1 bout 55 have DNA-binding sites identified by
DNA footprinting.
2 acterized using RNA and ATAC sequencing, and
DNA footprinting.
3 DNA footprinting also showed specific protection of the
4 We show by both mutational and
DNA footprinting analyses that the binding of nogalamyci
5 DNA-footprinting analyses revealed new transcriptional r
6 DNA footprinting analysis further demonstrated the speci
7 DNA footprinting analysis identified unique protein bind
8 DNA footprinting analysis of the cII transgene in AFB(1)
9 DNA footprinting analysis revealed a 37-bp region that i
10 Here we show by
DNA footprinting analysis that MPG, but not UDG, bound t
11 ng at the CR and M promoters was analyzed by
DNA footprinting and a range of biophysical techniques.
12 Exonuclease III mediated in vivo
DNA footprinting and dimethyl sulfate in vivo footprinti
13 We have used
DNA footprinting and fluorescence melting experiments to
14 By
DNA footprinting and gel retardation analysis, we demons
15 ron endonuclease with its DNA target site by
DNA footprinting and modification-interference approache
16 DNA footprinting and nuclease protection studies of PcrA
17 proximately 20 bp from the dyad was shown by
DNA footprinting and photoaffinity labeling using recomb
18 DNA footprinting and purine-base interference assays dem
19 DNA footprinting and single-molecule fluorescence experi
20 interactions with nucleosomes were mapped by
DNA footprinting and site-directed DNA and protein cross
21 egion I-deleted sigma holoenzyme observed by
DNA footprinting,
and are likely of significance to the
22 oying electrophoretic mobility-shift assays,
DNA footprinting,
and in silico analysis, we identified
23 Biochemical,
DNA footprinting,
and in vitro transcription assays indi
24 teraction evaluated by thermal denaturation,
DNA footprinting,
and in vitro transcription stop assays
25 ation interference, modification protection,
DNA footprinting,
and photocross-linking techniques.
26 Using
DNA footprinting as an assay, we show here that PriA als
27 Gel shift and
DNA footprinting assays demonstrate that the SspA protei
28 Furthermore, methylation interference
DNA footprinting assays showed increased nuclear protein
29 ies using electrophoretic mobility shift and
DNA footprinting assays showed that both Sp1 and Sp3 pro
30 nal fusion, gel mobility shift analyses, and
DNA footprinting assays were used to confirm the direct
31 electrophoresis, immunodot blot assays, and
DNA footprinting assays, we demonstrated a unique wavele
32 DNA footprinting confirmed that interaction of Dda with
33 DNA footprinting confirmed that MprA protected large sec
34 In vivo genomic
DNA footprinting confirms the presence of nuclear protei
35 Results of in vivo genomic
DNA footprinting experiments indicate that a protein(s)
36 DNA footprinting experiments revealed similarities betwe
37 Molecular docking simulations and
DNA footprinting experiments suggest a model where a PC4
38 DNA footprinting experiments were also conducted to furt
39 Previous
DNA footprinting experiments with C.AhdI have located th
40 region of A-tracts, a feature inferred from
DNA footprinting experiments.
41 osines protected by in vivo dimethyl sulfate
DNA footprinting (
GAAGAGTG) in a luciferase construct (-
42 Hydroxyl radical
DNA footprinting indicated that the site-specifically bo
43 ctrophoretic mobility shift assay (EMSA) and
DNA footprinting,
members of the Sp family (Sp1, Sp3, an
44 DNA footprinting of EcoSSB on wild-type and mutant promo
45 Using in vivo genomic
DNA footprinting of normal human epithelial cells (HaCaT
46 High-resolution
DNA footprinting of the DNA product of transposition att
47 DNA footprinting of the JBP.J-DNA complex with 1,10-phen
48 Using
DNA footprinting of the regions upstream of the liaXYZ a
49 Through systematic
DNA footprinting of the TNF (encoding tumour necrosis fa
50 DNA footprinting of the TxRE with 1, 10-phenanthroline-c
51 DNA footprinting of this fragment revealed a highly cons
52 of the phosphodiester backbone resulted in a
DNA-footprinting pattern similar to that observed with t
53 To test this, we analyzed pelA
DNA footprinting patterns with various combinations of F
54 he results from Western blotting, EMSAs, and
DNA footprinting reactions lead to the conclusion that A
55 of the protein-DNA interface by quantitative
DNA footprinting revealed new minor groove contacts and
56 DNA footprinting revealed that a major conformational di
57 nterrogation of the protein/DNA interface by
DNA footprinting showed similar accessibility to dimethy
58 Protein-
DNA footprinting showed that both genes were occupied by
59 In vivo
DNA footprinting shows a specific loss of occupancy at t
60 Using a combination of site-specific
DNA footprinting,
single-turnover unwinding assays, and
61 DNA footprinting studies confirmed the specific binding
62 DNA footprinting studies of PhoP-regulated promoters sho
63 DNA footprinting studies suggest that the RAG proteins i
64 ts of electrophoretic mobility shift assays,
DNA footprinting studies, and promoter-lac fusion experi
65 We also show using
DNA footprinting studies, that T7 ligase binds asymmetri
66 We have prepared novel
DNA footprinting substrates that contain all 64 symmetri
67 Using in-gel cleavage assays and
DNA footprinting techniques, I analyzed the catalytic ac
68 SWI/SNF was found by
DNA footprinting to contact tightly around one gyre of D
69 se electrophoretic mobility shift assays and
DNA footprinting to show that the DrHU N-terminal domain
70 DNA footprinting using exonucleaseIII and DNaseI, and me
71 died using equilibrium binding measurements,
DNA footprinting,
van't Hoff analysis and calorimetry.
72 As another approach, in vivo
DNA footprinting was used and identified protein protect
73 LEX data reanalysis, structural modeling and
DNA footprinting,
we propose that these proneural factor
74 The advent of
DNA footprinting with DNase I more than 35 years ago ena