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E Taioli

Showing results (71-80 of 124) with videos related to

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Biochemical and Biophysical Research Communications|February 13, 2001
Polymorphisms of drug-metabolizing enzymes in healthy nonagenarians and centenarians: difference at GSTT1 locusE Taioli, D Mari, C Franceschi, et al.
Environmental Health Perspectives|September 1, 1994
Occupational exposures to Cd, Ni, and Cr modulate titers of antioxidized DNA base autoantibodiesK Frenkel, J Karkoszka, B Cohen, et al.
European Journal of Neurology|January 26, 2007
Association of A313 G polymorphism (GSTP1*B) in the glutathione-S-transferase P1 gene with sporadic Parkinson's diseaseR Vilar, H Coelho, E Rodrigues, et al.
Clinical Transplants|September 30, 1999
Cadaver kidney allocation in the north Italy transplant program on the eve of the new millenniumG Sirchia, F Poli, M Cardillo, et al.
Minerva Anestesiologica|June 1, 2000
[Systemic and pulmonary vascular resistance in brain death]V Gravame, M Cardillo, G Paganoni, et al.
Leukemia Research|November 22, 2000
Deletion of parental GST genes as a possible susceptibility factor in the etiology of infant leukemiaS Garte, E Taioli, F Crosti, et al.
European Heart Journal|June 1, 1985
Role of blood pressure response to provocative tests in the prediction of hypertension in adolescentsM Radice, C Alli, F Avanzini, et al.
American Heart Journal|January 1, 1986
Left ventricular structure and function in normotensive adolescents with a genetic predisposition to hypertensionM Radice, C Alli, F Avanzini, et al.
Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association for Cancer Research, Cosponsored by the American Society of Preventive Oncology|February 10, 1998
Serum autoantibodies recognizing 5-hydroxymethyl-2'-deoxyuridine, an oxidized DNA base, as biomarkers of cancer risk in womenK Frenkel, J Karkoszka, T Glassman, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology|November 5, 1997
A common mutation in the methylenetetrahydrofolate reductase gene (C677T) increases the risk for deep-vein thrombosis in patients with mutant factor V (factor V:Q506)M Cattaneo, M Y Tsai, P Bucciarelli, et al.
Pageof 13

Showing results (71-80 of 124) with videos related to

Sort By:
Pageof 13
Biochemical and Biophysical Research Communications|February 13, 2001
Polymorphisms of drug-metabolizing enzymes in healthy nonagenarians and centenarians: difference at GSTT1 locusE Taioli, D Mari, C Franceschi, et al.
Environmental Health Perspectives|September 1, 1994
Occupational exposures to Cd, Ni, and Cr modulate titers of antioxidized DNA base autoantibodiesK Frenkel, J Karkoszka, B Cohen, et al.
European Journal of Neurology|January 26, 2007
Association of A313 G polymorphism (GSTP1*B) in the glutathione-S-transferase P1 gene with sporadic Parkinson's diseaseR Vilar, H Coelho, E Rodrigues, et al.
Clinical Transplants|September 30, 1999
Cadaver kidney allocation in the north Italy transplant program on the eve of the new millenniumG Sirchia, F Poli, M Cardillo, et al.
Minerva Anestesiologica|June 1, 2000
[Systemic and pulmonary vascular resistance in brain death]V Gravame, M Cardillo, G Paganoni, et al.
Leukemia Research|November 22, 2000
Deletion of parental GST genes as a possible susceptibility factor in the etiology of infant leukemiaS Garte, E Taioli, F Crosti, et al.
European Heart Journal|June 1, 1985
Role of blood pressure response to provocative tests in the prediction of hypertension in adolescentsM Radice, C Alli, F Avanzini, et al.
American Heart Journal|January 1, 1986
Left ventricular structure and function in normotensive adolescents with a genetic predisposition to hypertensionM Radice, C Alli, F Avanzini, et al.
Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association for Cancer Research, Cosponsored by the American Society of Preventive Oncology|February 10, 1998
Serum autoantibodies recognizing 5-hydroxymethyl-2'-deoxyuridine, an oxidized DNA base, as biomarkers of cancer risk in womenK Frenkel, J Karkoszka, T Glassman, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology|November 5, 1997
A common mutation in the methylenetetrahydrofolate reductase gene (C677T) increases the risk for deep-vein thrombosis in patients with mutant factor V (factor V:Q506)M Cattaneo, M Y Tsai, P Bucciarelli, et al.
Pageof 13