Identification of acquired somatic mutations in the gene encoding chromatin-remodeling factor ATRX in the α-thalassemia myelodysplasia syndrome (ATMDS)-Reference-Cited by-同舟云学术

Identification of acquired somatic mutations in the gene encoding chromatin-remodeling factor ATRX in the α-thalassemia myelodysplasia syndrome (ATMDS)

Published:2003-07-13 Issue:4 Volume:34 Page:446-449
ISSN:1061-4036
Container-title:Nature Genetics
language:en
Short-container-title:Nat Genet

Author:

Gibbons Richard J,Pellagatti Andrea,Garrick David,Wood William G,Malik Nicola,Ayyub Helena,Langford Cordelia,Boultwood Jacqueline,Wainscoat James S,Higgs Douglas R

Publisher

Springer Science and Business Media LLC

Subject

Genetics

Link

http://www.nature.com/articles/ng1213.pdf

Reference16 articles.

1. Higgs, D.R. et al. A review of the molecular genetics of the human α-globin gene cluster. Blood 73, 1081–1104 (1989).

2. Gibbons, R.J. & Higgs, D.R. The molecular-clinical spectrum of the ATR-X syndrome. Am. J. Med. Genet. 97, 204–212 (2000).

3. Gibbons, R.J., Picketts, D.J., Villard, L. & Higgs, D.R. Mutations in a putative global transcriptional regulator cause X-linked mental retardation with α-thalassemia (ATR-X syndrome). Cell 80, 837–845 (1995).

4. McDowell, T.L. et al. Localization of a putative transcriptional regulator (ATRX) at pericentromeric heterochromatin and the short arms of acrocentric chromosomes. Proc. Natl. Acad. Sci. USA 96, 13983–13988 (1999).

5. Berube, N.G., Smeenk, C.A. & Picketts, D.J. Cell cycle-dependent phosphorylation of the ATRX protein correlates with changes in nuclear matrix and chromatin association. Hum. Mol. Genet. 9, 539–547 (2000).

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