戻る
「早戻しボタン」を押すと検索画面に戻ります。 [閉じる]

コーパス検索結果 (１語後でソート)

通し番号をクリックするとPubMedの該当ページを表示します
1 , likely due to stabilization of the keratin heteropolymer.
2 aining the free energy of a typical designed heteropolymer.
3  extension of a short A-tail into a long A/U-heteropolymer.
4 izobium etli CE3 O antigen is a fixed-length heteropolymer.
5  by perturbing the chemical structure of the heteropolymer.
6 inued metabolism of this essential cell wall heteropolymer.
7 ion of two simplified models of protein-like heteropolymers.
8 ncovalent type I (K18, K19) and type II (K8) heteropolymers.
9 nover of FtsZ2 and FtsZA, respectively, from heteropolymers.
10 enerate diverse sequence-defined non-protein heteropolymers.
11 at is structurally related to UMOD but forms heteropolymers.
12 s which are assemblies of specific ESCRT-III heteropolymers.
13 DW-135/Y) have been identified to form these heteropolymers.
14 ent mutants reveal that FtsZ1 and FtsZ2 form heteropolymers.
15 nd select mRNAs and contributes U's into A/U heteropolymers.
16 o its ligands, resulting in the formation of heteropolymers.
17 n predicting the functional utility of novel heteropolymers.
18 (s) and the formation of high molecular mass heteropolymers.
19                While suberin is an insoluble heteropolymer, a number of soluble lipids can be extract
20                                The resulting heteropolymer adopts a dramatically different structure
21 hase molecular recognition (CoPhMoRe) uses a heteropolymer adsorbed onto and templated by a nanoparti
22  of poly(ethylene glycol) (PEG) phospholipid heteropolymers adsorbed onto near-infrared (nIR) fluores
23                                  The infused heteropolymers also facilitated rapid and quantitative b
24 osed during this transfer reaction, but both heteropolymer and CR1 are removed from the erythrocytes
25            The Langevin dynamics of a random heteropolymer and its dynamic glass transition are studi
26  encoded translation of diverse noncanonical heteropolymers and macrocycles.
27  primarily through interaction with FtsZ2 in heteropolymers and suggest that ARC3 activity is spatial
28 xical in light of what is known about random heteropolymers and the sensitivity of their properties t
29                        Keratins are obligate heteropolymers and, similarly to other IFs, they contain
30 ing that like mammalian NFs, lamprey NFs are heteropolymers, and that additional NF subunits may exis
31 inant of the mean pI of recombinant ferritin heteropolymers, and that ferritin microheterogeneity is
32  then cross-linked bispecific mAb complexes (heteropolymers, anti-CR1 x anti-phi X174) were infused i
33                                              Heteropolymers are important examples of self-assembling
34                          As a result, folded heteropolymers are predicted to display the kind of clos
35  when exposed to drought, the composition of heteropolymers are strategically varied across fine root
36  being a universal feature of all designable heteropolymers, as it is present also in natural protein
37 ecent evidence indicates these molecules are heteropolymers assembled from Bfr and Ftn subunits.
38        Mammalian neurofilaments are obligate heteropolymers assembled from three polypeptides, neurof
39 terface, consistent with roles in modulating heteropolymer assembly.
40 ular crowding that favors coalescence of the heteropolymer at the insert site and thus closure of the
41   This allows water to penetrate into folded heteropolymers at high pressure and break apart their hy
42       Spirocyclic adducts, in both homo- and heteropolymer background single-stranded DNA sequences,
43 rgy transfer to demonstrate the formation of heteropolymers between S and Z alpha1-antitrypsin.
44 ow information varies with activity in other heteropolymers, both biological and synthetic, may lead
45 dicate that not only may mixed variants form heteropolymers, but that this can causally lead to the d
46 4A suggesting that it disassembles ESCRT-III heteropolymers by affecting each component protein.
47 d 2, induces the postediting addition of A/U heteropolymers by KPAP1 poly(A) polymerase and RET1 term
48 o navigate random encounters(5,6); synthetic heteropolymers capable of emulating such interactions ca
49 sing two litter types that possessed similar heteropolymer chemistry, but different proportions of la
50                                 We revisit a heteropolymer collapse theory originally introduced to e
51 sic information about protein sequence using heteropolymer collapse theory.
52 from elementary sequence information using a heteropolymer collapse theory.
53  specific short and long range interactions (heteropolymer collapse).
