ライフサイエンスコーパス: abalone

1 ies of harvested, threatened, and endangered abalone.

2 ore distantly related gastropod, the Chilean abalone.

3 oth proteins from five species of California abalones.

4 ich are important fishery resources (such as abalones and red sea urchins), and they are harvested fo

5 specific gamete recognition proteins in both abalones and sea urchins, we predict that positive selec

6 ractants in red and green (Haliotis fulgens) abalone are only minor contributors to maintaining repro

7 High pressure processing (HPP) of post-rigor abalone at 300MPa for 10min extended the refrigerated sh

8 material of the shells of pearl oysters and abalone, consists mostly of aragonite (a form of CaCO3),

9 of the egg coat [vitelline envelope (VE)] of abalone eggs and to provide preliminary evidence regardi

10 n effectively doubles the target size of red abalone eggs, which in turn significantly increases fert

11 ow selection has acted on VE proteins during abalone evolution.

12 Lysins from seven California abalone exhibit species-specificity in binding to their

13 nducible factor-1beta (HIF-1beta) from small abalone Haliotis diversicolor were cloned.

14 Red abalone (Haliotis rufescens) nacre is a layered composit

15 We then evaluated abalone (Haliotis rufescens) settlement under ambient co

16 f L-tryptophan as a potent attractant to red abalone (Haliotis rufescens) sperm affords the opportuni

17 For red abalone (Haliotis rufescens), a large marine snail, the

18 front of nacre in gastropod shells from red abalone (Haliotis rufescens), using synchrotron spectrom

19 NA sequence (11,166 bp) of VERL from the red abalone (Haliotis rufescens).

20 coat of the non-vertebrate marine gastropod abalone (Haliotis spp.) is also known to contain a ZP do

21 ion proteins, lysin and 18-kDa protein, from abalone (Haliotis).

22 trea gigas (Bivalvia, Mollusca), the Pacific abalone, Haliotis discus hannai (Gastropoda, Mollusca),

23 layer of the shell and pearl produced by the abalone, Haliotis rufescens, a marine gastropod mollusc.

24 erm lysin dimer from Haliotis fulgens (green abalone) has been determined to 1.71 A by multiple isomo

25 on segments were sequenced from multiple red abalone individuals collected over a 1,200-km range.

26 h is illustrated with simulated data and the abalone lysin sperm data.

27 all fold of sp18 is similar to that of green abalone lysin; however, the surface features of the prot

28 Shucked abalone meats were processed at 100 or 300MPa for 5 or 1

29 he mixture of EDTA-soluble proteins found in abalone nacre are known to cause the nucleation and grow

30 Surprisingly, the abalone nacre data show the same ACC phases that are pre

31 ed in the pure system by nanomolar levels of abalone nacre proteins.

32 Here we report that bone, like abalone nacre, contains polymers with 'sacrificial bonds

33 toughness of another biocomposite material, abalone nacre, has been found.

34 a of peptides from purified VE proteins with abalone ovary EST sequences, identifying 9 of 10 ZP doma

35 rtality event, and its genetic effects on an abalone population.

36 the lysin dimer from Haliotis rufescens (red abalone) reveal a similar overall fold and conservation

37 Abalone settlement and metamorphosis increased from 11%

38 ed growth during exposure to increased pCO2, abalone settlement was unaffected by prior CCRA exposure

39 lcite seed crystal after the introduction of abalone shell proteins.

40 ably similar to biomineral structures in red abalone shells) and complex bilayers showing in situ col

41 s of natural materials, such as spider silk, abalone shells, and bone, has provided great insight int

42 e, we present the crystal structure of green abalone sp18 resolved to 1.86 A.

43 on mtDNA differentiation, four north Pacific abalone species diverged within the past 2 million years

44 n solved and the sequences of lysins from 20 abalone species have been determined.

45 complex and a sperm lysin alignment from 25 abalone species.

46 8 is an 18 kDa protein that is released from abalone sperm during the acrosome reaction.

47 Abalone sperm lysin is a 16 kDa acrosomal protein used b

48 Abalone sperm lysin is a 16-kDa acrosomal protein, which

49 Abalone sperm lysin is a nonenzymatic, 16-kDa protein th

50 se was strongly supported by our reanalysis (abalone sperm lysin), and one was weakly supported (babo

51 is evolutionarily related to lysin, a 16 kDa abalone sperm protein that dissolves the vitelline envel

52 Abalone sperm use 16 kDa lysin to create a hole in the e

53 In abalone, sperm lysin evolves rapidly by positive Darwini

54 The abalone spermatozoon has a large acrosomal vesicle conta

55 Studied most extensively in the abalone system, coevolution between adaptively diverging

56 he mature oocyte and propose that, as in the abalone system, concerted evolution may be involved in a

57 In abalone, the sperm protein lysin species-specifically cr

58 an sardine, prawn (six species), barramundi, abalone (three species), blue sprat, burrowing blackfish

59 Because abalone typically live in dense, multispecies aggregatio

60 er species shows that repeats 1 and 2 of red abalone VERL have not been subjected to concerted evolut

61 We found that otters feeding on abalone, which is the preferred prey in a resource-abund

62 dundancy in genera of CCRA providing cues to abalone, which may further buffer OA effects.

63 ficantly increase refrigerated shelf-life of abalone without affecting chemical or physical quality c