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An investigation on mutation strategies for fault injection into RDD-100 models
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PILOTAGE DU PARTAGE DES CONNAISSANCES DANS UNE COLLABORATION INTERORGANISATIO...
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Research and characterization of genes implicated in the catecholaminergic ve...
Catecholaminergic polymorphic ventricular tachycardia (CPVT) is a rare and severe inherited arrhythmogenic disorder, responsible for sudden death in young patients. It... -
Biophysical properties of mutant KCNQ1 S277L channels linked to hereditary lo...
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Identification and functional analysis of novel THAP1 mutations
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Clinical and molecular characterization of five patients with Succinyl-CoA:3-...
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Accumulation of flavonoids in an ntra ntrb mutant leads to tolerance to UV-C.
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Tendances d'évolution des loisirs sportifs de nature
This dataset has no description
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Model Driven Mutation Applied to Adaptative Systems Testing
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Trade-off between bile resistance and nutritional competence drives Escherich...
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Mutation stratégique des Chambres de Commerce et d'Industrie
Les Chambres de Commerce et d'Industrie régionales et locales sont dans une période décisive pour leur devenir. Elles ne parviendront à se développer et à être des... -
Qualité du conseil et mutation du service public
Un vif courant d'intérêt est né ces dernières années sur la nécessité de développer le professionnalisme des consultants en management qui devront affronter dès 1993... -
La nouvelle fabrique des experts
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La mutation fantasmée : le cas Cronenberg
Disponible en ligne, URL : www.cairn.info/revue-critique-2006-6-page-580.htm. -
Motor coordination in mice with hotfoot, Lurcher, and double mutations of the...
Grid2(ho/ho) is a loss of function gene mutation resulting in abnormal dendritic arborizations of Purkinje cells. These mutants were compared in a series of motor... -
Molecular Defects in Moroccan Patients with Ataxia-Telangiectasia.
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A cell-contact-regulated operon is involved in genetic variability in Neisser...
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Characterization of the phenotype associated with the masculinizing mutation ...
Rainbow trout has a strict genetic XX/XY sex determination system. However spontaneous masculinization has been observed in genetic females (XX) obtained through... -
Hematologically important mutations: the autosomal recessive forms of chronic...
International audience
