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Shaping the Future

Ming Guo, M.D., Ph.D.

Contact Information:

Lab Number:

310-794-4851

Office Phone Number:

310-206-9406

Work Phone Number:

(310) 794-1195

Laboratory Address:

Laboratory
Gonda 3309

UNITED STATES

Office Address:

Office
Gonda 3357A

UNITED STATES

Work Email Address:

mguo@mednet.ucla.edu

Websites:

  

Home Page:

     Health System

  

Laboratory:

     Guo Lab


Professor, Neurology

Molecular & Medical Pharmacology

Member, ACCESS Program: MBI IDP

Access Cell and Developmental Biology Home Area

Access Gene Regulation Home Area

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Brain Research Institute

Center for Duchenne Muscular Dystrophy

Center for Neurodegenerative Disease Studies

Neuroscience IDP

Faculty, Molecular, Cellular, and Integrative Physiology IDP


Awards and Honors:

UCLA School of Medicine
UCLA School of Medicine
UC Irvine Medical Center
UCLA School of Medicine

Detailed Biography:

Ming Guo, M.D., Ph.D., is Professor at UCLA Department of Neurology, Molecular and Medical Pharmacology. As a practicing Neurologist, she sees patients with memory disorders, neurodegenerative and neurogenetic disorders, referred from both domestic and international sources. As a researcher, her lab investigates molecular mechanisms of the two most common neurodegenerative disorders, Alzheimerís and Parkinsonís disease. Mutations in PINK1 and PARKIN lead to inherited forms of Parkinsonís disease. Her lab is one of the first two labs worldwide to report the function of PINK1, and to discover that PINK1, a mitochondria-localized serine-threonine kinase, and PARKIN, an E3 ubiquitin ligase, act in a common genetic pathway to regulate mitochondrial integrity and mitochondrial quality control. Her work has wide-range implications for controlling processes in aging, and other aging-related diseases including other neurodegenerative disorders, heart disease and metabolic disorders. Dr. Guo is an elected member of the American Neurological Association (ANA), and has received many awards. She is an Alfred P. Sloan Foundation fellow, a McKnight Neuroscience Foundation Brain Disorder Awardee, an Ellison Medical Foundation Senior Scholar in Aging, a Klingenstein-Simonís Fellow in Neuroscience, and the Klingenstein-Simon Foundation Robert H. Ebert Clinical Scholar. Her work is also supported by the National Institute of Health (NIH) EUREKA (Exceptional Unconventional Research Enabling Knowledge Acceleration) award. In addition, she was selected to receive the ANA Derek Denny Brown Neurological Scholar Award that is given to one or two awardees each year, and the John Walsh Young Investigator Award, which is given to one Assistant or Associate professor every three years for their research creativity at UCLA. Dr. Guo is actively involved in community service. She is Chair of the Board of Scientific Counselors at the National Institute of Neurological Disorders and Stroke (NIH/NINDS). She also serves as a member of a Blue Ribbon Panel for the NIH/NINDS, the ANA Scientific Program Advisory Committee, the Society of Neuroscience Program Committee, and the Scientific Advisory Committee of the A.P. Giannini Foundation in California.

Publications:

