101 research outputs found
Trace Element Patterns in Shells of Mussels (Bivalvia) Allow to Distinguish between Fresh- and Brackish-Water Coastal Environments of the Subarctic and Boreal Zone
- Author
- Publication venue
- MDPI
- Publication date
- 01/01/2023
- Field of study
The accumulation of trace metals in the shells of bivalves allows quantitative assessments of environmental pollution and helps to reconstruct paleo aquatic environments. However, the understanding on how marine and freshwater mollusks control the level of trace elements in their shells remains very limited. Here, we compared the trace element composition of marine and freshwater bivalves from boreal and subarctic habitats, using examples of widely distributed species of marine (Mytilus edulis, M. trossulus) and freshwater (Anodonta anatina, Unio sp., Beringiana beringiana) mussels. Sizable differences in several trace element concentrations were detected between different species, depending on their environmental niches. A multiparametric statistical treatment of the shell’s elemental composition allowed to distinguish the impact of external factors (water and sediment chemical composition) from active metabolic (biological) control. In particular, the obtained results demonstrated that Ba:Ca and Pb:Ca ratios in mussels’ shells are closely related to the primary productivity of aquatic ecosystems. The Mn:Ca ratio allowed to constrain the environmental conditions of mussels’ species depending on the trophic state of inhabited waterbody. Overall, the marine mussels exhibited stronger biological control of trace element accumulation, whereas trace element pattern in shells of freshwater mussels was chiefly controlled by environmental factors. The obtained results might help to use the trace element composition of bivalves in distinguishing marine and freshwater habitats of mollusks in paleo environments
A Dual Origin of the Xist Gene from a Protein-Coding Gene and a Set of Transposable Elements
- Author
- A Nekrutenko
- A Smit
- A Wutz
- AI Shevchenko
- Alexander I. Shevchenko
- C Chureau
- CJ Brown
- CJ Brown
- CM Johnston
- Eugeny A. Elisaphenko
- F Jeanmougin
- G Benson
- GV Glazko
- Igor B. Rogozin
- J Jurka
- JW Thomas
- L Duret
- L Elnitski
- LS Davidow
- MF Lyon
- N Brockdorff
- Neil Brockdorff
- Nikolay N. Kolesnikov
- RJ Britten
- S Kumar
- S Schwartz
- SC Chang
- SF Altschul
- Sudhindra Gadagkar
- Suren M. Zakian
- TA Hore
- Tatyana B. Nesterova
- TB Nesterova
- WR Pearson
- Z Yang
- ZC Yen
- Publication venue
- Public Library of Science
- Publication date
- 01/01/2008
- Field of study
X-chromosome inactivation, which occurs in female eutherian mammals is controlled by a complex X-linked locus termed the X-inactivation center (XIC). Previously it was proposed that genes of the XIC evolved, at least in part, as a result of pseudogenization of protein-coding genes. In this study we show that the key XIC gene Xist, which displays fragmentary homology to a protein-coding gene Lnx3, emerged de novo in early eutherians by integration of mobile elements which gave rise to simple tandem repeats. The Xist gene promoter region and four out of ten exons found in eutherians retain homology to exons of the Lnx3 gene. The remaining six Xist exons including those with simple tandem repeats detectable in their structure have similarity to different transposable elements. Integration of mobile elements into Xist accompanies the overall evolution of the gene and presumably continues in contemporary eutherian species. Additionally we showed that the combination of remnants of protein-coding sequences and mobile elements is not unique to the Xist gene and is found in other XIC genes producing non-coding nuclear RNA
Genome-wide sequence analyses of ethnic populations across Russia
- Author
- Antonik Alexey
- Balanovsky Oleg
- Brukhin Vladimir
- Cherkasov Nikolay
- Chernyaeva Ekaterina
- Davydova Tatyana K.
- Dobrynin Pavel
- Evsyukov Igor
- Glotov Andrey S.
- Gorbunova Anna
- Kliver Sergei
- Koepfli Klaus Peter
- Kolchanova Sofia
- Komissarov Alexei
- Krasheninnikova Ksenia
- Limborska Svetlana
- Logachev Anton
- Malov Sergey
- Noskova Ekaterina
- Novozhilov Alexey
- O'Brien Stephen J.
- Oleksyk Taras K.
- Osakovsky Vladimir
- Pavlova Olga A.
- Polev Dmitrii E.
- Puzyrev Valery
- Rotkevich Mikhail
- Shevchenko Andrey
- Sidorov Sviatoslav
- Simonov Serguei
- Sivtseva Tatyana M.
- Tamazian Gaik
- Ulantsev Vladimir
- Zhernakova Daria V.
- Zhuk Anna
- Publication venue
- 'Elsevier BV'
- Publication date
- 01/01/2020
- Field of study
The Russian Federation is the largest and one of the most ethnically diverse countries in the world, however no centralized reference database of genetic variation exists to date. Such data are crucial for medical genetics and essential for studying population history. The Genome Russia Project aims at filling this gap by performing whole genome sequencing and analysis of peoples of the Russian Federation. Here we report the characterization of genome-wide variation of 264 healthy adults, including 60 newly sequenced samples. People of Russia carry known and novel genetic variants of adaptive, clinical and functional consequence that in many cases show allele frequency divergence from neighboring populations. Population genetics analyses revealed six phylogeographic partitions among indigenous ethnicities corresponding to their geographic locales. This study presents a characterization of population-specific genomic variation in Russia with results important for medical genetics and for understanding the dynamic population history of the world's largest country
Genes flanking Xist in mouse and human are separated on the X chromosome in American marsupials
- Author
- Alexander I. Shevchenko
- C Chureau
- Christine Bird
- DW Cooper
- E Koina
- Eugeny A. Elisaphenko
- F Jeanmougin
- GB Sharman
- HK Evans
- Irina S. Zakharova
- JA Fantes
- JAM Graves
- JAM Graves
- JC Chow
- Jennifer R. Weidman
- JL VandeBerg
- John L. VandeBerg
- K Delaval
- L Duret
- Mark Ross
- MF Lyon
- MO Woodburne
- NB Rubtsov
- Neil Brockdorff
- Nicolay B. Rubtsov
- Nicolay N. Kolesnikov
- Nina A. Mazurok
- PB Samollow
- Randy L. Jirtle
- S Schwartz
- SF Altschul
