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  1. Article ; Online: Picking apart p values: common problems and points of confusion.

    Madjarova, Sophia J / Williams, Riley J / Nwachukwu, Benedict U / Martin, R Kyle / Karlsson, Jón / Ollivier, Mattheu / Pareek, Ayoosh

    Knee surgery, sports traumatology, arthroscopy : official journal of the ESSKA

    2022  Volume 30, Issue 10, Page(s) 3245–3248

    Abstract: Due to its frequent misuse, the p value has become a point of contention in the research community ... In this editorial, we seek to clarify some of the common misconceptions about p values and the hazardous ... issues related to p value interpretation in addition to problems such as p-hacking and statistical ...

    Abstract Due to its frequent misuse, the p value has become a point of contention in the research community. In this editorial, we seek to clarify some of the common misconceptions about p values and the hazardous implications associated with misunderstanding this commonly used statistical concept. This article will discuss issues related to p value interpretation in addition to problems such as p-hacking and statistical fragility; we will also offer some thoughts on addressing these issues. The aim of this editorial is to provide clarity around the concept of statistical significance for those attempting to increase their statistical literacy in Orthopedic research.
    MeSH term(s) Humans ; Orthopedics
    Language English
    Publishing date 2022-08-03
    Publishing country Germany
    Document type Editorial
    ZDB-ID 1159064-6
    ISSN 1433-7347 ; 0942-2056
    ISSN (online) 1433-7347
    ISSN 0942-2056
    DOI 10.1007/s00167-022-07083-3
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  2. Article ; Online: Structural basis of P[II] rotavirus evolution and host ranges under selection of histo-blood group antigens.

    Xu, Shenyuan / McGinnis, Kristen Rose / Liu, Yang / Huang, Pengwei / Tan, Ming / Stuckert, Michael Robert / Burnside, Riley Erin / Jacob, Elsa Grace / Ni, Shuisong / Jiang, Xi / Kennedy, Michael A

    Proceedings of the National Academy of Sciences of the United States of America

    2021  Volume 118, Issue 36

    Abstract: Group A rotaviruses cause severe gastroenteritis in infants and young children worldwide, with P[II ... structures of complexes of the major P[II] genogroup P[4] and P[8] genotype RV VP8* receptor-binding domains ... support the hypothesis that P[II] RV evolution progressed from animals to humans under the selection ...

    Abstract Group A rotaviruses cause severe gastroenteritis in infants and young children worldwide, with P[II] genogroup rotaviruses (RVs) responsible for >90% of global cases. RVs have diverse host ranges in different human and animal populations determined by host histo-blood group antigen (HBGA) receptor polymorphism, but details governing diversity, host ranges, and species barriers remain elusive. In this study, crystal structures of complexes of the major P[II] genogroup P[4] and P[8] genotype RV VP8* receptor-binding domains together with Lewis epitope-containing LNDFH I glycans in combination with VP8* receptor-glycan ligand affinity measurements based on NMR titration experiments revealed the structural basis for RV genotype-specific switching between ββ and βα HBGA receptor-binding sites that determine RV host ranges. The data support the hypothesis that P[II] RV evolution progressed from animals to humans under the selection of type 1 HBGAs guided by stepwise host synthesis of type 1 ABH and Lewis HBGAs. The results help explain disease burden, species barriers, epidemiology, and limited efficacy of current RV vaccines in developing countries. The structural data has the potential to impact the design of future vaccine strategies against RV gastroenteritis.
    MeSH term(s) Blood Group Antigens/immunology ; Crystallography, X-Ray ; Evolution, Molecular ; Host Specificity/genetics ; Humans ; Nuclear Magnetic Resonance, Biomolecular/methods ; Protein Conformation ; Rotavirus/chemistry ; Rotavirus/genetics ; Rotavirus/immunology ; Viral Nonstructural Proteins/chemistry ; Viral Vaccines/immunology
    Chemical Substances Blood Group Antigens ; Viral Nonstructural Proteins ; Viral Vaccines
    Language English
    Publishing date 2021-09-02
    Publishing country United States
    Document type Journal Article ; Research Support, Non-U.S. Gov't ; Research Support, U.S. Gov't, Non-P.H.S.
    ZDB-ID 209104-5
    ISSN 1091-6490 ; 0027-8424
    ISSN (online) 1091-6490
    ISSN 0027-8424
    DOI 10.1073/pnas.2107963118
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  3. Article: A Comparison of the P.C. and I.Q.

