ライフサイエンスコーパス: skate

1 nce of molecular motors - a process we term 'skating'.

2 the homologue in a primitive vertebrate, the skate.

3 elios, and Eos in Raja eglanteria (clearnose skate), a cartilaginous fish that is representative of a

4 Three skate AE isoforms (skAEs) are expressed, and at least sk

5 e ability of the basic domain of dynactin to skate along microtubules is used by dynein to maintain l

6 Prominent expression of Ikaros in skate also is found in the lymphoid Leydig organ and epi

7 rall most closely resembles mu chains of the skate and human and a new putative antigen binding molec

8 How have North Sea skate and shark assemblages changed since the early 20th

9 Pectoral fins of skates and rays, such as the little skate (Batoid, Leuco

10 hal versus 1.1 to 20 for ringed seal, arctic skate, and beluga whale, respectively).

11 Cartilaginous fish (sharks, skates, and rays) are in the oldest taxon of extant jawe

12 r organization in elasmobranch fish (sharks, skates, and rays) differs from that in other vertebrates

13 lved at all swimming speeds in the clearnose skate; and (iii) critical swimming protocols might misre

14 Sharks and skates are representatives of the earliest vertebrates w

15 ewer recreational activities such as in-line skating, are rapidly gaining the recognition they deserv

16 fins of skates and rays, such as the little skate (Batoid, Leucoraja erinacea), show a strikingly un

17 nic anions and steroids, including the major skate bile salt, scymnol sulfate.

18 In addition, in the skate but not the rat retina, retinal pigment epithelial

19 gous sequences from tetrapods, zebrafish and skate can drive reporter gene expression in mouse limbs

20 nel and rectifying Kv channel predicted from skate (cartilaginous fish) ampullary organ electrophysio

21 long-term declines, and the largest (common skate complex) became locally extirpated (as did angelsh

22 family revealed that perch Cx35 and Cx34.7, skate Cx35, and mouse Cx36 constitute a novel gamma subg

23 critically endangered species such as common skate (Dipturus batis) and angelshark (Squatina squatina

24 Upon hypotonic volume expansion, skate erythrocytes lose solutes via a pathway that requi

25 Skate erythrocytes possess numerous tyrosine kinases inc

26 Hypotonic volume expansion of skate erythrocytes rapidly stimulates the tyrosine phosp

27 OSTalpha-OSTbeta pairs from human, mouse, or skate) generated robust estrone 3-sulfate transport acti

28 Skate hepatocyte cDNA was amplified with degenerate olig

29 protein in the KI-IOV was identified as the skate homolog of the mammalian red cell anion exchanger

30 an unusual Sec tail, which is orthologous to skate IgX(short) cDNA.

31 22.5 million people participating in in-line skating in the United States in 1995, about 100,000 were

32 rentiation; it is found, in both the rat and skate, in the ventricular space that ultimately becomes

33 w pads, knee pads, and helmets in preventing skating injuries.

34 clasper development from pelvic fins of male skates is controlled by hormonal regulation of the Sonic

35 Further analyses showed that microtubule skating is a form of one-dimensional diffusion along the

36 s of the shark Scyliorhinus canicula and the skate Leucoraja erinacea and the absence of all HoxC gen

37 nts of the jaw, hyoid and gill arches of the skate Leucoraja erinacea derive from molecularly equival

38 expressed by electrosensory cells in little skate (Leucoraja erinacea) and functionally couple to me

39 he gills of a cartilaginous fish, the little skate (Leucoraja erinacea), are in fact endodermally der

40 embryos of a cartilaginous fish, the little skate (Leucoraja erinacea).

41 DiI tracing for up to 70 days in the little skate, Leucoraja erinacea, we show that lateral line pla

42 ction product was found and used to screen a skate liver cDNA library.

43 Thus, the skate liver P2Y receptor functions as a primitive P2Y AT

44 y analysis of nucleotide alignments show the skate opsin to be homologous to other rod opsins.

