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1 microinjection into the nucleus gracilis (n. gracilis).
2 ing of the dominant grass species (Bouteloua gracilis).
3 d also contains the cytosolic FBA of Euglena gracilis.
4  upregulated NPY via large fiber input to n. gracilis.
5 threshold myelinated fiber pathway to the n. gracilis.
6 the cyclic AMP-dependent kinase from Euglena gracilis.
7  and weaker in Porphyra purpurea and Euglena gracilis.
8  and in the rostral levels of the fasciculus gracilis.
9 behaviour of a long human muscle such as the gracilis.
10 VEs) in the genome of the microalgae Euglena gracilis.
11 e on a native amphibian species, Physalaemus gracilis.
12 s a model for flagellar mechanics in Euglena gracilis.
13 e Blancan, Megantereon hesperus and Smilodon gracilis.
14 psis requiring debridement of the transposed gracilis.
15  synthase dimer from mitochondria of Euglena gracilis, a member of the phylum Euglenozoa that also in
16                                      Euglena gracilis, a microalgal species of unicellular flagellate
17                                      Euglena gracilis, a photosynthetic and highly adaptable protist,
18 brucei, a lethal human parasite, and Euglena gracilis, a photosynthetic protist.
19 icra, Eubacterium nodatum, and Campylobacter gracilis, a significant positive correlation between sal
20 gical activities of Porphyra sp., Gracilaria gracilis, Alaria esculenta and Saccharina latissima extr
21  viruses integrated in the genome of Euglena gracilis, an ecologically and industrially relevant fres
22 s galbana, a Delta8 -desaturase from Euglena gracilis and a Delta5 -desaturase from Mortierella alpin
23                                              Gracilis and adductor longus biopsies were collected fro
24 ns and inhibited both producing organisms E. gracilis and C. elegans.
25 terior columns, and the bilateral fasciculus gracilis and cuneatus in the posterior columns.
26 cludes the putative istiodactylids Haopterus gracilis and Hongshanopterus lacustris.
27 the other two showing great similarity to C. gracilis and M. ovata AKs.
28             In contrast, AKs from Codonosiga gracilis and Monosiga ovata form a distinct cluster apar
29 ageenan seaweed producers whereas Gracilaria gracilis and O. pinnatifida were mostly agar producers.
30  the degradation compartment in the algae E. gracilis and observation of a network of membranes withi
31 ship between the mitochondrial genomes of E. gracilis and of the kinetoplastids, which is consistent
32 ly only poor nuclear genome assemblies of E. gracilis and Rhabdomonas costata are available, but ther
33                              Flowering of B. gracilis and soil respiration responded particularly str
34 ideo-rate metabolite imaging of live Euglena gracilis and statistical analysis of intracellular metab
35 ofiling in two representative algae, Euglena gracilis and the toxin-producing microalga Prymnesium pa
36 column sensory axons innervating the nucleus gracilis and white matter at the injury epicenter.
37 oduction by the dominant C4 grass (Bouteloua gracilis) and with increased abundance and production by
38 an appropriate brainstem target, the nucleus gracilis, and an inappropriate target, the reticular for
39 acteria, the photosynthetic excavate Euglena gracilis, and the heterokont Ochromonas spp.
40 rands of the chloroplast genome from Euglena gracilis are asymmetric with regards to nucleotide compo
41     The position and presence of spots in C. gracilis are determined by the epistatic interaction of
42 nd intravital microscopy to measure IMVR and gracilis artery diameter at baseline and during the hype
43   Control experiments identified the nucleus gracilis as the principal source of ascending projection
44                              The GEVEs in E. gracilis bear signatures of genomic erosion, including i
45                                              Gracilis biopsies were collected from TD patients underg
46 lizing inertial microfluidics to separate E. gracilis by a key shape parameter-cell aspect ratio (AR)
47 r also differs from Megantereon and Smilodon gracilis by having a very small mandibular flange.
