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1 mbrane lipid transfer protein present in the outer envelope.
2 proper delivery of cargo to the chloroplast outer envelope.
3 ave carotenoids localized in the chromoplast outer envelope.
4 xtensions (NDGD1 and NDGD2) targeting to the outer envelope.
5 is specifically incorporated into the viral outer envelope.
6 rvations of molecular lines that probe their outer envelopes.
7 culates called spermatophores composed of an outer envelope, an inner matrix, and a bolus of sperm.
8 e spontaneous insertion of proteins into the outer envelope and thylakoid, the role of cubic lipid st
9 These are the ER/plasmodesmata, chloroplast outer envelopes and membrane contact sites between them.
10 in-binding protein that was localized to the outer envelope based on susceptibility to proteinase K.
12 last-targeting sequence, was targeted to the outer envelope by an ATP-independent and protease-insens
13 eton within the yolk cell and defects in the outer enveloping cell layer, which are both known mediat
14 rmatophore regions, the inner matrix and the outer envelope, differ in their protein composition and
15 enables a temporal release of two drugs: the outer envelope first releases an anti-angiogenesis agent
18 the absence of energy, two components of the outer envelope import machinery, IAP86 and IAP75, cross-
20 fish, the embryonic epidermis consists of an outer enveloping layer (EVL) and an inner basal layer th
23 ency towards overproduction of the bacterial outer envelope, leading to the formation and release dur
24 f three distinct membrane systems, i.e., the outer envelope membrane (OEM), inner envelope membrane (
25 ificantly (10-fold) upregulated but those of outer envelope membrane (Toc159), stromal (hsp93, cpn60)
26 esidue did not block PDV1 insertion into the outer envelope membrane but did abolish its localization
27 ermediate which has completely traversed the outer envelope membrane but has not yet reached the stro
30 dependent formation of the translocon at the outer envelope membrane of chloroplasts (TOC) and TIC su
33 t of the import machinery [translocon at the outer envelope membrane of chloroplasts (Toc33), a 33-ki
35 75 is a protein translocation channel in the outer envelope membrane of chloroplasts and its presence
37 dicate that OEP40 is a "glucose-gate" in the outer envelope membrane of chloroplasts, facilitating se
38 ted that the TGD4 protein was present in the outer envelope membrane of chloroplasts, where it appear
39 , the protein-translocating channel from the outer envelope membrane of pea chloroplasts, in the geno
42 tified PLASTID DIVISION1 (PDV1), an integral outer envelope membrane protein, and its homolog PDV2 as
44 AKRA2, a targeting receptor for chloroplast outer envelope membrane proteins, binds chloroplast-spec
46 SFR2 protein is localized to the chloroplast outer envelope membrane, as revealed by the analysis of
47 iring steps: binding of the precursor to the outer envelope membrane, outer membrane transport, and i
48 of DAGK presence in the outer leaflet of the outer envelope membrane, phosphatidic acid accumulation
49 During energy-independent binding at the outer envelope membrane, preproteins interact with three
50 ing upon insertion of preproteins across the outer envelope membrane, supporting the proposal that bo
51 hatidic acid accumulation in the chloroplast outer envelope membrane, the location of MGDG synthase i
52 protein translocation channel at the plastid outer envelope membrane, Toc75, is essential for the via
67 mport is initiated by TOC (translocon at the outer envelope of chloroplasts) complexes in the plastid
71 d molecule, termed S881, is localized to the outer envelope of M. tuberculosis and negatively regulat
72 Because of its unique localization at the outer envelope of plastids, LACS9 was regarded as a cand
73 embrane of Gram-negative bacteria and of the outer envelope of the endosymbiotically derived organell
76 id (FFA) released is then transferred to the outer envelope of the plastid where it is reactivated to
78 a glycoprotein specifically localized to the outer envelope of vaccinia virus was shown to be encoded
79 n shown to be involved in the integration of outer envelope protein 14 (OEP14), whose outer membrane
80 tioning 1 (CHUP1) that encodes a chloroplast outer envelope protein constitutively induces stromules
81 A also binds specifically to the chloroplast OUTER ENVELOPE PROTEIN7 (OEP7) and is required for the b
82 specifies the mid-plastid positioning of the outer envelope proteins PDV1 and PDV2, which have parall
83 The Chlamydia family of human pathogens uses outer envelope proteins that are highly cross-linked by
85 s that were labeled with antibodies to other outer-envelope proteins and with protein A-colloidal gol
86 ptor (34-kD subunit of the translocon of the outer envelope) recognition in vitro, preprotein binding
87 segmentation; the presence or absence of an outer envelope; recombination frequency; duration of inf
88 rmation for targeting and insertion into the outer envelope resides in the N-terminal half of DGD1, b
91 e positioned on the cytosolic surface of the outer envelope, the stromal surface of the inner envelop
93 ntain the 75-kD component of the chloroplast outer envelope translocon (Toc75) and are capable of imp
94 ogenitor star must have retained much of its outer envelope until after helium fusion in the core was
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