ライフサイエンスコーパス: Eyed

1 Lateral-eyed afoveate animals use the subcortical accessory opti

2 hrough comparison with the aVOR of a lateral-eyed, afoveate mammal (Chinchilla lanigera).

3 atomy reveals that it was herbivorous, large-eyed and agile, with well-developed high-frequency heari

4 t the turtle is generally considered lateral-eyed and assumed to have eye movements instead like that

5 r-driven slow eye movements for both lateral-eyed and foveate species.

6 o official emissions inventories and a clear-eyed assessment of the most effective emission-finding t

7 nonresolving oculocardiac reflex, the "white-eyed" blowout fracture, and early enophthalmos or hypogl

8 Other predators, big-eyed bugs, and antlion larvae were insensitive to this d

9 In contrast, the lateral-eyed chinchilla faces different adaptive demands and thu

10 alanine, as compared to their river-dwelling eyed conspecifics.

11 a locus that maps just proximal to the pink-eyed dilution (p) locus in mouse chromosome 7, was initi

12 other melanocyte-specific genes such as pink-eyed dilution and Pmel 17 (silver), but not tyrosinase-r

13 at the underwhite locus and either the pink-eyed dilution locus or the melanocortin receptor 1 locus

14 phenotypes, similar to mutations at the pink-eyed dilution locus that is a model for type 2 oculocuta

15 Our data demonstrate that the pink-eyed dilution protein increases cellular sensitivity to

16 Mutations in the mouse p (pink-eyed dilution) and human P genes lead to melanosomal def

17 dly downregulating expression of the p (pink-eyed dilution) gene, while maintaining their cell fate.

18 analysis at four early life history stages; eyed egg, post hatch, first feeding and three weeks post

19 e mRNA for cathepsin D was detectable at the eyed embryo stage, and the expression of the gene increa

20 week-old rainbow trout (Oncorhynchus mykiss) eyed embryos.

21 water meniscus bisects the eyes of the "four-eyed" fish Anableps anableps, resulting in simultaneous

22 We tested this hypothesis in stalk-eyed flies by measuring the mating frequency of females

23 After emergence from the puparium, stalk-eyed flies of the family Diopsidae rapidly expand their

24 rect evidence from wild populations of stalk-eyed flies to support the hypothesis that male eyespan i

25 ed sex ratios in two sister species of stalk-eyed flies, Cyrtodiopsis dalmanni and C. whitei, are due

26 Females of the stalk-eyed fly Cyrtodiopsis dalmanni can mate several times ea

27 sexual ornament (male eye span) in the stalk-eyed fly Cyrtodiopsis dalmanni.

28 Several stalk-eyed fly species are known to exhibit X-linked meiotic d

29 In the diopsid stalk-eyed fly, Cyrtodiopsis dalmanni, sperm length and female

30 brain, we used Bodian staining in the stalk-eyed fly, Cyrtodiopsis whitei and compared it with devel

31 describe how sperm development in the stalk-eyed fly, Cyrtodiopsis whitei, influences progeny sex pr

32 n X-linked meiotic drive system in the stalk-eyed fly, Teleopsis dalmanni.

33 g of lateral eye incidence resolved the four-eyed fossil group as a member of the extant daddy-longle

34 s an adaptation related to primates' frontal-eyed, foveate status through comparison with the aVOR of

35 OR represents an adaptation to their forward-eyed, foveate status.

36 iversification of two sister species of four-eyed frogs of northeastern Brazil using single nucleotid

37 the ocular dominance columns formed in three-eyed frogs.

38 ammals and in experimentally-generated three-eyed frogs.

39 In analogy to three eyed-frogs, we generated three-eared frogs to assess to

40 a recombinant chromosome with the strong red-eyed GAL4 and a desired UAS-transgene construct may be d

41 iversion effect significantly benefits black-eyed guppies because they evade capture by rapidly pivot

42 ar pressure were studied in 24 healthy, blue-eyed humans.

43 Strabismic (cross-eyed) humans and animals show an imbalance between oppos

44 White-eyed individuals could also be recovered following a bli

45 influence of chromosome aberrations in light-eyed individuals.

46 s of environmental heterogeneity in the Dark-eyed Junco (Junco hyemalis) and its congeners.