48 middle and innermost plastid envelopes of E. gracilis by machinery homologous to the translocons of o
49    Overall, Streptococcus spp, Campylobacter gracilis, Capnocytophaga granulosa, Haemophilus parainfl
50 orrodens, Eubacterium nodatum, Campylobacter gracilis, Capnocytophaga sputigena, and Veillonella parv
51 CS-based isolation of top 0.5% lipid-rich E. gracilis cells with high viability, after inducing mutat
52             When the sequence of the Euglena gracilis chloroplast genome was reported in 1993 the alp
53 edicted to encode the mature form of Euglena gracilis chloroplast translational initiation factor 3 (
54 duction and beta-carotene protection, and L. gracilis components to deoxyribose protect.
55 al initiation factor 3 (IF3chl) from Euglena gracilis consists of an internal region homologous to pr
56 id, we isolated cyclic peptides from Euglena gracilis containing asparagine and non-proteinogenic ami
57 al initiation factor 3 (IF3chl) from Euglena gracilis contains a central region (homology domain) tha
58 oly-m-phenylenediamine (PPD) layer and an R. gracilis D-amino acid oxidase (RgDAAO) layer.
59 ed the H(2)O(2)-producing enzyme Rhodotorula gracilis D-amino acid oxidase (rgDAAO) selectively in as
60 on of DOM during blue grama grass (Bouteloua gracilis) decomposition and determine how these processe
61 g uptake, whereas DOM harvested from Euglena gracilis did not exhibit this same pronounced effect.
62 ids and polyamines, most abundant in Euglena gracilis DOM, were positively correlated to increase Hg
63                                      Euglena gracilis (E. gracilis) has been proposed as one of the m
64 ver forty euglenatide-like metabolites in E. gracilis, E. sanguinea and E. mutabilis, suggesting an i
65 Chlamydomonas reinhardtii (ChRe) and Euglena gracilis (EuGr), and HeLa cells in their native growth m
66           The most unusual feature of the P. gracilis eye is that its upward-looking portion is resol
67              Using proteomics of isolated E. gracilis flagella we identify nearly 1700 protein groups
68 entify significant adaptations within the E. gracilis flagellum, many of which are clearly linked to
69          Axons regenerating into the nucleus gracilis formed axodendritic synapses containing rounded
70 lete skeleton of a stem squamate, Bellairsia gracilis, from the Middle Jurassic epoch of Scotland, do
71 ist administration into the contralateral n. gracilis had no effect on injury-induced hypersensitivit
72 bored by the lactate-producing Campylobacter gracilis, had the strongest association with childhood d
73                                      Euglena gracilis harbours secondary green plastids, but an incom
74 re protocol including the surgical steps for gracilis harvest takes ~ 3 h.
75           The hyperiid amphipod Paraphronima gracilis has a pair of bi-lobed apposition compound eyes
76                         Euglena gracilis (E. gracilis) has been proposed as one of the most attractiv
77  situ in diverse Proteobacteria: Hylemonella gracilis, Helicobacter pylori, Campylobacter jejuni, Pse
78 ions placed into neighboring nuclei (nucleus gracilis, hypoglossal nucleus) served as controls.
79 t target led to reinnervation of the nucleus gracilis in a dose-related fashion, whereas NT-3 express
80 ccessfully healed.Thirty-six males underwent gracilis interposition for rectourethral fistulas, mainl
81                                              Gracilis interposition was performed in 53 patients.
82                  Two women required a second gracilis interposition.
83                 Seventeen women underwent 19 gracilis interpositions for 15 rectovaginal and 2 pouch-
84                          This analysis of B. gracilis intraspecific diversity across spatial scales w
85 trol serum or preabsorbed serum, into the n. gracilis ipsilateral to nerve injury reversed tactile, b
86 -ar gininamide trifluoroacetate, into the n. gracilis ipsilateral to the injury reversed tactile, but
87                                      Euglena gracilis is a photosynthetic flagellate possessing chlor
88 dition to muscle volume and weight since the gracilis is also completely removed from the leg.
89 predates the translocation event and that G. gracilis is an evolutionary intermediate between G. soja
90 trol, mild, severe) on blue grama (Bouteloua gracilis Kunth Lag.
