Qualcomm Sep 2012 - Oct 2015
Staff Pd Engineer
Broadcom Sep 2012 - Oct 2015
Principal Engineer, Physical Design
Toshiba America Electronic Components, Inc. Nov 1998 - Aug 2012
Staff Design Engineer
Education:
Purdue University 1994 - 1995
Masters, Master of Science In Electrical Engineering, Engineering
Wuhan University 1983 - 1987
Bachelors, Bachelor of Science, Electrical Engineering
Skills:
Ic Signal Integrity Timing Closure Soc Verilog Digital Signal Processors
Interests:
Children Environment Education Science and Technology Health
Lifesciences Data Analysis Biotechnology Bioinformatics Translational Medicine Tao Immunology Drug Development Biomarkers Statistics Biomarker Discovery Drug Discovery
Zeling Cai - San Diego CA, US Wei-Xing Shi - San Diego CA, US Xuejun P. Liu - San Diego CA, US Jiejun Wu - San Diego CA, US
Assignee:
Janssen Pharmaceutica N.V. - Beerse
International Classification:
A61K 39/00 C07K 14/00
US Classification:
4241841, 530300
Abstract:
Multiple myeloma (MM) is a clonal B cell malignancy and remains essentially incurable by conventional anti-tumor therapy. Patients with MM have a median survival of only three years. MM is characterized by proliferation and accumulation of mature plasma cells in the bone marrow (BM) leading to bone destruction, BM failure, anemia, and reduced immune function. The identification of MHC Class I, HLA-A2, associated peptides presented on multiple myeloma cells is an important step in developing immunotherapies for MM. Presented here are methods for creating activated T lymphocytes that are cytotoxic to both peptide loaded T2 target cells and multiple myeloma cell lines.
Identification Of Antigenic Peptides From Multiple Myeloma Cells
Zeling Cai - San Diego CA, US Wei-Xing Shi - San Diego CA, US Xuejun P. Liu - San Diego CA, US Jiejun Wu - San Diego CA, US
Assignee:
Janssen Pharmaceutica N.V. - Beerse
International Classification:
C12N 5/00 A61K 38/00 C07K 14/00
US Classification:
435375, 435405, 530327, 530328
Abstract:
Multiple myeloma (MM) is a clonal B cell malignancy and remains essentially incurable by conventional anti-tumor therapy. Patients with MM have a median survival of only three years. MM is characterized by proliferation and accumulation of mature plasma cells in the bone marrow (BM) leading to bone destruction, BM failure, anemia, and reduced immune function. The identification of MHC Class I, HLA-A2, associated peptides presented on multiple myeloma cells is an important step in developing immunotherapies for MM. Presented here are methods for creating activated T lymphocytes that are cytotoxic to both peptide loaded T2 target cells and multiple myeloma cell lines.
Identification Of Antigenic Peptides From Multiple Myeloma Cells
Zeling Cai - San Diego CA, US Wei-Xing Shi - San Diego CA, US Xuejun P. Liu - San Diego CA, US Jiejun Wu - San Diego CA, US
Assignee:
Janssen Pharmaceutica NV - Beerse
International Classification:
A61K 39/00 C07K 14/00
US Classification:
4241841, 530300
Abstract:
Multiple myeloma (MM) is a clonal B cell malignancy and remains essentially incurable by conventional anti-tumor therapy. Patients with MM have a median survival of only three years. MM is characterized by proliferation and accumulation of mature plasma cells in the bone marrow (BM) leading to bone destruction, BM failure, anemia, and reduced immune function. The identification of MHC Class I, HLA-A2, associated peptides presented on multiple myeloma cells is an important step in developing immunotherapies for MM. Presented here are methods for creating activated T lymphocytes that are cytotoxic to both peptide loaded T2 target cells and multiple myeloma cell lines.
