ライフサイエンスコーパス: metazoa

1 adhesion such as integrin beta subunits (all Metazoa).

2 xclusively in animal organisms (Protozoa and Metazoa).

3 chizosaccharomyces pombe) to hetero-nonamer (Metazoa).

4 premeiotic S phase remains poorly defined in metazoa.

5 sues can be traced to a soft tissue in early Metazoa.

6 by which to investigate protein function in metazoa.

7 asymmetric) within the division plane across Metazoa.

8 hat have been primarily studied in yeast and metazoa.

9 llular matrix is one defining feature of all Metazoa.

10 tRNAs, and two rRNAs) typically found in the metazoa.

11 nt of the phylum Placozoa at the root of the Metazoa.

12 and bacterial pathogens but are absent from metazoa.

13 has been implicated as a cause of ageing in metazoa.

14 al homologs, as opposed to homologs in other Metazoa.

15 ent and maintenance of tissue homeostasis in metazoa.

16 ly, it shares derived features unique to the Metazoa.

17 gous to lamins, the major lamina proteins of metazoa.

18 ct molecular clock cannot be assumed for the Metazoa.

19 n formation and morphogenesis throughout the metazoa.

20 arried out to determine its placement within Metazoa.

21 igands determines a variety of cell fates in metazoa.

22 the formation/function of tight-junctions in metazoa.

23 originally used later in development by all metazoa.

24 common ancestor of trichomonads, yeast, and metazoa.

25 f Fungi of approximately the same age as the Metazoa.

26 ic and regulatory evolution after WGD in the Metazoa.

27 of another--is a universal phenomenon in the Metazoa.

28 zation in many other contexts throughout the Metazoa.

29 e important modulators of origin activity in metazoa.

30 ence for origins has yet to be identified in metazoa.

31 ating conservation of NR functions among the Metazoa.

32 84 NR genes are 15 genes conserved among the Metazoa.

33 the greatest diversity of body plans in the Metazoa.

34 m cell specification may be ancestral to the Metazoa.

35 imeric CDK7-cyclin H-Mat1 in human and other metazoa.

36 ceptors that regulate cell fate decisions in metazoa.

37 aradigm for the complex origins found in the metazoa.

38 ment membrane (BM) proteins conserved in all metazoa.

39 le is known about the ORC-DNA interaction in metazoa.

40 hyly of Bilateria, Cnidaria, Ctenophora, and Metazoa.

41 and that may be linked to the origin of the Metazoa.

42 rged as regulators of gene expression across metazoa.

43 trast to their generally exonic locations in metazoa.

44 ell signalling evolved before the origins of metazoa.

45 ns that regulate cellular polyamine pools in metazoa.

46 lated in honey bees are conserved across the Metazoa.

47 from the common ancestral line of all other Metazoa.

48 before the origin of angiosperms, fungi, and metazoa.

49 ly component of the regulatory mechanisms of metazoa.

50 program in embryonic patterning in the lower Metazoa.

51 As from genes is an ubiquitous phenomenon in metazoa.

52 esses transposable elements in germ cells of Metazoa.

53 and gene expression are conserved among the Metazoa.

54 obacterium, replaced the ancestral enzyme in Metazoa.

55 d the cytoplasmic fates of messenger RNAs in metazoa.

56 an regulation and their evolution within the Metazoa.

57 ns unclear how UPF1 is activated outside the metazoa.

58 , transmembrane protein conserved throughout Metazoa.

59 BAF nucleosome-remodeling complex in vivo in metazoa.

60 verse transposable elements in germ cells of metazoa.

61 r to annotate data sets from taxa outside of Metazoa.

62 ys in a variety of cell types throughout the Metazoa.

63 bond, is evolutionarily conserved throughout Metazoa.

64 ce Ctenophora as the earliest lineage within Metazoa.

65 e thymidine kinase 2-like dNK gene family in metazoa.

66 ficity of Brachyury emerged at the origin of Metazoa.

67 onserved structures and functions across the Metazoa.

68 a noxious chemical sensor throughout much of Metazoa.

69 for coordinating developmental activities in metazoa.

70 apical polarity may be conserved throughout Metazoa.

71 m, evolved to diversify the transcriptome in metazoa.

72 tors (GPCRs), the largest receptor family in Metazoa.

