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1 developed hepatic steatosis characterized by microvesicular and macrovesicular lipid accumulation and
2  deep neural network-based model to quantify microvesicular and macrovesicular steatosis in the liver
3  to recognize and differentiate the areas of microvesicular and macrovesicular steatosis, and to quan
4 frozen-section biopsy to distinguish between microvesicular and macrovesicular steatosis.
5 s showed confluent parenchymal necrosis with microvesicular and macrovesicular steatosis.
6 rtal mononuclear infiltrates, hepatocellular microvesicular changes, cytoplasmic lipid droplets, and
7 ne COS7 and found that a cellugyrin-positive microvesicular compartment was present in all cell types
8 n fat synthesis were strongly activated, and microvesicular fat accumulated.
9 g almost exclusively in the third trimester; microvesicular fatty infiltration of hepatocytes causes
10 isomal beta-oxidation, development of severe microvesicular fatty liver, peroxisome assembly, cell de
11 e, the livers of ACOX -/- mice reveal severe microvesicular fatty metamorphosis of hepatocytes.
12 s, including reduced liver weight, transient microvesicular fatty metamorphosis, prolonged extramedul
13 r cell hyperplasia, erythrophagocytosis, and microvesicular fatty metamorphosis.
14 NI1/hSNF5 is completely absent from purified microvesicular fractions, it is specifically incorporate
15 a short-term treatment (5 days) that induces microvesicular hepatic steatosis and marked hypercholest
16 exposed larvae, including macrovesicular and microvesicular hepatic steatosis, as well as focal liver
17    We found that VLCAD-deficient hearts have microvesicular lipid accumulation, marked mitochondrial
18 ion by fibroblasts is controlled through the microvesicular release of EMMPRIN from tumor cells.
19 mal beta-oxidation system, exhibit extensive microvesicular steatohepatitis, leading to hepatocellula
20 ngly reduced (macrovesicular steatosis -34%; microvesicular steatosis -100%; inflammation -74%) and w
21          There was a significant increase in microvesicular steatosis accompanied by a marked reducti
22 al liver histology consisting of significant microvesicular steatosis and fatty Kupffer cells but no
23 s in the serum and induced chronic low-level microvesicular steatosis and inflammation in GWI vs Naiv
24 CV, there was an inverse correlation between microvesicular steatosis and level of autophagy (r = -0.
25 nodeficiency virus infection, which includes microvesicular steatosis and more severe hepatic injury
26  cholestasis and cirrhosis in the former and microvesicular steatosis and oncocytic transformation (m
27 tical information including the detection of microvesicular steatosis and quantitation of liver lipid
28                      Livers with even severe microvesicular steatosis can be reliably used for transp
29 ced biliary and liver damage and may promote microvesicular steatosis development during NAFLD progre
30 considered macrovesicular and 50% considered microvesicular steatosis important.
31 at-free diet and converted macrovesicular to microvesicular steatosis in B6.V-Lep(ob) obese mice as d
32 id screening of mitochondrial toxins-induced microvesicular steatosis in primary hepatocyte cultures.
33           Necropsy analysis revealed hepatic microvesicular steatosis in pubescent male homozygous mi
34              Loss of MCs prominently reduced microvesicular steatosis in zone 1 hepatocytes.
35 d liver damage and specifically up-regulated microvesicular steatosis in zone 1 hepatocytes.
36                                      Hepatic microvesicular steatosis is a hallmark of drug-induced h
37 transplanting livers with moderate to severe microvesicular steatosis is unknown.
38           Liver histology showed widespread, microvesicular steatosis on light-microscopic examinatio
39 acts/delays rapid progression of the hepatic microvesicular steatosis to the characteristic macrovesi
40                                              Microvesicular steatosis was the only ethanol-induced ch
41 ectron-microscopic examination showed severe microvesicular steatosis with severe mitochondrial injur
42 reated bcl-2 (-/+) mice displayed only early microvesicular steatosis without progression to extensiv
43  this virus developed diffuse hepatocellular microvesicular steatosis, an abnormal accumulation of in
44  higher degrees of necrosis, fibrosis stage, microvesicular steatosis, and ductular reaction among ot
45 rmal liver histology with macrovesicular and microvesicular steatosis, fatty Kupffer cells, extensive
46 itis with changes in hepatic tissues such as microvesicular steatosis, likely caused by an increase i
47 may progress to NASH when the liver displays microvesicular steatosis, lobular inflammation, and peri
48                     The liver showed diffuse microvesicular steatosis, marked periportal nuclear glyc
49 ocyte ballooning, which can be confused with microvesicular steatosis, whereas demonstration of an in
50                                  Blunting of microvesicular steatosis, which is restricted to few liv
51 he detection and characterization of hepatic microvesicular steatosis.
52 quate for the clinical evaluation of hepatic microvesicular steatosis.
53 han Oil Red O histology for the detection of microvesicular steatosis.
54  tool for the clinical evaluation of hepatic microvesicular steatosis.
55 ess that includes the development of hepatic microvesicular steatosis.
56 xacerbated hepatocyte damage, with extensive microvesicular steatosis.
57 e, progressive hepatocellular ballooning and microvesicular steatosis.
58 th were commonly identified risk factors for microvesicular steatosis.
59 ion of 40 allografts with moderate or severe microvesicular steatosis.
60 which the donor liver contained at least 30% microvesicular steatosis.
61 terized by liver inflammation, fibrosis, and microvesicular steatosis.
62 mers in microvesicles/exosomes and show that microvesicular TDP-43 is preferentially taken up by reci
63 n of tubular injury in all biopsy specimens: microvesicular tubular epithelial cytoplasmatic vacuoliz
64 ique, we provide evidence for preferentially microvesicular uptake as well as both soma-to-soma "hori