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1 by indirect calorimetry, as well as impaired thermoregulation.
2 e aspect to its well-documented functions in thermoregulation.
3 pth occupied, suggesting possible behavioral thermoregulation.
4  was not explained by novelty, locomotion or thermoregulation.
5  specialized fat tissue that is dedicated to thermoregulation.
6 s are abundant in the body and essential for thermoregulation.
7 c tone, cellular proliferative activity, and thermoregulation.
8 is involved in heat-induced hyperalgesia and thermoregulation.
9  dopaminergic circuits, pain perception, and thermoregulation.
10 REB deficient mice are limited to reward and thermoregulation.
11 functions associated with powered flight and thermoregulation.
12 ic structures involved in energy balance and thermoregulation.
13  and that 5-HT(2A) receptors are involved in thermoregulation.
14  dehydration, electrolyte imbalance and poor thermoregulation.
15 dentification of neural circuits involved in thermoregulation.
16 intenance of metabolic rate and adaptational thermoregulation.
17 ulating energy expenditure, body weight, and thermoregulation.
18  the C. elegans neural pathway that mediates thermoregulation.
19 ns including steroidogenesis, lipolysis, and thermoregulation.
20 ns such as foraging, predator avoidance, and thermoregulation.
21 achieved through natural host-driven dynamic thermoregulation.
22 asing resting metabolic rates, and improving thermoregulation.
23  by increasing metabolic and hydric costs of thermoregulation.
24 end projections to brain regions involved in thermoregulation.
25 al neurons serve as FS models with deficient thermoregulation.
26 iome contributes to host CRs in activity and thermoregulation.
27 ia-induced seizures as well as deficiency in thermoregulation.
28 litating access to scarce shade critical for thermoregulation.
29 ract with infection to influence patterns of thermoregulation.
30 variety of visual signals and potentially in thermoregulation.
31  which remarkably impacts their activity and thermoregulation.
32 entary and structural color productions, and thermoregulation.
33 ialized ability to burn calories as heat for thermoregulation.
34 piration, blood pressure, water balance, and thermoregulation.
35 after birth, and appropriate assistance with thermoregulation.
36 ties to shelter from their predators and for thermoregulation.
37 s a direct assessment of the limits of human thermoregulation.
38 heat and humidity exceeding limits for human thermoregulation.
39 et side effects, impacting thermosensing and thermoregulation.
40 ves as a previously unknown target of P57 in thermoregulation.
41 D2 (PGD(2)), we further explored its role in thermoregulation.
42 example of a protein with multiple layers of thermoregulation.
43 ature decrease, a negative feedback loop for thermoregulation.
44 increased anxiety-like behavior and improved thermoregulation.
45 gulation, including autonomic and behavioral thermoregulation.
46 ring acute cold exposure and is critical for thermoregulation.
47 cs of this species, coupled with behavioural thermoregulation.
48  (BAT), leading to impaired BAT function and thermoregulation.
49 ostasis and consequent metabolic control and thermoregulation.
50                Sweat glands are critical for thermoregulation.
51 creases BAT mass, with a resultant effect on thermoregulation.
52  (UCP1) and UCP3 are important for mammalian thermoregulation.
53 leasant cold stimuli as well as in mammalian thermoregulation.
54  and impairment in uncoupled respiration and thermoregulation.
55 nterrogate the neuronal circuitry underlying thermoregulation.
56                      Additionally, a role in thermoregulation, a defining feature of mammalian homeos
57 roclimate, predicts a moderate level of leaf thermoregulation across a broad air temperature gradient
58 e had impaired water repulsion and defective thermoregulation after water immersion.
59                                 Furthermore, thermoregulation and activity measurements in cilia muta
60 at MRR 5-HT1A receptors are also involved in thermoregulation and arousal.
61                      While infant behavioral thermoregulation and BAT thermogenesis have been extensi
62 affecting processes such as signal efficacy, thermoregulation and camouflage.
