ライフサイエンスコーパス: Petromyzon

1 n Ikaros-related gene has been identified in Petromyzon marinus (sea lamprey), a jawless vertebrate s

2 phalochordates (Branchiostoma), but occur in Petromyzon marinus (Sea Lamprey), a jawless vertebrate.

3 has been identified in a jawless vertebrate, Petromyzon marinus (sea lamprey).

4 the sequences of the Y1-subtype receptor of Petromyzon marinus and Lampetra fluviatilis to study the

5 orded from photoreceptors of the sea lamprey Petromyzon marinus and show that their rods have a singl

6 unit transcript was found in the sea lamprey Petromyzon marinus cDNA library.

7 ced cytidine deaminase-based CBE(7), and the Petromyzon marinus cytidine deaminase-based CBE Target-A

8 utants of the major Hb component, PMII, from Petromyzon marinus have been measured to test these mode

9 tch up to 75% of tagged invasive sea lamprey Petromyzon marinus in free-flowing streams.

10 Here, we show that sea lampreys (Petromyzon marinus L.) have cutaneous papillae located a

11 have been characterized in the sea lamprey (Petromyzon marinus L.), a basal vertebrate.

12 coding putative GHR and PRLR in sea lamprey (Petromyzon marinus) and Arctic lamprey (Lethenteron camt

13 rd, the NCBI Trace database for the lamprey (Petromyzon marinus) contains more than 18 million raw DN

14 steroids in vivo and ex vivo in sea lamprey (Petromyzon marinus) during the critical metamorphic peri

15 The hemoglobins of the Sea Lamprey (Petromyzon marinus) exist in an equilibrium between low

16 The sea lamprey (Petromyzon marinus) is a genetically programmed animal m

17 Here, we show in lampreys (Petromyzon marinus) of either sex that incremental stimu

18 Invasive sea lamprey (Petromyzon marinus) populations in North America have be

19 instem muscarinoceptive neurons in lampreys (Petromyzon marinus) that received parallel inputs from t

20 he basal jawless vertebrate the sea lamprey (Petromyzon marinus) to gain insight into its evolutionar

21 d brain responses of parasitic sea lampreys (Petromyzon marinus) to weak electric fields.

22 and two animal trajectories - a sea lamprey (Petromyzon marinus) tracked for 12 h and a wolf (Canis l

23 The lamprey (Petromyzon marinus) undergoes developmentally programmed

24 Here we show that in sea lampreys (Petromyzon marinus) VLRA and VLRB anticipatory receptors

25 ic acid biosynthesis ability in sea lamprey (Petromyzon marinus) which represent the most ancient ver

26 e from the milt (fish semen) of sea lamprey (Petromyzon marinus), a jawless fish that spawns in lek-l

27 Here, we show that the sea lamprey (Petromyzon marinus), a jawless vertebrate, undergoes a d

28 e such example could occur with sea lamprey (Petromyzon marinus), a parasitic invasive species in the

29 omparative genomic maps for the sea lamprey (Petromyzon marinus), a representative of an ancient line

30 Here we discovered that sea lamprey (Petromyzon marinus), a representative of extant jawless

31 Here, we show in the sea lamprey (Petromyzon marinus), a vertebrate invader of the Laurent

32 e for the population control of sea lamprey (Petromyzon marinus), an invasive species of the Laurenti

33 ark (Squalus acanthias) and the sea lamprey (Petromyzon marinus), exhibits broad-spectrum antiviral a

34 n the basal jawless vertebrate, sea lamprey (Petromyzon marinus), focusing on the SoxE (Sox8, Sox9 an

35 of a damaging invasive species, sea lamprey (Petromyzon marinus), in the Great Lakes, and the consequ

36 sequences are well conserved in sea lamprey (Petromyzon marinus), L. camtschaticum, and European broo

37 smic carbonic anhydrases in the sea lamprey (Petromyzon marinus), that has a complex life history mar

38 he tunicate (Boltenia villosa), the lamprey (Petromyzon marinus), the pufferfish (Fugu rubripes), and

39 ensively characterized in male sea lampreys (Petromyzon marinus), the status of GRCs in females has n

40 reticulospinal synapses of the sea lamprey (Petromyzon marinus), we found that this NEF inhibitor in

41 rliest known CFTR, expressed in sea lamprey (Petromyzon marinus), with unique structural features, al

42 n all vertebrates including the sea lamprey (Petromyzon marinus).

43 in the jawless vertebrate, the sea lamprey (Petromyzon marinus).

44 elus canis), and a jawless fish (the lamprey Petromyzon marinus).

45 uides reliable communication in sea lamprey (Petromyzon marinus).

46 spinal cord-transected larval sea lampreys (Petromyzon marinus).

47 /PRL family in an agnathan, the sea lamprey (Petromyzon marinus).

48 d, we have cloned Dlx genes from the lamprey Petromyzon marinus, an agnathan vertebrate that occupies

49 runk sympathetic neurons in the sea lamprey, Petromyzon marinus, an extant jawless vertebrate.

50 nd hindbrain segmentation in the sea lamprey Petromyzon marinus, an important jawless vertebrate mode

51 Tyrosinase and FGF8/17/18 in the sea lamprey Petromyzon marinus, and detail optimized parameters for

52 e (ir) system in the CNS of the sea lamprey, Petromyzon marinus.

53 edn, ednr and dlx genes in the sea lamprey, Petromyzon marinus.

54 al (RS) neurons in the brain of the lamprey, Petromyzon marinus.

55 nd their receptors genes in the sea lamprey, Petromyzon marinus.

56 the head-specific gene Otx from the lamprey Petromyzon marinus.

57 es have been isolated from a marine lamprey, Petromyzon marinus.

58 ish, that a small population of sea lamprey (Petromyzon marinus; Class Agnatha), arguably one of the

59 We studied this in larval sea lampreys (Petromyzon marinus; the sex of the animals was not taken