1,241 research outputs found
ending civil conflict through rebel demobilization
- Publication venue
- 'American Economic Association'
- Publication date
- 01/05/2020
- Field of study
We examine the role of FM radio in mitigating violent conflict. We collect original data on radio broadcasts encouraging defections during the Lord's Resistance Army (LRA) insurgency. This constitutes the first quantitative evaluation of an active counterinsurgency policy that encourages defections through radio messages. Exploiting random topography-driven variation in radio coverage along with panel variation at the grid-cell level, we identify the causal effect of messaging on violence. Broadcasting defection messages increases defections and reduces fatalities, violence against civilians, and clashes with security forces. Income shocks have opposing effects on both the conflict and the effectiveness of messaging.publishersversionpublishe
Maternal mortality and women’s political power
- Publication venue
- University of Warwick. Department of Economics
- Publication date
- 01/01/2021
- Field of study
Millions of women continue to die during and soon after childbirth, even where the knowledge and resources to avoid this are available. We posit that raising the share of women in parliament can trigger action. Leveraging the timing of gender quota legislation across developing countries, we identify sharp sustained reductions of 8–10 percent in maternal mortality. Investigating mechanisms, we find that gender quotas lead to increases in percentage points of 5–8 in skilled birth attendance and 4–8 in prenatal care utilization, alongside a decline in fertility of 6–7 percent and an increase in the schooling of young women of about 0.5 years. The results are robust to numerous robustness checks. They suggest a new policy tool for tackling maternal mortality
PREVALENCE OF INTESTINAL PARASITISM AND ASSOCIATED SYMPTOMATOLOGY AMONG HEMODIALYSIS PATIENTS
- Author
- Publication venue
- Universidade de São Paulo. Instituto de Medicina Tropical de São Paulo
- Publication date
- 01/04/2013
- Field of study
;Intestinal parasites are an important cause of morbidity and mortality. Immunocompromised individuals may develop more severe forms of these infections. Taking into account the immunity impairment in patients suffering from chronic renal failure (CRF), we will determine the prevalence and associated symptoms of intestinal parasites in these patients. Controls without CRF were used for comparison. Stool samples were collected and processed for microscopic identification of parasites using the Formalin-ether concentration method. For Cryptosporidium diagnosis, the ELISA technique was used. One hundred and ten fecal samples from hemodialysis patients were analyzed, as well as 86 from a community group used as control group. A result of 51.6% of intestinal parasites was observed in hemodialysis patients and 61.6% in the control group. Cryptosporidium and Blastocystis were the most common infections in patients with CRF (26.4% and 24.5%, respectively). Blastocystis was the most common infection in the control group (41.9%), however no individual was found positive for Cryptosporidium. Among the CRF patients, 73.6% were symptomatic, 54.3% of these tested positive for at least one parasite, in contrast to 44.8% in asymptomatic patients (p = 0.38). The most common symptoms in this group were flatulence (36.4%), asthenia (30.0%) and weight loss (30.0%). In the control group, 91.9% were symptomatic, 60.8% of