721 research outputs found
The Evolution of Compact Binary Star Systems
- Author
- A Ahmad
- A Blaauw
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- Z-W Liu
- ZW Liu
- ÉÉ Flanagan
- Publication venue
- 'Living Reviews'
- Publication date
- 03/01/2007
- Field of study
We review the formation and evolution of compact binary stars consisting of
white dwarfs (WDs), neutron stars (NSs), and black holes (BHs). Binary NSs and
BHs are thought to be the primary astrophysical sources of gravitational waves
(GWs) within the frequency band of ground-based detectors, while compact
binaries of WDs are important sources of GWs at lower frequencies to be covered
by space interferometers (LISA). Major uncertainties in the current
understanding of properties of NSs and BHs most relevant to the GW studies are
discussed, including the treatment of the natal kicks which compact stellar
remnants acquire during the core collapse of massive stars and the common
envelope phase of binary evolution. We discuss the coalescence rates of binary
NSs and BHs and prospects for their detections, the formation and evolution of
binary WDs and their observational manifestations. Special attention is given
to AM CVn-stars -- compact binaries in which the Roche lobe is filled by
another WD or a low-mass partially degenerate helium-star, as these stars are
thought to be the best LISA verification binary GW sources.Comment: 105 pages, 18 figure
Search for new phenomena in final states with an energetic jet and large missing transverse momentum in pp collisions at √ s = 8 TeV with the ATLAS detector
- Author
- Aad G
- Abbott B
- Abbott DC
- Abeling K
- Abhayasinghe DK
- Abidi SH
- AbouZeid OS
- Abraham NL
- Abramowicz H
- Abreu H
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- Abulaiti Y
- Acharya BS
- Achkar B
- Adachi S
- Adam L
- Adamczyk L
- Adamek L
- Adelman J
- Adersberger M
- Adiguzel A
- Adorni S
- Adye T
- Affolder AA
- Afik Y
- Agapopoulou C
- Agaras MN
- Aggarwal A
- Agheorghiesei C
- Aguilar-Saavedra JA
- Ahmadov F
- Ahmed WS
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- Aielli G
- Akatsuka S
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- Al Khoury K
- Alberghi GL
- Albert J
- Alderweireldt S
- Aleksa M
- Aleksandrov IN
- Alexa C
- Alexopoulos T
- Alfonsi A
- Alfonsi F
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- Ali B
- Aliev M
- Alimonti G
- Allaire C
- Allbrooke BMM
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- Zou R
- Zu Theenhausen HM
- Zwalinski L
- Publication venue
- 'Springer Science and Business Media LLC'
- Publication date
- 01/01/2015
- Field of study
Results of a search for new phenomena in final states with an energetic jet and large missing transverse momentum are reported. The search uses 20.3 fb−1 of √ s = 8 TeV data collected in 2012 with the ATLAS detector at the LHC. Events are required to have at least one jet with pT > 120 GeV and no leptons. Nine signal regions are considered with increasing missing transverse momentum requirements between Emiss T > 150 GeV and Emiss T > 700 GeV. Good agreement is observed between the number of events in data and Standard Model expectations. The results are translated into exclusion limits on models with either large extra spatial dimensions, pair production of weakly interacting dark matter candidates, or production of very light gravitinos in a gauge-mediated supersymmetric model. In addition, limits on the production of an invisibly decaying Higgs-like boson leading to similar topologies in the final state are presente
Measurement of the cross-section of high transverse momentum vector bosons reconstructed as single jets and studies of jet substructure in pp collisions at √s = 7 TeV with the ATLAS detector
