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1 spanning all domains of life, from humans to hyperthermophilic archaea.
2  in rRNA, tRNA, non-coding RNA and mRNA from hyperthermophilic archaea.
3  communities dominated by several species of hyperthermophilic Archaea.
4 d response mechanism that is present even in hyperthermophilic archaea.
5 ting experiments for bacteria and 90-99% for hyperthermophilic archaea.
6 ed to study its impact on DNA replication in hyperthermophilic Archaea.
7 like CPSase such as those present in several hyperthermophilic archaea.
8 ases are involved in peptide fermentation by hyperthermophilic archaea.
9 turally characterized mainly using WORs from hyperthermophilic archaea.
10 enzymes in sugar and peptide fermentation of hyperthermophilic archaea.
11 croscopy of three conjugative pili, two from hyperthermophilic archaea (Aeropyrum pernix and Pyrobacu
12 f structures and complete genomes of several hyperthermophilic archaea and bacteria revealed that org
13 bilizes tRNAs from thermophilic bacteria and hyperthermophilic archaea and is required for growth at
14 interaction with uracil is not restricted to hyperthermophilic archaea and that the polymerase from m
15                                              Hyperthermophilic archaea are close to the origin of lif
16 quences (ISs) are abundant and widespread in hyperthermophilic archaea, but few experimental studies
17  from common yeasts to extremophiles such as hyperthermophilic archaea can also generate high current
18            So far, little is known about how hyperthermophilic Archaea cope with such pyrimidine dama
19            The majority of viruses infecting hyperthermophilic archaea display unique virion architec
20 ) accumulates as a compatible solute in many hyperthermophilic archaea (e.g., Archaeoglobus fulgidus)
21       Here we describe a consortium of three hyperthermophilic archaea enriched from a continental ge
22 e that the intracellular proteins of certain hyperthermophilic archaea, especially the crenarchaea Py
23       Several enzymes of DNA metabolism from hyperthermophilic archaea exhibit unusual biochemical fe
24                                              Hyperthermophilic archaea grow at temperatures that dest
25    In particular, the approaches employed by hyperthermophilic archaea have been a general source of
26 f the DNA replication-associated proteins of hyperthermophilic archaea have yielded considerable insi
27                                           In hyperthermophilic archaea, however, TIM exists as a tetr
28    Inositol monophosphatase (EC 3.1.3.25) in hyperthermophilic archaea is thought to play a role in t
29 esults suggest that many DNA repair genes of hyperthermophilic archaea may not be recognized because
30                   Hsp16.5, isolated from the hyperthermophilic Archaea Methanococcus jannaschii, is a
31 o establish the key cell-cycle parameters of hyperthermophilic archaea of the genus Sulfolobus.
32 rs contained in a microbiome-associated with hyperthermophilic archaea of the order Sulfolobales reco
33                            Viruses infecting hyperthermophilic archaea of the phylum Crenarchaeota di
34 perties when compared even to Fds from other hyperthermophilic archaea or bacteria.
35 uctures of two ECNs from two major orders of hyperthermophilic archaea present in deep-sea hydrotherm
36  the TATA-box binding protein (TBP) from the hyperthermophilic archaea Pyrococcus woesei.
37 riginated in an extreme environment, such as hyperthermophilic archaea (Pyrococcus furiosus), are sig
38                            Divergence of the hyperthermophilic Archaea, Pyrococcus furiosus and Pyroc
39 d over a contiguous 16 kb region between two hyperthermophilic Archaea, Pyrococcus furiosus and Therm
40 esponses have been of particular interest in hyperthermophilic archaea, since these microbes live und
41 RNA-encoding DNA analysis places many of the hyperthermophilic Archaea (species with an optimum growt
42 ficity and binding mechanism of MCM from the hyperthermophilic Archaea Sulfolobus solfataricus on var
43                                  However, in hyperthermophilic archaea that live optimally at tempera
44         Cell extracts of the proteolytic and hyperthermophilic archaea Thermococcus litoralis, Thermo
45                            Viruses infecting hyperthermophilic archaea typically do not encode DNA po
46 s of recombination involving short ssDNAs in hyperthermophilic archaea, we evaluated oligonucleotide-