these tested positive for at least one parasite, in contrast to 71.4% in asymptomatic patients (p = 0.703). A significant difference between the two groups was observed with regard to symptoms, with bloating, postprandial fullness, and abdominal pain being more frequent in the control group than in the hemodialysis group (all p < 0.05). Comparing symptomatic with asymptomatic, there was no association in either group between symptoms or the prevalence of parasitic infection, nor with the type of parasite or with multiple parasitic infections. Patients with chronic renal failure are frequent targets for renal transplantation, which as well as the inherent immunological impairment of the disease itself, results in immunosuppression by medication. For this reason, carriers of intestinal parasites with pathogenic potential can develop serious clinical complications influencing the success of transplantation. This fact, coupled with the high prevalence of intestinal parasites and the dissociation between symptoms and infection in CRF patients, suggests that the stool test should be incorporated in routine propedeutics. Furthermore, preventive measures for the acquisition of parasites through the fecal-oral contamination route should be introduced.Doenças parasitárias infectam grande número de indivíduos em todo o mundo. Manifestações clínicas mais severas podem se apresentar em pacientes imunocomprometidos. Considerando o importante comprometimento imunológico observado em pacientes com insuficiência renal crônica (IRC), foi determinada a prevalência e sintomas associados a parasitoses intestinais nesses pacientes em comparação a controles saudáveis. Foram coletadas amostras fecais de cada participante e processadas para identificação microscópica dos parasitas pelo método de concentração por formol-éter. Foi utilizada a técnica de ELISA para identificar coproantígenos de Cryptosporidium. Foram analisadas 110 amostras fecais de pacientes em hemodiálise e 86 de um grupo controle comunitário. Cryptosporidium e Blastocystis foram as infecções mais freqüentes nos pacientes em hemodiálise (26,4% e 24,5%, respectivamente). Blastocystis foi a infecção mais freqüente no grupo controle (41,9%), entretanto nenhum indivíduo positivo para Cryptosporidium foi identificado. Considerando os pacientes com IRC, 73,6% eram sintomáticos, sendo 54,3% positivos para algum parasita, contra 44,8% nos assintomáticos (p = 0,38). Os sintomas mais frequentes neste grupo foram flatulência (36,4%), adinamia (30,0%) e perda de peso (30,0%). No grupo controle, 91,9% eram sintomáticos, sendo 60,8% positivos para algum parasita, contra 71,4% nos assintomáticos (p = 0,703). Em relação aos sintomas, houve diferença significativa entre os dois grupos, sendo que flatulência, plenitude pós-prandial, e dor abdominal foram mais freqüentes no grupo controle que nos pacientes em hemodiálise (todos p < 0,05). Comparando-se sintomáticos com assintomáticos, não houve associação entre a sintomatologia e a prevalência de parasitose, nem com o tipo de parasita, e nem com o poliparasitismo, nos dois grupos. Considerando que pacientes com IRC são frequentes alvos de transplante renal, resultando em imunossupressão por medicamentos, que é somada à deficiência imunológica inerente à própria doença. Os portadores de parasitas intestinais com potencial patogênico podem desenvolver sérias complicações clínicas que influenciam o sucesso do transplante. Este fato, aliado a alta prevalência de parasitas intestinais e dissociação entre os sintomas e infecção nesses pacientes, sugerem a incorporação do exame de fezes na propedêutica de rotina dos mesmos, juntamente com medidas preventivas para a aquisição de parasitas com rota de contaminação fecal-oral