54            We have constructed tri-molecular heteropolymer complexes consisting of b-mAb 9B9, SA, and
55 -wall carbon nanotubes (SWCNTs) wrapped with heteropolymers composed of hydrophobic and hydrophilic g
56                   It is often described as a heteropolymer comprised of polyaliphatic and polyaromati
57 polymer-chain nanoparticles formed by random heteropolymers comprising four or more components can di
58  BEAR reactions are used to generate protein heteropolymers containing a beta-backbone, gamma-backbon
59                      Protein and polypeptide heteropolymers containing non-alpha-backbone monomers ar
60                     The C(16) PEG2K Ceramide heteropolymer corona phase of SWCNTs allows selective bi
61 gest that both these models (homopolymer and heteropolymer) could be applicable depending on the solu
62                  Because the integrity of NF heteropolymers depends upon maintaining properly balance
63 ently linked to the FctA- and Cpa-containing heteropolymer derived from cell extracts.
64          They act by disassembling ESCRT-III heteropolymers during or after their proposed function i
65                Incubation of the erythrocyte-heteropolymer-E. coli complexes with freshly isolated hu
66 insert mutants to assess the strength of the heteropolymer-encoded folding signals that facilitate lo
67                                     For each heteropolymer ensemble, the level of segmental similarit
68 libraries and used the information to design heteropolymer ensembles as mixtures of disordered, parti
69   Amylovoran, a high molecular weight acidic heteropolymer exopolysaccharide, is a virulent factor of
70 pleen ferritin (HoSF), a naturally occurring heteropolymer ferritin of H and L-subunits (approximatel
71 recombinant H- and L-subunit homopolymer and heteropolymer ferritins and several site-directed H-subu
72 y more than 8 decades ago, recombinant human heteropolymer ferritins have never been synthesized, owi
73 elps to explain the widespread occurrence of heteropolymer ferritins in tissues of vertebrates.
74 allowing the synthesis of a full spectrum of heteropolymer ferritins, from H-rich to L-rich ferritins
75  two-state co-operative transition following heteropolymer formalism, whereas secondary structure for
76                          The regiocontrol of heteropolymer formation derives from the inability of th
77 the adult axon, the neurofilaments (NFs) are heteropolymers formed from the low (NFL), middle (NFM),
78 ucophytes, chloroplast division involves two heteropolymer-forming FtsZ isoforms: FtsZ1 and FtsZ2 in
79 nt structural studies indicate that a tektin heteropolymer forms a unique protofilament of flagellar
80    Suberin is a lipid and phenolic cell wall heteropolymer found in the roots and other organs of all
81  tests of the validity of REM as a model for heteropolymer freezing, freezing transition of random se
82 ghtly to the beta-1,4-linked glucose-mannose heteropolymer glucomannan.
83 mers, unlike the triplet, which are obligate heteropolymers, have supported a widely held view that a
84 mers, unlike the triplet, which are obligate heteropolymers, have supported a widely held view that p
85 s, we demonstrate sequence encoded nanoscale heteropolymers, helical polymers, 2D lattices, and mesos
86 (CR1) on E using a bispecific mAb complex, a heteropolymer (HP).
87              Monoclonal antibody (MAb)-based heteropolymers (HP) were used to simulate immune adheren
88          Lignin is a phenylpropanoid-derived heteropolymer important for the strength and rigidity of
89                 Lignin, an abundant aromatic heteropolymer in secondary plant cell walls, is the sing
90 lants is the presence of the phenolic lignin heteropolymer in xylem and other sclerified cell types.
91 t as in mammals, NFs in lamprey are obligate heteropolymers, in which NF-L is a required subunit.
92 cones, and depolymerized condensed flavonoid heteropolymers into flavanones, flavanols and (deoxy)ant
93 ess, the short A-tails are extended as (A/U) heteropolymers into structures previously thought to be
94 ss-linking of the cartilage type II collagen heteropolymer is an integral, early process in fibril as
95                The folding of a protein-like heteropolymer is studied by using direct simulation of a
96                          The exoskeletal PGN heteropolymer is the major determinant of cell shape and
97 hile the collapse of homopolymers and random heteropolymers is continuous and multi-phasic.
98 ion, which is a three-legged pinwheel-shaped heteropolymer, is a major component in the protein coats
99       Here we show that a more sophisticated heteropolymer Ising model can be constructed and fitted
100 is clathrin, which appears as a three-legged heteropolymer (known as a triskelion) that assembles int
101 dded to guide RNAs and rRNAs, while long A/U heteropolymers mark 3' ends of most mRNAs.
102                    Keratins 8 and 18 (K8/18) heteropolymers may regulate cell signaling via the known
103 f synthetic methyl methacrylate-based random heteropolymers (MMA-based RHPs) has displayed protein-li
104          The folding mechanism of a 125-bead heteropolymer model for proteins is investigated with Mo
105 mputer simulations of a well-studied lattice heteropolymer model, the first systematic test of this o
106            Numerical calculations on lattice heteropolymer models are presented to illustrate the key
107 s that the otherwise rapid folding of simple heteropolymer models becomes "glassy"-dominated by multi
108 this phenomenon, we report three examples of heteropolymer-nanotube recognition complexes for ribofla
109                                Unlike random heteropolymers, natural proteins fold into unique ordere
110                                  As obligate heteropolymers, NF assembly requires interactions betwee
111  homopolymer common antigen (A band) and the heteropolymer O antigen (B band), which impart serospeci
112 demands at each phase of regeneration for NF heteropolymers of differing composition in regrowing axo
113                     Vertebrate ferritins are heteropolymers of H and L subunits with only the H subun
114 toskeletal polymers of vertebrate axons, are heteropolymers of multiple NF subunit proteins.
