Publications by authors named "Anli Shu"

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DNA methylation age acceleration is associated with age of onset in Chinese spinocerebellar ataxia type 3 patients.
Jiahao Li, Anli Shu, Yimin Sun, Wanli Yang, Xuelin Tang

Neurobiol Aging· May 2022

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[Analysis of TGFBI gene mutation in a pedigree affected with corneal dystrophy].
Anli Shu, Gen Li, Hai Luo, Juan He, Xiaowen Hu

Zhonghua Yi Xue Yi Chuan Xue Za Zhi· October 2018

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[Analysis of chromosome regions 8q11.1-q13.3, 1q32-q34.3 and 14q31.1-q13.3 in a Chinese family with congenital preauricular fistula].
Jianwen Song, Yi Wu, Fayi Nie, Biyuan Wang, Yue Li, Anli Shu

Zhonghua Yi Xue Yi Chuan Xue Za Zhi· August 2015

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[Split hand/foot malformation: report of a family with 20 cases].
Anli Shu, Chua-nan Yi, Miao-miao Liu, Cui-qin Huang, She Chen, Shu-mei Yang

Zhonghua Yi Xue Yi Chuan Xue Za Zhi· August 2013

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Systematic screening for polymorphisms within the UGT1A6 gene in three Chinese populations and function prediction through structural modeling.
Yi Xing, Lun Yang, Lei Wang, Liyan Shao, Zhiyun Wei, Anli Shu

Pharmacogenomics· May 2009

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[Genetic analysis of a Chinese pedigree with split hand and foot malformation].
Jun Yang, Ling-han Gao, An-li Shu, Wei Qin, Guo-yin Feng

Zhonghua Yi Xue Yi Chuan Xue Za Zhi· December 2007

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Novel deletion mutation of DSRAD in a Chinese family with Dyschromatosis Symmetrica Hereditaria (DSH).
Qinghe Xing, Anli Shu, Lan Yu, Aiping Zhang, Jing DU

Eur J Dermatol· August 2007

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Differences in CYP3A41G genotype distribution and haplotypes of CYP3A4, CYP3A5 and CYP3A7 in 3 Chinese populations.
Jing Du, Lan Yu, Lei Wang, Aiping Zhang, Anli Shu

Clin Chim Acta· August 2007

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Screening for SNPs and haplotypes in the CYP3A7 gene in Chinese populations.
Jing Du, Yongyong Shi, Aiping Zhang, Lei Wang, Jiekun Xuan, Anli Shu

Pharmacogenomics· June 2007

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Systematic screening for polymorphisms in the CYP3A4 gene in the Chinese population.
Jing Du, Qinghe Xing, Lingyun Xu, Mingsheng Xu, Anli Shu

Pharmacogenomics· September 2006

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A novel mutation of PAX3 in a Chinese family with Waardenburg syndrome.
Wei Qin, Anli Shu, Xueqing Qian, Jianjun Gao, Qinghe Xing

Mol Vis· August 2006

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[Mutation analysis of 12S rRNA and tRNA-Ser(UCN) genes in a large Chinese family with maternally inherited nonsyndromic hearing loss by intermarriage].
An-li Shu, Bao-hu Ji, Wei Qin, Guo-yin Feng, Yu-zheng Nie

Zhonghua Yi Xue Yi Chuan Xue Za Zhi· June 2006

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[A family with nonsyndromic hearing impairment caused by intermarry].
An-Li Shu, Yu-Zheng Nie

Yi Chuan· July 2005

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[Mutation detection of COL1A1 gene in a pedigree with osteogenesis imperfecta].
Wei Qin, Jun-Xiang He, Jin Shi, Qing-He Xing, Jian-Juns Gao, An-Li Shu

Yi Chuan Xue Bao· March 2005

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A novel insertion mutation in the FOXL2 gene is detected in a big Chinese family with blepharophimosis-ptosis-epicanthus inversus.
Xueqing Qian, Anli Shu, Wei Qin, Qinghe Xing, Jianjun Gao

Mutat Res· October 2004

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[Genetic analysis of a Chinese pedigree with congenital synpolydactyly].
Wei Qin, An-Li Shu, Qing-He Xing, Mao-Sheng Yang, Guo-Yin Feng

Yi Chuan Xue Bao· October 2003

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