47 , we compared the feather morphology of Dark-eyed Junco (Junco hyemalis) populations established acro

48 Paridae, as well as to the non-storing dark-eyed junco (Junco hyemalis).

49 in wild-caught, breeding-condition male dark-eyed juncos (Junco hyemalis hyemalis) before and after e

50 in singing versus nonsinging adult male dark-eyed juncos (Junco hyemalis), leading us to hypothesize

51 ids that are not territorial in winter--dark-eyed juncos (Junco hyemalis), which seasonally flock, an

52 its, including migratory tendency, of yellow-eyed juncos along a continuous 1000-m elevational gradie

53 Urban dark-eyed juncos differ in bill shape and size in Los Angeles

54 timing in a non-migratory population of dark-eyed juncos Junco hyemalis.

55 positively related to the incidence of right-eyed looking.

56 covered his first Drosophila mutant, a white-eyed male.

57 e eye movements instead like that of lateral-eyed mammals, in which innervation of the superior obliq

58 n abduction of the eyes like that in frontal-eyed mammals.

59 The four-eyed milkweed beetle (Tetraopes tetrophthalmus) is an ab

60 served in Drosophila may be widespread among eyed, motile organisms.

61 ccessfully obtained multiple lines of orange-eyed OK371-GAL4 and elav-GAL4 that still maintain their

62 Black-eyed pea (Vigna unguiculata) is a legume species widely

63 ls to analyse transcript expression in black-eyed pea organs and to compare data with other legume sp

64 The black-eyed pea reference genotype has been used to generate a

65 five commonly edible seeds, fava bean, black-eyed pea, kidney bean, red lentil, and chickpea.

66 ts maximum content in day 5 sprouts of black-eyed peas (490 ug/100 g FW).

67 aximum on the fifth day in the case of black-eyed peas (861 ug/100 g Fresh Weight), white beans (755

68 in small organoids, recapitulating the small-eyed phenotype of mice with microphthalmia, while deleti

69 ions have an entirely white coat and a black-eyed phenotype similar to the phenotype of C(r)/C(r) or

70 he course of evolution to generate the stalk-eyed phenotype.

71 doderm pitx2c expression is dependent on one-eyed pinhead (EGF-CFC-related gene) and spadetail (tbx-t

72 ls Cyclops and Squint and their cofactor One-eyed pinhead (Oep) [10-14].

73 Although fez expression is present in one-eyed pinhead (oep) and cyclops (cyc) zebrafish mutants,

74 g mutants in the Nodal receptor cofactor one-eyed pinhead (oep) and the T-box transcription factors s

75 Loss of maternal and zygotic one-eyed pinhead (oep) does not alter expression of fgf3 or

76 Zebrafish one-eyed pinhead (oep) encodes a maternally and zygotically

77 The zebrafish locus one-eyed pinhead (oep) is essential for the formation of ant

78 The zebrafish EGF-CFC gene one-eyed pinhead (oep) is required zygotically for the forma

79 istently, opl was correctly expressed in one-eyed pinhead (oep) mutant embryos, where the prechordal

80 A comparison of the one-eyed pinhead (oep) mutant with the digital model of the

81 Similarly, zebrafish one-eyed pinhead (oep) mutants that have been rescued partia

82 The zebrafish one-eyed pinhead (oep) mutation disrupts embryonic developme

83 s Mixer, Xsox17, and HNF3beta; zebrafish One-eyed pinhead (Oep), a member of the Cripto/FRL-1/Cryptic

84 he zebrafish mutants cyclops, squint and one-eyed pinhead (oep), cause HPE.

85 In one-eyed pinhead (oep-) mutants, which are more completely d

86 oding the Cryptic protein) and zebrafish one-eyed pinhead (oep; refs 10, 11) are essential for the es

87 interact with zygotic mutant alleles of one-eyed pinhead (Zoep), leading to synergistic mesodermal d

88 egulated in the zebrafish midline mutant one-eyed pinhead and expressed predominantly in midline tiss

89 one-eyed pinhead and schmalspur are necessary for asymmetric

90 n addition to a role in Nodal signaling, One-eyed pinhead is required for aspects of cell movement, p

91 ant phenotype, cell behavior retains the one-eyed pinhead motility phenotype.

