Liao Shunyao相关文献与解析，生知库 | 链接生命科学的每一步

日期影响因子

Whole-exome sequencing of de novo genetic variants in a Chinese family with a sporadic case of congenital nonsyndromic hearing loss.

对中国一个散发性先天性非综合征性听力损失家族进行全外显子组测序，以检测新生基因变异

期刊:F1000Research

doi:10.12688/f1000research.27739.2

Hu Sijing, Zhang Hao, Liu Yunqiang, Liu Mohan, Li Jingjing, Liao Shunyao

发表日期：2021

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Novel compound heterozygous mutations of ALDH1A3 contribute to anophthalmia in a non-consanguineous Chinese family

ALDH1A3基因的新型复合杂合突变导致一个非近亲结婚的中国家族出现无眼症。

期刊:Genetics and Molecular Biology

影响因子:1.3

doi:10.1590/1678-4685-GMB-2016-0120

Liu, Yunqiang; Lu, Yongjie; Liu, Shasha; Liao, Shunyao

发表日期：2017

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Association of variants in CDKN2A/2B and CDKAL1 genes with gestational insulin sensitivity and disposition in pregnant Han Chinese women

CDKN2A/2B 和 CDKAL1 基因变异与汉族孕妇妊娠期胰岛素敏感性和代谢的相关性

doi:10.1111/jdi.12315

Mei, Jie; Liao, Shunyao; Liu, Yunqiang; Tan, Yuande; Wang, Hailian; Liang, Yaming; Dong, Xianjue; Song, Wenzhong; Gan, Lu; Deng, Shaoping

免疫/内分泌

发表日期：2015

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Expression of exogenous human hepatic nuclear factor-1α by a lentiviral vector and its interactions with Plasmodium falciparum subtilisin-like protease 2

利用慢病毒载体表达外源性人肝核因子-1α及其与恶性疟原虫枯草杆菌蛋白酶样蛋白酶2的相互作用

期刊:Korean Journal of Parasitology

影响因子:1.4

doi:10.3347/kjp.2011.49.4.431

Liao, Shunyao; Liu, Yunqiang; Zheng, Bing; Cho, Pyo Yun; Song, Hyun Ok; Lee, Yun-Seok; Jung, Suk-Yul; Park, Hyun

发表日期：2011

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