Characterization of a t(5;8)(q31;q21) translocation in a patient with mental retardation and congenital heart disease: implications for involvement of RUNX1T1 in human brain and heart development-Reference-Cited by-同舟云学术

Characterization of a t(5;8)(q31;q21) translocation in a patient with mental retardation and congenital heart disease: implications for involvement of RUNX1T1 in human brain and heart development

Published:2009-01-28 Issue:8 Volume:17 Page:1010-1018
ISSN:1018-4813
Container-title:European Journal of Human Genetics
language:en
Short-container-title:Eur J Hum Genet

Author:

Zhang Litu,Tümer Zeynep,Møllgård Kjeld,Barbi Gotthold,Rossier Eva,Bendsen Eske,Møller Rikke Steensbjerre,Ullmann Reinhard,He Jian,Papadopoulos Nickolas,Tommerup Niels,Larsen Lars Allan

Publisher

Springer Science and Business Media LLC

Subject

Genetics(clinical),Genetics

Link

http://www.nature.com/articles/ejhg2008269.pdf

Reference27 articles.

1. Erickson P, Gao J, Chang KS et al: Identification of breakpoints in t(8;21) acute myelogenous leukemia and isolation of a fusion transcript, AML1/ETO, with similarity to Drosophila segmentation gene, runt. Blood 1992; 80: 1825–1831.

2. Miyoshi H, Shimizu K, Kozu T, Maseki N, Kaneko Y, Ohki M : t(8;21) breakpoints on chromosome 21 in acute myeloid leukemia are clustered within a limited region of a single gene, AML1. Proc Natl Acad Sci USA 1991; 88: 10431–10434.

3. Miyoshi H, Kozu T, Shimizu K et al: The t(8;21) translocation in acute myeloid leukemia results in production of an AML1-MTG8 fusion transcript. EMBO J 1993; 12: 2715–2721.

4. Peterson LF, Boyapati A, Ahn EY et al: Acute myeloid leukemia with the 8q22;21q22 translocation: secondary mutational events and alternative t(8;21) transcripts. Blood 2007; 110: 799–805.

5. Yamagata T, Maki K, Mitani K : Runx1/AML1 in normal and abnormal hematopoiesis. Int J Hematol 2005; 82: 1–8.

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