- Author
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- Abdallah J
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- Zhemchugov A
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- Zobernig G
- Zoccoli A
- Zurzolo G
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- Publication venue
- 'IOP Publishing'
- Publication date
- 01/01/2014
- Field of study
This paper presents a measurement of the cross-section for high transverse momentum W and Z bosons produced in pp collisions and decaying to all-hadronic final states. The data used in the analysis were recorded by the ATLAS detector at the CERN Large Hadron Collider at a centre-of-mass energy of √s = 7 TeV;{\rm Te}{\rm V}andcorrespondtoanintegratedluminosityof4.6\;{\rm f}{{{\rm b}}^{-1}}.ThemeasurementisperformedbyreconstructingtheboostedWorZbosonsinsinglejets.ThereconstructedjetmassisusedtoidentifytheWandZbosons,andajetsubstructuremethodbasedonenergyclusterinformationinthejetcentre−of−massframeisusedtosuppressthelargemulti−jetbackground.Thecross−sectionforeventswithahadronicallydecayingWorZboson,withtransversemomentum{{p}_{{\rm T}}}\gt 320\;{\rm Ge}{\rm V}andpseudorapidity|\eta |\lt 1.9,ismeasuredtobe{{\sigma }_{W+Z}}=8.5\pm 1.7$ pb and is compared to next-to-leading-order calculations. The selected events are further used to study jet grooming techniques
Search for direct pair production of the top squark in all-hadronic final states in proton-proton collisions at s√=8 TeV with the ATLAS detector
- Author
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- Abbott B
- Abdallah J
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- Zhemchugov A
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- Zimine NI
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- Zoccoli A
- zur Nedden M
- Zurzolo G
- Zutshi V
- Zwalinski L
- Publication venue
- 'Springer Science and Business Media LLC'
- Publication date
- 01/01/2014
- Field of study
The results of a search for direct pair production of the scalar partner to the top quark using an integrated luminosity of 20.1fb−1 of proton–proton collision data at √s = 8 TeV recorded with the ATLAS detector at the LHC are reported. The top squark is assumed to decay via t˜→tχ˜01 or t˜→ bχ˜±1 →bW(∗)χ˜01 , where χ˜01 (χ˜±1 ) denotes the lightest neutralino (chargino) in supersymmetric models. The search targets a fully-hadronic final state in events with four or more jets and large missing transverse momentum. No significant excess over the Standard Model background prediction is observed, and exclusion limits are reported in terms of the top squark and neutralino masses and as a function of the branching fraction of t˜ → tχ˜01 . For a branching fraction of 100%, top squark masses in the range 270–645 GeV are excluded for χ˜01 masses below 30 GeV. For a branching fraction of 50% to either t˜ → tχ˜01 or t˜ → bχ˜±1 , and assuming the χ˜±1 mass to be twice the χ˜01 mass, top squark masses in the range 250–550 GeV are excluded for χ˜01 masses below 60 GeV
Search for pair-produced long-lived neutral particles decaying to jets in the ATLAS hadronic calorimeter in ppcollisions at √s=8TeV
- Author
- Aad G
- Abbott B
- Abdallah J
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- Sundermann JE
- Suruliz K
- Susinno G
- Sutton MR
- Suzuki Y
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- Swedish S
- Swiatlowski M
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- Sykora T
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- Taenzer J
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- Takai H
- Takashima R
- Takeda H
- Takeshita T
- Takubo Y
- Talby M
