244 related articles for article (PubMed ID: 31671722)
1. ATRX Contributes to MeCP2-Mediated Pericentric Heterochromatin Organization during Neural Differentiation.
Marano D; Fioriniello S; Fiorillo F; Gibbons RJ; D'Esposito M; Della Ragione F
Int J Mol Sci; 2019 Oct; 20(21):. PubMed ID: 31671722
[TBL] [Abstract][Full Text] [Related]
2. MeCP2 and Major Satellite Forward RNA Cooperate for Pericentric Heterochromatin Organization.
Fioriniello S; Csukonyi E; Marano D; Brancaccio A; Madonna M; Zarrillo C; Romano A; Marracino F; Matarazzo MR; D'Esposito M; Della Ragione F
Stem Cell Reports; 2020 Dec; 15(6):1317-1332. PubMed ID: 33296675
[TBL] [Abstract][Full Text] [Related]
3. Long non-coding RNA ChRO1 facilitates ATRX/DAXX-dependent H3.3 deposition for transcription-associated heterochromatin reorganization.
Park J; Lee H; Han N; Kwak S; Lee HT; Kim JH; Kang K; Youn BH; Yang JH; Jeong HJ; Kang JS; Kim SY; Han JW; Youn HD; Cho EJ
Nucleic Acids Res; 2018 Dec; 46(22):11759-11775. PubMed ID: 30335163
[TBL] [Abstract][Full Text] [Related]
4. ATRX interacts with H3.3 in maintaining telomere structural integrity in pluripotent embryonic stem cells.
Wong LH; McGhie JD; Sim M; Anderson MA; Ahn S; Hannan RD; George AJ; Morgan KA; Mann JR; Choo KH
Genome Res; 2010 Mar; 20(3):351-60. PubMed ID: 20110566
[TBL] [Abstract][Full Text] [Related]
5. Interaction between chromatin proteins MECP2 and ATRX is disrupted by mutations that cause inherited mental retardation.
Nan X; Hou J; Maclean A; Nasir J; Lafuente MJ; Shu X; Kriaucionis S; Bird A
Proc Natl Acad Sci U S A; 2007 Feb; 104(8):2709-14. PubMed ID: 17296936
[TBL] [Abstract][Full Text] [Related]
6. Abnormalities of cell packing density and dendritic complexity in the MeCP2 A140V mouse model of Rett syndrome/X-linked mental retardation.
Jentarra GM; Olfers SL; Rice SG; Srivastava N; Homanics GE; Blue M; Naidu S; Narayanan V
BMC Neurosci; 2010 Feb; 11():19. PubMed ID: 20163734
[TBL] [Abstract][Full Text] [Related]
7. MeCP2 links heterochromatin condensates and neurodevelopmental disease.
Li CH; Coffey EL; Dall'Agnese A; Hannett NM; Tang X; Henninger JE; Platt JM; Oksuz O; Zamudio AV; Afeyan LK; Schuijers J; Liu XS; Markoulaki S; Lungjangwa T; LeRoy G; Svoboda DS; Wogram E; Lee TI; Jaenisch R; Young RA
Nature; 2020 Oct; 586(7829):440-444. PubMed ID: 32698189
[TBL] [Abstract][Full Text] [Related]
8. MeCP2 dependent heterochromatin reorganization during neural differentiation of a novel Mecp2-deficient embryonic stem cell reporter line.
Bertulat B; De Bonis ML; Della Ragione F; Lehmkuhl A; Milden M; Storm C; Jost KL; Scala S; Hendrich B; D'Esposito M; Cardoso MC
PLoS One; 2012; 7(10):e47848. PubMed ID: 23112857
[TBL] [Abstract][Full Text] [Related]
9. Identification of epigenetic signature associated with alpha thalassemia/mental retardation X-linked syndrome.
Schenkel LC; Kernohan KD; McBride A; Reina D; Hodge A; Ainsworth PJ; Rodenhiser DI; Pare G; Bérubé NG; Skinner C; Boycott KM; Schwartz C; Sadikovic B
Epigenetics Chromatin; 2017; 10():10. PubMed ID: 28293299
[TBL] [Abstract][Full Text] [Related]