    Riley, Gordon L

    The Psychological clinic

    2017  Volume 18, Issue 9, Page(s) 261–265

    Language English
    Publishing date 2017-09-14
    Publishing country United States
    Document type Journal Article
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  4. Article: Rediscovery of Gasteranthus extinctus L.E.Skog & L.P.Kvist (Gesneriaceae) at multiple sites in western Ecuador

    Pitman, Nigel C. A. / White, Dawson M. / Andino, Juan Ernesto Guevara / Couvreur, Thomas L. P. / Fortier, Riley P. / Zapata, José Nicolás / Cornejo, Xavier / Clark, John L. / Feeley, Kenneth J. / Johnston, Mark K. / Lozinguez, Alix / Rivas-Torres, Gonzalo

    PhytoKeys. 2022 Apr. 15, v. 194

    2022  

    Abstract: AbstractWe report the rediscovery of the Critically Endangered cloud forest herb Gasteranthus extinctus, not seen since 1985. In 2019 and 2021, G. extinctus was recorded at five sites in the western foothills of the Ecuadorian Andes, 4–25 km from the ... ...

    Abstract AbstractWe report the rediscovery of the Critically Endangered cloud forest herb Gasteranthus extinctus, not seen since 1985. In 2019 and 2021, G. extinctus was recorded at five sites in the western foothills of the Ecuadorian Andes, 4–25 km from the type locality at the celebrated Centinela ridge. We describe the species’ distribution, abundance, habitat and conservation status and offer recommendations for further research and conservation efforts focused on G. extinctus and the small, disjunct forest remnants it occupies.
    Keywords Gesneriaceae ; conservation status ; habitats ; tropical montane cloud forests ; Andes region ; Ecuador
    Language English
    Dates of publication 2022-0415
    Size p. 33-46.
    Publishing place Pensoft Publishers
    Document type Article
    ZDB-ID 2579891-1
    ISSN 1314-2003 ; 1314-2011
    ISSN (online) 1314-2003
    ISSN 1314-2011
    DOI 10.3897/phytokeys.194.79638
    Database NAL-Catalogue (AGRICOLA)

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  5. Article ; Online: Clinical and Molecular Spectrum Associated with COL6A3 c.7447A>G p.(Lys2483Glu) Variant: Elucidating its Role in Collagen VI-related Myopathies.

    Villar-Quiles, Rocío N / Donkervoort, Sandra / de Becdelièvre, Alix / Gartioux, Corine / Jobic, Valérie / Foley, A Reghan / McCarty, Riley M / Hu, Ying / Menassa, Rita / Michel, Laurence / Gousse, Gaelle / Lacour, Arnaud / Petiot, Philippe / Streichenberger, Nathalie / Choumert, Ariane / Declerck, Léa / Urtizberea, J A / Sole, Guilhem / Furby, Alain /
    Cérino, Matthieu / Krahn, Martin / Campana-Salort, Emmanuelle / Ferreiro, Ana / Eymard, Bruno / Bönnemann, Carsten G / Bharucha-Goebel, Diana / Sumner, Charlotte J / Connolly, Anne M / Richard, Pascale / Allamand, Valérie / Métay, Corinne / Stojkovic, Tanya

    Journal of neuromuscular diseases

    2021  Volume 8, Issue 4, Page(s) 633–645

    Abstract: ... with the frequent COL6A3 missense variant c.7447A>G (p.Lys2483Glu).: Methods: We report the clinical and ...

