ライフサイエンスコーパス: heteropolymeric

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1 rochloride at pH 3.5, and renaturing to form heteropolymeric 24-mers.

2 ug effect on primer extension on M13 DNA and heteropolymeric 62-mer templates, where strand slippage

3 Compared with heteropolymeric assemblies of NF triplet proteins in mam

4 at the sequence features of A/T richness and heteropolymeric character discovered by in vitro berenil

5 ites in single molecules of homopolymeric or heteropolymeric DNA sequences.

6 unless there is an L-chain available to form heteropolymeric ferritin.

7 II collagen that matures from a cross-linked heteropolymeric fibril template of types II, IX, and XI

8 pare the structure and stability of homo and heteropolymeric fibrils formed from human beta2-microglo

9 erization of more than one protein sequence (heteropolymeric fibrils) is poorly understood.

10 redominantly into homopolymeric (rather than heteropolymeric) fibrils, which deposit mainly in separa

11 f DNA elongation by the G190E mutant RT on a heteropolymeric HIV-1 gag-based RNA template showed an o

12 suggest synemin functions as a component of heteropolymeric IFs and plays an important cytoskeletal

13 ious studies demonstrated that synemin forms heteropolymeric IFs with major IF proteins and contains

14 s by itself, but rather is incorporated into heteropolymeric IFs with vimentin.

15 Type I and type II keratins form the heteropolymeric intermediate filament cytoskeleton, whic

16 In animal models, the absence of heteropolymeric keratins 8 and 18 or the presence of mut

17 activity of native ferritins is due to their heteropolymeric nature.

18 Type 1 fimbriae of enterobacteria are heteropolymeric organelles of adhesion composed of FimH,

19 y, stoichiometry and subunit combinations of heteropolymeric P2X channels has been substantially eluc

20 We have recently described a heteropolymeric peptide-amphiphile system that forms org

21 lymerizing subunit of the 1,000-plus-subunit heteropolymeric pilus fiber.

22 ens rRNAs and mRNAs revealed the presence of heteropolymeric RNA 3' tails.

23 r catalytic activities and processivities on heteropolymeric RNA and DNA templates.

24 the dNTP substrate on both homopolymeric and heteropolymeric RNA and DNA templates.

25 s problem by employing a short, symmetrical, heteropolymeric RNA primer-template that we refer to as

26 following extension of 5'-(32)P-end-labeled, heteropolymeric RNA primer/templates.

27 of an RT with an oligodeoxynucleotide-primed heteropolymeric RNA template (a single processive cycle)

28 ingle-nucleotide incorporation assay using a heteropolymeric RNA template and DNA primers, we defined

29 Incorporation of nucleotides into a heteropolymeric RNA template as catalyzed by NS5B(Delta2

30 Using a synthetic heteropolymeric RNA template with dideoxycytidine at its

31 236L were analyzed for DNA polymerization on heteropolymeric RNA templates and RNase H degradation of

32 en investigated using both homopolymeric and heteropolymeric RNA templates.

33 Mutants retaining RNase H activity on a heteropolymeric RNA.DNA hybrid failed to support DNA str

34 ce for RNA hydrolysis from a HIV-1 gag-based heteropolymeric RNA/DNA hybrid in the presence of either

35 The realignment was discovered on the heteropolymeric sequence T5C5 and yields transcripts lac

36 bly is strongly stimulated by both homo- and heteropolymeric single-stranded DNA.

37 Moreover, these heteropolymeric structures allow units as short as tetra

38 ysis suggests that chemical heterogeneity in heteropolymeric systems leads to a decoupling between RE

39 he primary polynucleotide polymerase, adding heteropolymeric tails almost exclusively to 3' truncated

40 sphorylase not only synthesizes long, highly heteropolymeric tails in vivo, but also accounts for all

41 Defined heteropolymeric template-primer combinations and high-re

42 10-30-fold reduction in k(cat) on homo- and heteropolymeric template-primers, with no significant ch

43 contain various numbers (i.e., 6 to 23) of a heteropolymeric tetranucleotide (AGAT) repeat.

44 Homo- and heteropolymeric tracts of A and T demarcate nucleosome b

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