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1 ing a second microneedle introduced into the cisterna magna.
2 nduced by injecting 0.3 mL of blood into the cisterna magna.
3 throconidia of Coccidioides immitis into the cisterna magna.
4 ole blood, oxyhemoglobin and saline into the cisterna magna.
5 lobally through infusion into the CSF of the cisterna magna.
6 CSF was investigated by collecting CSF from cisterna magna.
7 with fluorescent dextrans injected into the cisterna magna.
10 n-a deficit that can be ameliorated by intra-cisterna magna administration of the naturally occurring
11 ld nanoparticles (AuNPs; 10-15 nm) via intra-cisterna magna administration, with tracking by SPECT im
12 s overexpressing IL-10 administered into the cisterna magna after stroke induces a switch of microgli
13 dose (1 x 10(14) vector genomes (vg)) in the cisterna magna and 25% at the thoracolumbar junction.
14 Rats were administered S1 or vehicle intra-cisterna magna and 7d later challenged with vehicle or L
15 dose, dose-escalation of combined BiT, intra-cisterna magna and intrathecal infusion in children with
21 hat track tracer particles injected into the cisterna magna (CM) of mouse brains have shown evidence
22 eport that transplantation of mGRPs into the cisterna magna did not result in increased mice survival
23 sed paramagnetic contrast (Gd-DOTA) into the cisterna magna during dynamic contrast-enhanced MRI to q
24 nto canine cerebrospinal fluid (CSF) via the cisterna magna (final viral titer in CSF, 10(9) pfu/ml).
25 of posterior fossa arachnoid cysts and mega cisterna magna findings independent of cerebellar volume
28 9 encoding canine GALC administered into the cisterna magna increased GALC enzyme activity, normalize
29 78 or by knock-down of EGFR expression using cisterna magna infusion of antisense oligodeoxynucleotid
32 i-17 MLNPs, delivered to 5XFAD mice by intra-cisterna magna injection, specifically deliver Anti-17 t
37 factor C (AAV8-VEGF-C) was injected into the cisterna magna of HE rats 1 day after surgery to induce
38 d fluorescent, 100 nm PEGylated-NPs into the cisterna magna of healthy mice and studied their distrib
40 nd large (~155 kDa) molecule agents into the cisterna magna of rats and then applied low, diagnostic-
41 ng kinetics (SILK) method to a rhesus monkey cisterna magna ported (CMP) nonhuman primate model, and
43 t temporomandibular joints (TMJs), or in the cisterna magna, respectively, to induce IL-1beta express