Zobrazeno 1 - 10
of 15
pro vyhledávání: '"Veronica Codoni"'
Autor:
Veronica Codoni, Yuna Blum, Mete Civelek, Carole Proust, Oscar Franzén, Cardiogenics Consortium, IDEM Leducq Consortium CADGenomics, Johan L. M. Björkegren, Wilfried Le Goff, Francois Cambien, Aldons J. Lusis, David-Alexandre Trégouët
Publikováno v:
G3: Genes, Genomes, Genetics, Vol 6, Iss 10, Pp 3361-3371 (2016)
Macrophages are key players involved in numerous pathophysiological pathways and an in-depth characterization of their gene regulatory networks can help in better understanding how their dysfunction may impact on human diseases. We here conducted a c
Externí odkaz:
https://doaj.org/article/6400e4b80771417f88d84779bd8eaf01
Autor:
Margaret O'Brien, Shridhar Parthasarathy, Eryn Fitch, Ingo Helbig, Roland Krause, Shiva Ganesan, Veronica Codoni, Katherine Crawford, Deanne Taylor, Colin A Ellis, Julie Xian, Peter D. Galer, David Lewis-Smith, Katherine L. Helbig, Michael C. Kaufman, Laura Conway
Publikováno v:
Genetics in Medicine
Purpose Pathogenic variants in SCN2A cause a wide range of neurodevelopmental phenotypes. Reports of genotype–phenotype correlations are often anecdotal, and the available phenotypic data have not been systematically analyzed. Methods We extracted
Autor:
Le Shu, Kei Hang K Chan, Guanglin Zhang, Tianxiao Huan, Zeyneb Kurt, Yuqi Zhao, Veronica Codoni, David-Alexandre Trégouët, Cardiogenics Consortium, Jun Yang, James G Wilson, Xi Luo, Daniel Levy, Aldons J Lusis, Simin Liu, Xia Yang
Publikováno v:
PLoS Genetics, Vol 13, Iss 9, p e1007040 (2017)
Cardiovascular diseases (CVD) and type 2 diabetes (T2D) are closely interrelated complex diseases likely sharing overlapping pathogenesis driven by aberrant activities in gene networks. However, the molecular circuitries underlying the pathogenic com
Externí odkaz:
https://doaj.org/article/9b65189309924c46a788c2d5b8b67fa5
Autor:
Veronica Codoni, Valeria Cardinali, Gianluca Schiavoni, Maria Paola Martelli, Andrea Marra, Stefano Ascani, Enrico Tiacci, Brunangelo Falini, Alessandra Venanzi, Giovanni Martino
Publikováno v:
New England Journal of Medicine
Two Cancers in CHIP A patient with clonal hematopoiesis of indeterminate potential (CHIP) received the diagnosis of lymphoma with activation of RHOA. Approximately 1 year later, NPM1-mutated acute ...
Autor:
François Cambien, Johan Björkegren, Yuna Blum, Veronica Codoni, Wilfried Le Goff, Oscar Franzén, Mete Civelek, David-Alexandre Trégouët, Carole Proust, Aldons J. Lusis
Publikováno v:
G3: Genes, Genomes, Genetics, Vol 6, Iss 10, Pp 3361-3371 (2016)
G3
G3, 2016, 6 (10), pp.3361-3371. ⟨10.1534/g3.116.033894⟩
G3: Genes|Genomes|Genetics
G3, Genetics Society of America, 2016, 6 (10), pp.3361-3371. ⟨10.1534/g3.116.033894⟩
G3
G3, 2016, 6 (10), pp.3361-3371. ⟨10.1534/g3.116.033894⟩
G3: Genes|Genomes|Genetics
G3, Genetics Society of America, 2016, 6 (10), pp.3361-3371. ⟨10.1534/g3.116.033894⟩
Cardiogenics Consortium, IDEM Leducq Consortium CADGenomics; International audience; Macrophages are key players involved in numerous pathophysiological pathways and an in-depth characterization of their gene regulatory networks can help in better un
Autor:
Yuna Blum, Henri Weidmann, Mete Civelek, Aldons J. Lusis, Zahia Touat-Hamici, Veronica Codoni, Ewa Ninio, Pauline Gaignard, Carole Proust, Francesca Iannacci, Sonia Karabina, Patrice Therond, François Cambien, Hervé Durand