- Siobhan Whitehead
- Suren M. Zakian
- T Haaf
- Tatiana V. Karamysheva
- Tatyana B. Nesterova
- TB Nesterova
- WR Pearson
- Publication venue
- Springer Netherlands
- Publication date
- 05/03/2007
- Field of study
X inactivation, the transcriptional silencing of one of the two X chromosomes in female mammals, achieves dosage compensation of X-linked genes relative to XY males. In eutherian mammals X inactivation is regulated by the X-inactive specific transcript (Xist), a cis-acting non-coding RNA that triggers silencing of the chromosome from which it is transcribed. Marsupial mammals also undergo X inactivation but the mechanism is relatively poorly understood. We set out to analyse the X chromosome in Monodelphis domestica and Didelphis virginiana, focusing on characterizing the interval defined by the Chic1 and Slc16a2 genes that in eutherians flank the Xist locus. The synteny of this region is retained on chicken chromosome 4 where other loci belonging to the evolutionarily ancient stratum of the human X chromosome, the so-called X conserved region (XCR), are also located. We show that in both M. domestica and D. virginiana an evolutionary breakpoint has separated the Chic1 and Slc16a2 loci. Detailed analysis of opossum genomic sequences revealed linkage of Chic1 with the Lnx3 gene, recently proposed to be the evolutionary precursor of Xist, and Fip1, the evolutionary precursor of Tsx, a gene located immediately downstream of Xist in eutherians. We discuss these findings in relation to the evolution of Xist and X inactivation in mammals
Combined Transfer of Human VEGF165 and HGF Genes Renders Potent Angiogenic Effect in Ischemic Skeletal Muscle
- Author
- A Efimenko
- Alexander Shevelev
- B Ferraro
- C Barreau
- DJ Wells
- DO Traktuev
- E Van Belle
- EM Rosen
- Evgeny Shevchenko
- F Bussolino
- F Sedighiani
- H Shigematsu
- HS Jang
- Igor Rybalkin
- Irina Beloglazova
- J Belch
- J Li
- J Wojta
- JA Wolff
- JD Schertzer
- JK Min
- JM Isner
- M Kowanetz
- M Shimamura
- ME Gerritsen
- N Arsic
- N Ferrara
- N Ferrara
- N Ferrara
- NA Mughal
- OA Antonova
- P Korpisalo
- Paolo Madeddu
- Pavel Makarevich
- PI Makarevich
- R Gupta
- R Gupta
- RJ Powell
- S Nikol
- S Sengupta
- SD Patil
- T Couffinhal
- Tatyana Vlasik
- TD Henry
- Vsevolod Tkachuk
- X Xin
- Y Gu
- Yelena Parfyonova
- YW Zhang
- Zoya Tsokolaeva
- Publication venue
- Public Library of Science
- Publication date
- 13/06/2012
- Field of study
Increased interest in development of combined gene therapy emerges from results of recent clinical trials that indicate good safety yet unexpected low efficacy of “single-gene” administration. Multiple studies showed that vascular endothelial growth factor 165 aminoacid form (VEGF165) and hepatocyte growth factor (HGF) can be used for induction of angiogenesis in ischemic myocardium and skeletal muscle. Gene transfer system composed of a novel cytomegalovirus-based (CMV) plasmid vector and codon-optimized human VEGF165 and HGF genes combined with intramuscular low-voltage electroporation was developed and tested in vitro and in vivo. Studies in HEK293T cell culture, murine skeletal muscle explants and ELISA of tissue homogenates showed efficacy of constructed plasmids. Functional activity of angiogenic proteins secreted by HEK293T after transfection by induction of tube formation in human umbilical vein endothelial cell (HUVEC) culture. HUVEC cells were used for in vitro experiments to assay the putative signaling pathways to be responsible for combined administration effect one of which could be the ERK1/2 pathway. In vivo tests of VEGF165 and HGF genes co-transfer were conceived in mouse model of hind limb ischemia. Intramuscular administration of plasmid encoding either VEGF165 or HGF gene resulted in increased perfusion compared to empty vector administration. Mice injected with a mixture of two plasmids (VEGF165+HGF) showed significant increase in perfusion compared to single plasmid injection. These findings were supported by increased CD31+ capillary and SMA+ vessel density in animals that received combined VEGF165 and HGF gene therapy compared to single gene therapy. Results of the study suggest that co-transfer of VEGF and HGF genes renders a robust angiogenic effect in ischemic skeletal muscle and may present interest as a potential therapeutic combination for treatment of ischemic disorders
Variability of Sequence Surrounding the Xist Gene in Rodents Suggests Taxon-Specific Regulation of X Chromosome Inactivation
- Author
- A Smit
- A Wutz
- Alexander I. Shevchenko
- Anastasia A. Malakhova
- B Courtier
- B Payer
- BR Migeon
- BR Migeon
- Brian P. Chadwick
- C Chureau
- C Chureau
- C Morey
- C Morey
- CL Tsai
- CM Johnston
- CS Xu
- CS Xu
- CS Xu
- D Tian
- DE Cohen
- E Debrand
- EA Elisaphenko
- Eugeny A. Elisaphenko
- EV Dementyeva
- F Jeanmougin
- FM Catzeflis
- G Benson
- GD Penny
- GF Kay
- I Okamoto
- J Zhao
- JC Chow
- JJ Jaeger
- JT Lee
- JT Lee
- KD Huynh
- M Prissette
- MF Lyon
- Neil Brockdorff
- Nina A. Mazurok
- P Clerc
- P Clerc
- P Navarro
- P Navarro
- RM Boumil
- S Rastan
- S Schwartz
- S Shibata
- SF Altschul
- SM Zakian
- Suren M. Zakian
- T Sado
- T Sado
- T Sado
- TA Hore
- Tatyana B. Nesterova
- TB Nesterova
- TB Nesterova
- TB Nesterova
- W Chao
- WR Pearson
- Y Marahrens
- ZC Yen
- Publication venue
- Public Library of Science
- Publication date
- 01/01/2011
- Field of study
One of the two X chromosomes in female mammalian cells is subject to inactivation (XCI) initiated by the Xist gene. In this study, we examined in rodents (voles and rat) the conservation of the microsatellite region DXPas34, the Tsix gene (antisense counterpart of Xist), and enhancer Xite that have been shown to flank Xist and regulate XCI in mouse. We have found that mouse regions of the Tsix gene major promoter and minisatellite repeat DXPas34 are conserved among rodents. We have also shown that in voles and rat the region homologous to the mouse Tsix major promoter, initiates antisense to Xist transcription and terminates around the Xist gene start site as is observed with mouse Tsix. A conservation of Tsix expression pattern in voles, rat and mice suggests a crucial role of the antisense transcription in regulation of Xist and XIC in rodents. Most surprisingly, we have found that voles lack the regions homologous to the regulatory element Xite, which is instead replaced with the Slc7a3 gene that is unassociated with the X-inactivation centre in any other eutherians studied. Furthermore, we have not identified any transcription that could have the same functions as murine Xite in voles. Overall, our data show that not all the functional elements surrounding Xist in mice are well conserved even within rodents, thereby suggesting that the regulation of XCI may be at least partially taxon-specific
