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Articles
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[hal-04522061] Time-Kill Analysis of Canine Skin Pathogens : A Comparison of Pradofloxacin and Marbofloxacin
26 mars, par ano.nymous@ccsd.cnrs.fr.invalid (Stefano Azzariti), Stefano AzzaritiTime-kill curves (TKCs) are more informative compared with the use of minimum inhibitory concentration (MIC) as they allow the capture of bacterial growth and the development of drug killing rates over time, which allows to compute key pharmacodynamic (PD) parameters. Our study aimed, using a (...) -
[hal-04514078] Archéologie terrestre
26 mars, par ano.nymous@ccsd.cnrs.fr.invalid (Virginie Motte), Virginie Motte[...] -
[hal-03808337] Ultrafast time-evolution of chiral Néel magnetic domain walls probed by circular dichroism in x-ray resonant magnetic scattering
26 mars, par ano.nymous@ccsd.cnrs.fr.invalid (Cyril Léveillé), Cyril LéveilléNon-collinear spin textures in ferromagnetic ultrathin films are attracting a renewed interest fueled by possible fine engineering of several magnetic interactions, notably the interfacial Dzyaloshinskii-Moriya interaction. This allows for the stabilization of complex chiral spin textures such (...) -
[hal-04522023] SUMOylation controls Hu antigen R posttranscriptional activity in liver cancer
26 mars, par ano.nymous@ccsd.cnrs.fr.invalid (Sofia Lachiondo-Ortega), Sofia Lachiondo-OrtegaThe posttranslational modification of proteins critically influences many biological processes and is a key mechanism that regulates the function of the RNA-binding protein Hu antigen R (HuR), a hub in liver cancer. Here, we show that HuR is SUMOylated in the tumor sections of patients with (...) -
[hal-04522006] The Rogdi knockout mouse is a model for Kohlschütter–Tönz syndrome
26 mars, par ano.nymous@ccsd.cnrs.fr.invalid (Alexandra Jimenez-Armijo), Alexandra Jimenez-ArmijoAbstract Kohlschütter–Tönz syndrome (KTS) is a rare autosomal recessive disorder characterized by severe intellectual disability, early-onset epileptic seizures, and amelogenesis imperfecta. Here, we present a novel Rogdi mutant mouse deleting exons 6–11- a mutation found in KTS patients (...)