73 ad mechanism to alter genetic information in metazoa.

74 the T-box family diversified at the onset of Metazoa.

75 s - many ciliate cells are larger than small metazoa.

76 ukaryotes prior to the origins of neurons in metazoa.

77 f ECM proteins to serve diverse functions in metazoa.

78 ran-Cambrian (578-510 Ma) diversification of Metazoa.

79 in allorecognition responses throughout the metazoa.

80 een groups of cells allowed the evolution of metazoa.

81 t, stress response, and energy metabolism in metazoa.

82 conserved master stress-response pathway in metazoa.

83 transcription factor binding sites among the metazoa.

84 ay, a major growth regulatory pathway within metazoa [4], but at least in some instances, the influen

85 cally important processes, and that for many metazoa, A-to-I conversion in coding regions may be the

86 All metazoa also have a membrane-associated Wee1p-like kinas

87 in addition to 55 genomes from invertebrate metazoa and 39 genomes from plants.

88 The formation of filopodia in Metazoa and Amoebozoa requires the activity of myosin 10

89 te decisions are likely to be conserved with metazoa and are providing insight into differentiation d

90 ein SAS-4 regulates centriole duplication in metazoa and basal body duplication in flagellated and ci

91 lex in a stem-holozoan, the ancestor of both Metazoa and Choanoflagellata, the protozoan group most c

92 ges (i.e., those with embryonic development, Metazoa and Embryophyta) have the most complex TF repert

93 y restricted to the supergroup Opisthokonta (Metazoa and Fungi), whereas proteins with the ELMOD orga

94 (Dd), a member of the Amoebazoa outgroup of Metazoa and Fungi, and show that it has a highly simplif

95 In metazoa and fungi, the catabolic dissimilation of cystei

96 BC10 is highly conserved across a range of metazoa and has been implicated in two forms of cancer.

97 ts determine an essential function of CDK in metazoa and identify a developmental role for regulated

98 This novel domain (NZF) is conserved in metazoa and is both present and functional in other prot

99 ned the differences between the proteomes of Metazoa and other eukaryotes.

100 analysis of published BiFC fragments used in metazoa and plants, and then developed an optimized sing

101 Genes related to Cdt1 have been found in Metazoa and plants, suggesting that the cooperation of C

102 ae in a common lineage distinct from that of metazoa and plants.

103 xual dimorphism is widespread throughout the metazoa and plays important roles in mate recognition an

104 al processes in a wide variety of organisms, metazoa and protists alike.

105 f the mechanism of cell cycle checkpoints in metazoa and provides a marker for studying the role of t

106 range of processes, including cytokinesis in Metazoa and some Archaea.

107 in visual system development throughout the metazoa and the function of Pax6 is evolutionarily conse

108 It comprises two major clades: (i) the Metazoa and their unicellular relatives and (ii) the Fun

109 Collagen IV networks are present in all metazoa and underlie epithelia as a component of basemen

110 3 orthologous families that were specific to Metazoa and were likely to have originated in their last

111 nts culminating in the emergence of animals (Metazoa) and new ecosystems.

112 hways not found in KEGG, from plants, fungi, metazoa, and actinobacteria; KEGG contains pathways not

113 each containing sequences from angiosperms, metazoa, and fungi.

114 ubiquitous sensory ability found across the Metazoa, and photoreceptive organs are intricate and div

115 inst PBGS orthologs from bacteria, protozoa, metazoa, and plants to elucidate the inhibitory spectrum

116 dherens junctions have only been detected in metazoa, and therefore we looked for them outside the an

117 r event in the stem lineage of Holozoa, i.e. Metazoa (animals) and their unicellular relatives, the C

118 ned at the molecular level, is unique to the Metazoa (animals).

119 seen during the split between fungi and the Metazoa approximately 1.0-1.2 Ga, at a time when oceanic

120 sly characterized modification guide RNAs in metazoa are encoded in and processed from introns.

121 The genomes of metazoa are organized at multiple scales.

122 studies of transcriptional regulation in the metazoa are significantly hindered by the absence of rea

123 ex systems, which control gene expression in metazoa, are helping researchers identify fundamental th

124 long and highly charged C-terminal tails, in metazoa as well as in yeast.

