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Biorxiv : the Preprint Server for Biology|February 23, 2026
The human plasma amino acids balance favours HIV replication in primary CD4 T lymphocytesLise Chauveau, Annemarie Fortuin, Arnaud Lecante, et al.
Scientific Reports|November 17, 2021
Probing the existence of non-thermal Terahertz radiation induced changes of the protein solution structureMartin A Schroer, Siawosch Schewa, Andrey Yu Gruzinov, et al.
Emerging Microbes & Infections|February 22, 2022
Usutu Virus escapes langerin-induced restriction to productively infect human Langerhans cells, unlike West Nile virusMarie-France Martin, Ghizlane Maarifi, Hervé Abiven, et al.
ASAIO Journal (American Society for Artificial Internal Organs : 1992)|October 23, 2004
Liver function during extracorporeal whole liver perfusion in a pig model of acute ischemic liver failureIsabelle Méchet, Franck Lhuillier, Marie Cécile Blanchet, et al.
Plos One|December 11, 2024
Diagnosis and treatment of occupational burnout in the Swiss outpatient sector: A national survey of healthcare professionals' attributes and attitudesIrina Guseva Canu, Roger Getzmann, Yara Shoman, et al.
American Journal of Human Genetics|April 17, 2007
Mutations in cytokine receptor-like factor 1 (CRLF1) account for both Crisponi and cold-induced sweating syndromesN Dagoneau, S Bellais, P Blanchet, et al.
The Ocular Surface|July 31, 2021
Tear metabolomics highlights new potential biomarkers for differentiating between Sjögren's syndrome and other causes of dry eyeGeoffrey Urbanski, Sophie Assad, Floris Chabrun, et al.
European Journal of Human Genetics : EJHG|May 23, 2013
Large deletions encompassing the TCOF1 and CAMK2A genes are responsible for Treacher Collins syndrome with intellectual disabilityMarie Vincent, Corinne Collet, Alain Verloes, et al.
Expert Opinion on Drug Metabolism & Toxicology|March 27, 2015
Effect of glucuronidation on transport and tissue accumulation of tyrosine kinase inhibitors: consequences for the clinical management of sorafenib and regorafenibCamille Tlemsani, Olivier Huillard, Jennifer Arrondeau, et al.
Human Mutation|June 20, 2014
Enrichment of LOVD-USHbases with 152 USH2A genotypes defines an extensive mutational spectrum and highlights missense hotspotsDavid Baux, Catherine Blanchet, Christian Hamel, et al.
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