Mutant Runx2 regulates amelogenesis and osteogenesis through a miR-185-5p-Dlx2 axis-Reference-Cited by-同舟云学术

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Mutant Runx2 regulates amelogenesis and osteogenesis through a miR-185-5p-Dlx2 axis

Published:2017-12 Issue:12 Volume:8 Page:
ISSN:2041-4889
Container-title:Cell Death & Disease
language:en
Short-container-title:Cell Death Dis

Author:

Chang Huaiguang,Wang Yue,Liu Haochen,Nan Xu,Wong Singwai,Peng Saihui,Gu Yajuan,Zhao Hongshan,Feng Hailan

Publisher

Springer Science and Business Media LLC

Subject

Cancer Research,Cell Biology,Cellular and Molecular Neuroscience,Immunology

Link

http://www.nature.com/articles/s41419-017-0078-4.pdf

Reference40 articles.

1. Mundlos, S. Cleidocranial dysplasia: clinical and molecular genetics. J. Med. Genet. 36, 177–182 (1999).

2. Chen, S. et al. Altered gene expression in human cleidocranial dysplasia dental pulp cells. Arch. Oral Biol. 50, 227–236 (2005).

3. Fukuta, Y. et al. Histological and analytical studies of a tooth in a patient with cleidocranial dysostosis. J. Oral Sci. 43, 85–89 (2001).

4. Bae, S. C. et al. PEBP2 alpha B/mouse AML1 consists of multiple isoforms that possess differential transactivation potentials. Mol. Cell Biol. 14, 3242–3252 (1994).

5. Otto, F., Kanegane, H. & Mundlos, S. Mutations in theRUNX2 gene in patients with cleidocranial dysplasia. Hum. Mutat. 19, 209–216 (2002).

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