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1 ion tissue and present at a reduced level in slender.
2                                 We find that slender actin filaments have a persistence length of app
3 he serotonin-immunoreactive cells are always slender and elongate, the PGP 9.5/NSE population compris
4                            SCI led to a more slender and elongated spine morphology.
5                    The appendage bears long, slender and equally spaced ventral spines furnished with
6  new, unexpectedly large-bodied taxon with a slender and ornamented skull from the Carnian Pekin Form
7 nd narrower width), and warbler finches have slender and pointed beaks, reflecting differences in the
8 in monomorphic slender forms and pleomorphic slender and stumpy forms has revealed that two regulator
9 tracortical axon projections from individual slender- and thick-tufted neurons, filled in vivo with b
10  layer 5 contains two excitatory cell types, slender- and thick-tufted neurons.
11 phogenesis can cooperate in the formation of slender arborized UB structures similar to those observe
12              The zeta cell has a small soma, slender axon, and compact, tufted, unistratified dendrit
13             The theta cell has a small soma, slender axon, and delicate, highly branched dendritic ar
14               The eta cell has a small soma, slender axon, and delicate, highly branched dendritic ar
15 migration of the spindle-shaped cell bodies, slender axonal processes grow along the opposite directi
16  extension zone of the developmental mutant, slender barley, compared with the wild type.
17          Drilling into solid substrates with slender beam-like structures is a mechanical challenge,
18 port chain present in the procyclic and long slender bloodstream forms of Trypanosoma brucei brucei w
19                                      In long slender bloodstream forms, the oxidation of glucose or g
20                                ES-attenuated slender bloodstream trypanosomes gain full developmental
21 hear flow, tank-treading red cells appear as slender bodies.
22 n contrast, the predictions of Stokeslet and slender body analyses agree with the laboratory measurem
23     We quantify this dynamical process for a slender body in a fluid by accounting for passive elasti
24  a subset of previously healthy women with a slender body morphotype, often with scoliosis and/or pec
25 cted using the resistive force theories, the slender body theories of Lighthill and Johnson, and the
26 ptotically small modelling approximations of slender body theory.
27             We present code implementing the slender body, regularized Stokeslet, and resistive force
28  unique fabrication process and a supporting slender-body hydrodynamics model.
29 speed in a Newtonian fluid, calculated using slender-body theories and a boundary-element method.
30 layed development, poor fertility, and short slender bristles.
31        Control skin formed normal elongated, slender buds with A-P orientation, but Wnt-7a overexpres
32 ampulla and an attached canal tube (long and slender canal portion), and, in some cases, a small port
33 ional infranuclear structure was composed of slender canaliculi that collected near or streamed to pl
34        However, the orientation of the long, slender CD155 molecule relative to the poliovirus surfac
35                                Filopodia are slender cellular protrusions that dynamically extend and
36 y visualized neurons were observed in a long slender column in the ventrolateral nucleus ambiguus (NA
37 ling resistance can be achieved by filling a slender column with a lightweight foam.
38 d link together, splitting the material into slender columns which then fail.
39 4n, is present at a greatly reduced level in slender compared with normal and encodes protochlorophyl
40 wo of the cDNAs, 7s and 8s, are increased in slender compared with normal.
41 ogonia bearing densely spaced, long, hollow, slender, conical papillae with multiple sharply pointed,
42 e epithelium for the lumen, retaining only a slender connection with basement membrane.
43 tial leaf area to be supported on relatively slender culms, are key traits contributing to the ecolog
44 , we report that basal cells extend long and slender cytoplasmic projections that not only reach towa
45        To clarify this issue, we generated a slender DeltaponA mutant that enabled high-resolution el
46 ottom one-fourth of the epithelium, extended slender dendrites to the epithelial surface, and possess
47  facial dysmorphia, mental retardation, long slender digits and genital anomalies.