FGF4 Independent Derivation of Trophoblast Stem Cells from the Common Vole
- Author
- A Bradley
- A Erlebacher
- A Ralston
- AA Avilion
- AG Smith
- AI Shevchenko
- Alexander G. Shilov
- Alexander I. Shevchenko
- Andrey P. Dyban
- Antonina I. Zhelezova
- B Feldman
- B Panning
- B Romeis
- BL Allen
- D Strumpf
- DA Rappolee
- DG Simmons
- E Arman
- E Heard
- E Notarianni
- E Notarianni
- EA Elisaphenko
- Ekaterina M. Noniashvili
- Elena V. Grigor'eva
- Eugeny A. Elisaphenko
- EW Carney
- GD Penny
- H Niwa
- I Chambers
- J Luo
- J Nichols
- J Rossant
- J Rossant
- J Schlessinger
- J Yan
- JA Thomson
- JA Thomson
- JB Lawrence
- JC Cross
- JC Cross
- JT Lee
- K Iwatsuki
- K Mitsui
- KH Graves
- KR Lescisin
- L Niswander
- M Amit
- M Guzman-Ayala
- M Hughes
- M Kibschull
- M Schmidt
- MJ Soares
- N Kirchhof
- NA Mazurok
- NA Mazurok
- Neil Brockdorff
- Nina A. Mazurok
- P Cartwright
- P Clerc
- Pavel A. Dyban
- R Grümmer
- R Haffner-Krausz
- Rafael Linden
- RL Gardner
- S Tanaka
- S Vassilieva
- SA Sheardown
- Sergey Ya. Slobodyanyuk
- SM Gartler
- SM Zakian
- SM Zakian
- Suren M. Zakian
- T Kunath
- T Matsuda
- Tatyana B. Nesterova
- TB Nesterova
- W Mak
- Publication venue
- Public Library of Science
- Publication date
- 01/01/2009
- Field of study
The derivation of stable multipotent trophoblast stem (TS) cell lines from preimplantation, and early postimplantation mouse embryos has been reported previously. FGF4, and its receptor FGFR2, have been identified as embryonic signaling factors responsible for the maintenance of the undifferentiated state of multipotent TS cells. Here we report the derivation of stable TS-like cell lines from the vole M. rossiaemeridionalis, in the absence of FGF4 and heparin. Vole TS-like cells are similar to murine TS cells with respect to their morphology, transcription factor gene expression and differentiation in vitro into derivatives of the trophectoderm lineage, and with respect to their ability to invade and erode host tissues, forming haemorrhagic tumours after subcutaneous injection into nude mice. Moreover, vole TS-like cells carry an inactive paternal X chromosome, indicating that they have undergone imprinted X inactivation, which is characteristic of the trophoblast lineage. Our results indicate that an alternative signaling pathway may be responsible for the establishment and stable proliferation of vole TS-like cells
Development and validation of HERWIG 7 tunes from CMS underlying-event measurements
- Author
- Aarrestad Thea Klaeboe,
- Aarup Petersen Henriette
- Abbaneo Duccio
- Abbiendi Giovanni
- Abbrescia Marcello
- Abdalla Hassan
- Abdullin Salavat
- Abercrombie Daniel
- Acharya Himal
- Acosta Darin
- Acosta John Gabriel,
- Adam Wolfgang
- Adams Eric
- Adams Mark Raymond,
- Adams Todd
- Adloff Catherine
- Adzic Petar
- Afanasiev Serguei
- Agapitos Antonis
- Agarwal Garvita
- Aggleton Robin
- Agram J-L
- AGRAM Jean-Laurent
- Aguilar-Benitez Manuel
- Ahmad Ashfaq
- Ahmad Muhammad
- Ahmed Asar
- Ahuja Sudha
- Akchurin Nural
- Akgun Bora
- Akpinar Alp
- Albajar Carmen
- Albergo Sebastiano
- Albert Andreas
- Albrow Michael
- Alcaraz Maestre Juan
- Aldaya Martin Maria
- Aldá Júnior Walter Luiz,
- Aleksandrov Aleksandar
- Alexakhin Vadim
- Alexander James
- Alhusseini Mohammad
- Alimena Juliette
- Alison John
- Allen Brandon
- Almond John
- Alvarez Gonzalez Barbara
- Alverson George
- Alves Gilvan,
- Aly Reham
- Alyari Maral
- Amapane Nicola
- Ambrogi Federico
- Amendola Chiara
- Amin Nick
- Amram Oz
- Amsler Claude
- Anagnostou Georgios
- Anderson Dustin
- Andrea Jeremy
- Andreev Vladimir
- Andreev Yuri,
- Andrews Michael Benjamin,
- Androsov Konstantin
- Ang L
- Antchev Georgy
- Antunovic Zeljko
- Apanasevich Leonard
- Apollinari Giorgio
- Appelt Eric
- Apresyan Artur
- Apyan Aram
- Araujo Mariana
- Arcaro Daniel
- Arcidiacono Roberta
- Arenton Michael Wayne,
- Argiro Stefano
- Arneodo Michele
- Aruta Caterina
- Asavapibhop Burin
- Asawatangtrakuldee Chayanit
- Asenov Patrick
- Asghar Muhammad Irfan,
- Asilar Ece
- Askew Andrew
- Asmuss Paul
- Assran Yasser
- Atakisi Ismail Okan,
- Atanasov Ivan
- Ather Mohsan Waseem,
- Attikis Alexandros
- Auffray Etiennette
- Aushev Tagir
- Auzinger Georg
- Avati Valentina
- Avery Paul
- Avila Carlos
- Awan Muhammad Imran Malik,
- Ayala Edy
- Aydogmus Sen Fatma
- Azarkin Maksim
- Azhgirey Igor
- Aziz Tariq
- Azzi Patrizia
- Azzurri Paolo
- Baarmand Marc M,
- Babaev Anton
- Babounikau Illia
- Bacchetta Nicola
- Bachiller Irene
- Bachtis Michail
- Backhaus Malte
- Baden A
- Baden Drew
- Baechler Joachim
- Bagliesi Giuseppe
- Bahinipati Seema
- Baillon Paul
- Bainbridge Robert
- Bakas Georgios
- Bakhshiansohi Hamed
- Baldenegro Barrera Cristian
- Ball Austin,
- Ban Yong
- Band Reyer
- Banerjee Sudeshna
- Banerjee Sunanda
- Bansal Sunil
- Barbagli Giuseppe
- Barberis Emanuela
- Bargassa Pedrame
- Baringer Philip
- Barnes Virgil E,
- Barney David
- Baron Owen
- Barrio Luna Mar
- Bartek Rachel
- Bartosik Nazar
- Bartók Márton
- Baselga Marta
- Bastos Diogo
- Battilana Carlo
- Baty Austin
- Bauerdick Lothar AT,
- Baur Sebastian
- Baxter Samuel
- Bayshev Igor
- Bean Alice
- Beauceron Stephanie
- Beaudette Florian
- Becerril Gonzalez Hugo
- Bechtel Janek
- Bedoya C,
- Beghin Diego
- Behera Prafulla Kumar,
- Behera Subash Chandra,
- Behnke Olaf
- Bein Samuel
- Belchior Batista Das Chagas Ewerton
- Belforte Stefano
- Bell Ken W,
- Bellan Riccardo
- Belloni Alberto
- Bellora Andrea
- Belyaev Alexander
- Belyaev Andrey
- Benaglia Andrea
- Benato Lisa
- Bencze Gyorgy
- Bendavid Joshua
- Benecke Anna
- Benelli Gabriele
- Beni Noemi
- Benitez Jose F,
- Benussi Luigi