63 , in addition to playing a conserved role in thermoregulation and chemosensation, is required for thi
64  To examine the role of nitric oxide (NO) on thermoregulation and control of breathing in obesity, aw
65 m, a genetically based trait associated with thermoregulation and crypsis.
66            LCN2 has a novel role in adaptive thermoregulation and diet-induced insulin resistance.
67 own adipose tissue (BAT) contributes to both thermoregulation and energy expenditure in rats through
68 sm that controls whole-body BAT activity for thermoregulation and energy homeostasis.
69 BAT function, with possible implications for thermoregulation and energy metabolism in drinkers.
70 nderlie the key physiological adaptations in thermoregulation and energy utilization that permitted h
71 ical model predicts that the energy costs of thermoregulation and flight, respectively, impose upper
72 L) and its receptor (PRLR) have an impact on thermoregulation and hair morphology phenotypes, giving
73 polating these findings clinically, impaired thermoregulation and hypothermia are potential risks in
74 DMH), a brain region known to be involved in thermoregulation and in stress responses, causes similar
75 nological basis have the potential to affect thermoregulation and increase the risk of heat injury.
76 tions, involving both direct effects through thermoregulation and indirect pathways through trophic i
77 nthesize the complexities of host behavioral thermoregulation and its impacts on various temperature-
78                                     Impaired thermoregulation and lowered average daily gains (ADG) r
79  and UCP5 may be involved in tissue-specific thermoregulation and metabolic changes associated with n
80 temperatures, may exert greater influence on thermoregulation and metabolism during the hibernation s
81 TRPV1- and TRPM8-neurons in thermosensation, thermoregulation and nociception, thus significantly ext
82 ompanied by adaptations in genes that govern thermoregulation and oxygen metabolism.
83 o demonstrate that increasing uncertainty in thermoregulation and parental investment of parasitic yo
84               Other brain regions related to thermoregulation and peripheral organs such as spleen, l
85 of butterfly wings potentially contribute to thermoregulation and provide an insight into butterflies
86       We dissect the molecular mechanisms of thermoregulation and report the structure of the CssA th
87 ting in normal thermal sensation relevant to thermoregulation and reproductive functions, HE TRPV1 ce
88 sults, infection and dehydration and enables thermoregulation and sensory perception.
89 nal autonomic and motor circuits involved in thermoregulation and sexual function.
90 DB thermosensitive neurons can modulate both thermoregulation and sleep-wake control.
91 e neurons are hypothesized to participate in thermoregulation and sleep-wake control.
92 insights into the role of microstructures in thermoregulation and suggest both evolutionary and physi
93                                      Newborn thermoregulation and the critical thermal maximum (CT(ma
94 n, which may be due to the interplay between thermoregulation and the habitat changes occurring in ea
95 drenaline reuptake inhibitor on performance, thermoregulation and the hormonal responses to exercise.
96                            In the context of thermoregulation and the maintenance of core temperature
97 f") - a state that is shaped by early social thermoregulation and through the social network.
98 dy were to develop a cell model of cutaneous thermoregulation and to determine the mechanisms underly
99  both female and male mice, their effects on thermoregulation and torpor bout initiation exhibit diff
100 e a response to opposed selection pressures, thermoregulation and water conservation, at different li
101 ine sweat glands are indispensable for human thermoregulation and, similar to other mammalian skin ap
102 e analogues, we propose that the benefits of thermoregulation and/or crypsis are likely to have contr
103 wo-component signal transduction systems for thermoregulation, and a ferritin uptake network.
104 al mechanisms underlying the drive to sleep, thermoregulation, and antinociception.
105 man and animal studies of muscle physiology, thermoregulation, and autonomic nervous system function.
106 hannel involved in cold temperature sensing, thermoregulation, and cold pain.
107  ANS are key regulators of immune responses, thermoregulation, and energy balance, functions that und
108 emodeling, lymph node organogenesis, central thermoregulation, and formation of a lactating mammary g
109 the environment and the costs of locomotion, thermoregulation, and maintenance.
110                 Reproduction, water balance, thermoregulation, and neuroendocrine functions are also
111 , memory, anxiety, cardiovascular responses, thermoregulation, and nociception.
