A novel GPR143 splicing mutation in a Chinese family with X-linked congenital nystagmus

Por Hu, Junjie, Liang, Desheng, Xue, Jinjie, Liu, Jing, Wu, Lingqian
Publicado em 2011

Mutation Analysis in Chinese Patients with Cornelia de Lange Syndrome

Por Zhong, Qiulian, Liang, Desheng, Liu, Jing, Xue, Jinjie, Wu, Lingqian
Publicado em 2012

A novel FOXL2 mutation in a Chinese family with blepharophimosis, ptosis, epicanthus inversus syndrome

Por Tan, Hu, Yang, Pu, Li, Haoxian, Pan, Qian, Liang, Desheng, Wu, Lingqian
Publicado no Hum Genome Var (2015)

Cryptic FMR1 mosaic deletion in a phenotypically normal mother of a boy with fragile X syndrome: case report

Por Luo, Shiyu, Huang, Wen, Xia, Qiuping, Xia, Yan, Du, Qian, Wu, Lingqian, Duan, Ranhui
Publicado no BMC Med Genet (2014)

A clear bias in parental origin of de novo pathogenic CNVs related to intellectual disability, developmental delay and multiple congenital anomalies

Por Ma, Ruiyu, Deng, Linbei, Xia, Yan, Wei, Xianda, Cao, Yingxi, Guo, Ruolan, Zhang, Rui, Guo, Jing, Liang, Desheng, Wu, Lingqian
Publicado no Sci Rep (2017)

Nonviral Gene Targeting at rDNA Locus of Human Mesenchymal Stem Cells

Por Hu, Youjin, Liu, Xionghao, Long, Panpan, Xiao, Di, Cun, Jintao, Li, Zhuo, Xue, Jinfeng, Wu, Yong, Luo, Sha, Wu, Lingqian, Liang, Desheng
Publicado em 2013

Three novel mutations of STK11 gene in Chinese patients with Peutz–Jeghers syndrome

Por Tan, Hu, Mei, Libin, Huang, Yanru, Yang, Pu, Li, Haoxian, Peng, Ying, Chen, Chen, Wei, Xianda, Pan, Qian, Liang, Desheng, Wu, Lingqian
Publicado no BMC Med Genet (2016)

Enhanced tumor growth inhibition by mesenchymal stem cells derived from iPSCs with targeted integration of interleukin24 into rDNA loci

Por Liu, Bo, Chen, Fei, Wu, Yong, Wang, Xiaolin, Feng, Mai, Li, Zhuo, Zhou, Miaojin, Wang, Yanchi, Wu, Lingqian, Liu, Xionghao, Liang, Desheng
Publicado no Oncotarget (2017)

Partial trisomy 2q33.3-q37.3 in a patient with an inverted duplicated neocentric marker chromosome

Por Ma, Ruiyu, Peng, Ying, Zhang, Yanghui, Xia, Yan, Tang, Guizhi, Chang, Jiazhen, Guo, Ruolan, Gui, Baoheng, Huang, Yanru, Chen, Chen, Liang, Desheng, Wu, Lingqian
Publicado no Mol Cytogenet (2015)

Eight-Shaped Hatching Increases the Risk of Inner Cell Mass Splitting in Extended Mouse Embryo Culture

Por Yan, Zheng, Liang, Hongxing, Deng, Li, Long, Hui, Chen, Hong, Chai, Weiran, Suo, Lun, Xu, Chen, Kuang, Yanping, Wu, Lingqian, Lu, Shengsheng, Lyu, Qifeng
Publicado no PLoS One (2015)

In situ genetic correction of F8 intron 22 inversion in hemophilia A patient-specific iPSCs

Por Wu, Yong, Hu, Zhiqing, Li, Zhuo, Pang, Jialun, Feng, Mai, Hu, Xuyun, Wang, Xiaolin, Lin-Peng, Siyuan, Liu, Bo, Chen, Fangping, Wu, Lingqian, Liang, Desheng
Publicado no Sci Rep (2016)

Targeting of the Human Coagulation Factor IX Gene at rDNA Locus of Human Embryonic Stem Cells

Por Liu, Xionghao, Wu, Yong, Li, Zhuo, Yang, Junlin, Xue, Jinfeng, Hu, Youjin, Feng, Mai, Niu, Wenbin, Yang, Qiurui, Lei, Ming, Xia, Jiahui, Wu, Lingqian, Liang, Desheng
Publicado em 2012

De Novo ring chromosome 11 and non-reciprocal translocation of 11p15.3-pter to 21qter in a patient with congenital heart disease

Por Peng, Ying, Ma, Ruiyu, Zhou, Yingjie, Xia, Yan, Wen, Juan, Zhang, Yanghui, Guo, Ruolan, Li, Haoxian, Pan, Qian, Zhang, Rui, Tang, Chengyuan, Liang, Desheng, Wu, Lingqian
Publicado no Mol Cytogenet (2015)

Characterization of Chromosomal Abnormalities in Pregnancy Losses Reveals Critical Genes and Loci for Human Early Development

Por Chen, Yiyun, Bartanus, Justin, Liang, Desheng, Zhu, Hongmin, Breman, Amy M, Smith, Janice L, Wang, Hua, Ren, Zhilin, Patel, Ankita, Stankiewicz, Pawel, Cram, David S, Cheung, Sau Wai, Wu, Lingqian, Yu, Fuli
Publicado no Hum Mutat (2017)