91  beta-(1->3)-glucan GPs from bacteria and E. gracilis, leading to their classification in glycoside h
92 n contrast to these active movements, the N. gracilis lid oscillation requires neither mechanical pre
93      The impact-driven oscillation of the N. gracilis lid represents a new kind of rapid plant moveme
94                             Reductions in B. gracilis may make this system more vulnerable to invasio
95 dditionally, we discuss the origin of the E. gracilis middle plastid envelope based on the lipid comp
96                Furthermore, we show that the gracilis muscle actually functions as a muscle with rela
97 ltrasound (1 MHz) was applied to exposed rat gracilis muscle after intravenous microbubble injection.
98                               Thus, the long gracilis muscle appears to be composed of relatively sho
99 ) were studied in cannulated and pressurized gracilis muscle arterioles ( approximately 75 microm in
100                                              Gracilis muscle arterioles ( approximately 80 micrometer
101 ed dilation and its mediation are altered in gracilis muscle arterioles of mice deficient in the gene
102 derwent repair of perineal fistula using the gracilis muscle between 1995 and 2007 was undertaken.
103 By detailing the relationship between canine gracilis muscle energy metabolism and contractile functi
104 rgery, we directly measured subject specific gracilis muscle force-length relationship in situ and pr
105 (n = 8, 3%)]; and 69 major procedures (24%) [gracilis muscle interposition (n = 32; 11%), coloanal or
106 this study was to review our experience with gracilis muscle interposition for complex perineal fistu
107 a unique surgical technique in which a human gracilis muscle is transferred from the thigh to the arm
108 a unique surgical technique in which a human gracilis muscle is transplanted from the thigh to the ar
109                                  Whole human gracilis muscle isometric length-tension relationships w
110                At matched sarcomere lengths, gracilis muscle mechanics and collagen architecture are
111                                          Rat gracilis muscle neuromuscular junctions were examined by
112 s (approximately 80 microm in diameter) from gracilis muscle of normotensive Wistar rats were cannula
113 in situ properties and function of the human gracilis muscle to validate this relationship.
114 e chart review of all patients who underwent gracilis muscle transposition for iatrogenic rectourethr
115 y was to review the authors' experience with gracilis muscle transposition in the treatment of iatrog
116                                          The gracilis muscle transposition is a safe and effective me
117                                              Gracilis muscle transposition is an effective surgical t
118  nine patients, the fistula healed following gracilis muscle transposition.
119 even men, mean age of 62 years, underwent 12 gracilis muscle transpositions for rectourethral fistula
120 turator nerve motor neurons which supply the gracilis muscle, as well as in the corresponding motor e
121 P < .05) increased in the semitendinosus and gracilis muscles 2 days after the marathon.
122 ging, whole mount imaging of vascular casted gracilis muscles, and immunostaining for CD31 in gastroc
123 ch AChE forms are maintained in intact adult gracilis muscles.
124 dult Sprague-Dawley rat fast-twitch anterior gracilis muscles.
125  normally innervated and otherwise untreated gracilis muscles; and (d) similar treatment with hCGRP(8
126 ly, we acquire a live, stable, lipid-rich E. gracilis mutant strain, named B1ZFeL, with 40% more lipi
127 or lidocaine microinjection into the nucleus gracilis (n. gracilis).
128 (RA) with or without electrically stimulated gracilis neosphincter (ESGN) was developed to address th
129 d through ascending pathways via the nucleus gracilis (NG) and is dependent on descending facilitator
130 merous in the spinal trigeminal, cuneate and gracilis nuclei whilst rarer in the lateral reticular nu
131 he lateral parabrachial nucleus, the cuneate/gracilis nuclei, and the pontocerebellar system.
132  massive axon degeneration in the fasciculus gracilis of mutant animals, as indicated by ultrastructu
133  the dorsal root ganglion (DRG) or in the n. gracilis of rats, became markedly upregulated at both si
134                    The ability to prepare E. gracilis of uniform shape at high purities has significa
135               NPY microinjection into the n. gracilis of uninjured rats elicited reversible tactile,
136              We also determined that average gracilis optimal fibre length is 12.9 cm.
137 ators were implanted to stimulate transposed gracilis or gluteus muscle.
138 ch has focused on the model organism Euglena gracilis, other members of the euglenids have now starte
139 pairment of paravertebral, vasti, sartorius, gracilis, peroneal and medial gastrocnemius muscles.
