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D25V apolipoprotein C-III variant causes dominant hereditary systemic amyloidosis and confers cardiovascular protective lipoprotein profile.
Valleix S, Verona G, Jourde-Chiche N, Nédelec B, Mangione PP, Bridoux F, Mangé A, Dogan A, Goujon JM, Lhomme M, Dauteuille C, Chabert M, Porcari R, Waudby CA, Relini A, Talmud PJ, Kovrov O, Olivecrona G, Stoppini M, Christodoulou J, Hawkins PN, Grateau G, Delpech M, Kontush A, Gillmore JD, Kalopissis AD, Bellotti V. Valleix S, et al. Among authors: kalopissis ad. Nat Commun. 2016 Jan 21;7:10353. doi: 10.1038/ncomms10353. Nat Commun. 2016. PMID: 26790392 Free PMC article.
A transgenic mouse model reproduces human hereditary systemic amyloidosis.
Chabert M, Rousset X, Colombat M, Lacasa M, Kakanakou H, Bourderioux M, Brousset P, Burlet-Schiltz O, Liepnieks JJ, Kluve-Beckerman B, Lambert G, Châtelet FP, Benson MD, Kalopissis AD. Chabert M, et al. Among authors: kalopissis ad. Kidney Int. 2019 Sep;96(3):628-641. doi: 10.1016/j.kint.2019.03.013. Epub 2019 Mar 28. Kidney Int. 2019. PMID: 31200944 Free article.
Molecular spectrum of autosomal dominant hypercholesterolemia in France.
Marduel M, Carrié A, Sassolas A, Devillers M, Carreau V, Di Filippo M, Erlich D, Abifadel M, Marques-Pinheiro A, Munnich A, Junien C; French ADH Research Network; Boileau C, Varret M, Rabès JP. Marduel M, et al. Hum Mutat. 2010 Nov;31(11):E1811-24. doi: 10.1002/humu.21348. Hum Mutat. 2010. PMID: 20809525 Free PMC article.
Lipids in metabolic diseases.
Dugail I, Kalopissis A, Miquel M, Rainteau D, Zachowski A, Forest C. Dugail I, et al. Biochimie. 2014 Jan;96:1-2. doi: 10.1016/j.biochi.2013.11.009. Biochimie. 2014. PMID: 24321080 No abstract available.
37 results