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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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