ライフサイエンスコーパス: temperature sense

1 to arousal, including nociception, pain and temperature sense.

2 al overview of the molecular determinants of temperature sensing.

3 t nothing is known about how it affects cold temperature sensing.

4 ion, localized Joule heating, and thermistic temperature sensing.

5 echanisms and implicate a specific region in temperature sensing.

6 ty of DsrA RNA are the thermometers for RpoS temperature sensing.

7 ribing for self-powered decoupled strain and temperature sensing.

8 d has been exploited in afterglow-indicating temperature sensing.

9 ging from thermoelectric power generators to temperature sensing.

10 source of progenitor cells for the pain- and temperature-sensing afferents, but also reveal a previou

11 device structures without feeding additional temperature sensing agents, (ii) bright phosphorescence

12 nd to temperature stimuli and participate in temperature sensing and acclimation.

13 d thermal radiation for applications such as temperature sensing and active radiative cooling.

14 the reaction chamber for real-time accurate temperature sensing and control.

15 his paper gives compelling evidence that the temperature sensing and mechanosensing of MSCs are inter

16 fibres and is involved in nociception, pain, temperature sensing and other experiences.

17 , we synthesize our current understanding of temperature sensing and response in plants.

18 mechanisms range from peristaltic pumping to temperature sensing and response to fluid flow variation

19 However, it remains unknown whether temperature sensing and responses are universal processe

20 ves both autonomous and organ-interdependent temperature sensing and signaling.

21 s imply TRPM8 input separates cool from warm temperature sensing and suggest other thermoreceptors al

22 n a wide range of biological functions, from temperature sensing and taste transduction to regulation

23 many functions in biology such as splicing, temperature sensing, and innate immunity.

24 verse physiological processes including core temperature sensing, apoptosis, and immune response.

25 tions suggest that the turret is part of the temperature-sensing apparatus in thermoTRP channels, and

26 Light and temperature sensing are important features of many organ

27 membrane exhibits not only the integrity and temperature sensing behaviour of the Ln-MOF powder but a

28 recently provided a proof of principle that temperature sensing by ion channels may diverge from the

29 Ambient temperature sensing by phytochrome B (PHYB) in Arabidops

30 t sensitivity is pertinent to the process of temperature sensing by the channel.

31 (BMI of 18-25) and obese subjects swallowed temperature-sensing capsules to measure core temperature

32 o be due to the existence of an unidentified temperature-sensing domain.

33 e general notion of the existence of modular temperature-sensing domains in temperature-sensitive ion

34 that PHYB plays an equally critical role in temperature sensing during the daytime.

35 large scaffold protein and key component of temperature sensing; ELF4, a small alpha-helical protein

36 has recently integrated more accurate tissue temperature sensing enabling temperature-controlled irri

37 d responses, is a description of the primary temperature-sensing event.

38 electrolytes (e.g. pH, sodium) together with temperature sensing for internal calibration.

39 ear if these auxiliary SLs contribute to the temperature-sensing function of the ROSE elements.

40 IMR was measured using a pressure- and temperature-sensing guidewire following percutaneous cor

41 LED and temperature sensing helical e-strips are demonstrated, a

42 accumulation plays an essential role in low temperature sensing in Arabidopsis, either indirectly mo

43 on of cell elongation in hypocotyls requires temperature sensing in cotyledons, followed by the gener

44 review recent progress in understanding how temperature sensing in four major pathways in Arabidopsi

45 e first transmembrane segment is crucial for temperature sensing in heat-activated vanilloid receptor

46 mperature dependence and are responsible for temperature sensing in mammals.

47 nsitive channels and significantly perturbed temperature sensing in temperature-sensitive wild-type c

48 is known about the molecular determinants of temperature sensing in the range between approximately 2

49 Here, we report video-rate upconversion temperature sensing in wide field using single-shot phot

50 g a cellular basis for perceptual changes in temperature sensing, including heat hypersensitivity, pe

51 munication and acts as a probe for real-time temperature sensing, including the monitoring of body te

52 Temperature sensing involves a built-in instability caus

53 sitivity of TPXZPhCor, high color-resolution temperature sensing is achieved.

54 g that the role of EYA in photoperiodism and temperature sensing is aided by the stabilizing action o

55 RNA-based temperature sensing is common in bacteria that live in f

56 Temperature sensing is crucial for homeotherms, includin

57 Our results indicate that temperature sensing is mainly dependent on the cooling r

58 polymer outperforms current state-of-the-art temperature sensing materials, including vanadium oxide,

59 Alternatively, temperature sensing may be confined to specific tissues

60 Hence, changes in DNA topology may be the temperature-sensing mechanism for virulence gene express

61 nociceptive sensor of noxious heat, but its temperature-sensing mechanism is yet to define.

62 ng independent stimuli but instead support a temperature-sensing mechanism that is coupled to charge

63 rmancy mechanism provides a highly adaptable temperature-sensing mechanism to control the timing of g

64 transition in order to properly decipher its temperature-sensing mechanism.

65 her show that olfactory receptor neurons and temperature-sensing neurons are required for successful

66 Temperature-sensing neurons in the Drosophila brain coop

67 Neural pathways, which couple temperature-sensing neurons to motor and autonomic outpu

68 cifically expressed in a subset of pain- and temperature-sensing neurons.

69 RNA thermometers are temperature-sensing non-coding RNAs that regulate the ex

70 ntegrate capabilities for flow, pressure and temperature sensing offer the potential for continuous m

71 diffusivity measurements of materials using temperature-sensing optical wireless integrated circuits

72 ssed in the prostate as well as in other non-temperature-sensing organs, and is regulated by downstre

73 ane architecture may exhibit a wide range of temperature-sensing phenotypes.

74 The flexible wireless multi-point temperature sensing probe is produced using micro-manufa

75 esolution (~0.65 m), distributed-fiber-optic temperature-sensing profile from a 1043-m borehole drill

76 nformed microneurography recordings revealed temperature-sensing properties across human sensory affe

77 l, UV-protective and antioxidant) and smart (temperature sensing) properties.

78 platelets, potentially having advanced high temperature sensing, radiation shielding, mechanical str

79 or-based microwave resonators achieve a wide temperature sensing range (30 to 205 degrees C) compared

80 ingle wavelength excitation and has a linear temperature sensing range that matches well with the phy

81 eversible thermal response, and (iv) tunable temperature sensing ranges by using different polymers.

82 examined the material's resistive emittance, temperature sensing, real-time metabolite monitoring per

83 h TRPV channels establish precise and robust temperature sensing remain elusive.

84 g of the structural mechanisms that underlie temperature sensing remains limited, in part due to the

85 In addition, we demonstrate that light and temperature sensing requires the photoreceptors LITE and

86 We report reaction temperature sensing (RTS)-based control to fundamentally

87 The temperature sensing structures within the channel have m

88 An infrared laser with a noncontact temperature sensing system was optimized for a 45 min PC

89 three of which are pain-sensing nociceptors, temperature-sensing thermoceptors, and itch-sensing prur

90 is a polymodal TRP channel involved in cold temperature sensing, thermoregulation, and cold pain.

91 nilloid 2 (TRPV2) channel is a member of the temperature-sensing thermoTRPV family.

92 We propose that a change in the coupling of temperature sensing to channel gating generates this sen

93 Mechanistically our findings indicate that temperature-sensing TRP channels may not contain a speci

94 the Pdot-RhB nanoparticle showed ratiometric temperature sensing under a single wavelength excitation

95 We present investigations into remote liquid temperature sensing with Raman spectroscopy using differ

96 ds in which nanothermometers can be used for temperature sensing within heterogeneous environments.