戻る
「早戻しボタン」を押すと検索画面に戻ります。

今後説明を表示しない

[OK]

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 sion of plant nodule-specific genes known as nodulins.
2  provide convincing evidence that microsomal nodulin-100 is phosphorylated in mature nodules, and tha
3 py, we documented that part of the total SS (nodulin-100) pool in mature soybean (Glycine max) nodule
4 ylation domain and site reside in microsomal nodulin-100.
5 epidermis, NIN restricts the extent of Early Nodulin 11 (ENOD11) expression and does so through compe
6 ) under control of the Medicago sativa EARLY NODULIN 12B promoter in our previously developed high-ir
7 noid legumes shown to possess putative early nodulin 2 (ENOD2) genes.
8  along with two other nodule-specific genes, nodulin-22 and nodulin-25.
9 unequal recombination event occurred between nodulin-25 and a nearby calmodulin, which gave rise to t
10  other nodule-specific genes, nodulin-22 and nodulin-25.
11                                              Nodulin 26 (NOD 26), a member of the aquaporin (AQP) wat
12                                              Nodulin 26 (nod26) is a major intrinsic protein that con
13                 Thus, the phosphorylation of nodulin 26 coincides with the establishment of mature ni
14 ing infected cells (16 days), phosphorylated nodulin 26 does not become pronounced until infected cel
15                         Liposomes containing nodulin 26 exhibited a high osmotic permeability (Pf = 0
16                                Reconstituted nodulin 26 exhibited a single-channel conductance of 3.8
17 eriments in Xenopus oocytes that showed that nodulin 26 facilitated glycerol flux in a manner indisti
18                                              Nodulin 26 intrinsic proteins (NIPs) are plant-specific,
19                  These results indicate that nodulin 26 is a multifunctional AQP that confers water a
20                                              Nodulin 26 is an aquaglyceroporin with a modest osmotic
21                                      Soybean nodulin 26 is expressed and targeted to the symbiosome m
22 s study, we show that the phosphorylation of nodulin 26 on Ser-262, which is catalyzed by a symbiosom
23 e developmental appearance and regulation of nodulin 26 phosphorylation in vivo.
24                                              Nodulin 26 phosphorylation is enhanced further by osmoti
25                                     Although nodulin 26 protein is detected first in differentiating
26                                              Nodulin 26 proteoliposomes also facilitate glycerol tran
27                           Water flux through nodulin 26 showed a low activation energy (Ea) (4.07 kca
28                                              Nodulin 26, a member of the major intrinsic protein/aqua
29 ilar to the archetype, soybean (Glycine max) nodulin 26, and another that is characteristic of Arabid
30 sembles the archetype of the family, soybean nodulin 26, and the NIP subgroup II, which is represente
31  shows that the protein differs from soybean nodulin 26, showing minimal water and glycerol transport
32 ater and solute transport characteristics of nodulin 26, we purified the protein from SMs and reconst
33 (PIPs), tonoplast intrinsic proteins (TIPs), nodulin 26-like intrinsic membrane proteins (NIPs), and
34                                          The nodulin 26-like intrinsic protein (NIP) subfamily in Ara
35 pecies when absorbed as silicic acid through nodulin 26-like intrinsic proteins (NIPs).
36 tructural and functional homology to soybean nodulin 26.
37 l as larger solutes that were impermeable to nodulin 26.
38                                        Plant nodulin-26 intrinsic proteins (NIPs) are members of the
39                                   Similarly, nodulin-26, which is closely related to AQP1, can act as
40    The SUS-binding peptides encoded by early nodulin 40 (ENOD40) specifically antagonized S170 phosph
41 ation, and it targeted a nodulin gene, Early Nodulin 93 (ENOD93).
42  barrel with topological similarity to plant nodulins and phytocyanins.
43 eved when the down-regulatory effect on late nodulins can be alleviated.
44 omo-oligomerization activities of the AtSfh1 nodulin domain and is an essential aspect of the polarit
45  uncharacterized Arabidopsis thaliana Sec14p-nodulin domain family, is a PITP that regulates a specif
46               We further suggest that Sec14p-nodulin domain proteins represent a family of regulators
47 n (PITP) domain linked to a carboxy-terminal nodulin domain.
48 ity (74%) to the soybean (Glycine max) early nodulin (ENOD) gene GmENOD93.
49  RNA using degenerate primers to be an early nodulin (ENOD)-like protein that is encoded by the expre
50                                    The early nodulin Enod2 gene encodes a putative hydroxyproline-ric
51 D40) are induced in lin, as is another early nodulin, ENOD20, a gene expressed during the differentia
52  that shares sequence homology with an early nodulin gene from a legume.
53 d during nodule formation, and it targeted a nodulin gene, Early Nodulin 93 (ENOD93).
54 n, and the accumulation of mRNA of the early nodulin gene, ENOD40.
55                             ENOD40, an early nodulin gene, is expressed following inoculation with Rh
56 ns, one of which coincides with a cluster of nodulin genes.
57                                            A nodulin-like gene was regulated only by Agrobacterium.
58 mino acid sequences, PtNIP1;1 belongs to the nodulin-like members of the major intrinsic protein supe
59 oup of female-specific small proteins, early nodulin-like proteins (ENODLs, or ENs), are required for
60         The predicted amino acid sequence of nodulin LjN70 revealed structural features characteristi
61  coiled-coil type structure, indicating that nodulin Nlj16 may interact with an as-yet-unidentified p
62 he predicted amino acid sequence analysis of nodulin Nlj16 revealed the presence of a long alpha-heli
63 LjNOD16, which encodes the L. japonicus late nodulin Nlj16.
64             Besides previously characterized nodulins, other examples of highly abundant nodule-speci
65  Here we identify the conserved AtSfh1 Sec14-nodulin protein as a novel effector of phosphoinositide
66           The data are consistent with Sec14-nodulin proteins controlling the lateral organization of
67 s a broadly conserved feature of plant Sec14-nodulin proteins, and that this strategy appeared only l
68                   Here, we report on RTP1, a nodulin-related MtN21 family gene in Arabidopsis that me
69 nts, protein degradation machinery, and some nodulins than plants inoculated with succinoglycan-defic
70 52, was previously characterized as an early nodulin that is expressed in roots and localized to the
71 d contains several nodule-specific proteins (nodulins) that perform unique functions for symbiosis.
72                                Various other nodulins were also strongly down-regulated, in particula

WebLSDに未収録の専門用語(用法)は "新規対訳" から投稿できます。