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4 in total

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

Authors: T Kondo; M P Bobek; R Kuick; B Lamb; X Zhu; A Narayan; D Bourc'his; E Viegas-Péquignot; M Ehrlich; S M Hanash
Journal: Hum Mol Genet Date: 2000-03-01 Impact factor: 6.150

2. Chromosome instability and immunodeficiency syndrome caused by mutations in a DNA methyltransferase gene.

Authors: G L Xu; T H Bestor; D Bourc'his; C L Hsieh; N Tommerup; M Bugge; M Hulten; X Qu; J J Russo; E Viegas-Péquignot
Journal: Nature Date: 1999-11-11 Impact factor: 49.962

3. Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2.

Authors: R E Amir; I B Van den Veyver; M Wan; C Q Tran; U Francke; H Y Zoghbi
Journal: Nat Genet Date: 1999-10 Impact factor: 38.330

4. Long-read sequence analysis of the MECP2 gene in Rett syndrome patients: correlation of disease severity with mutation type and location.

Authors: J P Cheadle; H Gill; N Fleming; J Maynard; A Kerr; H Leonard; M Krawczak; D N Cooper; S Lynch; N Thomas; H Hughes; M Hulten; D Ravine; J R Sampson; A Clarke
Journal: Hum Mol Genet Date: 2000-04-12 Impact factor: 6.150

4 in total

1 in total

Review 1. Epigenetics and airways disease.

Authors: Ian M Adcock; Paul Ford; Kazuhiro Ito; P J Barnes
Journal: Respir Res Date: 2006-02-06

1 in total