Search for novel genetic risk factors for venous thrombosis : a dual approach Minkelen, R. van

Peripheral blood cells were stained with HLA-A2.1 tetramers containing the tyrosinase368–376 peptide followed by staining with a panel of lineage antibodies, as described in

Blades and blade fragments seem to have been especially used for longitudinal motions, mainly on plant material (7/12). Flake and flake fragments are used in different motions on

In total, 287 aff ected sibling pairs with an objectively confi rmed venous thromboembolism at young age (index patients ≤45 years) were included in the Genetics In Familial

In the present study, we investigated whether genetic variants in eleven selected candidate genes, eight in the 7p region and three in the Xq region, contribute to the linkage

However, only the chromosome 7p linkage signal was genome-wide signifi cant (p=0.029). No evidence for linkage at the chromosome 7p region was found in the Vermont and GAIT

In Hoofdstuk 3.3 hebben we onderzocht of genetische varianten in elf geselecteerde kandidaatgenen, acht in het chromosoom 7p gebied (PDGFA, GPR30, CHST12, LFNG, GNA12, RAC1,

Na zijn afstuderen in 2003, is hij datz elfde jaar begonnen aan het door NWO gesubsidieerde onderzoek “Search for novel genetic risk factors for venous thrombosis: a dual

Marburg I variant van het factor VII-activerende protease hebben geen verhoogde kans op het krijgen van veneuze trombose..