The National Disease Research Interchange (NDRI) is the only not-for-profit organization supported by the NIH that provides a diverse collection of normal and diseased human biospecimens to biomedical researchers in academia, government and industry. The Human Tissue and Organ Research Resource (HTOR) of NDRI is an important resource to the biomedical research community because it provides high quality biospecimens, customized to researcher's requests, at an affordable cost. It is critical that HTOR expands its network of biospecimen acquisition sites to meet the increasing demands of researchers for human biospecimens for studies of both normal human physiology and the pathological basis of disease. This will be accomplished by, 1) communicating the HTOR mission and programs to the biomedical research community, as well as improving researcher application, protocol development and service delivery processes (Aim 1); 2) increasing the capacity and capability of the HTOR nationwide tissue acquisition network to procure and distribute greater quantities of high quality normal and disease human biospecimens of greater diversity (Aim 2); 3) maintaining HTOR compliance with current HHS, HIPAA and NIH guidelines and regulations governing donor consent, donor confidentiality, security of personal information, as well as HTOR personnel and researcher biohazard compliance (Aim 3); 4) expanding the National Rare Disease Biospecimen Resource and developing the National HIV Biospecimen Resource to provide greater service to the rare disease and HIV research communities, respectively (Aim 4), and 5) informing the government and scientific/lay public of the impact of HTOR-supported research projects on the biomedical research community and the resultant advances in medical research, as well as raising awareness of the value of human tissue donations for research (Aim 5). Implementation of this research plan will support the current trends in biomedical research that are placing greater emphasis on """"""""bench-to-bedside"""""""" translational research, biomarker development and pre-clinical drug development. ? ? ?
Pino, Christopher J; Westover, Angela J; Buffington, Deborah A et al. (2017) Bioengineered Renal Cell Therapy Device for Clinical Translation. ASAIO J 63:305-315 |
Westover, Angela J; Buffington, Deborah A; Johnston, Kimberly A et al. (2017) A bio-artificial renal epithelial cell system conveys survival advantage in a porcine model of septic shock. J Tissue Eng Regen Med 11:649-657 |
Dezzutti, Charlene S; Else, Laura J; Yandura, Sarah E et al. (2016) Distinct Pharmacodynamic Activity of Rilpivirine in Ectocervical and Colonic Explant Tissue. Antimicrob Agents Chemother 60:2765-70 |
Catterall, J B; Zura, R D; Bolognesi, M P et al. (2016) Aspartic acid racemization reveals a high turnover state in knee compared with hip osteoarthritic cartilage. Osteoarthritis Cartilage 24:374-81 |
Camci-Unal, Gulden; Newsome, David; Eustace, Brenda K et al. (2016) Fibroblasts Enhance Migration of Human Lung Cancer Cells in a Paper-Based Coculture System. Adv Healthc Mater 5:641-7, 626 |
Scott, Yanille M; Park, Seo Young; Dezzutti, Charlene S (2016) Broadly Neutralizing Anti-HIV Antibodies Prevent HIV Infection of Mucosal Tissue Ex Vivo. Antimicrob Agents Chemother 60:904-12 |
Wong, Marco D; Bingham, Karen; Moss, Emma et al. (2016) Recombinant Human Elastase Treatment of Cephalic Veins. Cardiovasc Pharm Open Access 5: |
Sroga, Gra?yna E; Wu, Ping-Cheng; Vashishth, Deepak (2015) Insulin-like growth factor 1, glycation and bone fragility: implications for fracture resistance of bone. PLoS One 10:e0117046 |
Myers, Meagan B; McKim, Karen L; Meng, Fanxue et al. (2015) Low-frequency KRAS mutations are prevalent in lung adenocarcinomas. Per Med 12:83-98 |
Sroga, Gra?yna E; Siddula, Alankrita; Vashishth, Deepak (2015) Glycation of human cortical and cancellous bone captures differences in the formation of Maillard reaction products between glucose and ribose. PLoS One 10:e0117240 |
Showing the most recent 10 out of 71 publications