The highly interactive infrastructure of Administrative Core A will facilitate effective scientific, administrative and fiscal oversight for the two institutions that comprise the Midwest Sickle Cell Center. Specific functions include: 1) Execution of administrative and budgetary functions;2) Provide scientific leadership within the Midwest Sickle Cell Center through the combined efforts of the Project and Core Leaders (the Internal Advisory Committee) and the External Advisory Committee;3) Coordinate teleconferences and face-to-face meetings between the two sites comprising the Midwest Sickle Cell Center, as well as between the Midwest Sickle Cell Center and central Comprehensive Sickle Cell Center (CSCC) activities;and 4) Develop, maintain and support a public and private access website that is linked to the Statistics and Data Management Center (SDMC). The operation of the proposed Sickle Cell Summer for Science Program for High School Students will take advantage of the existing infrastructure of two unique and highly successful summer high school programs: Apprenticeship in Medicine (AIM), a diversity program in place at the Medical College of Wisconsin, and the Ferring Scholars Program, an intense 3-year, meritbased, scientific mentoring program operated at Washington University School of Medicine. Each program annually will recruit 2 highly motivated students (4 total) for the Sickle Cell Summer for Science Program to cultivate their interests in the health care field.

Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
Specialized Center--Cooperative Agreements (U54)
Project #
5U54HL090503-04
Application #
8261340
Study Section
Special Emphasis Panel (ZHL1)
Project Start
Project End
Budget Start
2011-04-01
Budget End
2012-03-31
Support Year
4
Fiscal Year
2011
Total Cost
$110,395
Indirect Cost
Name
Medical College of Wisconsin
Department
Type
DUNS #
937639060
City
Milwaukee
State
WI
Country
United States
Zip Code
53226
Larson, M C; Karafin, M S; Hillery, C A et al. (2017) Phosphatidylethanolamine is progressively exposed in RBCs during storage. Transfus Med 27:136-141
Brandow, Amanda M; Panepinto, Julie A (2016) Clinical Interpretation of Quantitative Sensory Testing as a Measure of Pain Sensitivity in Patients With Sickle Cell Disease. J Pediatr Hematol Oncol 38:288-93
Larson, Michael C (2015) Free-flow electrophoresis to clean donated blood before transfusion at the point of care: a proof-of-concept study. Blood Transfus 13:342-4
Beverung, Lauren M; Varni, James W; Panepinto, Julie A (2015) Clinically meaningful interpretation of pediatric health-related quality of life in sickle cell disease. J Pediatr Hematol Oncol 37:128-33
Wandersee, Nancy J; Maciaszek, Jamie L; Giger, Katie M et al. (2015) Dietary supplementation with docosahexanoic acid (DHA) increases red blood cell membrane flexibility in mice with sickle cell disease. Blood Cells Mol Dis 54:183-8
Ataga, Kenneth I; Hinderliter, Alan; Brittain, Julia E et al. (2015) Association of pro-inflammatory high-density lipoprotein cholesterol with clinical and laboratory variables in sickle cell disease. Hematology 20:289-96
Yan, Xiaocai; Yan, Mingfei; Guo, Yihe et al. (2015) R-Ras Regulates Murine T Cell Migration and Intercellular Adhesion Molecule-1 Binding. PLoS One 10:e0145218
Xu, Hao; Wandersee, Nancy J; Guo, YiHe et al. (2014) Sickle cell disease increases high mobility group box 1: a novel mechanism of inflammation. Blood 124:3978-81
Brandow, Amanda M; Farley, Rebecca A; Panepinto, Julie A (2014) Neuropathic pain in patients with sickle cell disease. Pediatr Blood Cancer 61:512-7
Panepinto, Julie A; Torres, Sylvia; Bendo, Cristiane B et al. (2014) PedsQLâ„¢ Multidimensional Fatigue Scale in sickle cell disease: feasibility, reliability, and validity. Pediatr Blood Cancer 61:171-7

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