Yun, J., Puri, R.*, Yang, H.*, Lizzio, M., Wu, C., Sheng, Z.H. and Guo, M.   MUL1 acts in parallel to the PINK!/parkin pathway in regulating mitofusin and compensates for loss of PINK1/parkin, eLife, 2014; 3(e01958): (equal contribution).
Dauer WT, Guo M.   Multiplying messages LRRK beneath Parkinson disease, Cell, 2014; 157: 291-293.
Gross GG, Lone GM, Leung LK, Hartenstein V, Guo M.   X11/Mint genes control polarized localization of axonal membrane proteins in vivo, J. Neurosci. , 2013; 33: 8575-8586 (cover story).
Guo, M.   Drosophila as a model to study mitochondrial dysfunction in Parkinson's disease, Cold Spring Harb. Perspect. Med, 2012; a009944: .
J.C. Rochet, B.A. Hay and M. Guo   Molecular Insights into Parkinson's Disease, Progress in Molecular Biology and Translational Science, 2012; 107: 125-188.
M.W. Dodson, T. Zhang, C. Jiang, S. Chen and M. Guo   Roles of the Drosophila LRRK2 homolog in Rab7-dependent lysosomal positioning, Human Molecular Genetics, 2012; 21: 1350-1363.
B.A. Hay, C.H. Chen, C. M. Ward, H. Huang. J. T.Su, and M. Guo   Engineering the genomes of wild insect populations: Challenges, and opportunities provided by synthetic Medea selfish genetic elements, J. Insect Physiol. , 2010; 56: 1402-1413.
M. Guo   What have we learned from Drosophila models of Parkinson?s disease, Progress in Brain Research, 2010; 184: 3-17.
Li, H. and Guo, M.   Protein Degradation in Parkinson Disease Revisited: It's Complex , J. Clinical Invest, 2009; 119: 442-445.
Yun, J. Cao, J.H. Dodson, M.W Clark, I.E. Kapahi, P. Chowdhury, R.B. and Guo, M.   Loss-of-function analysis suggests that Omi/HtrA2 is not an essential component of the pink1/parkin pathway in vivo J. Neurosci, 2008; 28: 14500-14510.
Gross, G.G. Feldman, R. Ganguly, A. Wang, J. Yu, H. and Guo, M.   Role of X11 and ubiquilin as in vivo regulators of the amyloid precursor protein in Drosophila PLoS ONE, 2008; 3: e2495.
Deng, H. Dodson, M.W. Huang, H. Guo, M.   The Parkinson's disease genes pink1 and parkin promote mitochondrial fission and/or fusion in Drosophila PNAS, 2008; 105: 14503-14508.
Ganguly, A.*, Feldman, R.* and Guo, M.   ubiquilin antagonizes presenilin and promotes neurodegeneration Human Molecular Genetics, 2008; 17: 293-302. (Cover Story).
Chen, C., Huang, H., Ward, C., Su, J., Schaeffer, L., M. Guo and Hay, B.A.   A Synthetic Maternal-Effect Selfish Genetic Element Drives Population Replacement in Drosophila Science, 2007; 316: 597-600.
Dodson, M.W. and Guo, M.   Pink1, Parkin, DJ-1 and Mitochondrial Dysfunction in Parkinson's Disease Curr. Opin. Neurobiol, 2007; 17: 331-337.
Hay, B.A. and Guo, M.   Caspase-Dependent Cell Death in Drosophila Annu. Rev. Cell Dev. Biol, 2006; 22: 623-650.
Clark, I.E*., Dodson, M.W.*, Jiang, C.*, Cao, J.H., Huh, J.R., Seol, J.H., Yoo, S.J., Hay, B.A. and Guo, M.   Drosophila pink1 is required for mitochondrial function and interacts genetically with parkin Nature, 2006; 441: 1162-1166.
Hay, BA, Huh, JR and Guo, M   The genetics of cell death: approaches, insights and opportunities in Drosophila Nature Review Genetics , 2004; 5(12): 911-22.
Xu P, Guo M, Hay BA.   MicroRNAs and the regulation of cell death, Trends Genet, 2004; 20(12): 617-624.
Guo, M Hong, EJ Fernandes, J Zipursky, SL Hay, BA   A reporter for amyloid precursor protein gamma-secretase activity in Drosophila Human molecular genetics. , 2003; 12(20): 2669-78.
Hay, BA Guo, M   Coupling cell growth, proliferation, and death. Hippo weighs in Developmental cell. , 2003; 5(3): 361-3.
Xu, P Vernooy, SY Guo, M Hay, BA   The Drosophila microRNA Mir-14 suppresses cell death and is required for normal fat metabolism Current biology : , 2003; 13(9): 790-5.
Guo, M., Hay, B.   Cell proliferation and apoptosis, Curr Opin Cell Biol. , 1999; 11: 745-752.
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