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1 hat is compatible with a standard laboratory incubator.
2  image cell cultures directly from within an incubator.
3 revalent in vivo as they appear to be in the incubator.
4 track cell culture growth directly within an incubator.
5 hemical exposures was via a modified culture incubator.
6 on was 1.7%, 3-fold less than other reported incubators.
7 ted fluorescence imaging of cell cultures in incubators.
8 of a custom-built, demountable, microfluidic-incubator and a FTIR microscope coupled to a focal plane
9 g of an eight-channel coil integrated in the incubator and a separate four-channel surface coil.
10          Later, plates were placed in a 30 C incubator and observed for growth.
11              Lastly, we use the microfluidic-incubator and time-lapsed FTIR imaging to determine the
12  birth, Sprague-Dawley rats were placed into incubators and exposed to an atmosphere alternating betw
13 grants, friends and family, angel investors, incubators and industry partners from the perspective of
14  their system without the need for dedicated incubators and substantial monetary investments.
15 bility of cultivation in regular (non-CO(2)) incubators, are in progress.
16 erged from their cells into vials held in an incubator at 34C.
17 ually stimulated to initiate breathing in an incubator at 37 degrees C for 1 h in air.
18 pective detection instruments and a standard incubator at 37 degrees C, with TTD and CFU being monito
19 ) were heat-stressed in a prewarmed neonatal incubator at 44-47 degrees C until systolic blood pressu
20 edance measurements were performed inside an incubator at a constant frequency.
21 e incubated simultaneously in a conventional incubator at each of the time points.
22  1.5 T system with the use of a Nomag IC 1.5 incubator by Lammers Medical Technology Co., equipped wi
23 -matched control subjects receiving standard incubator care.
24 wn at various densities in standard in vitro incubator conditions do not have different pericellular
25 OWLS cuvette to be operated as a 1.5 ml mini-incubator, controlling both temperature and CO2 levels.
26 s of tissue contractile stresses inside cell incubator environments.
27 t limited to brain scans, with the use of an incubator equipped not only with head coil, but also wit
28                                          The incubator-equipped OWLS is readily applicable for delica
29              Even in humidified cell culture incubators, evaporation through PDMS and associated shif
30  work is the NSF-funded synthesis center, an incubator for community-led, innovative science.
31                  The use of an MR-compatible incubator for examinations of ill neonates is feasible a
32 investigated in a temperature gradient block incubator for temperatures ranging from -1 to 40 degrees
33 ropose that pollen may act as an "innovation incubator" for the birth of de novo genes.
34 were constructed and allowed to mature in an incubator in a facility approved for human-tissue manufa
35  microg/mL) and transferred to a pressurized incubator in which 30 mm Hg of pressure was applied for
36 in examinations using neonatal MR-compatible incubator (INC).
37                            The MR-compatible incubator increases the availability of MRI to newborns,
38 )Luer to allow for a convenient, sterile and incubator-independent time-lapse microscopic observation
39 hocytes are almost always conducted in CO(2) incubators maintained at atmospheric oxygen levels (atmo
40  that Culicoides cells might function as an "incubator" of viral variants.
41  new opportunities for easy integration into incubators or liquid handling systems.
42                                We found that incubator oxygen levels influenced lymphocyte proliferat
43 nation of warm, humid conditions in neonatal incubators, particularly in association with occlusive d
44 Dedicated neonatal coils integrated with the incubator permit more accurate diagnosis than the previo
45                             The microfluidic-incubator provides an optimal path length of 6-8 mum and
46  In an approach to this problem, we provided incubator-reared bees with opportunities to fly and see
47 rmia (CN) by placement in a servo-controlled incubator set to maintain rectal temperature at 37.4 deg
48  medium containing 10% FBS in a 37 degrees C incubator supplied with 5% CO(2), respectively.
49  medium containing 10% FBS in a 37 degrees C incubator supplied with 5% CO(2).
50 lood was cultured using the automated Bactec incubator system.
51 nature, and the setup was kept in a standard incubator under controlled conditions during the measure
52 ty of images obtained with the MR-compatible incubator was superior to that of images obtained with t
53 development: does the gut serve as a passive incubator where the first organisms randomly encountered
54 tal manipulation outside of the microfluidic-incubator, where assembly can be done just before the st
55 uclear cells (PBMCs) cultured in typical CO2 incubators, which are equilibrated with air (21% O2).
56 tic resonance (MR) imaging, an MR-compatible incubator with air, temperature, and humidity regulators
57 earts are excised, washed and cultured in an incubator with gentle agitation.
58 es, control of osmolarity and pH outside the incubator with Hibernate and density gradient separation
59 ons cultured for 7-10 days were placed in an incubator with levels set at 0.1%, 1%, and 3% O2 and wer
60 puter-controlled, infrared, water-jacked CO2 incubator with reduced oxygen control.

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