125 OSA-1, a cyclin-related protein conserved in metazoa, as a key component required to convert meiotic

126 icate that inferences about the evolution of Metazoa based on the Ctenophora-sister hypothesis are no

127 at DNA replication in multicellular animals (metazoa) begins at specific origins to which a pre-repli

128 large intracellular domain (ICD) present in metazoa (between transmembrane segments M3 and M4).

129 a, the group of Choanozoa that is closest to Metazoa, both the ancestral and the horizontally transfe

130 0 residues which also is highly conserved in Metazoa but is absent in Sc-Nup120.

131 shares many general cellular properties with metazoa, but has no identified cell suicide machinery.

132 ologs of ELL and EAF have been identified in metazoa, but it has been unclear whether such RNA polyme

133 otal regulator of eye development throughout Metazoa, but the direct upstream regulators of vertebrat

134 been implicated in age-associated decline in metazoa, but they have only been identified in extracell

135 l migration, survival and differentiation in metazoa by communicating signals bi-directionally across

136 In metazoa cap 1 (m(7)GpppNmp-RNA) is linked to higher leve

137 In Metazoa, Cdt1 is regulated by CRL4(Cdt2)-mediated ubiqui

138 xport protein Yra1 (ALY/RNA export factor in metazoa) cotranscriptionally associates with mRNA and de

139 of proteins involved in cell interactions in Metazoa demonstrates that these proteins evolved before

140 ia, protists, fungi, plants and invertebrate metazoa) designed to complement the availability of vert

141 In metazoa, distinct stress conditions activate different e

142 In metazoa, DNA elimination typically occurs in somatic cel

143 ur in a wide range of phyla, particularly in Metazoa, due to a reduced "proteomic constraint" on the

144 ing ATF4 control are conserved in the entire metazoa except nematoda.

145 Despite being bilaterally symmetric, most Metazoa exhibit clear, genetically determined left-right

146 egulate neuronal morphogenesis in developing metazoa (for review, see [1]).

147 Biomineralization is the process by which metazoa form hard minerals for support, defense, and fee

148 rucial role in safeguarding the germlines of metazoa from mobile DNA elements.

149 The evolution of the Metazoa from protozoans is one of the major milestones i

150 asement membranes that underlie epithelia in metazoa from sponge to human.

151 35 kDa), the heteromeric partner of CFD1 in metazoa, functions on its own in plants.

152 In metazoa, growth factors trigger conversion of Ras from a

153 etic position of the Chaetognatha within the Metazoa has long been uncertain, with conflicting or equ

154 nd the first sequence of a linear mtDNA from Metazoa - has been determined.

155 cysteine proteases in primitive protozoa and metazoa have suggested that this enzyme family is more d

156 Both land plants and metazoa have the capacity to reprogram differentiated ce

157 lution involved deployment of VWA domains by Metazoa in extracellular proteins involved in cell adhes

158 y marine demosponges, record the presence of Metazoa in the geological record before the end of the M

159 ADPGK is found in Archaea and metazoa; in Archaea, ADPGK participates in a glycolytic

160 lexity of the DNA damage response network in metazoa including the evolution of other BRCT domain-con

161 s that are required for cadherin function in Metazoa, including cytoskeleton organization, cell-subst

162 teraction is evolutionarily conserved across metazoa, indicating its significance.

163 Cell division in many metazoa is accompanied by the disassembly of the nuclear

164 The appearance of PONs in metazoa is likely to relate to innate immunity rather th

165 cell cycle and developmental transitions in metazoa is poorly understood.

166 CstF-64, a small region, highly conserved in metazoa, is responsible for interactions with two protei

167 In metazoa, lamin proteins preserve nuclear integrity and h

168 for the notion that origin specification in metazoa likely involves mechanisms other than simple rep

169 tions and lineage specific expansions in the metazoa lineage.

170 rphic histocompatibility loci common to many metazoa may have arisen or been maintained: to limit sup

171 The acquisition of O-GlcNAc signaling by metazoa may have facilitated the rapid and complex signa

172 to our knowledge, identified outside of the Metazoa, MBRTK1.

173 In metazoa multiple gamma-TuSCs assemble with other protein

174 Intercellular communication in metazoa not only requires autocrine, paracrine and exocr

175 In metazoa, nuclear pore complexes (NPCs) assemble from dis

176 ration was shown to occur in: (i) the LCA of Metazoa or (ii) independently in the Metazoan phyla.

