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71 results

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Page 1
GLI2 promoter hypermethylation in saliva of children with a respiratory allergy.
Langie SAS, Moisse M, Szarc Vel Szic K, Van Der Plas E, Koppen G, De Prins S, Louwies T, Nelen V, Van Camp G, Lambrechts D, Schoeters G, Vanden Berghe W, De Boever P. Langie SAS, et al. Among authors: moisse m. Clin Epigenetics. 2018 Apr 11;10:50. doi: 10.1186/s13148-018-0484-1. eCollection 2018. Clin Epigenetics. 2018. PMID: 29682088 Free PMC article.
Salivary DNA Methylation Profiling: Aspects to Consider for Biomarker Identification.
Langie SAS, Moisse M, Declerck K, Koppen G, Godderis L, Vanden Berghe W, Drury S, De Boever P. Langie SAS, et al. Among authors: moisse m. Basic Clin Pharmacol Toxicol. 2017 Sep;121 Suppl 3(Suppl Suppl 3):93-101. doi: 10.1111/bcpt.12721. Epub 2017 Feb 10. Basic Clin Pharmacol Toxicol. 2017. PMID: 27901320 Free PMC article. Review.
Meta-analysis of epigenome-wide association studies in neonates reveals widespread differential DNA methylation associated with birthweight.
Küpers LK, Monnereau C, Sharp GC, Yousefi P, Salas LA, Ghantous A, Page CM, Reese SE, Wilcox AJ, Czamara D, Starling AP, Novoloaca A, Lent S, Roy R, Hoyo C, Breton CV, Allard C, Just AC, Bakulski KM, Holloway JW, Everson TM, Xu CJ, Huang RC, van der Plaat DA, Wielscher M, Merid SK, Ullemar V, Rezwan FI, Lahti J, van Dongen J, Langie SAS, Richardson TG, Magnus MC, Nohr EA, Xu Z, Duijts L, Zhao S, Zhang W, Plusquin M, DeMeo DL, Solomon O, Heimovaara JH, Jima DD, Gao L, Bustamante M, Perron P, Wright RO, Hertz-Picciotto I, Zhang H, Karagas MR, Gehring U, Marsit CJ, Beilin LJ, Vonk JM, Jarvelin MR, Bergström A, Örtqvist AK, Ewart S, Villa PM, Moore SE, Willemsen G, Standaert ARL, Håberg SE, Sørensen TIA, Taylor JA, Räikkönen K, Yang IV, Kechris K, Nawrot TS, Silver MJ, Gong YY, Richiardi L, Kogevinas M, Litonjua AA, Eskenazi B, Huen K, Mbarek H, Maguire RL, Dwyer T, Vrijheid M, Bouchard L, Baccarelli AA, Croen LA, Karmaus W, Anderson D, de Vries M, Sebert S, Kere J, Karlsson R, Arshad SH, Hämäläinen E, Routledge MN, Boomsma DI, Feinberg AP, Newschaffer CJ, Govarts E, Moisse M, Fallin MD, Melén E, Prentice AM, Kajantie E, Almqvist C, Oken E, Dabelea D, Boezen HM, Melton PE, Wrig… See abstract for full author list ➔ Küpers LK, et al. Among authors: moisse m. Nat Commun. 2019 Apr 23;10(1):1893. doi: 10.1038/s41467-019-09671-3. Nat Commun. 2019. PMID: 31015461 Free PMC article.
Epigenetic effects of carbon nanotubes in human monocytic cells.
Öner D, Moisse M, Ghosh M, Duca RC, Poels K, Luyts K, Putzeys E, Cokic SM, Van Landuyt K, Vanoirbeek J, Lambrechts D, Godderis L, Hoet PH. Öner D, et al. Among authors: moisse m. Mutagenesis. 2017 Jan;32(1):181-191. doi: 10.1093/mutage/gew053. Epub 2016 Nov 13. Mutagenesis. 2017. PMID: 28011750
Whole-genome sequencing reveals a coding non-pathogenic variant tagging a non-coding pathogenic hexanucleotide repeat expansion in C9orf72 as cause of amyotrophic lateral sclerosis.
Herdewyn S, Zhao H, Moisse M, Race V, Matthijs G, Reumers J, Kusters B, Schelhaas HJ, van den Berg LH, Goris A, Robberecht W, Lambrechts D, Van Damme P. Herdewyn S, et al. Among authors: moisse m. Hum Mol Genet. 2012 Jun 1;21(11):2412-9. doi: 10.1093/hmg/dds055. Epub 2012 Feb 17. Hum Mol Genet. 2012. PMID: 22343411 Free PMC article.
71 results