112 mportant roles in mimicry, sexual selection, thermoregulation, and other adaptive processes in many g
113 tipredator defenses, parasitic exploitation, thermoregulation, and protection from ultraviolet light,
114 hological nucleus involved in feeding, fear, thermoregulation, and sexual activity.
115 ribute to the modulation of pain processing, thermoregulation, and sexual function in the spinal cord
116  mechanisms controlling feeding, metabolism, thermoregulation, and sleep overlap in the hypothalamus.
117 nd sufficient for autonomic cardiac control, thermoregulation, and survival, and targeting the overac
118 plays important roles in energy homeostasis, thermoregulation, and the maintenance of lung morphology
119 ent evidence suggests roles in AT expansion, thermoregulation, antigen presentation, and iron homeost
120 other constraints such as predation risk and thermoregulation are connected to this two-dimensional f
121                                Olfaction and thermoregulation are key functions for mammals.
122 changes, but the factors affecting butterfly thermoregulation are not fully understood.
123 ever, the effects of weightlessness on human thermoregulation are not well understood.
124 tributors to individual differences in human thermoregulation are physical attributes, including body
125  infrared wavelengths with potential ties to thermoregulation are relatively unknown.
126 iological roles for vagal afferents (e.g. in thermoregulation, arousal and fatigue) are being investi
127  insight into the role of adipose tissues in thermoregulation, as well as an alternative way to targe
128                                         Body thermoregulation at room temperature was also disrupted
129 in's temperature set-point while maintaining thermoregulation at that lower set point.
130 an important role in coupling metabolism and thermoregulation at the level of anterior hypothalamus.
131 emperature-sensitive neurons are involved in thermoregulation, because for eight decades they have on
132                            Changes in sleep, thermoregulation, behavioral activity, lipids, and catec
133           Rat pups are capable of behavioral thermoregulation, both in the nest and on a thermocline,
134 rozole (20 mug, p.o.) on cognition, anxiety, thermoregulation, brain estrogen content, and hippocampa
135 ses on routine neonatal care, resuscitation, thermoregulation, breast-feeding, "kangaroo" [skin-to-sk
136 tch (histamine and chloroquine) and impaired thermoregulation but did not impair mechanosensation or
137 MA, where ambient temperature interacts with thermoregulation, but not locomotor activity.
138  DNA sequences within papB were required for thermoregulation, but the PapB and PapI regulatory prote
139 gration of water/electrolyte homeostasis and thermoregulation, but we have a limited understanding th
140 peratures, suggesting the use of behavioural thermoregulation by caribou.
141     Specifically, we suggest that behavioral thermoregulation by the intermediate host may buffer the
142 ndividuals that fail to balance the costs of thermoregulation (by huddling in groups) with the costs
143 eaf area index, implying a certain degree of thermoregulation capability.
144 ipose tissues during cold is dispensable for thermoregulation, central FGF21 signaling is necessary f
145 lations in the SPZ, and different aspects of thermoregulation (circadian rhythm and fever response) a
146 nates, implying that this taxon did not have thermoregulation comparable to modern birds, but was abl
147 ulations depending more on microclimates for thermoregulation compared to Catalan populations.
148     In addition male piglets showed impaired thermoregulation compared to females.
149 ly spraying them directly, creates free-form thermoregulation composites, featuring an outstanding De
150                        Results indicate that thermoregulation constrains herbivore and insectivore ac
151  cost, as porpoises must maintain their high thermoregulation costs with a reduced energy intake.
152 rmanent and 4 (9%) transient ptosis, 5 (11%) thermoregulation difficulties, 4 (9%) a sensation of lef
153  with a severe defect in water repulsion and thermoregulation due to decreased production of sebaceou
154 ountercurrent heat exchange is associated to thermoregulation during blood-feeding.
155 ic drive to brown adipose tissue to maintain thermoregulation during cold.
156                    Its principal function is thermoregulation during exposure to a hot environment or
157 ehavioral mechanisms contribute to effective thermoregulation during huddling in the cold.