10. MeCP2 is required for global heterochromatic and nucleolar changes during activity-dependent neuronal maturation.
Singleton MK; Gonzales ML; Leung KN; Yasui DH; Schroeder DI; Dunaway K; LaSalle JM
Neurobiol Dis; 2011 Jul; 43(1):190-200. PubMed ID: 21420494
[TBL] [Abstract][Full Text] [Related]
11. Methyl CpG-binding proteins induce large-scale chromatin reorganization during terminal differentiation.
Brero A; Easwaran HP; Nowak D; Grunewald I; Cremer T; Leonhardt H; Cardoso MC
J Cell Biol; 2005 Jun; 169(5):733-43. PubMed ID: 15939760
[TBL] [Abstract][Full Text] [Related]
12. Retinal interneuron survival requires non-cell-autonomous Atrx activity.
Lagali PS; Medina CF; Zhao BY; Yan K; Baker AN; Coupland SG; Tsilfidis C; Wallace VA; Picketts DJ
Hum Mol Genet; 2016 Nov; 25(21):4787-4803. PubMed ID: 28173139
[TBL] [Abstract][Full Text] [Related]
13. Spatio-temporal dynamics and localization of MeCP2 and pathological mutants in living cells.
Marchi M; Guarda A; Bergo A; Landsberger N; Kilstrup-Nielsen C; Ratto GM; Costa M
Epigenetics; 2007 Sep; 2(3):187-97. PubMed ID: 17965612
[TBL] [Abstract][Full Text] [Related]
14. The chromatin remodeller ATRX facilitates diverse nuclear processes, in a stochastic manner, in both heterochromatin and euchromatin.
Truch J; Downes DJ; Scott C; Gür ER; Telenius JM; Repapi E; Schwessinger R; Gosden M; Brown JM; Taylor S; Cheong PL; Hughes JR; Higgs DR; Gibbons RJ
Nat Commun; 2022 Jun; 13(1):3485. PubMed ID: 35710802
[TBL] [Abstract][Full Text] [Related]
15. MeCP2 Rett mutations affect large scale chromatin organization.
Agarwal N; Becker A; Jost KL; Haase S; Thakur BK; Brero A; Hardt T; Kudo S; Leonhardt H; Cardoso MC
Hum Mol Genet; 2011 Nov; 20(21):4187-95. PubMed ID: 21831886
[TBL] [Abstract][Full Text] [Related]
16. Mutations of CDKL5 cause a severe neurodevelopmental disorder with infantile spasms and mental retardation.
Weaving LS; Christodoulou J; Williamson SL; Friend KL; McKenzie OL; Archer H; Evans J; Clarke A; Pelka GJ; Tam PP; Watson C; Lahooti H; Ellaway CJ; Bennetts B; Leonard H; Gécz J
Am J Hum Genet; 2004 Dec; 75(6):1079-93. PubMed ID: 15492925
[TBL] [Abstract][Full Text] [Related]
17. Pericentric heterochromatin generated by HP1 protein interaction-defective histone methyltransferase Suv39h1.
Muramatsu D; Singh PB; Kimura H; Tachibana M; Shinkai Y
J Biol Chem; 2013 Aug; 288(35):25285-25296. PubMed ID: 23836914
[TBL] [Abstract][Full Text] [Related]
18. Rett syndrome-causing mutations compromise MeCP2-mediated liquid-liquid phase separation of chromatin.
Wang L; Hu M; Zuo MQ; Zhao J; Wu D; Huang L; Wen Y; Li Y; Chen P; Bao X; Dong MQ; Li G; Li P
Cell Res; 2020 May; 30(5):393-407. PubMed ID: 32111972
[TBL] [Abstract][Full Text] [Related]
19. ATRX and DAXX: Mechanisms and Mutations.
Dyer MA; Qadeer ZA; Valle-Garcia D; Bernstein E
Cold Spring Harb Perspect Med; 2017 Mar; 7(3):. PubMed ID: 28062559
[TBL] [Abstract][Full Text] [Related]
20. A rare MeCP2_e1 mutation first described in a male patient with severe neonatal encephalopathy.
Soffer OD; Sidlow R
Am J Med Genet A; 2016 Jul; 170(7):1881-3. PubMed ID: 27090848
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