Perinatal maternal antibiotic exposure augments lung injury in offspring in experimental bronchopulmonary dysplasia
- Author
- Publication venue
- LSU Digital Commons
- Publication date
- 01/02/2020
- Field of study
Copyright © 2020 the American Physiological Society. During the newborn period, intestinal commensal bacteria influence pulmonary mucosal immunology via the gut-lung axis. Epidemiological studies have linked perinatal antibiotic exposure in human newborns to an increased risk for bronchopulmonary dysplasia, but whether this effect is mediated by the gut-lung axis is unknown. To explore antibiotic disruption of the newborn gut-lung axis, we studied how perinatal maternal antibiotic exposure influenced lung injury in a hyperoxia-based mouse model of bronchopulmonary dysplasia. We report that disruption of intestinal commensal colonization during the perinatal period promotes a more severe bronchopulmonary dysplasia phenotype characterized by increased mortality and pulmonary fibrosis. Mechanistically, metagenomic shifts were associated with decreased IL-22 expression in bronchoalveolar lavage and were independent of hyperoxia-induced inflammasome activation. Collectively, these results demonstrate a previously unrecognized influence of the gut-lung axis during the development of neonatal lung injury, which could be leveraged to ameliorate the most severe and persistent pulmonary complication of preterm birth
Single hadron response measurement and calorimeter jet energy scale uncertainty with the ATLAS detector at the LHC
- Author
- A. A. Abdelalim
- A. A. Carter
- A. A. Grillo
- A. A. Komar
- A. A. Minaenko
- A. A. Nepomuceno
- A. A. Snesarev
- A. A. Solodkov
- A. Abdesselam
- A. Ahmad
- A. Akiyama
- A. Aloisio
- A. Alonso
- A. Amorim
- A. Andreazza
- A. Angerami
- A. Anisenkov
- A. Annovi
- A. Antonaki
- A. Antonov
- A. Artamonov
- A. Astbury
- A. Astvatsatourov
- A. B. Fenyuk
- A. B. Lazarev
- A. Bangert
- A. Barashkou
- A. Barbaro Galtieri
- A. Baroncelli
- A. Battaglia
- A. Beddall
- A. Belloni
- A. Bertin
- A. Bingul
- A. Blondel
- A. Bocci
- A. Bogdanchikov
- A. Bogouch
- A. Borisov
- A. Boveia
- A. Braem
- A. Brandt
- A. Bruni
- A. C. König
- A. C. Martyniuk
- A. C. Schaffer
- A. Canepa
- A. Catinaccio
- A. Cattai
- A. Cerri
- A. Chafaq
- A. Cheplakov
- A. Chilingarov
- A. Christov
- A. Ciocio
- A. Clark
- A. Coccaro
- A. Cortes-Gonzalez
- A. D. Doxiadis
- A. D. Hawkins
- A. D. Hershenhorn
- A. D. Pilkington
- A. De Salvo
- A. De Santo
- A. Dell’Acqua
- A. Dewhurst
- A. Di Ciaccio
- A. Di Girolamo
- A. Di Mattia
- A. Di Simone
- A. Do Valle Wemans
- A. Doria
- A. Dos Anjos
- A. Dotti
- A. Dudarev
- A. D’Orazio
- A. E. Barton
- A. E. Kiryunin
- A. Engl
- A. Eppig
- A. Ereditato
- A. F. Saavedra
- A. Farbin
- A. Farilla
- A. Favareto
- A. Ferrari
- A. Ferrer
- A. Ferretto Parodi
- A. Filippas
- A. Filipčič
- A. Firan
- A. Floderus
- A. Formica
- A. Forti
- A. Foussat
- A. G. Buckley
- A. G. Goussiou
- A. G. Kholodenko
- A. G. Myagkov
- A. G. Olchevski
- A. G. Schamov
- A. Gaponenko
- A. Gemmell
- A. Gershon
- A. Gibson
- A. Glazov
- A. Gomes
- A. Gonidec
- A. Gorišek
- A. Guida
- A. Gupta
- A. Haas
- A. Hamilton
- A. Harvey
- A. Henrichs
- A. Hoecker
- A. Hoummada
- A. Huettmann
- A. I. Etienvre
- A. I. Kononov
- A. I. Mincer
