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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 familyHaematologica
accessLevelPublic
2022 337 183
Chemical modulators of fibrinogen production and their impact on venous thrombosisThrombosis and Haemostasis
accessLevelPublic
2021 260 206
A genetic modifier of venous thrombosis in zebrafish reveals a functional role for fibrinogen AαE in early hemostasisBlood Advances
accessLevelPublic
2020 211 162
Targeted mutation of zebrafish fga models human congenital afibrinogenemiaBlood
accessLevelRestricted
2014 704 5
Manipulating the quality control pathway in transfected cells: low temperature allows rescue of secretion-defective fibrinogen mutantsHaematologica
accessLevelPublic
2008 592 397
Quality control of fibrinogen secretion in the molecular pathogenesis of congenital afibrinogenemiaHuman molecular genetics
accessLevelRestricted
2005 663 4
Regulation of VEGF and VEGF receptor expression in the rodent mammary gland during pregnancy, lactation, and involutionDevelopmental dynamics
accessLevelRestricted
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 ischemiaThe American journal of pathology
accessLevelPublic
2000 592 326
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