Suny at Stony Brook
Professor
Stony Brook University
Professor
Education:
Columbia University In the City of New York 1982 - 1987
Skills:
Matlab C++ Powerpoint Physics Computer Science Teaching Statistics Algorithms R Programming Data Analysis Mathematica Statistical Modeling Research Machine Learning C
Web2Asia - Shanghai since Apr 2013
Graphic Design
SO-IL - Brooklyn Oct 2010 - Feb 2013
Communications Manager
Green Kids Media Jan 2012 - Apr 2012
Graphic Design
Emmis Communications Sep 2011 - Dec 2011
Graphic Design Intern
EDC | Center for Children and Technology Jun 2011 - Aug 2011
Graphic Design Intern
Education:
New York Institute of Technology-Old Westbury 2009 - 2011
BFA, Communication Arts
Skills:
Adobe Creative Suite Microsoft Office Mac OS X Final Cut Pro OS X InDesign Graphic Design
Languages:
English Chinese
Awards:
2012 Dean's Teach with Today’s Technology Challenge 1st Place The Dean's Teach with Today’s Technology Challenge is a challenge to School of Management (SoM) students to help them incorporate the newest and greatest Web 2.0 technologies into the curriculum. Our proposal integrated Web2.0 applications such as Twitter, Slideshare, YouTube, Facebook into a web interface at Wix.com to deliver knowledge content for the MGMT201 course. Interactive management games were also integrated into the content pages. The course content is portable to both Android and iOS based smart phones and also to tablets such as the iPad.
Xiamen University - Xiamen, Fujian, China since Jan 2012
Associate Professor
ISTC University of Illinois at Urbana-Champaign Apr 2010 - Dec 2011
Research Fellow
The Connecticut Agricultural Experiment Station Jun 2009 - Apr 2010
Post-doc
Education:
State University of New York at Stony Brook 2003 - 2009
Ph.D., Oceanography, Chemical and Physical
Xiamen University 2000 - 2003
M.S., Marine Chemistry
Xiamen University 1996 - 2000
B.S., Marine Chemistry
Us Patents
Compounds And Compositions As C-Kit Kinase Inhibitors
Vince YEH - San Diego CA, US Xiaolin LI - Emeryville CA, US Xiaodong LIU - San Diego CA, US Jon LOREN - San Diego CA, US Valentina MOLTENI - San Diego CA, US Juliet NABAKKA - San Diego CA, US Bao NGUYEN - San Diego CA, US Hank Michael James PETRASSI - Cardiff CA, US
The invention provides compounds and pharmaceutical compositions thereof, which are useful as protein kinase inhibitors, as well as methods for using such compounds to treat, ameliorate or prevent a condition associated with abnormal or deregulated kinase activity. In some embodiments, the invention provides methods for using such compounds to treat, ameliorate or prevent diseases or disorders that involve abnormal activation of c-kit or c-kit and PDGFR (PDGFRα, PDGFRβ) kinases.
Supramolecular Functionalization Of Graphitic Nanoparticles For Drug Delivery
Disclosed are nanoparticles, such as carbon nanotubes or other graphitic sheet materials having extended aromatic surfaces, which are used to deliver active agents such as drugs, labels or dyes (termed for convenience a “drug”) to the interior of cells. The nanoparticles are functionalized by a hydrophilic polymer or adsorption of an amphiphilic molecule to render them stable in suspension. The drug is therefore capable of release in the cell exterior. The drug is more rapidly released at lower pH, as found e.g., in tumor cells. The drug may also be linked to a branched chain hydrophilic polymer, so that each polymer molecule carries more than one drug bound by a cleavable linker.
- Basel, CH Xiaolin Li - Alameda CA, US Peichao Lu - Pleasant Hill CA, US Naomi Samadara Rajapaksa - Fremont CA, US David Charles Tully - Danville CA, US Xiaojing Michael Wang - Livermore CA, US Qian Zhao - Louisville CO, US
International Classification:
C07D 471/04 A61P 31/22
Abstract:
The invention provides compounds of Formula (I)as described herein, along with pharmaceutically acceptable salts, pharmaceutical compositions containing such compounds, and methods to use these compounds, salts and compositions for treating viral infections, particularly infections caused by herpesviruses.
