AARON OSBORNE, M.D., PH.D.
Osteopathic Medicine at Oakfield Dr, Brandon, FL

License number
Florida ME108215
Category
Osteopathic Medicine
Type
Emergency Medicine
Address
Address 2
119 Oakfield Dr, Brandon, FL 33511
18232 Clear Lake Dr, Lutz, FL 33548
Phone
(813) 571-5150
(813) 482-5599

Personal information

See more information about AARON OSBORNE at radaris.com
Name
Address
Phone
Aaron Osborne, age 42
440 Arizona Ave, Fort Lauderdale, FL 33312
(954) 306-6501
Aaron Osborne, age 52
10814 N Teegreen Rd, Tampa, FL 33612
Aaron Osborne
18232 Clear Lake Dr, Lutz, FL 33548
Aaron Osborne, age 70
440 Arizona Ave, Fort Lauderdale, FL 33312
(954) 581-1274
Aaron S Osborne
3620 3Rd St, Fort Lauderdale, FL 33311
(954) 585-2209

Professional information

See more information about AARON OSBORNE at trustoria.com
Aaron Osborne Photo 1
Dr. Aaron Osborne, Clearwater FL - MD (Doctor of Medicine)

Dr. Aaron Osborne, Clearwater FL - MD (Doctor of Medicine)

Specialties:
Emergency Medicine
Address:
EMCARE -SE REGION
18167 Us Highway 19 N SUITE 650, Clearwater 33764
(727) 507-2505 (Phone), (727) 507-3630 (Fax)
Emcare
119 Oakfield Dr, Brandon 33511
(800) 507-8874 (Phone)
Languages:
English
Education:
Medical School
University of South Florida / College of Medicine
Graduated: 2007


Aaron Osborne Photo 2
Aaron Osborne, Brandon FL

Aaron Osborne, Brandon FL

Specialties:
Emergency Medicine Physician
Address:
119 Oakfield Dr, Brandon, FL 33511


Aaron Osborne Photo 3
Assay For Transcriptionally Active Methylated Promoters

Assay For Transcriptionally Active Methylated Promoters

US Patent:
2007018, Aug 9, 2007
Filed:
Apr 16, 2007
Appl. No.:
11/735706
Inventors:
George Blanck - Tampa FL, US
Melissa Niesen - Tampa FL, US
Aaron Osborne - Lutz FL, US
Assignee:
UNIVERSITY OF SOUTH FLORIDA - Tampa FL
International Classification:
C12Q 1/68, C12Q 1/66
US Classification:
435006000, 435008000
Abstract:
A method of identifying genes that can be activated when methylated; as well as proteins that mediate such activation. The method allows identification of HLA-DRA silencing agents expected to be of therapeutic value in the treatment of inflammation associated with HLA-DRA expression.