- Beretvas Andrew
- Bergauer Thomas
- Berger Pirmin
- Berger Thomas
- Beri Suman Bala,
- Bermúdez Martínez Armando
- Bernardes Cesar Augusto,
- Bernet Colin
- Berry Douglas
- Berryhill Jeffrey
- Bertacchi Valerio
- Besancon Marc
- Beschi Andrea
- Bhal Eshwen
- Bhardwaj Ashutosh
- Bharti Monika
- Bhat Muzamil Ahmad,
- Bhat Pushpalatha C,
- Bhatnagar Vipin
- Bhattacharya Rajarshi
- Bhattacharya Saptaparna
- Bhattacharya Satyaki
- Bhattacharya Soham
- Bheesette Srinidhi
- Bhowmik Debabrata
- Bhowmik Sandeep
- Bhyun Ji Hwan,
- Bi Ran
- Bialkowska Helena
- Bianchini Lorenzo
- Bianco Michele
- Bianco Stefano
- Biasini Maurizio
- Biino Cristina
- Bilei Gian Mario,
- Bilin Bugra
- Bin Anuar Afiq Aizuddin,
- Bisello Dario
- Black Kevin
- Blekman Freya
- Blinov Vladimir
- Bloch Daniel
- Bloch Philippe
- Bloom Kenneth
- Bluj Michal
- Blumenfeld Barry
- Boccali Tommaso
- Bocci Andrea
- Bodek Arie
- Boimska Bozena
- Boletti Alessio
- Bologna Simone
- Bols Emil Sørensen,
- Bonacorsi Daniele
- Bonanomi Matteo
- Bonchev Miroslav
- Bonomally Shameena
- Boos Edouard
- Boran Fatma
- Borchsh Vladislav
- Borg Johan
- Borgonovi Lisa
- Bornheim Adolf
- Borras Kerstin
- Bortignon Pierluigi
- Bose Tulika
- Bossini Edoardo
- Botta Cristina
- Botta Valeria
- Boudoul Gaelle
- Bouhali Othmane
- Bourgatte Guillaume
- Bourilkov Dimitri
- Bozzo Marco
- Bragagnolo Alberto
- Braghieri Alessandro
- Braibant-Giacomelli Sylvie
- Brainerd Christopher
- BRANDAO MALBOUISSON Helena
- Brandt Stephanie
- Branson James G,
- Breedon Richard
- Breeze Shane
- Brew Christopher
- Brigliadori Luca
- Brigljevic Vuko
- Brinkerhoff Andrew
- Brivio Francesco
- Brochero Cifuentes Javier Andres,
- Brom J-M
- Brom Jean-Marie
- Brondolin Erica
- Brooke James John,
- Brown Robert M,
- Brunner David
- Bruno Giacomo
- Brzhechko Danyyl
- Brücken Erik
- Bucci Rachael
- Buccilli Andrew
- Buchanan James
- Buchmuller Oliver
- Buchot Perraguin Axel
- Bueghly James
- Bundock Aaron
- Bunichev Viacheslav
- Bunin Pavel
- Bunkowski Karol
- Buontempo Salvatore
- Burgo R,
- Burkett Kevin
- Burkle Bjorn
- Burt Kira
- Bury Florian Joel J
- Busson Philippe
- Busza Wit
- Butalla Stephen
- Butler Joel Nathan,
- Butler Philip H,
- Butz Erik
- Bylinkin Alexander
- Bylsma Ben
- Byszuk Adrian
- Cabrera Andrés
- Cabrillo Iban Jose,
- Cadamuro Luca
- Caillol Cécile
- Cakir Altan
- Calandri Alessandro
- Calderon De La Barca Sanchez Manuel
- Calderon Alicia
- Cali Ivan Amos,
- Call Kenneth
- Calligaris Luigi
- Calzaferri Simone
- Camen Camille
- Caminada Lea
- Campagnari Claudio
- Campanini Renato
- Campbell Alan
- Camporesi Tiziano
- Candelise Vieri
- Canelli Maria Florencia,
- Canepa Anadi
- Cankocak Kerem
- Capiluppi Paolo
- Cappati Alessandra
- Caputo Claudio
- Caraway Bryan
- Cardini Andrea
- Cardwell Bryan
- Carle Aurélien
- Carlin Roberto
- Carrera Jarrin Edgar
- Carrillo Montoya Camilo Andres,
- Carrillo Moreno Salvador
- Cartiglia Nicolo
- Carvalho Antunes De Oliveira Alexandra
- Carvalho Wagner
- Casarsa Massimo
- Caspart René
- Cassese Antonio
- Castaldi Rino
- Castaneda Hernandez Alfredo
- Castilla-Valdez Heriberto
- Castro Andrea
- Cavallari Francesca
- Cavallo Francesca Romana,
- Cavallo Nicola
- Cavanaugh Richard
- Ceard Ludivine
- Ceccarelli Rudy
- Cepaitis Vilius
- Cepeda Maria
- Cerati Giuseppe Benedetto,
- Cerci Salim
- Cerminara Gianluca
- Cerrada Marcos
- Cerri Olmo
- Cetorelli Flavia
- Chabert Eric Christian,
- Chadeeva Marina
- CHAHAL Gurpreet Singh,
- Chang Paoti
- Chang Philip
- Chanon Nicolas
- Chao Yuan
- Chapon Emilien
- Charaf Otman
- Charlot Claude
- Chatterjee Rajdeep Mohan,
- Chatterjee Suman
- Chauhan Shubhanshu
- Chauhan Sushil
- Chawla Ridhi
- Chazin Quero Barbara
- Checchia Paolo
- Chekhovsky Vladimir
- Chen Cheng
- Chen Guo-Ming,
- Chen He-Sheng,
- Chen Kai-Feng,
- Chen Mingshui
- Chen Po-Hsun,
- Chen Xuan
- Chen Yi
- Chen Yuan
- Chen Ziheng
- Chenarani Shirin
- Cheng Tongguang
- Cheng Yangyang
- Cherepanov Vladimir
- Chernyavskaya Nadezda
- Chertok Maxwell
- Cheung Harry,
- Chhibra Simranjit Singh,
- Chiarito Brandon
- Chinellato Jose
- Chlebana Frank
- Cho Sungwoong
- Choi Junho
- Choi Suyong
- Choi Young-Il
- Chou John Paul,
- Choudhary Brajesh C,
- Choudhury Somnath
- Chu Jennifer
- Chudasama Ruchi
- Chwalek Thorsten
- Ciangottini Diego
- Ciocci Maria Agnese,
- Cipriani Marco
- Ciriolo Vincenzo
- Cirkovic Predrag
- Citron Matthew
- Cittolin Sergio
- Ciulli Vitaliano
- Civinini Carlo
- Claes Daniel R,
- Clare Robert
- Clement Emyr
- Clerbaux Barbara
- Cockerill David JA,
- Coelho Eduardo
- Colaleo Anna
- Cole Joanne,
- Colino Nicanor
- Collard Caroline
- Colling David
- Cometti Simona
- Connor Patrick
- Consuegra Rodríguez Sandra
- Contardo Didier
- Conway John
- Conway Rylan
- Cooper Seth,
- Cooperstein Stephane
- Corcodilos Lucas
- Cornelis Tom
- Correia Silva Gilson
- Cosby Christopher
- Cossutti Fabio
- Costa Marco
- Costa Salvatore
- Coubez Xavier
- Couderc Fabrice
- Cousins Robert
- Covarelli Roberto
- Cox Bradley
- Cox Peter Timothy,
- Cranshaw Derek James,
- Creanza Donato
- Cremonesi Matteo
- Cristella Leonardo
- Croce D,
- Csanad Mate
- Csorgo Tamas Ferenc
- Cuevas Javier
- Cuffiani Marco
- Cumalat John Perry,
- Cummings Grace
- Cussans David
- Cutts David
- Czellar Sandor
- D'Alessandro Raffaello
- D'Alfonso Mariarosaria
- D'Enterria David
- D'Hondt Jorgen
- Da Costa E,
- Da Rold Alessandro
- Da Silveira Gustavo Gil,
- Dabrowski Anne
- Daci Nadir
- Dalchenko Mykhailo
- Dallavalle Gaetano-Marco,
- Damarseckin Serdal
- Damgov Jordan
- Danilov Vladyslav
- Daponte Vincenzo
- Darwish Mohamed Rashad,
- Das Pallabi
- Das Souvik
- Dasgupta Abhigyan
- Dash Dipika
- Daskalakis Georgios
- Dasu Sridhara
- Datta Abhisek
- Dauncey Paul
- David Tinoco Mendes Andre
- David A
- David Pieter
- Davies Gavin
- Davignon Olivier
- de Barbaro Pawel
- De Boer Wim
- De Bruyn Isabelle
- De Castro Manzano Pablo
- De Clercq Jarne
- De Cosa Annapaola
- De Filippis Nicola
- De Guio Federico
- De Iorio Agostino
- De Jesus Damiao Dilson
- De La Cruz Begona
- De La Cruz-Burelo Eduard
- De Lentdecker Gilles
- De Leo Ksenia
- De Moraes Gregores Eduardo
- De Palma Mauro
- De Roeck Albert
- De Souza Lemos Dener
- De Souza S,
- de Trocóniz Jorge F,
- De Wit Adinda
- De Wolf Eddi A,
