Vu, Dung

Title	Year	Hits	Downloads
Hypofibrinogenaemia caused by a novel FGG missense mutation (W253C) in the gamma chain globular domain impairing fibrinogen secretion	2005	360	1
Differential expression of LMO4 protein in Alzheimer's disease	2004	411	1
Congenital afibrinogenemia: identification and expression of a missense mutation in FGB impairing fibrinogen secretion	2003	423	0
Manipulating the quality control pathway in transfected cells: low temperature allows rescue of secretion-defective fibrinogen mutants	2008	446	311
Transcription regulator LMO4 interferes with neuritogenesis in human SH-SY5Y neuroblastoma cells	2003	463	3
Afibrinogénémie congénitale et contrôle de qualité de la sécrétion du fibrinogène	2006	464	3
In vitro rescue of FGA deletion by lentiviral transduction of afibrinogenemic patient's hepatocytes	2014	474	0
Molecular mechanisms accounting for fibrinogen deficiency: from large deletions to intracellular retention of misfolded proteins	2007	484	1
Expression and analysis of a split premature termination codon in FGG responsible for congenital afibrinogenemia: escape from RNA surveillance mechanisms in transfected cells	2004	491	0
Quality control of fibrinogen secretion in the molecular pathogenesis of congenital afibrinogenemia	2005	499	4
Prenatal diagnosis for congenital afibrinogenemia caused by a novel nonsense mutation in the FGB gene in a Palestinian family	2003	819	2
		5334	326

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