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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  a reduced Nod factor induction of the Early Nodulin 11 (MtENOD11) infection marker, and of the cytok
7 ) under control of the Medicago sativa EARLY NODULIN 12B promoter in our previously developed high-ir
8 noid legumes shown to possess putative early nodulin 2 (ENOD2) genes.
9  along with two other nodule-specific genes, nodulin-22 and nodulin-25.
10 unequal recombination event occurred between nodulin-25 and a nearby calmodulin, which gave rise to t
11  other nodule-specific genes, nodulin-22 and nodulin-25.
12                                              Nodulin 26 (NOD 26), a member of the aquaporin (AQP) wat
13                                              Nodulin 26 (nod26) is a major intrinsic protein that con
14                 Thus, the phosphorylation of nodulin 26 coincides with the establishment of mature ni
15 ing infected cells (16 days), phosphorylated nodulin 26 does not become pronounced until infected cel
16                         Liposomes containing nodulin 26 exhibited a high osmotic permeability (Pf = 0
17                                Reconstituted nodulin 26 exhibited a single-channel conductance of 3.8
18 eriments in Xenopus oocytes that showed that nodulin 26 facilitated glycerol flux in a manner indisti
19                                              Nodulin 26 intrinsic proteins (NIPs) are plant-specific,
20                  These results indicate that nodulin 26 is a multifunctional AQP that confers water a
21                                              Nodulin 26 is an aquaglyceroporin with a modest osmotic
22                                      Soybean nodulin 26 is expressed and targeted to the symbiosome m
23 s study, we show that the phosphorylation of nodulin 26 on Ser-262, which is catalyzed by a symbiosom
24 e developmental appearance and regulation of nodulin 26 phosphorylation in vivo.
25                                              Nodulin 26 phosphorylation is enhanced further by osmoti
26                                     Although nodulin 26 protein is detected first in differentiating
27                                              Nodulin 26 proteoliposomes also facilitate glycerol tran
28                           Water flux through nodulin 26 showed a low activation energy (Ea) (4.07 kca
29                                              Nodulin 26, a member of the major intrinsic protein/aqua
30 ilar to the archetype, soybean (Glycine max) nodulin 26, and another that is characteristic of Arabid
31 sembles the archetype of the family, soybean nodulin 26, and the NIP subgroup II, which is represente
32  shows that the protein differs from soybean nodulin 26, showing minimal water and glycerol transport
33 ater and solute transport characteristics of nodulin 26, we purified the protein from SMs and reconst
34 (PIPs), tonoplast intrinsic proteins (TIPs), nodulin 26-like intrinsic membrane proteins (NIPs), and
35 e examined solute selectivity for the barley Nodulin 26-like Intrinsic Protein (HvNIP2;1) embedded in
36                                          The nodulin 26-like intrinsic protein (NIP) subfamily in Ara
37 gulatory network analyses, we identified two NODULIN 26-LIKE INTRINSIC PROTEIN (NIP)-encoding genes,
38 pecies when absorbed as silicic acid through nodulin 26-like intrinsic proteins (NIPs).
39 tructural and functional homology to soybean nodulin 26.
40 l as larger solutes that were impermeable to nodulin 26.
41                                        Plant nodulin-26 intrinsic proteins (NIPs) are members of the
42                                   Similarly, nodulin-26, which is closely related to AQP1, can act as
43    The SUS-binding peptides encoded by early nodulin 40 (ENOD40) specifically antagonized S170 phosph
44                                        EARLY NODULIN 93 (ENOD93) has been genetically associated with
45 ation, and it targeted a nodulin gene, Early Nodulin 93 (ENOD93).
46  barrel with topological similarity to plant nodulins and phytocyanins.
47 eved when the down-regulatory effect on late nodulins can be alleviated.
48 omo-oligomerization activities of the AtSfh1 nodulin domain and is an essential aspect of the polarit
49  uncharacterized Arabidopsis thaliana Sec14p-nodulin domain family, is a PITP that regulates a specif
50               We further suggest that Sec14p-nodulin domain proteins represent a family of regulators
51 n (PITP) domain linked to a carboxy-terminal nodulin domain.
52 ity (74%) to the soybean (Glycine max) early nodulin (ENOD) gene GmENOD93.
53  RNA using degenerate primers to be an early nodulin (ENOD)-like protein that is encoded by the expre
54                                    The early nodulin Enod2 gene encodes a putative hydroxyproline-ric
55 D40) are induced in lin, as is another early nodulin, ENOD20, a gene expressed during the differentia
56  that shares sequence homology with an early nodulin gene from a legume.
57 d during nodule formation, and it targeted a nodulin gene, Early Nodulin 93 (ENOD93).
58 n, and the accumulation of mRNA of the early nodulin gene, ENOD40.
59                             ENOD40, an early nodulin gene, is expressed following inoculation with Rh
60 ns, one of which coincides with a cluster of nodulin genes.
61                                            A nodulin-like gene was regulated only by Agrobacterium.
62 mino acid sequences, PtNIP1;1 belongs to the nodulin-like members of the major intrinsic protein supe
63 oup of female-specific small proteins, early nodulin-like proteins (ENODLs, or ENs), are required for
64         The predicted amino acid sequence of nodulin LjN70 revealed structural features characteristi
65  coiled-coil type structure, indicating that nodulin Nlj16 may interact with an as-yet-unidentified p
66 he predicted amino acid sequence analysis of nodulin Nlj16 revealed the presence of a long alpha-heli
67 LjNOD16, which encodes the L. japonicus late nodulin Nlj16.
68             Besides previously characterized nodulins, other examples of highly abundant nodule-speci
69  Here we identify the conserved AtSfh1 Sec14-nodulin protein as a novel effector of phosphoinositide
70           The data are consistent with Sec14-nodulin proteins controlling the lateral organization of
71 s a broadly conserved feature of plant Sec14-nodulin proteins, and that this strategy appeared only l
72                   Here, we report on RTP1, a nodulin-related MtN21 family gene in Arabidopsis that me
73 nts, protein degradation machinery, and some nodulins than plants inoculated with succinoglycan-defic
74 52, was previously characterized as an early nodulin that is expressed in roots and localized to the
75 d contains several nodule-specific proteins (nodulins) that perform unique functions for symbiosis.
76                                Various other nodulins were also strongly down-regulated, in particula