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Proteins|May 10, 2002
ConsDock: A new program for the consensus analysis of protein-ligand interactionsNicodème Paul, Didier RognanBMC Bioinformatics|November 9, 2005
Identification of clustered microRNAs using an ab initio prediction methodAlain Sewer, Nicodème Paul, Pablo Landgraf, et al.AIDS (London, England)|September 28, 2021
Distinct antibody profiles in HLA-B∗57+, HLA-B∗57- HIV controllers and chronic progressorsJéromine Klingler, Nicodème Paul, Géraldine Laumond, et al.Plos One|November 3, 2015
Circulating Human Eosinophils Share a Similar Transcriptional Profile in Asthma and Other Hypereosinophilic DisordersCindy Barnig, Ghada Alsaleh, Nicolas Jung, et al.European Journal of Human Genetics : EJHG|July 7, 2016
Protein-altering MYH3 variants are associated with a spectrum of phenotypes extending to spondylocarpotarsal synostosis syndromeRaphael Carapito, Alice Goldenberg, Nicodème Paul, et al.Journal of Translational Autoimmunity|January 19, 2026
Systemic lupus pregnancies are characterized by an intrinsic pro-inflammatory monocyte transcriptome, driven by an aberrant miRNA signatureMarc Scherlinger, Eloi Schmauch, Raphaël Carapito, et al.Journal of Human Genetics|November 15, 2013
A new mutation in the C-SH2 domain of PTPN11 causes Noonan syndrome with multiple giant cell lesionsRaphael Carapito, Nicodème Paul, Meiggie Untrau, et al.Genome Biology and Evolution|April 27, 2017
Whole-Genome Sequencing of Seven Strains of Staphylococcus lugdunensis Allows Identification of Mobile Genetic ElementsXavier Argemi, Véronique Martin, Valentin Loux, et al.Scientific Reports|January 31, 2019
Multi-omics dataset to decipher the complexity of drug resistance in diffuse large B-cell lymphomaLuc-Matthieu Fornecker, Leslie Muller, Frédéric Bertrand, et al.Movement Disorders : Official Journal of the Movement Disorder Society|December 30, 2014
A de novo ADCY5 mutation causes early-onset autosomal dominant chorea and dystoniaRaphael Carapito, Nicodème Paul, Meiggie Untrau, et al.Pageof 4