Professor | Lu Daru | Asia Growth Partners

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Name	Lu Daru
Contact Information	drlu@fudan.edu.cn
Language ability	Chinese, English
Province	Shanghai

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Name

Lu Daru

Contact Information

drlu@fudan.edu.cn

Language ability

Chinese, English

Province

Shanghai

University/Lab Affiliation and Title	Fudan University
Faculty	Life Sciences
Academic Background & Achievements	1984-1988 Bachelor's Degree: Fudan University 1996 PhD in Genetics: Fudan University Achievement: Director of the Gene Technology Engineering Research Center of the Ministry of Education Achievement: Director of the National Health Commission Key Laboratory of Birth Defects and Reproductive Health Achievement: Executive Director/Deputy Secretary-General of the Chinese Genetics Society Achievement: Executive Director of the China Eugenics Association Achievement: Chairman of the Shanghai Genetics Society Achievement: Vice Chairman of the Shanghai Anthropology Society Achievement: Vice Chairman of the Shanghai Bioengineering Society
Work Experience	1996-present - Fudan University - Lecturer, Associate Professor, Professor, Distinguished Professor, Vice Dean of the School of Life Sciences
Awards	National Technological Invention Second Prize (1997): Second Contributor National Natural Science Second Prize (2007): Third Contributor Provincial and Ministerial Science and Technology First Prize: 5 times National Teaching Achievement Second Prize: 1 time National Excellent Doctoral Dissertation National Excellent Teacher China Youth Science and Technology Award National Candidate of the National Hundred, Thousand, and Ten Thousand Talent Project

University/Lab Affiliation and Title

Fudan University

Faculty

Life Sciences

Academic Background & Achievements

1984-1988 Bachelor's Degree: Fudan University
1996 PhD in Genetics: Fudan University
Achievement: Director of the Gene Technology Engineering Research Center of the Ministry of Education
Achievement: Director of the National Health Commission Key Laboratory of Birth Defects and Reproductive Health
Achievement: Executive Director/Deputy Secretary-General of the Chinese Genetics Society
Achievement: Executive Director of the China Eugenics Association
Achievement: Chairman of the Shanghai Genetics Society
Achievement: Vice Chairman of the Shanghai Anthropology Society
Achievement: Vice Chairman of the Shanghai Bioengineering Society

Work Experience

1996-present - Fudan University - Lecturer, Associate Professor, Professor, Distinguished Professor, Vice Dean of the School of Life Sciences

Awards

National Technological Invention Second Prize (1997): Second Contributor
National Natural Science Second Prize (2007): Third Contributor
Provincial and Ministerial Science and Technology First Prize: 5 times
National Teaching Achievement Second Prize: 1 time
National Excellent Doctoral Dissertation
National Excellent Teacher
China Youth Science and Technology Award
National Candidate of the National Hundred, Thousand, and Ten Thousand Talent Project

Areas of Focus	Gene Editing and Gene Therapy Genetic Diseases Birth Defects Molecular Detection and Gene Diagnosis Non-invasive Prenatal Testing for Monogenic Genetic Diseases Third-generation IVF Gene Testing
Publications	Two novel genetic variants in the STK38L and RAB27A genes are associated with glioma susceptibility, Chen H, Chen G, Li G, Zhang S, Chen H, Chen Y, Duggan D, Hu Z, Chen J, Zhao Y, Zhao Y, Huang H, Zheng SL, Trent JM, Yu L, Jiang D, Mo Z, Wang H, Mou Y, Jiang T, Mao Y, Xu J, Lu D, 2019 Shuttling SLC2A4RG is regulated by 14-3-3θ to modulate cell survival via caspase-3 and caspase-6 in human glioma, Yun D, Wang H, Wang Y, Chen Y, Zhao Z, Ma J, Ji Y, Huang Q, Chen J, Chen H, Lu D, 2019 Intracellular generation of single-strand template increases the knock-in efficiency by combining CRISPR/Cas9 with AAV, Xiao Q, Min T, Ma S, Hu L, Chen H, Lu D, 2018 New applications of CRISPR/Cas9 system on mutant DNA detection, Jia C, Huai C, Ding J, Hu L, Su B, Chen H, Lu D, 2018 Establishment of a Gene Detection System for Hotspot Mutations of Hearing Loss, Wang C, Wang S, Chen H, Lu D, 2018 Structural insights into DNA cleavage activation of CRISPR-Cas9 system, Huai C, Li G, Yao R, Zhang Y, Cao M, Kong L, Jia C, Yuan H, Chen H, Lu D, Huang Q, 2017 CRISPR/Cas9-mediated somatic and germline gene correction to restore hemostasis in hemophilia B mice, Huai C, Jia C, Sun R, Xu P, Min T, Wang Q, Zheng C, Chen H, Lu D, 2017 The establishment and application of preimplantation genetic haplotyping in embryo diagnosis for reciprocal and Robertsonian translocation carriers, Zhang S, Lei C, Wu J, Zhou J, Sun H, Fu J, Sun Y, Sun X, Lu D, Zhang Y, 2017

Areas of Focus

Gene Editing and Gene Therapy
Genetic Diseases
Birth Defects
Molecular Detection and Gene Diagnosis
Non-invasive Prenatal Testing for Monogenic Genetic Diseases
Third-generation IVF Gene Testing

Publications

Two novel genetic variants in the STK38L and RAB27A genes are associated with glioma susceptibility, Chen H, Chen G, Li G, Zhang S, Chen H, Chen Y, Duggan D, Hu Z, Chen J, Zhao Y, Zhao Y, Huang H, Zheng SL, Trent JM, Yu L, Jiang D, Mo Z, Wang H, Mou Y, Jiang T, Mao Y, Xu J, Lu D, 2019
Shuttling SLC2A4RG is regulated by 14-3-3θ to modulate cell survival via caspase-3 and caspase-6 in human glioma, Yun D, Wang H, Wang Y, Chen Y, Zhao Z, Ma J, Ji Y, Huang Q, Chen J, Chen H, Lu D, 2019
Intracellular generation of single-strand template increases the knock-in efficiency by combining CRISPR/Cas9 with AAV, Xiao Q, Min T, Ma S, Hu L, Chen H, Lu D, 2018
New applications of CRISPR/Cas9 system on mutant DNA detection, Jia C, Huai C, Ding J, Hu L, Su B, Chen H, Lu D, 2018
Establishment of a Gene Detection System for Hotspot Mutations of Hearing Loss, Wang C, Wang S, Chen H, Lu D, 2018
Structural insights into DNA cleavage activation of CRISPR-Cas9 system, Huai C, Li G, Yao R, Zhang Y, Cao M, Kong L, Jia C, Yuan H, Chen H, Lu D, Huang Q, 2017
CRISPR/Cas9-mediated somatic and germline gene correction to restore hemostasis in hemophilia B mice, Huai C, Jia C, Sun R, Xu P, Min T, Wang Q, Zheng C, Chen H, Lu D, 2017
The establishment and application of preimplantation genetic haplotyping in embryo diagnosis for reciprocal and Robertsonian translocation carriers, Zhang S, Lei C, Wu J, Zhou J, Sun H, Fu J, Sun Y, Sun X, Lu D, Zhang Y, 2017

Gene Editing Gene Therapy Hemophilia Thalassemia Pathogenic Genes Molecular Mechanisms Birth Defects Congenital Hypothyroidism Multiplex Gene Detection Low-Frequency Mutation Detection

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