158 multiple scales are critical for behavioural thermoregulation during periods of potential heat stress
159 gesting that muscle assumes a larger role in thermoregulation during starvation.
160  expected to influence body size by altering thermoregulation, energetics or food availability.
161 ding neural pathways for thermoreception and thermoregulation, experiments were performed on anaesthe
162 ions, including arousal, locomotor activity, thermoregulation, food intake, and memory.
163 erve sufficient reserves to fuel hunting and thermoregulation for return to cold seas.
164 o evidence of colour patterning, ecology and thermoregulation, fossil melanosomes can also carry a ph
165                  Consistent with behavioural thermoregulation, four of the five species were less lik
166 emoval and pay little attention to the basic thermoregulation function of sweat, showing limited evap
167 n the cold shock response (MSANTD4) and body thermoregulation (GRIA4).
168                                         Leaf thermoregulation has been documented in a handful of stu
169 ss impacts, including high metabolic cost of thermoregulation, hence access to microclimate refugia m
170  a region involved in the central control of thermoregulation, identified neurons that express both I
171 tions of the disease, would recapitulate the thermoregulation impairment observed in children with IN
172 oss during a fast, in partial restoration of thermoregulation in a cold challenge, and in inducing se
173 nce, and nanotechnology have now facilitated thermoregulation in a far more personalized and energy-s
174 lasma uridine governs energy homeostasis and thermoregulation in a mechanism involving adipocyte-depe
175  Circadian body temperature fluctuations and thermoregulation in a warm environment were also indisti
176 pigmentation could play an important role in thermoregulation in cold climates, while a range of comp
177 cies experiencing greater energy demands for thermoregulation in cold climates.
178 ls, devoid of 5-HT neurones, showing altered thermoregulation in cold stress (4 degrees C) and a redu
179 diverse range of non-visual roles, including thermoregulation in ectotherms.
180                   In line with this, altered thermoregulation in Gpr50(-/-) mice is associated with a
181  sweat glands are essential for sweating and thermoregulation in humans.
182 cussed, emphasizing the importance of social thermoregulation in maintaining physiological stability
183  and is required for glucose homeostasis and thermoregulation in OPA1 BKO mice by increasing energy e
184  of underlying brain injury causing impaired thermoregulation in out-of-hospital cardiac arrest patie
185                                              Thermoregulation in over-wintering clusters is thought t
186         To assess the global role of rppH in thermoregulation in P. syringae, RNA sequencing was used
187 about the underlying genetic determinants of thermoregulation in plant-pathogenic bacteria.
188 on MDMA neurotoxicity, core temperature, and thermoregulation in rats.
189 e NST could indeed play an important role in thermoregulation in species lacking BAT, we investigated
190 hesized to serve as a temperature sensor for thermoregulation in the cold.
191 otor responsiveness to cocaine, and improved thermoregulation in the cold.
192  These findings advance our understanding of thermoregulation in the distribution of natural colours.
193 against hyperthermia and alleviate defective thermoregulation in the elderly, and may provide a model
194  the snow leopard's daily temporal niche for thermoregulation in the future.
195 try processes for both internal and external thermoregulation in the human body.
196 contribution of TRPV4 to thermosensation and thermoregulation in vivo.
197                            Here we show that thermoregulation, in which the transcription of select R
198 ids resulted in impaired water repulsion and thermoregulation, increased rates of UVB-induced epiderm
199 d water loss, problems with electrolytes and thermoregulation, increased risk of local or systemic in
200                                              Thermoregulation is a complex intercommunicative functio
201                                   Behavioral thermoregulation is a defensive strategy employed by som
202  gene fusions and point mutations, that RhlR thermoregulation is a posttranscriptional effect depende
203                                    Autonomic thermoregulation is a recently acquired function, as it
204                             Morphine-induced thermoregulation is attenuated in CREB(alphaDelta) mutan
205 gh performance, particularly those for which thermoregulation is challenging or ecologically costly.
