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| Title | Published in | Access level | OA Policy | Year | Views | Downloads | |
|---|---|---|---|---|---|---|---|
| In vitro rescue of FGA deletion by lentiviral transduction of afibrinogenemic patient's hepatocytes | Journal of thrombosis and haemostasis |  | 2014 | 622 | 0 | ||
| Manipulating the quality control pathway in transfected cells: low temperature allows rescue of secretion-defective fibrinogen mutants | Haematologica |  | 2008 | 590 | 387 | ||
| Molecular mechanisms accounting for fibrinogen deficiency: from large deletions to intracellular retention of misfolded proteins | Journal of thrombosis and haemostasis | | 2007 | 616 | 1 | ||
| Afibrinogénémie congénitale et contrôle de qualité de la sécrétion du fibrinogène | MS. Médecine sciences | | 2006 | 593 | 3 | ||
| Hypofibrinogenaemia caused by a novel FGG missense mutation (W253C) in the gamma chain globular domain impairing fibrinogen secretion | Journal of medical genetics | | 2005 | 499 | 1 | ||
| Quality control of fibrinogen secretion in the molecular pathogenesis of congenital afibrinogenemia | Human molecular genetics | | 2005 | 663 | 4 | ||
| Expression and analysis of a split premature termination codon in FGG responsible for congenital afibrinogenemia: escape from RNA surveillance mechanisms in transfected cells | Blood | | 2004 | 648 | 0 | ||
| Differential expression of LMO4 protein in Alzheimer's disease | Neuropathology and applied neurobiology | | 2004 | 561 | 1 | ||
| Prenatal diagnosis for congenital afibrinogenemia caused by a novel nonsense mutation in the FGB gene in a Palestinian family | Blood | | 2003 | 952 | 0 | ||
| Transcription regulator LMO4 interferes with neuritogenesis in human SH-SY5Y neuroblastoma cells | Molecular brain research | | 2003 | 584 | 3 | ||
| Congenital afibrinogenemia: identification and expression of a missense mutation in FGB impairing fibrinogen secretion | Blood | | 2003 | 582 | 0 |
