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1 host early Darwinian molecular evolution at constant temperature.
2 s formed and assessment of G4 stability at a constant temperature.
3 ndred millivolts, we can trigger IM-PCR at a constant temperature.
4 ent with variations in mantle composition at constant temperature.
5 that undergo exponential amplification at a constant temperature.
6 inment to thermocycles versus photocycles in constant temperature.
7 hat became infectious (vector competence) at constant temperature.
8 ected scaling of metabolic rate with size at constant temperature.
9 racy comparable to the results obtained at a constant temperature.
10 y monitoring fluorescence at each cycle at a constant temperature.
11 dry weight as compared with those under the constant temperature.
12 d low-cost amplification of nucleic acids at constant temperatures.
13 vival of Gammarus pulex exposed to different constant temperatures.
14 o and pathogen thermal responses measured at constant temperatures.
15 sects that diverge from those predicted from constant temperatures.
16 e 'fundamental' norms derived under standard constant temperatures.
17 na for circadian leaf movement at a range of constant temperatures.
18 nted growth under continuous irradiation and constant temperatures.
19 der varying pressure conditions at different constant temperatures.
20 isture contents (30.0, 49.3, and 60.0%) at a constant temperature (144.57 C) to evaluate the changes
21 isture contents (30.0, 49.3, and 60.0%) at a constant temperature (144.57 degrees C) to evaluate the
22 s, our simulations used an atom-based model, constant temperature (274 K), and non-beta-hairpin initi
23 ric fields at a low field strength (0.4V/cm) constant temperature (65 degrees C) has a statistically
24 d to reversibly switch the particle array at constant temperature and blink the particles ON and OFF
25 y increasing the additive concentration at a constant temperature and by increasing temperature at a
29 length were carried out under conditions of constant temperature and pressure using periodic boundar
30 d classical molecular dynamics simulation at constant temperature and pressure with explicit solvent
31 th a shorter juvenile stage duration than in constant temperatures and a longer adult life span in mo
32 gh typically cosseted in the laboratory with constant temperatures and plentiful nutrients, microbes
33 constant conditions (continuous darkness and constant temperature) and is eliminated by period gene n
34 curves of helix formation induced by TFE at constant temperature, and the properties of these helix
35 traeus albidus (Oligochaeta) under different constant temperatures, and an FT regime were investigate
36 ity along Earth's surface needed to maintain constant temperatures, and has a global mean of 0.42 km
40 arrest with an initial shockable rhythm at a constant temperature between 32 degrees C and 36 degrees
41 red as a function of lipid molecular area at constant temperatures between 10 degrees C and 30 degree
42 function of lipid molecular area at various constant temperatures between 10 degrees C and 30 degree
43 support of these findings, saplings grown at constant temperature but exposed to an extended photoper
44 e when incubated for 21 days at 20 degrees C constant temperatures, but nearly 30% germinate after 21
45 rification in an aged woodchip bioreactor at constant temperature can effectively be modeled using ze
46 ween ultrahigh vacuum and 2 mbar of water at constant temperature causes oxidation state changes not
47 surement of NOE effects, 3JHN alpha coupling constants, temperature coefficients and residue-specific
51 rate that the rate of plant respiration at a constant temperature decreases monotonically with time t
52 reserving growth of spiral steps rotating at constant temperature-dependent angular velocities around
53 ir effect on (3)J(PH), the negative coupling constant, temperature-dependent chemical shifts due to r
54 its; and 3) while thermal suitability across constant temperatures did not perfectly capture fluctuat
55 y conformation when used in conjunction with constant temperature discontinuous molecular dynamics, a
56 otein dynamics when used in conjunction with constant-temperature discontinuous molecular dynamics, a
60 trait values substantially differ from both constant temperature experiments and rate summation; 2)
62 mperature-trait relationships observed under constant temperatures, fluctuating temperatures, and tho
63 oses: (1) it increases the eluent entropy at constant temperature (for approximately 35%); (2) it inc
64 t serves to generate stable water flow under constant temperature, for the study of flow-induced prot
65 table states, and seeds short simulations at constant temperature from each of them to quantitatively
66 es, but those hives also had higher and more constant temperatures from September until January than
67 cells grown at 33 degrees C was measured at constant temperature, from 10 degrees to 40 degrees C, a
68 ants in soil invertebrates under optimal and constant temperature has been widely reported, their upt
71 able of the predator was constructed at four constant temperatures, i.e. 15, 20, 25 and 30 degrees C,
72 s mass (M) loss as a function of time (t) at constant temperature in a dynamic inert nitrogen atmosph
75 l tubing, reduced column end nut mass, and a constant temperature in the column from heating the inle
76 n rates and reduced spore burden compared to constant temperatures in our focal host Daphnia magna ex
78 t future studies report ES at a standardized constant temperature, incorporate more manipulative trea
79 that undergoes self-sustained replication at constant temperature, increasing in copy number exponent
81 observation that the volume of a gas is, at constant temperature, inversely proportional to pressure
83 al effect increases with temperature and, at constant temperature, is invariant over a wide range of
84 linear averaging of trait values measured at constant temperatures-is commonly used to infer performa
86 ound a single cell, our approach can produce constant temperature jumps over 50 degrees C in submilli
89 t better convergence is achieved compared to constant temperature molecular dynamics simulation, with
90 rmal pressure, constant surface tension, and constant temperature (NP(N)gammaT) molecular dynamics (M
91 Compared to the natural situation (NS) at a constant temperature of 10 degrees C, both UTES systems
96 ised forward primers on specific rings, at a constant temperature of 37 degrees C and in less than 60
97 unts of DNA copies in less than an hour at a constant temperature of 37 degrees C, achieving a limit
99 lized to CO2 within 50 incubation years at a constant temperature of 5 degrees C, with vulnerability
100 tion, the simulation was run for 3.8 ns at a constant temperature of 50 degrees C and a constant pres
101 en and thermal degradation when exposed to a constant temperature of 50 degrees C, resulting in decre
102 Seeds were placed in germination chambers at constant temperatures of 5 +/- 0.5 to 40 +/- 0.5 degrees
103 coupled periodic self-motions in response to constant temperature or constant light sources: inside-o
105 ents are often performed under conditions of constant temperature or salinity or in flows with only s
106 EOP rate by more than 2-fold compared to the constant-temperature polarization rate (e.g., giving eff
107 elicited below 20 degrees C and that at any constant temperature, potentiation can be described by a
108 activity rhythm varied little when tested at constant temperatures ranging from 20 to 29 degrees C.
109 strate the assembly of DNA nanostructures at constant temperatures ranging from 4 degrees to 50 degre
111 temperature dependence of Rsoil by assuming constant temperature sensitivity and linearly interpolat
112 led embryos maintained in darkness and under constant temperature show elevated non-oscillating level
114 ship between volume and pressure of a gas at constant temperature." Some curricula may situate scienc
115 dence of the binding constant; the resulting constant-temperature system can then be described as a p
116 ifferent phases to coexist in equilibrium at constant temperature T and pressure P, the condition of
120 simulations leads to the conclusion that at constant temperature the size of fluid-phase domains, nf
122 nostic applications due to its simplicity of constant temperature, use of up to 4 to 6 primers (rende
125 are filled with CO2 and H2O and shaken in a constant-temperature water bath for at least 90 min.
126 s C slows parasite development compared with constant temperatures, whereas fluctuation around <21 de
128 decrease in the rate of plant respiration at constant temperature with the decrease in plant respirat
129 tes, but increased spore burden (relative to constant temperatures with the same mean) at 16 degrees
131 ynthesis and undergo mutual amplification at constant temperature, with apparent exponential growth a