Clark Atlanta University proposes to develop and implement a program addressing the impetus of the NIGMS/MORE Research Initiative for Scientific Enhancement (RISE) for its undergraduate and graduate students in the biological sciences and chemistry. The undergraduate component of the RISE program will provide students with specific enrichment activities. These include: 1) pre-freshman college preparatory courses; 2) group recitation sessions for key first-year courses (e.g., General Biology, General Chemistry); 3) required tutorials for courses such as General Biology, General Chemistry, Physics and Pre- calculus; and 4) a weekly meeting (RISE seminar) where topics of discussion will include adapting to college life, the challenges of being a science major, and the career options in the sciences. These academic enrichment activities will change as the student progresses through their academic programs so that they are appropriate for the developmental phase of the student. The undergraduate component will also contain a research apprenticeship requirement starting in the post-freshman summer. This apprenticeship experience will include workshops on specific research techniques and assignment to a research mentor (starting in the sophomore year) for actual research performance and subsequent research presentation. The goals of the combined academic enhancement and research apprenticeship are to retain students in the science major track especially during the freshman year; to increase the number to students who apply to and are accepted into graduate school, and to increase the number of students who successfully complete Ph.D. degree programs in the biomedical sciences. The graduate component of the RISE program will offer some academic enrichment but will mainly center on increased exposure of the students to cutting edge research technology, exposure to some of the most notable biomedical scientists today, opportunities for these student to do research with productive scientists, to present their research at national meetings in their field and to publish their results in peer-reviewed journals. The goals of the graduate RISE program are to: 1) increase the number of student who complete their Ph.D. program; 2) increase the number of publications authored doctoral students and 3) increase the number of degree recipients who enter into post-doctoral training.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Education Projects (R25)
Project #
5R25GM060414-02
Application #
6315490
Study Section
Minority Programs Review Committee (MPRC)
Program Officer
Poodry, Clifton A
Project Start
1999-09-30
Project End
2003-09-29
Budget Start
2000-09-30
Budget End
2001-09-29
Support Year
2
Fiscal Year
2000
Total Cost
$711,847
Indirect Cost
Name
Clark Atlanta University
Department
Biology
Type
Schools of Arts and Sciences
DUNS #
065325177
City
Atlanta
State
GA
Country
United States
Zip Code
30314
Scarlett, Kisha A; White, El-Shaddai Z; Coke, Christopher J et al. (2018) Agonist-induced CXCR4 and CB2 Heterodimerization Inhibits G?13/RhoA-mediated Migration. Mol Cancer Res 16:728-739
Burton, Liza J; Henderson, Veronica; Liburd, Latiffa et al. (2017) Snail transcription factor NLS and importin ?1 regulate the subcellular localization of Cathepsin L and Cux1. Biochem Biophys Res Commun 491:59-64
Morton, Derrick J; Patel, Divya; Joshi, Jugal et al. (2017) ID4 regulates transcriptional activity of wild type and mutant p53 via K373 acetylation. Oncotarget 8:2536-2549
Kong, Gui-Mei; Yu, Min; Gu, Zhongping et al. (2017) Selective small-chemical inhibitors of protein arginine methyltransferase 5 with anti-lung cancer activity. PLoS One 12:e0181601
Nichols, India S; Jones, Mary I; Okere, Chuma et al. (2017) Nitrergic neurons of the dorsal raphe nucleus encode information about stress duration. PLoS One 12:e0187071
Coke, Christopher J; Scarlett, Kisha A; Chetram, Mahandranauth A et al. (2016) Simultaneous Activation of Induced Heterodimerization between CXCR4 Chemokine Receptor and Cannabinoid Receptor 2 (CB2) Reveals a Mechanism for Regulation of Tumor Progression. J Biol Chem 291:9991-10005
Vo, Baohan T; Morton Jr, Derrick; Komaragiri, Shravan et al. (2013) TGF-? effects on prostate cancer cell migration and invasion are mediated by PGE2 through activation of PI3K/AKT/mTOR pathway. Endocrinology 154:1768-79
Don-Salu-Hewage, Ayesha S; Chan, Siu Yuen; McAndrews, Kathleen M et al. (2013) Cysteine (C)-x-C receptor 4 undergoes transportin 1-dependent nuclear localization and remains functional at the nucleus of metastatic prostate cancer cells. PLoS One 8:e57194
Shashikala, H B Mihiri; Nicolas, Chantel I; Wang, Xiao-Qian (2012) Tunable Doping in Graphene by Light-Switchable Molecules. J Phys Chem C Nanomater Interfaces 116:26102-26105
Chetram, Mahandranauth A; Odero-Marah, Valerie; Hinton, Cimona V (2011) Loss of PTEN permits CXCR4-mediated tumorigenesis through ERK1/2 in prostate cancer cells. Mol Cancer Res 9:90-102

Showing the most recent 10 out of 14 publications