Editorial
Copyright ©2006 Baishideng Publishing Group Co.
World J Gastroenterol. Dec 7, 2006; 12(45): 7250-7262
Published online Dec 7, 2006. doi: 10.3748/wjg.v12.i45.7250
Figure 1
Figure 1 Hepatocytic ultrastructure. Digitonin-treated biopsy specimen. The specimen is contrasted with aqueous uranyl acetate and lead citrate. Deposits of cholesterol-digitonin complexes (the view of “tender spoondrift clouds”) are seen in the cytoplasm close to the mitochondria. The mitochondrial membrane forms pseudopodia here and there (indicated by arrow).
Figure 2
Figure 2 Hepatocytic ultrastructure in PBC. Biopsy specimen. The specimen is contras-ted with aqueous uranyl acetate and lead citrate. Arrows indicate myelin-like and multilamellar structures with increased osmiophi-lia.
Figure 3
Figure 3 The scheme of liver biopsy specimen homogenization for quantitative adhesiometric study.
Figure 4
Figure 4 The scheme of mechanisms responsible for triggering and developing the major signs of PBC.
Figure 5
Figure 5 Ursodeoxycholic acid.
Figure 6
Figure 6 S-adenosyl-L-methionine.