- A. Irles Quiles
- A. Ishikawa
- A. J. Armbruster
- A. J. Barr
- A. J. Beddall
- A. J. Fowler
- A. J. Lankford
- A. J. Lowe
- A. J. Martin
- A. J. Tanasijczuk
- A. Jantsch
- A. Jeremie
- A. Juste Rozas
- A. K. Ciftci
- A. K. Morley
- A. Kaczmarska
- A. Kapliy
- A. Kasmi
- A. Kastanas
- A. Khanov
- A. Khodinov
- A. Khomich
- A. Khoroshilov
- A. Kiryunin
- A. Klier
- A. Klimentov
- A. Knue
- A. Kootz
- A. Korn
- A. Korol
- A. Kotwal
- A. Koutsman
- A. Krasznahorkay
- A. Kreisel
- A. Kruth
- A. Kugel
- A. Kupco
- A. L. Maslennikov
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- A. Larner
- A. Leger
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- A. Lewis
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- A. Zemla
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- A. Zoccoli
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- A.-E. Nuncio-Quiroz
- ATLAS Collaboration
- ATLAS Collaboration
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- T. Lenz
- T. Loddenkoetter
- T. Lohse
- T. M. Hong
- T. M. Liss
- T. Maeno
- T. Mashimo
- T. Masubuchi
- T. Matsushita
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- T. Mueller
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- T. Takeshita
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- T. Todorov
- T. Trefzger
- T. Vickey
- T. Vu Anh
- T. W. Jones
- T. Wenaus
- T. Wengler
- T. Yamamura
- T. Yamanaka
- T. Yamazaki
- T. Z. Kowalski
- T. Zhao
- T. Ženiš
- Th. D. Papadopoulou
- U. Bitenc
- U. Blumenschein
- U. Bratzler
- U. De Sanctis
- U. Husemann
- U. K. Yang
- U. Klein
- U. Kruchonak
- U. Landgraf
- U. Mallik
- U. Parzefall
- U. Schäfer
- U. Soldevila
- V. A. Bednyakov
- V. A. Gapienko
- V. A. Kantserov
- V. A. Kazanin
- V. A. Korotkov
- V. A. Kramarenko
- V. A. Mitsou
- V. A. Schegelsky
- V. Andrei
- V. B. Bobrovnikov
- V. B. Vinogradov
- V. Bansal
- V. Bartsch
- V. Boisvert
- V. Boldea
- V. Bortolotto
- V. Büscher
- V. Canale
- V. Castillo Gimenez
- V. Cavasinni
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- V. Chernyatin
- V. Cindro
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- V. D. Peshekhonov
- V. Dao
- V. E. Ozcan
- V. F. Chepurnov
- V. Ferrara
- V. G. Bondarenko
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- V. Giangiobbe
- V. Gilewsky
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- V. I. Rud
- V. I. Vassilakopoulos
- V. Ippolito
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- V. J. Guarino
- V. J. Martin
- V. Jain
- V. Juranek
- V. Kartvelishvili
- V. Kaushik
- V. Khovanskiy
- V. Kolesnikov
- V. Koreshev
- V. Kouskoura
- V. Kral
- V. Kukhtin
- V. Kus
- V. Lavorini
- V. Lendermann
- V. M. Kotov
- V. M. Romanov
- V. Malyshev
- V. Martinez Outschoorn
- V. Moeller
- V. N. Goryachev
- V. N. Gushchin
- V. Nguyen Thi Hong
- V. Nikolaenko
- V. O. Tikhomirov
- V. O’Shea
- V. P. Lombardo
- V. P. Maleev
- V. Paolone
- V. Perez Reale
- V. Polychronakos
- V. Pozdnyakov
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- V. Rojo
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- W. Bhimji
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- W. Dabrowski
- W. Davey
- W. Ehrenfeld
- W. F. Mader
- W. Fedorko
- W. Fernando
- W. G. Scott
- W. H. Bell
- W. Iwanski
- W. J. Dearnaley
- W. J. Mills
- W. J. Murray
- W. Ji
- W. K. Brooks
- W. Kozanecki
- W. L. Ebenstein
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- W. Lavrijsen
- W. Liebig
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- W. T. Meyer
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- W. Willis
