Hypomethylation of subtelomeric regions in ICF syndrome is associated with abnormally short telomeres and enhanced transcription from telomeric regions

Author： Yehezkel Shiran   Segev Yardena   Viegas-Pquignot Evani   Skorecki Karl   Selig Sara  

Publisher： Oxford University Press

ISSN： 1460-2083

Source： Human Molecular Genetics, Vol.17, Iss.18, 2008-09, pp. : 2776-2789

Disclaimer: Any content in publications that violate the sovereignty, the constitution or regulations of the PRC is not accepted or approved by CNPIEC.

Previous Menu Next

Abstract

Related content

A systematic search for DNA methyltransferase polymorphisms reveals a rare DNMT3L variant associated with subtelomeric hypomethylation

By El-Maarri Osman   Kareta Michael S.   Mikeska Thomas   Becker Tim   Diaz-Lacava Amalia   Junen Judith   Nsgen Nicole   Behne Frank   Wienker Thomas   Waha Andreas   Oldenburg Johannes   Chdin Frdric  

Human Molecular Genetics, Vol. 18, Iss. 10, 2009-05 ,pp. : 1755-1768

Oxford University Press

Access to resources Recommend Favorite

Whole-genome methylation scan in ICF syndrome: hypomethylation of non-satellite DNA repeats D4Z4 and NBL2

By Kondo Tadashi   Bobek Miroslav P.   Kuick Rork   Lamb Barbara   Zhu Xiaoxiang  

Human Molecular Genetics, Vol. 9, Iss. 4, 2000-03 ,pp. : 597-604

Oxford University Press

Access to resources Recommend Favorite

Sequence Comparison of Human and Yeast Telomeres Identifies Structurally Distinct Subtelomeric Domains

By Flint J.   Bates G. P.   Clark K.   Dorman A.   Willingham D.   Roe B. A.   Micklem G.   Higgs D. R.   Louis E. J.  

Human Molecular Genetics, Vol. 6, Iss. 8, 1997-01 ,pp. : 1305-1314

Oxford University Press

Access to resources Recommend Favorite

Comparative physical maps of the human and mouse Meckel syndrome critical regions

By Hentges Kathryn  

Mammalian Genome, Vol. 15, Iss. 4, 2004-04 ,pp. : 252-264

Springer Publishing Company

Access to resources Recommend Favorite

Inter- and intrachromosomal sub-telomeric rearrangements on 4q35: implications for facioscapulohumeral muscular dystrophy (FSHD) aetiology and diagnosis

By Padberg G.W.  

Human Molecular Genetics, Vol. 7, Iss. 8, 1998-08 ,pp. : 1207-1214

Oxford University Press

Access to resources Recommend Favorite