Professor | Xiuli Zhao | Asia Growth Partners

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Name	Xiuli Zhao
Contact Information	xiulizhao@ibms.pumc.edu.cn
Language ability	Chinese, English
Province	Beijing

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Name

Xiuli Zhao

Contact Information

xiulizhao@ibms.pumc.edu.cn

Language ability

Chinese, English

Province

Beijing

University/Lab Affiliation and Title	Peking Union Medical College
Faculty	Basic Medical Sciences
Academic Background & Achievements	1991 - Bachelor's degree in Biology: Hebei Normal University 2003 - Master's degree in Genetics: Southeast University Medical School 2006 - Doctorate in Medical Genetics: Peking Union Medical College 2008-2010 - Postdoctoral Research: Johns Hopkins University School of Medicine Achievement: Discovered pathogenic mutation Q50R in HOXD13 for syndactyly type V
Work Experience	1999-2000 - Lecturer: Hebei North University Medical School 2006-present - Professor: Peking Union Medical College, Institute of Basic Medical Sciences 2008-2010 - Postdoctoral Researcher: Johns Hopkins University School of Medicine
Awards	Chinese Medical Science Award Second Prize Ministry of Education Natural Science First Prize

University/Lab Affiliation and Title

Peking Union Medical College

Faculty

Basic Medical Sciences

Academic Background & Achievements

1991 - Bachelor's degree in Biology: Hebei Normal University
2003 - Master's degree in Genetics: Southeast University Medical School
2006 - Doctorate in Medical Genetics: Peking Union Medical College
2008-2010 - Postdoctoral Research: Johns Hopkins University School of Medicine
Achievement: Discovered pathogenic mutation Q50R in HOXD13 for syndactyly type V

Work Experience

1999-2000 - Lecturer: Hebei North University Medical School
2006-present - Professor: Peking Union Medical College, Institute of Basic Medical Sciences
2008-2010 - Postdoctoral Researcher: Johns Hopkins University School of Medicine

Awards

Chinese Medical Science Award Second Prize
Ministry of Education Natural Science First Prize

Areas of Focus	Monogenic Hereditary Bone Diseases Gene Diagnosis and Mutation Spectrum Gene Therapy for Monogenic Hereditary Diseases using Induced Stem Cells and Animal Models
Publications	A long noncoding RNA contributes to neuropathic pain by silencing Kcna2 in primary afferent neurons, Zhao X#, Tang Z, Zhang H, Atianjoh FE, Zhao JY, Liang L, Wang W, Guan X, Kao SC, Tiwari V, Gao YJ, Hoffman PN, Cui H, Li M, Dong X, Tao YX, 2013 Morphine tolerance and hyperalgesia mediated through mu opioid receptor-triggered activation of the mammalian target of rapamycin complex 1 pathway in dorsal horn neurons, Xu J, Zhao J, Zhao X#, LigonsD, Tiwari V, Atianjoh FE, Liang L, Zang W, Njoku D, Raja SN, Yaster M, Tao YX, 2014 Mutations in HOXD13 underlie syndactyly type V and a novel brachydactyly-syndactyly syndrome, Zhao X#, Sun M, Zhao J, Leyva JA, Zhu H, Yang W, Zeng X, Ao Y, Liu Q, Liu G, Lo WH, Jabs EW, Amzel LM, Shan X, Zhang X, 2007 A novel deletion in TNNI2 causes distal arthrogryposis in a large Chinese family with marked variability of expression, Jiang M, Zhao X#, Han WT, Bian CY, Li XF, Wang G, Ao Y, Li YQ, Yi DX, Zhe Y, Lo HY Wilson, Zhang X, Li JX, 2006 Absence of μ opioid receptor mRNA expression in astrocytes and microglia of rat spinal cord, Kao SC, Zhao X, Lee CY, Atianjoh FE, Gauda EB, Yaster M, Tao YX, 2012 Screening for AIP gene mutations in a Han Chinese pituitary adenoma cohort followed by LOH analysis, Cai F, Zhang YD, Zhao X, et al., 2013 Spinal cord protein interacting with C kinase 1 is required for the maintenance of complete Freund's adjuvant-induced inflammatory pain but not for incision-induced post-operative pain, Atianjoh FE, Yaster M, Zhao X, Takamiya K, Xia J, Gauda EB, Huganir RL, Tao YX, 2010 Expression and distribution of mTOR, p70S6K, 4E-BP1, and their phosphorylated counterparts in rat dorsal root ganglion and spinal cord dorsal horn, Xu JT, Zhao X, Yaster M, Tao YX, 2010 Three novel mutations of the EDA gene in Chinese patients with X-linked hypohidrotic ectodermal dysplasia, Zhao J, Hua R, Zhao X, Meng Y, Ao Y, Liu Q, Shang D, Sun M, Lo WH, Zhang X, 2008 一个角膜-鱼鳞病-耳聋综合征家系的致病突变分析, 李璐璐，李媛，林蔚，赵秀丽, 2017 应用PCR-HRM技术进行FGFR3热点突变的快速诊断, 李闪，汪涵，苏华，高劲松，赵秀丽, 2017 成骨不全症家系COL1A1/2的大片段缺失突变分析, 汪涵, 赵秀丽, 任秀智, 肖继芳, 张学, 2016 遗传性乳光牙本质家系致病基因突变的鉴定, 刘彦山，黄颖之，赵秀丽，张学, 2016 成骨不全症的COL1A1/2突变谱和基因诊断研究, 赵秀丽#，肖继芳，汪涵，任秀智，高劲松，吴易阳，卢超霞，孙悦，张学, 2015