177 te-have been purified and characterized from metazoa or their viruses.

178 ng in fission yeast and show that similar to metazoa, ORC binding is periodic during the cell cycle,

179 Metazoa possess protein disaggregase systems distinct fr

180 It appears that most metazoa possess sequences encoding a single highly conse

181 ila eye development but broadly conserved in metazoa, possesses dual functions as a transcriptional c

182 In metazoa, pre-mRNA 3' end formation occurs via two pathwa

183 ip between IBP39 and Inr-binding proteins in metazoa presents interesting evolutionary questions.

184 In Metazoa, promoters of transcriptionally active genes are

185 of a conserved nucleotide sequence that, in metazoa, promotes a +1 programmed ribosomal frameshift r

186 Understanding how metazoa protect their genomes from mutagenic retrovirus

187 OrthoVenn provides coverage of vertebrates, metazoa, protists, fungi, plants and bacteria for the co

188 lar and colonial protozoa closely related to Metazoa, provide a potential window into early animal ev

189 n of RtcB proteins in bacteria, archaea, and metazoa raises the prospect of an alternative enzymology

190 a protein resembles nonmuscle myosin-2s from metazoa rather than protozoa, though modulatory aspects

191 In metazoa, re-replication of DNA during a single S phase s

192 ponges (phylum Porifera) are early-diverging metazoa renowned for establishing complex microbial symb

193 n strategy to achieve cell type diversity in metazoa, results from binary cell-fate decisions in the

194 The gene order, although unique amongst Metazoa, shared the greatest number of gene boundaries a

195 In yeast and metazoa, structural maintenance of chromosome (SMC) comp

196 orax as Arthropoda and Chordata emerged from Metazoa suggesting that Taspase1 originated to regulate

197 e relationship between choanoflagellates and Metazoa, suggesting that comparison of the complement of

198 tilization and prior to pronuclear fusion in metazoa, suggesting that newly transcribed genes appear

199 ucity of peptidase families unique to higher metazoa suggests gains in proteolytic network complexity

200 ence of domains in repeats is more common in metazoa than in single cellular organisms.

201 adthrough is significantly more prevalent in Metazoa than previously recognized.

202 deaminase (ADAR1) is an ubiquitous enzyme in metazoa that edits pre-mRNA changing adenosine to inosin

203 rins are important adhesion receptors in all Metazoa that transmit conformational change bidirectiona

204 Reference genomes for metazoa that undergo DNA elimination are not available.

205 nd cleavage and polyadenylation, although in metazoa the replication-dependent histone mRNAs are proc

206 he center of discussions of the evolution of Metazoa, the biology of survival in extreme environments

207 ause neural systems are almost ubiquitous in metazoa, the constitutive expression of neuroglobin-like

208 es by directly modulating gene expression in Metazoa, the regulatory pathways for sensing and respond

209 nuclear proteins highly conserved throughout metazoa, the SR (serine/arginine) proteins.

210 Since their discovery in Metazoa, the three nuclear RNA polymerases (RNAPs) have

211 -1 was the first genetic locus identified in metazoa to affect the distribution of meiotic crossovers

212 nction throughout development and across the metazoa to regulate cell polarity.

213 ial process that occurs in female meiosis of metazoa to reset centriole number in the zygote at ferti

214 In metazoa, TREX is loaded on nascent RNA transcribed by RN

215 Ran interacts with the NPC of metazoa via two asymmetrically localized components, Nup

216 We conclude that evolution in the LCA of Metazoa was extensive and proceeded largely by gene dupl

217 in eukaryotes distantly related to yeast and metazoa, we characterized the Trypanosoma brucei SCC1 or

218 y governs cellular differentiation in higher metazoa, where Notch signals are transduced by the trans

219 sin, a novel metalloprotease present only in metazoa, whose activity appears to be essential for mito

220 c link between lineage-defining asymmetry of metazoa with unicellular eukaryotes.

221 Conversely, those metazoa with unlimited cellular replicability, by stavin

222 Whole-body regeneration is widespread in the Metazoa, yet little is known about how underlying molecu

223 cental mammals, early vertebrates, and early metazoa, yielding results consistent with, but more prec