San Diego Va Health Care Syst
Research Biologist
University of California, San Diego - School of Medicine
Director, Microcopy Imaging Core
University of California, San Diego
Professor
Genentech Nov 2003 - Dec 2004
Research Associate
Stanford University Nov 2001 - Nov 2003
Postdoctoral Fellow
Education:
Baylor College of Medicine 1994 - 1999
Doctorates, Doctor of Philosophy, Genetics, Philosophy
University of Kentucky 1992 - 1994
Masters, Biology
Fudan University 1988 - 1992
Bachelors, Genetics
Skills:
Molecular Biology Neuroscience Science Research Genetics
Us Patents
Method Chromosomal Rearrangement By Consecutive Gene Targeting Of Two Recombination Substrates To The Deletion Endpoints
Allan Bradley - Houston TX Ramiro Ramirez-Solis - Missouri City TX Hong Su - Houston TX Binhai Zheng - Houston TX
Assignee:
Baylor College of Medicine - Houston TX
International Classification:
C12Q 168
US Classification:
435 6, 4353201, 435462, 536 231
Abstract:
The present invention involves the creation of defined chromosomal deficiencies, inversions and duplications using Cre recombinase in ES cells transmitted into the mouse germ line. These chromosomal reconstructions can extend up to 3-4 cM. Chromosomal rearrangements are the major cause of inherited human disease and fetal loss. Additionally, translocations and deletions are recognized as major genetic changes that are causally involved in neoplasia. Chromosomal variants such as deletions and inversions are exploited commonly as genetic tools in organisms such as Drosophila. Mice with defined regions of segmental haploidy are useful for genetic screening and allow accurate models of human chromosomal diseases to be generated.
Method For Chromosomal Rearrangement By Consecutive Gene Targeting Of Two Recombination Substrates To The Deletion Endpoints
Allan Bradley - Houston TX Ramiro Ramirez-Solis - Missouri City TX Hong Su - Houston TX Binhai Zheng - Houston TX
Assignee:
Baylor College of Medicine - Houston TX
International Classification:
C12Q 168
US Classification:
435 6, 4351723, 4353201
Abstract:
The present invention involves the creation of defined chromosomal deficiencies, inversions and duplications using Cre recombinase in ES cells transmitted into the mouse germ line. These chromosomal reconstructions can extend up to 3-4 cM. Chromosomal rearrangements are the major cause of inherited human disease and fetal loss. Additionally, translocations and deletions are recognized as major genetic changes that are causally involved in neoplasia. Chromosomal variants such as deletions and inversions are exploited commonly as genetic tools in organisms such as Drosophila. Mice with defined regions of segmental haploidy are useful for genetic screening and allow accurate models of human chromosomal diseases to be generated.
Method For Chromosomal Rearrangement By Consecutive Gene Targeting Of Two Recombination Substrates To The Deletion Endpoints
Allan Bradley - Houston TX, US Ramiro Ramirez-Solis - Missouri City TX, US Hong Su - Houston TX, US Binhai Zheng - Houston TX, US
Assignee:
BAYLOR - Houston TX
International Classification:
A01K067/027
US Classification:
800/018000, 800/021000
Abstract:
The present invention involves the creation of defined chromosomal deficiencies, inversions and duplications using Cre recombinase in ES cells transmitted into the mouse germ line. These chromosomal reconstructions can extend up to 3-4 cM. Chromosomal rearrangements are the major cause of inherited human disease and fetal loss. Additionally, translocations and deletions are recognized as major genetic changes that are causally involved in neoplasia. Chromosomal variants such as deletions and inversions are exploited commonly as genetic tools in organisms such as Drosophila. Mice with defined regions of segmental haploidy are useful for genetic screening and allow accurate models of human chromosomal disease to be generated.
Method For Chromosomal Rearrangement By Consecutive Gene Targeting Of Two Recombination Substrates To The Deletion Endpoints
Allan Bradley - Houston TX Ramiro Ramirez-Solis - Missouri City TX Hong Su - Houston TX Binhai Zheng - Houston TX
International Classification:
C12Q 168 C12N 163 C12N 1587 C07H 2104
US Classification:
435 6
Abstract:
The present invention involves the creation of defined chromosomal deficiencies, inversions and duplications using Cre recombinase in ES cells transmitted into the mouse germ line. These chromosomal reconstructions can extend up to 3-4 cM. Chromosomal rearrangements are the major cause of inherited human disease and fetal loss. Additionally, translocations and deletions are recognized as major genetic changes that are causally involved in neoplasia. Chromosomal variants such as deletions and inversions are exploited commonly as genetic tools in organisms such as Drosophila. Mice with defined regions of segmental haploidy are useful for genetic screening and allow accurate models of human chromosomal diseases to be generated.
Youtube
INDIANA CAPONE - The China Adventure Begins
MHS Videography Teacher Jeff Capone explores the Bin Hai Foreign Langu...
Category:
Entertainment
Uploaded:
10 May, 2010
Duration:
2m 52s
News
Neural stem cells regenerate axons in severe spinal cord injury
Additional contributors to the study include Yaozhi Wang, Lori Graham, Karla McHale, Mingyong Gao, Di Wu, John Brock, Armin Blesch, Ephron S. Rosenzweig, Binhai Zheng and James M. Conner, UCSD Department of Neurosciences; Leif A. Havton, UCLA Department of Neurology; and Martin Marsala, UCSD Departm
Date: Sep 13, 2012
Category: Health
Source: Google
Nearly 30 Percent of New CIRM Awards go to UC San Diego Stem Cell Researchers
A binding sites of these proteins, the researchers will evaluate the importance of alternative splicing in neurological disease modeling and stem cell biology ultimately leading to advances in drug discovery and toxicology testing.Binhai Zheng, PhD, associate professor, Department of Neurosciences, was awarded $1,355,063 for his work to generate and characterize corticospinal neurons from hESCs, which are damaged or severely compromised in patients of spinal cord injury and ALS. To aid in this process, he and his colBinhai Zheng, PhD, associate professor, Department of Neurosciences, was awarded $1,355,063 for his work to generate and characterize corticospinal neurons from hESCs, which are damaged or severely compromised in patients of spinal cord injury and ALS. To aid in this process, he and his colleagues