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1 we show that TREK1, TREK2, and TRAAK readily coassemble.
2 associated in distinct complexes and do not coassemble.
3 essed with sigma3, with which it is known to coassemble.
4 te that HIV-1 and HIV-2 Gag can interact and coassemble.
5 amer-forming peptides and determine how they coassemble.
6 t with conventional actin and found it could coassemble.
7 ent isotypes within the Kv1 or Kv3 subfamily coassemble.
8 gly suggested that alpha7 and beta2 subunits coassemble.
9 resulting segregated beta-sheets can further coassemble.
10 o 13-fold, indicating that different SUR can coassemble.
12 shown that the alpha 2 and gamma 1 subunits coassemble and are incorporated into GABAA receptors whi
13 us expression systems, these subunits avidly coassemble and exhibit biophysical and pharmacological p
15 te that HIV-1 and HIV-2 Gag polyproteins can coassemble and functionally complement each other during
18 tion velocity that the ATDs of GluR6 and KA2 coassemble as a heterodimer of K(d) 11 nM, 32,000-fold l
19 ombinations of two or more DEG/ENaC subunits coassemble as heteromultimers to generate transient H(+)
20 on it is likely that different TRPC subunits coassemble as heterotetrameric structures to form smooth
21 terminal residue, phosphotyrosine vs lysine, coassemble as stacks of antiparallel beta-sheets with pr
22 er these data argue that UNC-49B and UNC-49C coassemble at the C. elegans neuromuscular junction.
23 pressed septins (Spn1, Spn2, Spn3, and Spn4) coassemble at the fusion site and are necessary for its
25 d thereby confer functional sensitivity upon coassembled channel subunits that are themselves not bou
26 tivated potassium channels (SK channels) are coassembled complexes of pore-forming SK alpha subunits
30 nally, the polyglutamine amyloid fibrils are coassembled from differently structured monomers, which
31 Synthetic vesicles have been assembled and coassembled from phospholipids, their modified versions,
32 o export from the endoplasmic reticulum (ER) coassembled from purified cargo adaptor Sec23-24 and Sec
33 ls explaining why certain subunits prefer to coassemble has been lacking in our understanding of glut
36 5 freely exchange between dimers but fail to coassemble in vitro with dodecameric plant cytosolic sHS
37 forming cationic semiconducting polymers can coassemble in water with cationic fullerene derivatives
38 s suggest that Cx43alpha1 and N-cadherin are coassembled in a multiprotein complex containing various
39 ments established that the two subunits were coassembled in the cerebellum along with the beta2 subun
41 nd graphene oxide sheets can be conveniently coassembled in water to yield a stable colloidal dispers
43 n pearl cells, the delta and sigma3 subunits coassemble into a heterodimer, whereas mu3 gets destroye
44 In mocha cells, the beta3 and mu3 subunits coassemble into a heterodimer, whereas the sigma3 subuni
47 ode two CPs (P2 and P4, respectively), which coassemble into approximately 450-A-diameter capsids.
