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Page 1
Identification of a DLG3 stop mutation in the MRX20 family.
Huyghebaert J, Mateiu L, Elinck E, Van Rossem KE, Christiaenssen B, D'Incal CP, McCormack MK, Lazzarini A, Vandeweyer G, Kooy RF. Huyghebaert J, et al. Among authors: mateiu l. Eur J Hum Genet. 2024 Mar;32(3):317-323. doi: 10.1038/s41431-024-01537-7. Epub 2024 Jan 25. Eur J Hum Genet. 2024. PMID: 38273165
ADNP dysregulates methylation and mitochondrial gene expression in the cerebellum of a Helsmoortel-Van der Aa syndrome autopsy case.
D'Incal C, Van Dijck A, Ibrahim J, De Man K, Bastini L, Konings A, Elinck E, Theys C, Gozes I, Marusic Z, Anicic M, Vukovic J, Van der Aa N, Mateiu L, Vanden Berghe W, Kooy RF. D'Incal C, et al. Among authors: mateiu l. Acta Neuropathol Commun. 2024 Apr 18;12(1):62. doi: 10.1186/s40478-024-01743-w. Acta Neuropathol Commun. 2024. PMID: 38637827 Free PMC article.
Transcriptomic and proteomic profiling of bi-partite and tri-partite murine iPSC-derived neurospheroids under steady-state and inflammatory condition.
Di Stefano J, Garcia-Pupo L, Di Marco F, Motaln H, Govaerts J, Van Breedam E, Mateiu LM, Van Calster S, Ricciardi L, Quarta A, Verstraelen P, De Vos WH, Rogelj B, Cicalini I, De Laurenzi V, Del Boccio P, FitzGerald U, Vanden Berghe W, Verhoye M, Pieragostino D, Ponsaerts P. Di Stefano J, et al. Among authors: mateiu lm. Brain Behav Immun. 2024 Oct;121:1-12. doi: 10.1016/j.bbi.2024.07.008. Epub 2024 Jul 17. Brain Behav Immun. 2024. PMID: 39002812
Loss of PPARα function promotes epigenetic dysregulation of lipid homeostasis driving ferroptosis and pyroptosis lipotoxicity in metabolic dysfunction associated Steatotic liver disease (MASLD).
Theys C, Vanderhaeghen T, Van Dijck E, Peleman C, Scheepers A, Ibrahim J, Mateiu L, Timmermans S, Vanden Berghe T, Francque SM, Van Hul W, Libert C, Vanden Berghe W. Theys C, et al. Among authors: mateiu l. Front Mol Med. 2024 Jan 8;3:1283170. doi: 10.3389/fmmed.2023.1283170. eCollection 2023. Front Mol Med. 2024. PMID: 39086681 Free PMC article.
Correction to: ADNP dysregulates methylation and mitochondrial gene expression in the cerebellum of a Helsmoortel-Van Der Aa syndrome autopsy case.
D'Incal C, Dijck AV, Ibrahim J, Man K, Bastini L, Konings A, Elinck E, Theys C, Gozes I, Marusic Z, Anicic M, Vukovic J, Aa NV, Mateiu L, Vanden Berghe W, Kooy RF. D'Incal C, et al. Among authors: mateiu l. Acta Neuropathol Commun. 2024 Oct 24;12(1):168. doi: 10.1186/s40478-024-01787-y. Acta Neuropathol Commun. 2024. PMID: 39449121 Free PMC article. No abstract available.
The Genetic Puzzle of Cerebral Palsy: Results of a Monocentric Study.
Thys L, Beysen D, Ceulemans B, Kenis S, Dielman C, Roelens F, Reyniers E, Mateiu L, Janssens K, Meuwissen M. Thys L, et al. Among authors: mateiu l. Pediatr Neurol. 2024 Dec;161:1-8. doi: 10.1016/j.pediatrneurol.2024.07.019. Epub 2024 Aug 5. Pediatr Neurol. 2024. PMID: 39213953
Heterozygous variants in CTR9, which encodes a major component of the PAF1 complex, are associated with a neurodevelopmental disorder.
Meuwissen M, Verstraeten A, Ranza E, Iwaszkiewicz J, Bastiaansen M, Mateiu L, Nemegeer M, Meester JAN, Afenjar A, Amaral M, Ballhausen D, Barnett S, Barth M, Asselbergh B, Spaas K, Heeman B, Bassetti J, Blackburn P, Schaer M, Blanc X, Zoete V, Casas K, Courtin T, Doummar D, Guerry F, Keren B, Pappas J, Rabin R, Begtrup A, Shinawi M, Vulto-van Silfhout AT, Kleefstra T, Wagner M, Ziegler A, Schaefer E, Gerard B, De Bie CI, Holwerda SJB, Abbot MA, Antonarakis SE, Loeys B. Meuwissen M, et al. Among authors: mateiu l. Genet Med. 2022 Jul;24(7):1583-1591. doi: 10.1016/j.gim.2022.04.003. Epub 2022 May 2. Genet Med. 2022. PMID: 35499524 Free article.
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