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  • 高通量测序技术与基因组学研究

    作者: 发布时间:2011-10-14 浏览次数:1885

    报告题目:高通量测序技术与基因组学研究

    报告人:高汉林博士(Assistant research Professor.Co-Director,Functional Genomics/Genome Sequencing Core,City of Hope National Medical Center)

    报告时间:2011年10月24日(周一)下午2:00

    报告地点:独墅湖校区炳麟图书馆720室

     

    高汉林博士简介

    EDUCATION/TRAINING

    The Ohio State University, Columbus, Ohio  Ph.D. 03/2001   Medical Genetics

    Harvard Medical School, Boston , MA   Postdoc.  07/2004   Molecular Genetics

    Harvard Medical School, Boston , MA   ABMG   07/2004  Clinical Molecular Genetics

    Positions and Employment

    2001-2004      Research Fellow, Harvard Medical School, Boston, MA     

    2004-2008   Co-Director, Clinical Molecular Diagnostics Laboratory, City of Hope Medical Center

    2004-     Assistant research professor, City of Hope Medical Center

    2008-2009   Associated Direcotor, DNA sequencing/Solexa Core lab, Beckman Research Institute of City   of Hope

    2009-     Co-Director, Function genome/genome sequencing Core lab, Beckman Research Institute of City of Hope     

    Awards and Honors

    2002-2003           Tosteson Postdoctoral Fellowship

    1996-2000           Bennett Fellowship, The Ohio State University

    1996                     University Fellowship, The Ohio State University

    1993                     Guang Hua Prize, Beijing Medical University

    1986-1990            Fellowship, Neimenggumeng Medical College

    Selected peer-reviewed publications

    1    Gao H, Huang KC, Yamasaki EF, Chan KK, Chohan L, Snapka RM.. XK469, selective topoisomerase II b poison. Proc. Natl. Acad. Sci. U.S.A. 1999;96:12168-12173. PMCID: PMC18430

    2    Gao H, Yamasaki EF, Chan KK, Shen LL, Snapka RM.  Chloroquinoxaline sulfoamide is a topoisomerase II a/b Poison. Cancer Research, 2000, 60:5937-5940 PMID: 11085507

    3    Gao H, Yamasaki EF, Chan KK, Shen LL, Snapka RM. DNA sequence specificity for topoisomerase II poisoning by the quinoxaline anticancer drugs XK469 and CQS. Mol Pharmacol. 2003; 63(6):1382-8. PMID: 12761349

    4    Huang KC, Gao H(co-first author), Yamasaki EF, Grabowski DR, Liu S, Shen LL, Chan KK, Ganapathi R, Snapka RM.  Topoisomerase II poisoning by ICRF-193. J Biol Chem. 2001; 276(48):44488-94. PMID:11577077

    5    Snapka RM, Gao H, Grabowski DR, Brill D, Chan KK, Li L, Li GC, Ganapathi R.  Cytotoxic mechanism of XK469: resistance of topoisomerase IIb knockout cells and inhibition of topoisomerase. Biochem Biophys Res Commun. 2001; 280(4):1155-60.

    6    Gao H, Boustany RM, Espinola JA, Cotman SL, Srinidhi L, Antonellis KA, Gillis T, Qin X, Liu S, Donahue LR, Bronson RT, Faust JR, Stout D, Haines JL, Lerner TJ, MacDonald ME. Mutations in a novel cln6-encoded transmembrane protein cause variant neuronal ceroid lipofuscinoses in man and mouse. Am J Hum Genet. 2002; 70(2):324-35 PMCID: PMC384912

    7    Fossale E, Wolf P, Espinola JA, Lubicz-Nawrocka T, Teed AM, Gao H, et al .  Membrane trafficking and mitochondrial abnormalities precede subunit c deposition in a cerebellar cell model of juvenile neuronal ceroid lipofuscinosis. BMC Neurosci. 2004 Dec 10;5(1):57. PMCID: PMC539297

    8    Zhang,J;Zhou,C;Yin,Y;Chen,L;Pardinas,J.R;Liu,T;Gao H;Saldivar-J.,S;Li,K  Detection of Known Mutations with DNA Polymerases: Its Pharmacogenetic Applications. Current Pharmacogenomics, 2006, 4, 121-131

