Zobrazeno 1 - 10
of 15
pro vyhledávání: '"Venetia Bazioti"'
Autor:
Venetia Bazioti, Anouk M. La Rose, Sjors Maassen, Frans Bianchi, Rinse de Boer, Benedek Halmos, Deepti Dabral, Emma Guilbaud, Arthur Flohr-Svendsen, Anouk G. Groenen, Alejandro Marmolejo-Garza, Mirjam H. Koster, Niels J. Kloosterhuis, Rick Havinga, Alle T. Pranger, Miriam Langelaar-Makkinje, Alain de Bruin, Bart van de Sluis, Alison B. Kohan, Laurent Yvan-Charvet, Geert van den Bogaart, Marit Westerterp
Publikováno v:
Nature Communications, Vol 13, Iss 1, Pp 1-23 (2022)
Cholesterol efflux is mediated by specific transporters in T cells. Here the authors show that when the ABCA1/ABCG1 cholesterol transporters are absent, peripheral T cell numbers are reduced but activation increased with a premature aging phenotype o
Externí odkaz:
https://doaj.org/article/cce4b1448a8b440488b90cdc27f0a71a
Autor:
Emmanouil Mavrogiannis, Quint A. J. Hagdorn, Venetia Bazioti, Johannes M. Douwes, Diederik E. Van Der Feen, Silke U. Oberdorf‐Maass, Marit Westerterp, Rolf M. F. Berger
Publikováno v:
Pulmonary Circulation, Vol 12, Iss 3, Pp n/a-n/a (2022)
Abstract Pulmonary arterial hypertension (PAH) is a fatal disease characterized by increased pulmonary arterial pressure, inflammation, and neointimal remodeling of pulmonary arterioles. Serum levels of interleukin (IL)‐1β and IL‐18 are elevated
Externí odkaz:
https://doaj.org/article/00ca98c48dea427ca494de673259cd0e
Autor:
Anouk M. La Rose, Anouk G. Groenen, Benedek Halmos, Venetia Bazioti, Martijn G.S. Rutten, Kishore A. Krishnamurthy, Mirjam H. Koster, Niels J. Kloosterhuis, Marieke Smit, Rick Havinga, Gilles Mithieux, Fabienne Rajas, Folkert Kuipers, Maaike H. Oosterveer, Marit Westerterp
Publikováno v:
Molecular Genetics and Metabolism Reports, Vol 31, Iss , Pp 100872- (2022)
Glycogen storage disease type 1a (GSD Ia) is an inborn error of carbohydrate metabolism. Despite severe hyperlipidemia, GSD Ia patients show limited atherogenesis compared to age-and-gender matched controls. Employing a GSD Ia mouse model that resemb
Externí odkaz:
https://doaj.org/article/a17931b37180404cb8818baa30ee324c
Autor:
Anouk G. Groenen, Anouk M. La Rose, Mengying Li, Venetia Bazioti, Arthur F. Svendsen, Niels J. Kloosterhuis, Albertina Ausema, Alle Pranger, M. Rebecca Heiner-Fokkema, Klary E. Niezen-Koning, Tom Houben, Ronit Shiri-Sverdlov, Marit Westerterp
Publikováno v:
Journal of Lipid Research, Vol 63, Iss 2, Pp 100167- (2022)
Niemann-Pick type C1 (NPC1) disease is a progressive lysosomal storage disorder caused by mutations of the NPC1 gene. While neurodegeneration is the most severe symptom, a large proportion of NPC1 patients also present with splenomegaly, which has be
Externí odkaz:
https://doaj.org/article/d9955d3f851b4a07a0a7d11d236a62ca
Autor:
Anouk M. La Rose, Venetia Bazioti, Joanne A. Hoogerland, Arthur F. Svendsen, Anouk G. Groenen, Martijn van Faassen, Martijn G.S. Rutten, Niels J. Kloosterhuis, Bertien Dethmers-Ausema, J. Hendrik Nijland, Gilles Mithieux, Fabienne Rajas, Folkert Kuipers, Michaël V. Lukens, Oliver Soehnlein, Maaike H. Oosterveer, Marit Westerterp
Publikováno v:
Molecular Metabolism, Vol 53, Iss , Pp 101265- (2021)
Objective: Glycogen storage disease type 1a (GSD Ia) is a rare inherited metabolic disorder caused by mutations in the glucose-6-phosphatase (G6PC1) gene. When untreated, GSD Ia leads to severe fasting-induced hypoglycemia. Although current intensive
Externí odkaz:
https://doaj.org/article/96f72353a8d648dbb58c1f3c0cd8e578
Autor:
Anouk G. Groenen, Venetia Bazioti, Isabelle A. van Zeventer, Lianmin Chen, Hilde E. Groot, Jan-Willem Balder, Alexandra Zhernakova, Pim van der Harst, Antoine Rimbert, Jan Albert Kuivenhoven, Jingyuan Fu, Marit Westerterp
Publikováno v:
Atherosclerosis
ATHEROSCLEROSIS, 343, 20-27. ELSEVIER IRELAND LTD
ATHEROSCLEROSIS, 343, 20-27. ELSEVIER IRELAND LTD
BACKGROUND AND AIMS: Leukocytosis, the expansion of white blood cells, is associated with increased cardiovascular risk. Studies in animal models have shown that high-density lipoprotein cholesterol (HDL-c) suppresses leukocytosis by mediating choles
