Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Trijnie Bos"'
Autor:
Amée M. Buziau, Maaike H. Oosterveer, Kristiaan Wouters, Trijnie Bos, Dean R. Tolan, Loranne Agius, Brian E. Ford, David Cassiman, Coen D.A. Stehouwer, Casper G. Schalkwijk, Martijn C.G.J. Brouwers
Publikováno v:
Molecular Metabolism, Vol 87, Iss , Pp 101984- (2024)
Objective: Stable isotope studies have shown that hepatic de novo lipogenesis (DNL) plays an important role in the pathogenesis of intrahepatic lipid (IHL) deposition. Furthermore, previous research has demonstrated that fructose 1-phosphate (F1P) no
Externí odkaz:
https://doaj.org/article/f788e7cbbd6b437a8180795a7483cdf6
Autor:
Martijn G. S. Rutten, Yu Lei, Joanne H. Hoogerland, Vincent W. Bloks, Hong Yang, Trijnie Bos, Kishore A. Krishnamurthy, Aycha Bleeker, Mirjam H. Koster, Rachel E. Thomas, Justina C. Wolters, Hilda van den Bos, Gilles Mithieux, Fabienne Rajas, Adil Mardinoglu, Diana C. J. Spierings, Alain de Bruin, Bart van de Sluis, Maaike H. Oosterveer
Publikováno v:
Cancer & Metabolism, Vol 11, Iss 1, Pp 1-11 (2023)
Abstract Background Glycogen storage disease type 1a (GSD Ia) is an inborn error of metabolism caused by a defect in glucose-6-phosphatase (G6PC1) activity, which induces severe hepatomegaly and increases the risk for liver cancer. Hepatic GSD Ia is
Externí odkaz:
https://doaj.org/article/176971327ab64839a0921d89e984a866
Autor:
Marije Boesjes, Vincent W Bloks, Jurre Hageman, Trijnie Bos, Theo H van Dijk, Rick Havinga, Henk Wolters, Johan W Jonker, Folkert Kuipers, Albert K Groen
Publikováno v:
PLoS ONE, Vol 9, Iss 12, p e115028 (2014)
The nuclear receptor FXR acts as an intracellular bile salt sensor that regulates synthesis and transport of bile salts within their enterohepatic circulation. In addition, FXR is involved in control of a variety of crucial metabolic pathways. Four F
Externí odkaz:
https://doaj.org/article/64e31ee85dd4492891216993898a5c4d
Autor:
Justina C. Wolters, Michel van Weeghel, Gilles Mithieux, Aycha Bleeker, Folkert Kuipers, Vincent W. Bloks, Fabienne Rajas, Yu Lei, Joanne A Hoogerland, Henk Wolters, Maaike H. Oosterveer, Trijnie Bos, Alain de Bruin, Brenda S. Hijmans, Rachel E. Thomas, Theo H. van Dijk, Riekelt H. Houtkooper
Publikováno v:
Hepatology (Baltimore, Md.)
Hepatology
Hepatology, Wiley-Blackwell, 2020, 72 (5), pp.1638-1653. ⟨10.1002/hep.31198⟩
Hepatology (Baltimore, Md.), 72(5), 1638-1653. John Wiley and Sons Ltd
Hepatology
Hepatology, Wiley-Blackwell, 2020, 72 (5), pp.1638-1653. ⟨10.1002/hep.31198⟩
Hepatology (Baltimore, Md.), 72(5), 1638-1653. John Wiley and Sons Ltd
International audience; Background and aims: Glycogen storage disease (GSD) type 1a is an inborn error of metabolism caused by defective glucose-6-phosphatase catalytic subunit (G6PC) activity. Patients with GSD 1a exhibit severe hepatomegaly due to
Autor:
Kishore Alagere Krishnamurthy, Ligia Akemi Kiyuna, Miriam Langelaar, Albert Gerding, Trijnie Bos, Dorenda Oosterhuis, Peter Olinga, Karen Van Eunen, Barbara Bakker, Maaike Oosterveer
Publikováno v:
Journal of Hepatology. 77:S539-S540
Autor:
Yu Lei, Henkjan J. Verkade, Vincent W. Bloks, Gilles Mithieux, Justina C. Wolters, Folkert Kuipers, Fabienne Rajas, Joanne A Hoogerland, Maaike H. Oosterveer, Jan Albert Kuivenhoven, Rebecca A. Haeusler, Niels L. Mulder, Aycha Bleeker, Jan Freark de Boer, Theo H. van Dijk, Trijnie Bos
Publikováno v:
Hepatology (Baltimore, Md.), 70(6), 2171-2184. John Wiley and Sons Ltd
Hepatology
Hepatology, Wiley-Blackwell, 2019, ⟨10.1002/hep.30778⟩
Hepatology, 70(6), 2171-2184. Wiley
Hepatology (Baltimore, Md.)
