204 related articles for article (PubMed ID: 21423757)
1. Nuclear scaffold attachment sites within ENCODE regions associate with actively transcribed genes.
Keaton MA; Taylor CM; Layer RM; Dutta A
PLoS One; 2011 Mar; 6(3):e17912. PubMed ID: 21423757
[TBL] [Abstract][Full Text] [Related]
2. Differential nuclear scaffold/matrix attachment marks expressed genes.
Linnemann AK; Platts AE; Krawetz SA
Hum Mol Genet; 2009 Feb; 18(4):645-54. PubMed ID: 19017725
[TBL] [Abstract][Full Text] [Related]
3. Multiple collagen I gene regulatory elements have sites of stress-induced DNA duplex destabilization and nuclear scaffold/matrix association potential.
Mielke C; Christensen MO; Westergaard O; Bode J; Benham CJ; Breindl M
J Cell Biochem; 2002; 84(3):484-96. PubMed ID: 11813254
[TBL] [Abstract][Full Text] [Related]
4. Association of the matrix attachment region recognition signature with coding regions in Caenorhabditis elegans.
Anthony A; Blaxter M
BMC Genomics; 2007 Nov; 8():418. PubMed ID: 18005410
[TBL] [Abstract][Full Text] [Related]
5. An unusual extended DNA loop attachment region is located in the human dystrophin gene.
Iarovaia OV; Borounova V; Vassetzky YS; Razin SV
J Cell Physiol; 2006 Nov; 209(2):515-21. PubMed ID: 16883579
[TBL] [Abstract][Full Text] [Related]
6. Identification of a candidate regulatory region in the human CD8 gene complex by colocalization of DNase I hypersensitive sites and matrix attachment regions which bind SATB1 and GATA-3.
Kieffer LJ; Greally JM; Landres I; Nag S; Nakajima Y; Kohwi-Shigematsu T; Kavathas PB
J Immunol; 2002 Apr; 168(8):3915-22. PubMed ID: 11937547
[TBL] [Abstract][Full Text] [Related]
7. Identifying Nuclear Matrix-Attached DNA Across the Genome.
Dobson JR; Hong D; Barutcu AR; Wu H; Imbalzano AN; Lian JB; Stein JL; van Wijnen AJ; Nickerson JA; Stein GS
J Cell Physiol; 2017 Jun; 232(6):1295-1305. PubMed ID: 27627025
[TBL] [Abstract][Full Text] [Related]
8. Mapping of structural and transcription-related matrix attachment sites in the alpha-globin gene domain of avian erythroblasts and erythrocytes.
Farache G; Razin SV; Rzeszowska-Wolny J; Moreau J; Targa FR; Scherrer K
Mol Cell Biol; 1990 Oct; 10(10):5349-58. PubMed ID: 2398893
[TBL] [Abstract][Full Text] [Related]
9. Enhanced expression of EGFP gene in CHSE-214 cells by an ARS element from mud loach (Misgurnus mizolepis).
Kim MS; Lim HS; Ahn SJ; Jeong YK; Kim CG; Lee HH
Plasmid; 2007 Nov; 58(3):228-39. PubMed ID: 17586046
[TBL] [Abstract][Full Text] [Related]
10. Breakpoint cluster regions of the AML-1 and ETO genes contain MAR elements and are preferentially associated with the nuclear matrix in proliferating HEL cells.
Iarovaia OV; Shkumatov P; Razin SV
J Cell Sci; 2004 Sep; 117(Pt 19):4583-90. PubMed ID: 15331666
[TBL] [Abstract][Full Text] [Related]
11. In-silico prediction and observations of nuclear matrix attachment.
Platts AE; Quayle AK; Krawetz SA
Cell Mol Biol Lett; 2006; 11(2):191-213. PubMed ID: 16847565
[TBL] [Abstract][Full Text] [Related]
12. Transcription factor binding sites in the matrix attachment region (MAR) of the chicken alpha-globin gene.
Boulikas T
J Cell Biochem; 1994 Aug; 55(4):513-29. PubMed ID: 7962181
[TBL] [Abstract][Full Text] [Related]
13. Chromatin loops are selectively anchored using scaffold/matrix-attachment regions.
Heng HH; Goetze S; Ye CJ; Liu G; Stevens JB; Bremer SW; Wykes SM; Bode J; Krawetz SA
J Cell Sci; 2004 Mar; 117(Pt 7):999-1008. PubMed ID: 14996931
[TBL] [Abstract][Full Text] [Related]
14. MAR/SAR elements flank the rat hst70 gene transcription unit.
Widłak W; Widłak P
Cell Mol Biol Lett; 2004; 9(1):123-33. PubMed ID: 15048156
[TBL] [Abstract][Full Text] [Related]
15. The human clotting factor VIII cDNA contains an autonomously replicating sequence consensus- and matrix attachment region-like sequence that binds a nuclear factor, represses heterologous gene expression, and mediates the transcriptional effects of sodium butyrate.
Fallaux FJ; Hoeben RC; Cramer SJ; van den Wollenberg DJ; Briët E; van Ormondt H; van Der Eb AJ
Mol Cell Biol; 1996 Aug; 16(8):4264-72. PubMed ID: 8754827
[TBL] [Abstract][Full Text] [Related]
16. High frequency of matrix attachment regions and cut-like protein x/CCAAT-displacement protein and B cell regulator of IgH transcription binding sites flanking Ig V region genes.
Goebel P; Montalbano A; Ayers N; Kompfner E; Dickinson L; Webb CF; Feeney AJ
J Immunol; 2002 Sep; 169(5):2477-87. PubMed ID: 12193717
[TBL] [Abstract][Full Text] [Related]
17. A nuclear matrix/scaffold attachment region co-localizes with the gypsy retrotransposon insulator sequence.
Nabirochkin S; Ossokina M; Heidmann T
J Biol Chem; 1998 Jan; 273(4):2473-9. PubMed ID: 9442099
[TBL] [Abstract][Full Text] [Related]
18. Silencing by nuclear matrix attachment distinguishes cell-type specificity: association with increased proliferation capacity.
Linnemann AK; Krawetz SA
Nucleic Acids Res; 2009 May; 37(9):2779-88. PubMed ID: 19276204
[TBL] [Abstract][Full Text] [Related]
19. Mapping of scaffold/matrix attachment regions in human genome: a data mining exercise.
Narwade N; Patel S; Alam A; Chattopadhyay S; Mittal S; Kulkarni A
Nucleic Acids Res; 2019 Aug; 47(14):7247-7261. PubMed ID: 31265077
[TBL] [Abstract][Full Text] [Related]
20. The limits of the DNase I-sensitive domain of the human apolipoprotein B gene coincide with the locations of chromosomal anchorage loops and define the 5' and 3' boundaries of the gene.
Levy-Wilson B; Fortier C
J Biol Chem; 1989 Dec; 264(35):21196-204. PubMed ID: 2592370
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
