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Medical Development

Location:
Hayward, CA
Posted:
April 12, 2014

Contact this candidate

Resume:

Yiguo Shen, Ph.D

***** ****** **, ****** ****** CA 94546

Cell Phone: 510-

***-****

Email:

*****.****@*****.***

CAREER OBJECTIVES

A Research & Development position in which molecule biology, cell

biology, biochemistry, and in vivo animal model applied towards new

medicine for human diseases.

PROFILE HIGHLIGHT

. Experienced veteran in molecular & cell biology, biochemistry and

genetics, human disease studies including transcription regulation,

protein expression & interaction, primary cell cultures,

inflammation and metabolite assays, in vivo viral delivery, animal

model and behaviours. Hands-on experience in lentivirus and

adenovirus constructs and in vivo gene delivery, conditional

knockout construction, stable siRNA knockdown cell lines etc.

. Superb communication skills, self motivated team player.

. Design, implement, analyze, and present experiments to demonstrate

feasibility and achieve project goals. Solve complex research and

development challenges independently and quickly.

EDUCATION

Ph.D. Genetics, Institute of Genetics, Chinese Academy of

Sciences, China, 2002.

B.S. Biology, University of Science and Technology of

China, China, 1997.

METROLOGY AND SKILLS

. DNA&RNA Techniques, Molecular Cloning, Library Construction, Virus

Construction, Conditional

Knockout Construction, Real-Time PCR, Confocal, Electron

Microscopy;

. Mammalian cell culture, Expression System, Protein Purification and

Interaction, ELISA, Enzymes activity Assay, Cell-based and

metabolites Assays;

. Mouse Genetics, Mapping and Mutation Cloning, Mouse Behaviour

Tests, Zero-maze, Open Field, Forced Swim, Stereotaxic Virus

Injection;

. Immunohistochemistry, Confocal, Transmission Electron Microscopy.

SELECTED SCHOLASTIC HONORS

. 2009 Bachmann Strauss Dystonia & Parkinson Foundation Grant

Award

. 2007 Dystonia Medical Research Foundation Fellowship

PROFESSIONAL EXPERIENCE

July, 2013 - Present: Senior Scientist, Manager of Bioassay Development,

Nvigen Inc., Santa Clara CA

. Develop novel method to quantify nanoparticle binding sensitivity,

capacity. Develop new reagents and protocols for non-hybridization

and hybridization based DNA-binding nanoparticles. Optimize assay

condition and improve nanoparticle recovery efficiency. Develop new

method for Antibody-based Cell Capture Assay in blood analysis.

. Provide technique support to various customers, and co-supervise

the product and catalogue development.

July, 2012 - June, 2013: Assistant Adjunct Professor, Veteran Affairs

Medical Center, San Francisco CA

Northern California Institute for Research&Education

. Discovered the molecular mechanism of the metabolism regulated

inflammatory responses through a C-terminal binding protein in the

microglia and macrophage. Revealed the role of metabolic NAD+/NADH

sensor protein in regulating NF-?B activated inflammatory pathway.

Wrote a manuscript titled "Bioenergetic State Regulates the

Inflammatory Response through NADH sensor CtBP", co-authored two

other publications.

July, 2010 -June, 2012: Associate Specialist, Veteran

Affairs Medical Center, San Francisco CA

Northern

California Institute for Research&Education

. Established an in vitro model of metabolism regulated inflammation

in macrophage and microglia, identified CtBP as the metabolism

sensor regulating pro-inflammatory genes transcription.

. Characterized the first PNKD mouse model and dissected the genetic

interaction between PNKD and RIMS genes by behaviour studies and

immunohistology.

. Collaborated with Dr. Wooping Ge in the Jan Lab at UCSF on

electrophysiology and identified short-term plasticity changes in

the PNKD knockout mouse.

. Wrote a manuscript "A protein mutated in paroxysmal dyskinesia

suppresses synaptic vesicle exocytosis through the active zone

protein RIM" (Submitted to Neuron), and co-authored one

publication.

. Independently conceived and wrote half of an NIH R01 grant

proposal. The proposal was reviewed and revised by the time I left.

July, 2007 -June, 2010: DMRF Fellow, Dept. of Neurology, University

of California, San Francisco CA

. Identified the inhibitory role of PNKD in neurotransmitter release

through its association with pre-synaptic protein RIMS; illustrated

this through protein interaction, isolation and Mass Spectrometry,

synaptic component isolation, immune-gold Transmission Electronic

Microscopy, TIRF, etc.

. Collaborated with Dr. Yulong Li in Richard Tsien Lab and Dr. Pascal

Kaeser in Thomas Sudhof lab at Stanford University on synaptic-

physiology using real-time imaging of synaptic release.

. Wrote a manuscript "Mutations in PNKD Causing Paroxysmal

Dyskinesia Alters Protein Cleavage and Stability" (Human Molecular

Genetics 2011).

