ライフサイエンスコーパス: dogfish

1 , while the average myosin head stiffness of dogfish (1.98 +/- 0.31 pN nm(-1)) is smaller than that o

2 es, and the gene content is identical in the dogfish, a member of the most basally branching lineage

3 We cloned the sAC ortholog from the dogfish, a shark that regulates blood A/B by absorbing a

4 The longer thin filaments in dogfish account for only part of this difference.

5 bipolar cells in both cartilaginous fishes (dogfish) and urodeles (salamanders), rod OFF bipolar cel

6 ased (spotted and starry ray, lesser-spotted dogfish) as did smooth-hound, likely benefiting from gre

7 the mammalian C/EBP alpha) to the two spiny dogfish C/EBP binding sequences are described.

8 shark Scyliorhinus canicula (lesser-spotted dogfish/catshark).

9 r example, Gly-ir cells were observed in the dogfish cerebellum, unlike the case in the Siberian stur

10 due (an amino acid found at position 1424 in dogfish CFTR) did not perturb AP-2 binding.

11 the region flanking the 5' end of the spiny dogfish CPSase III gene.

12 e promoter region, which suggests that spiny dogfish CPSase III might be subjected to transactivation

13 hough we did not detect lateral fin folds in dogfish embryos, Engrailed-1 expression suggests that th

14 Chondrichthyan dogfish embryos, however, use the primitive mechanism of

15 brates, we did not detect Shh transcripts in dogfish fin-buds, although dHand (a gene involved in est

16 Comparison of dogfish Gly-ir cell populations with those reported for

17 hey may contain chicken-GnRH-II (GnRH-II) or dogfish GnRH.

18 Gly-ir populations in the dogfish hypothalamus and telencephalon are notable in co

19 III (CPSase III) of Squalus acanthias (spiny dogfish) is a nuclear-encoded mitochondrial enzyme that

20 vestigated the conformation of NAD+ bound to dogfish lactate dehydrogenase (LDH) by using an NMR expe

21 species in certified reference materials of dogfish liver (DOLT-3) and dogfish muscle (DORM-2).

22 at, cod muscle, Greenland halibut muscle and dogfish liver (NRCC DOLT-4), with MMHg concentrations ra

23 Accuracy was evaluated using dogfish liver certified reference material (DOLT-3 NRC)

24 o check the accuracy of the method, "DOLT-5: Dogfish Liver" standard reference material was used and

25 ed method was evaluated by analyzing "DOLT:5 Dogfish Liver", "NIST SRM 1640a Trace elements in natura

26 Certified reference materials (CRM) DOLT-4 (Dogfish Liver) and TORT-2 (Lobster Hepatopancreas), and

27 The detailed structural analysis of dogfish MBP including several posttranslational modifica

28 ence materials of dogfish liver (DOLT-3) and dogfish muscle (DORM-2).

29 nch species (the skate Raja erinacea and the dogfish Mustelus canis), and a jawless fish (the lamprey

30 ) > sandbar (Carcharhinus plumbeus) > smooth dogfish (Mustelus canis).

31 impair odor tracking behavior of the smooth dogfish (Mustelus canis).

32 separations performed on tryptic digests of dogfish myelin basic protein (MBP) where eluting peaks 4

33 tractions of permeabilized white fibres from dogfish myotomal muscle at their physiological temperatu

34 e-clamped 'on' bipolar cells in dark-adapted dogfish retinal slices.

35 e-clamped 'on' bipolar cells in dark-adapted dogfish retinal slices.

36 obtained from bipolar cells in dark-adapted dogfish retinal slices.

37 r hair cells located in the labyrinth of the dogfish Scyliorhinus canicula, and find that it modulate

38 diffraction, to fast-twitch fibres from the dogfish (Scyliorhinus canicula).

39 previously isolated from the tissues of the dogfish shark (Squalus acanthias) and the sea lamprey (P

40 to isolate a 4.1-kb cDNA encoding a 1,027-aa dogfish shark (Squalus acanthias) kidney CaR.

41 shark (Carcharhinus limbatus), and the spiny dogfish shark (Squalus acanthias).

42 rom the embryo of an elasmobranch, the spiny dogfish shark S. acanthias.

43 nt deformable versions of the intestine of a dogfish shark, based on a tomogram of a biological sampl

44 sly isolated a V-NAR from an immunized spiny dogfish shark, named E06, that binds specifically and wi

45 developmental biology of the lesser spotted dogfish shark, Scyliorhinus canicula, make it ideal for

46 The oldest CFTR ortholog identified is from dogfish shark, which retains similar structural and func

47 low patterns in the wakes of freely swimming dogfish sharks and find that they have a ring-within-a-r

48 Corneas of rabbits and spiny dogfish sharks were de-epithelialized mechanically, subj

49 hair cells, we investigated inner ears from dogfish sharks, zebrafish, bullfrogs, Xenopus, turtles,

50 Similar to mammalian sAC, dogfish soluble adenylyl cyclase (dfsAC) is activated by

51 majority of samples were identified as Spiny Dogfish (Squalus acanthias), which is critically endange

52 the total myosin head working stroke in the dogfish than in the frog.

53 e cartilaginous fish, Scyliorhinus canicula (dogfish) using scanning electron microscopy and investig

54 pulations in the brain of the lesser spotted dogfish were studied by a glycine immunofluorescence met

55 contrast, the potential for overlap of spiny dogfish with prey species was enhanced by warming, expan

56 placodes and cranial sensory ganglia in the dogfish, with a focus on the epibranchial and lateral li

57 omparative morphometric analysis in lamprey, dogfish, zebrafish and mouse, we propose that elongation