272 related articles for article (PubMed ID: 19008940)
1. CTCF cis-regulates trinucleotide repeat instability in an epigenetic manner: a novel basis for mutational hot spot determination.
Libby RT; Hagerman KA; Pineda VV; Lau R; Cho DH; Baccam SL; Axford MM; Cleary JD; Moore JM; Sopher BL; Tapscott SJ; Filippova GN; Pearson CE; La Spada AR
PLoS Genet; 2008 Nov; 4(11):e1000257. PubMed ID: 19008940
[TBL] [Abstract][Full Text] [Related]
2. A SCA7 CAG/CTG repeat expansion is stable in Drosophila melanogaster despite modulation of genomic context and gene dosage.
Jackson SM; Whitworth AJ; Greene JC; Libby RT; Baccam SL; Pallanck LJ; La Spada AR
Gene; 2005 Feb; 347(1):35-41. PubMed ID: 15715978
[TBL] [Abstract][Full Text] [Related]
3. CTCF regulates ataxin-7 expression through promotion of a convergently transcribed, antisense noncoding RNA.
Sopher BL; Ladd PD; Pineda VV; Libby RT; Sunkin SM; Hurley JB; Thienes CP; Gaasterland T; Filippova GN; La Spada AR
Neuron; 2011 Jun; 70(6):1071-84. PubMed ID: 21689595
[TBL] [Abstract][Full Text] [Related]
4. Genomic context drives SCA7 CAG repeat instability, while expressed SCA7 cDNAs are intergenerationally and somatically stable in transgenic mice.
Libby RT; Monckton DG; Fu YH; Martinez RA; McAbney JP; Lau R; Einum DD; Nichol K; Ware CB; Ptacek LJ; Pearson CE; La Spada AR
Hum Mol Genet; 2003 Jan; 12(1):41-50. PubMed ID: 12490531
[TBL] [Abstract][Full Text] [Related]
5. Molecular genetics of hereditary spinocerebellar ataxia: mutation analysis of spinocerebellar ataxia genes and CAG/CTG repeat expansion detection in 225 Italian families.
Brusco A; Gellera C; Cagnoli C; Saluto A; Castucci A; Michielotto C; Fetoni V; Mariotti C; Migone N; Di Donato S; Taroni F
Arch Neurol; 2004 May; 61(5):727-33. PubMed ID: 15148151
[TBL] [Abstract][Full Text] [Related]
6. Dnmt1 deficiency promotes CAG repeat expansion in the mouse germline.
Dion V; Lin Y; Hubert L; Waterland RA; Wilson JH
Hum Mol Genet; 2008 May; 17(9):1306-17. PubMed ID: 18252747
[TBL] [Abstract][Full Text] [Related]
7. Xpa deficiency reduces CAG trinucleotide repeat instability in neuronal tissues in a mouse model of SCA1.
Hubert L; Lin Y; Dion V; Wilson JH
Hum Mol Genet; 2011 Dec; 20(24):4822-30. PubMed ID: 21926083
[TBL] [Abstract][Full Text] [Related]
8. Frequency of SCA1, SCA2, SCA3/MJD, SCA6, SCA7, and DRPLA CAG trinucleotide repeat expansion in patients with hereditary spinocerebellar ataxia from Chinese kindreds.
Tang B; Liu C; Shen L; Dai H; Pan Q; Jing L; Ouyang S; Xia J
Arch Neurol; 2000 Apr; 57(4):540-4. PubMed ID: 10768629
[TBL] [Abstract][Full Text] [Related]
9. Mutation of a single CTCF target site within the H19 imprinting control region leads to loss of Igf2 imprinting and complex patterns of de novo methylation upon maternal inheritance.