- Talyshev AA
- Tam JYC
- Tan KG
- Tanaka J
- Tanaka R
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- Tanaka S
- Tanasijczuk AJ
- Tannenwald BB
- Tannoury N
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- Tarem S
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- Thomas JP
- Thomas-Wilsker J
- Thompson AS
- Thompson EN
- Thompson PD
- Thompson PD
- Thompson RJ
- Thomsen LA
- Thomson E
- Thomson M
- Thong WM
- Thun RP
- Tian F
- Tibbetts MJ
- Tikhomirov VO
- Tikhonov YA
- Timoshenko S
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- Tisserant S
- Todorov T
- Todorova-Nova S
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- Touchard F
- Tovey DR
- Tran HL
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- Tremblet L
- Tricoli A
- Trigger IM
- Trincaz-Duvoid S
- Tripiana MF
- Trischuk W
- Trocme B
- Troncon C
- Trottier-McDonald M
- Trovatelli M
- True P
- Trzebinski M
- Trzupek A
- Tsarouchas C
- Tseng JC-L
- Tsiareshka PV
- Tsionou D
- Tsipolitis G
- Tsirintanis N
- Tsiskaridze S
- Tsiskaridze V
- Tskhadadze EG
- Tsukerman I
- Tsulaia V
- Tsuno S
- Tsybychev D
- Tudorache A
- Tudorache V
- Tuna AN
- Tupputi SA
- Turchikhin S
- Turecek D
- Turra R
- Tuts PM
- Tykhonov A
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- Tyndel M
- Uchida K
- Ueda I
- Ueno R
- Ughetto M
- Ugland M
- Uhlenbrock M
- Ukegawa F
- Unal G
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- Ungaro FC
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- Usai G
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- Vachon B
- Valencic N
- Valentinetti S
- Valero A
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- Van Den Wollenberg W
- Van Der Deijl PC
- van der Geer R
- van der Graaf H
- Van Der Leeuw R
- van der Ster D
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- Van Gemmeren P
- van Huysduynen LH
- Van Nieuwkoop J
- van Vulpen I
- Van Woerden MC
- Vanadia M
- Vandelli W
- Vanguri R
- Vaniachine A
- Vankov P
- Vannucci F
- Vaque FV
- Vardanyan G
- Vari R
- Varnes EW
- Varol T
- Varouchas D
- Vartapetian A
- Varvell KE
- Vazeille F
- Vazquez JGP
- Veatch J
- Veloso F
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- Veneziano S
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- Vercesi V
- Verducci M
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- Vermeulen JC
- Verzini MJA
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- Vetterli MC
- Viazlo O
- Vichou I
- Vickey T
- Viehhauser GHA
- Viel S
- Vigne R
- Villa M
- Vilucchi E
- Vincter MG
- Vinogradov VB
- Virzi J
- Vivarelli I
- Vlachos S
- Vladoiu D
- Vlasak M
- Vogel A
- Vokac P
- Volpi G
- Volpi M
- von der Schmitt H
- von Radziewski H
- von Toerne E
- Vorobel V
- Vorobev K
- Vos M
- Voss R
- Vossebeld JH
- Vranjes N
- Vrba V
- Vreeswijk M
- Vuanh T
- Vuillermet R
- Vukotic I
- Vykydal Z
- Wagner P
- Wagner W
- Wahlberg H
- Wahrmund S
- Wakabayashi J
- Walder J
- Walker R
- Walkowiak W
- Wall R
- Waller P
- Walls FMG
- Walsh B
- Wang C
- Wang C
- Wang F
- Wang H
- Wang H
- Wang J
- Wang J
- Wang K
- Wang R
- Wang SM
- Wang T
- Wang X
- Wanotayaroj C
- Warburton A
- Ward CP
- Wardrope DR
- Warsinsky M
- Washbrook A
- Wasicki C
- Watkins PM
- Watson AT
- Watson IJ
- Watson MF
- Watts G
- Watts S
- Waugh BM
- Webb S
- Weber MS
- Weber SW
- Webster JS
- Weidberg AR
- Weigell P
- Weinert B
- Weingarten J
- Weiser C
- Weits H
- Wells PS
- Wemans ADV
- Wenaus T
- Wendland D
- Weng Z
- Wengler T
- Wenig S
- Wermes N
- Werner M
- Werner P
- Wessels M
- Wetter J
- Whalen K
- White A
- White MJ
- White R
- White S
- Whiteson D
- Wicke D
- Wickens FJ
- Wiedenmann W
- Wielers M
- Wienemann P
- Wiglesworth C
- Wiik-Fuchs LAM
- Wijeratne PA