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0ff9c82cdb73e47eaff75813773a2798
https://doi.org/10.1016/j.atherosclerosis.2022.01.008
https://doi.org/10.1016/j.atherosclerosis.2022.01.008
Autor:
Venetia Bazioti, Anouk M. La Rose, Sjors Maassen, Frans Bianchi, Rinse de Boer, Emma Guilbaud, Arthur Flohr-Svendsen, Anouk G. Groenen, Alejandro Marmolejo-Garza, Mirjam H. Koster, Niels J. Kloosterhuis, Alle T. Pranger, Miriam Langelaar-Makkinje, Alain de Bruin, Bart van de Sluis, Alison B. Kohan, Laurent Yvan-Charvet, Geert van den Bogaart, Marit Westerterp
Atherosclerosis is a chronic inflammatory disease driven by hypercholesterolemia. During aging, T-cells accumulate cholesterol, which could lead to a pro-inflammatory phenotype. However, the role of cholesterol efflux pathways mediated by ATP-binding
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0f3f0739dddbc3921360c452fcf7e068
https://doi.org/10.1101/2022.04.10.487770
https://doi.org/10.1101/2022.04.10.487770
Autor:
Arthur Flohr Svendsen, Niels J. Kloosterhuis, Justina C. Wolters, Marieke Smit, Bart van de Sluis, Natalia Loaiza, Merel L. Hartgers, Geesje M. Dallinga-Thie, Mirjam H. Koster, Maaike Winkelmeijer, G. Kees Hovingh, Jan Albert Kuivenhoven, Laurens F. Reeskamp, Hans Jansen, Nicolette C. A. Huijkman, Aldo Grefhorst, Venetia Bazioti, Andrea Volta, J.W. Balder, Antoine Rimbert
Publikováno v:
Arteriosclerosis thrombosis and vascular biology, 40(4), 973-985. LIPPINCOTT WILLIAMS & WILKINS
Arteriosclerosis, thrombosis, and vascular biology, 40(4), 973-985. Lippincott Williams and Wilkins
Arteriosclerosis, thrombosis, and vascular biology, 40(4), 973-985. Lippincott Williams and Wilkins
Objective: STAP1 , encoding for STAP1 (signal transducing adaptor family member 1), has been reported as a candidate gene associated with familial hypercholesterolemia. Unlike established familial hypercholesterolemia genes, expression of STAP1 is ab
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b049a7bd1b0bb42725686d91351d7f09
http://www.scopus.com/inward/record.url?scp=85082388905&partnerID=8YFLogxK
http://www.scopus.com/inward/record.url?scp=85082388905&partnerID=8YFLogxK
Autor:
Venetia Bazioti
Cardiovascular disease (CVD) is one of the leading causes of death worldwide and atherosclerosis is the primary underlying cause. Main risk factors for atherosclerosis are elevated plasma low-density lipoprotein-cholesterol (LDL-c) levels and inflamm
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::65219e11b97226c18a4ae0361a76a644
https://hdl.handle.net/11370/e46f95f7-f356-4fbc-8d5b-0fa852a19338
https://hdl.handle.net/11370/e46f95f7-f356-4fbc-8d5b-0fa852a19338
Autor:
Bertien Dethmers-Ausema, Niels J. Kloosterhuis, Folkert Kuipers, Gilles Mithieux, Anouk M. La Rose, Martijn G S Rutten, Oliver Soehnlein, Joanne A Hoogerland, J Hendrik Nijland, Marit Westerterp, Fabienne Rajas, Maaike H. Oosterveer, Arthur Flohr Svendsen, Venetia Bazioti, Michaël V. Lukens, Martijn van Faassen, Anouk G. Groenen
Publikováno v:
Molecular metabolism
Molecular metabolism, Elsevier, 2021, pp.101265. ⟨10.1016/j.molmet.2021.101265⟩
Molecular metabolism, 53:101265, 1-14. ELSEVIER SCIENCE BV
Molecular Metabolism, Vol 53, Iss, Pp 101265-(2021)
Molecular Metabolism
Molecular metabolism, Elsevier, 2021, pp.101265. ⟨10.1016/j.molmet.2021.101265⟩
Molecular metabolism, 53:101265, 1-14. ELSEVIER SCIENCE BV
Molecular Metabolism, Vol 53, Iss, Pp 101265-(2021)
Molecular Metabolism
Objective Glycogen storage disease type 1a (GSD Ia) is a rare inherited metabolic disorder caused by mutations in the glucose-6-phosphatase (G6PC1) gene. When untreated, GSD Ia leads to severe fasting-induced hypoglycemia. Although current intensive
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a0fee94b82da6e1129feb4ffc5aac411
https://www.hal.inserm.fr/inserm-03257584/document
https://www.hal.inserm.fr/inserm-03257584/document