- Basel, CH Xiaolin Li - Alameda CA, US Peichao Lu - Pleasant Hill CA, US Naomi Samadara Rajapaksa - Fremont CA, US David Charles Tully - Danville CA, US Xiaojing Michael Wang - Livermore CA, US Qian Zhao - Louisville CO, US
International Classification:
C07D 471/04 A61P 31/22
Abstract:
The invention provides compounds of Formula (I)as described herein, along with pharmaceutically acceptable salts, pharmaceutical compositions containing such compounds, and methods to use these compounds, salts and compositions for treating viral infections, particularly infections caused by herpesviruses.
Zhigan JIANG - Shanghai, CN Jianhua XIA - Shanghai, CN Haiying HE - Shanghai, CN - Basel, CH Xiaolin LI - Alameda CA, US Peichao LU - Pleasant Hill CA, US Wosenu MERGO - Oakland CA, US Daniel MUTNICK - Concord CA, US Folkert RECK - Walnut Creek CA, US Alexey RIVKIN - Emeryville CA, US Colin Keith SKEPPER - Alameda CA, US Xiaojing Michael WANG - Livermore CA, US Yongjin XU - Castro Valley CA, US
This invention is in the field of medicinal chemistry and relates to compounds, and pharmaceutical compositions thereof, that inhibit bacterial gyrase. The compounds are useful as inhibitors of bacterial gyrase activity and bacterial infections, and have the structure of Formula (I)as further described herein. The invention further provides pharmaceutical compositions comprising a compound of Formula (I) and methods of using the compounds and compositions to treat bacterial infections.
Jiping Fu - Danville CA, US Subramanian Karur - Dublin CA, US Xiaolin Li - Alameda CA, US Peichao Lu - Pleasant Hill CA, US Wosenu Mergo - Oakland CA, US Alexey Rivkin - Emeryville CA, US Zachary Kevin Sweeney - Redwood City CA, US Meiliana Tjandra - Dublin CA, US Andrew Weiss - San Francisco CA, US Aregahegn Yifru - Pleasant Hill CA, US
Assignee:
NOVARTIS AG - Basel
International Classification:
A61K 38/13 A61K 45/06 C07K 7/64
Abstract:
The present invention provides a compound of formula I;or a pharmaceutically acceptable salt thereof, wherein R, R, R, R, R, and A-B are as defined herein, which are non-immunosuppressive, cyclophilin-binding, mPTP blockers and are therefore useful for the prevention or treatment of diseases or disorders such as HCV infection, stroke, multiple sclerosis, HBV infection, HPV infection, asthma, cancer, muscular dystrophy, sepsis, ischemia/reperfusion injury, and heart failure.
Compounds And Compositions As C-Kit Kinase Inhibitors
Jon Loren - San Diego CA, US Xiaolin Li - Emeryville CA, US Xiaodong Liu - San Diego CA, US Valentina Molteni - San Diego CA, US Juliet Nabakka - San Diego CA, US Bao Nguyen - San Diego CA, US Hank Michael James Petrassi - Cardiff CA, US Vince Yeh - San Diego CA, US Paul Vincent Rucker - Carlsbad CA, US
The invention provides compounds and pharmaceutical compositions thereof, which are useful as protein kinase inhibitors, as well as methods for using such compounds to treat, ameliorate or prevent a condition associated with abnormal or deregulated kinase activity. In some embodiments, the invention provides methods for using such compounds to treat, ameliorate or prevent diseases or disorders that involve abnormal activation of c-kit or c-kit and PDGFR (PDGFRα, PDGFRβ) kinases.
Jiping Fu - Danville CA, US Subramanian Karur - Dublin CA, US Xiaolin Li - Alameda CA, US Peichao Lu - Pleasant Hill CA, US Wosenu Mergo - Oakland CA, US Alexey Rivkin - Emeryville CA, US Zachary Kevin Sweeney - Redwood City CA, US Meiliana Tjandra - Dublin CA, US Andrew Weiss - San Francisco CA, US Aregahegn Yifru - Pleasant Hill CA, US
The present invention provides a compound of formula I;or a pharmaceutically acceptable salt thereof, wherein the variables R, R, R, R, R, and A-B are defined herein, which are non-immunosuppresive, cyclophilin-binding, mPTP blockers and are therefore useful for the prevention or treatment of diseases or disorders such as HCV infection, stroke, multiple sclerosis, HBV infection, HPV infection, asthma, cancer, muscular dystrophy, sepsis, ischemia/reperfusion injury, and heart failure.