    Abstract Background: Dominant and recessive autosomal pathogenic variants in the three major genes (COL6A1-A2-A3) encoding the extracellular matrix protein collagen VI underlie a group of myopathies ranging from early-onset severe conditions (Ullrich congenital muscular dystrophy) to milder forms maintaining independent ambulation (Bethlem myopathy). Diagnosis is based on the combination of clinical presentation, muscle MRI, muscle biopsy, analysis of collagen VI secretion, and COL6A1-A2-A3 genetic analysis, the interpretation of which can be challenging.
    Objective: To refine the phenotypical spectrum associated with the frequent COL6A3 missense variant c.7447A>G (p.Lys2483Glu).
    Methods: We report the clinical and molecular findings in 16 patients: 12 patients carrying this variant in compound heterozygosity with another COL6A3 variant, and four homozygous patients.
    Results: Patients carrying this variant in compound heterozygosity with a truncating COL6A3 variant exhibit a phenotype consistent with COL6-related myopathies (COL6-RM), with joint contractures, proximal weakness and skin abnormalities. All remain ambulant in adulthood and only three have mild respiratory involvement. Most show typical muscle MRI findings. In five patients, reduced collagen VI secretion was observed in skin fibroblasts cultures. All tested parents were unaffected heterozygous carriers. Conversely, two out of four homozygous patients did not present with the classical COL6-RM clinical and imaging findings. Collagen VI immunolabelling on cultured fibroblasts revealed rather normal secretion in one and reduced secretion in another. Muscle biopsy from one homozygous patient showed myofibrillar disorganization and rimmed vacuoles.
    Conclusions: In light of our results, we postulate that the COL6A3 variant c.7447A>G may act as a modulator of the clinical phenotype. Thus, in patients with a typical COL6-RM phenotype, a second variant must be thoroughly searched for, while for patients with atypical phenotypes further investigations should be conducted to exclude alternative causes. This works expands the clinical and molecular spectrum of COLVI-related myopathies.
    MeSH term(s) Adolescent ; Adult ; Aged ; Child ; Child, Preschool ; Collagen Type VI/genetics ; Female ; Heterozygote ; Humans ; Magnetic Resonance Imaging ; Male ; Middle Aged ; Muscle, Skeletal/pathology ; Muscular Diseases/genetics ; Muscular Dystrophies/genetics ; Mutation ; Phenotype ; Procollagen/genetics ; Young Adult
    Chemical Substances COL6A3 protein, human ; Collagen Type VI ; Procollagen
    Language English
    Publishing date 2021-03-22
    Publishing country Netherlands
    Document type Journal Article
    ISSN 2214-3602
    ISSN (online) 2214-3602
    DOI 10.3233/JND-200577
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  6. Article ; Online: Molecular Basis of Functional Effects of Phosphorylation of the C-Terminal Domain of the Rabies Virus P Protein.

    Zhan, Jingyu / Watts, Ericka / Brice, Aaron M / Metcalfe, Riley D / Rozario, Ashley M / Sethi, Ashish / Yan, Fei / Bell, Toby D M / Griffin, Michael D W / Moseley, Gregory W / Gooley, Paul R

    Journal of virology

    2022  Volume 96, Issue 9, Page(s) e0011122

    Abstract: The rabies virus (RABV) phosphoprotein (P protein) is expressed as several isoforms, which differ ... are poorly defined, but phosphorylation by protein kinase C (PKC) in the P protein C-terminal domain ... P ...