- Wildauer A
- Wildt MA
- Wilkens HG
- Will JZ
- Williams HH
- Williams S
- Willis C
- Willocq S
- Wilson A
- Wilson JA
- Wingerter-Seez I
- Winklmeier F
- Winter BT
- Wittgen M
- Wittig T
- Wittkowski J
- Wollstadt SJ
- Wolter MW
- Wolters H
- Wong KHY
- Wosiek BK
- Wotschack J
- Woudstra MJ
- Wozniak KW
- Wright M
- Wu M
- Wu SL
- Wu X
- Wu Y
- Wulf E
- Wyatt TR
- Wynne BM
- Xella S
- Xiao M
- Xu D
- Xu L
- Yabsley B
- Yacoob S
- Yakabe R
- Yamada M
- Yamaguchi H
- Yamaguchi Y
- Yamamoto A
- Yamamoto K
- Yamamoto S
- Yamamura T
- Yamanaka T
- Yamauchi K
- Yamazaki Y
- Yan Z
- Yang H
- Yang H
- Yang UK
- Yang Y
- Yanush S
- Yao L
- Yao W-M
- Yasu Y
- Yatsenko E
- Ye J
- Ye S
- Yeletskikh I
- Yen AL
- Yildirim E
- Yildiz HD
- Yilmaz M
- Yoosoofmiya R
- Yorita K
- Yoshida R
- Yoshihara K
- Young C
- Young CJS
- Youssef S
- Yu DR
- Yu J
- Yu J
- Yu JM
- Yuan L
- Yurkewicz A
- Yusuff I
- Zabinski B
- Zaidan R
- Zaitsev AM
- Zaman A
- Zambito S
- Zanello L
- Zanzi D
- Zeitnitz C
- Zeman M
- Zemla A
- Zengel K
- Zenin O
- Zenis T
- Zerwas D
- Zhang D
- Zhang F
- Zhang H
- Zhang J
- Zhang L
- Zhang X
- Zhang Z
- Zhao Z
- Zhemchugov A
- Zhong J
- Zhou B
- Zhou L
- Zhou N
- Zhu CG
- Zhu H
- Zhu J
- Zhu Y
- Zhuang X
- Zhukov K
- Zibell A
- Zieminska D
- Zimine NI
- Zimmermann C
- Zimmermann R
- Zimmermann S
- Zimmermann S
- Zinonos Z
- Ziolkowski M
- Zobernig G
- Zoccoli A
- zur Nedden M
- Zurzolo G
- Zutshi V
- Zwalinski L
- Publication venue
- 'Elsevier BV'
- Publication date
- 01/01/2014
- Field of study
The ATLAS detector at the Large Hadron Collider at CERN is used to search for the decay of a scalar boson to a pair of long-lived particles, neutral under the Standard Model gauge group, in 20.3fb−1of data collected in proton–proton collisions at √s=8TeV. This search is sensitive to long-lived particles that decay to Standard Model particles producing jets at the outer edge of the ATLAS electromagnetic calorimeter or inside the hadronic calorimeter. No significant excess of events is observed. Limits are reported on the product of the scalar boson production cross section times branching ratio into long-lived neutral particles as a function of the proper lifetime of the particles. Limits are reported for boson masses from 100 GeVto 900 GeV, and a long-lived neutral particle mass from 10 GeVto 150 GeV
The biopsychosocial model and chiropractic: a commentary with recommendations for the chiropractic profession
- Author
- A Ramond
- A Rooij de
- A Tsang
- BE Thorn
- BJ Palmer
- BK Humphreys
- BN Green
- C Hawk
- C Hawk
- C Johnson
- C Johnson
- C Johnson
- C Leboeuf-Yde
- C Sitges
- D Kopansky-Giles
- D Kopansky-Giles
- DH Novack
- DJ Gaskin
- DR Noll
- DT Wade
- FW Peabody
- G Goncalves
- G Kok
- G Waddell
- GBD 2015 Disease and Injury and Prevalence Collaborators
- GJY Peters
- GL Engel
- HT Ndetan
- I Axen
- ID Coulter
- IM Rosenstock
- JA Hayden
- JC Keating Jr
- JR Field
- KA Parish
- LT Moller
- MA Kaeser
- MW Evans
- MW Evans Jr
- R Russell
- RD Kerns
- RL Kane
- RR Edwards
- SI Innes
- TH Wideman
- WR Miller
- Publication venue
- 'Springer Science and Business Media LLC'
- Publication date
- 01/06/2017
- Field of study