92 lity defects are cell-autonomous; later, one-eyed pinhead mutant cells have a cell-autonomous tendenc

93 rmation dynamics in the maternal-zygotic one-eyed pinhead mutant, which is defective in mesoderm indu

94 ess a more severe phenotype than zygotic one-eyed pinhead mutants, cells of the dorsal margin exhibit

95 utants but exhibit defective motility in one-eyed pinhead mutants.

96 cryptic), Xenopus (FRL-1) and zebrafish (one-eyed pinhead), we show that all EGF-CFC genes share an i

97 in zygotic mutants for the EGF-CFC gene one-eyed pinhead, an essential cofactor for Nodal signaling,

98 re, we show that the zygotic function of one-eyed pinhead, the zebrafish EGF-CFC factor, is necessary

99 with mutants in nodal-related genes, in one-eyed pinhead, which is required for nodal signaling, and

100 We also show effective silencing of the one-eyed-pinhead and no-tail/brachyury genes.

101 ese processes such as sonic hedgehog and one-eyed-pinhead, cyclops is required for ventral midline pa

102 mutations of the genes no tail, chordin, one-eyed-pinhead, nacre and sparse, removing gene function f

103 municative content: caregivers increase wide-eyed positive affect, reduce neutral facial affect, redu

104 ected embryos produced families with colored-eyed progeny individuals, a transformation rate of 4%.

105 ese individuals produced more than 20% white-eyed progeny, with some producing up to 75%.

106 nd-inflicted prepupae metamorphosed to white-eyed pupae, all wound scars disappeared with the exuviae

107 abar (cn) gene was used to transform a white-eyed recipient strain of Ae. aegypti.

108 of a kynurenine hydroxylase-deficient, white-eyed recipient strain.

109 an cavefish, Astyanax mexicanus, consists of eyed river-dwelling surface populations and multiple ind

110 of Natural Understanding co-developed a Two-Eyed Seeing collaboration to learn more about these stur

111 To protect the Ocean, a "two-eyed seeing" approach combining Indigenous and western k

112 ical data for geographic samples of the four-eyed sleeper (Bostrychus sinensis), which reinforce the

113 These results and conclusions for the four-eyed sleeper are presented as a case study for future re

114 y in comparison with other mammalian lateral-eyed species.

115 veloping coho salmon embryos starting at the eyed stage to three concentrations of 6PPD-quinone twice

116 carapace forces the turtle to a more frontal-eyed state, perhaps the reason for the action of abducti

117 ss of G1 progeny, yielding several new white-eyed strains in the genetic background of the sequenced

118 The existence of eyed surface (surface fish) and blind cave (cavefish) dw

119 The characin fish, Astyanax mexicanus, has eyed surface and numerous blind cave populations.

120 al, and physiological evolution by comparing eyed surface populations and blind cave populations.

121 in the teleost Astyanax mexicanus, which has eyed surface-dwelling (surface fish) and blind cave-dwel

122 Astyanax mexicanus is a teleost with eyed surface-dwelling and eyeless cave-dwelling forms.

123 Astyanax mexicanus, a single species with an eyed surface-dwelling form (surface fish) and many blind

124 ivum (coriander) and Thunbergia alata (black-eyed Susan vine) produce unusual monoenoic fatty acids w

125 approach of females of the Australian orange-eyed tree frog (Litoria chloris) both in a laboratory ar

126 We examine the growth response of red-eyed treefrog tadpoles (Agalychnis callidryas) to cues f

127 he shaking (tremulation) display of male red-eyed treefrogs (Agalychnis callidryas) are a vibrational

128 ions by homologous recombination at the pink-eyed unstable (p(un)) locus is elevated in mice with mut

129 The pink-eyed unstable (p(un)) mutation in the C57BL/6J mouse is

130 The pink-eyed unstable (pun) mutation in the mouse is caused by d

131 eous homologous recombination using the pink-eyed unstable mouse model, in which we conditionally exc

132 an in vivo mouse model system with the pink-eyed unstable mutation, we demonstrate that the absence

133 lemetry to track three songbird species (Red-eyed Vireo, Swainson's Thrush, Wood Thrush) from coastal

134 We investigated patch fidelity of white-eyed vireos (Vireo griseus) based on reproductive succes

135 separation profile in comparison to the red-eyed, wild-type, Canton S fly.

136 he skull of Navaornis is toothless and large-eyed, with a vaulted cranium closely resembling the cond