ライフサイエンスコーパス: heavy water

1 ions, in particular deuterium oxide (D2 O or heavy water).

2 by growing C. elegans in the presence of 70% heavy water.

3 gG4 dimer formation at high concentration in heavy water.

4 ferent when mineralization is carried out in heavy water.

5 y-one patients with suspected NAFLD ingested heavy water ((2) H2 O, 50-mL aliquots) two to three time

6 n the incorporation of deuterium ((2)H) from heavy water ((2)H(2)O) into the deoxyribose moiety of pu

7 f the incorporation of deuterium ((2)H) from heavy water ((2)H(2)O) into the deoxyribose moiety of pu

8 he incorporation of deuterium ((2)H(2)) from heavy water ((2)H(2)O) into tubulin dimers and polymers

9 A heavy water ((2)H(2)O) labeling method recently develope

10 for estimating protein dynamics in vivo with heavy water ((2)H(2)O) using matrix-assisted laser desor

11 logical limitations have hampered the use of heavy water ((2)H(2)O), a convenient, universal biosynth

12 st to the longer term labeling achieved with heavy water ((2)H(2)O).

13 Participants were administered heavy water ((2)H(2)O; deuterium oxide) continuously for

14 rious forms of commercially available stable heavy water ((2)H2O, H2(18)O, and (2)H2(18)O).

15 Heavy water (2H2O) labeling has recently been developed

16 After a pulse administration of heavy water (2H2O), distinct, newly synthesized 2H-label

17 tope labelling of microbial populations with heavy water (a passive tracer) and (15) N ammonium in co

18 stitution of this marrow transit time in the heavy water analysis gave a better-defined blood half-li

19 LB/c controls were labeled continuously with heavy water, and splenic B cells and dendritic cells wer

20 t protein beta-crystallin in both normal and heavy-water-based solutions.

21 A monomer-dimer equilibrium was observed in heavy water buffer at low temperature.

22 ent increase as the temperature decreased in heavy water buffers.

23 tional spectra of cold, composition-selected heavy water clusters, D(+)(D2O)n, can be exploited to ca

24 ique was developed to measure the density of heavy water confined in a nanoporous silica matrix in a

25 Heavy water (D2O) has a distinct molecular vibration spe

26 Analysis of heavy water data sets yielded turnover rates consistent

27 Relative ion abundances of the light- and heavy-water digestion products, which are separated by 2

28 glyceride gain, mice were first administered heavy water for 5 weeks to label adipose triglycerides w

29 sed concentration, decreased temperature and heavy water from 8% to 25% in all buffers except for hig

30 entially labeled peptides in the presence of heavy water (H(2)(18)O), and performed LC/MS/MS analysis

31 TBW was measured by heavy water (H2O18 or D2O) dilution in 64 pediatric pati

32 urface, using isotopic mixtures of water and heavy water, have recently been performed.

33 kbone of PE with deuterium atoms from D(2)O (heavy water) in solvent.

34 Our results show that heavy water is capable of quantifying in situ single-cel

35 ty of isotope ratio mass spectrometry with a heavy water labeling approach to capture the full range

36 Heavy water labeling combined with sensitive tandem mass

37 ssible areas of concern regarding the use of heavy water labeling during plant growth.

38 Inpatient and outpatient heavy water labeling protocols resulted in (2)H label in

39 In both treatment groups, heavy water labeling revealed that after 2 h (study A),

40 otein turnover rates is accomplished using a heavy water labeling strategy.

41 Results of heavy-water labeling studies have challenged the notion

42 h rapidly and quantitatively measures stable heavy water levels in total body water.

43 ery similar for our "normal" and fictitious "heavy" water models.

44 ng data in healthy adult subjects using both heavy water (n = 4) and deuterium-labeled glucose (n = 9

45 to be strictly observed in the operation of heavy-water nuclear power plants is the mandatory regula

46 more-efficient operation and maintenance of heavy-water nuclear power plants.

47 a readily accessible amount, could provide a heavy-water output comparable to that of modern plants.

48 isotopic mixtures are processed annually for heavy-water production and tritium decontamination.

49 By switching from water to heavy water, the chemical conversion during photopolymer

50 By using heavy water to constrain cellular growth activity, we ca

51 he density data we obtained for the confined heavy water under these conditions are valuable to large

52 oods harvested from a hydroponic system with heavy water, vitamin A activity of stable isotope-labele

53 The increased second-order rate constant in heavy water was expected from ordering of this loop over

54 in the THz spectrum of deuterated glycine in heavy water, which allow us to separate the distinct mod

55 nged by stable isotope labeling studies with heavy water, which yielded estimates in excess of 3 days

56 was exposed to Ringer solution made up from heavy water, whose solvent isotope effect should reduce

57 e is digested with RNase T1 in 18O-labeled ("heavy") water with the 18O being incorporated at the 3'-