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1 cies other than hepatocellular carcinoma and fulminant hepatitis.
2 amined in two models: LPS-induced sepsis and fulminant hepatitis.
3 cessive copper accumulation in the liver and fulminant hepatitis.
4 also protected mice from endotoxin shock and fulminant hepatitis.
5 c HBV infection, but might prevent infantile fulminant hepatitis.
6 genotype 2a strain JFH-1 from a patient with fulminant hepatitis.
7 sion, and similar mortality from Fas-induced fulminant hepatitis.
8 BC, alcohol, primary biliary cirrhosis, and fulminant hepatitis.
9 maRII, leads to severe hemorrhage and lethal fulminant hepatitis.
10 agnosed 10 months after liver transplant for fulminant hepatitis.
11 ression in mice would reduce the severity of fulminant hepatitis.
12 HGV RNA is not causally related to non-A-E fulminant hepatitis.
13 f 14 of the 36 patients (38.8%) with non-A-E fulminant hepatitis.
14 blood product transfusion after the onset of fulminant hepatitis.
15 HCV-positive patients; no patients developed fulminant hepatitis.
16 agothrix lagotricha) that was suffering from fulminant hepatitis.
17 ase (CLD) has been associated with severe or fulminant hepatitis.
18 sig4 in mice ameliorates MHV-3-induced viral fulminant hepatitis.
19 management of gout, is known to cause fatal fulminant hepatitis.
20 hed experimental mouse model that mimics the fulminant hepatitis.
21 could potentially be a therapeutic agent for fulminant hepatitis.
22 The two prolines (P310 and P341 of Japanese fulminant hepatitis 1 [JFH-1]) contained in these motifs
23 that the H316N mutation rendered a Japanese fulminant hepatitis 1 chimeric HCV genome encoding the g
24 human hepatocytes infected with the Japanese fulminant hepatitis 1 HCV strain as well as in biopsies
25 cells, and approximately 90% in J6/Japanese fulminant hepatitis 1 HCV-infected cells without affecti
26 icon cells, approximately 70% in J6/Japanese fulminant hepatitis 1 HCV-transfected cells, and approxi
27 ent populations of immune cells and Japanese fulminant hepatitis-1 (JFH-1) HCV-infected Huh7.5 (cell
28 ted/founder virus, sucrose-purified Japanese fulminant hepatitis-1 (JFH-1), a virus encoding a lucife
30 and primary human hepatocytes with Japanese fulminant hepatitis-1 (JFH1) HCV cell culture system (HC
32 patient developed possibly treatment-related fulminant hepatitis 6 weeks after IPH4102 discontinuatio
33 th high prevalence in Japanese patients with fulminant hepatitis and chronic liver disease of unknown
34 were given LPS and D-galactosamine to induce fulminant hepatitis and MCC950 to specifically inhibit N
35 ida (intra-abdominal bleeding), Aspergillus (fulminant hepatitis), and cryptococcal (symptomatic cyto
37 2%) were admitted to hospital, two developed fulminant hepatitis, and one needed a liver transplant;
42 duced the severity of acetaminophen-mediated fulminant hepatitis, but was without effect on concanava
44 No major liver-related complications (e.g., fulminant hepatitis, decompensated liver, and hepatocell
46 ine hepatitis virus strain-3 (MHV-3)-induced fulminant hepatitis due to excessive macrophage-dependen
47 e increasingly recognized, and rare cases of fulminant hepatitis due to ICI hepatotoxicity have been
50 as been proposed as the etiological agent of fulminant hepatitis (FH) or hepatitis-associated aplasti
51 tic failure caused by drugs, the etiology of fulminant hepatitis (FH) remains unknown in many patient
55 oimmune hepatitis can present as an acute or fulminant hepatitis in the absence of pre-existent fibro
56 nfected mice showed decreased mortality from fulminant hepatitis induced by administration of LPS or
57 th ISIS 22023 completely protected mice from fulminant hepatitis induced by agonistic Fas antibody, b
60 culture model is permissive to HCV-Japanese fulminant hepatitis (JFH1) infection and produces very-l
61 re promoter of an HBV strain associated with fulminant hepatitis leading to highly (15-fold) enhanced
62 eristic patterns of liver regeneration after fulminant hepatitis may be seen at CT and MR imaging.
65 ssential for protection against ConA-induced fulminant hepatitis since only A3R-expressing mice were
67 nomic replicon cells or genotype 2a Japanese fulminant hepatitis type 1 (JFH-1) virus-infected hepato
68 We show that viral production of Japanese fulminant hepatitis type 1 increases 1,000-fold when cel
71 f severe end-stage liver diseases and infant fulminant hepatitis were significantly lower in the vacc
72 romoter mutant implicated in the outbreak of fulminant hepatitis, which was caused by the neighboring