ライフサイエンスコーパス: Ambystoma

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 ptasia pallida (Aiptasia) and the salamander Ambystoma maculatum-both of which exhibit endophotosymbi

20 ss for 1093 adult Arizona tiger salamanders (Ambystoma mavortium nebulosum) from a high elevation, po

21 histories of 717 Arizona tiger salamanders (Ambystoma mavortium nebulosum), we determined how annual

22 nces the rate of senescence in a salamander, Ambystoma mavortium nebulosum.

23 p of one of the larger linkage groups of the Ambystoma meiotic map.

24 tamorphic offspring from backcrosses between Ambystoma mexicanum (an obligate metamorphic-failure spe

25 We show that after tail amputation in Ambystoma mexicanum (Axolotl) the correct number and spa

26 hybrid combination of Ambystoma texanum and Ambystoma mexicanum (axolotl).

27 For example, the salamander Ambystoma mexicanum (the Mexican axolotl) is a model org

28 sing an interspecific meiotic mapping panel (Ambystoma mexicanum and A. tigrinum tigrinum; family Amb

29 ration individuals of interspecific crosses (Ambystoma mexicanum x Ambystoma tigrinum tigrinum) was c

30 dorsal root ganglia of Xenopus and axolotl (Ambystoma mexicanum) axons grow directly to the limb bud

31 target epigenetic mechanisms in an axolotl (Ambystoma mexicanum) embryo tail regeneration assay.

32 The Mexican axolotl (Ambystoma mexicanum) has a derived mode of development t

33 The axolotl (Mexican salamander, Ambystoma mexicanum) has become a very useful model orga

34 The Mexican axolotl (Ambystoma mexicanum) is a well-established tetrapod mode

35 The Mexican axolotl (Ambystoma mexicanum) is capable of fully regenerating am

36 ian mutants have been discovered in axolotl (Ambystoma mexicanum) populations, including several that

37 The axolotl (Ambystoma mexicanum) possesses a remarkable ability to r

38 The axolotl (Ambystoma mexicanum) provides critical models for studyi

39 After appendage amputation, the axolotl (Ambystoma mexicanum) regenerates missing structures thro

40 nerating limb tissue in the Mexican axolotl (Ambystoma mexicanum) that is indicative of cellular repr

41 erize gene expression responses of axolotls (Ambystoma mexicanum) to an emerging viral pathogen, Amby

42 metamorphosis in juvenile Mexican axolotls (Ambystoma mexicanum) using 5 and 50 nM T4, collected epi

43 rganization of genes in the Mexican axolotl (Ambystoma mexicanum), a species that presents relatively

44 g similar strategies in the Mexican axolotl (Ambystoma mexicanum), and the South African clawed toad

45 We fate-map this mesoderm in the axolotl (Ambystoma mexicanum), which retains external gills, and

46 olated an AHR cDNA from the Mexican axolotl (Ambystoma mexicanum).

47 itical for limb regeneration in the axolotl (Ambystoma mexicanum).

48 ence for 5 tiger salamander complex species (Ambystoma mexicanum, A. t. tigrinum, A. andersoni, A. ca

49 esoderm in the urodeles Ambystoma maculatum, Ambystoma mexicanum, and Taricha granulosa.

50 nly urodele salamanders, such as the axolotl Ambystoma mexicanum, can completely regenerate limbs as

51 In pond food webs, larvae of the salamander Ambystoma opacum occupy the intermediate predator trophi

52 s of selection from a gape-limited predator (Ambystoma opacum) and spatial location to explanations o

53 Ambystoma segments are estimated to be four to 51 times

54 EST-based PCR markers will better enable the Ambystoma system by facilitating development of new mole

55 g densities of a pair of larval salamanders (Ambystoma talpoideum and A. maculatum) in experimental m

56 n populations of predatory mole salamanders (Ambystoma talpoideum) within mesocosms and monitored a s

57 in a facultatively paedomorphic salamander, Ambystoma talpoideum.

58 using an interspecific hybrid combination of Ambystoma texanum and Ambystoma mexicanum (axolotl).

59 c interactions in small-mouthed salamanders, Ambystoma texanum.

60 mphibian species, Xenopus laevis (xArr1) and Ambystoma tigrinum (salArr1).

61 [Ca2+]i from isolated rods of the salamander Ambystoma tigrinum after incorporation of the fluorescen

62 nstrate that paedomorphic tiger salamanders (Ambystoma tigrinum complex) carry alleles at three moder

63 kinetics of inhibitory feedback currents in Ambystoma tigrinum cones and rods evoked by hyperpolariz

64 asured by recording postsynaptic currents in Ambystoma tigrinum horizontal or OFF bipolar cells evoke

65 se) and introduced Barred Tiger Salamanders (Ambystoma tigrinum mavortium) have been hybridizing for

66 and the introduced Barred Tiger Salamander (Ambystoma tigrinum mavortium).

67 +)] changes in cytoplasm and ER of rods from Ambystoma tigrinum retina using various dyes.

68 synaptic retinal neurons from the salamander Ambystoma tigrinum showed that the ribbon behaves like a

69 ee strains were used in the crossing design: Ambystoma tigrinum tigrinum (Att; metamorph), wild-caugh

70 equence tag (EST) markers were developed for Ambystoma tigrinum tigrinum (Eastern tiger salamander) a

71 ree region" and horizontal stripe pattern in Ambystoma tigrinum tigrinum (family Ambystomatidae) corr

72 rly larval pigment pattern in the salamander Ambystoma tigrinum tigrinum (family Ambystomatidae) is a

73 We captured wild salamander larvae (Ambystoma tigrinum tigrinum) and genotyped them at Amti-

74 interspecific crosses (Ambystoma mexicanum x Ambystoma tigrinum tigrinum) was consistent with Mendeli

75 ogous vaccinia virus system suggest that the Ambystoma tigrinum virus (ATV) eIF2alpha homologue (vIF2

76 ma mexicanum) to an emerging viral pathogen, Ambystoma tigrinum virus (ATV).

77 tor ribbon synapses of the tiger salamander (Ambystoma tigrinum) retina.

78 tes from intact, isolated larval salamander (Ambystoma tigrinum) retinas maintained in a 6.5-microL p

79 dy of ipRGCs in the larval tiger salamander (Ambystoma tigrinum), a nonmammalian vertebrate with a we

80 apses in the retina of the tiger salamander (Ambystoma tigrinum).

81 s isolated from the retina of the salamander Ambystoma tigrinum, changes in cytoplasmic calcium conce

82 epithelium and bulb in the tiger salamander, Ambystoma tigrinum, have elucidated a number of features

83 Na+/HCO3- cotransporter from the salamander Ambystoma tigrinum.

84 sequenced from the larval tiger salamander, Ambystoma tigrinum.

85 Genome size in Ambystoma was estimated to be 7291 cM, the largest linka