Zobrazeno 1 - 10
of 67
pro vyhledávání: '"J Antonie, Maassen"'
Autor:
Dorret I. Boomsma, P. Eline Slagboom, Gonneke Willemsen, Mark H.H. Kramer, Erwin Reiling, Elisabeth M. W. Eekhoff, Eco J. C. de Geus, Leen M 't Hart, Michaela Diamant, Jacqueline M. Dekker, Giel Nijpels, A.M.C. Simonis-Bik, Jeanine J. Houwing-Duistermaat, Timon W. van Haeften, Els C. van Hove, J. Antonie Maassen, Robert J. Heine
Publikováno v:
Diabetes
Diabetes, 59(1), 293-301
Bik-Simonis, A M C, Nijpels, M G A A M, van Haeften, T, Houwing-Duistermaat, J J, Boomsma, D I, Reiling, E, van Hove, E C, Diamant, M, Kramer, M H H, Heine, R J, Maassen, J A, Slagboom, P E, Willemsen, G, Dekker, J M, Eekhoff, E M W, de Geus, E J C & Hart, L M 2010, ' Gene variants in the novel type 2 diabetes loci CDC123/CAMK1D, THADA, ADAMTS9, BCL11A and MTNR1B affect different aspects of pancreatic beta cell function ', Diabetes, vol. 59, no. 1, pp. 293-301 . https://doi.org/10.2337/db09-1048
Diabetes, 59(1), 293-301. American Diabetes Association Inc.
Diabetes, 59(1), 293-301
Bik-Simonis, A M C, Nijpels, M G A A M, van Haeften, T, Houwing-Duistermaat, J J, Boomsma, D I, Reiling, E, van Hove, E C, Diamant, M, Kramer, M H H, Heine, R J, Maassen, J A, Slagboom, P E, Willemsen, G, Dekker, J M, Eekhoff, E M W, de Geus, E J C & Hart, L M 2010, ' Gene variants in the novel type 2 diabetes loci CDC123/CAMK1D, THADA, ADAMTS9, BCL11A and MTNR1B affect different aspects of pancreatic beta cell function ', Diabetes, vol. 59, no. 1, pp. 293-301 . https://doi.org/10.2337/db09-1048
Diabetes, 59(1), 293-301. American Diabetes Association Inc.
OBJECTIVE Recently, results from a meta-analysis of genome-wide association studies have yielded a number of novel type 2 diabetes loci. However, conflicting results have been published regarding their effects on insulin secretion and insulin sensiti
Autor:
Saskia G. C. van Elderen, Joost Doornbos, Einar H R van Essen, Herman H.P.J. Lemkes, Albert de Roos, Jan W. A. Smit, J. Antonie Maassen
Publikováno v:
van Elderen, S G C, Doornbos, J, van Essen, E H R, Lemkes, H H P J, Maassen, J A, Smit, J H A & de Roos, A 2009, ' Phosphorus-31 Magnetic Resonance Spectroscopy of Skeletal Muscle in Maternally Inherited Diabetes and Deafness A3243G Mitochondrial Mutation Carriers ', Journal of Magnetic Resonance Imaging, vol. 29, no. 1, pp. 127-131 . https://doi.org/10.1002/jmri.21620
Journal of Magnetic Resonance Imaging, 29(1), 127-131. John Wiley and Sons Inc.
Journal of Magnetic Resonance Imaging, 29(1), 127-131. John Wiley and Sons Inc.
Purpose To investigate high-energy phosphate metabolism in striated skeletal muscle of patients with Maternally Inherited Diabetes and Deafness (MIDD) syndrome. Materials and Methods In 11 patients with the MIDD mutation (six with diabetes mellitus [
Autor:
Knut Borch-Johnsen, Giel Nijpels, Torben Jørgensen, Yasmin H. Hamid, Jacqueline M. Dekker, Robert J. Heine, Torben Hansen, Oluf Pedersen, Erwin Reiling, Els C. van Hove, J. Antonie Maassen, Leen M 't Hart
Publikováno v:
Diabetes. 55:3193-3196
The short-chain l-3-hydroxyacyl-CoA dehydrogenase (SCHAD) protein is involved in the penultimate step of mitochondrial fatty acid oxidation. Previously, it has been shown that mutations in the corresponding gene (HADHSC) are associated with hyperinsu
Publikováno v:
Experimental and Clinical Endocrinology & Diabetes. 114:168-174
We have identified two locations with novel multiplasmic length variants in the mitochondrial DNA of a family with diabetes and deafness. At nt568 in the D-loop, the 6-bp polycytidine tract was found to be variable in length up to a total of 12 resid
Publikováno v:
Molecular endocrinology (Baltimore, Md.), 20(8), 1786-1795. The Endocrine Society
The stimulation of cells with physiological concentrations of insulin induces a variety of responses, e.g. an increase in glucose uptake, induction of glycogen and protein synthesis, and gene expression. One of the determinants regulating insulin-med
Autor:
Karoly Szuhai, Anton K. Raap, Peter J. Svensson, George M.C. Janssen, J. Antonie Maassen, Roshan S. Jahangir Tafrechi
Publikováno v:
Mutation Research/Fundamental and Molecular Mechanisms of Mutagenesis. 578:43-52
The pathobiochemical pathways determining the wide variability in phenotypic expression of mitochondrial DNA (mtDNA) mutations are not well understood. Most pathogenic mtDNA mutations induce a general defect in mitochondrial respiration and thereby A
Autor:
Rob C. G. van de Ven, J. Antonie Maassen, Peter J.A. van den Broek, Gerard C.M. van der Zon, Merlijn Bazuine
Publikováno v:
Biochemical pharmacology, 68(1), 105-112. Elsevier Inc.
Recently, it was shown that rottlerin inhibits insulin-stimulated glucose uptake and reduces intracellular adenosine triphosphate (ATP) levels in 3T3-L1 adipocytes, suggesting that these two events are causally linked. However, several other reports
Autor:
Fausto Machicao, Robert J. Heine, Andreas Fritsche, Jacqueline M. Dekker, Leen M 't Hart, Timon W. van Haeften, Cornelia M. van Duijn, Giel Nijpels, Michael Stumvoll, Ingrid Rietveld, Hans U. Häring, J. Antonie Maassen
Publikováno v:
Diabetes. 53:S26-S30
IGFs are important regulators of pancreatic β-cell development, growth, and maintenance. Mutations in the IGF genes have been found to be associated with type 2 diabetes, myocardial infarction, birth weight, and obesity. These associations could res
Autor:
Merlijn Bazuine, Françoise Carlotti, Philippe Pognonec, Tuija Kekarainen, J. Antonie Maassen, Jurgen Seppen, Rob C. Hoeben
Publikováno v:
Molecular therapy, 9(2), 209-217. Nature Publishing Group
Obesity is associated with many serious afflictions such as cardiovascular disease, cancer, and diabetes. One of the main cellular systems used to study the underlying physiological and biological processes is the 3T3-L1 preadipocyte differentiation
Autor:
R.J. Heine, Giel Nijpels, George M.C. Janssen, Leen M 't Hart, Roshan S. Jahangir Tafrechi, Herman H.P.J. Lemkes, Anton K. Raap, J. Antonie Maassen, Einar H R van Essen
Publikováno v:
Diabetes. 53:S103-S109
Mutations in mitochondrial DNA (mtDNA) associate with various disease states. A few mtDNA mutations strongly associate with diabetes, with the most common mutation being the A3243G mutation in the mitochondrial DNA-encoded tRNA(Leu,UUR) gene. This ar