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1  the diminutive allele resulted in increased thermosensitivity.
2 with Ser322 phosphomutants displayed altered thermosensitivity.
3 temperature-dependent transition with a high thermosensitivity.
4 so identifying portable modules that specify thermosensitivity.
5 e region that robustly reduces the channel's thermosensitivity.
6 at of wild-type levels and further increases thermosensitivity.
7 en firing rate thermosensitivity and current thermosensitivity.
8 stitute the underlying mechanism of neuronal thermosensitivity.
9 m-induced depolarization determines neuronal thermosensitivity.
10  spore viability, slow growth, and increased thermosensitivity.
11 ive phenotype but partially rescued ydj1-151 thermosensitivity.
12 , suggesting a likely cause of the increased thermosensitivity.
13 of Akt or ERK1 and -2 kinases increased cell thermosensitivity.
14 here were reductions in both firing rate and thermosensitivity.
15  bicuculline had no change in firing rate or thermosensitivity.
16 exhibited reductions in both firing rate and thermosensitivity.
17 ns, although these neurons had a higher mean thermosensitivity.
18 ture of Cooling Cell cilia endings and their thermosensitivity.
19 t exhibit unique substrate specificities and thermosensitivities.
20 rating that individual PBs possess different thermosensitivities.
21 there was no correlation between firing rate thermosensitivity and current thermosensitivity.
22 drogel to investigate effects on the polymer thermosensitivity and gelation properties.
23 ivation by amylopectin, response to citrate, thermosensitivity and the processivity of glucan chain e
24 s between neuronal activity (firing rate and thermosensitivity) and tissue survival as a function of
25 major differences in sequence specificities, thermosensitivities, and structural features, all orthol
26 es: spontaneous DNA damage, chromosome loss, thermosensitivity, and acute sensitivity to genotoxic ag
27  There were no differences in firing rate or thermosensitivity between 350 and 450 microm slices; but
28 se impaired the sweating onset threshold and thermosensitivity (both P < 0.01).
29 Our work reveals the bidirectional change of thermosensitivity by injury and suggests that the crosso
30        These findings indicate that reducing thermosensitivity can be critical for TRP channel functi
31  specialized class of neurons, the degree of thermosensitivity can be strongly modulated by synaptic
32 iciency and near elimination of the splicing thermosensitivity characteristic of MuSVts110 were obser
33 osensory-specific TRPA1 isoform with reduced thermosensitivity compared to the previously described i
34                     Changes in POAH neuronal thermosensitivity could be a component of the mechanism
35 he present study compared discharge rate and thermosensitivity (discharge rate change/degree C) of WS
36  discharge in NREM sleep exhibited increased thermosensitivity during NREM sleep compared to wakefuln
37 he dorsal HDB, 65% of the neurons maintained thermosensitivity during SB.
38 ignificant differences in membrane potential thermosensitivity for the different neuronal types.
39                                The change in thermosensitivity from wakefulness to NREM sleep was cor
40 that gene deletions resulting in the highest thermosensitivity generally are not the same as those tr
41                    TTX decreased the current thermosensitivity in most neurones, but there were no re
42 charge during NREM sleep exhibited decreased thermosensitivity in NREM sleep.
43 P amplitude contributed to an enhancement of thermosensitivity in some neurones.
44 f TOC1 and its close homologue PRR5 restores thermosensitivity in the evening, whereas TOC1 overexpre
45 died, 37 (25%) neurons met the criterion for thermosensitivity including 17 warm-sensitive (WSNs) and
46 ed9-1 double mutant by restoring germination thermosensitivity, indicating that both NCED4 genes enco
47 is supports studies suggesting that neuronal thermosensitivity is controlled, not by resting currents
48 sting temperature, and we find that arterial thermosensitivity is tuned to this temperature, making m
49 e activation segment, the core driver of CLK thermosensitivity, is observed across all eukaryotic kin
50                                          The thermosensitivity of 24 WSNs and 31 CSNs from the medial
51 d to determine the mechanisms underlying the thermosensitivity of alpha2C-ARs.
52  have identified mutations that suppress the thermosensitivity of an ipl1-2 mutant.
53 f those mutant groES alleles to suppress the thermosensitivity of bacteria bearing the dnaA46 mutatio
54 minCDE might at least partially suppress the thermosensitivity of ftsZ84, which can form colonies bel
55 and 1.0 microM doses) on the firing rate and thermosensitivity of HDB neurons.
56                      The onset threshold and thermosensitivity of local sweat rate and forearm blood
57  the influence of loaded DOX crystals on the thermosensitivity of LTSLs and their therapeutic efficac
58                               We studied the thermosensitivity of neurons in the rat horizontal limb
59  the Q(A)/Q(A)(-) redox couple and increased thermosensitivity of photosystem II (PSII), suggesting s
60 pable of either enhancing or suppressing the thermosensitivity of SCN neurones.
61  dosage of the division gene zipA suppresses thermosensitivity of the ftsZ84 mutant by stabilizing th
62                                          The thermosensitivity of the neurons in the diagonal band of
63                      The ability to tune the thermosensitivity of the polymer in order to compensate
64 d here indicate that the previously reported thermosensitivity of the respiratory complexes of abc1/c
65 orylation of Orp2 suppress or exacerbate the thermosensitivity of the spb70 mutants, respectively, in
66 and its close homolog, TRPV6, do not exhibit thermosensitivity or ligand-dependent activation but are
67 iciency in coenzyme Q had a much more severe thermosensitivity phenotype for these oxidative endpoint
68    To study the basic mechanisms of neuronal thermosensitivity, rat hypothalamic tissue slices were u
69       SSE1-dependent suppression of ydj1-151 thermosensitivity required the wild-type ATP-binding dom
70 c efficiency at low temperatures and greater thermosensitivity than their mesophilic counterparts.
71 nal mutations cause basal, but not acquired, thermosensitivity that occurs in conjunction with hypera
72                     Therefore, this mirrored thermosensitivity, together with the matched thresholds,
73                     Of 34 neurons tested for thermosensitivity under SB, 11 were WS, 4 were CS and 19
74 ecular level, GR28B(D) misexpression confers thermosensitivity upon diverse cell types, suggesting th
75                            We found that AFD thermosensitivity, which exceeds that of most biological
76  PIF4 target genes show circadian rhythms of thermosensitivity, with minimum responsiveness in the ev