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1 ies of harvested, threatened, and endangered abalone.
2 ore distantly related gastropod, the Chilean abalone.
3 slow-growth, temperate invertebrates such as abalone.
4 fects pigs, and abalone virus, which infects abalone.
5 oth proteins from five species of California abalones.
6 nica caused increased iodine accumulation in abalone, accompanied by reduced synthesis of thyroid hor
7 ing future restoration aquaculture for pinto abalone and determining their ideal habitat and potentia
8 bility of early life history stages of pinto abalone and inform hatchery practices under future clima
9 o OA is critical to the continued success of abalone and other shellfish production, and these mitiga
10 ich are important fishery resources (such as abalones and red sea urchins), and they are harvested fo
11 specific gamete recognition proteins in both abalones and sea urchins, we predict that positive selec
12 ractants in red and green (Haliotis fulgens) abalone are only minor contributors to maintaining repro
13 age that includes African swine fever virus, abalone asfarvirus, and giant viral sequences recently f
14 High pressure processing (HPP) of post-rigor abalone at 300MPa for 10min extended the refrigerated sh
15 increases in the energetic demands of pinto abalone caused by ocean acidification during winter will
16 material of the shells of pearl oysters and abalone, consists mostly of aragonite (a form of CaCO3),
17 on Survey and four other datasets (Tasmanian Abalone data, Boston Housing crime rate data, Los Angele
18 viduals.m(2)), biomass, number of aggregated abalone, egg production, and proportion of individuals b
19 of the egg coat [vitelline envelope (VE)] of abalone eggs and to provide preliminary evidence regardi
20 n effectively doubles the target size of red abalone eggs, which in turn significantly increases fert
23 g in the closure in 2018 of the recreational abalone fishery worth an estimated $44 M and the collaps
24 ulation, strong RCP scenarios can affect red abalone growth as well as reduce fertilization during ex
25 We evaluated the population status of green abalone, H. fulgens, by conducting (1) an assessment of
28 ntative marine benthic invertebrate, the red abalone Haliotis rufescens, to a highly varying multi-st
32 s entire mollusk shells from red and rainbow abalone (Haliotis rufescens and Haliotis iris) at variou
33 i(A) with physiological measurements for red abalone (Haliotis rufescens) and purple urchin (Strongyl
36 f L-tryptophan as a potent attractant to red abalone (Haliotis rufescens) sperm affords the opportuni
38 the effects of OA on two populations of red abalone (Haliotis rufescens), a marine mollusc important
39 front of nacre in gastropod shells from red abalone (Haliotis rufescens), using synchrotron spectrom
41 coat of the non-vertebrate marine gastropod abalone (Haliotis spp.) is also known to contain a ZP do
43 trea gigas (Bivalvia, Mollusca), the Pacific abalone, Haliotis discus hannai (Gastropoda, Mollusca),
44 layer of the shell and pearl produced by the abalone, Haliotis rufescens, a marine gastropod mollusc.
46 erm lysin dimer from Haliotis fulgens (green abalone) has been determined to 1.71 A by multiple isomo
48 on segments were sequenced from multiple red abalone individuals collected over a 1,200-km range.
51 all fold of sp18 is similar to that of green abalone lysin; however, the surface features of the prot
54 he mixture of EDTA-soluble proteins found in abalone nacre are known to cause the nucleation and grow
59 a of peptides from purified VE proteins with abalone ovary EST sequences, identifying 9 of 10 ZP doma
60 by conducting (1) an assessment of the green abalone population around Guadalupe Island through subti
61 work, we report for the first time the green abalone population status at Guadalupe Island and a posi
63 MRs combined with good management could help abalone populations in the short term in Guadalupe Islan
65 the lysin dimer from Haliotis rufescens (red abalone) reveal a similar overall fold and conservation
66 ts are disproportionally deleterious for red abalone, revealing how species-specific physiologies mod
68 ed growth during exposure to increased pCO2, abalone settlement was unaffected by prior CCRA exposure
70 ably similar to biomineral structures in red abalone shells) and complex bilayers showing in situ col
71 s of natural materials, such as spider silk, abalone shells, and bone, has provided great insight int
72 ive aquaculture conditions demonstrated that abalone sourced from a strong upwelling region were tole
74 on mtDNA differentiation, four north Pacific abalone species diverged within the past 2 million years
76 o abalone (Haliotis kamtschatkana), the only abalone species native to Washington, declined by 97% in
82 se was strongly supported by our reanalysis (abalone sperm lysin), and one was weakly supported (babo
83 is evolutionarily related to lysin, a 16 kDa abalone sperm protein that dissolves the vitelline envel
89 he mature oocyte and propose that, as in the abalone system, concerted evolution may be involved in a
91 an sardine, prawn (six species), barramundi, abalone (three species), blue sprat, burrowing blackfish
94 er species shows that repeats 1 and 2 of red abalone VERL have not been subjected to concerted evolut
99 ficantly increase refrigerated shelf-life of abalone without affecting chemical or physical quality c