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1 ons disrupting mitochondrial biogenesis in a multicellular eukaryote.
2 enetic characterization of a La homolog in a multicellular eukaryote.
3 tion of the downstream signaling events in a multicellular eukaryote.
4 itis elegans, the first completely sequenced multicellular eukaryote.
5 n nuclear dynamics and genome integrity in a multicellular eukaryote.
6 y of histone variant utilization in a simple multicellular eukaryote.
7 he genome-wide rate of gene duplication in a multicellular eukaryote.
8 ing a role in specific mRNA translation in a multicellular eukaryote.
9 e-surely rivals (if not exceeds) that of the multicellular eukaryotes.
10 any aspects of cell and tissue physiology in multicellular eukaryotes.
11 ine monophosphate arose before the origin of multicellular eukaryotes.
12 ) (PAR) is critical for genomic stability in multicellular eukaryotes.
13 ggest that it may be essential in many other multicellular eukaryotes.
14 splicing and the profile of mature mRNAs in multicellular eukaryotes.
15 es cell proliferation and differentiation in multicellular eukaryotes.
16 ses in genome complexity from prokaryotes to multicellular eukaryotes.
17 systematic expansion of the genetic codes of multicellular eukaryotes.
18 le strand DNA breaks in somatic cells of all multicellular eukaryotes.
19 weakly negative such correlation is seen in multicellular eukaryotes.
20 in subunits or effectors may be conserved in multicellular eukaryotes.
21 ant progress has been made in measuring U in multicellular eukaryotes.
22 tylglucosamine (O-GlcNAc) is abundant in all multicellular eukaryotes.
23 essential, pathway that is ubiquitous in all multicellular eukaryotes.
24 ing functional diversity during evolution of multicellular eukaryotes.
25 toskeletal organisation and cell polarity in multicellular eukaryotes.
26 s and higher plants, and probably among most multicellular eukaryotes.
27 t difficult genomic components to analyze in multicellular eukaryotes.
28 volved independently of the H3.3 variants of multicellular eukaryotes.
29 that specify cell fate during development in multicellular eukaryotes.
30 early developmental events characteristic of multicellular eukaryotes.
31 prokaryotes, occurring almost exclusively in multicellular eukaryotes.
32 dic glycans are essential for the biology of multicellular eukaryotes.
33 to the high complexity of transcriptomes of multicellular eukaryotes.
34 sequence motifs are highly conserved across multicellular eukaryotes.
35 ) is a recently identified NAT found only in multicellular eukaryotes.
36 presence and biological functions of 6mA in multicellular eukaryotes.
37 ver, this mechanism has not been observed in multicellular eukaryotes.
38 transcription factors reprogram cell fate in multicellular eukaryotes.
39 to development, homeostasis, and immunity in multicellular eukaryotes.
40 ng the transcriptome in both single cell and multicellular eukaryotes.
41 al AGO paralogs have been well documented in multicellular eukaryotes.
42 ns for responses to nutrient fluctuations in multicellular eukaryotes.
43 velopmental hourglass pattern across complex multicellular eukaryotes.
44 ry that first responds to viral infection in multicellular eukaryotes.
45 prokaryotes and eukaryotes, and even between multicellular eukaryotes.
46 re evolutionarily conserved between uni- and multicellular eukaryotes.
47 apply to both single-celled prokaryotes and multicellular eukaryotes.
48 einforces cell fate in bilaterally symmetric multicellular eukaryotes.
49 pe-specific activation of gene expression in multicellular eukaryotes.
50 reveal a species-specific feature of IRE1 in multicellular eukaryotes.
51 scription factor family that is conserved in multicellular eukaryotes.
52 r altered-self leads to immune activation in multicellular eukaryotes.
53 (DNA) double-strand break repair pathway in multicellular eukaryotes.
54 intron boundaries of pre-mRNA transcripts in multicellular eukaryotes.
55 okaryotes, unicellular eukaryotes, and small multicellular eukaryotes.
56 comparable experiments have not been done in multicellular eukaryotes.
57 ntially infectious microorganisms that enter multicellular eukaryotes.
