Zobrazeno 1 - 10
of 122
pro vyhledávání: '"G. Mollet"'
Autor:
F. C. Tilley, C. Arrondel, C. Chhuon, M. Boisson, N. Cagnard, M. Parisot, G. Menara, N. Lefort, I. C. Guerrera, C. Bole-Feysot, A. Benmerah, C. Antignac, G. Mollet
Publikováno v:
Scientific Reports, Vol 11, Iss 1, Pp 1-13 (2021)
Abstract Several studies have reported WDR73 mutations to be causative of Galloway–Mowat syndrome, a rare disorder characterised by the association of neurological defects and renal-glomerular disease. In this study, we demonstrate interaction of W
Externí odkaz:
https://doaj.org/article/167c8a987f01465c88c9cb66da245073
Autor:
João Pedro Marto, Ana Sofia Carvalho, Inês G. Mollet, Marcelo Mendonça, Manuel Salavisa, Bruna Meira, Marco Fernandes, Filipa Serrazina, Gonçalo Cabral, Rita Ventura, André Sobral‐Pinho, Hans C. Beck, Helena L. A. Vieira, Miguel Viana‐Baptista, Rune Matthiesen
Publikováno v:
Journal of the American Heart Association: Cardiovascular and Cerebrovascular Disease, Vol 12, Iss 22 (2023)
Background Blood biomarkers are a potential tool for early stroke diagnosis. We aimed to perform a pilot and exploratory study on untargeted blood biomarkers in patients with suspected stroke by using mass spectrometry analysis. Methods and Results T
Externí odkaz:
https://doaj.org/article/14e84b612146400794cafcbe834cc7cf
Autor:
Inês G. Mollet, Helena L. A. Vieira, Marcelo Mendonça, João Pedro Marto, Miguel Viana Baptista
Publikováno v:
Molecular Neurobiology
Stroke is one of the main causes of neurological disability worldwide and the second cause of death in people over 65 years old, resulting in great economic and social burden. Ischemic stroke accounts for 85% of total cases, and the approved therapie
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0d608a11d2dd164f888ee5a126a65f71
https://doi.org/10.1007/s12035-021-02585-6
https://doi.org/10.1007/s12035-021-02585-6
Autor:
Sanela Kjellqvist, Christian Klose, Michal A. Surma, George Hindy, Inês G. Mollet, Anna Johansson, Patrick Chavaux, Johan Gottfries, Kai Simons, Olle Melander, Céline Fernandez
Publikováno v:
Journal of the American Heart Association: Cardiovascular and Cerebrovascular Disease, Vol 5, Iss 12 (2016)
BackgroundDiabetes mellitus (DM) and cardiovascular disease are associated with dyslipidemia, but the detailed lipid molecular pattern in both diseases remains unknown. Methods and ResultsWe used shotgun mass spectrometry to determine serum levels of
Externí odkaz:
https://doaj.org/article/6e19ae8b74264bf7b979e481028f9bc0
Autor:
Maria E Bernabeu-Herrero, Dilip Patel, Adrianna Bielowka, Sindu Srikaran, Patricia Chaves Guerrero, Fatima S Govani, Inês G Mollet, Michela Noseda, Micheala A. Aldred, Claire L Shovlin
In order to identify cellular phenotypes resulting from nonsense (gain of stop/premature termination codon) variants, we devised a framework of analytic methods that minimised confounder contributions, and applied to blood outgrowth endothelial cells
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::81cdff8980d68fa0ddb4a45f4b60f228
https://doi.org/10.1101/2021.12.05.471269
https://doi.org/10.1101/2021.12.05.471269
Akademický článek
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Akademický článek
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K zobrazení výsledku je třeba se přihlásit.
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Autor:
Maria Paula Macedo, Inês G. Mollet
Distinct plasma microRNA profiles associate with different disease features. Elevated plasma microRNA hsa-miR-193b-3p has been reported in patients with pre-diabetes where early liver dysmetabolism plays a crucial role. MicroRNA target databases reve
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a1bc96045922fc03ca85c6614a324505
https://doi.org/10.1101/2021.01.22.427820
https://doi.org/10.1101/2021.01.22.427820
Autor:
Claire L Shovlin, Gillian Angus, Richard A Manning, Grace N Okoli, Fatima S Govani, Kay Elderfield, Graeme M Birdsey, Inês G Mollet, Michael A Laffan, Francesco A Mauri
Publikováno v:
PLoS ONE, Vol 5, Iss 2, p e9154 (2010)
Coagulation factor VIII (FVIII) deficiency leads to haemophilia A. Conversely, elevated plasma levels are a strong predictor of recurrent venous thromboemboli and pulmonary hypertension phenotypes in which in situ thromboses are implicated. Extrahepa
Externí odkaz:
https://doaj.org/article/1ee1cca344154c9baa88b450f4f448dd
Autor:
Inês G. Mollet, Malin Fex, Lisa M. Nicholas, Bérengère Valtat, Nils Wierup, Lena Eliasson, Mia Abels, Deepak Jain, Hindrik Mulder, Lotta Andersson, Anya Medina
Publikováno v:
Molecular Metabolism
Molecular Metabolism, Vol 6, Iss 7, Pp 651-663 (2017)
Molecular Metabolism, Vol 6, Iss 7, Pp 651-663 (2017)
Objective Insulin release from pancreatic β-cells is controlled by plasma glucose levels via mitochondrial fuel metabolism. Therefore, insulin secretion is critically dependent on mitochondrial DNA (mtDNA) and the genes it encodes. Mitochondrial tra
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::83dcd7ba5105a325832e60c6a31d48dc
https://doi.org/10.1016/j.molmet.2017.05.005
https://doi.org/10.1016/j.molmet.2017.05.005