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Nature Structural & Molecular Biology|October 13, 2015
The chaperone αB-crystallin uses different interfaces to capture an amorphous and an amyloid clientAndi Mainz, Jirka Peschek, Maria Stavropoulou, et al.
Metabolism: Clinical and Experimental|August 11, 2016
Effects of lifestyle intervention on left ventricular regional myocardial function in metabolic syndrome patients from the RESOLVE randomized trialJuan Serrano-Ferrer, Edward Crendal, Guillaume Walther, et al.
Journal of Animal Science|February 24, 2021
The Blonde d'Aquitaine T3811>G3811 mutation in the myostatin gene: association with growth, carcass, and muscle phenotypes in veal calvesAurélie Vinet, Claire Bouyer, Lionel Forestier, et al.
American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation|April 1, 1988
Hypoxemia during hemodialysis: a critical review of the factsM Cardoso, P Vinay, B Vinet, et al.
Molecular and Cellular Neurosciences|October 10, 2001
Doublecortin interacts with mu subunits of clathrin adaptor complexes in the developing nervous systemG Friocourt, P Chafey, P Billuart, et al.
Optics Express|May 5, 2019
HV discharges triggered by dual- and triple-frequency laser filamentsThomas Produit, Pierre Walch, Guillaume Schimmel, et al.
Bioorganic & Medicinal Chemistry Letters|September 27, 2006
Inhibitors of Plasmepsin II-potential antimalarial agentsOlivier Corminboeuf, Guillaume Dunet, Mehdi Hafsi, et al.
Frontiers in Bioengineering and Biotechnology|July 9, 2024
Biphasic bone substitutes coated with PLGA incorporating therapeutic ions Sr2+ and Mg2+: cytotoxicity cascade and in vivo response of immune and bone regenerationYanru Ren, Ole Jung, Milijana Batinic, et al.
Food Chemistry|November 24, 2015
Characterization of fruit development and potential health benefits of arrayan (Luma apiculata), a native berry of South AmericaLida Fuentes, Mónika Valdenegro, María-Graciela Gómez, et al.
Journal of Medical Genetics|April 1, 1994
Linkage analysis of families with severe childhood autosomal recessive muscular dystrophy in Morocco indicates genetic homogeneity of the disease in north AfricaF el Kerch, A Sefiani, K Azibi, et al.
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