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Susan Marie Byrne, 687 Bentley Ln, Kates Corner, MA 01824

Susan Byrne Phones & Addresses

7 Bentley Ln, Chelmsford, MA 01824    978-2561209   

Roy, UT   

Waltham, MA   

Belmont, MA   

Work

Position: Administration/Managerial

Education

Degree: Associate degree or higher

Mentions for Susan Marie Byrne

Career records & work history

Lawyers & Attorneys

Susan Byrne Photo 1

Susan Byrne - Lawyer

ISLN:
908617928
Admitted:
1986
University:
The University of Michigan, B.A., 1980
Law School:
The University of Toledo, J.D., 1986

Medicine Doctors

Susan M. Byrne

Specialties:
Psychiatry, Child & Adolescent Psychiatry
Work:
Child & Family Wellness Center
646 Main St, Port Jefferson, NY 11777
631-9818300 (phone) 631-9818400 (fax)
Languages:
English
Description:
Ms. Byrne works in Port Jefferson, NY and specializes in Psychiatry and Child & Adolescent Psychiatry.

License Records

Susan Beth Byrne

Licenses:
License #: 2014-000166 - Active
Category: Marriage and Family Therapy
Issued Date: Jun 12, 2014
Expiration Date: Jun 12, 2019
Type: ADC Intern

Susan Beth Byrne

Licenses:
License #: 2014-000166 - Active
Category: Marriage and Family Therapy
Issued Date: Jun 12, 2014
Expiration Date: Jun 12, 2019
Type: ADC Intern

Susan Beth Byrne

Licenses:
License #: 2014-000166 - Active
Category: Marriage and Family Therapy
Issued Date: Jun 12, 2014
Expiration Date: Jun 12, 2019
Type: ADC Intern

Publications & IP owners

Us Patents

Methods For Increasing Efficiency Of Nuclease-Mediated Gene Editing In Stem Cells

US Patent:
2019012, May 2, 2019
Filed:
Apr 19, 2017
Appl. No.:
16/094011
Inventors:
- Cambridge MA, US
Susan M. Byrne - Brookline MA, US
International Classification:
C12N 15/90
C12N 9/22
C12N 5/074
C12N 5/0793
C12N 5/0775
C12N 5/0735
Abstract:
Inhibiting p53 or Bax can be used to improve nuclease-mediated gene targeting frequencies in stem cells. This inhibition can be achieved, e.g., by overexpression of anti-apoptosis proteins or by silencing or reducing p53 or Bax expression. This technique can be used in conjunction with other rapidly developing CRISPR technologies, including improvements in specificity, other types of nucleases, and further enrichment, screening, and selection schemes, to expand the use of stem cells in experimental studies and tissue engineering for therapeutic purposes.

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