- Deelen Nikkie
- Defranchis Matteo Maria,
- Deile Mario
- Dejardin Marc
- Del Burgo Riccardo
- Del Re Daniele
- Delaere Christophe
- Delannoy Andrés G,
- Delannoy Hugo
- Delcourt Martin
- Delgado Peris Antonio
- Delgado Andrea
- Dell'Orso Roberto
- Della Negra Michel
- Della Ricca Giuseppe
- Dell’orso R
- Demaria Natale
- Demina Regina
- Demiragli Zeynep
- Demiroglu Zuhal Seyma,
- Denegri Daniel
- Depasse Pierre
- Derdzinski Mark
- Dermenev Alexander
- Dev Nabarun
- Dewanjee Ram Krishna,
- Dezoort Gage
- Dhammage Deshitha Chamikara Wickramarathna
- Dharmaratna Welathantri GD,
- Dhingra Nitish
- Di Croce Davide
- Di Domenico M R
- Di Florio Adriano
- Di Marco Emanuele
- Di Maria Riccardo
- Di Mattia Alessandro
- Di Pilato Antonio
- Diab Batoul
- Diamantopoulou Magda
- Diaz Daniel
- Didukh Leonid
- Diemoz Marcella
- Dierlamm Alexander
- Dildick Sven
- Dilsiz Kamuran
- Dimitrov Anton
- Dimova Tatyana
- Dinardo Mauro Emanuele,
- Dini Paolo
- Diotalevi Tommaso
- Dissertori Günther
- Dittmann Jay
- Dittmar Michael
- Dittmer Susan
- Dobson Marc
- Dobur Didar
- Dogra Sunil
- Dolek Furkan
- Dolen James
- Domenico M,
- Dominguez Aaron
- Domínguez Damiani Daniela
- Donato Silvio
- Donegà Mauro
- Donertas Izzeddin Suat,
- Dordevic Milos
- Dorfer Christian
- Dorigo Tommaso
- Dorney Brian
- Doroba Krzysztof
- Dorsett Alex
- Dozen Candan
- Dragicevic Marko
- Dremin Igor
- Dreyer Torben
- Droll Alexander
- Duarte Campderros Jordi
- Duarte Javier
- Dube Sourabh
- Dubinin Mikhail
- Dudko Lev
- Dugad Shashikant
- Duh Yi-ting,
- Dulemba Joseph Lynn,
- Dumanoglu Isa
- Dupont Niels
- Durgut Süleyman
- Duric Senka
- Durkin Lloyd Stanley,
- Dutta Dipanwita
- Dutta Irene
- Dutta Suchandra
- Dutta Valentina
- Dziwok Christian
- Dünser Marc
- D’alessandro R
- D’alfonso M
- D’enterria D
- D’hondt J
- Ebrahimi Aliakbar
- Eckerlin Guenter
- Ecklund Karl Matthew,
- Eckstein Doris
- Eerola Paula
- Ehataht Karl
- Eich Melanie
- Eichhorn Thomas
- El Mamouni Houmani
- El Morabit Karim
- Eliseev Dmitry
- Elkafrawy Tamer
- Elliott-Peisert Anna
- Ellis Katherine Victoria,
- Elmer Peter
- Elmetenawee Walaa
- Elvira Victor Daniel,
- Elwood Adam
- Eminizer Margaret
- Emriskova Natalia
- Eno Sarah Catherine,
- Epshteyn Vladimir
- Erbacher Robin
- Erdmann Martin
- Erdmann Wolfram
- Erice Carlos
- Erodotou Eleni
- Errico Filippo
- Erö Janos
- Escalante Del Valle Alberto
- Eskut Eda
- Estevez Banos Luis Ignacio,
- Etesami Seyed Mohsen,
- Eusebi Ricardo
- Evangelou Ioannis
- Evans Andrew
- Evdokimov Olga
- Everaerts Pieter
- Eysermans Jan
- Fabbri Fabrizio
- Fabozzi Francesco
- Faccioli Pietro
- Fackeldey Peter
- Fallavollita Francesco
- Fallon Colin
- Falmagne Guillaume
- Faltermann Nils
- Fanfani Alessandra
- Fang Wenxing
- Fangmeier Caleb
- Fanò Livio
- Fasanella Daniele
- Faure Jean-Louis,
- Favart Laurent
- Fay Jean
- Fedi Giacomo
- Feindt Finn
- Felcini Marta
- Feld Lutz
- Feng Yongbin
- Ferbel Thomas
- Ferencek Dinko
- Ferguson Thomas
- Fernandez Bedoya Cristina
- Fernandez Menendez Javier
- Fernandez Perez Tomei T,
- Fernandez Marcos
- Fernández Manteca Pedro José,
- Fernández Ramos Juan Pablo,
- Ferri Federico
- Ferro Fabrizio
- Field Richard D,
- Fienga Francesco
- Finco Linda
- Finger Michael
- Finger Miroslav
- Fiore Luigi
- Fiorendi Sara
- Fiori Francesco
- Fiorina Davide
- Fischer Benjamin
- Flacher Henning
- Flix Jose
- Florent Alice
- Flores Chad
- Florez Carlos
- Flöh Kevin
- Flügge Günter
- Focardi Ettore
- Folgueras Santiago
- Fonseca De Souza Sandro
- Fontaine J-C
- Fontaine Jean-Charles
- Fontanesi Elisa
- Ford William T,
- Forthomme Laurent
- Foudas Costas
- Fouz Maria Cruz,
- Fraga Jorge
- Francis Brian
- Francois Brieuc
- Frankenthal Andre
- Franzoni Giovanni
- Freed Sarah
- Freeman Jim
- Freer Chad
- Frueboes Tomasz
- Fruehwirth Rudolf
- Fröhlich Alexander
- Frühwirth R
- Fulcher Jonathan
- Funk Garrett
- Funk Wolfgang
- Gadallah Mahmod Moussa Abdelkhalek,
- Gadek Tomasz
- Galanti Mario
- Gallinaro Michele
- Gallo Elisabetta
- Galloni Camilla
- Gandrajula Reddy Pratap,
- Gandrakota Abhijith
- Ganjour Serguei
- Gao Xuyang
- Garbers Christoph
- Garcia Fuentes Francisco Ignacio
- Garcia F
- Garcia-Bellido Aran
- García Alonso Andrea
- Garg Rocky Bala,
- Garutti Erika
- Gary J William,
- Gascon Susan
- Gasparini Fabrizio
- Gasparini Ugo
- Gastler Daniel
- Gavrilenko Mikhail
- Gavrilov Genady
- Gavrilov Vladimir
- Gecse Zoltan
- Geiser Achim
- Gelmi Andrea
- Gelé Denis
- Gennai Simone
- Geralis Theodoros
- Gerber Cecilia Elena,
- Gerosa Raffaele
- Gershtein Yuri
- Geurts Frank JM,
- Ghezzi Alessio
- Ghiasi Shirazi Seyyed Mohammad Amin,
- Ghosh Saranya
- Ghosh Shamik
- Giacomelli Paolo
- Giammanco Andrea
- Giani Simone
- Gianneios Paraskevas
- Giannini Leonardo
- Giassi Alessandro
- Giffels Manuel
- Gigi Dominique
- Gilbert Andrew
- Gilbert Dylan
- Giljanovic Duje
- Gill Karl
- Gilmore Jason
- Giommi Luca
- Giraldi Angela
- Givernaud Alain
- Glege Frank
- Gleyzer Sergei V,
- Gninenko Sergei
- Go Yeonju
- Godinovic Nikola
- Goerlach Ulrich
- Goh Junghwan
- Gokbulut Gul
- Gola Mohit
- Goldouzian Reza
- Goldstein Joel
- Golf Frank
- Golovtcov Victor
- Golubev Nikolai
- Golutvin Igor
- Gomber Bhawna
- Gomez Ceballos Guillelmo
- Gomez Gervasio
- Goncharov Maxim
- Gonzalez Caballero Isidro
- Gonzalez Lopez Oscar
- González Fernández Juan Rodrigo,
- Gorbunov Ilya
- Gottmann Artur
- Gottschalk Erik
- Gouskos Loukas
- Gouzevitch Maxime
- Govoni Pietro
- Goy Lopez Silvia
- Grab Christoph
- Grandi Claudio
- Granier de Cassagnac Raphael
- Gras Philippe
- Gray Lindsey
- Grebenyuk Anastasia
- Green Dan
- Greenberg Bennett
- Greene Senta
- Gregores E,
- Grimault Clément
- Grippo Maria Teresa,
- Gritsan Andrei,
- Grohsjean Alexander
- Gruchala Marek
- Grunewald Martin
- Grynyov Boris
- Grzanka Leszek
- Grünendahl Stefan
- Guchait Monoranjan
- Guerrero Daniel
- Guiducci Luigi
- Guilbaud Maxime
- Gul Muhammad
- Guler Yalcin
- Gulhan Doga
- Gunnellini Paolo
- Gunter Thoth
- Guo Qianying
- Gupta Rajat
- Gurpinar guler Emine
- Gurrola Alfredo
- Gurtu Atul
- Gutay Laszlo
- Guthoff Moritz
- Guts Sergey
- Gutsche Oliver
- Guzzi Luca
- Gómez Espinosa Tirso Alejandro,
- Górski Maciej
- Gülmez Erhan
- Ha Seungkyu
- Habibullah Redwan
- Haddad Yacine
- Hadjiiska Roumyana