Identification Of Antigenic Peptides From Multiple Myeloma Cells
Zeling Cai - San Diego CA, US Wei-Xing Shi - San Diego CA, US Xuejun P. Liu - San Diego CA, US Jiejun Wu - San Diego CA, US
Assignee:
Janssen Pharmaceutica NV - Beerse
International Classification:
C12N 5/00 C12N 5/08
US Classification:
435325, 435372
Abstract:
Multiple myeloma (MM) is a clonal B cell malignancy and remains essentially incurable by conventional anti-tumor therapy. Patients with MM have a median survival of only three years. MM is characterized by proliferation and accumulation of mature plasma cells in the bone marrow (BM) leading to bone destruction, BM failure, anemia, and reduced immune function. The identification of MHC Class I, HLA-A2, associated peptides presented on multiple myeloma cells is an important step in developing immunotherapies for MM. Presented here are methods for creating activated T lymphocytes that are cytotoxic to both peptide loaded T2 target cells and multiple myeloma cell lines.
Gene Expression Profiling Of Antidepressant Action In The Brain
Pascal Bonaventure - San Diego CA, US Hongqing Quo - San Diego CA, US Xuejun Liu - San Diego CA, US Fredrik Kamme - San Diego CA, US Bernhard Meurers - La Jolla CA, US Josepha Leysen - Oud-Turnhout, BE Margot Bakker - Breda, NL
International Classification:
A61K048/00 C12Q001/68 C12M001/34
US Classification:
514/044000, 435/006000, 435/287200
Abstract:
Implementing gene expression to study drug action in the central nervous system is complicated by functional heterogeneity because of the existence of many different neuronal subtypes within the mammalian brain. The integration of laser capture microdissection (LCM) and RNA amplification with cDNA microarray technology allows for large-scale gene expression analysis at cellular level. Using this approach, we have generated gene expression profiles of imipramine, a reference antidepressant, and a new putative antidepressant, novelR1 in several laser-captured brain nuclei (locus coeruleus, dorsal raphe, hypothalamic paraventricular nucleus and hippocampus) of rats subjected to the chronic mild stress model (CMS) of depression.
Methods And Systems Of Biomolecular Sequence Matching
Xiang Yao - San Diego CA, US Heng Dai - San Diego CA, US Albert Leung - San Diego CA, US Bin Tian - San Diego CA, US Wei Zhao - San Diego CA, US Xuejun Liu - San Diego CA, US Joseph Ciervo - San Diego CA, US Simon Smith - San Diego CA, US Jackson Wan - San Diego CA, US
International Classification:
G06F019/00 G01N033/48 G01N033/50
US Classification:
702/020000
Abstract:
The present invention relates to methods and systems for database comparison and database searching and matching, and specifically to database comparison and database searching and matching of databases containing biomolecular sequences as well as databases comprising matched sequences, as well as the use of databases comprising matched biomolecular sequences. In addition, a database comprising matched sequences or a database comprising matched biomolecular sequences may be accessed via a graphical user interface.
Methods And Algorithms For Performing Quality Control During Gene Expression Profiling On Dna Microarray Technology
Anton Bittner - Escondido CA, US Andrew Carmen - San Diego CA, US Albert Leung - San Diego CA, US Xuejun Liu - San Diego CA, US Simon Smith - San Diego CA, US Li Sun - Carlsbad CA, US Jackson Wan - San Diego CA, US Huinian Xiao - San Diego CA, US Xiang Yao - San Diego CA, US Lynn Yieh - San Diego CA, US
International Classification:
C12Q001/68 G06F019/00 G01N033/48 G01N033/50
US Classification:
435/006000, 702/020000
Abstract:
Methods and algorithms for quality control in gene expression profiling on DNA microarray technology are disclosed including methods and algorithms for assessing quality control of the printing of a DNA microarray, the preparation of an RNA sample, the labeling of probes, the hybridization between a DNA microarray and probes, the result of washing procedures, the result of scanning procedures, and for quantifying the gene expression data produced by imaging the hybridized DNA microarray.
Synthesis Of 4-Chlorokynurenines And Intermediates
The invention relates to an overall enantio-specific synthesis of 4-chlorokynurenine compounds, in particular L-4-chlorokynurenine, with improved yields. Large-scale syntheses are disclosed. The invention also relates to novel intermediates in the synthesis of L-4-chlorokynurenine.