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Genetic mouse models of neurodegenerative diseases.
Trancikova A, Ramonet D, Moore DJ. Trancikova A, et al. Among authors: ramonet d. Prog Mol Biol Transl Sci. 2011;100:419-82. doi: 10.1016/B978-0-12-384878-9.00012-1. Prog Mol Biol Transl Sci. 2011. PMID: 21377633 Review.
Dopaminergic neuronal loss, reduced neurite complexity and autophagic abnormalities in transgenic mice expressing G2019S mutant LRRK2.
Ramonet D, Daher JP, Lin BM, Stafa K, Kim J, Banerjee R, Westerlund M, Pletnikova O, Glauser L, Yang L, Liu Y, Swing DA, Beal MF, Troncoso JC, McCaffery JM, Jenkins NA, Copeland NG, Galter D, Thomas B, Lee MK, Dawson TM, Dawson VL, Moore DJ. Ramonet D, et al. PLoS One. 2011 Apr 6;6(4):e18568. doi: 10.1371/journal.pone.0018568. PLoS One. 2011. PMID: 21494637 Free PMC article.
The single-molecule mechanics of the latent TGF-β1 complex.
Buscemi L, Ramonet D, Klingberg F, Formey A, Smith-Clerc J, Meister JJ, Hinz B. Buscemi L, et al. Among authors: ramonet d. Curr Biol. 2011 Dec 20;21(24):2046-54. doi: 10.1016/j.cub.2011.11.037. Epub 2011 Dec 8. Curr Biol. 2011. PMID: 22169532 Free article.
SUCLG2 identified as both a determinator of CSF Aβ1-42 levels and an attenuator of cognitive decline in Alzheimer's disease.
Ramirez A, van der Flier WM, Herold C, Ramonet D, Heilmann S, Lewczuk P, Popp J, Lacour A, Drichel D, Louwersheimer E, Kummer MP, Cruchaga C, Hoffmann P, Teunissen C, Holstege H, Kornhuber J, Peters O, Naj AC, Chouraki V, Bellenguez C, Gerrish A; International Genomics of Alzheimer's Project (IGAP); Alzheimer's Disease Neuroimaging Initiative (ADNI); Heun R, Frölich L, Hüll M, Buscemi L, Herms S, Kölsch H, Scheltens P, Breteler MM, Rüther E, Wiltfang J, Goate A, Jessen F, Maier W, Heneka MT, Becker T, Nöthen MM. Ramirez A, et al. Among authors: ramonet d. Hum Mol Genet. 2014 Dec 15;23(24):6644-58. doi: 10.1093/hmg/ddu372. Epub 2014 Jul 15. Hum Mol Genet. 2014. PMID: 25027320 Free PMC article.
Mitochondrial alterations in Parkinson's disease: new clues.
Vila M, Ramonet D, Perier C. Vila M, et al. Among authors: ramonet d. J Neurochem. 2008 Oct;107(2):317-28. doi: 10.1111/j.1471-4159.2008.05604.x. Epub 2008 Aug 30. J Neurochem. 2008. PMID: 18680555 Free article. Review.
Common variants in the HLA-DQ region confer susceptibility to idiopathic achalasia.
Gockel I, Becker J, Wouters MM, Niebisch S, Gockel HR, Hess T, Ramonet D, Zimmermann J, Vigo AG, Trynka G, de León AR, de la Serna JP, Urcelay E, Kumar V, Franke L, Westra HJ, Drescher D, Kneist W, Marquardt JU, Galle PR, Mattheisen M, Annese V, Latiano A, Fumagalli U, Laghi L, Cuomo R, Sarnelli G, Müller M, Eckardt AJ, Tack J, Hoffmann P, Herms S, Mangold E, Heilmann S, Kiesslich R, von Rahden BH, Allescher HD, Schulz HG, Wijmenga C, Heneka MT, Lang H, Hopfner KP, Nöthen MM, Boeckxstaens GE, de Bakker PI, Knapp M, Schumacher J. Gockel I, et al. Among authors: ramonet d. Nat Genet. 2014 Aug;46(8):901-4. doi: 10.1038/ng.3029. Epub 2014 Jul 6. Nat Genet. 2014. PMID: 24997987
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