An APOA5 3′ UTR Variant Associated with Plasma Triglycerides Triggers APOA5 Downregulation by Creating a Functional miR-485-5p Binding Site

Authors: Caussy, C., Charrière, S., Marçais, C., Di Filippo, M., Sassolas, A. s., Delay, M., Euthine, V., Jalabert, A., Lefai, E., Rome, S.

Source: AMERICAN JOURNAL OF HUMAN GENETICS. 94(1):129-134

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Clinical and electrophysiological characteristics of neuropathy associated with Tangier disease

Authors: Zyss, J., Béhin, A., Couvert, P., Bouhour, F. o., Sassolas, A. s., Kolev, I., Denys, V., Vial, C., Lacour, A., Carrié, A.

Source: JOURNAL OF NEUROLOGY -BERLIN-. 259(6):1222-1226

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Identification of two novel mutations and long-term follow-up in abetalipoproteinemia: a report of four cases

Authors: Chardon, L., Sassolas, A. s., Dingeon, B., Michel-Calemard, L., Bovier-Lapierre, M., Moulin, P., Lachaux, A.

Source: EUROPEAN JOURNAL OF PEDIATRICS. 168(8):983-989

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Association of APOA5 −1131T>C and S19W gene polymorphisms with both mild hypertriglyceridemia and hyperchylomicronemia in type 2 diabetic patients

Authors: Charriere, S., Bernard, S., Aqallal, M., Merlin, M., Billon, S. p., Perrot, L., Le Coquil, E., Sassolas, A. s., Moulin, P., Marcais, C.

Source: CLINICA CHIMICA ACTA. 394(1-2):99-103

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