Interaction of Aminoglycosides with Human Mitochondrial 12S rRNA Carrying the Deafness-Associated Mutation

Por Qian, Yaping, Guan, Min-Xin
Publicado em 2009

Next generation sequencing technologies in medical genetics

Por Valencia, C. Alexander., Pervaiz, M. Ali., Husami, Ammar., Qian, Yaping., Zhang, Kejian.
Publicado em 2013

Low dose naltrexone administration in morphine dependent rats attenuates withdrawal-induced norepinephrine efflux in forebrain

Por Van Bockstaele, Elisabeth J., Qian, Yaping, Sterling, Robert C., Page, Michelle E.
Publicado em 2008

Combined Immune Deficiency in a Patient with a Novel NFKB2 Mutation

Por Lindsley, Andrew W., Qian, Yaping, Valencia, C. Alexander, Shah, Kara, Zhang, Kejian, Assa’ad, Amal
Publicado no J Clin Immunol (2014)

Calpains mediate axonal cytoskeleton disintegration during Wallerian degeneration

Por Ma, Marek, Ferguson, Toby A., Schoch, Kathleen M., Li, Jian, Qian, Yaping, Shofer, Frances S., Saatman, Kathryn E., Neumar, Robert W.
Publicado em 2013

Cosegregation of the ND4 G11696A mutation with the LHON-associated ND4 G11778A mutation in a four generation Chinese family

Por Qu, Jia, Li, Ronghua, Zhou, Xiangtian, Tong, Yi, Yang, Li, Chen, Jie, Zhao, Fuxing, Lu, Chunjie, Qian, Yaping, Lu, Fan, Guan, Min-Xin
Publicado em 2006

Mutational analysis of the mitochondrial 12S rRNA gene in Chinese pediatric subjects with aminoglycoside-induced and non-syndromic hearing loss

Por Li, Zhiyuan, Li, Ronghua, Chen, Jianfu, Liao, Zhisu, Zhu, Yi, Qian, Yaping, Xiong, Sudao, Heman-Ackah, Selena, Wu, Jianbo, Choo, Daniel I., Guan, Min-Xin
Publicado em 2005

Mitochondrial tRNA(Thr) G15927A mutation may modulate the phenotypic manifestation of ototoxic 12S rRNA A1555G mutation in four Chinese families

Por Wang, Xinjian, Lu, Jianxin, Zhu, Yi, Yang, Aifen, Yang, Li, Li, Ronghua, Chen, Bobei, Qian, Yaping, Tang, Xiaowen, Wang, Jindan, Zhang, Xue, Guan, Min-Xin
Publicado em 2008

Very high penetrance and occurrence of Leber’s hereditary optic neuropathy in a large Han Chinese pedigree carrying the ND4 G11778A mutation

Por Zhou, Xiangtian, Zhang, Hongxing, Zhao, Fuxin, Ji, Yanchun, Tong, Yi, Zhang, Juanjuan, Zhang, Yu, Yang, Li, Qian, Yaping, Lu, Fan, Qu, Jia, Guan, Min-Xin
Publicado em 2010

Leber's Hereditary Optic Neuropathy Is Associated with the T3866C Mutation in Mitochondrial ND1 Gene in Three Han Chinese Families

Por Zhou, Xiangtian, Qian, Yaping, Zhang, Juanjuan, Tong, Yi, Jiang, Pingping, Liang, Min, Dai, Xianning, Zhou, Huihui, Zhao, Fuxin, Ji, Yanchun, Mo, Jun Qin, Qu, Jia, Guan, Min-Xin
Publicado em 2012

Deep Sequencing Reveals Novel Genetic Variants in Children with Acute Liver Failure and Tissue Evidence of Impaired Energy Metabolism

Por Valencia, C. Alexander, Wang, Xinjian, Wang, Jin, Peters, Anna, Simmons, Julia R., Moran, Molly C., Mathur, Abhinav, Husami, Ammar, Qian, Yaping, Sheridan, Rachel, Bove, Kevin E., Witte, David, Huang, Taosheng, Miethke, Alexander G.
Publicado no PLoS One (2016)

Cosegregation of the G7444A Mutation in the Mitochondrial COI/tRNA(Ser(UCN)) Genes with the 12S rRNA A1555G Mutation in a Chinese Family with Aminoglycoside-induced and Nonsyndromi...

Por Yuan, Huijun, Qian, Yaping, Xu, Yanjun, Cao, Juyang, Bai, Linna, Shen, Weidong, Ji, Fei, Zhang, Xin, Kang, Dongyang, Mo, Jun Qin, Greinwald, John H., Han, Dongyi, Zhai, Suoqiang, Young, Wie-Yen, Guan, Min-Xin
Publicado em 2005

Mitochondrial haplotypes may modulate the phenotypic manifestation of the deafness-associated 12S rRNA 1555A>G mutation

Por Lu, Jianxin, Qian, Yaping, Li, Zhiyuan, Yang, Aifen, Zhu, Yi, Li, Ronghua, Yang, Li, Tang, Xiaowen, Chen, Bobei, Ding, Yu, Li, Yongyan, You, Junyan, Zheng, Jing, Tao, Zhihua, Zhao, Fuxin, Wang, Jindan, Sun, Dongmei, Zhao, Jianyue, Meng, Yanzi, Guan, Min-Xin
Publicado em 2009

The struggle to find reliable results in exome sequencing data: filtering out Mendelian errors

Por Patel, Zubin H., Kottyan, Leah C., Lazaro, Sara, Williams, Marc S., Ledbetter, David H., Tromp, hbGerard, Rupert, Andrew, Kohram, Mojtaba, Wagner, Michael, Husami, Ammar, Qian, Yaping, Valencia, C. Alexander, Zhang, Kejian, Hostetter, Margaret K., Harley, John B., Kaufman, Kenneth M.
Publicado em 2014

Mutation in TRMU Related to Transfer RNA Modification Modulates the Phenotypic Expression of the Deafness-Associated Mitochondrial 12S Ribosomal RNA Mutations

Por Guan, Min-Xin, Yan, Qingfeng, Li, Xiaoming, Bykhovskaya, Yelena, Gallo-Teran, Jaime, Hajek, Petr, Umeda, Noriko, Zhao, Hui, Garrido, Gema, Mengesha, Emebet, Suzuki, Tsutomu, Castillo, Ignacio del, Peters, Jennifer Lynne, Li, Ronghua, Qian, Yaping, Wang, Xinjian, Ballana, Ester, Shohat, Mordechai, Lu, Jianxin, Estivill, Xavier, Watanabe, Kimitsuna, Fischel-Ghodsian, Nathan
Publicado em 2006

Clinical Impact and Cost-Effectiveness of Whole Exome Sequencing as a Diagnostic Tool: A Pediatric Center’s Experience

Por Valencia, C. Alexander, Husami, Ammar, Holle, Jennifer, Johnson, Judith A., Qian, Yaping, Mathur, Abhinav, Wei, Chao, Indugula, Subba Rao, Zou, Fanggeng, Meng, Haiying, Wang, Lijun, Li, Xia, Fisher, Rachel, Tan, Tony, Hogart Begtrup, Amber, Collins, Kathleen, Wusik, Katie A., Neilson, Derek, Burrow, Thomas, Schorry, Elizabeth, Hopkin, Robert, Keddache, Mehdi, Harley, John Barker, Kaufman, Kenneth M., Zhang, Kejian
Publicado no Front Pediatr (2015)