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Binhai Zheng

age ~54

from San Diego, CA

Also known as:
  • Bin Hai Zheng
  • Dinghai Zheng
  • I Zheng
Phone and address:
6324 Golden Lily Way, San Diego, CA 92130
858 792-0330

Binhai Zheng Phones & Addresses

  • 6324 Golden Lily Way, San Diego, CA 92130 • 858 792-0330
  • 4176 Calle Isabelino, San Diego, CA 92130
  • 400 Ortega Ave, Mountain View, CA 94040 • 650 965-8087
  • San Francisco, CA
  • Auburndale, MA
  • 1800 El Paseo St, Houston, TX 77054 • 713 799-8763
  • Pacifica, CA

Work

  • Company:
    San diego va health care syst
    Nov 2018
  • Position:
    Research biologist

Education

  • Degree:
    Doctorates, Doctor of Philosophy
  • School / High School:
    Baylor College of Medicine
    1994 to 1999
  • Specialities:
    Genetics, Philosophy

Skills

Molecular Biology • Neuroscience • Science • Research • Genetics

Industries

Research

Resumes

Binhai Zheng Photo 1

Research Biologist

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Location:
6324 Golden Lily Way, San Diego, CA 92101
Industry:
Research
Work:
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

    view source
  • US Patent:
    6395487, May 28, 2002
  • Filed:
    Apr 19, 2000
  • Appl. No.:
    09/552219
  • Inventors:
    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

    view source
  • US Patent:
    6461818, Oct 8, 2002
  • Filed:
    Apr 19, 2000
  • Appl. No.:
    09/552626
  • Inventors:
    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

    view source
  • US Patent:
    20030084467, May 1, 2003
  • Filed:
    Jul 30, 2002
  • Appl. No.:
    10/209615
  • Inventors:
    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

    view source
  • US Patent:
    60776676, Jun 20, 2000
  • Filed:
    Jun 26, 1997
  • Appl. No.:
    8/883616
  • Inventors:
    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

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  • 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

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  • 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
  • Date: May 04, 2011
  • Category: Health
  • Source: Google

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