115         In the serogroups W and Y, these are heteropolymers of the repeating units (-->6)-alpha-d-Gal
116           Keratin intermediate filaments are heteropolymers of type I and type II polypeptides that c
117                 Here, we show that synthetic heteropolymers, once constrained onto a single-walled ca
118      It should now be possible to extend the heteropolymer paradigm to a live pathogen in a primate m
119                      A cell wall made of the heteropolymer peptidoglycan (PG) surrounds most bacteria
120 etween the inserted homopolymer and flanking heteropolymer portions of the unfolded protein.
121 lyketides are a class of biologically active heteropolymers produced by assembly line-like multiprote
122                      The 24-subunit ferritin heteropolymer protein shell consists of light (L) and he
123                                These unusual heteropolymers represent unique examples of a conjugatio
124                        Assembled as obligate heteropolymers requiring NF-L and substoichiometric amou
125 that rodent neurofilaments (NF) are obligate heteropolymers requiring NF-L plus either NF-M or NF-H f
126 a secondary pectinase hydrolyzing the pectic heteropolymer, rhamnogalacturonan I (RG-I).
127 bout 1,300 metalloproteins, we design random heteropolymers (RHPs) as enzyme mimics based on one-pot
128                                       Random heteropolymers (RHPs) consisting of three or more comono
129 tructured channel, four-monomer-based random heteropolymers (RHPs)(14) can mimic membrane proteins an
130  accommodate the use of both homopolymer and heteropolymer RNA templates lacking uridylates and can b
131  We have generated bispecific mAb complexes (heteropolymer(s), HP), which contain a mAb specific for
132 ar environment by systematically varying the heteropolymer segment distribution and the strength of t
133      We show that a Gaussian distribution of heteropolymer segments, coupled with strong lamin-chroma
134 distributions for different distributions of heteropolymer segments.
135 ly an "active learning" strategy to identify heteropolymer sequences that break this correlation.
136 gnificantly more foldable than purely random heteropolymer sequences.
137                    Lignins, complex aromatic heteropolymers, stiffen and fortify secondary cell walls
138 hage previously cleared to the liver via the heteropolymer system was phagocytosed and destroyed.
139                         Lignin is a phenolic heteropolymer that is deposited in secondary-thickened c
140                         Septin monomers form heteropolymers that in turn associate into a variety of
141 ent in their molecular mass assemble to form heteropolymers that produce a structure-providing intrac
142 ared cross-linked, bispecific mAb complexes (heteropolymers) that facilitate rapid and quantitative b
143         However, in the design of artificial heteropolymers the control over the single chain self-as
144 ytoplasmic membrane with a net-like, elastic heteropolymer, the peptidoglycan sacculus, to protect th
145 tional evidence for the potential utility of heteropolymers to facilitate the safe and rapid clearanc
146 tained predominantly B-type homopolymers and heteropolymers up to 12-mers (3400 Da).
147                 The formation of crosslinked heteropolymers was also explored with networks containin
148 o L subunit composition of purified ferritin heteropolymers was analyzed by SDS-PAGE and capillary ge
149 ent extensive crosslinking on their own, but heteropolymers were not observed in multiprotein network
150 ade in previous in vivo experiments in which heteropolymers were used to facilitate clearance of inno
151 proteins can produce beta-linked glucomannan heteropolymers when supplied both GDP-mannose and GDP-gl
152 ormation generation from random sequences of heteropolymers, where unfavorable Shannon entropy is ove
153 formational mobility of peptides and related heteropolymers while simultaneously altering their prope
154 ormation modes with minimal bond changes and heteropolymers whose folding pathway selections are cont
155 izobium etli CE3 O antigen is a fixed-length heteropolymer with O methylation being the predominant t
156 nant O-polysaccharide (OPS) is an unbranched heteropolymer with repeating d-glucose and 6-deoxy-l-tal
157                   In addition, FctA formed a heteropolymer with the putative collagen-binding protein
158 ynthetically accessible and provides (AB)(n) heteropolymers with an alternating backbone and alternat
159  resulted in the formation of high molecular heteropolymers with FnBPA only, suggesting a specificity
160 an be a powerful tool in the design of novel heteropolymers with tuned stereochemical properties.

 
Page Top