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1 r prospecting in poorly studied species like elasmobranchs.
2 f blood-feeding marine parasites of fish and elasmobranchs.
3 acellular proteins in the urea-rich cells of elasmobranchs.
4  in holocephalans is more similar to that of elasmobranchs.
5 irst homologs of MAGP1 in monotremes, birds, elasmobranchs and agnathans, and the first MAGP2 genes i
6  fish pallium may be more segregated than in elasmobranchs and anurans and have some surprising simil
7 y between the separate profundal ganglion of elasmobranchs and basal actinopterygians and the ophthal
8 olute concentrated in the urea-rich cells of elasmobranchs and coelacanth to offset the damaging effe
9 orm of supplemental provisioning utilized by elasmobranchs and variation in reproductive modes likely
10 s of rapid evolution in the amphibia and the elasmobranchs, and several bursts in the teleosts.
11                          If sharks and other elasmobranchs are similarly affected, this could have si
12 es in the distribution and occurrence of the elasmobranch assemblage of the southern North Sea, based
13 ), another well-known protective osmolyte of elasmobranchs, at 0.1-0.3 mol L(-1) was also confirmed u
14 e potential importance of biofluorescence in elasmobranch behavior and biology.
15 rimates, marine and terrestrial mammals, and elasmobranchs but does not recognize insulin.
16  inferred from single-molecule studies of an elasmobranch Cl(-) channel and later confirmed by crysta
17 n the future; therefore, parallel changes in elasmobranch communities in other regions are to be expe
18 The repeated evolution of biofluorescence in elasmobranchs, coupled with a visual adaptation to detec
19  (PCBs), but has not been well documented in elasmobranchs despite their propensity to accumulate hig
20 mined neurexins in the electric organ of the elasmobranch electric fish.
21                                          The elasmobranch electrosensory system is the most thoroughl
22                   Oculomotor organization in elasmobranch fish (sharks, skates, and rays) differs fro
23 systems such as the ampullae of Lorenzini of elasmobranch fish are involved, these results strongly s
24  act as salinity sensors in both teleost and elasmobranch fish.
25 suggest a loss of the entire HoxC cluster in elasmobranch fishes and represent evidence for the natur
26                                              Elasmobranch fishes are among a broad range of taxa beli
27                                              Elasmobranch fishes, including sharks, rays, and skates,
28 d sensitivity in living organisms, including elasmobranch fishes, is the result of a highly evolved,
29 characterised in teleost fish and studies in elasmobranchs have failed to identify nociceptors.
30 s-1970s, and historical target fisheries for elasmobranchs; (ii) climate change, currently favouring
31 e hypothesis that the reticular formation of elasmobranches is complexly organized into many of the s
32 icture of trunk neural crest development for elasmobranchs is yet to be developed.
33 likely influences the extent to which female elasmobranchs may maternally offload contaminants.
34 und stingray (Urobatis halleri) as a coastal elasmobranch model, we examined maternal offloading proc
35 er this innervation pattern is unique to the elasmobranchs, or is the ancestral pattern for cartilagi
36 , here documented to have impacted North Sea elasmobranchs over the past century, are likewise impact
37          Two main conditions are observed in elasmobranchs (shark and rays) and osteichthyans (bony f
38  with respect to branchial ray distribution--elasmobranchs (sharks and batoids) possess a series of r
39                                              Elasmobranchs (sharks and rays) first appeared >400 mill
40 t (the killifish Fundulus heteroclitus), two elasmobranch species (the skate Raja erinacea and the do
41 stem cell line derived from the embryo of an elasmobranch, the spiny dogfish shark S. acanthias.
42  a representative of the sister group to the elasmobranchs, the holocephalans (ratfish).
43 or inferring habitat residency of euryhaline elasmobranchs via chemical analysis of vertebrae.
44 a concentrations found in urea-rich cells of elasmobranches, we have found time-dependent effects on
45 rine, here reported for the first time in an elasmobranch, which was present at substantially lower c

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