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1 derate to severe collagen deposition seen as perisinusoidal and bridging fibrosis using H&E, Trichome
2 chronic ASH with macrophage inflammation and perisinusoidal and pericellular fibrosis to AH in 57% (1
5 mice reveals that quiescent Cxcl12-creER(+) perisinusoidal BMSCs differentiate into cortical bone os
6 orm to sinusoidal endothelial cells or other perisinusoidal cells, such as hepatic stellate cells, wo
7 ntiation with altered EC gene expression and perisinusoidal ECM deposition and angiocrine dysregulati
10 lls and Tcf21(+) stromal cells thus create a perisinusoidal EMH niche in the spleen, which is necessa
11 tic steatosis, substantial inflammation, and perisinusoidal fibrosis (i.e., steatohepatitis), associa
12 r and portal inflammation scores (P < 0.01), perisinusoidal fibrosis (P < 0.001), and NAS > or =5 (P
13 ic hepatosclerosis in which there is diffuse perisinusoidal fibrosis (type IV collagen) without zonal
16 he mean steatosis (1.6 vs. 2.16, P <.04) and perisinusoidal fibrosis scores (0.35 vs. 0.9, P <.049) w
17 ne deletion in 129/Ola mice triggers hepatic perisinusoidal fibrosis that was detectable from 15 week
24 d by steatosis, ballooning degeneration, and perisinusoidal fibrosis; type 2 was characterized by ste
26 d, it is now apparent that the activation of perisinusoidal hepatic stellate cells, which is a key ev
29 sponsible for sinusoidal capillarization and perisinusoidal matrix deposition, impairing vascular exc
30 ied in PCE in ARLD biopsies and broken dense perisinusoidal mature elastic fibres in explanted livers
31 ing CXCR4-CXCL12-dependent migration towards perisinusoidal megakaryocytes, plucking neutrophils acti
33 IgD(hi) B cells can occupy an extravascular perisinusoidal niche in the bone marrow in addition to t
35 ations of the aged HSC niche and unveil that perisinusoidal niches are uniquely preserved and thereby
36 and non-dividing HSCs thus reside mainly in perisinusoidal niches with Lepr(+)Cxcl12(high) cells thr
39 circulating monocytes transmigrated into the perisinusoidal space and acquired the liver-associated t
40 thin the metaphysis of long bones not in the perisinusoidal space and are needed for bone development
42 onectin in normal liver was localized to the perisinusoidal space surrounding the periportal and the
43 brinogen in normal liver is localized to the perisinusoidal space surrounding the periportal region.
47 epatic stellate and endothelial cells create perisinusoidal vascular HSC niche in the developing live