ライフサイエンスコーパス: thermal transition

1 kinetic parameters for the first step of the thermal transition.

2 ing, the papain fragments exhibited a single thermal transition.

3 tion of diffusion coefficients, close to the thermal transition.

4 the activation of acute responses to sudden thermal transitions.

5 esters is triglyceride-rich, does not have a thermal transition above 0 degrees C, and exhibits impai

6 Thermal transition analysis of snap-to-it probes with co

7 ut lack the ability to undergo a cooperative thermal transition and are substantially less resistant

8 The midpoints of the thermal transition and chemical denaturing curves (repre

9 polypeptides and the relation to the inverse thermal transition are discussed.

10 Thermal transitions are continuous, with a strong compos

11 The MCM protein shows a single thermal transition at 67 degrees C.

12 The thermal transition at pH 6.8 leads to a protein state th

13 Electron microscopy shows that the thermal transition at pH 6.8 results in fibril formation

14 lues show that the protein has a distinctive thermal transition at pH 6.8.

15 lization from the neutral pH value, with two thermal transitions at 24 and 27 degrees C.

16 The RAD52(1--192) mutant had only two thermal transitions at 47.6 and 100.9 degrees C (labeled

17 BS sample was found to undergo a cooperative thermal transition between 70 and 75 degrees C, consiste

18 The results display a thermal transition between different backbone conformati

19 al stability, decreasing the midpoint of the thermal transition by almost 40 degrees C.

20 an provide spatially resolved information on thermal transitions by applying a novel algorithm to ima

21 C, fully hydrated C16:0-LacCer shows complex thermal transitions characteristic of polymorphic behavi

22 hermore, we demonstrate structure-controlled thermal transitions, conjugation to human lysozyme throu

23 ignificant difference in the midpoint of the thermal transition curves (DeltaTm of 21.8 degrees C) an

24 A three-state thermodynamic analysis of the thermal transition curves gives a total DeltaH(0) of unf

25 denaturation: melting temperature, width of thermal transition, deltaG, deltaH, deltaS, and deltaCp.

26 eak as a function of temperature gives sharp thermal transitions for both peptides, similar to those

27 Furthermore, the thermal transitions for Ca(2+)- and Mg(2+)-regenerated b

28 The thermal transitions for the holo form follow the same pa

29 ifferential scanning calorimetry revealed no thermal transitions for these proteins in the range 15-1

30 The thermal transitions for these two domains are superimpos

31 cholesteryl ester-rich core that undergoes a thermal transition from a liquid crystalline to an isotr

32 rod and tropomyosin, for which non-two-state thermal transitions have been observed.

33 Thermal transitions identified at (150 +/- 10) degrees C

34 pectra of complex polymer systems undergoing thermal transitions, illustrated by application to sever

35 ake at ambient temperature are overcome by a thermal transition in the apo-protein structure.

36 Using a host polymer with a thermal transition in the regime of interest, we demonst

37 This review focuses on the nature of the non-thermal transitions in semiconductors under femtosecond

38 The three thermal transitions in this model were assigned as follo

39 V-vis spectra, and XRD all indicate that the thermal transition is due to a crystal-crystal phase tra

40 This worm-to-sphere thermal transition is essentially irreversible on heatin

41 TPgammaS and AMP-PNP, however, only a single thermal transition is observed at temperatures slightly

42 d where almost complete reversibility of the thermal transitions is attained.

43 Three thermal transitions (labeled A, B, and C) were observed

44 From thermal transition measurements in the presence of low-m

45 The irreversible thermal transition (melting), monitored by the appearanc

46 Thermal, transition metal-catalysed, and also two differ

47 e is 12.4 +/- 0.3 kJ mol(-1) (pH 5), and the thermal transition midpoint is 59 +/- 1 degrees C (pH 7)

48 of the Scl2 protein all showed a very sharp thermal transition near 36 degrees C, indicating a highl

49 Furthermore, the unique nature of the thermal transition observed for this system offers up co

50 The loss of thermal transition observed in DPC confirms that the pro

51 alorimetry (DSC) showed that an irreversible thermal transition occurred at approximately 39 degrees

52 nteractions are also shown by a calorimetric thermal transition of low cooperativity, and the extende

53 nt of this model, it is found that the major thermal transition of SA in 1% SDS is reversible.

54 The thermal transition of the beta2 subunit below 60 degrees

55 The thermal transitions of fibrillar collagen are investigat

56 t fiber fortification did not interfere with thermal transitions of surimi myosin and actin.

57 o deionized bacteriorhodopsin (dI-bR) on the thermal transitions of the protein secondary structure h

58 The thermal transitions of the TTTT, TTTC, and AAAA octamers

59 The thermal transitions of the two derivatives at neutral pH

60 on by Ferguson analysis and by observing its thermal transition profile; the two molecules behave vir

61 Thermal transition profiles suggest a premelting transit

62 The observed thermal transition represents the unfolding of the four-

63 allowed the previously reported 75 degrees C thermal transition seen in the excess heat capacity func

64 ith high fidelity, confirmed by native PAGE, thermal transition study, and Ferguson analysis.

65 decreased whereas fatty acids increased the thermal transition temperature of firefly luciferase.

66 The thermal transition temperature of swim bladder ASC (35.0

67 The thermal transition temperatures measured by circular dic

68 and bovine fibrinogen as model proteins, the thermal transition temperatures of proteins in dilute an

69 xes with the C-C mismatch cross-link have UV thermal transition temperatures that are 25 degrees C hi

70 culation of a broad distribution of midpoint thermal-transition temperatures measured by the nuclear

71 gesting that virion surface proteins undergo thermal transitions that expose cysteine residues to mod

72 d arenarone broadened the native-to-unfolded thermal transition (Tm), quite different to the large in

73 hodopsin, the primary photoproduct K makes a thermal transition to the L intermediate, which prepares

74 In contrast, BHBmon shows a broad thermal transition, typical of multistate unfolding for

75 ally altered with the appearance of a second thermal transition up to 10 degrees C higher in the pres

76 The thermal transitions were asymmetric, and the temperature

77 Only noncooperative thermal transitions were observed for the PHF samples in

78 were asymmetric, and the temperatures of the thermal transitions were scan rate dependent.

79 ion parameters obtained from the fits to the thermal transitions were used to assess the kinetic stab

80 reversible, endothermic, and very asymmetric thermal transition with a concentration-dependent transi