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1 ose response between approximately 1 and 200 micromole.
2 than 0.4% for acetate samples larger than 5 micromoles.
3 found to more completely remove the nano- to micromole amounts of anions (and cations) in HPAE fracti
4 ivity kept the amount of material limited to micromole amounts, spectra of the highly luminescent com
6 moderate suction, Gd3+ provided at about 0.5 micromole at the extracellular face of the membrane prom
7 onenal appears inactive at concentrations <1 micromole but displays both stimulatory and inhibitory e
8 xylic acids have the potential to supply 4-5 micromoles C hr(-1)g(-1) fresh weight to the soil soluti
9 crease represent the release of around 10-50 micromoles Ca(2+) per litre cytoplasmic volume from boun
15 (NOS), NG-monomethyl-L-arginine (L-NMMA; 50 micromoles/kg body weight infused simultaneously with VE
19 CM-DTT), was designed and synthesized at the micromole level by reaction of dithiothreitol with triti
21 d-light intensity at the root surface to 100 micromoles m-1 s-1 or supplementing with 6% blue light.
22 roots exposed to constant red light (300-500 micromoles m-2 s-1) did not accumulate chlorophyll in th
25 of inorganic phosphate was produced for each micromole of maltose transferred to glycogen, and 56% of
27 xide-supported catalyst, yield around 22,000 micromoles of acetic acid per gram of catalyst, or aroun
32 tic acid per gram of catalyst, or around 230 micromoles of methanol per gram of catalyst, respectivel
33 MMA concentration expressed as the ratio of micromoles of MMA to millimoles of creatinine (uMMA rati
34 The wild-type enzyme gave specific activity (micromoles of Pi per hour per milligram of expressed H+,
37 s only a commonly available plate reader and micromole per liter concentrations of polyphosphate.
38 = 1.03-1.47, p = 0.022); for each additional micromole per liter unit (mumol/l) of non-Cp copper, the
42 tolerance (mean 35.4 [SE 4.0] vs 60.6 [7.2] micromoles per kg lean body mass per min; p=0.023) owing
43 ctose) switched net hepatic glucose balance (micromoles per kilogram per minute) from output (11.3 +/
44 take (14.7 +/- 1.7) and net lactate balance (micromoles per kilogram per minute) from uptake (6.5 +/-
45 phosphate (P) was found to be highest (~0.24 micromoles per kilogram per year) in the vicinity of the
46 dissolution rates, ranging from 0.003 to 1.2 micromoles per kilogram per year, are observed beginning
49 The amplitude of the changes reached several micromoles per liter when detected with the low-affinity
50 urea (millimoles per liter), and creatinine (micromoles per liter) levels; longer hospital stay (in d
52 4 (192.0) ng/mL, respectively (to convert to micromoles per liter, multiply by 0.00489; P = .07).
53 When the concentrations of biomarkers are at micromoles per liter, such as for sarcosine, which was r
55 The CO2 concentration was elevated to 1200 micromoles per mole, and water and nutrients were suppli
56 WF plus 12 hours dim incandescent (INC) at 5 micromoles per square meter per second and a control tre
57 sed well under continuous irradiation at 400 micromoles per square meter per second and under 12 hour
58 continuous photosynthetic photon flux of 200 micromoles per square meter per second cool-white fluore
59 a control treatment of 12 hours light at 400 micromoles per square meter per second CWF and 12 hours
60 quare meter per second CWF; (c) 12 hours 400 micromoles per square meter per second CWF plus 12 hours
61 square meter per second; (d) 12 hours [400] micromoles per square meter per second CWF plus 12 hours
62 -white fluorescent (CWF); (b) continuous 400 micromoles per square meter per second CWF; (c) 12 hours
63 24-hour continuous irradiation at 560 to 580 micromoles per square meter per second from either metal
64 onducted under continuous irradiation of 400 micromoles per square meter per second of photosynthetic
67 e same photosynthetic photon flux (PPF), 200 micromoles per square meter per second, but with phytoch
68 er per second CWF plus 12 hours dim CWF at 5 micromoles per square meter per second; (d) 12 hours [40
69 photosynthetic photon fluxes (PPF, 400-2080 micromoles per square meter per second; 22-150 moles per
71 d requires approximately 60 min and utilizes micromole quantities of the secondary alcohol being test
75 The automated screening was conducted on micromole scale at a rate of one fully characterized rea
76 hase methodologies offer rapid assembly on a micromole scale sufficient for biophysical characterizat
77 Finally, the procedure was miniaturized to micromole scales by integrating soluble battery chemistr
78 These methods are suitable for large-scale (micromole to millimole) production of oligonucleotides a
79 t, the mean conversion of 13C-CA to 13C-DCA (micromoles) was greater (P < 0.05) on study days 3, 4, a