ライフサイエンスコーパス: canary

1 he 1st year, males were housed with pairs of canaries.

2 redominant mutant isoform in white recessive canaries.

3 hite recessive with yellow and red breeds of canaries.

4 ombination on DCX expression in adult female canaries.

5 neuronal addition to the HVC of adult female canaries.

6 ian archipelagos of the Azores, Madeira, and Canaries.

7 n the caudomedial neostriatum (NCM) of adult canaries.

8 product of crossing red siskins with common canaries [7].

9 Here we examine the song of the domesticated canary, a complex singer whose song consists of syllable

10 NK protein in the brain of zebra finches and canaries after presentation of song playbacks.

11 CANARY allows the noninvasive risk stratification of lun

12 of targetable mutations (50-gene-panel) and CANARY analysis of the preoperative (</=3 months) high r

13 Whole genome alignments between the canary and 13 genomes throughout the bird taxa show a mu

14 thropods of the volcanic archipelagos of the Canary and Hawaiian Islands to address whether there is

15 - and estrogen-sensitive specifically in the canary and that are involved in rewiring of neurons migh

16 Canaries appear to lack the protein, but it can be induc

17 The two major radiations identified in the Canaries are correlated with distinct ecological habitat

18 e consistent across three of the four EBUSs (Canary, Benguela and Humboldt, but not California).

19 is of lung adenocarcinoma was analyzed using CANARY blinded to clinical data.

20 ulation of neuronal replacement in the adult canary brain and suggest that the effects of testosteron

21 copy, we determined that the VZ of the adult canary brain is composed of three main cell types (A, B,

22 dy the presence of this protein in the adult canary brain.

23 ct neuron recruitment equally throughout the canary brain.

24 tomy of the inner ear of Belgian Waterslager canaries (BWC) have demonstrated myriad malformations as

25 CANARY characterizes nodules by the distribution of nine

26 thers and several tissues of white recessive canaries, consistent with a genetic defect in carotenoid

27 Our results suggest that CANARY could ultimately facilitate individualized manage

28 My experimental evidence from captive canaries demonstrates a marginal cost of begging through

29 ng nucleus higher vocal center (HVC) in male canaries did not change seasonally when its borders were

30 nto the lowermost mantle: Ascension, Azores, Canary, Easter, Samoa, and Tahiti.

31 g TP53 (n = 5) had a good prognosis based on CANARY features.

32 Moreover, isolated adult canary forebrain endothelial cells secreted MMP2, and VE

33 The canary genome sequence and complementary expression anal

34 assembly and annotation of a female 1.2-Gbp canary genome.

35 Studies in zebra finches and canaries have now identified the gene responsible for re

36 Among the testosterone-regulated genes of canary HVC, 20% lack estrogen response elements and 4 to

37 ubspecies, the males did not vocalize to the canaries in courtship tests but showed incompetent court

38 udied this question by castrating adult male canaries in late summer and quantifying their song in ea

39 rates, and annual plants) may be inaccurate 'canaries in the coal mine' for CC without pertinent demo

40 uter-Aided Nodule Assessment and Risk Yield (CANARY) is quantitative imaging analysis software that p

41 The cell walls of leaf base tissues of the Canary Island date palm (Phoenix canariensis) contain li

42 ia bravoana), is an endemic lacertid of this Canary Island that lives confined to a very restricted a

43 Basques and Canary Islanders are clearly associated with modern Euro

44 ributed 16%-31% autosomal ancestry to modern Canary Islanders, here represented by two individuals fr

45 northeast Atlantic were highest north of the Canary Islands (280-980 pg/L) and decreased with latitud

46 st-generation hybrid individuals between the Canary Islands and Columbia strains also showed a cytosi

47 haeological dating for the settlement of the Canary Islands and Remote Oceania and also, given certai

48 olonization of most permanent streams on the Canary Islands by M. aspersus.

49 Most of the PH1 alleles detected in the Canary Islands carry the Ile-244 --> Thr (I244T) mutatio

50 The two sheep breeds native to the Canary Islands display distinctly different resistant ph

51 t that the alliance probably occurred in the Canary Islands during the late Miocene or early Pliocene

52 to three or more-times larger than subaerial Canary Islands flank collapses.

