234 related articles for article (PubMed ID: 22595875)
1. Whole-genome bisulfite DNA sequencing of a DNMT3B mutant patient.
Heyn H; Vidal E; Sayols S; Sanchez-Mut JV; Moran S; Medina I; Sandoval J; Simó-Riudalbas L; Szczesna K; Huertas D; Gatto S; Matarazzo MR; Dopazo J; Esteller M
Epigenetics; 2012 Jun; 7(6):542-50. PubMed ID: 22595875
[TBL] [Abstract][Full Text] [Related]
2. Satellite 2 methylation patterns in normal and ICF syndrome cells and association of hypomethylation with advanced replication.
Hassan KM; Norwood T; Gimelli G; Gartler SM; Hansen RS
Hum Genet; 2001 Oct; 109(4):452-62. PubMed ID: 11702227
[TBL] [Abstract][Full Text] [Related]
3. DNA methyltransferase 3B (DNMT3B) mutations in ICF syndrome lead to altered epigenetic modifications and aberrant expression of genes regulating development, neurogenesis and immune function.
Jin B; Tao Q; Peng J; Soo HM; Wu W; Ying J; Fields CR; Delmas AL; Liu X; Qiu J; Robertson KD
Hum Mol Genet; 2008 Mar; 17(5):690-709. PubMed ID: 18029387
[TBL] [Abstract][Full Text] [Related]
4. Defective de novo methylation of viral and cellular DNA sequences in ICF syndrome cells.
Tao Q; Huang H; Geiman TM; Lim CY; Fu L; Qiu GH; Robertson KD
Hum Mol Genet; 2002 Sep; 11(18):2091-102. PubMed ID: 12189161
[TBL] [Abstract][Full Text] [Related]
5. Subtelomeric methylation distinguishes between subtypes of Immunodeficiency, Centromeric instability and Facial anomalies syndrome.
Toubiana S; Velasco G; Chityat A; Kaindl AM; Hershtig N; Tzur-Gilat A; Francastel C; Selig S
Hum Mol Genet; 2018 Oct; 27(20):3568-3581. PubMed ID: 30010917
[TBL] [Abstract][Full Text] [Related]
6. DNA methyltransferase 3B mutations linked to the ICF syndrome cause dysregulation of lymphogenesis genes.
Ehrlich M; Buchanan KL; Tsien F; Jiang G; Sun B; Uicker W; Weemaes CM; Smeets D; Sperling K; Belohradsky BH; Tommerup N; Misek DE; Rouillard JM; Kuick R; Hanash SM
Hum Mol Genet; 2001 Dec; 10(25):2917-31. PubMed ID: 11741835
[TBL] [Abstract][Full Text] [Related]
7. Heterochromatic genes undergo epigenetic changes and escape silencing in immunodeficiency, centromeric instability, facial anomalies (ICF) syndrome.
Brun ME; Lana E; Rivals I; Lefranc G; Sarda P; Claustres M; Mégarbané A; De Sario A
PLoS One; 2011 Apr; 6(4):e19464. PubMed ID: 21559330
[TBL] [Abstract][Full Text] [Related]
8. Genome-Wide DNA Methylation Analysis Identifies Novel Hypomethylated Non-Pericentromeric Genes with Potential Clinical Implications in ICF Syndrome.
Simo-Riudalbas L; Diaz-Lagares A; Gatto S; Gagliardi M; Crujeiras AB; Matarazzo MR; Esteller M; Sandoval J
PLoS One; 2015; 10(7):e0132517. PubMed ID: 26161907
[TBL] [Abstract][Full Text] [Related]
9. A Novel Mutation in a Critical Region for the Methyl Donor Binding in DNMT3B Causes Immunodeficiency, Centromeric Instability, and Facial Anomalies Syndrome (ICF).
