192 related articles for article (PubMed ID: 22378288)
1. 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]
2. 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]
3. 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]
4. Immunodeficiency, centromeric region instability, facial anomalies syndrome (ICF).
Ehrlich M; Jackson K; Weemaes C
Orphanet J Rare Dis; 2006 Mar; 1():2. PubMed ID: 16722602
[TBL] [Abstract][Full Text] [Related]
5. 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]
6. 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]
7. 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]
8. 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]
9. ICF, an immunodeficiency syndrome: DNA methyltransferase 3B involvement, chromosome anomalies, and gene dysregulation.
Ehrlich M; Sanchez C; Shao C; Nishiyama R; Kehrl J; Kuick R; Kubota T; Hanash SM
Autoimmunity; 2008 May; 41(4):253-71. PubMed ID: 18432406
[TBL] [Abstract][Full Text] [Related]
10. [Clinical and genetic manifestations of immunodeficiency, centromeric instability, and facial anomalies syndrome: a case report and literature review].
Hu SC; Wang YB; Sun Q; Liu XR; Sun LL; Cui GM
Zhonghua Er Ke Za Zhi; 2019 Jan; 57(1):55-59. PubMed ID: 30630233
[No Abstract] [Full Text] [Related]
11. 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]
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. Expanding the mutation spectrum in ICF syndrome: Evidence for a gender bias in ICF2.
van den Boogaard ML; Thijssen PE; Aytekin C; Licciardi F; Kıykım AA; Spossito L; Dalm VASH; Driessen GJ; Kersseboom R; de Vries F; van Ostaijen-Ten Dam MM; Ikinciogullari A; Dogu F; Oleastro M; Bailardo E; Daxinger L; Nain E; Baris S; van Tol MJD; Weemaes C; van der Maarel SM
Clin Genet; 2017 Oct; 92(4):380-387. PubMed ID: 28128455
[TBL] [Abstract][Full Text] [Related]
14. 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]
15. Subcellular distribution of HP1 proteins is altered in ICF syndrome.
Luciani JJ; Depetris D; Missirian C; Mignon-Ravix C; Metzler-Guillemain C; Megarbane A; Moncla A; Mattei MG
Eur J Hum Genet; 2005 Jan; 13(1):41-51. PubMed ID: 15470359
[TBL] [Abstract][Full Text] [Related]
16. Novel
Aminorroaya A; Rayzan E; Shahkarami S; Seyedpour S; Zoghi S; Aryan Z; Somekh I; Rohlfs M; Klein C; Esmaeilzadeh H; Rezaei N
Endocr Metab Immune Disord Drug Targets; 2023; 23(3):410-415. PubMed ID: 35996251
[TBL] [Abstract][Full Text] [Related]
17. 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]
18. 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]
19. Immunodeficiency, Centromeric Region Instability, and Facial Anomalies Syndrome (ICF) in a Boy with Variable Clinical and Immunological Presentations.
Bemanian MH; Arshi S; Nabavi M; Vafaee-Shahi M; Fallahpour M; Shokri S; Rezaeifar A; Shahzadi H; Atashrazm F
Iran J Allergy Asthma Immunol; 2021 Apr; 20(2):249-254. PubMed ID: 33904683
[TBL] [Abstract][Full Text] [Related]
20. Structural basis of ICF-causing mutations in the methyltransferase domain of DNMT3B.
Lappalainen I; Vihinen M
Protein Eng; 2002 Dec; 15(12):1005-14. PubMed ID: 12601140
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]