53 entanglement-swapping experiment between the Canary Islands of La Palma and Tenerife, verifying the p

54 fferent tissues from two small fishes of the Canary Islands that constitute an important level of the

55 fer of cattle from the Iberian Peninsula and Canary Islands to the Caribbean laid the foundation for

56 aspersus (Trichoptera, Limnephilidae) on the Canary Islands was investigated by studying allozyme var

57 rk, different types of gofio produced in the Canary Islands were characterized on the basis of physic

58 ping data from F2 individuals derived from a Canary Islands x Columbia cross revealed that NOR2 accou

59 ations (France, Portugal, Continental Spain, Canary Islands, and Cape Verde) were analysed by headspa

60 of the flowering plant Arabidopsis thaliana (Canary Islands, Cape Verde Islands, and Columbia).

61 ffinity of the aboriginal inhabitants of the Canary Islands, commonly known as Guanches, are poorly u

62 otii, Bolle 1862) on the island of Tenerife (Canary Islands, Spain) using spatially explicit models t

63 d crosses between two species endemic to the Canary Islands, the self-compatible (SC) species Tolpis

64 light over a distance of 143 km between two Canary Islands, which is 50x greater than the maximum di

65 similar to allied genera now present on the Canary Islands.

66 ch many originate from mass movements in the Canary Islands.

67 Western Pacific Ocean, from the Caribbean to Canary Islands.

68 demic to the southern archipelago--e.g., the Canary Islands.

69 growth, and final subaerial emergence of the Canary Islands.

70 of HVC neurons born in the fall, when adult canaries learn a new song, are still present 8 mo later,

71 ated songs were reprogrammed to form typical canary phrasing.

72 When presented with a female canary, POM-T birds copulated at a rate comparable to bi

73 The RV144 HIV-1 trial of the canary pox vector (ALVAC-HIV) plus the gp120 AIDSVAX B/E

74 Johns Hopkins University (JHU); Canary Prostate Active Surveillance Study (PASS); Univer

75 CANARY risk groups were compared using survival analysis

76 tified into the Good, Intermediate, and Poor CANARY risk groups yielded distinct progression-free sur

77 nd Fluorogold) to show that RA of adult male canaries (Serinus canaria) and zebra finches (taeniopygi

78 ion paradigm in two additional bird species: canaries (Serinus canaria) and zebra finches (Taeniopygi

79 ial preoptic nucleus (POM) of castrated male canaries (Serinus canaria) increase song rate but do not

80 nd neuron recruitment in the brains of adult canaries (Serinus canaria), a species well-known for its

81 ng of red siskins (Spinus cucullata), common canaries (Serinus canaria), and "red factor" canaries, w

82 stinct features of birdsong using adult male canaries (Serinus canaria), which show extensive seasona

83 We investigated this question in adult male canaries (Serinus canaria), which show extensive vocal p

84 te actions of estrogens regulate birdsong in canaries (Serinus canaria).

85 center of both adult male zebra finches and canaries (Serinus canaria).

86 Neurons in female canaries (Serinus canarius) that project to Area X of th

87 h vocal center (HVC), a nucleus of the adult canary (Serinus canaria) brain that plays a critical rol

88 in seasonally breeding songbirds such as the canary (Serinus canaria) that learns new songs in adulth

89 The white recessive breed of the common canary (Serinus canaria), which carries an autosomal rec

90 r (a motor nucleus) and other song nuclei of canaries, Serinus canaria, and zebra finches, Taeniopygi

91 The high vocal center (HVC) of adult male canaries, Serinus canaria, is necessary for the producti

92 to the high vocal center (HVC) of adult male canaries, Serinus canaria.

93 ophic factor (BDNF) in the HVC of adult male canaries, Serinus canaria.

94 Based on their parametric CANARY signatures, all the lung adenocarcinoma nodules w

95 In the morning, male canaries sing within minutes after light onset.

96 e elements to the hormone-sensitivity of the canary singing behavior, we identify seasonal testostero

97 tes, which suggests that innate rules govern canary song development.

98 Canary song is hierarchically structured: Short stereoty

99 We show that presentation of individual canary song syllables results in distinct expression pat

100 egulated in the skin and liver of red factor canaries, strongly implicating CYP2J19 as the ketolase t

101 to 60 years; wind change is equivocal in the Canary system.

102 In male canaries, T regulates expression of the microtubule-asso

103 In our study setting, canaries that are naive to malaria infection routinely s

104 ntrogressed from red siskins into red factor canaries that are required for red coloration.

105 Neurons formed in adult canaries were labeled with [(3)H]-thymidine and examined

106 canaries (Serinus canaria), and "red factor" canaries, which are the hybrid product of crossing red s

107 We placed canaries with different immunologic backgrounds (e.g., n