Acute brainstem haemorrhage as a presenting feature of high-grade glioma

Por Aghajan, Yasmin, Levy, Michael L, Mo, Jun Qin, Crawford, John Ross
Publicado no BMJ Case Rep (2016)

Vav3 oncogene activates estrogen receptor and its overexpression may be involved in human breast cancer

Por Lee, Kiwon, Liu, Yin, Mo, Jun Qin, Zhang, Jinsong, Dong, Zhongyun, Lu, Shan
Publicado em 2008

Medullary thyroid cancer in a 9-week-old infant with familial MEN 2B: Implications for timing of prophylactic thyroidectomy

Por Shankar, Roopa Kanakatti, Rutter, Michael J, Chernausek, Steven D, Samuels, Paul J, Mo, Jun Qin, Rutter, Meilan M
Publicado em 2012

Targeted Overexpression of Vav3 Oncogene in Prostatic Epithelium Induces Nonbacterial Prostatitis and Prostate Cancer

Por Liu, Yin, Mo, Jun Qin, Hu, Qiande, Boivin, Gregory, Levin, Linda, Lu, Shan, Yang, Dianer, Dong, Zhongyun, Lu, Shan
Publicado em 2008

The tRNA(Met) 4435A>G mutation in the mitochondrial haplogroup G2a1 is responsible for maternally inherited hypertension in a Chinese pedigree

Por Lu, Zhongqiu, Chen, Hong, Meng, Yanzi, Wang, Yan, Xue, Ling, Zhi, Shaoce, Qiu, Qiaomeng, Yang, Li, Mo, Jun Qin, Guan, Min-Xin
Publicado em 2011

Mitochondrial tRNA Variants in Chinese Subjects With Coronary Heart Disease

Por Qin, Yanwen, Xue, Ling, Jiang, Pingping, Xu, Meifen, He, Yiqun, Shi, Suxue, Huang, Yangyiyi, He, Jiqiang, Mo, Jun Qin, Guan, Min‐Xin
Publicado em 2014

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

Contribution of the tRNA(Ile) 4317A→G mutation to the phenotypic manifestation of the deafness-associated mitochondrial 12S rRNA 1555A→G mutation

Por Meng, Feilong, He, Zheyun, Tang, Xiaowen, Zheng, Jing, Jin, Xiaofen, Zhu, Yi, Ren, Xiaoyan, Zhou, Mi, Wang, Meng, Gong, Shasha, Mo, Jun Qin, Shu, Qiang, Guan, Min-Xin
Publicado no J Biol Chem (2018)

The 12S rRNA A1555G mutation in the mitochondrial haplogroup D5a is responsible for maternally inherited hypertension and hearing loss in two Chinese pedigrees

Por Chen, Hong, Zheng, Jing, Xue, Ling, Meng, Yanzi, Wang, Yan, Zheng, Bingjiao, Fang, Fang, Shi, Suxue, Qiu, Qiaomeng, Jiang, Pingping, Lu, Zhongqiu, Mo, Jun Qin, Lu, Jianxin, Guan, Min-Xin
Publicado em 2012

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