2005 — 2011 |
Amlaner, Charles Easton, Richard Powers, Susan (co-PI) [⬀] Williams, Robert (co-PI) [⬀] Jones, Elizabeth Brown, Elizabeth Beilfuss, Meredith Gatrell, Jay (co-PI) [⬀] |
N/AActivity Code Description: No activity code was retrieved: click on the grant title for more information |
The Robert Noyce Scholars Program At Indiana State University @ Indiana State University
The Robert Noyce Scholars Program at Indiana State University (ISU) is increasing the number and retention rate of licensed secondary school teachers in science and mathematics in high-need schools in the Indianapolis Public School system. Noyce Scholars are recruited from among transfer students entering ISU from two-year institutions, as well as from transitioning professionals with backgrounds in science and mathematics. Undergraduates receive scholarships to support their teacher training, and graduate students, entering ISU's Transition to Teaching program, receive stipends to offset the costs of attendance at ISU. Twenty-six future teachers are being trained and mentored in a well-established teacher education program, which builds on a long-standing partnership between ISU and the Professional Development Schools in the Indianapolis area. Students in the program take coursework that integrates both Indiana Academic Standards into content area training, as well as a problem-based learning approach to teaching science and mathematics. Noyce Scholars commit to teaching in the Indianapolis Public Schools for two years for each year of the scholarship. The intellectual merit of the project includes an evaluation of the effect of targeted teacher training for the urban environment as a strategy for transforming the urban setting into a learning tool for both students and teachers in training. ISU is also using its Noyce program to assess the value of problem-based learning in urban settings. The broader impacts include more and better STEM teachers and improved learning outcomes in an urban school district.
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0.94 |
2008 — 2012 |
Brown, Elizabeth |
P01Activity Code Description: For the support of a broadly based, multidisciplinary, often long-term research program which has a specific major objective or a basic theme. A program project generally involves the organized efforts of relatively large groups, members of which are conducting research projects designed to elucidate the various aspects or components of this objective. Each research project is usually under the leadership of an established investigator. The grant can provide support for certain basic resources used by these groups in the program, including clinical components, the sharing of which facilitates the total research effort. A program project is directed toward a range of problems having a central research focus, in contrast to the usually narrower thrust of the traditional research project. Each project supported through this mechanism should contribute or be directly related to the common theme of the total research effort. These scientifically meritorious projects should demonstrate an essential element of unity and interdependence, i.e., a system of research activities and projects directed toward a well-defined research program goal. |
A Genetic Risk Profile in Longitudinal Systemic Lupus Erythematosus (Sle) Cohorts @ University of Alabama At Birmingham
4H-Imidazol-4-one, 2-amino-1,5-dihydro-1-methyl-; ACR; Accounting; Active Follow-up; Address; Admixture; African; African American; Afro American; Afroamerican; Allele Frequency; American; American College of Radiology; Articulation; Autoimmune; Autoimmune Process; Biologic Marker; Biological Markers; Biostatistics Core; Black Populations; Black or African American; Blood Serum; CREA; Causality; Characteristics; Classification; Clinic; Clinical; Clinical Management; Collaborations; Complex; Condition; Coupled; Creatinine; Data; Development; Disease; Disease Progression; Disorder; ESRD; End stage renal failure; End-Stage Kidney Disease; Enrollment; Environment; Environmental Factor; Environmental Risk Factor; Epistasis; Epistasis, Genetic; Epistatic Deviation; Ethnic Origin; Ethnicity; Ethnicity aspects; Etiology; European; Evaluation; Evolution; Exhibits; Flare; Fostering; Foundations; GWAS; Gene Frequency; Genes; Genetic; Genetic Epistasis; Genetic Predisposition; Genetic Predisposition to Disease; Genetic Risk; Genetic Susceptibility; Genome; Glomerular Filtration Rate; Goals; Hispanic Americans; Hispanic Populations; Hispanics; Hispanics or Latinos; Human; Human, General; Individual; Infrastructure; Inherited Predisposition; Inherited Susceptibility; Institution; Interaction Deviation; International; Investigation; Joints; Kidney; Latino Population; Lupus; Lupus Erythematosus; Lupus Erythematosus Disseminatus; Lupus Erythematosus, Systemic; Lupus Glomerulonephritis; Lupus Nephritis; Man (Taxonomy); Man, Modern; Maps; Measures; Mediating; Mexico; Modeling; Molecular Marker; Morbidity; Morbidity - disease rate; Mortality; Mortality Vital Statistics; Musculoskeletal Pain Disorder; Natural History; North America; Organ; Outcome; P01 Mechanism; P01 Program; Patients; Persons; Phenotype; Population; Population Study; Prevalence; Principal Investigator; Program Project Grant; Program Research Project Grants; Programs (PT); Programs [Publication Type]; Proteins; Proteinuria; Puerto Rico; QTL; Quantitative Trait Loci; Race; Racial Group; Rate; Relative; Relative (related person); Renal