Pant V; Kurukuti S; Pugacheva E; Shamsuddin S; Mariano P; Renkawitz R; Klenova E; Lobanenkov V; Ohlsson R
Mol Cell Biol; 2004 Apr; 24(8):3497-504. PubMed ID: 15060168
[TBL] [Abstract][Full Text] [Related]
10. Spinocerebellar ataxia 7 (SCA7).
Lebre AS; Brice A
Cytogenet Genome Res; 2003; 100(1-4):154-63. PubMed ID: 14526176
[TBL] [Abstract][Full Text] [Related]
11. Epigenetics DNA methylation in the core ataxin-2 gene promoter: novel physiological and pathological implications.
Laffita-Mesa JM; Bauer PO; Kourí V; Peña Serrano L; Roskams J; Almaguer Gotay D; Montes Brown JC; Martínez Rodríguez PA; González-Zaldívar Y; Almaguer Mederos L; Cuello-Almarales D; Aguiar Santiago J
Hum Genet; 2012 Apr; 131(4):625-38. PubMed ID: 22037902
[TBL] [Abstract][Full Text] [Related]
12. [The clinical features and gene mutation analysis in a pedigree of spinocerebellar ataxia type 7].
Yin XZ; Zhang BR; Wu DW; Tian J; Zhang H
Yi Chuan; 2007 Jun; 29(6):688-92. PubMed ID: 17650485
[TBL] [Abstract][Full Text] [Related]
13. CTCF binding is not the epigenetic mark that establishes post-fertilization methylation imprinting in the transgenic H19 ICR.
Matsuzaki H; Okamura E; Fukamizu A; Tanimoto K
Hum Mol Genet; 2010 Apr; 19(7):1190-8. PubMed ID: 20047949
[TBL] [Abstract][Full Text] [Related]
14. Molecular pathogenesis and cellular pathology of spinocerebellar ataxia type 7 neurodegeneration.
Garden GA; La Spada AR
Cerebellum; 2008; 7(2):138-49. PubMed ID: 18418675
[TBL] [Abstract][Full Text] [Related]
15. Very large (CAG)(n) DNA repeat expansions in the sperm of two spinocerebellar ataxia type 7 males.
Monckton DG; Cayuela ML; Gould FK; Brock GJ; Silva R; Ashizawa T
Hum Mol Genet; 1999 Dec; 8(13):2473-8. PubMed ID: 10556295
[TBL] [Abstract][Full Text] [Related]
16. Massive CAG repeat expansion and somatic instability in maternally transmitted infantile spinocerebellar ataxia type 7.
Trang H; Stanley SY; Thorner P; Faghfoury H; Schulze A; Hawkins C; Pearson CE; Yoon G
JAMA Neurol; 2015 Feb; 72(2):219-23. PubMed ID: 25506882
[TBL] [Abstract][Full Text] [Related]
17. Novel CTCF binding at a site in exon1A of BCL6 is associated with active histone marks and a transcriptionally active locus.
Batlle-López A; Cortiguera MG; Rosa-Garrido M; Blanco R; del Cerro E; Torrano V; Wagner SD; Delgado MD
Oncogene; 2015 Jan; 34(2):246-56. PubMed ID: 24362533
[TBL] [Abstract][Full Text] [Related]
18. Tissue- and age-specific DNA replication patterns at the CTG/CAG-expanded human myotonic dystrophy type 1 locus.
Cleary JD; Tomé S; López Castel A; Panigrahi GB; Foiry L; Hagerman KA; Sroka H; Chitayat D; Gourdon G; Pearson CE
Nat Struct Mol Biol; 2010 Sep; 17(9):1079-87. PubMed ID: 20711191
[TBL] [Abstract][Full Text] [Related]
19. Epigenetic regulation of the human retinoblastoma tumor suppressor gene promoter by CTCF.
De La Rosa-Velázquez IA; Rincón-Arano H; Benítez-Bribiesca L; Recillas-Targa F
Cancer Res; 2007 Mar; 67(6):2577-85. PubMed ID: 17363576
[TBL] [Abstract][Full Text] [Related]
20. CTCF haploinsufficiency destabilizes DNA methylation and predisposes to cancer.
Kemp CJ; Moore JM; Moser R; Bernard B; Teater M; Smith LE; Rabaia NA; Gurley KE; Guinney J; Busch SE; Shaknovich R; Lobanenkov VV; Liggitt D; Shmulevich I; Melnick A; Filippova GN
Cell Rep; 2014 May; 7(4):1020-9. PubMed ID: 24794443
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]