ライフサイエンスコーパス: hagfish

1 ish (cyclostomes, represented by lamprey and hagfish).

2 metals can be taken up by the integument of hagfish.

3 ecame cyclostomes, which include lamprey and hagfish.

4 VLR genes (VLRA and VLRB) have been found in hagfish.

5 d are orthologs of Wnt9 genes from shark and hagfish.

6 g, striped bass, thresher shark, and Pacific hagfish.

7 two VLR isotypes occurs in both lampreys and hagfishes.

8 ste buds was previously known in the skin of hagfishes.

9 like cells, but not on erythrocytes from the hagfish, a primitive agnathan vertebrate lacking markers

10 Features of ECs that are shared between hagfish and gnathostomes can be inferred to have already

11 The last common ancestor of hagfish and gnathostomes was also the last common ancest

12 possibility of convergent evolution between hagfish and gnathostomes.

13 ation pattern whereas primitive vertebrates (hagfish and lamprey) have patterns that are typical of v

14 As such, the genomes of the jawless fish (hagfish and lamprey) offer the best possibility for find

15 Hagfish and lampreys are the only living representatives

16 studies recover a monophyletic Cyclostomata (hagfish and lampreys as closest relatives).

17 surveys, that Cyclostomata is monophyletic: hagfish and lampreys share 4 unique microRNA families, 1

18 he living jawless vertebrates (cyclostomes), hagfishes and lampreys, provide scarce information about

19 yclostomes (jawless vertebrates-lampreys and hagfish) and gnathostomes (jawed vertebrates-cartilagino

20 microRNA expression patterns among lamprey, hagfish, and gnathostome organs, implying that the role

21 ) of jawless vertebrates such as lamprey and hagfish are composed of highly diverse modular leucine-r

22 Lampreys and hagfish are primitive jawless vertebrates capable of mou

23 Lamprey and hagfish are surviving representatives of the most ancien

24 ing jawless vertebrates such as lampreys and hagfishes, are the sister group of living jawed vertebra

25 was obtained from mRNA isolated from Pacific hagfish brain using rapid amplification of cDNA ends (RA

26 Lampreys and hagfishes, by contrast, are thought to have noncollageno

27 n, mouse Down syndrome critical region 1, or hagfish coagulation factor X genes.

28 y have consequences for human health through hagfish consumption.

29 The defensive slime of hagfishes contains thousands of intermediate filament pr

30 l of this study was to determine whether the hagfish endothelium displays phenotypic heterogeneity.

31 Here we show that the brain of the inshore hagfish (Eptatretus burgeri), another cyclostome group,

32 g an in vitro technique, the skin of Pacific hagfish (Eptatretus stouti) was shown to take up nickel

33 Indeed, Pacific hagfish exposed acutely to severe sustained hypercarbia

34 uirts, the closest invertebrate relatives of hagfish, failed to reveal evidence of an intact vwf gene

35 fish, and further studies of the lamprey and hagfish genomes will determine just how explosive the Bi

36 As in the Sea lamprey, the incomplete hagfish germ-line VLR-A and -B genes are modified in lym

37 In contrast, we found hagfish gills to be associated with a tremendous capacit

38 ver, in the most basal extant craniates, the hagfishes, gills play only a minor role in gas exchange.

39 This sensory modality of hagfishes has no direct homolog in vertebrates and appea

40 surviving jawless vertebrates, lampreys and hagfish, instead solved the receptor diversification pro

41 Cyclostomes, the lampreys and hagfish, instead use leucine-rich repeat proteins to con

42 immunity in jawless vertebrates (lamprey and hagfish) is mediated by lymphocytes that undergo combina

43 te systems and the Schreiner organ system of hagfishes, it is concluded that Schreiner organs are not

44 Assay of hagfish liver demonstrated vitamin K-dependent carboxyla

45 e of Xenopus lymphocytes and tumor cells and hagfish lymphocyte-like cells by a process that requires

46 fish (Opsanus tau), chicken (Gallus gallus), hagfish (Myxine glutinosa), horseshoe crab (Limulus poly

47 nctional vwf gene is present in the Atlantic hagfish, Myxine glutinosa We found a single vwf transcri

48 brates and appears to be a specialization of hagfishes, perhaps derived from the primitive somatosens

49 wf formed high-molecular-weight multimers in hagfish plasma and in stably transfected CHO cells.

50 The hagfish sequence showed low conservation with the mammal

51 ad analogs, and end with a discussion of how hagfish slime may have evolved.

52 e orthologous VLR genes in both lampreys and hagfish suggests that this anticipatory receptor system

53 Lamprey and hagfish, the extant jawless vertebrates, have an alterna

54 Lamprey and hagfish, the living representatives of jawless vertebrat

55 nd the presence of two types of VLR genes in hagfish, the only other order of contemporary jawless ve

56 of vertebrate cartilage, and we report that hagfishes, the sister group to lampreys, also have Col2a

57 Hagfishes thwart attacks by fish predators by producing

58 Immunohistochemical analyses of hagfish tissues and blood revealed Vwf expression in end

59 Electron microscopic studies of hagfish tissues demonstrated the presence of Weibel-Pala

60 ylogenetic analysis indicate that the unique hagfish VLR is the counterpart of lamprey VLRA and the p

61 Here we have identified a third hagfish VLR, which undergoes somatic assembly to generat

62 f lamprey VLRA and the previously identified hagfish "VLRA" is the lamprey VLRC counterpart.

63 Hagfish Vwf formed high-molecular-weight multimers in ha

64 The sequence of the Pacific hagfish was most homologous with the human mu opioid rec

65 for a burrowing, benthic scavenger, such as hagfish, which are likely to be exposed to relatively en

66 Lampreys and hagfish, which together are known as the cyclostomes or