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1 elus canis), and a jawless fish (the lamprey Petromyzon marinus).
2  spinal cord-transected larval sea lampreys (Petromyzon marinus).
3 n all vertebrates including the sea lamprey (Petromyzon marinus).
4  in the jawless vertebrate, the sea lamprey (Petromyzon marinus).
5 al (RS) neurons in the brain of the lamprey, Petromyzon marinus.
6 e (ir) system in the CNS of the sea lamprey, Petromyzon marinus.
7 nd their receptors genes in the sea lamprey, Petromyzon marinus.
8  the head-specific gene Otx from the lamprey Petromyzon marinus.
9 es have been isolated from a marine lamprey, Petromyzon marinus.
10          Here, we show that the sea lamprey (Petromyzon marinus), a jawless vertebrate, undergoes a d
11 omparative genomic maps for the sea lamprey (Petromyzon marinus), a representative of an ancient line
12         Here we discovered that sea lamprey (Petromyzon marinus), a representative of extant jawless
13            Here, we show in the sea lamprey (Petromyzon marinus), a vertebrate invader of the Laurent
14 e for the population control of sea lamprey (Petromyzon marinus), an invasive species of the Laurenti
15 d, we have cloned Dlx genes from the lamprey Petromyzon marinus, an agnathan vertebrate that occupies
16  the sequences of the Y1-subtype receptor of Petromyzon marinus and Lampetra fluviatilis to study the
17 orded from photoreceptors of the sea lamprey Petromyzon marinus and show that their rods have a singl
18 Tyrosinase and FGF8/17/18 in the sea lamprey Petromyzon marinus, and detail optimized parameters for
19 unit transcript was found in the sea lamprey Petromyzon marinus cDNA library.
20 rd, the NCBI Trace database for the lamprey (Petromyzon marinus) contains more than 18 million raw DN
21 ark (Squalus acanthias) and the sea lamprey (Petromyzon marinus), exhibits broad-spectrum antiviral a
22          The hemoglobins of the Sea Lamprey (Petromyzon marinus) exist in an equilibrium between low
23 n the basal jawless vertebrate, sea lamprey (Petromyzon marinus), focusing on the SoxE (Sox8, Sox9 an
24 utants of the major Hb component, PMII, from Petromyzon marinus have been measured to test these mode
25 tch up to 75% of tagged invasive sea lamprey Petromyzon marinus in free-flowing streams.
26                             The sea lamprey (Petromyzon marinus) is a genetically programmed animal m
27 sequences are well conserved in sea lamprey (Petromyzon marinus), L. camtschaticum, and European broo
28                   Here, we show in lampreys (Petromyzon marinus) of either sex that incremental stimu
29 n Ikaros-related gene has been identified in Petromyzon marinus (sea lamprey), a jawless vertebrate s
30 phalochordates (Branchiostoma), but occur in Petromyzon marinus (Sea Lamprey), a jawless vertebrate.
31 has been identified in a jawless vertebrate, Petromyzon marinus (sea lamprey).
32 instem muscarinoceptive neurons in lampreys (Petromyzon marinus) that received parallel inputs from t
33 smic carbonic anhydrases in the sea lamprey (Petromyzon marinus), that has a complex life history mar
34 he tunicate (Boltenia villosa), the lamprey (Petromyzon marinus), the pufferfish (Fugu rubripes), and
35 he basal jawless vertebrate the sea lamprey (Petromyzon marinus) to gain insight into its evolutionar
36 d brain responses of parasitic sea lampreys (Petromyzon marinus) to weak electric fields.
37 and two animal trajectories - a sea lamprey (Petromyzon marinus) tracked for 12 h and a wolf (Canis l
38                                 The lamprey (Petromyzon marinus) undergoes developmentally programmed
39           Here we show that in sea lampreys (Petromyzon marinus) VLRA and VLRB anticipatory receptors
40  reticulospinal synapses of the sea lamprey (Petromyzon marinus), we found that this NEF inhibitor in
41 ic acid biosynthesis ability in sea lamprey (Petromyzon marinus) which represent the most ancient ver

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