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- X. Ju
- X. Lei
- X. Li
- X. Lou
- X. Portell Bueso
- X. Prudent
- X. Ruan
- X. S. Anduaga
- X. Sun
- X. Wu
- X. Zhang
- X. Zhuang
- Y. A. Kurochkin
- Y. A. Tikhonov
- Y. Arai
- Y. Azuma
- Y. B. Pan
- Y. Bai
- Y. Benhammou
- Y. Coadou
- Y. Davygora
- Y. Doi
- Y. F. Ryabov
- Y. Fang
- Y. Gusakov
- Y. Hasegawa
- Y. Hernández Jiménez
- Y. Homma
- Y. Ikegami
- Y. Ilchenko
- Y. Jiang
- Y. Kataoka
- Y. Komori
- Y. Kulchitsky
- Y. Liu
- Y. Mahalalel
- Y. Makida
- Y. Ming
- Y. Munwes
- Y. Nagasaka
- Y. Nakahama
- Y. Ninomiya
- Y. Okumura
- Y. Oren
- Y. Pylypchenko
- Y. Rozen
- Y. S. Gao
- Y. Silver
- Y. Smirnov
- Y. Sugaya
- Y. Suzuki
- Y. Suzuki
- Y. Takahashi
- Y. Takubo
- Y. Tanaka
- Y. Tayalati
- Y. Unno
- Y. V. Grishkevich
- Y. Wu
- Y. Xie
- Y. Yamazaki
- Y. Yang
- Y. Yang
- Y. Yao
- Y. Yasu
- Y. Zhou
- Y. Zhu
- Y. Zolnierowski
- Yu. M. Sviridov
- Z. Czyczula
- Z. D. Greenwood
- Z. Dolezal
- Z. Drasal
- Z. Hajduk
- Z. Hubacek
- Z. Kohout
- Z. L. Ren
- Z. Liang
- Z. Marshall
- Z. Meng
- Z. Qian
- Z. Qin
- Z. Rurikova
- Z. V. Krumshteyn
- Z. van Kesteren
- Z. Weng
- Z. Yan
- Z. Yang
- Z. Zajacova
- Z. Zenonos
- Z. Zhan
- Z. Zhang
- Z. Zhao
- Z. Zinonos
- Publication venue
- 'Springer Science and Business Media LLC'
- Publication date
- 06/03/2012
- Field of study
The uncertainty on the calorimeter energy response to jets of particles is
derived for the ATLAS experiment at the Large Hadron Collider (LHC). First, the
calorimeter response to single isolated charged hadrons is measured and
compared to the Monte Carlo simulation using proton-proton collisions at
centre-of-mass energies of sqrt(s) = 900 GeV and 7 TeV collected during 2009
and 2010. Then, using the decay of K_s and Lambda particles, the calorimeter
response to specific types of particles (positively and negatively charged
pions, protons, and anti-protons) is measured and compared to the Monte Carlo
predictions. Finally, the jet energy scale uncertainty is determined by
propagating the response uncertainty for single charged and neutral particles
to jets. The response uncertainty is 2-5% for central isolated hadrons and 1-3%
for the final calorimeter jet energy scale.Comment: 24 pages plus author list (36 pages total), 23 figures, 1 table,
submitted to European Physical Journal
Measurement of the inclusive and dijet cross-sections of b-jets in pp collisions at sqrt(s) = 7 TeV with the ATLAS detector
- Author
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- Abbott B
- Abdallah J
- Abdelalim AA
- Abdesselam A
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- Abolins M
- Abramowicz H
- Abreu H
- Acerbi E
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- Zhemchugov A
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- Zieminska D
- Zilka B
- Zimmermann R
- Zimmermann S
- Zimmermann S
- Ziolkowski M
- Zitoun R
- Zivkovic L
- Zmouchko VV
- Zobernig G
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- Zolnierowski Y
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- zur Nedden M
- Zutshi V
- Zwalinski L
- Publication venue
- 'Springer Science and Business Media LLC'
- Publication date
- 31/12/2010
- Field of study
The inclusive and dijet production cross-sections have been measured for jets
containing b-hadrons (b-jets) in proton-proton collisions at a centre-of-mass
energy of sqrt(s) = 7 TeV, using the ATLAS detector at the LHC. The
measurements use data corresponding to an integrated luminosity of 34 pb^-1.