48                                        Their slender distal limb bones resemble those of Asiatic asse
49 e, erectoides, semibrachytic, semidwarf, and slender dwarf mutant groups.
50 nder (MS), long-slender (LS), and extra-long slender (ELS).
51 ructures, and mechanical properties of their slender emergent stalks or leaves.
52 ortant functional implications: although the slender feather shafts of Archaeopteryx and Anchiornis m
53 e (gp26) crystallized at acidic pH reveals a slender fiber containing an N-terminal "trimer of hairpi
54     Here we show by electron tomography that slender fibrils connect curved protofilaments directly t
55 ilaments that were connected to chromatin by slender fibrils.
56 28 does confer limited protection, whereas a slender figure yielding a body mass index < 22-24 increa
57 st, where parasites exist as a proliferative slender form or a G0-arrested stumpy form, and the tsets
58     Dissection of this region in monomorphic slender forms and pleomorphic slender and stumpy forms h
59 apidly in the mammalian bloodstream as long, slender forms, but at higher population densities they t
60 ransmissible stumpy forms from proliferative slender forms.
61  stumpy-specific surface transporter PAD1 in slender forms.
62  forms of the parasite exist: proliferative 'slender' forms and arrested 'stumpy' forms that are resp
63 ut downstream from the site of action of the Slender gene product.
64 ds, GA 2-oxidation is controlled by the SLN (SLENDER) gene, a mutation of which produces seedlings ch
65         The purified particles carry a novel slender horn structure projecting from the vertex opposi
66 ll size with body mass in ceratopsids, while slender humeri in the largest stegosaurs may be the resu
67 gulation requires LONG HYPOCOTYL IN FAR RED1/SLENDER IN CANOPY SHADE1 and phytochrome A, which functi
68 he constitutive gibberellin response mutant, slender, in the absence of exogenous GA3.
69 -population genetic correlation for tall and slender individuals (r = -0.80, 95% CI = -0.95, -0.60),
70 ring limbs and covered by tergites with long slender lateral spines.
71   Although expression of 7s was increased in slender leaf tissue, the increase was much less extreme
72  adults, and larvae have extremely elongate, slender legs with pectinate pretarsal claws and lacking
73 ether as the Sphenosuchia, with fully erect, slender limbs; their relationships, however, are poorly
74 eletal abnormalities including shorter, more slender long bones with decreased mechanical strength as
75          All were aerobic glucose-oxidizing, slender, long, curved gram-negative rods that utilized x
76 s short-bold (SB), medium-slender (MS), long-slender (LS), and extra-long slender (ELS).
77 ively tall orbital region and proportionally slender maxilla, a feature documented in the early 20(th
78 act structures and the formation of multiple slender membrane protrusions capped by actin spikes.
79 ates owing to the bending-induced failure of slender microcolumns created between sets of secondary c
80 he anaphase B spindle in fission yeast has a slender morphology and must elongate against compressive
81 lls deficient in CycE1/CYC2 displayed a long slender morphology, whereas those lacking CycB2 assumed
82  categories, such as short-bold (SB), medium-slender (MS), long-slender (LS), and extra-long slender
83                                       In the slender mutant, GAMyb and alpha-amylase are highly expre
84 a spine head isolated from the dendrite by a slender neck, indicates a potential role in isolating in
85 ism; furthermore, gannets and boobies have a slender neck, which is potentially the weakest part of t
86              A primary cilium is a solitary, slender, non-motile protuberance of structured microtubu
87  which produces seedlings characterized by a slender or hyper-elongated phenotype.
88 on of a natural or artificial snake or other slender organism that "swims" on land by propagating ret
89 of cell-to-cell "linker" in the form of long slender outgrowths and branches.
90               In mammals, proliferating long slender parasites transform into non-diving short stumpy
91 llele co-segregating with the characteristic slender phenotype.
