ライフサイエンスコーパス: higher vertebrate

1 ay shed new light on hypoxia and ischemia in higher vertebrates.

2 des for neonatal learning in most species of higher vertebrates.

3 as grown to include 19 identified members in higher vertebrates.

4 ns the same number of genes as the genome of higher vertebrates.

5 terize the alpha(2)beta(2) tetrameric Hbs of higher vertebrates.

6 ate their axons is a striking peculiarity of higher vertebrates.

7 genetically conserved in some DH segments of higher vertebrates.

8 engers and which impedes viral infections in higher vertebrates.

9 formation of any primary sensory neurons in higher vertebrates.

10 within myelinated fiber tracts in the CNS of higher vertebrates.

11 is conserved from Caenorhabditis elegans to higher vertebrates.

12 o that found in other vertebrates, including higher vertebrates.

13 during late gastrula/early neurula stage in higher vertebrates.

14 regeneration in urodeles and its absence in higher vertebrates.

15 quence homology with p53 proteins from other higher vertebrates.

16 is homologous to the alternative pathway in higher vertebrates.

17 to their force-transmitting counterparts in higher vertebrates.

18 samine residues, is an essential molecule of higher vertebrates.

19 imes more common in the DNA of bacteria than higher vertebrates.

20 few polypeptide hormones never described in higher vertebrates.

21 ntestinal system matures in a manner akin to higher vertebrates.

22 ns with microbes have not been determined in higher vertebrates.

23 LPM), where SHF progenitors are specified in higher vertebrates.

24 n of v2r gene expression during evolution of higher vertebrates.

25 contribute to retinoic acid biosynthesis in higher vertebrates.

26 ltage-gated sodium and potassium channels in higher vertebrates.

27 the complex routes to initiate locomotion in higher vertebrates.

28 ve relatively recent evolutionary origins in higher vertebrates.

29 pivotal antiviral innate immune response in higher vertebrates.

30 idual neuronal cell types from C. elegans to higher vertebrates.

31 ulating the cell cycle at multiple stages in higher vertebrates.

32 set of the many clotting factors observed in higher vertebrates.

33 al 1,25-dihydroxyvitamin D3 [1,25(OH)2D3] in higher vertebrates.

34 missing data or assembly problems present in higher vertebrates.

35 al stage exhibits high similarity to that of higher vertebrates.

36 ary for initiation of neural tube closure in higher vertebrates.

37 me is highly conserved between zebrafish and higher vertebrates.

38 rs characterized here in a fish and those of higher vertebrates.

39 s of clade B intracellular serpin members in higher vertebrates.

40 ural projections has not been established in higher vertebrates.

41 ures in common with the neurogenic niches of higher vertebrates.

42 being more akin to the arterial trunk(s) of higher vertebrates.

43 ication of immune receptors is a hallmark of higher vertebrates.

44 bout why lens regeneration does not occur in higher vertebrates.

45 the contralateral side of the floor plate in higher vertebrates.

46 duction channels have not been identified in higher vertebrates.

47 pond to major overt behaviors, occurs in all higher vertebrates.

48 d patterns of expression within the heart of higher vertebrates.

49 represents a model for organ regeneration in higher vertebrates.

50 ucture homologous to the limbic structure of higher vertebrates.

51 pecialized in the detection of pheromones in higher vertebrates.

52 iological properties to nociceptors found in higher vertebrates.

53 icant challenge in annotating the genomes of higher vertebrates.

54 the regulation of Tbx4 and Tbx5 differs from higher vertebrates.

55 limb positioning, identity and patterning in higher vertebrates.

56 ccurs through the Tbx4 and Tbx5 genes, as in higher vertebrates.

57 e understanding of myogenic specification in higher vertebrates.

58 d by organisms ranging from bacteria through higher vertebrates.

59 erning is not reported for rodents and other higher vertebrates, a nonlinear regression analysis conf

60 ficity for the 13-14 double bond retained in higher vertebrates and also the evolutionarily preserved

61 of the fibril forming family of collagens in higher vertebrates and its heterotrimeric form is compri

62 tream of FGF-induced neural specification in higher vertebrates and provide insight into the signalli

63 mesodermal initiation of otic development in higher vertebrates and show that the mesoderm can direct

64 y narrower in teleosts compared with that in higher vertebrates, and can be accounted for in part by

65 ust activity exceeds that of CYP17 from most higher vertebrates, and likely explains why virtually no

66 lutionarily conserved between Drosophila and higher vertebrates, and that this genetically tractable

67 es comprise large portions of the genomes of higher vertebrates, and the available genomic data allow

68 for embryonic vascular pattern formation in higher vertebrates, and VEGFA is a necessary component o

69 The forelimbs of higher vertebrates are composed of two portions: the app

70 Higher vertebrates are extremely sensitive to LPS, but l

71 Arthropods and higher vertebrates both possess appendages, but these ar

72 ons of prolactin (PRL) have been reported in higher vertebrates, but are less well established in tel

73 CpG-rich islands, like the Surfeit genes in higher vertebrates, but these Fugu CpG islands are simil

74 The vestibular organs of the inner ear of higher vertebrates control balance, and their counterpar

75 The AID/APOBEC family of enzymes in higher vertebrates converts cytosines in DNA or RNA to u

76 The muscle actins in higher vertebrates display highly conserved amino acid s

77 Limb growth in higher vertebrate embryos is initially due to the outgro

78 Around the time of gastrulation in higher vertebrate embryos, inductive interactions direct

79 rns of DH segments typically associated with higher vertebrates evolved early in vertebrate phylogeny

80 ping with the evidence that Pc-G homologs in higher vertebrates exist in related pairs, we report her

81 otransposon family and was "domesticated" in higher vertebrates for synaptic functions.