The b-jets are identified using either a lifetime-based method, where secondary
decay vertices of b-hadrons in jets are reconstructed using information from
the tracking detectors, or a muon-based method where the presence of a muon is
used to identify semileptonic decays of b-hadrons inside jets. The inclusive
b-jet cross-section is measured as a function of transverse momentum in the
range 20 < pT < 400 GeV and rapidity in the range |y| < 2.1. The bbbar-dijet
cross-section is measured as a function of the dijet invariant mass in the
range 110 < m_jj < 760 GeV, the azimuthal angle difference between the two jets
and the angular variable chi in two dijet mass regions. The results are
compared with next-to-leading-order QCD predictions. Good agreement is observed
between the measured cross-sections and the predictions obtained using POWHEG +
Pythia. MC@NLO + Herwig shows good agreement with the measured bbbar-dijet
cross-section. However, it does not reproduce the measured inclusive
cross-section well, particularly for central b-jets with large transverse
momenta.Comment: 10 pages plus author list (21 pages total), 8 figures, 1 table, final
version published in European Physical Journal
Jet energy measurement with the ATLAS detector in proton-proton collisions at root s=7 TeV
- Author
- Aad G
- Abbott B
- Abdallah J
- Abdelalim AA
- Abdesselam A
- Abdinov O
- Abi B
- Abolins M
- Abramowicz H
- Abreu H
- Acerbi E
- Acharya BS
- Adams DL
- Addy TN
- Adelman J
- Aderholz M
- Adomeit S
- Adragna P
- Adye T
- Aefsky S
- Aguilar-Saavedra JA
- Aharrouche M
- Ahlen SP
- Ahles F
- Ahmad A
- Ahsan M
- Aielli G
- Akdogana T
- Akesson TPA
- Akimoto G
- Akimov AV
- Akiyama A
- Aktas A
- Alam MA
- Alam MS
- Albert J
- Albrand S
- Aleksa M
- Aleksandrov IN
- Alessandria F
- Alexa C
- Alexander G
- Alexandre G
- Alexopoulos T
- Alhroob M
- Aliev M
- Alimonti G
- Alison J
- Aliyev M
- Allport PP
- Allwood-Spiers SE
- Almenar CC
- Almond J
- Aloisio A
- Alon R
- Alonso A
- Alviggi MG
- Amako K
- Amaral P
- Amelung C
- Ammosov VV
- Amorim A
- Amoros G
- Amram N
- Anastopoulos C
- Ancu LS
- Andari N
- Andeen T
- Anders CF
- Anders G
- Anderson KJ
- Andreazza A
- Andrei V
- Andrieux M-L
- Anduaga XS
- Angerami A
- Anghinolfi F
- Anh TV
- Anjos N
- Annovi A
- Antonaki A
- Antonelli M
- Antonov A
- Antos J
- Anulli F
- Aoun S
- Apolle R
- Arabidze G
- Aracena I
- Arai Y
- Aranda CP
- Arce ATH
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- Publication venue
- 'Springer Science and Business Media LLC'
- Publication date
- 01/03/2013
- Field of study
The jet energy scale and its systematic uncertainty are determined for jets measured with the ATLAS detector at the LHC in proton-proton collision data at a centre-of-mass energy of √s = 7TeV corresponding to an integrated luminosity of 38 pb-1. Jets are reconstructed with the anti-kt algorithm with distance parameters R=0. 4 or R=0. 6. Jet energy and angle corrections are determined from Monte Carlo simulations to calibrate jets with transverse momenta pT≥20 GeV and pseudorapidities {pipe}η{pipe}<4. 5. The jet energy systematic uncertainty is estimated using the single isolated hadron response measured in situ and in test-beams, exploiting the transverse momentum balance between central and forward jets in events with dijet topologies and studying systematic variations in Monte Carlo simulations. The jet energy uncertainty is less than 2. 5 % in the central calorimeter region ({pipe}η{pipe}<0. 8) for jets with 60≤pT<800 GeV, and is maximally 14 % for pT<30 GeV in the most forward region 3. 2≤{pipe}η{pipe}<4. 5. The jet energy is validated for jet transverse momenta up to 1 TeV to the level of a few percent using several in situ techniques by comparing a well-known reference such as the recoiling photon pT, the sum of the transverse momenta of tracks associated to the jet, or a system of low-pT jets recoiling against a high-pT jet. More sophisticated jet calibration schemes are presented based on calorimeter cell energy density weighting or hadronic properties of jets, aiming for an improved jet energy resolution and a reduced flavour dependence of the jet response. The systematic uncertainty of the jet energy determined from a combination of in situ techniques is consistent with the one derived from single hadron response measurements over a wide kinematic range. The nominal corrections and uncertainties are derived for isolated jets in an inclusive sample of high-pT jets. Special cases such as event topologies with close-by jets, or selections of samples with an enhanced content of jets originating from light quarks, heavy quarks or gluons are also discussed and the corresponding uncertainties are determined. © 2013 CERN for the benefit of the ATLAS collaboration
