Cleidocranial dysplasia and RUNX2-clinical phenotype-genotype correlation-Reference-Cited by-同舟云学术

Cleidocranial dysplasia and RUNX2-clinical phenotype-genotype correlation

Published:2016-06-30 Issue:5 Volume:90 Page:393-402
ISSN:0009-9163
Container-title:Clinical Genetics
language:en
Short-container-title:Clin Genet

Author:

Jaruga A.¹²,Hordyjewska E.¹²,Kandzierski G.³,Tylzanowski P.¹⁴

Affiliation:

1. Department of Biochemistry and Molecular Biology; Medical University; Lublin Poland

2. Postgraduate School of Molecular Medicine; Warsaw Poland

3. Children Orthopaedic and Rehabilitation Department; Medical University of Lublin; Lublin Poland

4. Laboratory for Developmental and Stem Cell Biology, Department of Development and Regeneration, Skeletal Biology and Engineering Research Centre; University of Leuven; Leuven Belgium

Funder

Narodowe Centrum Nauki

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/cge.12812/fullpdf

Reference92 articles.

1. AML1, the target of multiple chromosomal translocations in human leukemia, is essential for normal fetal liver hematopoiesis;Okuda;Cell,1996

2. T. K et al. t(8;21) breakpoints on chromosome 21 in acute myeloid leukemia are clustered within a limited region of a single gene, AML1;Miyoshi;Proc Natl Acad Sci USA,1991

3. Targeted disruption of Cbfa1 results in a complete lack of bone formation owing to maturational arrest of osteoblasts;Komori;Cell,1997

4. Cbfa1, a candidate gene for cleidocranial dysplasia syndrome, is essential for osteoblast differentiation and bone development;Otto;Cell,1997

5. Causal relationship between the loss of RUNX3 expression and gastric cancer;Li;Cell,2002

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