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1 ements, as well as within a nuclear scaffold/matrix attachment region.
2 s present in human follicular lymphoma, is a matrix attachment region.
3 es being approximately equal near a centered matrix attachment region.
4 y general DNase I sensitivity and flanked by matrix attachment regions.
5 extraction-resistant protein structure, via matrix attachment regions.
6 formed to the consensus sequence for nuclear matrix attachment regions.
7 nucleosomal DNA and association with nuclear matrix attachment regions.
8 and are typically identified within various matrix attachment regions.
9 at sequences known as scaffold-attachment or matrix-attachment regions.
10 borhood of HS4 is not like that of canonical matrix attachment regions, and its incorporation into th
12 000 controls identified SNPs in the scaffold/matrix attachment region as among the most likely causal
13 T cell) derived cDNA library, using SATB1 (a matrix attachment region binding protein) as the bait, y
14 longs to the same family as SATB1, a nuclear matrix-attachment region binding protein implicated in t
18 ancer (E micro ) with and without associated matrix attachment regions (E micro MAR) into lentivirus
19 None of the DNase I-hypersensitive sites/matrix attachment regions, either alone or in combinatio
21 interference (RNAi) constructs, PTG and its matrix-attachment-region flanked version MPG, into the e
22 ther the TNF locus to the nuclear matrix via matrix attachment region formation, potentially promotin
23 ts of the core enhancer flanked by 5' and 3' matrix attachment regions, has been implicated in contro
24 of rearrangement, we replaced the endogenous matrix attachment region/Igk intronic enhancer (MiE(kapp
26 ions of the core enhancer and its associated matrix attachment regions in the endogenous IgH locus, w
27 d by DNase I-hypersensitive sites (DHSs) and matrix-attachment regions, in expressing and non-express
28 d by DNase I hypersensitive sites (DHSs) and matrix-attachment regions, in expressing and non-express
29 f cis-regulatory elements in which a nuclear matrix attachment region is in close proximity to an enh
30 nd identified one of the core factors as the matrix attachment region (MAR) binding protein, SATB1, w
31 ion of chromatin with the nuclear matrix via matrix attachment region (MAR) DNA is considered to be o
33 ronic enhancer (iE kappa) and its associated matrix attachment region (MAR) during B cell development
34 human breast tumor tissues that recognizes a matrix attachment region (MAR) in the immediate vicinity
36 The chromatin fragments were enriched in a matrix attachment region (MAR) sequence compared with a
37 nd pUC18 plasmids containing various nuclear matrix attachment region (MAR) sequences suggest that DN
38 Attachment of DNA to the nuclear matrix via matrix attachment region (MAR) sequences, and interactio
39 antially impaired by deletion of the nuclear matrix attachment region (MAR) which flanks the intron-e
40 uctural boundary is represented by a nuclear matrix attachment region (MAR), situated about 3 kb 5' o
44 keratin 18 (K18) gene and synthetic nuclear matrix attachment regions (MAR) composed of the binding
46 ally binds to nuclear matrix attachment DNA (matrix attachment region, MAR) from a breast carcinoma c
47 he human CD8 gene complex, we mapped nuclear matrix attachment regions (MARs) and DNase I hypersensit
52 used this system to determine whether human matrix attachment regions (MARs) can function as insulat
53 oth plant and animal systems have shown that matrix attachment regions (MARs) can increase expression
56 different configurations of flanking nuclear matrix attachment regions (MARs) encompassing the protam
59 ified as a protein that bound to the nuclear matrix attachment regions (MARs) of the immunoglobulin h
60 ion of chromatin with the nuclear matrix via matrix attachment regions (MARs) on the DNA is considere
61 Previous studies have identified nuclear matrix attachment regions (MARs) that are closely associ
62 ganization of the c-myc locus is provided by matrix attachment regions (MARs) that define a domain la
64 ed AT islands exhibit sequence attributes of matrix attachment regions (MARs), domains that organize
66 gH) intronic enhancer, Emicro, by binding to matrix attachment regions (MARs), sites necessary for DN
68 eb site provides a tool for the detection of matrix attachment regions (MARs), which can be used to i
70 says (NMBAs) define certain DNA sequences as matrix attachment regions (MARs), which often have cis-a
71 ear cellular sequences identified as nuclear matrix attachment regions (MARs), while integrations in
79 s domain exhibits characteristics of nuclear matrix attachment regions (MARs): an exceptionally inten
81 rolling this transcription also requires the matrix-attachment regions (MARs) that flank the intronic
82 DNA: a human fragment of alphoid repeat DNA, matrix-attachment regions (MARs), and the hepatocyte con
84 bone, promoter, rhodopsin gene, and scaffold/matrix attachment region) of the vectors were evaluated
85 in fiber to the nuclear matrix, known as the matrix attachment region or scaffold attachment region (
86 ial pitfall of functional studies of nuclear matrix attachment regions outside of their natural chrom
88 s (NPs) containing a plasmid with a scaffold matrix attachment region (S/MAR) and vitelliform macular
89 e strategy to successfully generate scaffold/matrix attachment region (S/MAR) DNA plasmid vectors con
90 by activator Zif-VP64, based on the Scaffold/Matrix Attachment Region (S/MAR) for episomal retention
96 ns (BURs) are typically found in scaffold or matrix attachment regions (SARs/MARs) that are thought t
97 ct recruitment of SMAR1/HDAC1 complex to the matrix attachment region site present in the Slug promot
98 associations with gene regulatory elements, matrix attachment regions, stress-induced DNA duplex des
99 be distinct from the domains created by the matrix attachment regions that typically flank smaller,
100 fragment lying just upstream from a centered matrix attachment region--the same region that was also
101 oter, 5' UTR, 3' UTR, double terminator, and matrix attachment region, to modify the TMV-based pJL-TR
103 with allele-specific effects and a scaffold/matrix attachment region were characterized and, through