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1 s: periportal, intermediate or midzonal, and perivenous.
2 plot analysis of glutamine synthesis versus perivenous ammonia concentration revealed that TauT KO h
3 ated encephalomyelitis, the co-occurrence of perivenous and confluent demyelination in some individua
4 planted cells was shifted from periportal to perivenous areas by targeted hepatic ablations with carb
6 eriportal regions of hepatic acinus, whereas perivenous areas were weakly stained or were stain-free.
9 ced iodine concentration appears to diminish perivenous artifact and to result in improved arterial e
13 f the lobule was taken up by the most distal perivenous cells; this distal perivenous uptake was grea
14 of the total glucokinase of the liver; this perivenous concentration of glucokinase was greatly redu
16 s demyelination cohort, 10 patients had only perivenous demyelination and three also had confluent de
23 d cortical demyelination was found among six perivenous demyelination patients, all of whom had encep
25 efined acute disseminated encephalomyelitis (perivenous demyelination), but misdiagnosed acute dissem
28 of mice and the expression of periportal and perivenous hepatocyte markers was determined by polymera
31 in kidney proximal tubule S3 segments and in perivenous hepatocytes, consistent with the sites of hig
34 P450 inducibility was originally greater in perivenous hepatocytes; however, periportal cells rapidl
36 that demyelination can occur independent of perivenous inflammatory changes and supports the presenc
39 mprove vein grafts and shows that preserving perivenous lymphatic vessels or promoting autologous lym
40 -derived venous samples, contributing to the perivenous macrophage accumulation and functional lympha
41 mice were initially treated with halothane, perivenous necrosis and an infiltration of CD11b(+) Gr-1
42 lidated clinical diagnostic criteria but its perivenous pathological findings distinguish it from mul
43 ibility occurs in the periportal (PP) and/or perivenous (PV) zones in response to hypoxia/reoxygenati
45 F-injected fluorescent tracers can reach the perivenous space by passing through these arteriovenous
46 p-AQP4 drives overall convective flow toward perivenous space, i.e., glymphatics, whereas n-AQP4 may
47 omolecules can traverse from periarterial to perivenous spaces, with transfer occurring at sites of o
51 aging features associated with MS, including perivenous T2-weighted hyperintense lesions and focal le
53 periportal-type (wild-type beta-catenin) and perivenous-type (mutant beta-catenin), which expressed n
54 he most distal perivenous cells; this distal perivenous uptake was greatly diminished in maternal low
55 ointensity, periependymal brainstem lesions, perivenous white matter lesions, Dawson's fingers, curve
57 of hypoxia and lower gluconeogenesis in the perivenous zone as compared to the rest of the organ.
58 tion of GS in hepatocytes outside the normal perivenous zone was accompanied by a reduction in the ex