root ganglia.
Vroman R, Hunter RS, Wood MJ, Davis OC, Malfait Z, George DS, Ren D, Tavares-Ferreira D, Price TJ, Miller RJ, Malfait AM, Malfait F, Miller RE, Syx D. Vroman R, et al. Among authors: malfait f. Front Mol Neurosci. 2023 Aug 17;16:1232447. doi: 10.3389/fnmol.2023.1232447. eCollection 2023. Front Mol Neurosci. 2023. PMID: 37664243 Free PMC article.
Somatic symptoms, pain, catastrophizing and the association with disability among children with heritable connective tissue disorders.
de Koning LE, Warnink-Kavelaars J, van Rossum MA, Bosman D, Menke LA, Malfait F, de Boer R, Oosterlaan J, Engelbert RHH, Rombaut L; Pediatric Heritable Connective Tissue Disorders Study Group. de Koning LE, et al. Among authors: malfait f. Am J Med Genet A. 2023 Jul;191(7):1792-1803. doi: 10.1002/ajmg.a.63204. Epub 2023 Apr 26. Am J Med Genet A. 2023. PMID: 37186039
164 results