There is an increasing awareness, interest and acceptance of the biopsychosocial (BPS) model by all health care professionals involved with patient care. The areas of spine care and pain medicine are no exception, and in fact, these areas of health care are a major centerpiece of the movement from the traditional biomedical model to a BPS model of patient assessment and delivery of care. The chiropractic approach to health care has a history that is grounded in key aspects of the BPS model. The profession has inherently implemented certain features of the BPS model throughout its history, perhaps without a full understanding or realization. The purpose of this paper is to present an overview of the BPS model, its relationship with spine care and pain management, and to discuss the BPS model, particularly psychosocial aspects, in the context of its historical relationship with chiropractic. We will also provide recommendations for the chiropractic profession as it relates to successful adoption of a full integration of the BPS model
Predicting infectious complications in neutropenic children and young people with cancer (IPD protocol)
- Author
- A Marshall
- A Marshall
- B Phillips
- B Phillips
- C Duncan
- C Oude Nijhuis
- D Heney
- D Tallon
- DC West
- DG Altman
- DG Altman
- DG Altman
- DG Altman
- DG Altman
- DR Hargrave
- E Orudjev
- EP Baorto
- EW Steyerberg
- F Freycon
- FE Harrell Jr
- I Hann
- I Hann
- I Hrynaszkiewicz
- J Klastersky
- J Mant
- JA Hayden
- JAC Sterne
- JC Chisholm
- JD Chamberlain
- K Broeze
- K Pritchard-Jones
- KG Lucas
- KGM Moons
- KS Khan
- L Fern
- L Kitanovski
- LA Stewart
- M Boragina
- M Diepold
- M Soker
- M Trivella
- ME Santolaya
- ME Santolaya
- MG Kris
- MI Spasova
- MMG Leeflang
- N Partridge
- N Stabell
- O Teuffel
- P Riikonen
- P Royston
- P Royston
- P Royston
- PIP Rondinelli
- R Simon
- RA Ammann
- RA Ammann
- RA Ammann
- RA Ammann
- RD Riley
- RD Riley
- RJ Klaassen
- SW Alexander
- WR Rackoff
- Publication venue
- BioMed Central
- Publication date
- 01/01/2012
- Field of study
<p>Abstract</p> <p>Background</p> <p>A common and potentially life-threatening complication of the treatment of childhood cancer is infection, which frequently presents as fever with neutropenia. The standard management of such episodes is the extensive use of intravenous antibiotics, and though it produces excellent survival rates of over 95%, it greatly inconveniences the three-fourths of patients who do not require such aggressive treatment. There have been a number of studies which have aimed to develop risk prediction models to stratify treatment. Individual participant data (IPD) meta-analysis in therapeutic studies has been developed to improve the precision and reliability of answers to questions of treatment effect and recently have been suggested to be used to answer questions regarding prognosis and diagnosis to gain greater power from the frequently small individual studies.</p> <p>Design</p> <p>In the IPD protocol, we will collect and synthesise IPD from multiple studies and examine the outcomes of episodes of febrile neutropenia as a consequence of their treatment for malignant disease. We will develop and evaluate a risk stratification model using hierarchical regression models to stratify patients by their risk of experiencing adverse outcomes during an episode. We will also explore specific practical and methodological issues regarding adaptation of established techniques of IPD meta-analysis of interventions for use in synthesising evidence derived from IPD from multiple studies for use in predictive modelling contexts.</p> <p>Discussion</p> <p>Our aim in using this model is to define a group of individuals at low risk for febrile neutropenia who might be treated with reduced intensity or duration of antibiotic therapy and so reduce the inconvenience and cost of these episodes, as well as to define a group of patients at very high risk of complications who could be subject to more intensive therapies. The project will also help develop methods of IPD predictive modelling for use in future studies of risk prediction.</p
Exploring Cell Tropism as a Possible Contributor to Influenza Infection Severity
