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 | 337 | 183 | |||
| Chemical modulators of fibrinogen production and their impact on venous thrombosis | Thrombosis and Haemostasis | 2021 | 260 | 206 | |||
| A genetic modifier of venous thrombosis in zebrafish reveals a functional role for fibrinogen AαE in early hemostasis | Blood Advances | 2020 | 211 | 162 | |||
| Targeted mutation of zebrafish fga models human congenital afibrinogenemia | Blood | 2014 | 704 | 5 | |||
| Manipulating the quality control pathway in transfected cells: low temperature allows rescue of secretion-defective fibrinogen mutants | Haematologica | 2008 | 592 | 397 | |||
| Quality control of fibrinogen secretion in the molecular pathogenesis of congenital afibrinogenemia | Human molecular genetics | 2005 | 663 | 4 | |||
| Regulation of VEGF and VEGF receptor expression in the rodent mammary gland during pregnancy, lactation, and involution | Developmental dynamics | 2000 | 645 | 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 | 592 | 326 |
