Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 2157
Gene Symbol: F8
F8
1.000 Biomarker disease BEFREE Here, we generated a porcine model of hemophilia A by nuclear transfer cloning from F8-targeted fibroblasts. 23209578 2012
Entrez Id: 2157
Gene Symbol: F8
F8
1.000 AlteredExpression disease LHGDN Factor VIII-specific memory B cells in patients with hemophilia A. 17958750 2007
Entrez Id: 2157
Gene Symbol: F8
F8
1.000 Biomarker disease BEFREE In children with haemophilia A and a history of target-joint and/or FVIII inhibitor, abnormalities may occur in the long bones as were revealed by pQCT, where low trabecular density and weak cortical bone quality in upper and lower extremities, respectively, were confirmed. 30088693 2018
Entrez Id: 2157
Gene Symbol: F8
F8
1.000 Biomarker disease BEFREE Our data show a correlation between FVIII:C and thrombin generation testing with a clear differentiation between patients with haemophilia and normal controls. 24452774 2014
Entrez Id: 2157
Gene Symbol: F8
F8
1.000 AlteredExpression disease BEFREE The Fc fusion has no impact on FVIII-specific activity. rFVIIIFc has comparable acute efficacy as rFVIII in treating tail clip injury in HemA mice, and fully corrects whole blood clotting time (WBCT) in HemA dogs immediately after dosing. 22246033 2012
Entrez Id: 2157
Gene Symbol: F8
F8
1.000 AlteredExpression disease BEFREE Together, these technologies contribute to an AAV-fVIII vector that confers sustained, curative levels of fVIII at a minimal dose in hemophilia A mice. 29552578 2018
Entrez Id: 2157
Gene Symbol: F8
F8
1.000 AlteredExpression disease BEFREE To determine its capacity for in vivo excision and/or genomic integration, Ad/AAV/FVIIIDelta761-1639 was injected by tail vein into three groups of hemophilia A mice (2 x 10(11) vp [n = 3]; 4 x 10(11) vp [n = 3]; 8 x 10(11) vp [n = 3]), with clear concentration-dependent increase in FVIII activity (range 160-510 mU/ml; plasma activity 16%-51% of normal). 15269828 2004
Entrez Id: 2157
Gene Symbol: F8
F8
1.000 GeneticVariation disease LHGDN The spectrum of mutations in Southern Spanish patients with hemophilia A and identification of 28 novel mutations. 15921397 2005
Entrez Id: 2157
Gene Symbol: F8
F8
1.000 Biomarker disease BEFREE Given the decades of experience using sheep to study both normal physiology and a wide array of diseases and the high homology between human and sheep FVIII, this new model will enable a better understanding of HA and facilitate the development and testing of novel treatments that can directly translate to HA patients. 19943872 2010
Entrez Id: 2157
Gene Symbol: F8
F8
1.000 Biomarker disease BEFREE The manifestation of hemophilia A, a common hereditary bleeding disorder in humans, is caused by abnormalities in the factor VIII (FVIII) gene. 11179760 2001
Entrez Id: 2157
Gene Symbol: F8
F8
1.000 GeneticVariation disease LHGDN Identification of 217 unreported mutations in the F8 gene in a group of 1,410 unselected Italian patients with hemophilia A. 18217193 2008
Entrez Id: 2157
Gene Symbol: F8
F8
1.000 GeneticVariation disease UNIPROT Experience of a single Italian center in genetic counseling for hemophilia: from linkage analysis to molecular diagnosis. 10800171 2000
Entrez Id: 2157
Gene Symbol: F8
F8
1.000 GeneticVariation disease BEFREE SUMMARY: Background We have previously demonstrated that von Willebrand factor (VWF) is essential in platelet-specific FVIII (2bF8) gene therapy of hemophilia A (HA) with inhibitory antibodies (inhibitors). 30609275 2019
Entrez Id: 2157
Gene Symbol: F8
F8
1.000 GeneticVariation disease UNIPROT Precise carrier diagnosis in families with haemophilia A: use of conformation sensitive gel electrophoresis for mutation screening and polymorphism analysis. 9569180 1998
Entrez Id: 2157
Gene Symbol: F8
F8
1.000 GeneticVariation disease LHGDN Characterization of a causative mutation of hemophilia A identified in the promoter region of the factor VIII gene (F8). 17944985 2008
Entrez Id: 2157
Gene Symbol: F8
F8
1.000 Biomarker disease BEFREE Moreover, CD4(+)CD25(+) Tregs from tolerized mice adoptively transferred dominant tolerance in syngeneic hFVIII plasmid-treated hemophilia A mice and reduced the production of antibodies against FVIII. 18574023 2008
Entrez Id: 2157
Gene Symbol: F8
F8
1.000 Biomarker disease BEFREE Potential uses of platelet-directed therapeutics will be discussed, focusing on targeted delivery of urokinase as a thromboprophylactic agent and FVIII for the treatment of hemophilia A patients with intractable inhibitors. 26149015 2015
Entrez Id: 2157
Gene Symbol: F8
F8
1.000 GeneticVariation disease UNIPROT Independent occurrence of the novel Arg2163 to His mutation in the factor VIII gene in three unrelated families with haemophila A with different phenotypes. Mutations in brief no. 126. Online. 10215414 1998
Entrez Id: 2157
Gene Symbol: F8
F8
1.000 GeneticVariation disease LHGDN Detection of large duplications within the factor VIII gene by MLPA. 18752578 2008
Entrez Id: 2157
Gene Symbol: F8
F8
1.000 GeneticVariation disease UNIPROT Mild hemophilia A resulting from Arg-to-Leu substitution in exon 26 of the factor VIII gene. 2495245 1989
Entrez Id: 2157
Gene Symbol: F8
F8
1.000 AlteredExpression disease BEFREE To date, research in the field of gene therapy for haemophilia has largely relied on retroviruses, adenoviruses and adeno-associated viruses as transfer vectors and the major aims will be to achieve stable longlasting in vivo expression of factors VIII or IX (FVIII or FIX) at therapeutic levels. 11554929 2001
Entrez Id: 2157
Gene Symbol: F8
F8
1.000 Biomarker disease BEFREE Thus, a significant number of haemophilia patients form antibodies, called inhibitors, which neutralize the procoagulant functions of therapeutic cofactors FVIII (haemophilia A) or FIX (haemophilia B). 24762281 2014
Entrez Id: 2157
Gene Symbol: F8
F8
1.000 AlteredExpression disease BEFREE This study suggested that a single administration of an advanced generation LV carrying the human FVIII cDNA resulted in elevation of FVIII level in immune competent rats, and that this gene transfer approach to the skeletal muscle could be an effective tool in treatment of hemophilia A. 20046514 2010
Entrez Id: 2157
Gene Symbol: F8
F8
1.000 GeneticVariation disease UNIPROT Eleven novel mutations in the factor VIII gene from Brazilian hemophilia A patients. 7579394 1995
Entrez Id: 2157
Gene Symbol: F8
F8
1.000 Biomarker disease BEFREE Type and intensity of FVIII exposure on inhibitor development in PUPs with haemophilia A. A patient-level meta-analysis. 25631402 2015