ライフサイエンスコーパス: periductal

1 Portal and periductal accumulation of all other cell types examined

2 nflammation was also associated with reduced periductal accumulation of CD24(+) oval cells and abroga

3 NOD mouse AIP was associated with severe periductal and parenchymal inflammation of the exocrine

4 D and T2D, the patterns were different, with periductal and perivascular fibrosis occurring more freq

5 stin-expressing CAFs were spatially found at periductal and perivascular margins, were enriched at ly

6 ressing lymphocytes were detected within the periductal areas of PSC patients.

7 fect of the FoxO1 transgene on the number of periductal beta cells.

8 tor (HGF) on the proliferation of ductal and periductal cells after their activation with 2-acetylami

9 numbers of [3H]thymidine-labeled ductal and periductal cells expanding into the liver acinus.

10 acts as a mitogenic stimulus for ductal and periductal cells, growth factors are necessary for survi

11 es of 2-AAF were used to activate ductal and periductal cells, whereafter growth factors were infused

12 ult hepatocytes, cholangiocytes, and SOX9(+) periductal cells.

13 s expressed on T cells that accumulated in a periductal distribution in diseased tissue.

14 over, the mammary clock is controlled by the periductal extracellular matrix in vivo, which contribut

15 gland, uPARAP/Endo180 is widely expressed in periductal fibroblast-like mesenchymal cells that line m

16 mal fibroblasts in malignant tissue and both periductal fibroblasts and residual myoepithelial cells

17 avbeta6 integrin, which is closely linked to periductal fibrogenesis.

18 (FPA-FTIR) microspectroscopy to characterize periductal fibrosis and bile duct cells progressing to C

19 lopment in pediatric patients to progressive periductal fibrosis and cancer.

20 atosis, dilatation of portal lymphatics, and periductal fibrosis did not show a significant differenc

21 vealed positive correlations between biliary periductal fibrosis during opisthorchiasis and CagA and

22 dministration causes hyperplasia of PBGs and periductal fibrosis in EHBT.

23 wall thickening of some portal arteries, and periductal fibrosis in Fut2(-/-)(high) mice more than Fu

24 Intense foci of inflammation and periductal fibrosis in the liver and kidneys of wild-typ

25 rocirculatory disturbances, mild (secondary) periductal fibrosis, and sensitivity toward human bile s

26 inflammation of the biliary system leads to periductal fibrosis, which is a precursor of CCA, the fl

27 sion and redistributions of lymphocytes from periductal foci to acini.

28 and the acquisition of lymphoid features in periductal foci.

29 progressive organization and maintenance of periductal foci.

30 death of lymphocytes, particularly in dense periductal foci.

31 These observations show that periductal hematolymphoid and stromal cells are the sour

32 l liver, and the production was localized to periductal hematolymphoid cells, which had the morpholog

33 itate the study of the biology of ductal and periductal hepatic cell types, including progenitors.

34 lation, intrahepatic biliary duct cysts with periductal hyperplasia, and pancreatic dysplasia with cy

35 oss the damaged biliary epithelia and affect periductal immune cells.

36 Furthermore, periductal immunoglobulin deposits and serum antibodies

37 The noninsulinomas are often periductal in location, express none of the four major i

38 neonatal cholangiopathy, characterized by a periductal infiltrate composed of CD4(+) and CD8(+) T ce

39 ase, lymph node involvement, bile duct type, periductal infiltration).

40 NZM2328 female mice developed severe chronic periductal inflammation in both submandibular and lacrim

41 owed stronger hBD-1 expression in ducts with periductal inflammation, as indicated by the immunostain

42 did not induce pancreatitis, parenchymal or periductal inflammatory cell accumulation, ductal hyperp

43 Furthermore, periductal inflammatory infiltrates were shown to be a p

44 There is dramatic periductal lymphocytic infiltration in the pancreata of

45 filtration toward the development of SS-like periductal lymphoid aggregates within 2 wk from AdV deli

46 is of unknown etiology includes the entities periductal mastitis and idiopathic granulomatous mastiti

47 me during the budding stage and localizes to periductal mesenchymal cells with an increasing proximal

48 and senescent cholangiocytes can modify the periductal microenvironment through their ability to sec

49 Acute biliary obstruction leads to periductal myofibroblasts and fibrosis, the origin of wh

50 d production is localized to stellate cells, periductal neutrophils, and stromal cells, which typical

51 imal biliary tree), intralobular bile ducts, periductal "null" mononuclear cells, and peribiliary hep

52 of the noninsulinoma tumors, their apparent periductal origin, and the ability of these cells to par

53 ed with a marked induction of the peripheral periductal oval cell/stem cell compartment of the liver.

54 agen were found in the biliary epithelia and periductal region.

55 nflammatory lesions develop initially in the periductal regions of the salivary glands and escalate a

56 facultative stem cells termed oval cells in periductal regions.

57 Periductal sections from all animals were reviewed by a

58 roteinases were fibroblast-like cells in the periductal stroma and stromal cells surrounding the coll

59 ryogenesis and then in the myoepithelium and periductal stroma in the adult.

60 Wnt5a protein is secreted and localizes to periductal stroma, extracellular matrix and epithelial c

61 whereas Msx-2 expression was confined to the periductal stroma.

62 Also, samples of periductal stromal breast tissue were consistently hyper

63 ntraductal growth but are slow to invade the periductal tissues and slow to metastasize.

64 ted with redistribution of immune cells from periductal to interacinar sites and enhanced immunoreact

65 TLA+ and CD18+ cells were redistributed from periductal to interacinar sites during pregnancy and aft