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1 ir species, the American robin and the house sparrow.
2 field sparrow from the more aggressive song sparrow.
3 to some degree pre-encoded in white-crowned sparrows.
4 that controls song behavior in white-crowned sparrows.
5 tion typically removes circulating T in tree sparrows.
6 a pedigreed insular population of wild house sparrows.
7 dial amygdala of field sparrows but not song sparrows.
8 the song system in adult male white-crowned sparrows.
9 d cerebrosides in the SC compared with mesic sparrows.
10 ty in RA was not altered by deafening in the sparrows.
11 ain in breeding-condition male white-crowned sparrows 2 days prior to T withdrawal and shifting them
12 ying neural representations of song in swamp sparrows, a species in which juveniles learn and practic
13 nd for communication between neighbors (song sparrows address or reply to a neighbor with a song they
14 ons for a threatened songbird, the saltmarsh sparrow (Ammodramus caudacutus), in a region where sea l
15 rea, dorsal arcopallium, and optic tectum in sparrow and was essentially undetectable in zebra finch.
18 issue, we castrated adult male white-crowned sparrows and rapidly shifted them to short-day photoperi
20 phrase types characteristic of white-crowned sparrows and, thus, could contribute to innate song reco
23 he suppression of winter aggression in field sparrows, because similar winter differences were found
24 ely to threaten the persistence of saltmarsh sparrows beyond 2060 and could cause extinction as soon
26 We here confirm earlier findings that swamp sparrows categorically perceive the notes that constitut
27 lts from a 20-year study of free-living song sparrows confirm that attractive males contribute more o
28 easonal changes in the song nuclei, the song sparrows continued to sing the same number of different
29 er quality data analysis, the application of SPARROW controls for confounding factors such as hydrolo
30 d susceptibility to infection we observed in sparrows, coupled with their presence in poultry houses,
33 t common mammal species captured while house sparrows, European starlings, rock pigeons, swallows, an
35 ensorimotor neurons in freely behaving swamp sparrows expressed categorical auditory responses to cha
36 analyses further identify groups (New World sparrows, finches, and vireos) disproportionally affecte
38 st recognized, or more subordinate levels - 'sparrow', for example - which require additional percept
39 , M. Hashimoto, K. Nakanishi, J. Dillon & J. Sparrow, for the biosynthesis of A2E: (i) condensation o
40 that a certain class of neurons in the swamp sparrow forebrain displays a precise auditory-vocal corr
42 examined the population genetics of 576 song sparrows from 23 populations using seven microsatellite
44 d lipid composition of the SC of adult house sparrows from two populations, one living in the deserts
45 e a northward shift in current White-crowned sparrow habitat range and a 20-60% increase in their pre
48 In a field study, we show that a young song sparrow (i) selects his songs from three or four older b
49 d to acute myeloid leukemia expression data, SPARROW identifies an apoptotic biomarker (PYCARD) for a
50 We showed previously that in white-throated sparrows, immediate early gene responses in the auditory
58 We fitted animal models to 38 years of song sparrow (Melospiza melodia) phenology and pedigree data
61 e examine song type representations in swamp sparrows (Melospiza georgiana), a multiple song type spe
62 attributes of Area X in wild adult male song sparrows (Melospiza melodia) captured during the spring
65 c paternity and pedigree data from wild song sparrows (Melospiza melodia) to partition variance in ea
66 illa), which seasonally flock, and male song sparrows (Melospiza melodia), which are territorial year
71 does not exceed 20 cm, whereas White-crowned sparrows nested only under shrubs between 20 cm and 1 m
74 ncreases observed in the abundances of house sparrow (Passer domesticus) and spotted dove (Streptopel
75 s France, screening populations of the house sparrow (Passer domesticus) for malaria (Plasmodium reli
76 marked females in eight populations of house sparrows (Passer domesticus) from North America and Euro
77 tion: songs composed of single white-crowned sparrow phrases and songs played in reverse elicited voc
83 enile, long-distance migrating white-crowned sparrows rapidly recognize and correct for a continent-w
84 of the SC in desert and mesic nestling house sparrows reared in low and high humidity and compared ou
85 se inhibitors in vivo in adult white-crowned sparrows rescued neurons within the hormone-sensitive so
87 g circuitry was incompletely developed, male sparrows sang less stereotyped songs than males at day 2
89 as capable of detecting anti-WN IgM in house sparrow serum samples from laboratory-infected birds but
90 able when wild, adult, free-ranging chipping sparrows sing at dawn than when they sing during the day
91 expression data with a novel method, namely SPARROW ( SPAR: se selected exp R: essi O: n regulators
92 show how a migratory songbird, the chipping sparrow (Spizella passerina), achieves prompt and precis
93 brains in spring and winter from male field sparrows (Spizella pusilla), which seasonally flock, and
94 were collected from wild ducks, geese, owls, sparrows, swallows, and starlings and from sentinel duck
96 seasonally breeding adult male white-crowned sparrows, the song system nucleus HVC loses approximatel
97 l U.S. Geological Survey water-quality model SPARROW to investigate whether spatial differences in co
100 the sensorimotor nucleus HVC in anesthetized sparrows to assess neuronal responsiveness to songs in t
101 posed estrogen-primed, female white-throated sparrows to conspecific male song and looked for evidenc
102 Waterborne transmission from inoculated sparrows to contact chickens was absent, while 25% of sp
103 We exposed adult male Gambel's white-crowned sparrows to either short-day photoperiod or long-day pho
107 strildidae and a limited number of emberizid sparrows) using antibodies against 10 neuropeptides and
112 to contact chickens was absent, while 25% of sparrows were infected via waterborne transmission from
115 o model songbird species, the white-throated sparrow (Zonotrichia albicollis) and zebra finch (Taenio
116 l behavior and plumage in the white-throated sparrow (Zonotrichia albicollis) is linked to an inversi
117 polymorphism (ZAL2(m)) in the white-throated sparrow (Zonotrichia albicollis) is linked to variation
120 dressed this issue in Gambel's white-crowned sparrow (Zonotrichia leucophrys gambelii), a songbird th
121 rder--is such a feature in the white-crowned sparrow (Zonotrichia leucophrys), the authors tutored ma
122 ensory systems in experienced white-throated sparrows (Zonotrichia albicollis) captured in southern O
123 ort-term flocks for wintering golden-crowned sparrows (Zonotrichia atricapilla) across three years an
124 e studied two populations of rufous-collared sparrows (Zonotrichia capensis) that breed, only 25 km a
125 rols song behavior in Gambel's white-crowned sparrows (Zonotrichia leucophrys gambelii) and examined
126 aught wild adult male Gambel's white-crowned sparrows (Zonotrichia leucophrys gambelii) during spring
127 r injected in RA of adult male white-crowned sparrows (Zonotrichia leucophrys gambelii) in breeding o
129 arius lapponicus) and Gambel's White-crowned sparrows (Zonotrichia leucophrys gambelii) with modeled
131 rs of the HVC in male Gambel's white-crowned sparrows (Zonotrichia leucophrys gambelii): Nissl staini
134 ays to show that male mountain white-crowned sparrows, Zonotrichia leucophrys oriantha, must learn to
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