- Author
- A Handel
- A Handel
- A Hindmarsh
- A Ibrecevic
- A Pekosz
- AS Perelson
- AS Perelson
- AU Neumann
- B Hancioglua
- BP Holder
- Brian E. Davies
- C Beauchemin
- C Cheung
- Catherine A. A. Beauchemin
- CI Thompson
- D van Riel
- D van Riel
- DY Oh
- FG Hayden
- GA Bocharov
- GAF Seber
- H Dahari
- H Miao
- Hana M. Dobrovolny
- HW Hethcote
- HY Lee
- I Li
- J Nicholls
- J Nicholls
- J Stevens
- JW Eaton
- K Shinya
- L Glaser
- L Kaiser
- LA Perrone
- M Chan
- M Nowak
- MA Kaufman
- MA Nowak
- Marc J. Baron
- MD de Jong
- MD de Jong
- MN Matrosovich
- MN Matrosovich
- MN Matrosovich
- Nelson L. Jumbe
- O Diekmann
- P Baccam
- P Eizenberg
- P van den Driessche
- R Coombes
- RA Saenz
- Ralph Tripp
- RC Larson
- RG Crystal
- RJH Payne
- RJH Payne
- Ronald Gieschke
- RS Fritz
- S Yamada
- SH Bajaria
- SH Seo
- SH Seo
- SM Hsieh
- T Kogure
- VV Ganusov
- WR Gallaher
- ZY Ning
- Publication venue
- Public Library of Science
- Publication date
- 23/11/2010
- Field of study
Several mechanisms have been proposed to account for the marked increase in severity of human infections with avian compared to human influenza strains, including increased cytokine expression, poor immune response, and differences in target cell receptor affinity. Here, the potential effect of target cell tropism on disease severity is studied using a mathematical model for in-host influenza viral infection in a cell population consisting of two different cell types. The two cell types differ only in their susceptibility to infection and rate of virus production. We show the existence of a parameter regime which is characterized by high viral loads sustained long after the onset of infection. This finding suggests that differences in cell tropism between influenza strains could be sufficient to cause significant differences in viral titer profiles, similar to those observed in infections with certain strains of influenza A virus. The two target cell mathematical model offers good agreement with experimental data from severe influenza infections, as does the usual, single target cell model albeit with biologically unrealistic parameters. Both models predict that while neuraminidase inhibitors and adamantanes are only effective when administered early to treat an uncomplicated seasonal infection, they can be effective against more severe influenza infections even when administered late
Bioprospecting the African Renaissance: The new value of muthi in South Africa
- Author
- A Appadurai
- A Ashforth
- A Ashforth
- A Ashforth
- A Cheik Diop
- A Geri
- A Kleinman
- A Kuper
- A Lakoff
- A Petryna
- AB Cunningham
- African Biosciences Initiative
- AP Dold
- B Berlin
- B Latour
- B Latour
- B Latour
- B-E Wyk van
- C Hayden
- C Leslie
- C Shackelton
- C Smith
- C Waldby
- D Posey
- D Posey
- D Turnbull
- F Barth
- Food and Agriculture Organization of the United Nations (FAO)
- G Lund
- H Ngubane
- Hanspeter CW Reihling
- J Botha
- J Keirungi
- J Pottier
- J Rosenthal
- JT Wreford
- K Peterson
- K Sunder Rajan
- KD Knorr-Cetina
- L Nader
- M Brown
- M Callon
- M Mander
- M Nichter
- M Nichter
- M Wolfson
- Medicines and Medical Devices Regulatory Authority Act
- ML Cocks
- MM Koyama
- N Rose
- NEPAD
- P Folb
- P Rabinow
- P Rabinow
- PL Berger
- Portfolio Committee on Health
- R Coombe
- R Nigh
- R Ostergard
- R Wynberg
- R Wynberg
- S Brush
- S Brush
- S Franklin
- S Geest van
- S Greene
- Select Committee on Social Services
- SPN Mativandlela
- T Eisner
- T Eisner
- T Mbeki
- T Wegener
- U Hoering
- WIPO
- World Health Organisation
- Worldbank
- WR Reid
- Y Dezalay
- Publication venue
- 'Springer Science and Business Media LLC'
- Publication date
- 01/01/2008
