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1 microinjection into the nucleus gracilis (n. gracilis).
2 and weaker in Porphyra purpurea and Euglena gracilis.
3 and in the rostral levels of the fasciculus gracilis.
4 e Blancan, Megantereon hesperus and Smilodon gracilis.
5 psis requiring debridement of the transposed gracilis.
6 d also contains the cytosolic FBA of Euglena gracilis.
7 upregulated NPY via large fiber input to n. gracilis.
8 threshold myelinated fiber pathway to the n. gracilis.
9 the cyclic AMP-dependent kinase from Euglena gracilis.
12 icra, Eubacterium nodatum, and Campylobacter gracilis, a significant positive correlation between sal
13 s galbana, a Delta8 -desaturase from Euglena gracilis and a Delta5 -desaturase from Mortierella alpin
18 ageenan seaweed producers whereas Gracilaria gracilis and O. pinnatifida were mostly agar producers.
19 ship between the mitochondrial genomes of E. gracilis and of the kinetoplastids, which is consistent
20 ideo-rate metabolite imaging of live Euglena gracilis and statistical analysis of intracellular metab
22 oduction by the dominant C4 grass (Bouteloua gracilis) and with increased abundance and production by
23 an appropriate brainstem target, the nucleus gracilis, and an inappropriate target, the reticular for
24 rands of the chloroplast genome from Euglena gracilis are asymmetric with regards to nucleotide compo
26 Control experiments identified the nucleus gracilis as the principal source of ascending projection
27 lizing inertial microfluidics to separate E. gracilis by a key shape parameter-cell aspect ratio (AR)
29 Overall, Streptococcus spp, Campylobacter gracilis, Capnocytophaga granulosa, Haemophilus parainfl
30 CS-based isolation of top 0.5% lipid-rich E. gracilis cells with high viability, after inducing mutat
32 edicted to encode the mature form of Euglena gracilis chloroplast translational initiation factor 3 (
33 al initiation factor 3 (IF3chl) from Euglena gracilis consists of an internal region homologous to pr
34 al initiation factor 3 (IF3chl) from Euglena gracilis contains a central region (homology domain) tha
36 ed the H(2)O(2)-producing enzyme Rhodotorula gracilis D-amino acid oxidase (rgDAAO) selectively in as
40 ist administration into the contralateral n. gracilis had no effect on injury-induced hypersensitivit
44 t target led to reinnervation of the nucleus gracilis in a dose-related fashion, whereas NT-3 express
45 ccessfully healed.Thirty-six males underwent gracilis interposition for rectourethral fistulas, mainl
49 trol serum or preabsorbed serum, into the n. gracilis ipsilateral to nerve injury reversed tactile, b
50 -ar gininamide trifluoroacetate, into the n. gracilis ipsilateral to the injury reversed tactile, but
51 n contrast to these active movements, the N. gracilis lid oscillation requires neither mechanical pre
54 ltrasound (1 MHz) was applied to exposed rat gracilis muscle after intravenous microbubble injection.
55 ) were studied in cannulated and pressurized gracilis muscle arterioles ( approximately 75 microm in
57 ed dilation and its mediation are altered in gracilis muscle arterioles of mice deficient in the gene
58 derwent repair of perineal fistula using the gracilis muscle between 1995 and 2007 was undertaken.
59 By detailing the relationship between canine gracilis muscle energy metabolism and contractile functi
60 (n = 8, 3%)]; and 69 major procedures (24%) [gracilis muscle interposition (n = 32; 11%), coloanal or
61 this study was to review our experience with gracilis muscle interposition for complex perineal fistu
63 s (approximately 80 microm in diameter) from gracilis muscle of normotensive Wistar rats were cannula
64 e chart review of all patients who underwent gracilis muscle transposition for iatrogenic rectourethr
65 y was to review the authors' experience with gracilis muscle transposition in the treatment of iatrog
69 even men, mean age of 62 years, underwent 12 gracilis muscle transpositions for rectourethral fistula
70 turator nerve motor neurons which supply the gracilis muscle, as well as in the corresponding motor e
72 ging, whole mount imaging of vascular casted gracilis muscles, and immunostaining for CD31 in gastroc
75 normally innervated and otherwise untreated gracilis muscles; and (d) similar treatment with hCGRP(8
76 ly, we acquire a live, stable, lipid-rich E. gracilis mutant strain, named B1ZFeL, with 40% more lipi
78 (RA) with or without electrically stimulated gracilis neosphincter (ESGN) was developed to address th
79 d through ascending pathways via the nucleus gracilis (NG) and is dependent on descending facilitator
80 merous in the spinal trigeminal, cuneate and gracilis nuclei whilst rarer in the lateral reticular nu
81 massive axon degeneration in the fasciculus gracilis of mutant animals, as indicated by ultrastructu
82 the dorsal root ganglion (DRG) or in the n. gracilis of rats, became markedly upregulated at both si
88 Compared to sympatric N. rafflesiana, N. gracilis pitchers secreted more nectar under the lid and
92 ella pyrenoidsa, Chlorella vulgaris, Euglena gracilis, Scenedesmus obliquus, and Chlamydomonas reinha
93 -CS) coatings containing a mixture of Lippia gracilis Schauer genotypes (EOM) on the shelf life of gu
95 ecent advances in the mass cultivation of E. gracilis that have enabled the cost-effective production
98 treptococci, Parvimonas micra, Campylobacter gracilis, Treponema socranskii, Dialister pneumosintes,
101 diameter DRG cells, and the NPY-IR in the n. gracilis was blocked by dorsal rhizotomy or dorsal colum
103 and flagellar shapes of specimens of Euglena gracilis We achieved this task by using high-speed 2D im
106 cribe a new trapping mechanism for Nepenthes gracilis which has evolved a unique, semi-slippery wax c
108 olumn neurons, a caudal extension of nucleus gracilis, whose connections to the thalamus are spared i
109 l focusing dynamic equilibrium positions, E. gracilis with different ARs ranging from 1 to 7 are dire
110 cient selective breeding of live oil-rich E. gracilis with fluorescence-activated cell sorting (FACS)
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