- Hadley Mary
- Hadley Nicholas John,
- Hagopian Sharon
- Hagopian Vasken
- Hahn Kristan Allan,
- Haj Ahmad Wael
- Hajdu Csaba
- Hakala John
- Hakimi Alexandre
- Halkiadakis Eva
- Hall Geoffrey
- Haller Johannes
- Hamel De Monchenault Gautier
- Hamilton David
- Hangal Dhanush Anil,
- Hansen Peter
- Hanson Gail
- Haranko Mykyta
- Harb Ali
- Harder Kristian
- Harper Sam
- Harrington Charles
- Harris Philip
- Harris Robert M,
- Hart Andrew
- Hartmann Frank
- Hasegawa Satoshi
- Hashemi Bobak
- Hassan Qamar
- Hatakeyama Kenichi
- Haubrich Nicholas
- Hauser Jay
- Havukainen Joona
- Hay Lauren
- Haytmyradov Maksat
- He He
- Heath Greg P,
- Heath Helen F,
- Hebbeker Thomas
- Hegde Vinay
- Hegeman Jeroen
- Heidecker Christoph
- Heikkilä Jaana Kristiina,
- Heindl Maximilian
- Heintz Ulrich
- Heller Ryan
- Henderson Conor
- Hensel Carsten
- Heredia-De La Cruz Ivan
- Hernandez Jose M,
- Herndon Matthew
- Hervé Alain
- Herwig Theodor Christian,
- Higginbotham Samuel
- Hildreth Michael
- Hill Christopher
- Hiltbrand Joshua
- Hindrichs Otto
- Hinzmann Andreas
- Hirosky Robert
- Hirschauer James
- Hits Dmitry
- Hlushchenko Olena
- Hobson Peter R,
- Hoepfner Kerstin
- Hofman David Jonathan,
- Hogan Julie Managan,
- Hoh Siew Yan,
- Hohlmann Marcus
- Hollar Jonathan
- Hong Byung-Sik
- Hoorani Hafeez R,
- Horisberger Roland
- Hortiangtham Apichart
- Horvath Dezso
- Hos Ilknur
- Hou George Wei-Shu
- Hou W-S
- Hsu Dylan
- Hu Miao
- Hu Zhen
- Huang Tao
- Hughes Elliot
- Huh Changgi
- Hurtado Anampa Kenyi
- Husemann Ulrich
- Hussain Usama
- Huwiler Marc
- Hwang Chanwook
- Iaselli Giuseppe
- Iashvili Ia
- Iaydjiev Plamen
- Iemmi Fabio
- Ignatenko Mikhail
- Iiyama Yutaro
- Iles Gregory
- Ille Bernard
- Incandela Joe
- Ince Merve
- Ingram Quentin
- Innocente Vincenzo
- Ioannou Aimilios
- Iorio Alberto Orso Maria,
- Iqbal Muhammad Ansar,
- Isidori Tommaso
- Isik Candan
- Isildak Bora
- Iuzhakov Aleksandr
- Ivanchenko V
- Ivanov Andrew
- Ivanov Todor
- Ivanov Yury
- Ivantchenko Vladimir
- Jabeen Shabnam
- Jafari Abideh
- Jain Sandhya,
- Jain Shilpi,
- James Thomas
- Janjam Ravi
- Janot Patrick
- Janssen Xavier
- Jaramillo Johny
- Jarry Patrick
- Jayananda M,
- Jayatilaka Bodhitha
- Jeitler Manfred
- Jeng Geng-Yuan,
- Jensen Frank
- Jeon Dajeong
- Jeon Sihyun
- Jeong Yongho
- Jessop Colin
- Jha Vishwajeet
- Jindariani Sergo
- Jofrehei Arash
- Johns Willard
- Johnson Kurtis F,
- Johnson Marvin
- Jomhari Nur Zulaiha,
- Jones Matthew
- Josa Maria Isabel,
- Joshi Bhargav Madhusudan,
- Joshi Umesh
- Joyce Matthew
- Jung Andreas Werner,
- Jung Hannes
- Juodagalvis Andrius
- Kaadze Ketino
- Kachanov Vassili
- Kadastik Mario
- Kaestli Hans-Christian,
- Kailasapathy Balashangar
- Kalbhor Pritam
- Kalinin Alexey
- Kalinowski Artur
- Kalogeropoulos Alexis
- Kalsi Amandeep Kaur,
- Kamon Teruki
- Kangal Evrim Ersin,
- Kansal Bhumika
- Kanuganti Ankush Reddy,
- Kaplan Steven
- Kapoor Anshul
- Kar Chandiprasad
- Kara Ozgun
- Karacheban Olena
- Karancsi János
- Karapinar Guler
- Karapostoli Georgia
- Karasavvas Dimitrios
- Karathanasis George
- Karavdina Anastasia
- Karchin Paul Edmund,
- Kardapoltsev Leonid
- Karimäki Veikko
- Karjavine Vladimir
- Karmakar Saikat
- Karmgard Daniel John,
- Karneyeu Anton
- Kasem A
- Kasemann Matthias
- Kasieczka Gregor
- Kaspar Jan
- Katkov Igor
- Katsoulis Panagiotis
- Kaur Amandeep
- Kaur Sandeep
- Kaveh Hessamoddin
- Kaya Mithat
- Kaya Ozlem
- Kayis Topaksu Aysel
- Kaynak Berkan
- Kazana Malgorzata
- Keicher Philip
- Keller Henning
- Kello Tomas
- Kellogg Richard G,
- Keshri Sumit
- Khakzad Mohsen
- Khalil Sadia
- Khan Akram
- Khan Wajid Ali,
- Kharchilava Avto
- Khristenko Viktor
- Khukhunaishvili Aleko
- Khurana Raman
- Khvastunov Illia
- Kiani Bilal
- Kieseler Jan
- Kilminster Benjamin
- Kilpatrick Matthew
- Kim Bobae
- Kim Dong Hee,
- Kim Doyeong
- Kim Gui Nyun,
- Kim Hyunchul
- Kim Hyunsoo,
- Kim Hyunyong
- Kim Jae Sung,
- Kim Ji Hyun,
- Kim Junho
- Kim Min Suk,
- Kim Mugeon
- Kim Tae Jeong,
- Kim Victor
- Kim Yongsun
- Kiminsu Ugur
- King Jack
- Kinnunen Ritva
- Kirakosyan Martin
- Kirsanov Mikhail
- Kirschenmann Henning
- Klabbers Pamela
- Klanner Robert
- Klein Daniel
- Klein Katja
- Kleinwort Claus
- Klijnsma Thomas
- Klima Boaz
- Klute Markus
- Klyukhin Vyacheslav
- Knolle Joscha
- Ko Byeonghak
- Ko Sanghyun
- Ko Winston
- Kodolova Olga
- Koeth Timothy
- Kogler Roman
- Kokkas Panagiotis
- Kolberg Ted
- Kole Gouranga
- Kolosova Marina
- Komaragiri Jyothsna Rani,
- Komm Matthias
- Komurcu Yildiray
- Konecki Marcin
- Konigsberg Jacobo
- Konstantinou Sotiroulla
- Konstantinov Dmitri
- Kontaxakis Pantelis
- Kopp Gillian
- Koppenhöfer Roland
- Koraka Charis Kleio,
- Kortelainen Matti J,
- Korytov Andrey
- Kothekar Kunal
- Kotlinski Danek
- Kousouris Konstantinos
- Kovac Marko
- Kovalskyi Dmytro
- Krammer Natascha
- Krasnikov Nikolai
- Kratochwil Nicolaus
- Kravchenko Ilya
- Kreczko Lukasz
- Kress Thomas
- Krikler Benjamin
- Krintiras Georgios
- Krofcheck David
- Krohn Michael
- Krolikowski Jan
- Kropivnitskaya Anna
- Krupa Jeffrey
- Krutelyov Vyacheslav
- Krücker Dirk
- Kubota Yuichi
- Kucher Inna
- Kukral Ota
- Kumar Verma Ravindra
- Kumar Arun
- Kumar Ashok
- Kumar Deepak
- Kumar Sanjeev
- Kumar Vineet
- Kumari Priyanka
- Kunori Shuichi
- Kuo Chia-Ming,
- Kutzner Viktor
- Kuznetsova Ekaterina
- Kveton Antonin
- Kwan Stephanie
- Kwok Ka Hei Martin,
- Kwon Hyejin
- Kyberd Paul
- Kyriacou Savvas
- Kyriakis Aristotelis
- Köseyan Ohannes Kamer,
- La Cruz I. Heredia-De
- Laflotte Ian
- Laird Edward
- Laktineh Imad Baptiste,
- Lam Tyler
- Lamichhane Kamal
- Lammel Stephan
- Lampén Tapio
- Lanaro Armando
- Lander Richard
- Landsberg Greg
- Lanev Alexander
- Lange Clemens
- Lange David
- Lange Johannes
- Lange Torben
- Lange Wolfgang
- Langenegger Urs
- Langford Jonathon
- Lannon Kevin
- Lariccia Paolo
- Lassila-Perini Kati
- Lath Amitabh
- Latino Giuseppe
- Lattaud Hugues
- Lau Ka Tung,
- Laurila Santeri
- Lawhorn Jay Mathew,
- Layer Lukas
- Le Bihan A-C
- Le Bihan Anne-Catherine
- Lechner Lukas
- Lecoq Paul
- Ledovskoy Alexander
- Lee Haneol
- Lee Heewon
- Lee Jangbae
- Lee Jason Sang Hun,
- Lee Jeongeun
- Lee Kisoo
- Lee Kyeongpil
- Lee Kyong Sei,
- Lee Sangeun
- Lee Seh Wook,
- Lee Sung Won,
- Lee Y-J
- Lee Yen-Jie