    Abstract The rabies virus (RABV) phosphoprotein (P protein) is expressed as several isoforms, which differ in nucleocytoplasmic localization and microtubule (MT) association, mediated by several sequences, including nuclear localization (NLS) and export (NES) sequences. This appears to underpin a functional diversity enabling multiple functions in viral replication and modulation of host biology. Mechanisms regulating trafficking are poorly defined, but phosphorylation by protein kinase C (PKC) in the P protein C-terminal domain (P
    MeSH term(s) Animals ; Cell Nucleus/metabolism ; Molecular Chaperones ; Phosphorylation ; Protein Isoforms/genetics ; Protein Isoforms/metabolism ; Rabies virus/genetics ; Rabies virus/metabolism ; Viral Structural Proteins
    Chemical Substances Molecular Chaperones ; P phosphoprotein, Rabies virus ; Protein Isoforms ; Viral Structural Proteins
    Language English
    Publishing date 2022-04-11
    Publishing country United States
    Document type Journal Article
    ZDB-ID 80174-4
    ISSN 1098-5514 ; 0022-538X
    ISSN (online) 1098-5514
    ISSN 0022-538X
    DOI 10.1128/jvi.00111-22
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    Zs.A 609: Show issues Location:
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  7. Article ; Online: Palladium-Catalyzed C-P Bond-Forming Reactions of Aryl Nonaflates Accelerated by Iodide.

    McErlain, Holly / Riley, Leanne M / Sutherland, Andrew

    The Journal of organic chemistry

    2021  Volume 86, Issue 23, Page(s) 17036–17049

    Abstract: An iodide-accelerated, palladium-catalyzed C-P bond-forming reaction of aryl nonaflates is ... with coupling to other P(O)H compounds for the synthesis of aryl phosphonates and an aryl phosphinate ... The straightforward synthesis of stable, isolable aryl nonaflates, in combination with the rapid C-P bond-forming ...

    Abstract An iodide-accelerated, palladium-catalyzed C-P bond-forming reaction of aryl nonaflates is described. The protocol was optimized for the synthesis of aryl phosphine oxides and was found to be tolerant of a wide range of aryl nonaflates. The general nature of this transformation was established with coupling to other P(O)H compounds for the synthesis of aryl phosphonates and an aryl phosphinate. The straightforward synthesis of stable, isolable aryl nonaflates, in combination with the rapid C-P bond-forming reaction allows facile preparation of aryl phosphorus target compounds from readily available phenol starting materials. The synthetic utility of this general strategy was demonstrated with the efficient preparation of an organic light-emitting diode (OLED) material and a phosphonophenylalanine mimic.
    MeSH term(s) Catalysis ; Iodides ; Oxides ; Palladium
    Chemical Substances Iodides ; Oxides ; Palladium (5TWQ1V240M)
    Language English
    Publishing date 2021-11-02
    Publishing country United States
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 123490-0
    ISSN 1520-6904 ; 0022-3263
    ISSN (online) 1520-6904
    ISSN 0022-3263
    DOI 10.1021/acs.joc.1c02172
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  8. Article ; Online: The impact of delayed treatment of uncomplicated P. falciparum malaria on progression to severe malaria: A systematic review and a pooled multicentre individual-patient meta-analysis.

    Mousa, Andria / Al-Taiar, Abdullah / Anstey, Nicholas M / Badaut, Cyril / Barber, Bridget E / Bassat, Quique / Challenger, Joseph D / Cunnington, Aubrey J / Datta, Dibyadyuti / Drakeley, Chris / Ghani, Azra C / Gordeuk, Victor R / Grigg, Matthew J / Hugo, Pierre / John, Chandy C / Mayor, Alfredo / Migot-Nabias, Florence / Opoka, Robert O / Pasvol, Geoffrey /
    Rees, Claire / Reyburn, Hugh / Riley, Eleanor M / Shah, Binal N / Sitoe, Antonio / Sutherland, Colin J / Thuma, Philip E / Unger, Stefan A / Viwami, Firmine / Walther, Michael / Whitty, Christopher J M / William, Timothy / Okell, Lucy C

    PLoS medicine

    2020  Volume 17, Issue 10, Page(s) e1003359

    Abstract: ... at the health facility (odds ratio [OR] = 1.33, 95% CI: 1.07-1.64 for a delay of >24 hours versus ≤24 hours; p = 0.009 ... in children, with an OR of 2.79 (95% CI:1.92-4.06; p < 0.001) for a delay of 2-3 days and 5.46 (95% CI: 3.49-8 ... 53; p < 0.001) for a delay of >7 days, compared with receiving treatment within 24 hours from symptom ...

