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1 mal or plant multicellular organisms (higher eucaryotes).
2 ical characteristics of RNase P from a lower eucaryote.
3 Erf2 plays a role in Ras localization in all eucaryotes.
4 tion early in the evolution of multicellular eucaryotes.
5 d in the outer mitochondrial membrane of all eucaryotes.
6 ally incorporated opposite abasic lesions in eucaryotes.
7 nces occur with high frequency in the DNA of eucaryotes.
8 E-Cdk2 and subsequent G(1) arrest in higher eucaryotes.
9 d in the outer mitochondrial membrane of all eucaryotes.
10 sitol 1 (or 4) monophosphatases from various eucaryotes.
11 ns are widely distributed in procaryotes and eucaryotes.
12 of critically shortened telomeres in higher eucaryotes.
13 urally identical to those produced by higher eucaryotes.
14 hly conserved WD domain protein found in all eucaryotes.
15 g chromatin structure and gene expression in eucaryotes.
16 shed is its role in the protection of higher eucaryotes against oxygen toxicity through destruction o
18 ospholipid cardiolipin (CL) is ubiquitous in eucaryotes and is unique in structure, subcellular local
19 rence reflected a general difference between eucaryotes and procaryotes, we now extended the analysis
20 -genome random BAC fingerprint analysis of a eucaryote, and have provided a model essential to effort
21 range of variation in bacteria, archaea, and eucaryotes as well as chemical probing and cross-linking
22 lls differs from the pathway found in higher eucaryotes, as indicated by the fact that glycoproteins
23 p of four stacked heptameric rings, which in eucaryotes assemble from 14 different but related subuni
25 pair in mammalian cells, as opposed to lower eucaryotes, but HRR has recently been implicated in crit
28 ese motifs to search for homologous genes in eucaryotes demonstrated the presence of rnhB genes in a
29 ophilic bacteria and from an amitochondriate eucaryote each contain four domains which are phylogenet
30 lded polypeptides and has been purified from eucaryotes, gram-positive actinomycetes, and archaea.
32 ocessing pathways of insect cells and higher eucaryotes imposes a significant limitation on their use
35 of critically shortened telomeres in higher eucaryotes is presumed to be mediated by nonhomologous e
37 f this RNA from diverse organisms, including eucaryotes, primarily fungi, but also a limited set of v
38 icA polypeptide resembles choline kinases of eucaryotes, suggesting that the pathway for choline inco
39 dehydrogenases (GSH-FDH) in procaryotes and eucaryotes suggests this enzyme plays a central and univ
40 12- to 13-nucleotide-long oligomers, and in eucaryotes they result in excision of the damage in the
41 properties similar to small introns in lower eucaryotes, we studied the small second intron from the
42 sential membrane proteins in procaryotes and eucaryotes, which use the energy of the transmembrane el
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