58 zing principle of gene expression in diverse multicellular eukaryotes.
59 the lack of unbiased genome-wide screens in multicellular eukaryotes.
60 he mitochondrial genomes of plants and other multicellular eukaryotes.
61 rgence of differentiation and development in multicellular eukaryotes.
62 e is similar to heterochromatin formation in multicellular eukaryotes.
63 utionary forces that drive their assembly in multicellular eukaryotes.
64 ties in culturing isolated live meiocytes of multicellular eukaryotes.
65 els function as cellular sensors in uni- and multicellular eukaryotes.
66 mere cap in Arabidopsis, and likely in other multicellular eukaryotes.
67 be far more frequent in prokaryotes than in multicellular eukaryotes.
68 ated transcriptional gene silencing (TGS) in multicellular eukaryotes.
69 rtant regulatory roles in the development of multicellular eukaryotes.
70 hanism for patterning and differentiation in multicellular eukaryotes.
71 regulation of many developmental pathways in multicellular eukaryotes.
72 ing the regulation of developmental genes in multicellular eukaryotes.
73 ay for the repair of double-strand breaks in multicellular eukaryotes.
74 ht to occur only rarely between bacteria and multicellular eukaryotes.
75 terms of gene structure relative to those of multicellular eukaryotes.
76 ional regulators that control development in multicellular eukaryotes.
77 mune system to combat bacterial infection in multicellular eukaryotes.
78 ikely required for cell proliferation in all multicellular eukaryotes.
79 nicellular eukaryotes, which have fewer than multicellular eukaryotes.
80 with a third Rio3 subfamily present only in multicellular eukaryotes.
81 R-G protein modules that may be conserved in multicellular eukaryotes.
83 mutation rates are similar to those in other multicellular eukaryotes (about 4 x 10(-9) per site per
84 balance that is not ordinarily achievable in multicellular eukaryotes, allowing the impact to be stro
85 co-ordination of key regulatory functions in multicellular eukaryotes, also reside within the cellulo
86 ell fusion is common during organogenesis in multicellular eukaryotes, although the molecular mechani
87 ion that an Xrn1p homolog degrades mRNA in a multicellular eukaryote and contributes to the miRNA-med
89 ndicated that COP8 is highly conserved among multicellular eukaryotes and is also similar to a subuni
90 that vastly increases proteomic diversity in multicellular eukaryotes and is associated with organism
92 es of Hsps in the stress physiology of whole multicellular eukaryotes and the tissues and organs they
93 factor (BAF or BANF1) is highly conserved in multicellular eukaryotes and was first identified for it
94 is present in prokaryotes and fungi (but not multicellular eukaryotes) and is an important member of
95 rder is a common phenomenon, particularly in multicellular eukaryotes, and is responsible for importa
96 ween prokaryotes, unicellular eukaryotes and multicellular eukaryotes are accompanied by orders-of-ma
100 air (DDR) in prokaryotes and unicellular and multicellular eukaryotes are similar, but the associatio
103 il marine phototrophs, including macroscopic multicellular eukaryotes, before and after each Snowball
104 l for nutrient transport and gas exchange in multicellular eukaryotes, but how connections between di
106 ecay have been identified, particularly from multicellular eukaryotes, but pinpointing the cellular c
107 rder-based signaling is further modulated in multicellular eukaryotes by alternative splicing, for wh
110 f novel signaling axes in the TOR network in multicellular eukaryotes, concentrating especially on am
113 ther, our results reveal that bacteria, like multicellular eukaryotes, couple danger sensing to the a
117 of the genes involved in the development of multicellular eukaryotes encode large, multidomain prote
120 Alternative splicing is a crucial process in multicellular eukaryote, facilitated by the assembly of
121 ng replication and a common strategy used in multicellular eukaryotes for regulating post-replicative
122 ous end joining (NHEJ) is a major pathway in multicellular eukaryotes for repairing double-strand DNA
123 at plays an essential function in protecting multicellular eukaryotes from neurodegeneration, cancer,
128 data suggests that regulatory mechanisms in multicellular eukaryotes have evolved in such a manner t
129 s a major physiological constraint for which multicellular eukaryotes have evolved robust cellular me
130 han those known to occur in prokaryotes, but multicellular eukaryotes have experienced elevations in
131 toplasmic, and mitochondrial proteins within multicellular eukaryotes have hydroxyl groups of specifi
132 less is known about the XRN-like proteins of multicellular eukaryotes; however, differences in their
133 dings extend the paradigm from yeast ARS1 to multicellular eukaryotes, implicating ORC as a determina
135 ing together a tremendously large dataset of multicellular eukaryotes, including all living species o
136 ine (aza-dC) can derepress silenced genes in multicellular eukaryotes, including animals and plants.