Publikováno v:
Cardiovascular Research
Cardiovascular Research, 2016, 112 (3), pp.702-713. ⟨10.1093/cvr/cvw217⟩
Cardiovascular Research, Oxford University Press (OUP), 2016, 112 (3), pp.702-713. ⟨10.1093/cvr/cvw217⟩
Cardiovascular Research, 2016, 112 (3), pp.702-713. ⟨10.1093/cvr/cvw217⟩
Cardiovascular Research, Oxford University Press (OUP), 2016, 112 (3), pp.702-713. ⟨10.1093/cvr/cvw217⟩
Aims Lipid phosphate phosphatase 3; type 2 phosphatidic acid phosphatase β (LPP3; PPAP2B ) is a transmembrane protein dephosphorylating and thereby terminating signalling of lipid substrates including lysophosphatidic acid (LPA) and sphingosine-1-ph
Autor:
Jean-Sébastien Hulot, Nathalie Mougenot, Michel Clergue, Anne-Marie Lompré, Carole Proust, Veronica Codoni, David-Alexandre Trégouët, Fabrice Atassi, Jeremy Berthuin, Alexandre Marchand
Publikováno v:
Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease. 1862:611-621
We identified murine miR-322, orthologous to human miR-424, as a new regulator of insulin receptor, IGF-1 receptor and sirtuin 4 mRNA in vitro and in vivo in the heart and found that miR-322/424 is highly expressed in the heart of mice. C57Bl/6N mice
Autor:
Zeyneb Kurt, Daniel Levy, David-Alexandre Trégouët, Veronica Codoni, Kei Hang K. Chan, Le Shu, Yuqi Zhao, Simin Liu, Jun Yang, Xia Yang, James G. Wilson, Guanglin Zhang, Xi Luo, Tianxiao Huan, Aldons J. Lusis
Publikováno v:
PLoS Genetics
PLoS Genetics, Public Library of Science, In press, ⟨10.1371/journal.pgen.1007040⟩
PLoS Genetics, In press, ⟨10.1371/journal.pgen.1007040⟩
PLoS Genetics, Vol 13, Iss 9, p e1007040 (2017)
PLoS Genetics, Public Library of Science, In press, ⟨10.1371/journal.pgen.1007040⟩
PLoS Genetics, In press, ⟨10.1371/journal.pgen.1007040⟩
PLoS Genetics, Vol 13, Iss 9, p e1007040 (2017)
Cardiovascular diseases (CVD) and type 2 diabetes (T2D) are closely interrelated complex diseases likely sharing overlapping pathogenesis driven by aberrant activities in gene networks. However, the molecular circuitries underlying the pathogenic com
Autor:
Zeyneb Kurt, Aldons J. Lusis, Xia Yang, Veronica Codoni, Brian J. Bennett, Calvin Pan, Richard C. Davis, David-Alexandre Trégouët, Yuqi Zhao, Bin Zhang
Publikováno v:
Arteriosclerosis, Thrombosis, and Vascular Biology. 36
Coronary artery disease (CAD) remains one of leading causes of death worldwide. Although the genetic heritability of CAD has been estimated to be 40 to 60%, only ~10% can be explained by the genetic loci uncovered from recent large-scale human GWAS.
Autor:
Aldons J. Lusis, Mete Civelek, Eric J. Topol, Nilesh J. Samani, Ingrid Braenne, Johan Björkegren, Tom R. Webb, Jeanette Erdmann, Stephen E. Hamby, Hassan Foroughi Asl, Baiba Vilne, Xia Yang, Heribert Schunkert, Veronica Codoni, Benedikt Reiz, David-Alexandre Trégouët, Ke Hao, Antonio Fabio Di Narzo, Yuqi Zhao, Andrew D. Johnson, Eric E. Schadt, Lingyao Zeng
Publikováno v:
Arteriosclerosis, thrombosis, and vascular biology. 35(10)
Objective— Genome-wide association studies have to date identified 159 significant and suggestive loci for coronary artery disease (CAD). We now report comprehensive bioinformatics analyses of sequence variation in these loci to predict candidate c