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1 s present in human follicular lymphoma, is a matrix attachment region.
2 es being approximately equal near a centered matrix attachment region.
3  extraction-resistant protein structure, via matrix attachment regions.
4 y general DNase I sensitivity and flanked by matrix attachment regions.
5 formed to the consensus sequence for nuclear matrix attachment regions.
6 nucleosomal DNA and association with nuclear matrix attachment regions.
7  and are typically identified within various matrix attachment regions.
8 at sequences known as scaffold-attachment or matrix-attachment regions.
9 borhood of HS4 is not like that of canonical matrix attachment regions, and its incorporation into th
10                       Insulator elements and matrix attachment regions are essential for the organiza
11 T cell) derived cDNA library, using SATB1 (a matrix attachment region binding protein) as the bait, y
12 longs to the same family as SATB1, a nuclear matrix-attachment region binding protein implicated in t
13                      We report here that the matrix attachment region-binding protein SATB1 interacts
14                          These sperm nuclear matrix attachment regions delimit the DNase I-sensitive
15 lts suggest that NPM associates with nuclear matrix attachment region DNA in heat-shocked cells.
16 ancer (E micro ) with and without associated matrix attachment regions (E micro MAR) into lentivirus
17     None of the DNase I-hypersensitive sites/matrix attachment regions, either alone or in combinatio
18 o, suggesting that it may also function as a matrix attachment region element.
19 ther the TNF locus to the nuclear matrix via matrix attachment region formation, potentially promotin
20 ts of the core enhancer flanked by 5' and 3' matrix attachment regions, has been implicated in contro
21 of rearrangement, we replaced the endogenous matrix attachment region/Igk intronic enhancer (MiE(kapp
22 m of the TNF gene (HSS-7), which serves as a matrix attachment region in monocytes.
23 ions of the core enhancer and its associated matrix attachment regions in the endogenous IgH locus, w
24 d by DNase I-hypersensitive sites (DHSs) and matrix-attachment regions, in expressing and non-express
25 d by DNase I hypersensitive sites (DHSs) and matrix-attachment regions, in expressing and non-express
26 f cis-regulatory elements in which a nuclear matrix attachment region is in close proximity to an enh
27 nd identified one of the core factors as the matrix attachment region (MAR) binding protein, SATB1, w
28 ion of chromatin with the nuclear matrix via matrix attachment region (MAR) DNA is considered to be o
29        SATB1 is a cell type-specific nuclear matrix attachment region (MAR) DNA-binding protein, pred
30 ronic enhancer (iE kappa) and its associated matrix attachment region (MAR) during B cell development
31 human breast tumor tissues that recognizes a matrix attachment region (MAR) in the immediate vicinity
32                            We find a nuclear matrix attachment region (MAR) present within the NRE of
33   The chromatin fragments were enriched in a matrix attachment region (MAR) sequence compared with a
34 nd pUC18 plasmids containing various nuclear matrix attachment region (MAR) sequences suggest that DN
35  Attachment of DNA to the nuclear matrix via matrix attachment region (MAR) sequences, and interactio
36 antially impaired by deletion of the nuclear matrix attachment region (MAR) which flanks the intron-e
37 uctural boundary is represented by a nuclear matrix attachment region (MAR), situated about 3 kb 5' o
38                                              Matrix attachment region (MAR)-binding proteins have bee
39 ative neonatal promoter, a DMR and an active Matrix Attachment Region (MAR).
40 origin of replication is a prominent nuclear matrix attachment region (MAR).