    Abstract Background: Delay in receiving treatment for uncomplicated malaria (UM) is often reported to increase the risk of developing severe malaria (SM), but access to treatment remains low in most high-burden areas. Understanding the contribution of treatment delay on progression to severe disease is critical to determine how quickly patients need to receive treatment and to quantify the impact of widely implemented treatment interventions, such as 'test-and-treat' policies administered by community health workers (CHWs). We conducted a pooled individual-participant meta-analysis to estimate the association between treatment delay and presenting with SM.
    Methods and findings: A search using Ovid MEDLINE and Embase was initially conducted to identify studies on severe Plasmodium falciparum malaria that included information on treatment delay, such as fever duration (inception to 22nd September 2017). Studies identified included 5 case-control and 8 other observational clinical studies of SM and UM cases. Risk of bias was assessed using the Newcastle-Ottawa scale, and all studies were ranked as 'Good', scoring ≥7/10. Individual-patient data (IPD) were pooled from 13 studies of 3,989 (94.1% aged <15 years) SM patients and 5,780 (79.6% aged <15 years) UM cases in Benin, Malaysia, Mozambique, Tanzania, The Gambia, Uganda, Yemen, and Zambia. Definitions of SM were standardised across studies to compare treatment delay in patients with UM and different SM phenotypes using age-adjusted mixed-effects regression. The odds of any SM phenotype were significantly higher in children with longer delays between initial symptoms and arrival at the health facility (odds ratio [OR] = 1.33, 95% CI: 1.07-1.64 for a delay of >24 hours versus ≤24 hours; p = 0.009). Reported illness duration was a strong predictor of presenting with severe malarial anaemia (SMA) in children, with an OR of 2.79 (95% CI:1.92-4.06; p < 0.001) for a delay of 2-3 days and 5.46 (95% CI: 3.49-8.53; p < 0.001) for a delay of >7 days, compared with receiving treatment within 24 hours from symptom onset. We estimate that 42.8% of childhood SMA cases and 48.5% of adult SMA cases in the study areas would have been averted if all individuals were able to access treatment within the first day of symptom onset, if the association is fully causal. In studies specifically recording onset of nonsevere symptoms, long treatment delay was moderately associated with other SM phenotypes (OR [95% CI] >3 to ≤4 days versus ≤24 hours: cerebral malaria [CM] = 2.42 [1.24-4.72], p = 0.01; respiratory distress syndrome [RDS] = 4.09 [1.70-9.82], p = 0.002). In addition to unmeasured confounding, which is commonly present in observational studies, a key limitation is that many severe cases and deaths occur outside healthcare facilities in endemic countries, where the effect of delayed or no treatment is difficult to quantify.
    Conclusions: Our results quantify the relationship between rapid access to treatment and reduced risk of severe disease, which was particularly strong for SMA. There was some evidence to suggest that progression to other severe phenotypes may also be prevented by prompt treatment, though the association was not as strong, which may be explained by potential selection bias, sample size issues, or a difference in underlying pathology. These findings may help assess the impact of interventions that improve access to treatment.
    MeSH term(s) Antimalarials/therapeutic use ; Benin/epidemiology ; Community Health Workers ; Disease Progression ; Gambia/epidemiology ; Humans ; Malaria/drug therapy ; Malaria/epidemiology ; Malaria, Falciparum/drug therapy ; Malaria, Falciparum/epidemiology ; Malaysia/epidemiology ; Mozambique/epidemiology ; Plasmodium falciparum/pathogenicity ; Tanzania/epidemiology ; Time-to-Treatment/economics ; Uganda/epidemiology ; Yemen/epidemiology ; Zambia/epidemiology
    Chemical Substances Antimalarials
    Keywords covid19
    Language English
    Publishing date 2020-10-19
    Publishing country United States
    Document type Journal Article ; Meta-Analysis ; Research Support, N.I.H., Extramural ; Research Support, Non-U.S. Gov't ; Systematic Review
    ZDB-ID 2185925-5
    ISSN 1549-1676 ; 1549-1277
    ISSN (online) 1549-1676
    ISSN 1549-1277
    DOI 10.1371/journal.pmed.1003359
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  9. Article ; Online: Linear Dichroism Activity of Chiral Poly(p‑Aryltriazole) Foldamers