137 members of the NiaP family are conserved in multicellular eukaryotes, including human, pointing to p
138 roRNAs (miRNAs) are regulatory RNAs found in multicellular eukaryotes, including humans, where they a
139 t an affinity with cellularly differentiated multicellular eukaryotes, including stem-group animals o
140 entified in homologous proteins from several multicellular eukaryotes, including the model plant Arab
141 the situation previously reported for other multicellular eukaryotes, interaction between developmen
142 of a secreted variant of this enzyme from a multicellular eukaryote is very unusual and is suggestiv
143 fying cis-regulatory elements, or motifs, in multicellular eukaryotes is more difficult compared to u
144 nship has been shown in both prokaryotes and multicellular eukaryotes, it has not been demonstrated b
145 translational modification widespread across multicellular eukaryotes, its biological functions remai
146 s of cellular neighborhoods of two different multicellular eukaryotes: lab-evolved 'snowflake' yeast
147 pecific histone mark has not been studied in multicellular eukaryotes, mainly because the Rtt109 enzy
151 that the Gaoyuzhuang fossils record benthic multicellular eukaryotes of unprecedentedly large size.
153 on of a conserved enzymatic oxygen sensor in multicellular eukaryotes opens routes to better understa
154 It represents parts of a larger organism (multicellular eukaryote or a colony), likely with greate
155 mammalian systems but predominantly focus on multicellular eukaryotes owing to the additional complex
157 regime that dominates the evolution of most multicellular eukaryotes provides ample material for fun
158 is substantially more efficient than in any multicellular eukaryote, recommending it as the outstand
159 ryotes, the evolutionary mechanisms by which multicellular eukaryotes recover from deleterious mutati
161 structural features of centromeres from most multicellular eukaryotes remain to be characterized, rec
162 pora crassa, a convenient model organism for multicellular eukaryotes, remained largely undefined.
166 m is quite profound, and from single cell to multicellular eukaryotes significant similarities exist
167 rongly correlates with its GC content in all multicellular eukaryotes studied regardless of genome si
168 sion is triggered by nutrient starvation, in multicellular eukaryotes, such as plants, it is under de
170 iological hypotheses of gene regulation in a multicellular eukaryote that can be tested by medium-thr
171 pecies richness across 1,397 major clades of multicellular eukaryotes that collectively account for m
172 ng and parasitic unicellular, and even small multicellular, eukaryotes) that exclusively rely on ferm
174 nuity in genomic scaling from prokaryotes to multicellular eukaryotes, the divergent patterns of mito
175 ion are understood at the molecular level in multicellular eukaryotes, the elucidation of similar pro
176 phylogenetic level, for both unicellular and multicellular eukaryotes, the energetic expense per unit
177 which proteins encoded in the genomes of two multicellular eukaryotes, the nematode Caenorhabditis el
178 Complete genomic sequence is known for two multicellular eukaryotes, the nematode Caenorhabditis el
180 h dimorphic sexes have evolved repeatedly in multicellular eukaryotes, their origins are unknown.
184 y is widely observed in both unicellular and multicellular eukaryotes, usually associated with adapta
185 igh mannose N-glycans extracted from various multicellular eukaryotes which are not glycosylation mut
186 -methyladenine (6mA) is relatively scarce in multicellular eukaryotes, which has facilitated the deve
188 sils provide the strongest evidence yet that multicellular eukaryotes with decimetric dimensions and
189 (WGD) is a major factor in the evolution of multicellular eukaryotes, yet by doubling the number of