Citations

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Showing 10 of 107969 citations.

Signal Peptide Peptidase:  Biochemical Properties and Modulation by Nonsteroidal Antiinflammatory Drugs
Nyborg, Andrew C., Iwata, Nobuhisa , Diehl, Thekla S., Golde, Todd E. , Sato, Toru , Saido, Takaomi C. , Wolfe, Michael S.

Biochemistry | June 27, 2006 | Volume: 45 | Issue: 28 | Pages: 8649-8656

10.1021/bi060597g | PMID 16834339 Get It

Impact of acute blood pressure variability on ischemic stroke outcome
Stead, L. G., Gilmore, R.M. , Vedula, K.C., Weaver, Amy L. , Decker, Wyatt W., Brown, Robert D. , Ganti, Latha , Stead, L. G.

Neurology | June 26, 2006 | Volume: 66 | Issue: 12 | Pages: 1878-1881

10.1212/01.wnl.0000219628.78513.b5 | PMID 16801654 Get It

Preventing Cardiovascular Disease and Diabetes
Eckel, Robert H. , Kahn, Richard , Robertson, Rose Marie , Rizza, Robert A.

Diabetes Care | June 26, 2006 | Volume: 29 | Issue: 7 | Pages: 1697-1699

10.2337/dc06-9911 | PMID 16801605 Get It

Physical training and metabolic supplementation reduce spontaneous atherosclerotic plaque rupture and prolong survival in hypercholesterolemic mice
Napoli, Claudio , Williams‐Ignarro, Sharon, Nigris, Filomena de , Lerman, Lilach O. , D’Armiento, Francesco Paolo , Crimi, Ettore , Byrns, Russell E., Casamassimi, Amelia , Lanza, Alessandro , Gombos, F, Sica, Vincenzo, Ignarro, Louis J.

Proceedings of the National Academy of Sciences | June 26, 2006 | Volume: 103 | Issue: 27 | Pages: 10479-10484

10.1073/pnas.0602774103 | PMID 16801544 Get It

Moderate physical exercise (PE) combined with metabolic treatment (MT) (antioxidants and l -arginine) are well known to reduce atherosclerotic lesion formation in hypercholesterolemic mice. However, the long-term beneficial effects on unstable atheroma remain poorly understood. We started early PE training in large groups of 6-week-old hypercholesterolemic mice (by graduated swimming) alone or in combination with nutritional supplementation (1.0% vitamin E added to the chow and 0.05% vitamin C and 6% l -arginine added to the drinking water). Inactive controls did not receive PE. The spontaneous development of atherosclerotic plaque rupture (associated with advanced atherosclerosis) and survival rates were evaluated. Moderate PE elicited an increase in plasma levels of nitric oxide. Early combined treatment with PE and MT in the hypercholesterolemic mice significantly reduced lesions (also detected noninvasively at 10 months) and spontaneous atherosclerotic plaque rupture and prolonged survival more effectively than each intervention alone. Thus, early concerted actions of MT and PE improve the natural history of atherosclerotic lesions and reduce the plaque instability in hypercholesterolemic mice.
A phase I study of chlorozotocin (NSC 178248)
Kovach, John S., Moertel, Charles G., Schutt, Allen J., Frytak, Stephen, Rubin, Joseph, O’Connell, Michael J. , Ingle, James N.

Cancer | June 26, 2006 | Volume: 43 | Issue: 6 | Pages: 2189-2196

10.1002/1097-0142(197906)43:6<2189::aid-cncr2820430605>3.0.co;2-# | PMID 156580 Get It

Estrogen replacement therapy withdrawal and regression of metastatic breast cancer
Dhodapkar, Madhav V. , Ahmann, David L., Ingle, James N.

Cancer | June 25, 2006 | Volume: 75 | Issue: 1 | Pages: 43-46

10.1002/1097-0142(19950101)75:1<43::aid-cncr2820750109>3.0.co;2-# | PMID 7804976 Get It

Primary reticulum‐cell sarcoma of bone
McCormack, Lawrence J., Ivins, John C., Dahlin, David C., Johnson, Einer W.

Cancer | June 24, 2006 | Volume: 5 | Issue: 6 | Pages: 1182-1192

10.1002/1097-0142(195211)5:6<1182::aid-cncr2820050615>3.0.co;2-# | PMID 12998025 Get It

Reactive Oxygen Species–Mediated Mitochondria-to-Nucleus Signaling: A Key to Aging and Radical-Caused Diseases
Störz, Peter

Science's STKE | June 24, 2006 | Volume: 2006 | Issue: 332 | Pages: No page available

10.1126/stke.3322006re3 | PMID 16639035 Get It

Mitochondria-generated reactive oxygen species have been implicated as a common feature that connects aging of organisms and age-related diseases. Efficient elimination of these radicals by antioxidants correlates with increased life span. Understanding how the mitochondrion signals to the nucleus to regulate antioxidant proteins might be a key to aging processes and treatment of human diseases.