Genetic polymorphisms of PAX1 are functionally associated with different PUMC types of adolescent idiopathic scoliosis in a northern Chinese Han population

Author:

Liu Gang,Liu Sen,Li Xiaoxin,Chen Jia,Chen Weisheng,Zuo Yuzhi,Liu Jiaqi,Niu Yuchen,Lin Mao,Zhao Sen,Long Bo,Zhao Yanxue,Ye Yongyu,Zhang Jianguo,Shen Jianxiong,Qiu Guixing,Wu Zhihong,Wu Nan

Funder

National Natural Science Foundation of China

Beijing Natural Science Foundation

Beijing Nova Program

Central Level Public Interest Program for Scientific Research Institute

PUMC

CAMS

Peking Union Medical College Hospital

2016 PUMCH Science Fund for Junior Faculty

2016 Milstein Medical Asian American Partnership Foundation Fellowship Award in Translational Medicine

National Key Research and Development Program of China

Publisher

Elsevier BV

Subject

Genetics,General Medicine

Reference33 articles.

1. Aberrant Pax1 and Pax9 expression in Jarcho-Levin syndrome: report of two Caucasian siblings and literature review;Bannykh;Am. J. Med. Genet. A,2003

2. SNP rs11190870 near LBX1 is associated with adolescent idiopathic scoliosis in southern Chinese;Fan;J. Hum. Genet.,2012

3. Association of PAX1 gene polymorphisms with susceptibility to congenital scoliosis in Chinese Han population;Fei;Zhonghua Yi Xue Za Zhi,2008

4. Notochord-dependent expression of MFH1 and PAX1 cooperates to maintain the proliferation of sclerotome cells during the vertebral column development;Furumoto;Dev. Biol.,1999

5. Association between common variants near LBX1 and adolescent idiopathic scoliosis replicated in the Chinese Han population;Gao;PLoS One,2013

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