45 the similarity of the cytoplasmic domains of skate opsin to those of blue-sensitive visual pigments.

46 n action resembling that of flatfish such as skates or rays.

47 Skate orthologs of mammalian GATA-3, GATA-1, EBF-1, Pax-

48 Srds represents the skate orthologue of mammalian peripherin/rds genes.

49 Human, mouse, and skate OSTalpha proteins are predicted to contain seven t

50 human P2Y(2), rat P2Y(6), human P2Y(11), or skate P2Y receptors in oocytes resulted in modulation of

51 ply ancestral patterns of gene expression in skate pectoral fins, shedding light on the molecular mec

52 The 5' and 3' untranslated regions of the skate peripherin/rds (srds) cDNA were isolated by the ra

53 To determine the cellular function of the skating phenomenon, dynein and the dynactin microtubule-

54 Cartilaginous fishes (e.g., sharks and skates) possess a postcranial dermal skeleton consisting

55 to functionally complement the corresponding skate proteins by measuring transport of [3H]estrone 3-s

56 The all-rod retina of skate provides a comparatively simple system in which to

57 The tissue-specific expression patterns of skate PU.1 and Spi-C suggest that these genes share regu

58 s are highly conserved between mammalian and skate PU.1, in marked contrast to lamprey Spi, in which

59 sed a negatively buoyant fish, the clearnose skate Raja eglanteria, and took two approaches: a classi

60 heteroclitus), two elasmobranch species (the skate Raja erinacea and the dogfish Mustelus canis), and

61 ce suggests that hepatocytes from the little skate Raja erinacea express a primitive P2Y ATP receptor

62 rily primitive marine vertebrate, the little skate Raja erinacea, was screened for taurocholate trans

63 t diverging jawed vertebrates, the clearnose skate (Raja eglanteria).

64 Volume expansion of little skate (Raja erinacea) erythrocytes increases the affinit

65 Skates (Raja erinacea and R. ocellata) are among the few

66 a proteins recently identified in the little skate, Raja erinacea, even though the latter exhibit onl

67 In the little skate, Raja erinacea, the electrosensory primary afferen

68 Chondrichthyans (sharks, skates, rays and holocephalans) possess paired appendage

69 ep in the volume-activated taurine efflux in skate red cells.

70 Sharks and skates represent the earliest vertebrates with an adapti

71 ast two of the four Ikaros family members in skate resemble the patterns observed in mammals, i.e., i

72 Both immunohistochemistry in the adult skate retina and in situ hybridizations in the adult rat

73 ve cloned and analyzed the opsin cDNA from a skate retina library.

74 molecular basis of visual adaptation in the skate retina, we have cloned and analyzed the opsin cDNA

75 uxes from horizontal cells isolated from the skate retina.

76 A skate retinal cDNA library was screened using a mouse pe

77 ue of peripherin/rds was identified from the skate retinal cDNA library.

78 bridization to clone a novel connexin from a skate retinal cDNA library.

79 indicate alterations in the interactions of skate rhodopsin with other proteins in the phototransduc

80 However, skate rods are unusual in that they are capable of adapt

81 in the posterior half of the pectoral fin of skate, shark, and zebrafish but in the anterior side of

82 enerate primers and R. eglanteria (clearnose skate) spleen cDNA as template.

83 The receptor was expressed widely in skate tissue and was expressed to a similar extent in ot

84 on and fate-mapping approaches in the little skate to demonstrate that Shh secretion from a signallin

85 mobranch fishes, including sharks, rays, and skates, use specialized electrosensory organs called amp

86 had and whether or not they performed trick skating, was 9.5 (95 percent confidence interval, 2.6 to

87 rovided by batoid fish such as stingrays and skates, we created a biohybrid system that enables an ar

88 earned a motor skill, such as cycling or ice-skating, we can rapidly generalize to novel tasks, such

89 ically isolated external horizontal cells of skate were examined using whole-cell voltage-clamp techn