206 mote winter survival when food is scarce and thermoregulation is challenging.
207 nkeys), demonstrating that TRPV1 function in thermoregulation is conserved from rodents to primates.
208                                   Behavioral thermoregulation is critical for survival across animals
209 are sensitive to cold, indicating that their thermoregulation is defective.
210   A combination of blunted HCVR and abnormal thermoregulation is known to occur with dysfunction of t
211 riability but evidence for plant behavioural thermoregulation is limited.
212 s the sweating response, whereas behavioural thermoregulation is maintained.
213                                  In mammals, thermoregulation is mediated by the preoptic area of ant
214                                              Thermoregulation is not only ecologically important; it
215                                              Thermoregulation is one of the most vital functions of t
216  a significantly lower maximum T(w) at which thermoregulation is possible even with minimal metabolic
217                         We suggest that leaf thermoregulation is widespread in both space and time, a
218  a region that contains neurons that control thermoregulation, is the main locus at which histamine a
219 ine gland density are required for efficient thermoregulation, it is unclear if these changes are lin
220 gnificant role for delta opioid receptors in thermoregulation, it is unclear whether delta receptors
221  (size, wings), behavior (activity patterns, thermoregulation), life cycles, and ecophysiology (cold
222 for these two species indicate that variable thermoregulation likely existed among the non-avian dino
223 an adaptation to special challenges, such as thermoregulation, locomotion in dense forests, or endura
224 , with applications in robotic transformers, thermoregulation, mechanical memories in hysteresis loop
225 sting a trade-off between predation risk and thermoregulation mediated by body size.
226 such as the preoptic area (altered sleep and thermoregulation), medulla (adrenal corticosteroid respo
227                       A relationship between thermoregulation, metabolism, and the host response to i
228 d, on the basis of heat-balance models, that thermoregulation might have been important in the evolut
229  are widely accepted in animal but not human thermoregulation models.
230  are widely accepted in animal but not human thermoregulation models.
231           In this study, we investigated the thermoregulation of B. seminalis TC3.4.2R3 at 28 degrees
232 ar to BAT and is essential for intravascular thermoregulation of cold acclimation.
233                                              Thermoregulation of immune defence could offer an adapti
234                                              Thermoregulation of leaf temperature (T(leaf) ) may fost
235  direct temperature effects representing the thermoregulation of photosynthesis were negligible.
236 e RNA thermometers are the main mechanism of thermoregulation of QS-dependent gene expression in P. a
237 ation of the molecular mechanism involved in thermoregulation of QS-dependent virulence-factor produc
238 e nonpermissive temperature, suggesting that thermoregulation of region 1 may be exerted through vari
239        Intriguingly, RppH is involved in the thermoregulation of ribosome-associated proteins, as wel
240 ently suggested to play an important role in thermoregulation of species lacking brown adipose tissue
241 ia coli mediates RNA turnover, contribute to thermoregulation of syfA.
242  sera revealed that some proteins exhibiting thermoregulation of synthesis elicited antibody response
243 e nearly poikilothermic, with no evidence of thermoregulation of T(leaf) towards a homeostatic value.
244 hanism may explain the role of alpha2-ARs in thermoregulation of the cutaneous circulation.
245                                              Thermoregulation of the thorax allows endothermic insect
246 stem-loop structure was sufficient to confer thermoregulation on the reporter, while sequences furthe
247 e hypothalamus in the homeostatic control of thermoregulation or goal-oriented behaviors during wakef
248 iological functions including UV protection, thermoregulation, oxidant scavenging, arthropod immunity
249 onse to mitochondrial stress is required for thermoregulation, partially by increasing FGF21 expressi
250 t functions of colour lightness in anurans - thermoregulation, pathogen and UVB protection - and broa
251                 Nest building is involved in thermoregulation, positive motivational states, and moto
252 cur and coincide with the periods of altered thermoregulation produced by systemic administration of
253 aphical habitats, but the molecular basis of thermoregulation remains poorly understood.
