ライフサイエンスコーパス: coassemble into

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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 e an intrinsic capacity of RNP components to coassemble into either large semiliquids or solid lattic

11 that overexpressed Drosophila Sas-6 and Ana2 coassemble into extended tubules (SAStubules) that bear

12 osed of all-l and all-d peptides, but rather coassemble into fibrils that contain alternating L- and

13 When mixed, 3R tau and 4R tau coassemble into heterogeneous filaments.

14 We show that NM II isoforms coassemble into heterotypic filaments in a variety of se

15 conditions, smitin and smooth muscle myosin coassemble into irregular aggregates containing large si

16 Therefore, different SUR subtypes can coassemble into K(ATP) channels with distinct metabolic

17 On stimulation, Dyn2 and cortactin coassemble into large, circular structures on the dorsal

18 r CA proteins from two different viruses can coassemble into mature cores of infectious viruses, we e

19 beta3 is coassembled into microtubules with beta1, the sole beta-

20 The proteins can coassemble into particles together with full-length, wil

21 (v) the UL26.5 and UL80.5 proteins will not coassemble into scaffold structures.

22 All dendritic dipeptides were shown to coassemble into single columns regardless of their stere

23 d cationic amphiphiles of unequal charge can coassemble into small buckled vesicles and present a phy

24 n CE cell nuclei, ferritin and ferritoid are coassembled into stable complex(es) present in embryonic

25 Ribonucleoproteins (RNPs) often coassemble into supramolecular bodies with regulated dyn

26 nvestigate how GluN1 and GluN2 type subunits coassemble into tetramers.

27 However, if hCA and sCA can coassemble into the same core structure to form a mixed

28 If hCA and sCA cannot coassemble into the same core when equal amounts of sCA

29 Our results indicate that hCA and sCA can coassemble into the same mature core to produce infectio

30 e this, HIV-1 and HIV-2 Gag polyproteins can coassemble into the same particle and their genomes can

31 egulated cytoskeleton-associated protein are coassembled into the same RNA granules and targeted to d

32 cated that adherens junction components were coassembled into these structures along with desmosomal

33 Meanwhile, NR1, NR2, and NR3 appear to coassemble into triheteromeric receptors in neurons, but

34 enin, and beta-catenin, but not plakoglobin, coassemble into Triton X-100 insoluble (TX-insoluble) st

35 and chimeric CP-TMOF (20:1 ratio) that were coassembled into virus particles in infected Nicotiana t

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