    Jake G. Carter / Rueben Pfukwa / Liam Riley / James H. R. Tucker / Alison Rodger / Timothy R. Dafforn / Bert Klumperman

    ACS Omega, Vol 6, Iss 48, Pp 33231-

    2021  Volume 33237

    Keywords Chemistry ; QD1-999
    Language English
    Publishing date 2021-11-01T00:00:00Z
    Publisher American Chemical Society
    Document type Article ; Online
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

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  10. Article ; Online: Observation of Charge-Dependent Azimuthal Correlations in p-Pb Collisions and Its Implication for the Search for the Chiral Magnetic Effect.

    Khachatryan, V / Sirunyan, A M / Tumasyan, A / Adam, W / Asilar, E / Bergauer, T / Brandstetter, J / Brondolin, E / Dragicevic, M / Erö, J / Flechl, M / Friedl, M / Frühwirth, R / Ghete, V M / Hartl, C / Hörmann, N / Hrubec, J / Jeitler, M / König, A /
    Krätschmer, I / Liko, D / Matsushita, T / Mikulec, I / Rabady, D / Rad, N / Rahbaran, B / Rohringer, H / Schieck, J / Strauss, J / Waltenberger, W / Wulz, C-E / Dvornikov, O / Makarenko, V / Zykunov, V / Mossolov, V / Shumeiko, N / Suarez Gonzalez, J / Alderweireldt, S / De Wolf, E A / Janssen, X / Lauwers, J / Van De Klundert, M / Van Haevermaet, H / Van Mechelen, P / Van Remortel, N / Van Spilbeeck, A / Abu Zeid, S / Blekman, F / D'Hondt, J / Daci, N / De Bruyn, I / Deroover, K / Lowette, S / Moortgat, S / Moreels, L / Olbrechts, A / Python, Q / Tavernier, S / Van Doninck, W / Van Mulders, P / Van Parijs, I / Brun, H / Clerbaux, B / De Lentdecker, G / Delannoy, H / Fasanella, G / Favart, L / Goldouzian, R / Grebenyuk, A / Karapostoli, G / Lenzi, T / Léonard, A / Luetic, J / Maerschalk, T / Marinov, A / Randle-Conde, A / Seva, T / Vander Velde, C / Vanlaer, P / Vannerom, D / Yonamine, R / Zenoni, F / Zhang, F / Cimmino, A / Cornelis, T / Dobur, D / Fagot, A / Garcia, G / Gul, M / Khvastunov, I / Poyraz, D / Salva, S / Schöfbeck, R / Sharma, A / Tytgat, M / Van Driessche, W / Yazgan, E / Zaganidis, N / Bakhshiansohi, H / Beluffi, C / Bondu, O / Brochet, S / Bruno, G / Caudron, A / De Visscher, S / Delaere, C / Delcourt, M / Francois, B / Giammanco, A / Jafari, A / Jez, P / Komm, M / Krintiras, G / Lemaitre, V / Magitteri, A / Mertens, A / Musich, M / Nuttens, C / Piotrzkowski, K / Quertenmont, L / Selvaggi, M / Vidal Marono, M / Wertz, S / Beliy, N / Aldá Júnior, W L / Alves, F L / Alves, G A / Brito, L / Hensel, C / Moraes, A / Pol, M E / Rebello Teles, P / Belchior Batista Das Chagas, E / Carvalho, W / Chinellato, J / Custódio, A / Da Costa, E M / Da Silveira, G G / De Jesus Damiao, D / De Oliveira Martins, C / Fonseca De Souza, S / Huertas Guativa, L M / Malbouisson, H / Matos Figueiredo, D / Mora Herrera, C / Mundim, L / Nogima, H / Prado Da Silva, W L / Santoro, A / Sznajder, A / Tonelli Manganote, E J / Vilela Pereira, A / Ahuja, S / Bernardes, C A / Dogra, S / Fernandez Perez Tomei, T R / Gregores, E M / Mercadante, P G / Moon, C S / Novaes, S F / Padula, Sandra S / Romero Abad, D / Ruiz Vargas, J C / Aleksandrov, A / Hadjiiska, R / Iaydjiev, P / Rodozov, M / Stoykova, S / Sultanov, G / Vutova, M / Dimitrov, A / Glushkov, I / Litov, L / Pavlov, B / Petkov, P / Fang, W / Ahmad, M / Bian, J G / Chen, G M / Chen, H S / Chen, M / Chen, Y / Cheng, T / Jiang, C H / Leggat, D / Liu, Z / Romeo, F / Shaheen, S M / Spiezia, A / Tao, J / Wang, C / Wang, Z / Zhang, H / Zhao, J / Ban, Y / Chen, G / Li, Q / Liu, S / Mao, Y / Qian, S J / Wang, D / Xu, Z / Avila, C / Cabrera, A / Chaparro Sierra, L F / Florez, C / Gomez, J P / González Hernández, C F / Ruiz Alvarez, J D / Sanabria, J C / Godinovic, N / Lelas, D / Puljak, I / Ribeiro Cipriano, P M / Sculac, T / Antunovic, Z / Kovac, M / Brigljevic, V / Ferencek, D / Kadija, K / Mesic, B / Micanovic, S / Sudic, L / Susa, T / Attikis, A / Mavromanolakis, G / Mousa, J / Nicolaou, C / Ptochos, F / 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Ojalvo, I / Perry, T / Pierro, G A / Polese, G / Ruggles, T / Savin, A / Smith, N / Smith, W H / Taylor, D / Woods, N

    Physical review letters

    2017  Volume 118, Issue 12, Page(s) 122301

    Abstract: Charge-dependent azimuthal particle correlations with respect to the second-order event plane in p ... particles, are of similar magnitude in p-Pb and PbPb collisions at the same multiplicities. These results ...

    Abstract Charge-dependent azimuthal particle correlations with respect to the second-order event plane in p-Pb and PbPb collisions at a nucleon-nucleon center-of-mass energy of 5.02 TeV have been studied with the CMS experiment at the LHC. The measurement is performed with a three-particle correlation technique, using two particles with the same or opposite charge within the pseudorapidity range |η|<2.4, and a third particle measured in the hadron forward calorimeters (4.4<|η|<5). The observed differences between the same and opposite sign correlations, as functions of multiplicity and η gap between the two charged particles, are of similar magnitude in p-Pb and PbPb collisions at the same multiplicities. These results pose a challenge for the interpretation of charge-dependent azimuthal correlations in heavy ion collisions in terms of the chiral magnetic effect.
    Language English
    Publishing date 2017-03-24
    Publishing country United States
    Document type Journal Article
    ZDB-ID 208853-8
    ISSN 1079-7114 ; 0031-9007
    ISSN (online) 1079-7114
    ISSN 0031-9007
    DOI 10.1103/PhysRevLett.118.122301
    Database MEDical Literature Analysis and Retrieval System OnLINE

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