Disease, End-Stage; Reporting; Research; Research Infrastructure; Research Program Projects; Rheumatic Diseases; Rheumatism; Risk; Risk Factors; SLE; SLE - Lupus Erythematosus, Systemic; Serum; Severities; Signature Molecule; Site; Socio-economic status; Socioeconomic Status; Spanish Americans; Spanish Origin; Statistical Methods; Status, Socioeconomic; Stocks, Racial; Structure; Systematics; Systemic Lupus Erythematosus; Systemic Lupus Erythmatosus; Testing; Texas; Therapeutic Intervention; Time; Urinary System, Kidney; Visit; abstracting; allelic frequency; base; biomarker; black American; cohort; cost; design; designing; disease causation; disease etiology; disease/disorder; disease/disorder etiology; disorder etiology; disseminated lupus erythematosus; enroll; environment effect on gene; environmental risk; ethnic minority; ethnic minority population; follow-up; gene environment interaction; gene product; gene x gene interaction; genetic epidemiology; genetic epistases; genetic etiology; genetic mechanism of disease; genetic vulnerability; genome sequencing; genome wide association scan; genome wide association studies; genome wide association study; genome-wide scan; genomewide association scan; genomewide association studies; genomewide association study; genomewide scan; health disparities; health disparity; hispanic community; indexing; insight; intervention therapy; low socioeconomic status; multidisciplinary; novel; prognostic; programs; prospective; racial and ethnic; racial/ethnic; renal; social; socioeconomic; socioeconomically; socioeconomics; systemic lupus erythematosis; time use; tool; trait; trend; whole genome association studies; whole genome association study
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0.931 |
2009 — 2015 |
Wallace, Carolyn Gonser, Rusty (co-PI) [⬀] Tuttle, Elaina (co-PI) [⬀] Seung, Eulsun Collins, Denise (co-PI) [⬀] Powers, Susan (co-PI) [⬀] Speer, James Brown, Elizabeth Gatrell, Jay (co-PI) [⬀] |
N/AActivity Code Description: No activity code was retrieved: click on the grant title for more information |
The Robert Noyce Scholars Program At Indiana State University: Phase Ii Scholarship & Stipend @ Indiana State University
This Phase II project is awarding forty-one scholarships to twenty- three students fulfilling the requirements to become secondary mathematics and science teachers. Undergraduate scholarship recipients are selected from eligible mathematics majors and those interested in seeking a double major of biology, chemistry or physics and science education. A third year of scholarship support is available to the double majors. Individuals with a prior STEM degree may receive a one-year scholarship. The Noyce Scholars are enrolled in a teacher preparation program utilizing innovative problem-based learning pedagogies and clinical field experiences in high needs settings.
Vigo County School Corporation, the fifth largest public school district in Indiana, has partnered with Indiana State University in the Professional Development Schools program for the past fourteen years. This school system with a mix of urban, suburban and rural areas provides a range of field experiences for the Noyce scholars. The close relationship between the university and the Vigo schools is exemplified by more than half the Vigo County school teachers holding a degree from Indiana State University.
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0.94 |
2021 |
Brown, Elizabeth |
K99Activity Code Description: To support the initial phase of a Career/Research Transition award program that provides 1-2 years of mentored support for highly motivated, advanced postdoctoral research scientists. |
The Neural Basis For Aging-Dependent Decline in Taste Function
PROJECT SUMMARY Deficits in chemosensory processing are associated with healthy aging, as well as numerous neurodegenerative disorders including Alzheimer?s Disease (AD). In many cases, chemosensory deficits are harbingers of neurodegenerative disease, and understanding the mechanistic basis for these changes may provide insight into fundamental dysfunction associated with aging and neurodegeneration. The genetic and physiological accessibility of chemosensory neurons and their defined higher order processing centers provide a unique opportunity to investigate the effects of aging-related processes on neural function, including sensory responsiveness, plasticity, and synaptic connectivity. The fruit fly, Drosophila melanogaster, is a powerful model for studying chemosensation, aging, and aging-related pathologies, yet the effects of aging on chemosensation remain largely unexplored in this model, particularly with respect to taste. A large genetic toolkit combined with functional imaging allow for cell-type specific manipulation of taste circuits. Numerous models of AD been developed in Drosophila that largely phenocopy two hallmarks of AD: amyloid beta (A?)-mediated toxicity and tauopathy caused by hyperphosphorylation of the Tau protein. My preliminary findings reveal that taste perception and taste memory deteriorate with age, and this is exacerbated in a fly model of AD. Here, I will examine the physiological and molecular basis for age-associated reduction in taste and taste memory in models of natural and pathological aging. These experiments build on my expertise in chemosensory processing and functional imaging, while providing training in aging and genomic approaches.
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0.951 |