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1 termediate compartment (ERGIC) and cis-Golgi cisterna.
2 ments layered in front of the cis-most Golgi cisterna.
3 trols the structural organization of a Golgi cisterna.
4 cles, balanced by the appearance of numerous cisternas.
5 s containing dihydroxyphenylalanine-positive cisterna and 50 nm vesicles.
6 g of HBV virions occurs in the intracellular cisterna and that tetherin colocalizes with HBV virions
7  structures on the cis side of the cis-Golgi cisterna and the cis-most cisterna, but is not detected
8 e of the cis-Golgi cisterna and the cis-most cisterna, but is not detected in more distal compartment
9 that PtdIns4P is enriched on the trans-Golgi cisterna, but surprisingly, Vps74 (the orthologue of hum
10  controls the structural features of a Golgi cisterna by regulating its association to curvature-gene
11                  To retrospectively evaluate cisterna chyli (CC) enhancement on magnetic resonance (M
12                                          The cisterna chyli can mimic the appearance of an enlarged r
13                                          The cisterna chyli was variably located at T12-L1 (n=11), at
14 ER tubules from being pulled from the mother cisterna into the bud and strongly suggests that Rtns/Yo
15                               The flat Golgi cisterna is a highly conserved feature of eukaryotic cel
16 stable compartments model predicts that each cisterna is a long-lived structure that retains a charac
17 isternal maturation model predicts that each cisterna is a transient structure that matures from earl
18 nto canine cerebrospinal fluid (CSF) via the cisterna magna (final viral titer in CSF, 10(9) pfu/ml).
19 ing cerebellar vermis hypoplasia (CVH), mega-cisterna magna (MCM) and DWM.
20           This reduction is blocked by intra-cisterna magna administration of the anti-inflammatory c
21 n-a deficit that can be ameliorated by intra-cisterna magna administration of the naturally occurring
22 HMGB-1 antagonist BoxA was injected into the cisterna magna before IS.
23 acranial pressure (ICP) was monitored with a cisterna magna catheter.
24 itored continuously using intra-arterial and cisterna magna catheters, respectively.
25                  Direct infusion of EGF into cisterna magna caused up-regulation of proliferating cel
26 78 or by knock-down of EGFR expression using cisterna magna infusion of antisense oligodeoxynucleotid
27 ng, FIV(IL-1Ra) vector was injected into the cisterna magna of Col1-IL-1betaXAT mice.
28 ng kinetics (SILK) method to a rhesus monkey cisterna magna ported (CMP) nonhuman primate model, and
29                   Bombesin injected into the cisterna magna potently inhibits gastric acid secretion
30 t temporomandibular joints (TMJs), or in the cisterna magna, respectively, to induce IL-1beta express
31  injected intrathecally, at the level of the cisterna magna, with human leukemic cells.
32 ing a second microneedle introduced into the cisterna magna.
33 nduced by injecting 0.3 mL of blood into the cisterna magna.
34 throconidia of Coccidioides immitis into the cisterna magna.
35 ole blood, oxyhemoglobin and saline into the cisterna magna.
36  CSF was investigated by collecting CSF from cisterna magna.
37  with fluorescent dextrans injected into the cisterna magna.
38 jecting Group B Streptococcus (GBS) into the cisterna magnae of rabbits.
39 BV virions were tethered in the lumen of the cisterna membrane under tetherin expression.
40                          A physical model of cisterna morphology led us to propose that sphingomyelin
41 le to release of calcium from the subsurface cisterna of the OHC, perhaps triggered by CICR from the
42 tween the plasma membrane and the subsurface cisterna of the outer hair cell.
43 ce of clathrin-coated buds on the trans-most cisterna only.
44                               The trans-most cisterna produces exclusively clathrin-coated buds, wher
45 clear Ca(2+) stores, as assayed by a nuclear cisterna-targeted Ca(2+) indicator.
46  perhaps triggered by CICR from the synaptic cisterna; the two time scales of efferent action may res
47 roteins are transported by vesicles from one cisterna to the next.
48 d rbet1 do not appear beyond the first Golgi cisterna, whereas syntaxin 5 and membrin penetrate deepl
49 e models, Golgi residents remain in the same cisterna, whereas, according to cisternal maturation, Go
50 COPII-containing budding zone on a single ER cisterna, which is adjacent to budding zones found on di

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