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1 3 domain expressed at levels comparable with human factor VIII.
2 murine, bovine, and porcine factor V and in human factor VIII.
3 for Glu2181-Val2243 significantly less than human factor VIII.
4 sequence for Thr2253-Tyr2332 equally well as human factor VIII.
5 5 (AAV5) vector encoding a B-domain-deleted human factor VIII (AAV5-hFVIII-SQ) in nine men with seve
6 in vivo, we achieved long-term expression of human factors VIII and IX (hFVIII and hFIX) in mouse mod
8 Thus, the inhibitory antibody response to human factor VIII can be reduced by mutagenesis of a B-c
9 n 1b alpha promoter to drive expression of a human factor VIII cDNA construct, transgenic lines were
13 racterize the immune response to recombinant human factor VIII (fVIII) and to study new approaches fo
16 hemophilia A that encodes a B-domain-deleted human factor VIII (FVIII) protein controlled by a hepato
18 III deficiency require frequent infusions of human factor VIII (hFVIII) concentrates to treat life-th
23 eno-associated virus (rAAV) vectors encoding human factor VIII (hFVIII) were systematically evaluated
25 aining an EF1alpha enhancer/promoter driving human factors VIII (hFVIII) or IX (hFIX) complementary D
29 ld greater than recombinant B-domain-deleted human factor VIII levels by transient and stable express
30 purified recombinant B domain-deleted (BDD) human factor VIII molecules containing mutations at R484
32 e and subsequent inactivation of recombinant human factor VIII (rhFVIII) and human factor VIIIa (rhFV
34 he full-length complementary DNA sequence of human factor VIII), second-generation full-length produc
36 actor VIII-deficient background that express human factor VIII under control of the involucrin promot
37 elper-dependent adenoviral vector expressing human factor VIII was administered i.v. to neonatal hemo
38 For this purpose two-dimensional crystals of human factor VIII were grown onto phosphatidylserine-con