Viegas-Péquignot E - Search Results

1

Regulation of DNA methylation activity through Dnmt3L promoter methylation by Dnmt3 enzymes in embryonic development.

Hu YG, Hirasawa R, Hu JL, Hata K, Li CL, Jin Y, Chen T, Li E, Rigolet M, Viegas-Péquignot E, Sasaki H, Xu GL. Hu YG, et al. Among authors: viegas pequignot e. Hum Mol Genet. 2008 Sep 1;17(17):2654-64. doi: 10.1093/hmg/ddn165. Epub 2008 Jun 10. Hum Mol Genet. 2008. PMID: 18544626

2

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. Jiang YL, et al. Among authors: viegas pequignot e. Hum Mutat. 2005 Jan;25(1):56-63. doi: 10.1002/humu.20113. Hum Mutat. 2005. PMID: 15580563

3

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. Yehezkel S, et al. Among authors: viegas pequignot e. Hum Mol Genet. 2008 Sep 15;17(18):2776-89. doi: 10.1093/hmg/ddn177. Epub 2008 Jun 16. Hum Mol Genet. 2008. PMID: 18558631

4

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. Xu GL, et al. Nature. 1999 Nov 11;402(6758):187-91. doi: 10.1038/46052. Nature. 1999. PMID: 10647011

5

An embryonic-like methylation pattern of classical satellite DNA is observed in ICF syndrome.

Jeanpierre M, Turleau C, Aurias A, Prieur M, Ledeist F, Fischer A, Viegas-Pequignot E. Jeanpierre M, et al. Hum Mol Genet. 1993 Jun;2(6):731-5. doi: 10.1093/hmg/2.6.731. Hum Mol Genet. 1993. PMID: 8102570

6

Early prenatal diagnosis of ICF syndrome by mutation detection.

Rigolet M, Grégoire A, Lefort G, Blanchet P, Courbes C, Rodière M, Sarda P, Viegas-Péquignot E. Rigolet M, et al. Among authors: viegas pequignot e. Prenat Diagn. 2007 Nov;27(11):1075-8. doi: 10.1002/pd.1826. Prenat Diagn. 2007. PMID: 17705213 No abstract available.

7

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. Kondo T, et al. Hum Mol Genet. 2000 Mar 1;9(4):597-604. doi: 10.1093/hmg/9.4.597. Hum Mol Genet. 2000. PMID: 10699183

8

The epigenetic imprinting defect of patients with Beckwith-Wiedemann syndrome born after assisted reproductive technology is not restricted to the 11p15 region.

Rossignol S, Steunou V, Chalas C, Kerjean A, Rigolet M, Viegas-Pequignot E, Jouannet P, Le Bouc Y, Gicquel C. Rossignol S, et al. Among authors: viegas pequignot e. J Med Genet. 2006 Dec;43(12):902-7. doi: 10.1136/jmg.2006.042135. Epub 2006 Jul 6. J Med Genet. 2006. PMID: 16825435 Free PMC article.

9

alpha-satellite DNA methylation in normal individuals and in ICF patients: heterogeneous methylation of constitutive heterochromatin in adult and fetal tissues.

Miniou P, Jeanpierre M, Bourc'his D, Coutinho Barbosa AC, Blanquet V, Viegas-Péquignot E. Miniou P, et al. Hum Genet. 1997 Jun;99(6):738-45. doi: 10.1007/s004390050441. Hum Genet. 1997. PMID: 9187666

10

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. Miniou P, et al. Hum Mol Genet. 1994 Dec;3(12):2093-102. doi: 10.1093/hmg/3.12.2093. Hum Mol Genet. 1994. PMID: 7881405

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