592 related articles for article (PubMed ID: 10647011)
1. 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]
2. 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]
3. 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]
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. 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]
6. 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]
7. 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]
8. 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]
9. 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]
10. A novel deletion in ZBTB24 in a Lebanese family with immunodeficiency, centromeric instability, and facial anomalies syndrome type 2.
Chouery E; Abou-Ghoch J; Corbani S; El Ali N; Korban R; Salem N; Castro C; Klayme S; Azoury-Abou Rjeily M; Khoury-Matar R; Debo G; Germanos-Haddad M; Delague V; Lefranc G; Mégarbané A
Clin Genet; 2012 Nov; 82(5):489-93. PubMed ID: 21906047
[TBL] [Abstract][Full Text] [Related]
11. Chromosome instability in ICF syndrome: formation of micronuclei from multibranched chromosomes 1 demonstrated by fluorescence in situ hybridization.
Sawyer JR; Swanson CM; Wheeler G; Cunniff C
Am J Med Genet; 1995 Mar; 56(2):203-9. PubMed ID: 7625446
[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. [Abnormal condensation of the heterochromatin of chromosomes 1, 9 and 16].
Sakiyama Y
Ryoikibetsu Shokogun Shirizu; 2000; (32):289-91. PubMed ID: 11212720
[No Abstract] [Full Text] [Related]
14. Clinical spectrum of immunodeficiency, centromeric instability and facial dysmorphism (ICF syndrome).
Hagleitner MM; Lankester A; Maraschio P; Hultén M; Fryns JP; Schuetz C; Gimelli G; Davies EG; Gennery A; Belohradsky BH; de Groot R; Gerritsen EJ; Mattina T; Howard PJ; Fasth A; Reisli I; Furthner D; Slatter MA; Cant AJ; Cazzola G; van Dijken PJ; van Deuren M; de Greef JC; van der Maarel SM; Weemaes CM
J Med Genet; 2008 Feb; 45(2):93-9. PubMed ID: 17893117
[TBL] [Abstract][Full Text] [Related]
15. 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]
16. 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]
17. 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]
18. Multibranched chromosomes in the ICF syndrome: immunodeficiency, centromeric instability, and facial anomalies.
Turleau C; Cabanis MO; Girault D; Ledeist F; Mettey R; Puissant H; Prieur M; de Grouchy J
Am J Med Genet; 1989 Mar; 32(3):420-4. PubMed ID: 2729362
[TBL] [Abstract][Full Text] [Related]
19. Mutations in DNA methyltransferase DNMT3B in ICF syndrome affect its regulation by DNMT3L.
Xie ZH; Huang YN; Chen ZX; Riggs AD; Ding JP; Gowher H; Jeltsch A; Sasaki H; Hata K; Xu GL
Hum Mol Genet; 2006 May; 15(9):1375-85. PubMed ID: 16543361
[TBL] [Abstract][Full Text] [Related]
20. 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]
[Next] [New Search]