The proposed training program seeks to continue to provide multidisciplinary postgraduate research training in academic nephrology to individuals who have previously earned M.D., and/or Ph.D. degrees. Individuals accepted into this program will spend three or more years in essentially full-time laboratory research. The program will be enriched with a regularly scheduled series of lectures and seminars; participants are also encouraged to enroll in some formal postgraduate course work within Harvard University. It is our belief that the most important component of the proposed program is the intense and virtually undisturbed involvement of trainees in ongoing research projects within the applicant institution, with close and continuous supervision provided by faculty preceptors who are themselves the recipients and principal investigators of NIH supported research programs. Emphasis will be placed on integration of basic and applied nephrology. The domain of training opportunities in basic research will include the physiological, cellular and molecular biological bases of solute and fluid exchanges across renal epithelia and endothelia, physiology and pharmacology of vasoactive hormones, the immunological and non-immunological mechanisms operating in renal diseases, and the immunobiology of transplantation. These basic approaches will also be applied, wherever possible, to clinically relevant areas of investigation, including the creation of animal models of deranged functions of the kidney; extensive of immunological techniques to better define T cell recognition of cell surface antigens, and subsequent gene activation systems that lead to inflammatory immune responses, or to tolerance; the nature and control of effector mechanisms in graft rejection in animal models and in human transplant recipients. Techniques represented include protein and nucleic acid biochemistry, molecular biology, cell and tissue culture, immunocytochemistry, membrane fractionation, electrophysiology, micropuncture, and whole animal procedures.

Agency
National Institute of Health (NIH)
Institute
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Type
Institutional National Research Service Award (T32)
Project #
2T32DK007527-18
Application #
6499708
Study Section
Diabetes, Endocrinology and Metabolic Diseases B Subcommittee (DDK)
Program Officer
Rankin, Tracy L
Project Start
1985-07-01
Project End
2007-06-30
Budget Start
2002-07-01
Budget End
2003-06-30
Support Year
18
Fiscal Year
2002
Total Cost
$325,525
Indirect Cost
Name
Brigham and Women's Hospital
Department
Type
DUNS #
071723621
City
Boston
State
MA
Country
United States
Zip Code
02115
Borges, Thiago J; Murakami, Naoka; Machado, Felipe D et al. (2018) March1-dependent modulation of donor MHC II on CD103+ dendritic cells mitigates alloimmunity. Nat Commun 9:3482
Garlo, Katherine G; White, William B; Bakris, George L et al. (2018) Kidney Biomarkers and Decline in eGFR in Patients with Type 2 Diabetes. Clin J Am Soc Nephrol 13:398-405
Kishi, Seiji; Minato, Masanori; Saijo, Atsuro et al. (2018) IgA Nephropathy after Nivolumab Therapy for Postoperative Recurrence of Lung Squamous Cell Carcinoma. Intern Med 57:1259-1263
Prochaska, Megan; Taylor, Eric; Ferraro, Pietro Manuel et al. (2018) Relative Supersaturation of 24-Hour Urine and Likelihood of Kidney Stones. J Urol 199:1262-1266
Uehara, Mayuko; Solhjou, Zhabiz; Banouni, Naima et al. (2018) Ischemia augments alloimmune injury through IL-6-driven CD4+ alloreactivity. Sci Rep 8:2461
Gupta, Navin; Susa, Koichiro; Yoda, Yoko et al. (2018) CRISPR/Cas9-based Targeted Genome Editing for the Development of Monogenic Diseases Models with Human Pluripotent Stem Cells. Curr Protoc Stem Cell Biol 45:e50
Murakami, Naoka; Ding, Yanli; Cohen, David J et al. (2018) Recurrent membranous nephropathy and acute cellular rejection in a patient treated with direct anti-HCV therapy (ledipasvir/sofosbuvir). Transpl Infect Dis 20:e12959
Hundemer, Gregory L; Curhan, Gary C; Yozamp, Nicholas et al. (2018) Cardiometabolic outcomes and mortality in medically treated primary aldosteronism: a retrospective cohort study. Lancet Diabetes Endocrinol 6:51-59
Feng, Di; Notbohm, Jacob; Benjamin, Ava et al. (2018) Disease-causing mutation in ?-actinin-4 promotes podocyte detachment through maladaptation to periodic stretch. Proc Natl Acad Sci U S A 115:1517-1522
Leon, Juliette; Pérez-Sáez, María José; Uffing, Audrey et al. (2018) Effect of Combined Gluten-Free, Dairy-Free Diet in Children With Steroid-Resistant Nephrotic Syndrome: An Open Pilot Trial. Kidney Int Rep 3:851-860

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