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1 tion of the downstream signaling events in a multicellular eukaryote.
2 ons disrupting mitochondrial biogenesis in a multicellular eukaryote.
3 enetic characterization of a La homolog in a multicellular eukaryote.
4 itis elegans, the first completely sequenced multicellular eukaryote.
5 y of histone variant utilization in a simple multicellular eukaryote.
6 he genome-wide rate of gene duplication in a multicellular eukaryote.
7 ses in genome complexity from prokaryotes to multicellular eukaryotes.
8 systematic expansion of the genetic codes of multicellular eukaryotes.
9 le strand DNA breaks in somatic cells of all multicellular eukaryotes.
10 weakly negative such correlation is seen in multicellular eukaryotes.
11 in subunits or effectors may be conserved in multicellular eukaryotes.
12 ant progress has been made in measuring U in multicellular eukaryotes.
13 tylglucosamine (O-GlcNAc) is abundant in all multicellular eukaryotes.
14 essential, pathway that is ubiquitous in all multicellular eukaryotes.
15 ing functional diversity during evolution of multicellular eukaryotes.
16 toskeletal organisation and cell polarity in multicellular eukaryotes.
17 s and higher plants, and probably among most multicellular eukaryotes.
18 t difficult genomic components to analyze in multicellular eukaryotes.
19 volved independently of the H3.3 variants of multicellular eukaryotes.
20 that specify cell fate during development in multicellular eukaryotes.
21 early developmental events characteristic of multicellular eukaryotes.
22 re evolutionarily conserved between uni- and multicellular eukaryotes.
23 prokaryotes, occurring almost exclusively in multicellular eukaryotes.
24 apply to both single-celled prokaryotes and multicellular eukaryotes.
25 einforces cell fate in bilaterally symmetric multicellular eukaryotes.
26 pe-specific activation of gene expression in multicellular eukaryotes.
27 reveal a species-specific feature of IRE1 in multicellular eukaryotes.
28 scription factor family that is conserved in multicellular eukaryotes.
29 r altered-self leads to immune activation in multicellular eukaryotes.
30 (DNA) double-strand break repair pathway in multicellular eukaryotes.
31 ) is a recently identified NAT found only in multicellular eukaryotes.
32 intron boundaries of pre-mRNA transcripts in multicellular eukaryotes.
33 okaryotes, unicellular eukaryotes, and small multicellular eukaryotes.
34 ntially infectious microorganisms that enter multicellular eukaryotes.
35 zing principle of gene expression in diverse multicellular eukaryotes.
36 the lack of unbiased genome-wide screens in multicellular eukaryotes.
37 he mitochondrial genomes of plants and other multicellular eukaryotes.
38 e is similar to heterochromatin formation in multicellular eukaryotes.
39 al AGO paralogs have been well documented in multicellular eukaryotes.
40 utionary forces that drive their assembly in multicellular eukaryotes.
41 ties in culturing isolated live meiocytes of multicellular eukaryotes.
42 els function as cellular sensors in uni- and multicellular eukaryotes.
43 mere cap in Arabidopsis, and likely in other multicellular eukaryotes.
44 be far more frequent in prokaryotes than in multicellular eukaryotes.
45 ated transcriptional gene silencing (TGS) in multicellular eukaryotes.
46 rtant regulatory roles in the development of multicellular eukaryotes.
47 hanism for patterning and differentiation in multicellular eukaryotes.
48 regulation of many developmental pathways in multicellular eukaryotes.
49 ing the regulation of developmental genes in multicellular eukaryotes.
50 ay for the repair of double-strand breaks in multicellular eukaryotes.
51 ht to occur only rarely between bacteria and multicellular eukaryotes.
52 terms of gene structure relative to those of multicellular eukaryotes.
53 ional regulators that control development in multicellular eukaryotes.
54 mune system to combat bacterial infection in multicellular eukaryotes.
55 ikely required for cell proliferation in all multicellular eukaryotes.
56 nicellular eukaryotes, which have fewer than multicellular eukaryotes.
57 with a third Rio3 subfamily present only in multicellular eukaryotes.
58 R-G protein modules that may be conserved in multicellular eukaryotes.
59 ine monophosphate arose before the origin of multicellular eukaryotes.
60 ) (PAR) is critical for genomic stability in multicellular eukaryotes.
61 prokaryotes and eukaryotes, and even between multicellular eukaryotes.
62 ggest that it may be essential in many other multicellular eukaryotes.
63 splicing and the profile of mature mRNAs in multicellular eukaryotes.
64 es cell proliferation and differentiation in multicellular eukaryotes.
