8 research outputs found
Characterization and Structure of Pineapple Stem Inhibitor of Cysteine Proteinases
- Publication venue
- 'Walter de Gruyter GmbH'
- Publication date
- Field of study
Structure-Function Relationship of Bromelain Isoinhibitors from Pineapple Stem
- Author
- Publication venue
- 'Walter de Gruyter GmbH'
- Publication date
- Field of study
Reduced Attentional Engagement Contributes to Deficits in Prefrontal Inhibitory Control in Schizophrenia
- Author
- Ammons
- Andreasen
- Andreasen
- Clementz
- Clementz
- Clementz
- Corbetta
- Cornblatt
- Curtis
- Dorris
- Everling
- Everling
- First
- Fischer
- Fukushima
- Funahashi
- Gooding
- Hamilton
- Harris
- Hutton
- Hutton
- James L. Reilly
- John A. Sweeney
- Johnston
- Keedy
- Keedy
- Margret S.H. Harris
- Matcheri S. Keshavan
- Matsue
- McDowell
- Moore
- Muller
- Munoz
- Munoz
- Nuechterlein
- Overall
- Perlstein
- Pierrot-Deseilligny
- Posner
- Reilly
- Salgado-Pineda
- Saslow
- Sereno
- Smyrnis
- Sweeney
- Sweeney
- Tin T. Khine
- Wang
- Weber
- Publication venue
- 'Elsevier BV'
- Publication date
- Field of study
Mucoid impaction of the bronchi in relation to asthma and plastic bronchitis
- Author
- A. D. Morgan
- A. M. W. ("mucoid
- Ash B.
- Ash B.
- Burgi H.
- Churchill Bettmann
- E. Keegan
- Gerrits J.C.
- Glynn A.A.
- Greer A.E.
- Harvey C.
- Huber H.L.
- Izzo R.A.
- Jezierski P.V.
- Johnson R.Sleigh
- Kee J.clin Path
- Keeley R.L.A.
- Leggat P. 0
- Lendrum A.C.
- Leopold J.G.
- Luke C.M.
- Malamud T.
- Mannes P.
- Merica F.W.
- Mulligan P.B.
- Naylor B.
- Nunzi A.
- Paulson D.L.
- Perlstein R.N.
- Rakower J.
- Rodenbaugh F.H.
- Sanerkin N.G.
- Shaw R.R.
- Sheehan V.A.
- Smith W.G.
- Spencer H.
- Trounce J.R.
- Tsai S.H.
- Urschel H.C.
- W. Bogomoletz
- Walker I.C.
- Waring W.W.
- Welsh R.A.
- Wilson W.
- Publication venue
- 'BMJ'
- Publication date
- Field of study
Representative Conducting Oxides
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- (4.132) A. Narath D.C. Barham
- A Alexandrov
- A Barone
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- A Ono
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- E
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- SE Barrett
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- See for example, F.C. Nix, W. Shockley
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- Y. Tokura
- Ya.G. Ponomarev B.A. Aminov, M.A. Hein, H. Heinrichs, V.Z. Kresin, G. MĂĽller, H. Piel, K. Rosner, S.V. Tchesnokov, E.B. Tsokur, D. Wehler, K. Winzer, A.V. Yaryagin
- YJ Uemura
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- Z Schlesinger
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- ZZ Sheng
- ZZ Sheng
- ZZ Wang
- Publication venue
- 'Springer Science and Business Media LLC'
- Publication date
- 01/01/2000
- Field of study
Enzyme Handbook
- Author
- 339-349
- [10]Siffert O., Emöd, I.
- [11] Fricker L.D., Snyder, S.H.
- [11] Taylor A., Volz, K.W., Lipscomb, W.N., Takemoto, L. J.
- [3] Schmidt U., Weller, D., Holder, A.
- [9]Fujiwara K., Tsuru, D.
- [hie J.N., Dure, L.S.
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- “ (Turk V., Neville, M.
- Publication venue
- 'Springer Science and Business Media LLC'
- Publication date
- 01/01/1991
- Field of study
Proteinase inhibitors and their function in plants: A review
- Author
- A. Benchekroun
- A. Favel
- A. Groover
- A. Heibges
- A. Heitz
- A. Ishikawa
- A. Lecardonnel
- A. Lyons
- A. Nagasue
- A. Ojima
- A. Polanowski
- A. Pusztai
- A. Ritonja
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- 'Springer Science and Business Media LLC'
- Publication date
- Field of study
Antiinflammatory therapy with canakinumab for atherosclerotic disease
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- Abaci F.
- Abbate A.
- Abdullakutty J.
- Abhaichand R.
- Abhyankar A.
- Abib E.Jr.
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- Publication venue
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- Field of study
BACKGROUND: Experimental and clinical data suggest that reducing inflammation without affecting lipid levels may reduce the risk of cardiovascular disease. Yet, the inflammatory hypothesis of atherothrombosis has remained unproved. METHODS: We conducted a randomized, double-blind trial of canakinumab, a therapeutic monoclonal antibody targeting interleukin-1β, involving 10,061 patients with previous myocardial infarction and a high-sensitivity C-reactive protein level of 2 mg or more per liter. The trial compared three doses of canakinumab (50 mg, 150 mg, and 300 mg, administered subcutaneously every 3 months) with placebo. The primary efficacy end point was nonfatal myocardial infarction, nonfatal stroke, or cardiovascular death. RESULTS: At 48 months, the median reduction from baseline in the high-sensitivity C-reactive protein level was 26 percentage points greater in the group that received the 50-mg dose of canakinumab, 37 percentage points greater in the 150-mg group, and 41 percentage points greater in the 300-mg group than in the placebo group. Canakinumab did not reduce lipid levels from baseline. At a median follow-up of 3.7 years, the incidence rate for the primary end point was 4.50 events per 100 person-years in the placebo group, 4.11 events per 100 person-years in the 50-mg group, 3.86 events per 100 person-years in the 150-mg group, and 3.90 events per 100 person-years in the 300-mg group. The hazard ratios as compared with placebo were as follows: in the 50-mg group, 0.93 (95% confidence interval [CI], 0.80 to 1.07; P=0.30); in the 150-mg group, 0.85 (95% CI, 0.74 to 0.98; P=0.021); and in the 300-mg group, 0.86 (95% CI, 0.75 to 0.99; P=0.031). The 150-mg dose, but not the other doses, met the prespecified multiplicity-adjusted threshold for statistical significance for the primary end point and the secondary end point that additionally included hospitalization for unstable angina that led to urgent revascularization (hazard ratio vs. placebo, 0.83; 95% CI, 0.73 to 0.95; P=0.005). Canakinumab was associated with a higher incidence of fatal infection than was placebo. There was no significant difference in all-cause mortality (hazard ratio for all canakinumab doses vs. placebo, 0.94; 95% CI, 0.83 to 1.06; P=0.31). CONCLUSIONS: Antiinflammatory therapy targeting the interleukin-1β innate immunity pathway with canakinumab at a dose of 150 mg every 3 months led to a significantly lower rate of recurrent cardiovascular events than placebo, independent of lipid-level lowering. Copyright © 2017 Massachusetts Medical Society