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Computational protein design with a generalized Born solvent model: applicati...
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Risk factors and clinical presentation of venous thromboembolism according to...
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Interrelation of hyperhomocysteinemia and inherited risk factors for venous t...
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High frequency of factor V Leiden in surgical patients with symptomatic venou...
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Fibrinogen Aalpha-Thr312Ala and factor XIII-A Val34Leu polymorphisms in idiop...
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Characterization of a hepatitis B and hepatitis delta virus receptor binding ...
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Eight previously unidentified mutations found in the OA1 ocular albinism gene.
BACKGROUND: Ocular albinism type 1 (OA1) is an X-linked ocular disorder characterized by a severe reduction in visual acuity, nystagmus, hypopigmentation of the... -
Hematologically important mutations: the autosomal recessive forms of chronic...
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First report on the co-inheritance of beta-globin IVS-I-5 (G-->C) thalassemia...
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Prevalence of molecular markers of Plasmodium falciparum drug resistance in D...
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A novel function for spumaretrovirus integrase: an early requirement for inte...
Retroviral integration is central to viral persistence and pathogenesis, cancer as well as host genome evolution. However, it is unclear why integration appears... -
Comparative proteomics as a new tool for exploring human mitochondrial tRNA d...
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[EGFR activating mutation in lung adenocarcinoma: risk factor of thromboembol...
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Identification of a functional destruction box in the Xenopus laevis aurora-A...
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Inherited genetic variants in autism-related CNTNAP2 show perturbed trafficki...
International audience