48 e an intrinsic capacity of RNP components to coassemble into either large semiliquids or solid lattic
49 that overexpressed Drosophila Sas-6 and Ana2 coassemble into extended tubules (SAStubules) that bear
50 osed of all-l and all-d peptides, but rather coassemble into fibrils that contain alternating L- and
53 conditions, smitin and smooth muscle myosin coassemble into irregular aggregates containing large si
56 r CA proteins from two different viruses can coassemble into mature cores of infectious viruses, we e
60 d cationic amphiphiles of unequal charge can coassemble into small buckled vesicles and present a phy
65 Our results indicate that hCA and sCA can coassemble into the same mature core to produce infectio
66 e this, HIV-1 and HIV-2 Gag polyproteins can coassemble into the same particle and their genomes can
68 enin, and beta-catenin, but not plakoglobin, coassemble into Triton X-100 insoluble (TX-insoluble) st
69 Finally, we show that ESCRT-II and ESCRT-III coassemble into ~65 nm diameter rings indicative of a ca
70 The colloidal nanodisks and nanorods are coassembled into AB-, AB2-, and AB6-type binary arrays d
72 n CE cell nuclei, ferritin and ferritoid are coassembled into stable complex(es) present in embryonic
73 egulated cytoskeleton-associated protein are coassembled into the same RNA granules and targeted to d
74 cated that adherens junction components were coassembled into these structures along with desmosomal
75 and chimeric CP-TMOF (20:1 ratio) that were coassembled into virus particles in infected Nicotiana t
77 dent increases in cell surface expression of coassembled Kv1.1 and Kv1.2, while coassembly with Kv1.1
78 ed shape, morphology, and surface pattern by coassembling MAMs of block copolymers (BCPs) and NPAMs c
81 faceted polyhedra with diverse symmetries by coassembling oppositely charged molecules of different s
82 nts self-assembles, the molecules can either coassemble, or self-sort, where a preference for like-li
83 c engineering of M13 viruses can allow us to coassemble other functional materials (e.g., catalysts a
84 lls identified a class of genes that rapidly coassemble p300 and RNA polymerase II (pol II) following
87 in which crystalline lamellae made up of the coassembled proteorhodopsin and charged lipid molecules
88 or inhomogeneous shells, we demonstrate that coassembled shells with two elastic components buckle in
90 ones containing a free C-terminus results in coassembled structures, as demonstrated by circular dich
94 wo bifunctional protein building blocks that coassemble to form a bioelectrocatalytic hydrogel that c
97 and KCNQ3 ion channel pore-forming subunits coassemble to form a heteromeric voltage-gated potassium
98 are coordinately rescued and therefore might coassemble to form a heteromultimeric GABA receptor.
100 nown to encode K(+) channel monomers and can coassemble to form hetero-tetrameric K(+) channels.
101 l data imply that different HCN isoforms may coassemble to form heteromeric channel complexes, but li
102 have now found that Slick and Slack subunits coassemble to form heteromeric channels that differ from
103 ucts reveals that the family of polypeptides coassemble to form heteromeric IMPDH complexes, suggesti
106 r Cx isoforms found in the cochlea, and they coassemble to form hybrid (heteromeric and heterotypic)
107 A) receptor alpha4 and delta subunits, which coassemble to form receptors mediating tonic inhibition,
108 e limiting components of gamma-secretase and coassemble to form the active enzyme in mammalian cells.
109 tural proteins, L1 and L2, can spontaneously coassemble to form virus-like particles, currently avail
110 the alpha4, beta2, and alpha5 gene products coassemble to produce epibatidine-binding receptors.
111 of the KCNQ channel family, KCNQ2 and KCNQ3, coassemble to underlie the M current in the nervous syst
112 nition using aptamers and peptide substrates coassembled to a central semiconductor quantum dot (QD).
113 native subunits, the native subunit and PCS coassemble, traffic to the plasma membrane, and place th
118 defective in GTP binding and hydrolysis can coassemble with and stimulate GTP hydrolysis by wild-typ
122 ment of Cav2 channels in the brain, directly coassemble with Cav2.2 channels upon heterologous coexpr
123 ith age in monkey prefrontal cortex, and can coassemble with delta subunits to form functional GABA(A
129 ysiological evidence that the pi subunit can coassemble with either alpha5beta3 or alpha5beta3gamma3
130 sly introduced into hippocampal neurons, can coassemble with endogenous NR1 and NR2A and can reduce t
131 , in which four channel-tethered RCK domains coassemble with four soluble (untethered) RCK domains.
133 mossy fiber synapses where they most likely coassemble with GluR6 subunits to form functional hetero
134 Gag proteins of endogenous retroviruses can coassemble with HIV-1 Gag and modulate the late phase of
135 Furthermore, HERV-K(CON) Gag was found to coassemble with HIV-1 Gag, as demonstrated by (i) proces
136 Multiple K(+) channel alpha-subunits that coassemble with Hk, including Shaker, Ether-a-go-go, and
139 eart, KCNQ1 voltage-gated potassium channels coassemble with KCNE1 beta-subunits to generate the IKs
140 nificantly, we show that Kir2.6 subunits can coassemble with Kir2.1 and Kir2.2 in vitro and in vivo.
