戻る
「早戻しボタン」を押すと検索画面に戻ります。 [閉じる]

コーパス検索結果 (１語後でソート)

通し番号をクリックするとPubMedの該当ページを表示します
1 the TrmB metabolic GRN in the model archaeon Halobacterium salinarum.
2 ystems analysis of the Cu stress response of Halobacterium salinarum.
3 duced proton pump in the halophilic archaeon Halobacterium salinarum.
4 cts of iron homeostasis in the model species Halobacterium salinarum.
5 acterium Anabaena flos-aquae and the archaea Halobacterium salinarum.
6 h functions as a light-driven proton pump in Halobacterium salinarum.
7 e purple membrane of the salt marsh archaeon Halobacterium salinarum.
8 found in the purple membrane of the archaeon Halobacterium salinarum.
9 the cell membrane of the halophilic organism Halobacterium salinarum.
10 e inserted into the membrane of the archaeon Halobacterium salinarum.
11 gh its bound transducer HtrI in the archaeon Halobacterium salinarum.
12 ervation with the rhodopsins of the archaeon Halobacterium salinarum.
13 nsitive phototaxis responses in the archaeon Halobacterium salinarum.
14 entifying how this differs from the archaeon Halobacterium salinarum.
15 aturally expressed in the purple membrane of Halobacterium salinarum.
16      Using this method, we demonstrated that Halobacterium salinarum, a hypersaline-adapted archaeal
17 conditions of limited iron, the extremophile Halobacterium salinarum, a salt-loving archaeon, mounts
18                 Sensory rhodopsin I (SRI) in Halobacterium salinarum acts as a receptor for single-qu
19  transcriptional response is identifiable in Halobacterium salinarum, an archaeal model organism.
20  and bR-containing purple membranes (PMs) of Halobacterium salinarum and demonstrated that this cell
21                  Halophilic archaea, such as Halobacterium salinarum and Natronobacterium pharaonis,
22 helix, visual pigment-like proteins found in Halobacterium salinarum and related halophilic Archaea.
23                 Using bacteriorhodopsin from Halobacterium salinarum and the translocon SecYEG from E
24 e Bacteria (termed HemAT-Hs for the archaeon Halobacterium salinarum, and HemAT-Bs for Bacillus subti
25 noparticles into the purple membrane (PM) of Halobacterium salinarum archaea, which can unidirectiona
26 otein A, a beta-barrel, eubacterial MP, (ii) Halobacterium salinarum bacteriorhodopsin, an alpha-heli
27 pic protein bacterioopsin, the apoprotein of Halobacterium salinarum bacteriorhodopsin.
28 d a homologous gene replacement strategy for Halobacterium salinarum based on ura3, which encodes the
29 iorhodopsin, the light-driven proton pump of Halobacterium salinarum, consists of the membrane apopro
30                                              Halobacterium salinarum displays four distinct kinetic f
31 ious research revealed that the haloarchaeon Halobacterium salinarum encodes four diphtheria toxin re
32 d oxidative stress responses of the archaeon Halobacterium salinarum exposed to ionizing radiation (I
33 ss conditions in the model archaeal organism Halobacterium salinarum For yeast, our method correctly
34 the first sensory rhodopsins in the archaeon Halobacterium salinarum, genome projects have revealed a
35 stribution of Z-DNA-forming sequences in the Halobacterium salinarum GRB chromosome was analyzed by d
36  (Chroococcidiopsis cubana cyanobacteria and Halobacterium salinarum halophilic archaea) to detect th
37 I), a repellent phototaxis receptor found in Halobacterium salinarum, has several homologous residues
38 -terminal regions of HemAT from the archaeon Halobacterium salinarum (HemAT-Hs) and from the Gram-pos
39 ers in the phototaxis system of the archaeon Halobacterium salinarum, HtrI and HtrII, are methyl-acce
40 yptic peptides from bovine serum albumin and Halobacterium salinarum in a high throughput liquid chro
41                    Dodecin from the archaeal Halobacterium salinarum is a riboflavin storage device.
42          Signal transduction in the archaeon Halobacterium salinarum is mediated by three distinct su
43  sole histone encoded in the model halophile Halobacterium salinarum, is not involved in DNA packagin
44 I and the mutant D73E, both reconstituted in Halobacterium salinarum lipids, using FTIR difference sp
45 s a dimer when functionally expressed in the Halobacterium salinarum membrane.
46 y rhodopsin II (SRII) by flash photolysis of Halobacterium salinarum membranes genetically engineered
47               Sensory rhodopsin II (SRII) in Halobacterium salinarum membranes is a phototaxis recept
48 s carry out light-driven proton transport in Halobacterium salinarum membranes.
49 have constructed a model for this process in Halobacterium salinarum NRC-1 through the data-driven di
50 al lineages: a photoheterotrophic halophile (Halobacterium salinarum NRC-1), a hydrogenotrophic metha
51 rotein and in the extended C-terminus of the Halobacterium salinarum protein.
52 roton pump bacteriorhodopsin in the archaeon Halobacterium salinarum requires coordinate synthesis of
53 treme halophiles, Halobacterium halobium and Halobacterium salinarum, retain entrapped carboxyfluores
54  A fusion protein in which the C-terminus of Halobacterium salinarum sensory rhodopsin I (SRI) is con
55                                              Halobacterium salinarum sensory rhodopsin II (HsSRII) is
56    The spectral tuning of halorhodopsin from Halobacterium salinarum (shR) during anion transport was
57 epellent phototaxis receptor in the archaeon Halobacterium salinarum, similar to visual pigments in i
58 low for the archaea using the model organism Halobacterium salinarum sp. NRC-1 and demonstrate its ap
59 alorhodopsin, Jaws, derived from Haloarcula (Halobacterium) salinarum (strain Shark) and engineered t
60 dation, we discovered an RNase (VNG2099C) in Halobacterium salinarum that is transcriptionally co-reg
61 eless HtrI, a phototaxis transducer found in Halobacterium salinarum that transmits signals from the
62                        In the model archaeon Halobacterium salinarum, the transcription factor TrmB r
63                              Chimeras of the Halobacterium salinarum transducers HtrI and HtrII were
64  As a test case, bacteriorhodopsin (bR) from Halobacterium salinarum was crystallized from a bicellar
65                                              Halobacterium salinarum was used as the model organism a
66     The deletion of halA in the haloarchaeon Halobacterium salinarum, whose cells are consistently ro
67  dried purple membrane patches purified from Halobacterium salinarum with infrared vibrational scatte
68 membranes (formed from lipids extracted from Halobacterium salinarum), yet systematic analyses based