92 ression of SUN is positively correlated with slender phenotypes in cotyledon, leaflet, and floral org
93 ing realization that photoinduced bending of slender photoreactive single crystals is surprisingly co
94                       Microtubules are long, slender polymers of alphabeta-tubulin found in all eukar
95            During polarization the uropod (a slender posterior appendage) forms at the site of the MT
96 ted cells display a condensed cell body with slender processes that traverse the area formerly covere
97 ls from astrocytomas of all grades had long, slender processes, were usually bipolar, and their cell
98 ther, represented by a partial skeleton with slender proportions, is a new basal coelurosaur closely
99               Many feathers exhibit a short, slender rachis with alternating barbs and a uniform seri
100 ual electrostatic repulsion, then NFs in the slender regenerating neurites should be lightly phosphor
101  (the number of NFs per micrometer) in these slender regenerating neurites was twice that in their pa
102  and the possible contributions of opposing 'slender retainer' and 'stumpy inducer' arms described.
103  accumulation of the GA signaling repressors Slender Rice-1 (SLR1) and SLR1 Like-1 (SLRL1) and concom
104 reveal a prominent role of the DELLA protein Slender Rice1 (SLR1) in the resistance toward (hemi)biot
105 f the DELLA protein and central GA repressor SLENDER RICE1 (SLR1).
106  an amino-terminal tail-attachment domain, a slender shaft, and a carboxyl-terminal domain composed o
107 partially migratory population having a more slender, shallow-bodied morphology than fish from closed
108 pport known feeding ecology for both African slender-snouted crocodile and alligator, and suggest tha
109 codilians: two longistrine taxa, the African slender-snouted crocodile Mecistops cataphractus and the
110                    Results show that African slender-snouted crocodile skulls are more resistant to b
111 ibaum(R), modified Bibaum(R), triple leader, slender spindle and Solaxe, were evaluated based on agro
112                                          The slender spindle training system showed the highest cumul
113 less than a millisecond by rapidly coiling a slender stalk anchoring it to a nearby surface.
114 he cell body is attached to a substrate by a slender stalk containing a polymeric structure-the spasm
115 rted on the ciliary cap, one function of the slender stalk may be to expose the cap to greater drag f
116 ucing strain that overproduced HAA exhibited slender swarming tendrils.
117 ation but is more primitive in having short, slender, symmetrical remiges.
118 ilament with a short, rigid head and a long, slender tail on which cardiomyocytes are selectively cul
119 ia-bearing arms, drumstick-shaped legs and a slender tail, features that were probably widespread amo
120 cZ) mice, beta-gal (BDNF) is present in long slender taste cells, as well as pyriform taste cells.
121 lation comprise two morphological types--one slender, the other broader and pyriform.
122 larity and produces an unexpectedly long and slender thread.
123  is the density-dependent differentiation of slender to stumpy cells.
124                                          The slender to stumpy differentiation is a density-dependent
125 se dormancy and reversible initiation of the slender-to-stumpy differentiation pathway.
126                  These data suggest that the slender-to-stumpy transformation of T. brucei may not be
127 y of the complexes have a similar shape of a slender triangle.
128 n showed fluorescence in tips cells of long, slender trichomes that is consistent with acyl sugar ace
129  two distinct compartments: small puncta and slender tubules.
130 midal-cell classes in layers 2/3, 4, and the slender-tufted and thick-tufted pyramidal cells of layer
131                     In rat vibrissal cortex, slender-tufted neurons carry motion and phase informatio
132  cortex receive input of whisker motion from slender-tufted neurons onto their apical tuft dendrites
133                                   Individual slender-tufted neurons showed elaborate and dense innerv
134 h soma locations intermingling with those of slender-tufted ones display less dense intracortical axo
135                                              Slender tunnels sensitively capture tumor cells with sli
136 form as submicron beads along the lengths of slender, unbranched micropodia.
137 exhibit unusual wing kinematics; their long, slender wings flap at remarkably high frequencies for th
138 ifferent types of zoids were identified, the slender zoid derived from reduced CycE1/CYC2 expression

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