82 at there are approximately : 20 000 genes in higher vertebrate genomes and the experimental verificat

83 pment in all animal species examined, and in higher vertebrates has an additional role in sensory org

84 on of signaling and transcription factors in higher vertebrates has led to the proposal that a neural

85 ority of primary and secondary bile acids in higher vertebrates have a 3alpha-hydroxyl group.

86 Retinal Muller glia in higher vertebrates have been reported to possess progeni

87 is role; TRPN1 is absent from the genomes of higher vertebrates, however, and has not been localized

88 In contrast to higher vertebrates, Hoxb13 is expressed not only in the

89 ramework for performing comparative tests in higher vertebrates in which network linkages may be more

90 the hypothalamus in gonadotropin release in higher vertebrates including birds is well established.

91 In higher vertebrates, including birds and mammals, the vas

92 ive in most fish species and two paralogs in higher vertebrates, including birds and mammals.

93 cending dopaminergic pathway is conserved to higher vertebrates, including mammals.

94 In higher vertebrates, interferons (IFNs) mediate the innat

95 CNS regeneration in higher vertebrates is a long sought after goal in neuros

96 though the biochemistry of Hox regulation in higher vertebrates is complex, the actual spatiotemporal

97 Slc5a12 in higher vertebrates is likely responsible for the electro

98 est that anterior expansion of expression in higher vertebrates is linked to the formation of the han

99 Resistance to virus infections in higher vertebrates is mediated in part through catalysis

100 The D2 mRNA of higher vertebrates is over 6 kilobases (kb), and no comp

101 Virus replication in higher vertebrates is restrained by IFNs that cause cell

102 The peripheral nervous system (PNS) of higher vertebrates is segmented to align the spinal nerv

103 or of innate immunity to viral infections in higher vertebrates, is required for a complete IFN antiv

104 wer vertebrates; although it is vestigial in higher vertebrates, it is a necessary precursor for the

105 which will undoubtedly have applicability to higher vertebrate kidney development.

106 light chains, the type III genes align with higher vertebrate lambda genes.

107 Higher vertebrates learn to recognize complex conspecifi

108 Neurons in the CNS of higher vertebrates lose their ability to regenerate thei

109 One pathway that is shared by all higher vertebrates makes an ongoing comparison of intera

110 mbrane protein of peripheral nerve myelin in higher vertebrates, mediating homoadhesion of the multip

111 ral-to-dorsal order, as has been observed in higher vertebrates, nor did we find evidence of a neural

112 e the biomineralized structures--otoconia in higher vertebrates or otoliths in fish--that deflect the

113 is the most abundant gap junction protein in higher vertebrate organisms and has been shown to be inv

114 ish epidermis is very different from that of higher vertebrates, our study shows that DeltaNp63 has e

115 In higher vertebrates, reactive gliosis resulting from inju

116 understood (although they are ubiquitous in higher vertebrates), receive input from multiple pathway

117 nation of high spatiotemporal resolution and higher vertebrate relevance for quantitative neuropharma

118 , particularly pertaining to regeneration in higher vertebrates, remains an interesting and mostly op

119 lycanopathies, as disruption of this gene in higher vertebrates results in early embryonic lethality.

120 skeletal, cardiac, vascular, and enteric) in higher vertebrates show distinct expression patterns and

121 nces were found to be highly conserved among higher vertebrate species that have acquired extraembryo

122 ugh adult neurogenesis has been conserved in higher vertebrates such as primates and humans, timing o

123 conserved, stress-associated, expression in higher vertebrates suggests that ISG15 is an important c

124 Throughout the developing nervous system of higher vertebrates, synaptic connections are concurrentl

125 t Brachyury plays a more significant role in higher vertebrates than lower vertebrates.

126 ) is a tightly regulated endoribonuclease of higher vertebrates that is catalytically active only aft

127 that encodes a simpler protein compared with higher vertebrates, the most striking difference being t

128 provide evidence suggesting that, as in the higher vertebrates, the precursor cells maintaining adul

129 In higher vertebrates, the primordium of the nervous system

130 However, unlike higher vertebrates, the zebrafish appears to be capable

131 this enzyme and the carbonic anhydrases from higher vertebrates, there are structural similarities in

132 iven the complexity of the nervous system in higher vertebrates this is a daunting task.

133 Analogous to the actions of insulin in higher vertebrates, those in Drosophila include expansio

134 d as a possible stress resistance protein in higher vertebrates to maintain chaperone activity under

135 e the diverse IgL organizations in early and higher vertebrates, two elements essential to generating

136 In contrast, unlike higher vertebrates, we did not detect Shh transcripts in

137 required for the maturation of antibodies in higher vertebrates, where it promotes somatic hypermutat

138 Although evolution has provided the higher vertebrates with complex adult kidneys, they cont

139 n approach to inactivate in vivo function in higher vertebrates with high temporal and spatial specif

140 are considerably more diverse than those of higher vertebrates, with evidence of "intron gain" in ma

141 together, these data demonstrate that, as in higher vertebrates, zebrafish SHF progenitors are specif