Hepatology
Hepatology, Wiley-Blackwell, 2019, ⟨10.1002/hep.30778⟩
Hepatology, 70(6), 2171-2184. Wiley
Hepatology (Baltimore, Md.)
It is well-established that, besides facilitating lipid absorption, bile acids act as signaling molecules that modulate glucose and lipid metabolism. Bile acid metabolism, in turn, is controlled by several nutrient-sensitive transcription factors. Al
Autor:
Folkert Kuipers, Amanda C. M. Pronk, Gilles Mithieux, Karen van Eunen, Trijnie Bos, Dirk-Jan Reijngoud, Sander Kooijman, Terry G J Derks, Joanne A Hoogerland, Fabian Peeks, Henk Wolters, Theo H. van Dijk, Albert Gerding, Aycha Bleeker, Rick Havinga, Brenda S. Hijmans, Patrick C.N. Rensen, Maaike H. Oosterveer, Fabienne Rajas, Justina C. Wolters
Publikováno v:
Journal of Inherited Metabolic Disease
Journal of Inherited Metabolic Disease, Springer Verlag, 2021, Online ahead of print. ⟨10.1002/jimd.12380⟩
Journal of Inherited Metabolic Disease, 44(4). SPRINGER
Journal of Inherited Metabolic Disease, 44(4), 879-892. WILEY
Journal of Inherited Metabolic Disease, Springer Verlag, 2021, Online ahead of print. ⟨10.1002/jimd.12380⟩
Journal of Inherited Metabolic Disease, 44(4). SPRINGER
Journal of Inherited Metabolic Disease, 44(4), 879-892. WILEY
Prevention of hypertriglyceridemia is one of the biomedical targets in Glycogen Storage Disease type 1a (GSD Ia) patients, yet it is unclear how hypoglycemia links to plasma triglyceride (TG) levels. We analyzed whole-body TG metabolism in normoglyce
Autor:
Theo H. van Dijk, Claus Kremoser, Marleen Schonewille, Albert K. Groen, Jan Freark de Boer, Vincent W. Bloks, Folkert Kuipers, Renze Boverhof, Antonio Moschetta, Justina C. Wolters, Ronald P.J. Oude Elferink, Jan M. van Deursen, Angelika Jurdzinski, Henkjan J. Verkade, Jan Albert Kuivenhoven, Henk Wolters, Trijnie Bos, Marije Boesjes
Publikováno v:
Gastroenterology, 152, 5, pp. 1126-1138.e6
Gastroenterology, 152, 1126-1138.e6
Gastroenterology, 152(5), 1126-1138. W B SAUNDERS CO-ELSEVIER INC
Gastroenterology, 152(5), 1126-1138.e6. W.B. Saunders Ltd
Gastroenterology, 152, 1126-1138.e6
Gastroenterology, 152(5), 1126-1138. W B SAUNDERS CO-ELSEVIER INC
Gastroenterology, 152(5), 1126-1138.e6. W.B. Saunders Ltd
Contains fulltext : 174424.pdf (Publisher’s version ) (Closed access) BACKGROUND & AIMS: The role of the intestine in the maintenance of cholesterol homeostasis increasingly is recognized. Fecal excretion of cholesterol is the last step in the athe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::209629ad22b7de8e385e2dcc56df9034
https://hdl.handle.net/2066/174424
https://hdl.handle.net/2066/174424
Autor:
Henkjan J. Verkade, Albert K. Groen, Marije Boesjes, Marleen Schonewille, Folkert Kuipers, Jan M. van Deursen, Ronald P.J. Oude Elferink, Trijnie Bos, Theo H. van Dijk, Angelika Jurdzinski, Claus Kremoser, Jan F de Boer, Renze Boverhof, Vincent W. Bloks, Henk Wolters, Antonio Moschetta
