Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Mariëlle J. Tempelman"'
Autor:
Rianne C. Scholman, Sanne Hiddingh, Beatriz Malvar Fernandez, Wilco de Jager, Barbara Giovannone, Mariëlle J. Tempelman, Jenny Meerding, Berent J. Prakken, Mariska E. A. van Dijk
Publikováno v:
Cytokine. 106
Diagnosis of complex disease and response to treatment is often associated with multiple indicators, both clinical and laboratorial. With the use of biomarkers, various mechanisms have been unraveled which can lead to better and faster diagnosis, pre
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b8848cec20047edbd610ab4838b7843e
https://pubmed.ncbi.nlm.nih.gov/29089178
https://pubmed.ncbi.nlm.nih.gov/29089178
Autor:
Yvonne T. van der Schouw, Diederick E. Grobbee, Mark Roest, Mariëlle J. Tempelman, Philip G. de Groot, Jan J. Sixma, Jan Dirk Banga
Publikováno v:
American Journal of Epidemiology. 153:673-679
Methylenetetrahydrofolate reductase (MTHFR) is involved in the reduction of 5,10-methylenetetrahydrofolate to 5-methyltetrahydrofolate. A 677 C/T single nucleotide polymorphism localized in the MTHFR gene is associated with both thermolability and re
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::51d1d69896321944effec05d1623c3e8
https://doi.org/10.1093/aje/153.7.673
https://doi.org/10.1093/aje/153.7.673
Autor:
Yvonne T. van der Schouw, Diederick E. Grobbee, Jan J. Sixma, Philip G. de Groot, Jan Dirk Banga, Mark Roest, Mariëlle J. Tempelman
Publikováno v:
Circulation. 101:67-70
Background —A common 4G allele of a 4G/5G polymorphism in the promoter region of the plasminogen activator inhibitor-1 (PAI-1) gene is associated with increased transcription of the PAI-1 protein, which may lead to decreased fibrinolysis. It has th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::02755bb0121fd20336b4f9d6bc8b257c
https://doi.org/10.1161/01.cir.101.1.67
https://doi.org/10.1161/01.cir.101.1.67
Publikováno v:
Thrombosis and Haemostasis. 80:791-797
SummaryThe presence of antiphospholipid antibodies (aPL) is strongly correlated with venous and arterial thrombosis, fetal loss and thrombocytopenia. This relation is called the antiphospholipid syndrome (APS). It is well recognized that thrombosis r
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e313e7be90995dfded6ae5388b3bc63c
https://doi.org/10.1055/s-0037-1615360
https://doi.org/10.1055/s-0037-1615360
Autor:
Yvonne T. van der Schouw, Jan Dirk Banga, Jo J. M. Marx, Bart de Valk, Mark Roest, Mariëlle J. Tempelman, Philip G. de Groot, Jan J. Sixma
Publikováno v:
Circulation. 100(12)
Background —The genetic background of hereditary hemochromatosis ( HH ) is homozygosity for a cysteine-to-tyrosine transition at position 282 in the HFE gene. Heterozygosity for HH is associated with moderately increased iron levels and could be a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a7f532d1595b7413033c5b44cb630f71
https://pubmed.ncbi.nlm.nih.gov/10491367
https://pubmed.ncbi.nlm.nih.gov/10491367
Autor:
Yvonne T. van der Schouw, Diederick E. Grobbee, Mark Roest, Jan J. Sixma, Mariëlle J. Tempelman, Jan Dirk Banga, Philip G. de Groot
Publikováno v:
American journal of epidemiology. 149(7)
Factor V Arg506Gln is the most common genetic risk factor for venous thrombosis and is associated with myocardial infarction in young women, especially among smokers. The authors studied the relation of factor V Arg506Gln to cardiovascular mortality
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9a9e9440767cfe15a632729bd31ea4ee
https://pubmed.ncbi.nlm.nih.gov/10192314
https://pubmed.ncbi.nlm.nih.gov/10192314