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1 x-chromosome loci in a salamander amphibian (Ambystoma).
2 0 Gbp) is a major determinant of map size in Ambystoma.
3  numbers were reduced in lineages leading to Ambystoma and Xenopus.
4  two larval salamanders, intraguild predator Ambystoma annulatum and intraguild prey A. maculatum.
5      Overall, mitochondrial transcription in Ambystoma approximated the pattern observed in other ver
6 s where native California Tiger Salamanders (Ambystoma californiense) and introduced Barred Tiger Sal
7 ive, threatened California Tiger Salamander (Ambystoma californiense) and the introduced Barred Tiger
8 ow extensive conservation of synteny between Ambystoma, chicken, and human, and a positive correlatio
9 re ordered among linkage groups defining the Ambystoma genome, and we show that these same chromosoma
10 respond to the 14 haploid chromosomes in the Ambystoma genome.
11 ing locus (ambysex) in the tiger salamander (Ambystoma) genome.
12 most vertebrate species, linkage map size in Ambystoma is not strongly correlated with chromosome arm
13 somes map to neighboring regions of a common Ambystoma linkage group 2 (ALG2).
14 ajectories in a natural population of larval Ambystoma macrodactylum using function-valued quantitati
15  amblystomatis enter cells of the salamander Ambystoma maculatum forming an endosymbiosis.
16 ed and Holtfreter confirmed that ectoderm of Ambystoma maculatum salamander embryos could form brain
17 ival in 10 populations of salamander larvae (Ambystoma maculatum).
18 esis of superficial mesoderm in the urodeles Ambystoma maculatum, Ambystoma mexicanum, and Taricha gr
19 p of one of the larger linkage groups of the Ambystoma meiotic map.
20 tamorphic offspring from backcrosses between Ambystoma mexicanum (an obligate metamorphic-failure spe
21        We show that after tail amputation in Ambystoma mexicanum (Axolotl) the correct number and spa
22  hybrid combination of Ambystoma texanum and Ambystoma mexicanum (axolotl).
23                  For example, the salamander Ambystoma mexicanum (the Mexican axolotl) is a model org
24 sing an interspecific meiotic mapping panel (Ambystoma mexicanum and A. tigrinum tigrinum; family Amb
25 ration individuals of interspecific crosses (Ambystoma mexicanum x Ambystoma tigrinum tigrinum) was c
26  dorsal root ganglia of Xenopus and axolotl (Ambystoma mexicanum) axons grow directly to the limb bud
27                         The Mexican axolotl (Ambystoma mexicanum) has a derived mode of development t
28             The axolotl (Mexican salamander, Ambystoma mexicanum) has become a very useful model orga
29                         The Mexican axolotl (Ambystoma mexicanum) is capable of fully regenerating am
30 nerating limb tissue in the Mexican axolotl (Ambystoma mexicanum) that is indicative of cellular repr
31 erize gene expression responses of axolotls (Ambystoma mexicanum) to an emerging viral pathogen, Amby
32  metamorphosis in juvenile Mexican axolotls (Ambystoma mexicanum) using 5 and 50 nM T4, collected epi
33 rganization of genes in the Mexican axolotl (Ambystoma mexicanum), a species that presents relatively
34 g similar strategies in the Mexican axolotl (Ambystoma mexicanum), and the South African clawed toad
35    We fate-map this mesoderm in the axolotl (Ambystoma mexicanum), which retains external gills, and
36 olated an AHR cDNA from the Mexican axolotl (Ambystoma mexicanum).
37 ence for 5 tiger salamander complex species (Ambystoma mexicanum, A. t. tigrinum, A. andersoni, A. ca
38 esoderm in the urodeles Ambystoma maculatum, Ambystoma mexicanum, and Taricha granulosa.
39 nly urodele salamanders, such as the axolotl Ambystoma mexicanum, can completely regenerate limbs as
40  In pond food webs, larvae of the salamander Ambystoma opacum occupy the intermediate predator trophi
41 s of selection from a gape-limited predator (Ambystoma opacum) and spatial location to explanations o
42                                              Ambystoma segments are estimated to be four to 51 times
43 EST-based PCR markers will better enable the Ambystoma system by facilitating development of new mole
44 g densities of a pair of larval salamanders (Ambystoma talpoideum and A. maculatum) in experimental m
45  in a facultatively paedomorphic salamander, Ambystoma talpoideum.
46 using an interspecific hybrid combination of Ambystoma texanum and Ambystoma mexicanum (axolotl).
47 [Ca2+]i from isolated rods of the salamander Ambystoma tigrinum after incorporation of the fluorescen
48 nstrate that paedomorphic tiger salamanders (Ambystoma tigrinum complex) carry alleles at three moder
49  kinetics of inhibitory feedback currents in Ambystoma tigrinum cones and rods evoked by hyperpolariz
50 asured by recording postsynaptic currents in Ambystoma tigrinum horizontal or OFF bipolar cells evoke
51 se) and introduced Barred Tiger Salamanders (Ambystoma tigrinum mavortium) have been hybridizing for
52  and the introduced Barred Tiger Salamander (Ambystoma tigrinum mavortium).
53 +)] changes in cytoplasm and ER of rods from Ambystoma tigrinum retina using various dyes.
54 synaptic retinal neurons from the salamander Ambystoma tigrinum showed that the ribbon behaves like a
55 ee strains were used in the crossing design: Ambystoma tigrinum tigrinum (Att; metamorph), wild-caugh
56 equence tag (EST) markers were developed for Ambystoma tigrinum tigrinum (Eastern tiger salamander) a
57 ree region" and horizontal stripe pattern in Ambystoma tigrinum tigrinum (family Ambystomatidae) corr
58 rly larval pigment pattern in the salamander Ambystoma tigrinum tigrinum (family Ambystomatidae) is a
59          We captured wild salamander larvae (Ambystoma tigrinum tigrinum) and genotyped them at Amti-
60 interspecific crosses (Ambystoma mexicanum x Ambystoma tigrinum tigrinum) was consistent with Mendeli
61 ogous vaccinia virus system suggest that the Ambystoma tigrinum virus (ATV) eIF2alpha homologue (vIF2
62 ma mexicanum) to an emerging viral pathogen, Ambystoma tigrinum virus (ATV).
63 tor ribbon synapses of the tiger salamander (Ambystoma tigrinum) retina.
64 tes from intact, isolated larval salamander (Ambystoma tigrinum) retinas maintained in a 6.5-microL p
65 dy of ipRGCs in the larval tiger salamander (Ambystoma tigrinum), a nonmammalian vertebrate with a we
66 apses in the retina of the tiger salamander (Ambystoma tigrinum).
67 s isolated from the retina of the salamander Ambystoma tigrinum, changes in cytoplasmic calcium conce
68 epithelium and bulb in the tiger salamander, Ambystoma tigrinum, have elucidated a number of features
69  Na+/HCO3- cotransporter from the salamander Ambystoma tigrinum.
70  sequenced from the larval tiger salamander, Ambystoma tigrinum.
71                               Genome size in Ambystoma was estimated to be 7291 cM, the largest linka

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