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1 idges membranes through opposite ends of its elongated structure.
2 ts (PUF repeats) arranged side by side in an elongated structure.
3 ge Stokes radius (14.3 nm), indicative of an elongated structure.
4 ht cysteine residues distributed through the elongated structure.
5 (2+) biases the ensemble toward a moderately elongated structure.
6 he separase-securin complex assumes a highly elongated structure.
7 shion and are disorted to form a wider, less elongated structure.
8 d after deglycosylation, again indicating an elongated structure.
9 revealing paraspeckles with dynamic, twisted elongated structures.
10 n is partially opened, generating a slightly elongated structure and exposing the hydrophobic core.
11 signaling elements of YopN at one end of an elongated structure and the secretion regulating TyeA bi
12 ed and membrane-bound VWF are stretched into elongated structures and become the core of aggregates t
13 aining seven pairs of Ala-Pro, which form an elongated structure, and two pairs of lysines located ne
14 se in which assemblies of chirally selective elongated structures are observed in this size range of
20 dimerization activity and conferred a highly elongated structure, characteristic of native GRP94, to
21 n conformers formed at high temperature have elongated structures, consistent with unfolded forms of
22 amide] (piperazinyl-piperidine) with a rigid elongated structure containing two basic groups and NBI-
25 ot terminate and continue to grow into large elongated structures following actomyosin disruption.
26 imental timescales are observed: a family of elongated structures for n = 18 to 39 and a series of mo
27 s emerges as a key issue in the formation of elongate structures from compact ones by directed migrat
28 ata suggest that all three proteins share an elongated structure, identical Stokes radius (60 A), and
30 ing the generation of specialized actin-rich elongated structures in response to bioactive signaling
31 acture of glass fibers, and the formation of elongated structures in volcanic eruptions known as Pele
35 cell lines, rp3 was found associated with an elongated structure located in the layer of cytoplasm ab
36 ly, electron microscopy images confirmed the elongated structure of AgI/II and enabled building a com
37 Using analytical ultracentrifugation, the elongated structure of IgG3 was determined from the redu
39 red to be elongated and conferred a somewhat elongated structure on segments containing this subdomai
40 peared as randomly oriented hyperreflective, elongated structures on in vivo confocal microscopy imag
42 , physical and structural analyses, revealed elongated structures protruding from the surface (length
43 the dimer subunits, resulting in an overall elongated structure relative to the more compact structu
45 ificant axial asymmetry, consistent with the elongated structure seen for other for ankyrin repeat pr
46 example to be determined, contrasts with the elongated structures seen for EGF-module pairs having sh
47 ificantly higher charge states and with more elongated structures than those formed by premixing the
48 intrinsic propensity to oligomerize into an elongated structure that activates the signaling adaptor
51 forkhead-associated domain, and MxiK has an elongated structure that interacts with the IR via MxiG(
53 a homodimer of 116 amino acids and adopts an elongated structure that resembles the shape of a bent 2
54 ng of low charge states to a distribution of elongated structures that are observed as highly charged
59 with 6 and 8 methylene units formed dynamic elongated structures, while those with 10 and 12 units y
61 and sgAi9 leads to the formation of an oval elongated structure with a neutral charge resulting in 1
62 of the MASP-2 CUB1-EGF-CUB2 dimer reveals an elongated structure with a prominent concave surface tha
64 solved to 18 A displayed the tetramer as an elongated structure with an apparent 2-fold symmetry.
65 ions suggest that TnT N47 might fold into an elongated structure with at least one high-affinity meta
66 of the Atg17-Atg31-Atg29 complex reveals an elongated structure with Atg29 located at the opposing e
67 omodimeric CrISA1 structure reveals a unique elongated structure with monomers connected end-to-end.
70 undergoes morphogenetic movements, producing elongated structures with a notochord and ventral neural
71 gregates break symmetry autonomously to form elongated structures with an anterior-posterior pattern.
72 erical aggregates, which, upon aging, formed elongated structures with significantly reduced antibact
73 uld be rare, appearing in adaptive optics as elongated structures with variable orientation and no fo
74 ly disordered, but it maintained an extended elongated structure, with hydrophobic clusters and resid
75 emonstrate that the monomer is a two-domain, elongated structure, with the smaller domain coupling tw