    9    Zeng WQ, Gao H, Brueton L, Hutchin T, Gray G, Chakrapani A, Olpin S, Shih VE. Fumarase deficiency caused by homozygous of P131R mutation on partial uniparental isodisomy of Chromosome 1. Am J Med Genet A. 2006;140(9):1004-9. PMID:16575891

    10  Adegbola A, Gao H, Sommer S, Browning M.. A Novel Mutation in JARID1C / SMCX Associated with Autism Spectrum Disorder (ASD). Am J Med Genet A 2008 Feb 15;146(4):505-11. PMID:18203167

    11  Liang S, Bass HN, Gao H, Astbury C, Jamehdor MR, Qu Y. A Pseudo-full Mutation in Fragile X Assay Resulted from a Novel Base Change Abolishing an EcoRI Restriction Site Journal of Molecular Diagnostics, 2008;. 10 (5):469-474

    12  Weng L, Wu X, Gao H(co-first author), Mu B, Li X, Wang J, Guo C,  Jin J, Chen Z, Covarrubias M, Yuan YC, Weiss LM, Wu H. MicroRNA profiling of clear cell renal cell carcinoma by whole genome small RNA deep sequencing of paired frozen and formalin-fixed paraffin-embedded tissue specimens. J Pathol. 2010 Sep;222(1):41-51. PMID: 20593407

    13  Tao R, Wei D, Gao H, Liu Y, Depinho RA, Dong XC. Hepatic FoxOs regulate lipid metabolism via modulation of expression of the nicotinamide phosphoribosyltransferase gene. J Biol Chem. 2011 Apr 22;286(16):14681-90. PMCID: PMC3077665

    14  Duldulao MP, Lee W, Le M, Chen Z, Li W, Wang J, Gao H, Li H, Kim J, Garcia-Aguilar J, Gene Expression Variations in Microsatellite Stable and Unstable Colon Cancer Cells J Surg Res. 2011 Jul 7. [Epub ahead of print] PMID: 21816436

    15  Sun G, Wu X,  Wang J, Li H,  Gao H, Rossi J, Yen Y True” Small RNAome Revealed by a Bias-Reducing Strategy in Profiling Small RNAs Using Solexa.  RNA (2011 in press)

    Research Support

    5R37ES006070-19    PFEIFER (PI)     04/28/10-04/30/14

    UV DAMAGE, REPAIR, AND MUTAGENESIS

    The goal of this study is the molecular mechanisms of UV damage, repair and mutagenesis. CpG-methylated mutation will be studied using Next Generation DNA sequencing technology.

     

    5R01CA084469-11     PFEIFER (PI)      03/01/10-02/28/14

    CPG METHYLATION AND MUTATION

    The goal of this study is Transcriptional gene silencing by hypermethylation of CpG islands spanning the promoter regions of genes. CpG-methylated mutation will be studied using Next Generation DNA sequencing technology.

     

    CBCRP IDEA, Emily Wang      7/1/2010-12/31/2011

    Identify Blood-based MiRNA Markers of NCT Response in Breast Cancer.

     

    1R01MH094599    LU (PI)    6/15/11-3/31-2016

    EPIGENOMIC MODIFICATIONS IN MAMMALIAN NEUROGENESIS

    The goal of this study is to understand how epigenomic modifications in neural stem/progenitor cells contribute to the control of a dynamic balance between the state of self-renewal and differentiation. 

     

    5R01AG036041-03      PFEIFER (PI)      9/15/2009-8/31/2014                         

    AGING AND THE UNSTABLE EPIGENOME

    To study epigenetic changes are a hallmark of the aging process. 

     

    1R01NS075393-01   LU (PI)     5/1/2011-2/29/2016

    MOLECULAR GENETIC ANALYSIS OF MAMMALIAN NEURONAL DIFFERENTIATION

    Our proposed study on identification and characterization of causal factors in neural progenitor cell regulation  to provide insight into how self-renewal and differentiation are regulated, which has direct implication on future regenerative medicine and is also useful for understanding of tumor development.

     

    1R01HL106089-01       NATARAJAN (PI)     1/1/2011-12/31/2015

    TRANSCRIPTIONAL REGULATION BY ANGIOTENSIN II IN VASCULAR SMOOTH MUSCLE CELLS

    Our goal is to evaluate such epigenetic and miR mechanisms in Ang II actions in order to unravel new therapeutic targets.