390 related articles for article (PubMed ID: 11702227)
1. 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]
2. Hypomethylation of subtelomeric regions in ICF syndrome is associated with abnormally short telomeres and enhanced transcription from telomeric regions.
Yehezkel S; Segev Y; Viegas-Péquignot E; Skorecki K; Selig S
Hum Mol Genet; 2008 Sep; 17(18):2776-89. PubMed ID: 18558631
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. DNMT3B mutations and DNA methylation defect define two types of ICF syndrome.
Jiang YL; Rigolet M; Bourc'his D; Nigon F; Bokesoy I; Fryns JP; Hultén M; Jonveaux P; Maraschio P; Mégarbané A; Moncla A; Viegas-Péquignot E
Hum Mutat; 2005 Jan; 25(1):56-63. PubMed ID: 15580563
[TBL] [Abstract][Full Text] [Related]
5. 3D position of pericentromeric heterochromatin within the nucleus of a patient with ICF syndrome.
Dupont C; Guimiot F; Perrin L; Marey I; Smiljkovski D; Le Tessier D; Lebugle C; Baumann C; Bourdoncle P; Tabet AC; Aboura A; Benzacken B; Dupont JM
Clin Genet; 2012 Aug; 82(2):187-92. PubMed ID: 21554265
[TBL] [Abstract][Full Text] [Related]
6. Chromosome instability and immunodeficiency syndrome caused by mutations in a DNA methyltransferase gene.
Xu GL; Bestor TH; Bourc'his D; Hsieh CL; Tommerup N; Bugge M; Hulten M; Qu X; Russo JJ; Viegas-Péquignot E
Nature; 1999 Nov; 402(6758):187-91. PubMed ID: 10647011
[TBL] [Abstract][Full Text] [Related]
7. Overexpression of a splice variant of DNA methyltransferase 3b, DNMT3b4, associated with DNA hypomethylation on pericentromeric satellite regions during human hepatocarcinogenesis.
Saito Y; Kanai Y; Sakamoto M; Saito H; Ishii H; Hirohashi S
Proc Natl Acad Sci U S A; 2002 Jul; 99(15):10060-5. PubMed ID: 12110732
[TBL] [Abstract][Full Text] [Related]
8. Three novel DNMT3B mutations in Japanese patients with ICF syndrome.
Shirohzu H; Kubota T; Kumazawa A; Sado T; Chijiwa T; Inagaki K; Suetake I; Tajima S; Wakui K; Miki Y; Hayashi M; Fukushima Y; Sasaki H
Am J Med Genet; 2002 Sep; 112(1):31-7. PubMed ID: 12239717
[TBL] [Abstract][Full Text] [Related]
9. 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]
10. Expression of mRNA for DNA methyltransferases and methyl-CpG-binding proteins and DNA methylation status on CpG islands and pericentromeric satellite regions during human hepatocarcinogenesis.
Saito Y; Kanai Y; Sakamoto M; Saito H; Ishii H; Hirohashi S
Hepatology; 2001 Mar; 33(3):561-8. PubMed ID: 11230735
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. X inactivation-specific methylation of LINE-1 elements by DNMT3B: implications for the Lyon repeat hypothesis.
Hansen RS
Hum Mol Genet; 2003 Oct; 12(19):2559-67. PubMed ID: 12925568
[TBL] [Abstract][Full Text] [Related]
13. DNA CpG hypomethylation induces heterochromatin reorganization involving the histone variant macroH2A.
Ma Y; Jacobs SB; Jackson-Grusby L; Mastrangelo MA; Torres-Betancourt JA; Jaenisch R; Rasmussen TP
J Cell Sci; 2005 Apr; 118(Pt 8):1607-16. PubMed ID: 15784683
[TBL] [Abstract][Full Text] [Related]
14. CpG methylation modifies the genetic stability of cloned repeat sequences.
Nichol K; Pearson CE
Genome Res; 2002 Aug; 12(8):1246-56. PubMed ID: 12176932
[TBL] [Abstract][Full Text] [Related]
15. Loss of pericentromeric DNA methylation pattern in human glioblastoma is associated with altered DNA methyltransferases expression and involves the stem cell compartment.
Fanelli M; Caprodossi S; Ricci-Vitiani L; Porcellini A; Tomassoni-Ardori F; Amatori S; Andreoni F; Magnani M; De Maria R; Santoni A; Minucci S; Pelicci PG
Oncogene; 2008 Jan; 27(3):358-65. PubMed ID: 17653095
[TBL] [Abstract][Full Text] [Related]
16. DNA hypomethylation, cancer, the immunodeficiency, centromeric region instability, facial anomalies syndrome and chromosomal rearrangements.
Ehrlich M
J Nutr; 2002 Aug; 132(8 Suppl):2424S-2429S. PubMed ID: 12163705
[TBL] [Abstract][Full Text] [Related]
17. DNA hypomethylation and unusual chromosome instability in cell lines from ICF syndrome patients.
Tuck-Muller CM; Narayan A; Tsien F; Smeets DF; Sawyer J; Fiala ES; Sohn OS; Ehrlich M
Cytogenet Cell Genet; 2000; 89(1-2):121-8. PubMed ID: 10894953
[TBL] [Abstract][Full Text] [Related]
18. Whole-genome methylation scan in ICF syndrome: hypomethylation of non-satellite DNA repeats D4Z4 and NBL2.
Kondo T; Bobek MP; Kuick R; Lamb B; Zhu X; Narayan A; Bourc'his D; Viegas-Péquignot E; Ehrlich M; Hanash SM
Hum Mol Genet; 2000 Mar; 9(4):597-604. PubMed ID: 10699183
[TBL] [Abstract][Full Text] [Related]
19. Genetic variation in ICF syndrome: evidence for genetic heterogeneity.
Wijmenga C; Hansen RS; Gimelli G; Björck EJ; Davies EG; Valentine D; Belohradsky BH; van Dongen JJ; Smeets DF; van den Heuvel LP; Luyten JA; Strengman E; Weemaes C; Pearson PL
Hum Mutat; 2000 Dec; 16(6):509-17. PubMed ID: 11102980
[TBL] [Abstract][Full Text] [Related]
20. Abnormal methylation pattern in constitutive and facultative (X inactive chromosome) heterochromatin of ICF patients.
Miniou P; Jeanpierre M; Blanquet V; Sibella V; Bonneau D; Herbelin C; Fischer A; Niveleau A; Viegas-Péquignot E
Hum Mol Genet; 1994 Dec; 3(12):2093-102. PubMed ID: 7881405
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
