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HHS Recovery Act Recipient Reporting Readiness Tool

Step 4. Review and Copy the Grant Awards Data

TAGGS provides some – but not all – of the data needed for the Recipient Report. Recipients are responsible for directly collecting and reporting all required data to FederalReporting.gov. Data that HHS does not currently collect are highlighted in yellow. Do not copy this highlighted information. Please enter the appropriate data for your organization in these required fields. For assistance with entering these data please contact FederalReporting.gov.

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Award Detail for: SPECIFIC AMYLOID-BETA OLIGOMER APTAMERS
UNIVERSITY OF MINNESOTA, OFFICE OF STUDENT FINANCE AID
DUNS Number: 555917996
106 PLEASANT SE, 210 FRASER HL
MINNEAPOLIS, MN 55455
Recipient Report: Grant or Loan
Prime Recipient

Reporting Information
Award Type Award Number Final Report
Grant 1RC1AG035870-01 Recipient responsible for this data

Award Recipient Information
Recipient DUNS Number Recipient Account Number Recipient Congressional District
555917996 Recipient responsible for this data 5

Award Information
Funding Agency Code Awarding Agency Code Award Date
7529 7529 09-22-2009
Amount of Award Sub Account Number for Program Source (TAS)  
$ 369,833 Recipient responsible for this data
Program Source (TAS)* CFDA Number 
750845 93.701
Total Number of Sub Awards to Individuals Total Amount of Sub Awards to Individuals
Recipient responsible for this data Recipient responsible for this data
Total Number of Payments to Vendors less than $25,000/award Total Amount of Payments to Vendors less than $25,000/award
Recipient responsible for this data Recipient responsible for this data
Total Number of Sub Awards less than $25,000/award Total Amount of Sub Awards less than $25,000/award
Recipient responsible for this data Recipient responsible for this data
Award Description
DESCRIPTION (provided by applicant): The central focus of this proposal explores how to fill a technological gap - the detection of specific A¿ oligomers in living subjects. The development of new techniques for measuring specific A¿ oligomers in living individuals will enable us to investigate how long individuals that are producing A¿*56, A¿ dimers and A¿ trimers may live before clinically recognizable signs of AD emerge. This project may improve both our understanding of the processes that initiate AD and our ability to diagnose it in its earliest stages, by determining whether specific A¿ oligomers appear early enough in AD to become a target for therapies aimed at preventing the illness altogether. If successful, the work could benefit millions of people in America and the world. Recently, in collaboration with researchers at Rush University, we found that A¿*56 levels were elevated in many elderly individuals with no cognitive impairment who, presumably, would have developed AD had they lived longer. We also showed that distinct A¿ oligomers were elevated in different phases of the development and progression of AD. Other researchers have missed these intricate patterns in the rise and fall of distinct A¿ oligomers, because they used tests which measure A¿ oligomers in bulk, without distinguishing between distinct species. One test of our hypothesis, that A¿*56 initiates AD, is to observe the long-term consequences of A¿*56 in the brain. However, since we cannot monitor A¿*56 in the brains of living subjects, we will instead measure A¿*56 in readily accessible test specimens, preferably blood, but also spinal fluid. Using our current immunoblotting methods we can detect A¿*56 in brain and spinal fluid, but not in blood. This suggests that the levels of A¿*56 in blood are extremely low, or absent. However, there is indirect evidence in APP transgenic mice that A¿*56 is present in the blood. In the past few years, researchers in the laboratory of Dr. Srinand Sreevatsan developed DNA aptamers capable of detecting the scrapie isoform of the prion protein in the blood of scrapie-infected sheep, at levels far below the detection threshold of immunoblotting methods. Lately, researchers at the Mayo Clinic led by Dr. Ronald Petersen completed enrollment of nearly 2,000 elderly residents of Rochester, Minnesota, in a longitudinal study of genetic, biomarker, and imaging aspects of aging and very early cognitive problems, and have agreed to make spinal fluid and blood samples available to us. In this Challenge grant application, we propose to collaborate with Dr. Sreevatsan to develop DNA aptamers which detect specific A¿ oligomers, and to use these aptamers to measure distinct A¿ oligomers, including A¿*56, in the spinal fluid and blood of the Mayo Clinic cohort. PUBLIC HEALTH RELEVANCE: The central focus of this proposal explores how to fill a technological gap - the detection of specific A¿ oligomers in living subjects. The development of new techniques for measuring specific A¿ oligomers in living individuals will enable us to investigate how long individuals that are producing A¿*56, A¿ dimers and A¿ trimers may live before clinically recognizable signs of AD emerge. This project may improve both our understanding of the processes that initiate AD and our ability to diagnose it in its earliest stages, by determining whether specific A¿ oligomers appear early enough in AD to become a target for therapies aimed at preventing the illness altogether. If successful, the work could benefit millions of people in America and the world.

Project Information
Project Name or
Project/Program Title
Project Status Total Federal Amount ARRA Funds
Received/Invoiced
SPECIFIC AMYLOID-BETA OLIGOMER APTAMERS Recipient responsible for this data Recipient responsible for this data
Number of Jobs Description of Jobs Created
Recipient responsible for this data Recipient responsible for this data
Quarterly Activities/Project Description
Recipient responsible for this data
 
Activity Code (NAICS or NTEE-NPC)
1Recipient responsible for this data2Recipient responsible for this data
3Recipient responsible for this data4Recipient responsible for this data
5Recipient responsible for this data6Recipient responsible for this data
7Recipient responsible for this data8Recipient responsible for this data
9Recipient responsible for this data10Recipient responsible for this data
Total Federal Amount of ARRA
Expenditure
Total Federal ARRA
Infrastructure Expenditure
Infrastructure Contact Name
Recipient responsible for this data Recipient responsible for this data Recipient responsible for this data
Infrastructure Contact Email Infrastructure Contact Phone Infrastructure Contact Phone Ext.
Recipient responsible for this data Recipient responsible for this data Recipient responsible for this data
Infrastructure Contact Street Address 1 Infrastructure Contact Street Address 2 Infrastructure Contact Street Address 3
106 PLEASANT SE, 210 FRASER HL Not Available Recipient responsible for this data
Infrastructure City Infrastructure State Infrastructure ZIP Code+4
MINNEAPOLIS MN 55455
Infrastructure Purpose and Rationale
Recipient responsible for this data

Primary Place of Performance
Street Address 1 Street Address 2 City
2101 6TH ST SE Recipient responsible for this data MINNEAPOLIS
State Zip Code+4 Congressional District
MN 55455 5
Country  
US

Recipient Highly Compensated Officers
Prime Recipient Indication of Reporting Applicability # Officer Name Officer Compensation
Recipient responsible for this data 1 Recipient responsible for this data Recipient responsible for this data
2 Recipient responsible for this data Recipient responsible for this data
3 Recipient responsible for this data Recipient responsible for this data
4 Recipient responsible for this data Recipient responsible for this data
5 Recipient responsible for this data Recipient responsible for this data

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USE IN THE RECIPIENT REPORT

The information provided by this tool is baseline data that the Recipient should include in the Recipient Report that must be submitted to FederalReporting.gov beginning October 1, 2009. The data from this tool can be cut and pasted directly into the Recipient Report.