254                                     Apparent thermoregulation resulted from fixed diel activity patte
255        Here we report an additional layer of thermoregulation resulting in lower eftM mRNA transcript
256           Neonates with HIE display impaired thermoregulation, resulting in spontaneous hypothermia.
257 y critical inter-individual factors of human thermoregulation, resulting in unreliable and unrealisti
258 ted in feeding behavior, energy homeostasis, thermoregulation, reward seeking, addiction, and materna
259 ross animals, in part because of its role in thermoregulation: small ears conserve heat, while large
260             Pigmentation also affects floral thermoregulation, suggesting climate warming may additio
261 defense, immune surveillance, UV protection, thermoregulation, sweating, lubrication, pigmentation, t
262          General anaesthetics greatly impair thermoregulation, synchronously reducing the thresholds
263 spectively, we propose an autonomous textile thermoregulation system that could intelligently provide
264 at TRPM8 is a universal cold receptor in the thermoregulation system.
265 tissues, which were instead dependent on the thermoregulation tactic employed by an organism, being c
266 mentous covering that probably functioned in thermoregulation, tactile sensing, signalling and aerody
267 me climate change effects through behavioral thermoregulation that can be captured by mechanistic mod
268 me climate change effects through behavioral thermoregulation that can be captured by mechanistic mod
269  evaluate predictions from a novel theory of thermoregulation that synthesizes energy budget and carb
270      Within the central neural circuitry for thermoregulation, the balance between excitatory and inh
271                                Self-adaptive thermoregulation, the mechanism living organisms use to
272 terface for light capture, gas exchange, and thermoregulation, the potential contributions of leaves
273  appeared to match predictions of behavioral thermoregulation theory, fine-scale examination revealed
274  on taste and ingestive behaviors, pain, and thermoregulation, this review is intended to provide a c
275 d water is a vital resource that facilitates thermoregulation through evaporative cooling, especially
276 hange implementations equipped with adaptive thermoregulation to drive Monte Carlo optimization proce
277 must be considered in addition to behavioral thermoregulation to explain habitat selection decisions.
278 ed in diverse aspects of their ecology, from thermoregulation to mimicry.
279 e to novel conditions or may use behavioural thermoregulation to reduce their exposure to stressful m
280 to general principles of thermosensation and thermoregulation, unachievable using the rodent model al
281 e-stimulated insulin secretion and defective thermoregulation upon fasting.
282      The lig fragment successfully conferred thermoregulation upon the beta-galactosidase reporter in
283 dy provides new evidence that TRPV1 controls thermoregulation upstream of the SNS, providing a potent
284                                  His work on thermoregulation, vasopressin, perinatal programming, an
285 nce of two buffering mechanisms: behavioural thermoregulation versus fine-scale microclimate selectio
286 Then, we demonstrated these neurons' role in thermoregulation via chemogenetics.
287 Therefore, the role of 5-HT(2A) receptors in thermoregulation was assessed in two rat models of ovari
288                              This failure of thermoregulation was caused by impaired shivering and no
289 no changes in hypothalamic E2 were observed, thermoregulation was disrupted by letrozole in females o
290                                     Impaired thermoregulation was evident in Mfap2(-/-) mice prior to
291 ance understanding of TRPV1 contributions to thermoregulation, we measured the effects of a TRPV1 rec
292 e the roles of 5-HT neurons in breathing and thermoregulation, we took advantage of a unique conditio
293 , the potential detrimental effects of SI on thermoregulation were discussed, emphasizing the importa
294 pring and summer when environmental costs of thermoregulation were low, but reducing that precision i
295 ndicates that in social insect tasks such as thermoregulation, where temperature may provide a global
296 ciated with PPT1 deficiency, that of altered thermoregulation, which is associated with impaired lipo
297 region-wide demographic trends and butterfly thermoregulation, which may be due to the interplay betw
298  at both temperatures, contrasting with papB thermoregulation, which was not greatly altered by limit
299  brown coloration may have a limited role in thermoregulation, while light brown-yellow does not have
300 AAs playing a role in photon dissipation and thermoregulation with a possible role in contributing to

 
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