Publikováno v:
Arteriosclerosis, Thrombosis, and Vascular Biology. 36
High plasma cholesterol levels increase the risk of cardiovascular disease (CVD). Transintestinal Cholesterol Excretion (TICE) is a recently emerged pathway of cholesterol removal and has the potential to lower plasma cholesterol levels and confer pr
Autor:
Hans R. Waterham, Theo Boer, L. P. ten Kate, Trijnie Bos, Gerrit Smit, J. M. M. Rondeel, Dirk Reijngoud, Klaziena Niezen-Koning, A. van Assen, Jaap H. Ruiter, J. G. Loeber, Terry G J Derks, R. J. A. Wanders
Publikováno v:
Journal of inherited metabolic disease, 31(1), 88-96. Springer Netherlands
Journal of Inherited Metabolic Disease, 31(1), 88-96. Springer Netherlands
Journal of Inherited Metabolic Disease, 31(1), 88-96. SPRINGER
Derks, T G J, Boer, T S, van Assen, A, Bos, T, de Ruiter, J, Waterham, H R, Niezen-Koning, K E, Wanders, R J A, Rondeel, J M M, Loeber, J G, ten Kate, L P, Smit, G P A & Reijngoud, D J 2008, ' Neonatal screening for medium-chain acyl-CoA dehydrogenase (MCAD) deficiency in The Netherlands: the importance of enzyme analysis to ascertain true MCAD deficiency ', Journal of Inherited Metabolic Disease, vol. 31, no. 1, pp. 88-96 . https://doi.org/10.1007/s10545-007-0492-3
Journal of Inherited Metabolic Disease, 31(1), 88-96. Springer Netherlands
Journal of Inherited Metabolic Disease, 31(1), 88-96. SPRINGER
Derks, T G J, Boer, T S, van Assen, A, Bos, T, de Ruiter, J, Waterham, H R, Niezen-Koning, K E, Wanders, R J A, Rondeel, J M M, Loeber, J G, ten Kate, L P, Smit, G P A & Reijngoud, D J 2008, ' Neonatal screening for medium-chain acyl-CoA dehydrogenase (MCAD) deficiency in The Netherlands: the importance of enzyme analysis to ascertain true MCAD deficiency ', Journal of Inherited Metabolic Disease, vol. 31, no. 1, pp. 88-96 . https://doi.org/10.1007/s10545-007-0492-3
The outcome was determined of population-wide neonatal screening for medium-chain acyl-CoA dehydrogenase (MCAD) deficiency using tandem mass spectrometry (MS/MS) in The Netherlands, between October 2003 and September 2005. Prospective population-wide
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bf279e6d6ee87075ad71b110706d4d73
https://pure.amc.nl/en/publications/neonatal-screening-for-mediumchain-acylcoa-dehydrogenase-mcad-deficiency-in-the-netherlands-the-importance-of-enzyme-analysis-to-ascertain-true-mcad-deficiency(8e383323-b68b-4de7-8b08-2f5dc24aeff2).html
https://pure.amc.nl/en/publications/neonatal-screening-for-mediumchain-acylcoa-dehydrogenase-mcad-deficiency-in-the-netherlands-the-importance-of-enzyme-analysis-to-ascertain-true-mcad-deficiency(8e383323-b68b-4de7-8b08-2f5dc24aeff2).html