140                                      Clarkia gracilis petals each have a single red-purple spot that
141                               Analysis of E. gracilis' phototactic accumulation dynamics over a broad
142     Compared to sympatric N. rafflesiana, N. gracilis pitchers secreted more nectar under the lid and
143 rally been assumed that the two innermost E. gracilis plastid envelopes originated from the primary p
144 hips and hence predicted functions of the E. gracilis plastid proteome.
145                            COI cDNAs from E. gracilis possess short 5' and 3' untranslated transcribe
146 tion, and provides evidence that suggests G. gracilis, rather than G. soja, as the ancestor of cultiv
147      We show that the trapping success of N. gracilis relies on the combination of material stiffness
148                                        The E.gracilis rpoA gene is the distal cistron of a multigene
149 hich raised the question of the origin of E. gracilis's middle plastid envelope.
150 ella pyrenoidsa, Chlorella vulgaris, Euglena gracilis, Scenedesmus obliquus, and Chlamydomonas reinha
151 -CS) coatings containing a mixture of Lippia gracilis Schauer genotypes (EOM) on the shelf life of gu
152                                    Bouteloua gracilis seeds were planted in sterilized sand with (ino
153       Shape is an important biomarker for E. gracilis, serving as an indicator of biological clock st
154 d Native (Mentha Spicata L) and Scotch (M. x gracilis Sole) are the main producers of spearmint type
155 of wild (Glycine soja) and semiwild (Glycine gracilis) soybeans, and domestication of cultivated soyb
156 ution of petal pigmentation patterning in C. gracilis ssp.
157  the basal region ('cup') in the petal of C. gracilis ssp.
158 e(s) involved in petal coloration in Clarkia gracilis ssp.
159 ution of petal pigmentation patterning in C. gracilis ssp. sonomensis.
160  the basal region ('cup') in the petal of C. gracilis ssp. sonomensis.
161 e(s) involved in petal coloration in Clarkia gracilis ssp. sonomensis.
162 mposition of whole cells of the pigmented E. gracilis strain Z and two bleached mutants that lack det
163 lL We determined the lipid composition of E. gracilis strain Z mitochondria and plastids, and of plas
164 ecent advances in the mass cultivation of E. gracilis that have enabled the cost-effective production
165 ity and capacity for adaptation in Bouteloua gracilis, the dominant species in the Central US shortgr
166 of essential oil of Thymus zygis, subspecies gracilis, thymol chemotype).
167              This patient underwent a second gracilis transposition, which uneventfully healed.
168  the case of the swimming microalgae Euglena gracilis trapped in light-defined billiard geometries.
169 treptococci, Parvimonas micra, Campylobacter gracilis, Treponema socranskii, Dialister pneumosintes,
170                                    Nepenthes gracilis uses the impact of rain drops to catapult insec
171                     Finally, in isolated rat gracilis vessels, rauwolscine completely inhibited the L
172 diameter DRG cells, and the NPY-IR in the n. gracilis was blocked by dorsal rhizotomy or dorsal colum
173 e extent to which phenotypic diversity in B. gracilis was correlated with climate.
174 ein (PBP) pigments from red algae Gracilaria gracilis was optimized using maceration, ultrasound-assi
175                                           C. gracilis was the dominant Campylobacter species found in
176 and flagellar shapes of specimens of Euglena gracilis We achieved this task by using high-speed 2D im
177 hesis in chloroplasts of the protist Euglena gracilis We show that, rather than comparable uncoupling
178 60 gene from the euglenoid protozoan Euglena gracilis were cloned and sequenced.
179 urements of the behavior of the alga Euglena gracilis when exposed to controlled light fields.
180                        Actual testing of the gracilis where experimental data is measured takes place
181 cribe a new trapping mechanism for Nepenthes gracilis which has evolved a unique, semi-slippery wax c
182          We also identify a locus in Euglena gracilis, which is similarly required for Z-ISO activity
183 olumn neurons, a caudal extension of nucleus gracilis, whose connections to the thalamus are spared i
184 l focusing dynamic equilibrium positions, E. gracilis with different ARs ranging from 1 to 7 are dire
185 cient selective breeding of live oil-rich E. gracilis with fluorescence-activated cell sorting (FACS)

 
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