141 either Kvbeta1.2 or Kvbeta1.3, both of which coassemble with Kv1.5 and induce fast inactivation.
144 ypical rapid desensitization, and they could coassemble with native P2X2 subunits in pheochromocytoma
146 and the need for the synthesized proteins to coassemble with nuclear-encoded subunits have had substa
147 PARs) is observed when pore-forming subunits coassemble with or without auxiliary subunits, respectiv
148 ked inactivation, suggesting that Kv3.1b may coassemble with other members of the Kv3 subfamily.
149 that NF180 could not self-assemble but could coassemble with rat NFL, suggesting the existence of add
151 ostsynaptic density, however, AMPA receptors coassemble with transmembrane AMPA receptor regulatory p
152 in Xenopus laevis oocytes, two NR3 subunits coassemble with two NR1 subunits to form a glycine-gated
153 two-hybrid assay, since these same molecules coassemble with wild-type Gag into Ty1 virus-like partic
154 gnated dominant negative (DN), were found to coassemble with wild-type PA and generate defective hept
157 ctenophore Shaker subfamily channel subunits coassembled with cnidarian and mouse Shaker subunits, bu
160 tors require two copies of the GluN1 subunit coassembled with GluN2 (and/or GluN3) subunits into a he
164 rehybridized with a thiolated short DNA) was coassembled with mercaptohexanol onto the gold surface o
167 nst a 70-kDa human ELP and showed that ELP70 coassembled with MTs in HeLa cell extracts and colocaliz
169 he QD was used as a central nanoplatform and coassembled with peptides or oligonucleotides that were
170 nvelope proteins (E1 or E2) were efficiently coassembled with the wild-type HBV S protein into subvir
171 eas irreversible binding results when tau is coassembled with tubulin into a tau-microtubule copolyme
172 ortant aspects of effector secretion: (i) It coassembles with a second regulator (Pcr1) on the inner
176 CN1b, an integral subunit of Na(V) channels, coassembles with and modulates the biophysical propertie
177 rotrimer, [alpha1(V)]2alpha2(V), and it both coassembles with and regulates type I collagen-fibril di
179 raphy experiments demonstrated that Caskin 1 coassembles with CASK on the immobilized cytoplasmic tai
180 y that beta-filagenin is a core protein that coassembles with either myosin or paramyosin in C. elega
183 KCNE1 encoding a transmembrane protein which coassembles with K+ channels mediating slow K+, I(Ks), c
184 s from the colon, stomach, and kidney, KCNE3 coassembles with KCNQ1 to form K(+) channels that are vo
185 t that a splice variant of the Kv3.4 subunit coassembles with Kv3.1 subunits in rat brain FS neurons.
188 Therefore, K(V)LQT1 is the subunit that coassembles with minK to form I(Ks) channels and I(Ks) d
191 ed rectifier K+ channel Kv1.1 (Kv1.1N206Tag) coassembles with other K+ channels of the Kv1 subfamily
192 quitously expressed cytoplasmic protein that coassembles with pallidin and the muted protein in the B
193 In the colon, stomach, and kidney, KCNE3 coassembles with the alpha-subunit KCNQ1 to form K(+) ch
195 heart, has rapid deactivation kinetics, and coassembles with the longer isoform in Xenopus oocytes.
196 he intermediate filament (IF) protein nestin coassembles with vimentin and promotes the disassembly o
197 s a single-transmembrane domain protein that coassembles with voltage-gated K+ channel KVS-1 in the n
199 functionally distinct potassium channels by coassembling with KCNE ancillary subunits MinK and MiRP2
200 can also form slower activating channels by coassembling with MinK-related peptide 2 (MiRP2), a sing
201 in division by specifically interacting and coassembling with the guanosine triphosphate-bound form
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