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Title | Published in | Access level | OA Policy | Year | Views | Downloads | |
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In vitro rescue of FGA deletion by lentiviral transduction of afibrinogenemic patient's hepatocytes | Journal of thrombosis and haemostasis | 2014 | 572 | 0 | |||
Manipulating the quality control pathway in transfected cells: low temperature allows rescue of secretion-defective fibrinogen mutants | Haematologica | 2008 | 529 | 350 | |||
Molecular mechanisms accounting for fibrinogen deficiency: from large deletions to intracellular retention of misfolded proteins | Journal of thrombosis and haemostasis | 2007 | 561 | 1 | |||
Afibrinogénémie congénitale et contrôle de qualité de la sécrétion du fibrinogène | MS. Médecine sciences | 2006 | 557 | 3 | |||
Hypofibrinogenaemia caused by a novel FGG missense mutation (W253C) in the gamma chain globular domain impairing fibrinogen secretion | Journal of medical genetics | 2005 | 446 | 1 | |||
Quality control of fibrinogen secretion in the molecular pathogenesis of congenital afibrinogenemia | Human molecular genetics | 2005 | 594 | 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 | 581 | 0 | |||
Differential expression of LMO4 protein in Alzheimer's disease | Neuropathology and applied neurobiology | 2004 | 507 | 1 | |||
Prenatal diagnosis for congenital afibrinogenemia caused by a novel nonsense mutation in the FGB gene in a Palestinian family | Blood | 2003 | 892 | 0 | |||
Transcription regulator LMO4 interferes with neuritogenesis in human SH-SY5Y neuroblastoma cells | Molecular brain research | 2003 | 537 | 3 | |||
Congenital afibrinogenemia: identification and expression of a missense mutation in FGB impairing fibrinogen secretion | Blood | 2003 | 505 | 0 |