ライフサイエンスコーパス: temperature sense

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

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

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

4 echanisms and implicate a specific region in temperature sensing.

5 echanisms and implicate a specific region in temperature sensing.

6 al overview of the molecular determinants of temperature sensing.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

27 Temperature sensing involves a built-in instability caus

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

29 Temperature sensing is crucial for homeotherms, includin

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

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

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

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

34 Temperature-sensing neurons in the Drosophila brain coop

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

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

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

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

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

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

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

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

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

44 The temperature sensing structures within the channel have m

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

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

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

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

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