Measurement of the production cross section for W-bosons in association with jets in pp collisions at s=7 TeV with the ATLAS detector
- Author
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- Zarzhitsky P
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- Zhan Z
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- Zitoun R
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- ¿eni¿ T
- Åsman B
- Øye O
- Publication venue
- Publication date
- 01/01/2011
- Field of study
Essential versus accessory aspects of cell death: recommendations of the NCCD 2015
- Author
- A Ciechanover
- A Criollo
- A Degterev
- A Degterev
- A Degterev
- A Gross
- A Hochreiter-Hufford
- A Kaczmarek
- A Linkermann
- A Linkermann
- A Linkermann
- A Linkermann
- A Nagasaka
- A Oberst
- A Oberst
- A Pogrebniak
- A Rebbaa
- A Strasser
- A Villunger
- AA Fatokun
- AA Mailleux
- AC Schinzel
- AD Dam
- AG Fraser
- AJ Schile
- AM Chinnaiyan
- AM Chinnaiyan
- AM Choi
- AM Verhagen
- AU Lindner
- AV Vaseva
- B D Dynlacht
- B Joseph
- B La Scola
- B La Scola
- B Levine
- B R Stockwell
- B Zhivotovsky
- B Zhivotovsky
- BA Gibson
- BB Wolf
- BH Han
- C Borner
- C Brenner
- C Brenner
- C Brenner
- C Brenner
- C Du
- C Garrido
- C Garrido
- C López-Otín
- C M Rodrigues
- C Munoz-Pinedo
- C Muñoz-Pinedo
- C Scaffidi
- C Scheller
- C Volbracht
- C Volbracht
- CM Haynes
- CO Bellamy
- CP Baines
- CP Baines
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- D Chandra
- D Denton
- D Denton
- D Denton
- D Denton
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- D R Green
- D Raoult
- D Ren
- D Vercammen
- D Vercammen
- D Vercammen
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- DA Fruman
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- DR Green
- DV Krysko
- DV Krysko
- DW Zhang
- E Basso
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- E H Baehrecke
- E H Cheng
- E Laane
- E Lugli
- E Murphy
- E Noch
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- E Tasdemir
- E White
- E White
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- EA Slee
- EA Slee
- EH Baehrecke
- EJ Park
- F Basit
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- F Cecconi
- F Gonzalvez
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- F Verrier
- FC Kischkel
- FH Igney
- G A Rabinovich
- G Denecker
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- G Kroemer
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- H Walczak
- H Wang
- H Yoshida
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- H-U Simon
- HI Roach
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- HL Tang
- I Amelio
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- I Vitale
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- IP Nezis
- J A Cidlowski
- J E Chipuk
- J H Prehn
- J Hitomi
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- J Li
- J M Abrams
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- J M Penninger
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- J Sosna
- J Wu
- J Yang
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- J Zhao
- J-C Marine
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- JA Rickard
- JC Reed
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- JG Albeck
- JH Shin
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- JS Long
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- JW Upton
- K Bianchi
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- L Altucci
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- M Annicchiarico-Petruzzelli
- M Arundine
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- M Campanella
- M Campanella
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- NJ Curtin
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- O Kepp
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- P Bouillet
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- P J Jost
- P Kraft
- P Li
- P Mazzarello
- P Meier
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- P Nicotera
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- P Schotte
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- P Vandenabeele
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- RM del Moral
- RU Janicke
