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David Cameron

Researcher at University of Oslo

Publications -  1765
Citations -  141776

David Cameron is an academic researcher from University of Oslo. The author has contributed to research in topics: Large Hadron Collider & Breast cancer. The author has an hindex of 154, co-authored 1586 publications receiving 126067 citations. Previous affiliations of David Cameron include Universidade Nova de Lisboa & Cameron International.

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Differential top-antitop cross-section measurements as a function of observables constructed from final-state particles using pp collisions at s√=7 TeV in the ATLAS detector

Georges Aad, +2920 more
TL;DR: In this article, various differential cross-sections are measured in top-quark pair (t (t) over bar) events produced in proton-proton collisions at a centre-of-mass energy of root s = 7 TeV at the LHC with the ATLAS detector.
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Search for direct stau production in events with two hadronic τ-leptons in s =13 TeV pp collisions with the ATLAS detector

Georges Aad, +2943 more
- 28 Feb 2020 - 
TL;DR: In this article, a search for the direct production of the supersymmetric partners of staus (staus) in final states with two hadronically decaying leptons is presented.
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Measurement of the top quark pair cross section with ATLAS in pp collisions at √{ s} = 7 TeV using final states with an electron or a muon and a hadronically decaying τ lepton

Georges Aad, +2867 more
- 22 Oct 2012 - 
TL;DR: In this article, the top quark pair cross section with ATLAS in pp collisions at root s = 7 TeV using final states with an electron or a muon and a hadronically decaying tau lepton.
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Measurement of the top quark mass in the tt → lepton+jets and tt → dilepton channels using √s = 7 TeV ATLAS data

Georges Aad, +2816 more
TL;DR: In this article, the top quark mass was measured in the channels t (t) over bar-to-lepton+jets and t (T) over lepton-b-jets (lepton = e, mu) based on ATLAS data recorded in 2011 at the LHC with a proton-proton center-of-mass energy of root s = 7 TeV and correspond to an integrated luminosity of 4.6 fb(-1).
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In situ detection of HER2:HER2 and HER2:HER3 protein-protein interactions demonstrates prognostic significance in early breast cancer.

TL;DR: It is demonstrated that in situ detection of HER2 and HER2:3 protein:protein complexes can be performed robustly and reproducibly in clinical specimens, provides novel prognostic information and opens a significant novel opportunity to probe the clinical impact of cellular signalling processes.