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1 Finally, we show that ESCRT-II and ESCRT-III coassemble into ~65 nm diameter rings indicative of a ca
2 h chemically distinct monomers spontaneously coassemble into a dynamic, functional structure.
3 n pearl cells, the delta and sigma3 subunits coassemble into a heterodimer, whereas mu3 gets destroye
4   In mocha cells, the beta3 and mu3 subunits coassemble into a heterodimer, whereas the sigma3 subuni
5                              Peripherin also coassembles into a single network of filaments containin
6     The colloidal nanodisks and nanorods are coassembled into AB-, AB2-, and AB6-type binary arrays d
7 st seven distinct beta-tubulin isotypes that coassemble into all cellular microtubules.
8 ulin isotypes are freely interchangeable and coassemble into all classes of microtubules.
9 ode two CPs (P2 and P4, respectively), which coassemble into approximately 450-A-diameter capsids.
10 arge-complementary peptides that selectively coassemble into B-sheet nanofibers when mixed together b
11  cytosol in which proteins and nucleic acids coassemble into compartments.
12 e an intrinsic capacity of RNP components to coassemble into either large semiliquids or solid lattic
13 that overexpressed Drosophila Sas-6 and Ana2 coassemble into extended tubules (SAStubules) that bear
14 osed of all-l and all-d peptides, but rather coassemble into fibrils that contain alternating L- and
15                When mixed, 3R tau and 4R tau coassemble into heterogeneous filaments.
16                  We show that NM II isoforms coassemble into heterotypic filaments in a variety of se
17  conditions, smitin and smooth muscle myosin coassemble into irregular aggregates containing large si
18        Therefore, different SUR subtypes can coassemble into K(ATP) channels with distinct metabolic
19           On stimulation, Dyn2 and cortactin coassemble into large, circular structures on the dorsal
20         In vitro, MinC and MinD are known to coassemble into linear polymers; therefore, we monitored
21  blocks and functional coronal segments were coassembled into low-dispersity, one-dimensional archite
22 r CA proteins from two different viruses can coassemble into mature cores of infectious viruses, we e
23                                     beta3 is coassembled into microtubules with beta1, the sole beta-
24 isotypes of alpha- and beta-tubulin that can coassemble into MTs.
25                             The proteins can coassemble into particles together with full-length, wil
26 o P22 assembly assay where portal protein is coassembled into procapsid-like particles (PLPs).
27  (v) the UL26.5 and UL80.5 proteins will not coassemble into scaffold structures.
28       All dendritic dipeptides were shown to coassemble into single columns regardless of their stere
29 d cationic amphiphiles of unequal charge can coassemble into small buckled vesicles and present a phy
30 n CE cell nuclei, ferritin and ferritoid are coassembled into stable complex(es) present in embryonic
31              Ribonucleoproteins (RNPs) often coassemble into supramolecular bodies with regulated dyn
32 nvestigate how GluN1 and GluN2 type subunits coassemble into tetramers.
33                  However, if hCA and sCA can coassemble into the same core structure to form a mixed
34                        If hCA and sCA cannot coassemble into the same core when equal amounts of sCA
35    Our results indicate that hCA and sCA can coassemble into the same mature core to produce infectio
36 e this, HIV-1 and HIV-2 Gag polyproteins can coassemble into the same particle and their genomes can
37 egulated cytoskeleton-associated protein are coassembled into the same RNA granules and targeted to d
38 cated that adherens junction components were coassembled into these structures along with desmosomal
39 amily of six alpha-chains (alpha1 to alpha6) coassemble into three distinct protomers that form supra
40       Meanwhile, NR1, NR2, and NR3 appear to coassemble into triheteromeric receptors in neurons, but
41 enin, and beta-catenin, but not plakoglobin, coassemble into Triton X-100 insoluble (TX-insoluble) st
42 troscopy indicate that CATCH(+) and CATCH(-) coassemble into two-component nanofibers instead of self
43  and chimeric CP-TMOF (20:1 ratio) that were coassembled into virus particles in infected Nicotiana t