66 mutation rates are similar to those in other multicellular eukaryotes (about 4 x 10(-9) per site per
67 co-ordination of key regulatory functions in multicellular eukaryotes, also reside within the cellulo
68 ell fusion is common during organogenesis in multicellular eukaryotes, although the molecular mechani
69 ion that an Xrn1p homolog degrades mRNA in a multicellular eukaryote and contributes to the miRNA-med
71 ndicated that COP8 is highly conserved among multicellular eukaryotes and is also similar to a subuni
72 that vastly increases proteomic diversity in multicellular eukaryotes and is associated with organism
74 es of Hsps in the stress physiology of whole multicellular eukaryotes and the tissues and organs they
75 factor (BAF or BANF1) is highly conserved in multicellular eukaryotes and was first identified for it
76 is present in prokaryotes and fungi (but not multicellular eukaryotes) and is an important member of
77 rder is a common phenomenon, particularly in multicellular eukaryotes, and is responsible for importa
78 ween prokaryotes, unicellular eukaryotes and multicellular eukaryotes are accompanied by orders-of-ma
81 air (DDR) in prokaryotes and unicellular and multicellular eukaryotes are similar, but the associatio
84 l for nutrient transport and gas exchange in multicellular eukaryotes, but how connections between di
86 ecay have been identified, particularly from multicellular eukaryotes, but pinpointing the cellular c
87 rder-based signaling is further modulated in multicellular eukaryotes by alternative splicing, for wh
95 of the genes involved in the development of multicellular eukaryotes encode large, multidomain prote
98 ous end joining (NHEJ) is a major pathway in multicellular eukaryotes for repairing double-strand DNA
99 at plays an essential function in protecting multicellular eukaryotes from neurodegeneration, cancer,
103 data suggests that regulatory mechanisms in multicellular eukaryotes have evolved in such a manner t
104 han those known to occur in prokaryotes, but multicellular eukaryotes have experienced elevations in
105 less is known about the XRN-like proteins of multicellular eukaryotes; however, differences in their
106 dings extend the paradigm from yeast ARS1 to multicellular eukaryotes, implicating ORC as a determina
107 ing together a tremendously large dataset of multicellular eukaryotes, including all living species o
108 ine (aza-dC) can derepress silenced genes in multicellular eukaryotes, including animals and plants.
109 members of the NiaP family are conserved in multicellular eukaryotes, including human, pointing to p
110 roRNAs (miRNAs) are regulatory RNAs found in multicellular eukaryotes, including humans, where they a
111 t an affinity with cellularly differentiated multicellular eukaryotes, including stem-group animals o
112 entified in homologous proteins from several multicellular eukaryotes, including the model plant Arab
113 the situation previously reported for other multicellular eukaryotes, interaction between developmen
114 of a secreted variant of this enzyme from a multicellular eukaryote is very unusual and is suggestiv
115 fying cis-regulatory elements, or motifs, in multicellular eukaryotes is more difficult compared to u
116 nship has been shown in both prokaryotes and multicellular eukaryotes, it has not been demonstrated b
117 translational modification widespread across multicellular eukaryotes, its biological functions remai
118 pecific histone mark has not been studied in multicellular eukaryotes, mainly because the Rtt109 enzy
121 that the Gaoyuzhuang fossils record benthic multicellular eukaryotes of unprecedentedly large size.
123 is substantially more efficient than in any multicellular eukaryote, recommending it as the outstand
124 ryotes, the evolutionary mechanisms by which multicellular eukaryotes recover from deleterious mutati
125 structural features of centromeres from most multicellular eukaryotes remain to be characterized, rec
126 pora crassa, a convenient model organism for multicellular eukaryotes, remained largely undefined.
128 m is quite profound, and from single cell to multicellular eukaryotes significant similarities exist
129 rongly correlates with its GC content in all multicellular eukaryotes studied regardless of genome si
131 iological hypotheses of gene regulation in a multicellular eukaryote that can be tested by medium-thr
132 pecies richness across 1,397 major clades of multicellular eukaryotes that collectively account for m
134 nuity in genomic scaling from prokaryotes to multicellular eukaryotes, the divergent patterns of mito
135 which proteins encoded in the genomes of two multicellular eukaryotes, the nematode Caenorhabditis el
136 Complete genomic sequence is known for two multicellular eukaryotes, the nematode Caenorhabditis el
138 h dimorphic sexes have evolved repeatedly in multicellular eukaryotes, their origins are unknown.
141 sils provide the strongest evidence yet that multicellular eukaryotes with decimetric dimensions and
142 (WGD) is a major factor in the evolution of multicellular eukaryotes, yet by doubling the number of
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