5 research outputs found
Tamoxifen for prevention of breast cancer: extended long-term follow-up of the IBIS-I breast cancer prevention trial
- Author
- Abdi E
- Anderson E
- Atkinson C
- Baum M
- Beith J
- Bird A
- Birrell S
- Blamey R
- Blum R
- Boyages J
- Buser K
- Campbell I
- Cawthorn S
- Cawthorne Simon
- Chapman C
- Chipman M
- Coates A
- Collins J P
- Craft P
- Cuzick J
- Denton L
- Dewar J
- Dowsett M
- Earl H
- Eccles D
- Edwards R
- Evans G
- Fallowfield L
- Fentiman I
- Forbes J F
- Forbes John F
- Friedlander M
- Garcia J
- Gebski V
- George W
- Gilbert F J
- Godbolt P
- Goldhirsch A
- Hamed H
- Hanby A
- Hart S
- Hearne J
- Henry A
- Hirst C
- Holcombe C
- Holli Kaija
- Howell A
- Kealy R
- Kirk J
- Lansdown M
- Lee M
- Lennard T
- Lindsay D
- MacKay J
- MacMichael K
- MacNeil F
- Maddox P
- Mansel R
- McAleese P
- Melmeth A
- Mitine C
- Newton A
- Normand C
- Odling-Smee W
- Oivanen T
- Pagani O
- Paksec L
- Powles T
- Raytor Z
- Richmond B
- Robertson J
- Sainsbury R
- Sauven P
- Seccombe M
- Sestak Ivana
- Simes R J
- Stewart R
- Stotter A
- Thompson A
- Thornto R
- Toy J
- Twentyman P
- Underhill C
- Vergine Beata
- Ward R
- White S
- Wilkinson A
- Wilkinson S
- Williamson J
- Wynne C
- Publication venue
- 'Elsevier BV'
- Publication date
- 11/12/2014
- Field of study
© Cuzick et al. Open Access article distributed under the terms of CC BY.http://dx.doi.org/10.1016/S1470-2045(14)71171-
An Investigation into the Cognition Behind Spontaneous String Pulling in New Caledonian Crows
- Author
- A Reiner
- AAS Weir
- AAS Weir
- AH Taylor
- AH Taylor
- AH Taylor
- Alex H. Taylor
- B Heinrich
- B Heinrich
- B Heinrich
- B Osthaus
- C Plinius
- Colin Allen
- D Kirsh
- D Werdenich
- DR Brown
- Felipe S. Medina
- G Dücker
- G Rehkämper
- Gavin R. Hunt
- GR Hunt
- GR Hunt
- I Pepperberg
- J Piaget
- Jennifer C. Holzhaider
- Lindsay J. Hearne
- M Hauser
- M Wilson
- MA Vince
- NJ Emery
- NJ Emery
- Russell D. Gray
- RW Gibbs Jr
- U Seibt
- W Köhler
- Publication venue
- Public Library of Science
- Publication date
- 01/01/2010
- Field of study
The ability of some bird species to pull up meat hung on a string is a famous example of spontaneous animal problem solving. The “insight” hypothesis claims that this complex behaviour is based on cognitive abilities such as mental scenario building and imagination. An operant conditioning account, in contrast, would claim that this spontaneity is due to each action in string pulling being reinforced by the meat moving closer and remaining closer to the bird on the perch. We presented experienced and naïve New Caledonian crows with a novel, visually restricted string-pulling problem that reduced the quality of visual feedback during string pulling. Experienced crows solved this problem with reduced efficiency and increased errors compared to their performance in standard string pulling. Naïve crows either failed or solved the problem by trial and error learning. However, when visual feedback was available via a mirror mounted next to the apparatus, two naïve crows were able to perform at the same level as the experienced group. Our results raise the possibility that spontaneous string pulling in New Caledonian crows may not be based on insight but on operant conditioning mediated by a perceptual-motor feedback cycle
Reviews and bibliographical notices
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- Balfour Edward
- Ballard Edward
- Baly William
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- Coghlan John
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- Snow John
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- Tod David
- Tucker J. H.
- Watson Eben
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Edoxaban versus warfarin in patients with atrial fibrillation
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- Young C
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- Yukhno E
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- Zachar A
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- Zamorano JL
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- Zarpentin C
- Zateyshchikov D
- Zateyshchikova A
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- Zhang HQ
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- Zubeeva G
- Zyatenkova E
- Åkerberg A
- Östberg S
- Ŝpinar J
- Publication venue
- 'Massachusetts Medical Society'
- Publication date
- 01/01/2013
- Field of study
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125374.pdf (publisher's version ) (Open Access)BACKGROUND: Edoxaban is a direct oral factor Xa inhibitor with proven antithrombotic effects. The long-term efficacy and safety of edoxaban as compared with warfarin in patients with atrial fibrillation is not known. METHODS: We conducted a randomized, double-blind, double-dummy trial comparing two once-daily regimens of edoxaban with warfarin in 21,105 patients with moderate-to-high-risk atrial fibrillation (median follow-up, 2.8 years). The primary efficacy end point was stroke or systemic embolism. Each edoxaban regimen was tested for noninferiority to warfarin during the treatment period. The principal safety end point was major bleeding. RESULTS: The annualized rate of the primary end point during treatment was 1.50% with warfarin (median time in the therapeutic range, 68.4%), as compared with 1.18% with high-dose edoxaban (hazard ratio, 0.79; 97.5% confidence interval [CI], 0.63 to 0.99; P<0.001 for noninferiority) and 1.61% with low-dose edoxaban (hazard ratio, 1.07; 97.5% CI, 0.87 to 1.31; P=0.005 for noninferiority). In the intention-to-treat analysis, there was a trend favoring high-dose edoxaban versus warfarin (hazard ratio, 0.87; 97.5% CI, 0.73 to 1.04; P=0.08) and an unfavorable trend with low-dose edoxaban versus warfarin (hazard ratio, 1.13; 97.5% CI, 0.96 to 1.34; P=0.10). The annualized rate of major bleeding was 3.43% with warfarin versus 2.75% with high-dose edoxaban (hazard ratio, 0.80; 95% CI, 0.71 to 0.91; P<0.001) and 1.61% with low-dose edoxaban (hazard ratio, 0.47; 95% CI, 0.41 to 0.55; P<0.001). The corresponding annualized rates of death from cardiovascular causes were 3.17% versus 2.74% (hazard ratio, 0.86; 95% CI, 0.77 to 0.97; P=0.01), and 2.71% (hazard ratio, 0.85; 95% CI, 0.76 to 0.96; P=0.008), and the corresponding rates of the key secondary end point (a composite of stroke, systemic embolism, or death from cardiovascular causes) were 4.43% versus 3.85% (hazard ratio, 0.87; 95% CI, 0.78 to 0.96; P=0.005), and 4.23% (hazard ratio, 0.95; 95% CI, 0.86 to 1.05; P=0.32). CONCLUSIONS: Both once-daily regimens of edoxaban were noninferior to warfarin with respect to the prevention of stroke or systemic embolism and were associated with significantly lower rates of bleeding and death from cardiovascular causes. (Funded by Daiichi Sankyo Pharma Development; ENGAGE AF-TIMI 48 ClinicalTrials.gov number, NCT00781391.)