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1 her feeding nor social stimuli did not alter feeding behaviour.
2 rain as a major modulatory centre underlying feeding behaviour.
3 tides that regulate the sleep-wake cycle and feeding behaviour.
4 hes, which correspond to a more generalistic feeding behaviour.
5 takeout, influencing sex-specific mating and feeding behaviour.
6 omated and high-throughput quantification of feeding behaviour.
7 ression or ablation eliminates sugar-induced feeding behaviour.
8 e production and release from the liver, and feeding behaviour.
9 f body fat stores to adaptive adjustments of feeding behaviour.
10 roles in regulating growth, development and feeding behaviour.
11 ntrol the choice between social and solitary feeding behaviour.
12 -deficient mice show alterations of baseline feeding behaviour.
13 ctions in the mammalian brain, in particular feeding behaviour.
14 tinergic neurons exert a tonic inhibition of feeding behaviour.
15 ought to function as a central stimulator of feeding behaviour.
16 ch abolished optogenetically induced hedonic feeding behaviour.
17 andard model that captures the complexity of feeding behaviour.
18 esity in mice, with no change in movement or feeding behaviour.
19 y and quantity of prey might influence their feeding behaviours.
20 from zona incerta (ZI) for the regulation of feeding behaviours.
21 ventral tegmental area (VTA) encoded hedonic feeding behaviours.
22 basic drives (for example, for social versus feeding behaviour(1-3)) can exert potent influences on e
25 on of a single Fdg neuron induces asymmetric feeding behaviour and ablation of a single Fdg neuron di
30 in the diet, has important consequences for feeding behaviour and is a possible factor involved in f
32 unusual and unique context of the extra-oral feeding behaviour and pentaradial body plan of an echino
33 t rates, which provide insight into how host feeding behaviour and physiology may affect transmission
34 ring US04, indicating plasticity in reindeer feeding behaviour, and potentially overall increased lic
35 mptoms of depression, including dysregulated feeding behaviour, anhedonia and behavioural despair.
37 ghlights host traits related to movement and feeding behaviour as important determinants of whether s
38 vector arthropods differ in life histories, feeding behaviour as well as reproductive strategies, th
39 environmental tolerance and an opportunistic feeding behaviour, as assessed by the study of environme
41 let aggression by 30% and tended to increase feeding behaviour by 35% the first 24 h post-weaning.
42 vity of subcortical networks and to regulate feeding behaviour by dynamic reorganization of functiona
43 lony area is expected to impair its peculiar feeding behaviour by limiting the exploitable dimensiona
45 hat modifying rhythmic behaviours (including feeding behaviour) can dramatically impact the 24 h rhyt
47 cate that the interaction of temperature and feeding behaviour could be a major ecological determinan
48 ents and shows that the temporal dynamics of feeding behaviour depends on the severity and stage of t
50 ur analysis demonstrates that the changes in feeding behaviour evoked by the anorectic agents investi
51 from electrophysiological studies describing feeding behaviour experiments where resistance mechanism
54 mammalian brain to regulate many aspects of feeding behaviour, from food-seeking to meal termination
55 s system signalling mechanisms in regulating feeding behaviour have been largely uncharacterized.
58 n simulations, multiple but not preferential feeding behaviour in mosquitos reduced the accuracy of f
62 caudolateral orbital frontal cortex predict feeding behaviour independently of meal-related sensory
63 are well established, the interplay between feeding behaviour, infection and immune function remains
65 lammation, immune functions, mood disorders, feeding behaviour, neuroprotection, diabetes mellitus an
66 are keystone grazers in reef ecosystems, yet feeding behaviour of adults causes physical damage and m
71 hat stochastic resonance enhances the normal feeding behaviour of paddlefish (Polyodon spathula), whi
73 ndings resolve long debated questions on the feeding behaviour of Phytomyxea, suggesting an unrecogni
74 discuss how mycorrhizal fungi can affect the feeding behaviour of S. avenae in wheat, inducing suscep
76 nt, reproduction, attraction, settlement and feeding behaviour on two naturally susceptible varieties
77 brainstem, which in turn control elements of feeding behaviour operating on short and long timescales
79 ty and calcium imaging simultaneously during feeding behaviour reveals that the Fdg neurons respond t
80 hese differences support the hypothesis that feeding behaviour selects for specific gut bacterial com
81 precisely engaged to bidirectionally control feeding behaviours subject to, for example, social influ
82 s then excite brain regions known to mediate feeding behaviour, such as the lateral parabrachial nucl
83 ties, and provides information on the infant-feeding behaviours that were practised by prehistoric hu
84 ive neurons was causally linked to increased feeding behaviour; this effect was selective as, by cont
85 ng whole body energy balance by coordinating feeding behaviour through the hypothalamus in conjunctio
86 single Fdg neuron distorts the sugar-induced feeding behaviour to become asymmetric, indicating the d
87 indings indicate that dopamine adapts future feeding behaviour to the availability of food by signifi
88 e contribution of these distinct circuits to feeding behaviour using optogenetic and pharmacogenetic
89 eeders world-wide, indicating the changes in feeding behaviour we document here may not be sufficient
90 e species' entire spring activity season and feeding behaviours were quantified with camera traps at
92 filaria location are exploited by the vector feeding-behaviour whereas adult survival is enhanced by