. Independently conceived and wrote a grant proposal for Bachmann

Strauss Dystonia & Parkinson Foundation. The proposal was approved

and funded for one year.

March, 2002 -June, 2007: Postdoctoral Fellow, Dept. of Neurology,

University of California, San Francisco CA

Howard Hughes Medical Institute

. Identified a point-mutation that causes cleavage fault and

subsequent protein stability fault in the human dyskinesia disease

gene PNKD.

. Analyzed the enzymatic activity of PNKD and collaborated with Dr.

Sunil Ojha in Patricia Babbitt lab at UCSF to simulate the

substrate binding motif and to screen possible compounds docking

through KEGG.

. Identified and characterized the transcription bi-regulator

activity of Atrophin proteins.

. Mouse forebrain development mutants screening and map-based cloning

of Megalin nonsense point mutation.

. Delivered 2 first-author (Journal of Biological Chemistry, Cellular

Molecular Life Sciences) and 2 co-author publications to help

secure research funding.

. Independently conceived and wrote a fellowship proposal for

Dystonia Medical Research Foundation. Proposal was approved and

funded for two years.

SELECTED PUBLICATIONS

1. Yiguo Shen, Angela Brennan, Yong Huang, Raymond Swanson. Bioenergetic

State Regulates the Inflammatory Response through NADH sensor CtBP

(Manuscript in Preparation).

2. Yiguo Shen, Wooping Ge, Yulong Li, Pascal Kaeser, Hsien-Yang Lee,

Richard Tsien, Thomas C. Sudhof, Lily Jan, Ying-Hui Fu, Louis J. Ptacek.

A protein mutated in paroxysmal dyskinesia suppresses synaptic vesicle

exocytosis through the active zone protein RIM (Submitted).

3. Tina Lam, Angela Brennan-Minnella, Seok Joon Won, Yiguo Shen, Colleen

Hefner, Yejie Shi, Dandan Sun, Raymond Swanson. Intracellular pH

reduction prevents excitotoxic and ischemic neuronal death by inhibiting

NADPH oxidase (In Revision).

4. Angela Brennan, Yiguo Shen, Raymond Swanson. Phosphoinositide 3-kinase

couples NMDA receptor activation to superoxide release and propagation

of excitotoxic injury. Cell Death and Disease. 2013, 4: e580.

5. Reno Reyes, Angela Brennan, Yiguo Shen, Ylva Baldwin, Raymond Swanson.

Activation of Neuronal NMDA Receptors Induces Superoxide-Mediated

Oxidative Stress in Neighboring Neurons and Astrocytes. Journal of

Neuroscience. 2012, 32:129**-*****.

6. Hsien-yang Lee, Junko Nakayama, Ying Xu, Xueliang Fan, Maha Karouani,

Yiguo Shen, Emmanuel N. Pothos, Ellen J. Hess, Ying-Hui Fu, Robert H.

Edwards and Louis J. Ptacek. Dopamine dysregulation in a mouse model of

paroxysmal nonkinesigenic dyskinesia. Journal of Clinical Investigation.

2012, 122:507-518.

7. Yiguo Shen, Hsien-Yang Lee, Joel Rawson, Sunil Ojha, Patricia Babbitt,

Ying-Hui Fu, and Louis J. Ptacek. Mutations in PNKD Causing Paroxysmal

Dyskinesia Alters Protein Cleavage and Stability. Human Molecular

Genetics. 2011, 20:2322-2332.

8. Yiguo Shen, Andrew S. Peterson. Atrophins, emerging roles in development

and neurodegenerative disease. Cellular and Molecular Life Sciences.

2009, 66:437 - 446.

9. Yiguo Shen, Gena Lee, Youngshik Choe, J. Susie Zoltewicz, Andrew S.

Peterson. Functional architecture of atrophins. Journal of Biological

Chemistry. 2007, 282: 5037-5044.

10. Scott R. May, Amir M. Ashique, Mattias Karlen, Baolin Wang, Yiguo Shen,

Konstantinos Zarbalis, Jeremy Reiter, Johan Ericson, Andrew S. Peterson.

Loss of the retrograde motor for IFT disrupts localization of Smo to

cilia and prevents the expression of both activator and repressor

functions of Gli. Developmental Biology. 2005, 287:378-389.

11. Konstantinos Zarbalis, Scott R. May, Yiguo Shen, Marc Ekker, John L. R.

Rubenstein, Andrew S. Peterson. A Focused and Efficient Genetic

Screening Strategy in the Mouse: Identification of Mutations That

Disrupt Cortical Development. PLoS Biology 2004, 2:1177-1187.

REFERENCES:

Dr. Andrew Peterson

Director, Department of Molecular Biology, Genentech

Tel: 650-***-****

Email: ********.******@****.***

Dr. Ziyin Li

Assistant Professor, Department of Microbiology and Molecular genetics,

Texas Medical Center

Tel: 281-***-****

Email: *****.**@***.***.***



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