Aug 2012 to 2000 Student Assistant to Cooperative Education & Internship OfficeKing Emmanuel Baptist Church Washington, DC Aug 2009 to Mar 2012 Audio/Video TechnicianKing Emmanuel Baptist Church Washington, DC Aug 2011 to Jan 2012 Food Service WorkerOffice of Exhibits Central Landover, MD Feb 2011 to May 2011 (Internship) Safety Administrative AssistantDC Summer Youth Program Washington, DC Jul 2009 to Jul 2010 Clerical Assistant, Department of Mental Health
Education:
MONTGOMERY COLLEGE Takoma Park, MD 2013 AASMCKINLEY TECHNOLOGY HIGH SCHOOL Washington, DC 2009 Diploma
Wyche T Coleman MD 1633 Marvel St, Coushatta, LA 71019 3189329980 (phone), 3189329906 (fax)
Education:
Medical School Louisiana State University School of Medicine at Shreveport Graduated: 2007
Languages:
English
Description:
Dr. Carter graduated from the Louisiana State University School of Medicine at Shreveport in 2007. He works in Coushatta, LA and specializes in Family Medicine. Dr. Carter is affiliated with Christus Coushatta Health Care Center.
Isbn (Books And Publications)
Soil Quality for Crop Production and Ecosystem Health
- Denver CO, US Richard Tobin - Aurora CO, US Nabanita Mukherjee - Aurora CO, US David Norris - Englewood CO, US Martin D.` Carter - Golden CO, US
International Classification:
A61K 31/519 A61K 39/395 A61K 31/635 A61P 35/00
Abstract:
Disclosed herein are methods for using therapeutic compounds, for example BH3 mimetics such as MCL1 inhibitors, to treat patients that may have failed to respond to targeted or immunotherapy treatments. In several embodiments, methods for treating such patients include combining MCL1 inhibitors with immunotherapies to enhance immunotherapy treatment. For example, the combination of MCL1 inhibitors with immunotherapies is used to treat cancer, such as melanoma. In some embodiments, MCL1 inhibitory compounds and therapies may be useful in treating tissues or tumors having one or more MDSC cell expressing high levels of MCL1. In some embodiments, MCL1 and BCL2 inhibitory compounds and therapies comprising same may be used to treat one or more melanomas, for example cutaneous melanoma, melanoma subtypes selected from uveal, acral, and mucosal. In some embodiments, MCL1 inhibitory compounds and therapies comprising same may be used to treat one or more melanomas, for example uveal melanoma. In many embodiments the targeted cells or tissues may not have BRAF mutations.