نتایج جستجو برای: f8 protein
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INTRODUCTION In this article, we present a comparative immunohistochemical evaluation of four clinical-stage antibodies (L19, F16, G11 and F8) directed against splice isoforms of fibronectin and of tenascin-C for their ability to stain synovial tissue alterations in rheumatoid arthritis patients. Furthermore we have evaluated the therapeutic potential of the most promising antibody, F8, fused t...
Activated leukocyte cell adhesion molecule (ALCAM/CD166), a member of the immunoglobulin superfamily with five extracellular immunoglobulin-like domains, promotes heterophilic (ALCAM-CD6) and homophilic (ALCAM-ALCAM) cell-cell interactions. Here we describe a fully human single-chain antibody fragment (scFv) directed to ALCAM/CD166. We selected the I/F8 scFv from a phage display library of huma...
Absence or decreased activity of the F8 protein causes hemophilia A (HA) which is characterized by the occurrence of spontaneous bleeding. Mutations in the F8 gene, located at the telomeric end of the long arm of the X chromosome, have been identified as the cause of HA. Such mutations include the intron 22 and intron 1 inversions hot spots, point mutations (nonsense and missense mutations) tha...
Haemophilia A is a common X-linked recessive disorder caused by mutations in F8 leading to deficiency or dysfunction of coagulant factor VIII (FVIII). Despite tremendous improvements in mutation screening methods, in a small group of patients with FVIII deficiency suffering from haemophilia A, no DNA change can be found. In these patients, analysis reveals no causal mutations even after sequenc...
Worker Preferences Firm Preferences w1 : [f1] f2 f3 f4 f5 f6 f7 f8 f1 : [w1] w2 w3 w4 w5 w6 w7 w8 w2 : f1 [f2] f3 f4 f5 f6 f7 f8 f2 : w1 [w2] w3 w4 w5 w6 w7 w8 w3 : f1 f2 [f3] f4 f5 f6 f7 f8 f3 : w1 w2 [w3] w4 w5 w6 w7 w8 w4 : f1 f2 f3 [f4] f5 f6 f7 f8 f4 : w1 w2 w3 [w4] w5 w6 w7 w8 w5 : f1 f2 f3 f4 [f5] f6 f7 f8 f5 : w1 w2 w3 w4 [w5] w6 w7 w8 w6 : f1 f2 f3 f4 f5 [f6] f7 f8 f6 : w1 w2 w3 w4 w5 ...
Von Willebrand factor (VWF) is the carrier protein of the anti-haemophilic Factor VIII (FVIII) in plasma. It has been reported that the infusion of FVIII concentrate in haemophilia A patients results in lowered VWF plasma levels. However, the impact of F8-deficiency on VWF plasma levels in F8-/y mice is unresolved. In order to avoid confounding variables, we back-crossed F8-deficient mice onto ...
Hemophilia A (HA) is a bleeding disorder caused by deficiency of functional plasma clotting factor VIII (FVIII). Genetic mutations in the gene encoding FVIII (F8) have been extensively studied. Over a thousand different mutations have been reported in the F8 gene. These span a diverse range of mutation types, namely, missense, splice-site, deletions of single and multiple exons, inversions, etc...
Methylation, CpG island, promoter, intron 1 Haemophilia A is the most common X-linked inherited coagulation disorder caused by a deficiency of the factor VIII protein (FVIII). A plethora of different mutations in the factor VIII gene (F8) have been identified as causative for this bleeding disease including a few promoter mutations. However, in approximately 2-5% of all haemophilic patients, th...
Hemophilia A and B are coagulation disorders resulting from the loss of functional coagulation factor VIII (FVIII) or factor IX proteins, respectively. Gene therapy for hemophilia with adeno-associated virus vectors has shown efficacy in hemophilia B patients. Although hemophilia A patients are more prevalent, the development of therapeutic adeno-associated virus vectors has been impeded by the...
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