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Journal of Hypertension|June 24, 2015
New developments in the pathogenesis of obesity-induced hypertensionVasilios Kotsis, Peter Nilsson, Guido Grassi, et al.
Atherosclerosis|February 23, 2010
Association of selected ABC gene family single nucleotide polymorphisms with postprandial lipoproteins: results from the population-based Hortega studyRosario Abellán, María Luisa Mansego, Sergio Martínez-Hervás, et al.
International Journal of Molecular Sciences|October 22, 2011
Different impacts of cardiovascular risk factors on oxidative stressMaria L Mansego, Josep Redon, Sergio Martinez-Hervas, et al.
Plos One|October 4, 2011
High-throughput analysis of promoter occupancy reveals new targets for Arx, a gene mutated in mental retardation and interneuronopathiesMarie-Lise Quillé, Solenne Carat, Sylvia Quéméner-Redon, et al.
Journal of Hypertension|June 10, 2009
Prognostic value of blood pressure in patients with high vascular risk in the Ongoing Telmisartan Alone and in combination with Ramipril Global Endpoint Trial studyPeter Sleight, Josep Redon, Paolo Verdecchia, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|September 9, 2010
Histone gammaH2AX and poly(ADP-ribose) as clinical pharmacodynamic biomarkersChristophe E Redon, Asako J Nakamura, Yong-Wei Zhang, et al.
Methods in Molecular Biology (Clifton, N.J.)|November 9, 2010
γ-H2AX detection in peripheral blood lymphocytes, splenocytes, bone marrow, xenografts, and skinChristophe E Redon, Asako J Nakamura, Olivier Sordet, et al.
Journal of Medical Genetics|April 3, 2004
Microarray based comparative genomic hybridisation (array-CGH) detects submicroscopic chromosomal deletions and duplications in patients with learning disability/mental retardation and dysmorphic featuresC Shaw-Smith, R Redon, L Rickman, et al.
Frontiers in Cell and Developmental Biology|July 29, 2024
Exploring the origins of neurodevelopmental proteasomopathies associated with cardiac malformations: are neural crest cells central to certain pathological mechanisms?Virginie Vignard, Alban-Elouen Baruteau, Bérénice Toutain, et al.
Human Mutation|April 10, 2026
Cellular Functional Analyses of ARX Variants Reveal New Insights Into Genotype-Phenotype Correlations in Neurodevelopmental Disorders Among Male and Female PatientsRasha Faraj, Audrey Farrugia, Anna C E Hurst, et al.
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