CD
| Title | Published in | Access level | OA Policy | Year | Views | Downloads | |
|---|---|---|---|---|---|---|---|
| A homozygous duplication of the FGG exon 8-intron 8 junction causes congenital afibrinogenemia. Lessons learned from the study of a large consanguineous Turkish family | Haematologica |  | 2022 | 348 | 278 | ||
| Chemical modulators of fibrinogen production and their impact on venous thrombosis | Thrombosis and Haemostasis | | 2021 | 271 | 277 | ||
| A genetic modifier of venous thrombosis in zebrafish reveals a functional role for fibrinogen AαE in early hemostasis | Blood Advances | | 2020 | 218 | 251 | ||
| Targeted mutation of zebrafish fga models human congenital afibrinogenemia | Blood |  | 2014 | 712 | 5 | ||
| Manipulating the quality control pathway in transfected cells: low temperature allows rescue of secretion-defective fibrinogen mutants | Haematologica | | 2008 | 602 | 429 | ||
| Quality control of fibrinogen secretion in the molecular pathogenesis of congenital afibrinogenemia | Human molecular genetics | | 2005 | 672 | 4 | ||
| Regulation of VEGF and VEGF receptor expression in the rodent mammary gland during pregnancy, lactation, and involution | Developmental dynamics | | 2000 | 652 | 0 | ||
| Hypoxia-inducible angiopoietin-2 expression is mimicked by iodonium compounds and occurs in the rat brain and skin in response to systemic hypoxia and tissue ischemia | The American journal of pathology | | 2000 | 605 | 380 |
