ライフサイエンスコーパス: deoxyribonuclease I

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1 a, which was abrogated by preincubation with deoxyribonuclease-I.

2 acute liver failure plasma with and without deoxyribonuclease-I.

3 selective serine 3 cofilin kinase binds to a deoxyribonuclease I affinity column, whereas the nonspec

4 odified 3'-phosphate of oligonucleotides and deoxyribonuclease I and ribonuclease H cleavages.

5 lease A) and six acidic proteins (myoglobin, deoxyribonuclease I, beta-lactoglobulin A, beta-lactoglo

6 A deoxyribonuclease I binding assay shows that the number

7 Detection of pointed ends in situ using deoxyribonuclease I binding demonstrates that this incre

8 reated wild-type MLEC were hypersensitive to deoxyribonuclease I compared with wild-type cells, demon

9 Employing deoxyribonuclease I (DNase I) as a model enzyme template

10 are concentrated in regulatory DNA marked by deoxyribonuclease I (DNase I) hypersensitive sites (DHSs

11 It was demonstrated previously that deoxyribonuclease I (DNase I) is a highly active renal e

12 Bovine pancreatic deoxyribonuclease I (DNase I) is a nuclease of relativel

13 Bovine pancreatic deoxyribonuclease I (DNase I) is a well characterised en

14 Recombinant human deoxyribonuclease I (DNase I) is an important clinical a

15 Deoxyribonuclease I (DNase I) is an important enzyme tha

16 Although deoxyribonuclease I (DNase I) was used to probe the stru

17 Human deoxyribonuclease I (DNase I), an enzyme recently approv

18 Human deoxyribonuclease I (DNase I), an enzyme used to treat c

19 ty (71 and 63% similarity), respectively, to deoxyribonuclease I (DNase I).

20 nalised with dornase alfa (recombinant human deoxyribonuclease I, DNase), demonstrating DNA degradati

21 Deoxyribonuclease I (DNaseI) hypersensitivity analyses i

22 They belong to nine different proteins (deoxyribonuclease I, enolase, hen egg-white lysozyme, hu

23 Deoxyribonuclease I footprint analysis of the minimal pr

24 tituted in vitro transcription reactions and deoxyribonuclease I footprinting assays confirmed the ab

25 Deoxyribonuclease I footprinting identified a specific s

26 We used genomic deoxyribonuclease I footprinting to map nucleotide resol

27 Deoxyribonuclease I footprinting was used to identify a

28 Gel-shift and deoxyribonuclease-I footprinting assays revealed four DN

29 Deoxyribonuclease I forms a very tight complex with acti

30 The identification of a tissue-specific deoxyribonuclease I hypersensitive site approximately 3k

31 portant transcriptional regulatory elements, deoxyribonuclease I hypersensitive site mapping studies

32 Colon-specific deoxyribonuclease I hypersensitive sites (DHS) have been

33 d single nucleotide polymorphisms (SNPs) and deoxyribonuclease I hypersensitive sites (DHSs) from 112

34 locus control region (LCR) composed of five deoxyribonuclease I hypersensitive sites (HSs).

35 Analysis of transcription factor motifs in deoxyribonuclease I hypersensitive sites at cell-type-sp

36 A 3.5-kb fragment containing one of these deoxyribonuclease I hypersensitive sites, located -14 kb

37 However, removal of SWI/SNF left a deoxyribonuclease I-hypersensitive site specifically at

38 cs of regulatory DNA, we mapped >1.3 million deoxyribonuclease I-hypersensitive sites (DHSs) in 45 mo

39 Myeloid-cell-specific, deoxyribonuclease-I-hypersensitive sites localized to th

40 ility as detected by histone acetylation and deoxyribonuclease I hypersensitivity.

41 i to digestion with micrococcal nuclease and deoxyribonuclease I, indicating that chromatin structure

42 l protein (CLC); carboxypeptidase A3 (CPA3); deoxyribonuclease I-like 3 (DNASE1L3); IL-1beta (IL1B);

43 ous ATP-actin structures from complexes with deoxyribonuclease I, profilin, and gelsolin, monomeric A

44 Deoxyribonuclease I protection assays confirmed the pres

45 markers acetyl-H4 and H4K20m, and regions of deoxyribonuclease I-sensitive chromatin compared with co

46 iple histone marks and Pol II, as well as in deoxyribonuclease I sensitivity and nucleosome positioni

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