- Lee Yonghoon
- Lefeld Anthony
- Leggat Duncan
- Legger Federica
- Lehti Sami
- Lelas Damir
- Lelek Aleksandra
- Lemaitre Vincent
- Lemos D,
- Lenz Teresa
- Lenzi Bruno
- Lenzi Piergiulio
- Leonardo Nuno
- Leontsinis Stefanos
- Lesauvage Antoine
- Lesko Zachary
- Lethuillier Morgan
- Letts James
- Levchuk Leonid
- Levin Andrew
- Lezki Samet
- León Holgado Jaime
- Li Ang
- Li Qiang
- Li Wei
- Li Wenzhao
- Li You-ying,
- Liao Hongbo
- Lidrych Jindrich
- Ligabue Franco
- Liko Dietrich
- Lim Jaehoon
- Lin Willis
- Linacre Jacob
- Lincoln Don
- Lindsey Cole
- Lindén Tomas
- Lipinski Martin
- Lipka Katerina
- Lipton Ron
- Lista Luca
- Litomin Aliaksandr
- Litov Leander
- Liu Miaoyuan
- Liu Tiehui
- Liu Zhenan
- Liyanage Kalpanie
- Lizzo Mattia
- Lo Meo Sergio
- Lo Kin Ho,
- Lobanov Artur
- Locci Elizabeth
- Loeliger Andrew
- Lohan Manisha
- Lohmann Wolfgang
- Lokhtin Igor
- Long Kenneth
- Long Owen Rosser,
- Longo Egidio
- Lontkovskyi Denys
- Lopez-Fernandez Ricardo
- Loukas Demetrios
- Loukas Nikitas
- Lourenco Carlos
- Loveless Richard
- Lowette Steven
- Lu Meng
- Lu Nan
- Lu R-S
- Lu Rong-Shyang
- Lucchini Marco Toliman,
- Luckey Paul David,
- Luo Jingyu
- Luo Sifu
- Lustermann Werner
- Luukka Panja-Riina
- Lychkovskaya Natalia
- Lykken Joseph
- Lyon A-M
- Lyon Anne-mazarine
- Lyons Louis
- Lyu Xudong
- Lökös Sándor
- Macchiolo Anna
- MacDonald Emily
- Mackay Catherine Kirsty,
- Madhusudanan Sreekala Jithin
- Madigan Gabriel
- Madlener Thomas
- Madrid Christopher
- Maeshima Kaori
- Maggi Giorgio
- Maggi Marcello
- Maghrbi Yasser
- Magnan A-M
- Magnan Anne-Marie
- Maguire Charles
- Mahakud Bibhuprasad
- Mahmoud Mohammed,
- Maier Benedikt
- Maier Stefan
- Maity Manas
- Major Péter
- Majumder Devdatta
- Majumder Gobinda
- Makarenko Inna
- Makarenko Vladimir
- Maksimovic Petar
- Mal Prolay
- Malagalage Kithsiri
- Malakhov Alexander
- Malara Andrea
- Malawski Maciej
- Malberti Martina
- Malcles Julie
- Malgeri Luca
- Malhotra Shivali
- Malik Sarah
- Malik Sudhir
- Mallampalli Abhishikth
- Mallios Stavros
- Malvezzi Sandra
- Manca Elisabetta
- Mandal Koushik
- Mandorli Giulio
- Manganelli Nicholas
- Manitara Kalliopi
- Mankel Rainer
- Mannelli Marcello
- Manolopoulos Konstantinos
- Manousakis-Katsikakis Arkadios
- Mans Jeremy
- Manthos Nikolaos
- Mantilla Cristina
- Mantovani Giancarlo
- Manzoni Riccardo Andrea,
- Mao Jiajing
- Mao Yajun
- Maravin Yurii
- Marcellini Stefano
- Marchesini Ivan
- Margjeka Ilirjan
- Margoni Martino
- Mariani Valentina
- Marinelli Nancy
- Marini Andrea Carlo,
- Mariotti Chiara
- Marlow Daniel
- Marsh Bennett
- Martelli Arabella
- Martin Perez Cristina
- Martinez Rivero Celso
- Martinez Ruiz del Arbol Pablo
- Martinez German
- Martins Jordan
- Marzocchi Badder
- Masciovecchio Mario
- Maselli Silvia
- Masetti Gianni
- Mason David
- Massironi Andrea
- Mastrolorenzo Luca
- Matchev Konstantin
- Matorras Francisco
- Matos Figueiredo Diego
- Matveev Viktor
- Mavromanolakis Georgios
- May Samuel
- Mazumdar Kajari
- Mcalister Ian
- Mcbride Patricia
- Mccoll Nickolas
- Mcdermott Kevin
- Mcginn Christopher
- Mclean Christine
- Mcmaster Brooks
- Medina Jaime Miguel
- Meena Meena
- Mehta Ankita
- Mei Hualin
- Mei Kelvin
- Meijers Frans
- Meinhard Maren Tabea,
- Meiring Peter
- Mejia Guisao Jhovanny
- Melo Da Costa Eliza
- Melo De Almeida Miqueias
- Melo Andrew
- Melzer-Pellmann I-A
- Melzer-Pellmann Isabell-Alissandra
- Menasce Dario
- Meneguzzo Anna Teresa,
- Menendez Nicholas
- Meng Fanbo
- Mengke Tielige
- Menichelli Mauro
- Meola Sabino
- Mercadante Pedro G,
- Meridiani Paolo
- Merkel Petra
- Merlin Jeremie Alexandre,
- Merlo J-P
- Merlo Jean-Pierre
- Merschmeyer Markus
- Mersi Stefano
- Meschi Emilio
- Meschini Marco
- Mesic Benjamin
- Messineo Alberto
- Mestvirishvili Alexi
- Metwally Josry
- Metzler Marius
- Meuser Danilo
- Meyer Andreas Bernhard,
- Meyer Arnd
- Meyer Mareike
- Micheli Francesco
- Migliore Ernesto
- Mignerey Alice,
- Mijuskovic Jelena
- Mikulec Ivan
- Mikuni Vinicius Massami,
- Milenovic Predrag
- Millet Philipp
- Mills Corrinne
- Milosevic Jovan
- Milosevic Vukasin
- Minafra Nicola
- Mirabito Laurent
- Mironov Camelia
- Misheva Milena
- Mishra Dipak Kumar,
- Mishra Tribeni
- Missiroli Marino
- Mitchell Tyler
- Mitra Soureek
- Mitselmakher Guenakh
- Mitsyn Valeri Valentinovitch,
- Mnich Joachim
- Mocellin Giovanni
- Modak Atanu
- Moeller Anthony
- Mohamed Amr
- Mohamed Ashraf
- Mohammadi Najafabadi Mojtaba
- Mohammadi Abdollah
- Mohammed Yasser
- Mohrman Kelci
- Moisenz Petr
- Molinatti Umberto
- Molnar Jozsef
- Monaco Vincenzo
- Mondal Kuntal
- Mondal Spandan
- Monroy Jose
- Montagna Paolo
- Montalvo Roy
- Monteil Ennio
- Monteno Marco
- Monti Fabio
- Moon Chang-Seong,
- Moon Dong Ho,
- Moortgat Filip
- Moortgat Seth
- Mora Herrera Clemencia
- Moraes Arthur
- Moran Dermot
- Morelos Pineda Antonio
- Moroni Luigi
- Morse David Michael,
- Morton Alexander
- Moscatelli Francesco
- Moureaux Louis
- Mousa Jehad
- Mozer Matthias Ulrich,
- Mrenna Stephen
- Mudholkar Tanmay
- Mueller Ryan
- Muhammad Alibordi
- Mukherjee Soumya
- Mukherjee Swagata
- Mulargia Roberto
- Mulders Martijn
- Mulhearn Michael
- Mulholland Troy
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- Muraleedharan Nair Bindhu Vinaya Krishnan,
- Murillo Quijada Javier Alberto,
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- Sahoo Niladribihari
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- Tuominiemi Jorma
- Turini Nicola
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- Wu Zhenbin
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- Wulz Claudia-Elisabeth
- Wuyckens Sophie
- Wyslouch Bolek
- Wöhrmann Clemens
- Würthwein Frank
- Xia Fan
- Xiao Jie
- Xiao Meng
- Xiao rui
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- Yang Yu Chul,
- Yao Yao
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- Yi Kai
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- Yoo Hwi Dong,
- Yoo Jaehyeok
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- Yu David
- Yu Geum Bong,
- Yu Intae
- Yu Shin-Shan,
- Yuan Li
- Yuan Siqi
- Yuldashev Bekhzod S,
- Yumiceva Francisco
- Yusli Mohd Nizam,
- Zabi Alexandre
- Zacharopoulou Anna
- Zahid Sema
- Zaleski Shawn
- Zalewski Piotr
- Zanetti Marco
- Zarubin Anatoli