Rechavi E; Lev A; Eyal E; Barel O; Kol N; Barhom SF; Pode-Shakked B; Anikster Y; Somech R; Simon AJ
J Clin Immunol; 2016 Nov; 36(8):801-809. PubMed ID: 27734333
[TBL] [Abstract][Full Text] [Related]
10. DNA methylation in disease: Immunodeficiency, Centromeric instability, Facial anomalies syndrome.
Vukic M; Daxinger L
Essays Biochem; 2019 Dec; 63(6):773-783. PubMed ID: 31724723
[TBL] [Abstract][Full Text] [Related]
11. The DNMT3B DNA methyltransferase gene is mutated in the ICF immunodeficiency syndrome.
Hansen RS; Wijmenga C; Luo P; Stanek AM; Canfield TK; Weemaes CM; Gartler SM
Proc Natl Acad Sci U S A; 1999 Dec; 96(25):14412-7. PubMed ID: 10588719
[TBL] [Abstract][Full Text] [Related]
12. The ICF syndrome, a DNA methyltransferase 3B deficiency and immunodeficiency disease.
Ehrlich M
Clin Immunol; 2003 Oct; 109(1):17-28. PubMed ID: 14585272
[TBL] [Abstract][Full Text] [Related]
13. Persistent epigenetic memory impedes rescue of the telomeric phenotype in human ICF iPSCs following DNMT3B correction.
Toubiana S; Gagliardi M; Papa M; Manco R; Tzukerman M; Matarazzo MR; Selig S
Elife; 2019 Nov; 8():. PubMed ID: 31738163
[TBL] [Abstract][Full Text] [Related]
14. DNMT3b protects centromere integrity by restricting R-loop-mediated DNA damage.
Shih HT; Chen WY; Wang HY; Chao T; Huang HD; Chou CH; Chang ZF
Cell Death Dis; 2022 Jun; 13(6):546. PubMed ID: 35688824
[TBL] [Abstract][Full Text] [Related]
15. Non-random length distribution of individual telomeres in immunodeficiency, centromeric instability and facial anomalies syndrome, type I.
Sagie S; Edni O; Weinberg J; Toubiana S; Kozlovski T; Frostig T; Katzin N; Bar-Am I; Selig S
Hum Mol Genet; 2017 Nov; 26(21):4244-4256. PubMed ID: 28973513
[TBL] [Abstract][Full Text] [Related]
16. ICF-specific DNMT3B dysfunction interferes with intragenic regulation of mRNA transcription and alternative splicing.
Gatto S; Gagliardi M; Franzese M; Leppert S; Papa M; Cammisa M; Grillo G; Velasco G; Francastel C; Toubiana S; D'Esposito M; Angelini C; Matarazzo MR
Nucleic Acids Res; 2017 Jun; 45(10):5739-5756. PubMed ID: 28334849
[TBL] [Abstract][Full Text] [Related]
17. Structure of DNMT3B homo-oligomer reveals vulnerability to impairment by ICF mutations.
Gao L; Guo Y; Biswal M; Lu J; Yin J; Fang J; Chen X; Shao Z; Huang M; Wang Y; Wang GG; Song J
Nat Commun; 2022 Jul; 13(1):4249. PubMed ID: 35869095
[TBL] [Abstract][Full Text] [Related]
18. DNA replication is altered in Immunodeficiency Centromeric instability Facial anomalies (ICF) cells carrying DNMT3B mutations.
Lana E; Mégarbané A; Tourrière H; Sarda P; Lefranc G; Claustres M; De Sario A
Eur J Hum Genet; 2012 Oct; 20(10):1044-50. PubMed ID: 22378288
[TBL] [Abstract][Full Text] [Related]
19. Epigenetic alteration of microRNAs in DNMT3B-mutated patients of ICF syndrome.
Gatto S; Della Ragione F; Cimmino A; Strazzullo M; Fabbri M; Mutarelli M; Ferraro L; Weisz A; D'Esposito M; Matarazzo MR
Epigenetics; 2010 Jul; 5(5):427-43. PubMed ID: 20448464
[TBL] [Abstract][Full Text] [Related]
20. Novel compound heterozygous mutations in UHRF1 are associated with atypical immunodeficiency, centromeric instability and facial anomalies syndrome with distinctive genome-wide DNA hypomethylation.
Unoki M; Velasco G; Kori S; Arita K; Daigaku Y; Yeung WKA; Fujimoto A; Ohashi H; Kubota T; Miyake K; Sasaki H
Hum Mol Genet; 2023 Apr; 32(9):1439-1456. PubMed ID: 36458887
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