- RW Oppenheim
- S A Aaronson
- S A Lipton
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- S Dolma
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- S He
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- S Kumar
- S Kumar
- S Melino
- S Morioka
- S Renolleau
- S Tan
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- S W Tait
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- SA Lakhani
- SA Susin
- SB Bratton
- SC Chow
- SJ Dixon
- SJ Dixon
- SJ Kim
- SJ Martin
- SJ Martin
- SM Knoblach
- SM Laster
- SM Srinivasula
- SN Willis
- SW Tait
- SW Tait
- SW Tait
- SW Tait
- SW Tait
- SW Yu
- SW Yu
- SY Chen
- T Hirsch
- T Ide
- T Kaufmann
- T Lindsten
- T M Dawson
- T Nakagawa
- T Nakamura
- T Panaretakis
- T Rudel
- T Tenev
- T Vanden Berghe
- T Vanden Berghe
- T Vanden Berghe
- T Vanden Berghe
- T Vanden Berghe
- TG Cotter
- TJ Daish
- TJ Fan
- TM Caserta
- U Moll
- V De Laurenzi
- V Giorgio
- V Gogvadze
- V L Dawson
- V Labi
- V M Dixit
- V Nikoletopoulou
- W Fiers
- W G Wood
- W Han
- W Han
- W Hou
- W Malorni
- W S El-Deiry
- W Zhang
- WJ Kaiser
- WJ Kaiser
- WS Yang
- WW Chen
- X Chen
- X Li
- X Liu
- X Luo
- X Pan
- XM Yin
- Y Ben-Neriah
- Y Dondelinger
- Y Dondelinger
- Y Eguchi
- Y Fuchs
- Y Li
- Y Liu
- Y Rong
- Y Shi
- Y Tsujimoto
- Y Wang
- Y Zaltsman
- YP Ow
- YS Cho
- Z Cai
- Z Song
- Z Wang
- Z Zakeri
- ZA Dunai
- Publication venue
- 'Springer Science and Business Media LLC'
- Publication date
- 01/01/2014
- Field of study
Cells exposed to extreme physicochemical or mechanical stimuli die in an uncontrollable manner, as a result of their immediate structural breakdown. Such an unavoidable variant of cellular demise is generally referred to as ‘accidental cell death’ (ACD). In most settings, however, cell death is initiated by a genetically encoded apparatus, correlating with the fact that its course can be altered by pharmacologic or genetic interventions. ‘Regulated cell death’ (RCD) can occur as part of physiologic programs or can be activated once adaptive responses to perturbations of the extracellular or intracellular microenvironment fail. The biochemical phenomena that accompany RCD may be harnessed to classify it into a few subtypes, which often (but not always) exhibit stereotyped morphologic features. Nonetheless, efficiently inhibiting the processes that are commonly thought to cause RCD, such as the activation of executioner caspases in the course of apoptosis, does not exert true cytoprotective effects in the mammalian system, but simply alters the kinetics of cellular demise as it shifts its morphologic and biochemical correlates. Conversely, bona fide cytoprotection can be achieved by inhibiting the transduction of lethal signals in the early phases of the process, when adaptive responses are still operational. Thus, the mechanisms that truly execute RCD may be less understood, less inhibitable and perhaps more homogeneous than previously thought. Here, the Nomenclature Committee on Cell Death formulates a set of recommendations to help scientists and researchers to discriminate between essential and accessory aspects of cell death
ACBD5 and VAPB mediate membrane associations between peroxisomes and the ER
- Author
- Publication venue
- The Rockefeller University Press
- Publication date
- 22/12/2016
- Field of study
Peroxisomes (POs) and the endoplasmic reticulum (ER) cooperate in cellular lipid metabolism and form tight structural associations, which were first observed in ultrastructural studies decades ago. PO–ER associations have been suggested to impact on a diverse number of physiological processes, including lipid metabolism, phospholipid exchange, metabolite transport, signaling, and PO biogenesis. Despite their fundamental importance to cell metabolism, the mechanisms by which regions of the ER become tethered to POs are unknown, in particular in mammalian cells. Here, we identify the PO membrane protein acyl-coenzyme A–binding domain protein 5 (ACBD5) as a binding partner for the resident ER protein vesicle-associated membrane protein-associated protein B (VAPB). We show that ACBD5–VAPB interaction regulates PO–ER associations. Moreover, we demonstrate that loss of PO–ER association perturbs PO membrane expansion and increases PO movement. Our findings reveal the first molecular mechanism for establishing PO–ER associations in mammalian cells and report a new function for ACBD5 in PO–ER tethering
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