41  keratin 18 (K18) gene and synthetic nuclear matrix attachment regions (MAR) composed of the binding
42                                      Nuclear matrix attachment regions (MAR) have been implicated in
43 ally binds to nuclear matrix attachment DNA (matrix attachment region, MAR) from a breast carcinoma c
44 he human CD8 gene complex, we mapped nuclear matrix attachment regions (MARs) and DNase I hypersensit
45                                              Matrix attachment regions (MARs) are DNA sequences that
46                                              Matrix attachment regions (MARs) are operationally defin
47                                              Matrix attachment regions (MARs) are thought to particip
48                                              Matrix attachment regions (MARs) can be operationally de
49  used this system to determine whether human matrix attachment regions (MARs) can function as insulat
50 oth plant and animal systems have shown that matrix attachment regions (MARs) can increase expression
51                                        Human matrix attachment regions (MARs) can insulate transgene
52                                              Matrix attachment regions (MARs) comprise a set of AT-ri
53 different configurations of flanking nuclear matrix attachment regions (MARs) encompassing the protam
54                                      Nuclear matrix attachment regions (MARs) flanking the immunoglob
55          We have identified the locations of matrix attachment regions (MARs) in these homologous chr
56 ified as a protein that bound to the nuclear matrix attachment regions (MARs) of the immunoglobulin h
57 ion of chromatin with the nuclear matrix via matrix attachment regions (MARs) on the DNA is considere
58     Previous studies have identified nuclear matrix attachment regions (MARs) that are closely associ
59 ganization of the c-myc locus is provided by matrix attachment regions (MARs) that define a domain la
60      The inserted fragment includes flanking matrix attachment regions (MARs), an origin of bidirecti
61 ed AT islands exhibit sequence attributes of matrix attachment regions (MARs), domains that organize
62                   The positions of predicted matrix attachment regions (MARs), possibly related to re
63 gH) intronic enhancer, Emicro, by binding to matrix attachment regions (MARs), sites necessary for DN
64           A specific class of DNA sequences, matrix attachment regions (MARs), was found to be in com
65 eb site provides a tool for the detection of matrix attachment regions (MARs), which can be used to i
66                                      Nuclear matrix attachment regions (MARs), which flank the immuno
67 says (NMBAs) define certain DNA sequences as matrix attachment regions (MARs), which often have cis-a
68 ear cellular sequences identified as nuclear matrix attachment regions (MARs), while integrations in
69  and association of transcription factors at matrix attachment regions (MARs).
70 ore intronic enhancer (Emu) and its flanking matrix attachment regions (MARs).
71  sequences were shown to function as nuclear matrix attachment regions (MARs).
72 ear matrix via specific DNA fragments called matrix attachment regions (MARs).
73 mu enhancer is dependent on flanking nuclear matrix attachment regions (MARs).
74 of specific transcription factors near these matrix attachment regions (MARs).
75 ing, and transcription factor association at matrix attachment regions (MARs).
76 s domain exhibits characteristics of nuclear matrix attachment regions (MARs): an exceptionally inten
77                                              Matrix-attachment regions (MARs) are DNA elements that a
78 rolling this transcription also requires the matrix-attachment regions (MARs) that flank the intronic
79 DNA: a human fragment of alphoid repeat DNA, matrix-attachment regions (MARs), and the hepatocyte con
80 element and two 310-350-bp flanking scaffold/matrix attachment regions named MARsEmu.
81 bone, promoter, rhodopsin gene, and scaffold/matrix attachment region) of the vectors were evaluated
82 in fiber to the nuclear matrix, known as the matrix attachment region or scaffold attachment region (
83 ial pitfall of functional studies of nuclear matrix attachment regions outside of their natural chrom
84 ermore, we demonstrate that HS1 is a nuclear matrix attachment region, referred to as MARbeta.
85 s (NPs) containing a plasmid with a scaffold matrix attachment region (S/MAR) and vitelliform macular
86 pisomal retention properties of the scaffold/matrix attachment region (S/MAR).
87                                     Scaffold/matrix attachment regions (S/MARs) and locus control reg
88                                  Scaffold or matrix attachment regions (S/MARs) are found in all euka
89          This may be achieved using scaffold/matrix attachment regions (S/MARs) that establish loop d
90 cally identified within nuclear scaffold- or matrix-attachment regions (S/MARs).
91 ns (BURs) are typically found in scaffold or matrix attachment regions (SARs/MARs) that are thought t
92 ct recruitment of SMAR1/HDAC1 complex to the matrix attachment region site present in the Slug promot
93  associations with gene regulatory elements, matrix attachment regions, stress-induced DNA duplex des
94  be distinct from the domains created by the matrix attachment regions that typically flank smaller,
95 fragment lying just upstream from a centered matrix attachment region--the same region that was also
96 ase sensitivity flanked by 5' and 3' nuclear matrix attachment regions was defined.
97                  Surprisingly, the 5' and 3' matrix attachment regions were dispensable for these pro

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