Areas of Focus

Monogenic Hereditary Bone Diseases Gene Diagnosis and Mutation Spectrum
Gene Therapy for Monogenic Hereditary Diseases using Induced Stem Cells and Animal Models

Publications

A long noncoding RNA contributes to neuropathic pain by silencing Kcna2 in primary afferent neurons, Zhao X#, Tang Z, Zhang H, Atianjoh FE, Zhao JY, Liang L, Wang W, Guan X, Kao SC, Tiwari V, Gao YJ, Hoffman PN, Cui H, Li M, Dong X, Tao YX, 2013
Morphine tolerance and hyperalgesia mediated through mu opioid receptor-triggered activation of the mammalian target of rapamycin complex 1 pathway in dorsal horn neurons, Xu J, Zhao J, Zhao X#, LigonsD, Tiwari V, Atianjoh FE, Liang L, Zang W, Njoku D, Raja SN, Yaster M, Tao YX, 2014
Mutations in HOXD13 underlie syndactyly type V and a novel brachydactyly-syndactyly syndrome, Zhao X#, Sun M, Zhao J, Leyva JA, Zhu H, Yang W, Zeng X, Ao Y, Liu Q, Liu G, Lo WH, Jabs EW, Amzel LM, Shan X, Zhang X, 2007
A novel deletion in TNNI2 causes distal arthrogryposis in a large Chinese family with marked variability of expression, Jiang M, Zhao X#, Han WT, Bian CY, Li XF, Wang G, Ao Y, Li YQ, Yi DX, Zhe Y, Lo HY Wilson, Zhang X, Li JX, 2006
Absence of μ opioid receptor mRNA expression in astrocytes and microglia of rat spinal cord, Kao SC, Zhao X, Lee CY, Atianjoh FE, Gauda EB, Yaster M, Tao YX, 2012
Screening for AIP gene mutations in a Han Chinese pituitary adenoma cohort followed by LOH analysis, Cai F, Zhang YD, Zhao X, et al., 2013
Spinal cord protein interacting with C kinase 1 is required for the maintenance of complete Freund's adjuvant-induced inflammatory pain but not for incision-induced post-operative pain, Atianjoh FE, Yaster M, Zhao X, Takamiya K, Xia J, Gauda EB, Huganir RL, Tao YX, 2010
Expression and distribution of mTOR, p70S6K, 4E-BP1, and their phosphorylated counterparts in rat dorsal root ganglion and spinal cord dorsal horn, Xu JT, Zhao X, Yaster M, Tao YX, 2010
Three novel mutations of the EDA gene in Chinese patients with X-linked hypohidrotic ectodermal dysplasia, Zhao J, Hua R, Zhao X, Meng Y, Ao Y, Liu Q, Shang D, Sun M, Lo WH, Zhang X, 2008
一个角膜-鱼鳞病-耳聋综合征家系的致病突变分析, 李璐璐，李媛，林蔚，赵秀丽*, 2017
应用PCR-HRM技术进行FGFR3热点突变的快速诊断, 李闪，汪涵，苏华，高劲松，赵秀丽*, 2017
成骨不全症家系COL1A1/2的大片段缺失突变分析, 汪涵, 赵秀丽*, 任秀智, 肖继芳, 张学, 2016
遗传性乳光牙本质家系致病基因突变的鉴定, 刘彦山，黄颖之，赵秀丽*，张学, 2016
成骨不全症的COL1A1/2突变谱和基因诊断研究, 赵秀丽#，肖继芳，汪涵，任秀智，高劲松，吴易阳，卢超霞，孙悦，张学, 2015

Genetics Bone Diseases Mutation Diagnosis Gene Therapy Stem Cells Animal Models Monogenic Hereditary Research

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