- Field of study
This article gives an overview of anthropological research on bioprospecting in general and of available literature related to bioprospecting particularly in South Africa. It points out how new insights on value regimes concerning plant-based medicines may be gained through further research and is meant to contribute to a critical discussion about the ethics of Access and Benefit Sharing (ABS). In South Africa, traditional healers, plant gatherers, petty traders, researchers and private investors are assembled around the issues of standardization and commercialization of knowledge about plants. This coincides with a nation-building project which promotes the revitalization of local knowledge within the so called African Renaissance. A social science analysis of the transformation of so called Traditional Medicine (TM) may shed light onto this renaissance by tracing social arenas in which different regimes of value are brought into conflict. When medicinal plants turn into assets in a national and global economy, they seem to be manipulated and transformed in relation to their capacity to promote health, their market value, and their potential to construct new ethics of development. In this context, the translation of socially and culturally situated local knowledge about muthi into global pharmaceuticals creates new forms of agency as well as new power differentials between the different actors involved
Testosterone, cortisol, and serotonin as key regulators of social aggression: A review and theoretical perspective
- Author
- A Bechara
- A Glenn
- A Popma
- A Raine
- A Ratka
- AA Marsh
- AJ Cleare
- AJ Tilbrook
- B Derntl
- BC Trainor
- C Eisenegger
- D Terburg
- D Terburg
- David Terburg
- DJ Hawes
- DM Hayden-Hixson
- DR Rosell
- EA Phelps
- EJ Hermans
- EJ Hermans
- EJ Hermans
- EO Johnson
- Estrella R. Montoya
- G Fink
- H Karst
- H Soderstrom
- J Dabbs
- J Decety
- J Honk van
- J Honk van
- J Honk van
- J Honk van
- J Honk van
- J Honk van
- J Honk van
- J Honk van
- J Schulkin
- J Schulkin
- J Schulkin
- Jack van Honk
- JD Higley
- JM Peer van
- JM Reul
- JMG Williams
- K Pajer
- L Bevilacqua
- LJ Siever
- M Carrillo
- M Cima
- M Linnoila
- M Virkunnen
- M Wirth
- MJ Crockett
- MJ Crockett
- MJ Henckens
- NY Oei
- P Francesco Ferrari
- P Putman
- P Putman
- P Putman
- P Putman
- P Putman
- PA Arnett
- Peter A. Bos
- PH Mehta
- PH Mehta
- PH Mehta
- PJ Zak
- PV Piazza
- R Böhnke
- R Huber
- R Wood
- RJ Nelson
- RJR Blair
- RJR Blair
- RJR Blair
- RJR Blair
- S Sarkey
- SB Manuck
- SP Taylor
- TC Burnham
- TW Buchanan
- V Viau
- W Guth
- WG Frankle
- WJ Cassano
- WR Lovallo
- Y Kuepper
- Publication venue
- Springer US
- Publication date
- 01/01/2011
- Field of study
In human and non-human animals the steroid hormones cortisol and testosterone are involved in social aggression and recent studies suggest that these steroids might jointly regulate this behavior. It has been hypothesized that the imbalance between cortisol and testosterone levels is predictive for aggressive psychopathology, with high testosterone to cortisol ratio predisposing to a socially aggressive behavioral style. In this review, we focus on the effects of cortisol and testosterone on human social aggression, as well as on how they might modulate the aggression circuitry of the human brain. Recently, serotonin is hypothesized to differentiate between impulsive and instrumental aggression, and we will briefly review evidence on this hypothesis. The aim of this article is to provide a theoretical framework for the role of steroids and serotonin in impulsive social aggression in humans
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