ライフサイエンスコーパス: Lymnaea

1 wal [4, 5] and feeding [6] in the pond snail Lymnaea.

2 o 6.2 mM for Aplysia and 0.12 to 0.22 mM for Lymnaea.

3 In the isolated CNS of Lymnaea, a peptidergic neuron termed VD4 makes monosynap

4 Using the Lymnaea acetylcholine-binding protein as a surrogate of

5 that has the highest known affinity for the Lymnaea AChBP and also potently blocks the alpha7 nAChR

6 on are possible for approximately 56% of the Lymnaea AChBP sequence, covering primarily the outer sur

7 r of 4,6-disubstituted 2-aminopyrimidines to Lymnaea AChBP, with different molecular variants exhibit

8 ide that was purified and characterized from Lymnaea albumen gland extracts.

9 f nitric oxide (NO) production in the CNS of Lymnaea, an established model for molecular analysis of

10 In this work, homomeric AChBPs from Lymnaea and Aplysia snails were used as in situ template

11 ing substituted anabaseines with AChBPs from Lymnaea, Aplysia, and Bulinus species and correlated the

12 Secretions of the exocrine albumen gland of Lymnaea are packaged in the eggs of an egg mass before t

13 s contingent upon trophic factors present in Lymnaea brain-conditioned medium.

14 the albumen gland produces large amounts of Lymnaea epidermal growth factor.

15 the development of the embryo, for example, Lymnaea epidermal growth factor.

16 This is the maximum feeding rate of intact Lymnaea in sucrose.

17 In the snail, Lymnaea, motoneurons such as the B4, B8, and B4CL cells

18 atively damped swelling-tension responses of Lymnaea neurons (no BAPTA) were consistent with feedback

19 hods to measure Ca2+ channel inactivation in Lymnaea neurons-one method, based upon the conventional

20 t membrane tension of swelling and shrinking Lymnaea neurons.

21 In the feeding system of the mollusc Lymnaea, one of the best-studied rhythmical networks, in

22 Specifically, the electrically synapsed Lymnaea pedal dorsal A cluster neurons were used to stud

23 al approach, we demonstrate that the mollusc Lymnaea performs a sophisticated form of decision-making

24 g masses of the freshwater gastropod mollusc Lymnaea provide a microenvironment for developing embryo

25 e of a single-trial conditioning paradigm in Lymnaea solves this problem.

26 a soluble acetylcholine-binding protein from Lymnaea stagnali.

27 availability in the model freshwater species Lymnaea stagnalis (Gastropoda).

28 ith distinct pharmacological profiles [i.e., Lymnaea stagnalis (Ls) AChBP of low neonicotinoid and hi

29 2 and the acetylcholine-binding protein from Lymnaea stagnalis (Ls-AChBP) confirms Ls-AChBP as struct

30 , we chronically exposed freshwater snails ( Lymnaea stagnalis ) to synthetic water spiked with Cu th

31 alifornica, Pleurobranchaea californica, and Lymnaea stagnalis -three well-recognized models in cellu

32 erred to as model I, was built from both the Lymnaea stagnalis acetylcholine binding protein (AChBP)

33 constructed from the human alpha(7) AChR and Lymnaea stagnalis acetylcholine binding protein (AChBP),

34 tinic acetylcholine receptor (nAChR) and the Lymnaea stagnalis acetylcholine binding protein (Ls-AChB

35 L112Q, and M114T, into the binding pocket of Lymnaea stagnalis acetylcholine-binding protein (Ls-AChB

36 Lymnaea stagnalis efficiently accumulated (65)Cu after a

37 r and reward, and research on the pond snail Lymnaea stagnalis elucidated the role of a behavior-init

38 e of Cu were evaluated in the benthic grazer Lymnaea stagnalis following 4-5 h exposures to Cu adsorb

39 entity over a stretch of 294 residues with a Lymnaea stagnalis G-protein-linked receptor (LSGLR).

40 rates Gammarus pulex, Gammarus fossarum, and Lymnaea stagnalis illustrates the approach.

41 ly, we trained intact specimens of the snail Lymnaea stagnalis in a single conditioning trial using a

42 lower than reported for the freshwater snail Lymnaea stagnalis in similar experiments.

43 Lymnaea stagnalis is a model species that has relatively

44 ic behaviour we show that the feeding CPG of Lymnaea stagnalis is itself associated with another, and

45 ted during the maturation of the pond snail, Lymnaea stagnalis L., applying light and electron micros

46 The snail Lymnaea stagnalis produces a neuropeptide precursor prot

47 tral nervous system of the gastropod mollusk Lymnaea stagnalis produces a soluble protein that specif

48 re of the acetylcholine binding protein from Lymnaea stagnalis to model the chicken alpha7 agonist-bi

49 ntified neurons in the CNS of the pond snail Lymnaea stagnalis to study the role of endogenous NO sig

50 nervous system (CNS) of the freshwater snail Lymnaea stagnalis was conducted.

51 First, heterozygous (Dd) pond snails Lymnaea stagnalis were self-fertilised or backcrossed, a

52 re of the acetylcholine-binding protein from Lymnaea stagnalis with NS9283, a stoichiometry selective

53 these transposon families in the pond snail Lymnaea stagnalis, a cosmopolitan vector of trematodes i

54 re of the acetylcholine-binding protein from Lymnaea stagnalis, a nicotinic receptor surrogate.

55 protein (AChBP) from the fresh water snail, Lymnaea stagnalis, shows it to be a structural homolog o

56 using central neurons from the invertebrate Lymnaea stagnalis, we demonstrate that menin coordinates

57 te circuit generating feeding in the mollusk Lymnaea stagnalis, we identified three independent pathw

58 ontaining the learning circuits of the snail Lymnaea stagnalis.

59 bound to acetylcholine binding protein from Lymnaea stagnalis.

60 ferent identified neurons in the pond snail, Lymnaea stagnalis.

61 ng buccal neurons from the freshwater snail, Lymnaea stagnalis.

62 the binding protein previously derived from Lymnaea stagnalis.

63 e binding protein (AChBP) found in the snail Lymnaea stagnalis.

64 the isolated central nervous system (CNS) of Lymnaea stagnalis.

65 ed buccal feeding neurons in the pond snail, Lymnaea stagnalis.

66 ntral nervous system of the freshwater snail Lymnaea stagnalis.

67 etopleura, the limpet Tectura, and the snail Lymnaea, the MAPK pathway is activated in the 3D cell bu

68 rs to produce significant amounts of a novel Lymnaea trypsin inhibitor (LTI), a second peptide that w

69 Using the molluscan model system Lymnaea, we investigate here whether LTM formation is as

70 Using associative learning in Lymnaea, we show that reconsolidation after the retrieva