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1 tides that regulate the sleep-wake cycle and feeding behaviour.
2 hes, which correspond to a more generalistic feeding behaviour.
3 takeout, influencing sex-specific mating and feeding behaviour.
4 omated and high-throughput quantification of feeding behaviour.
5 ression or ablation eliminates sugar-induced feeding behaviour.
6 e production and release from the liver, and feeding behaviour.
7 f body fat stores to adaptive adjustments of feeding behaviour.
8 roles in regulating growth, development and feeding behaviour.
9 ntrol the choice between social and solitary feeding behaviour.
10 -deficient mice show alterations of baseline feeding behaviour.
11 ctions in the mammalian brain, in particular feeding behaviour.
12 tinergic neurons exert a tonic inhibition of feeding behaviour.
13 ought to function as a central stimulator of feeding behaviour.
14 rain as a major modulatory centre underlying feeding behaviour.
16 on of a single Fdg neuron induces asymmetric feeding behaviour and ablation of a single Fdg neuron di
20 in the diet, has important consequences for feeding behaviour and is a possible factor involved in f
21 t rates, which provide insight into how host feeding behaviour and physiology may affect transmission
22 mptoms of depression, including dysregulated feeding behaviour, anhedonia and behavioural despair.
24 ghlights host traits related to movement and feeding behaviour as important determinants of whether s
25 environmental tolerance and an opportunistic feeding behaviour, as assessed by the study of environme
26 vity of subcortical networks and to regulate feeding behaviour by dynamic reorganization of functiona
29 ents and shows that the temporal dynamics of feeding behaviour depends on the severity and stage of t
32 mammalian brain to regulate many aspects of feeding behaviour, from food-seeking to meal termination
33 s system signalling mechanisms in regulating feeding behaviour have been largely uncharacterized.
38 caudolateral orbital frontal cortex predict feeding behaviour independently of meal-related sensory
41 hat stochastic resonance enhances the normal feeding behaviour of paddlefish (Polyodon spathula), whi
42 discuss how mycorrhizal fungi can affect the feeding behaviour of S. avenae in wheat, inducing suscep
44 nt, reproduction, attraction, settlement and feeding behaviour on two naturally susceptible varieties
46 ty and calcium imaging simultaneously during feeding behaviour reveals that the Fdg neurons respond t
47 hese differences support the hypothesis that feeding behaviour selects for specific gut bacterial com
48 s then excite brain regions known to mediate feeding behaviour, such as the lateral parabrachial nucl
49 ng whole body energy balance by coordinating feeding behaviour through the hypothalamus in conjunctio
50 single Fdg neuron distorts the sugar-induced feeding behaviour to become asymmetric, indicating the d
51 indings indicate that dopamine adapts future feeding behaviour to the availability of food by signifi
52 e contribution of these distinct circuits to feeding behaviour using optogenetic and pharmacogenetic
54 filaria location are exploited by the vector feeding-behaviour whereas adult survival is enhanced by
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