- Zarucki Mateusz
- Zecchinelli Angelo Giacomo,
- Zenaiev Oleksandr
- Zenz Seth Conrad,
- Zeuner Wolfram Dietrich,
- Zghiche Amina
- Zhang Aobo
- Zhang Fengwangdong
- Zhang Huaqiao
- Zhang Jingyu
- Zhang Sijing
- Zhang Wenyu
- Zhang Yi
- Zhang Zhicai
- Zhao Jingzhou
- Zhemchugov Evgenii
- Zhokin Alexander
- Zhu De Hua,
- Zhu Ren-Yuan,
- Ziemons Tim
- Zientek Margaret
- Zlebcik Radek
- Zobec Joze
- Zoi Irene
- Zolkapli Zukhaimira
- Zorbakir Ibrahim Soner,
- Zorbilmez Caglar
- Zotto Pierluigi
- Zou David
- Zucchetta Alberto
- Zuo Xunwu
- Zuolo Davide
- Zygala Lara
- Álvarez Fernández Adrian
- Özçelik Özlem
- Publication venue
- 'Springer Science and Business Media LLC'
- Publication date
- 01/01/2020
- Field of study
This paper presents new sets of parameters (“tunes”) for the underlying-event model of the HERWIG7 event generator. These parameters control the description of multiple-parton interactions (MPI) and colour reconnection in HERWIG7, and are obtained from a fit to minimum-bias data collected by the CMS experiment at s=0.9, 7, and 13Te. The tunes are based on the NNPDF 3.1 next-to-next-to-leading-order parton distribution function (PDF) set for the parton shower, and either a leading-order or next-to-next-to-leading-order PDF set for the simulation of MPI and the beam remnants. Predictions utilizing the tunes are produced for event shape observables in electron-positron collisions, and for minimum-bias, inclusive jet, top quark pair, and Z and W boson events in proton-proton collisions, and are compared with data. Each of the new tunes describes the data at a reasonable level, and the tunes using a leading-order PDF for the simulation of MPI provide the best description of the dat
Measurement of prompt open-charm production cross sections in proton-proton collisions at root s=13 TeV
- Author
- Aarrestad Thea Klaeboe
- Aarup Petersen Henriette
- Abbaneo Duccio
- Abbiendi Giovanni
- Abbrescia Marcello
- Abdelalim Ahmed Ali
- Abdullin Salavat
- Abercrombie Daniel
- Abu Zeid Shimaa
- Acharya Himal
- Acosta Darin
- Acosta John Gabriel
- Adam Wolfgang
- Adams Eric
- Adams Mark Raymond
- Adams Todd
- Adloff Catherine
- Adzic Petar
- Afanasiev Serguei
- Agapitos Antonis
- Agarwal Garvita
- Aggleton Robin
- Agram Jean-Laurent
- Aguilar-Benitez Manuel
- Ahmad Ashfaq
- Ahmad Muhammad
- Ahmed Asar
- Ahuja Sudha
- Akchurin Nural
- Akgun Bora
- Akpinar Alp
- Albajar Carmen
- Albergo Sebastiano
- Albert Andreas
- Albrow Michael
- Alcaraz Maestre Juan
- Aldaya Martin Maria
- Aldá Júnior Walter Luiz
- Aleksandrov Aleksandar
- Alexakhin Vadim
- Alexander James
- Alhusseini Mohammad
- Alimena Juliette
- Alison John
- Allen Brandon
- Almond John
- Alvarez Gonzalez Barbara
- Alverson George
- Alves Gilvan
- Aly Reham
- Alyari Maral
- Amapane Nicola
- Ambrogi Federico
- Amendola Chiara
- Amin Nick
- Amram Oz
- Amsler Claude
- Anagnostou Georgios
- Anderson Dustin
- Andrea Jeremy
- Andreev Vladimir
- Andreev Yu.
- Andreev Yuri
- Andrews Michael Benjamin
- Androsov Konstantin
- Antchev Georgy
- Antunovic Zeljko
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- Zahid Sema
- Zaleski Shawn
- Zalewski Piotr
- Zanetti Marco
- Zarubin Anatoli
- Zarucki Mateusz
- Zecchinelli Angelo Giacomo
- Zenaiev Oleksandr
- Zenz Seth Conrad
- Zeuner Wolfram Dietrich
- Zghiche Amina
- Zhang Aobo
- Zhang Fengwangdong
- Zhang Huaqiao
- Zhang Jingyu
- Zhang Sijing
- Zhang Wenyu
- Zhang Yi
- Zhang Zhicai
- Zhao Jingzhou
- Zhokin Alexander
- Zhu De Hua
- Zhu Ren-Yuan
- Ziemons Tim
- Zientek Margaret
- Zlebcik Radek
- Zobec Joze
- Zoi Irene
- Zolkapli Zukhaimira
- Zorbakir Ibrahim Soner
- Zorbilmez Caglar
- Zotto Pierluigi
- Zou David
- Zucchetta Alberto
- Zuo Xunwu
- Zuolo Davide
- Zygala Lara
- Álvarez Fernández Adrian
- Özçelik Özlem
- Publication venue
- Publication date
- 01/01/2020
- Field of study
The production cross sections for prompt open-charm mesons in proton-proton collisions at a center-of-mass energy of 13TeV are reported. The measurement is performed using a data sample collected by the CMS experiment corresponding to an integrated luminosity of 29 nb(-1). The differential production cross sections of the D*(+/-), D-+/-, and D-0 ((D) over bar (0)) mesons are presented in ranges of transverse momentum and pseudorapidity 4 < p(T) < 100 GeV and vertical bar eta vertical bar < 2.1, respectively. The results are compared to several theoretical calculations and to previous measurements.Peer reviewe
An embedding technique to determine ττ backgrounds in proton-proton collision data
- Author
- Aarrestad Thea Klaeboe
- Abbaneo Duccio
- Abbiendi Giovanni
- Abbrescia Marcello
- Abdullin Salavat
- Abdulsalam Abdulla
- Abercrombie Daniel
- Acharya Himal
- Ackert Andrew
- Acosta Darin
- Acosta John Gabriel
- Adam Wolfgang
- Adams Mark Raymond
- Adams Todd
- Adzic Petar
- Afanasiev Serguei
- Agapitos Antonis
- Agaras Merve Nazlim
- Aggleton Robin
- Agram Jean-Laurent
- Ahmad Ashfaq
- Ahmad Muhammad, 1
- Ahmad Muhammad, 2
- Ahuja Sudha
- Akbiyik Melike
- Akchurin Nural
- Akgun Bora
- Al-bataineh Ayman
- Albajar Carmen
- Albergo Sebastiano
- Albert Andreas
- Albrow Michael
- Alcaraz Maestre Juan
- Aldaya Martin Maria
- Aleksandrov Aleksandar
- Alexander James
- Alhusseini Mohammad
- Alimena Juliette
- Allen Brandon
- Almond John
- Alverson George
- Alves Fábio Lúcio
- Alves Gilvan
- Alyari Maral
- Amapane Nicola
- Ambrogi Federico
- Amendola Chiara
- Amin Nick
- Amsler Claude
- Anagnostou Georgios
- Anderson Dustin
- Andrea Jeremy
- Andreev Vladimir
- Andreev Yuri
- Andrews Michael Benjamin
- Androsov Konstantin
- Antonelli Louis
- Antropov Iurii
- Antunovic Zeljko
- Apanasevich Leonard
- Apollinari Giorgio
- Apresyan Artur
- Apyan Aram
- Araujo Mariana
- Arcaro Daniel
- Arcidiacono Roberta
- Arenton Michael Wayne
- Argiro Stefano
- Arndt Till
- Arneodo Michele
- Asavapibhop Burin
- Asawatangtrakuldee Chayanit
- Asghar Muhammad Irfan
- Asilar Ece
- Askew Andrew
- Atakisi Ismail Okan
- Ather Mohsan Waseem
- Attikis Alexandros
- Auffray Etiennette
- Aushev Tagir
- Autermann Christian
- Auzinger Georg
- Avdeeva Ekaterina
- Avery Paul
- Avila Carlos
- Ayala Edy
- Azarkin Maksim
- Azhgirey Igor
- Aziz Tariq
- Azzi Patrizia
- Azzolini Virginia
- Azzurri Paolo
- Baarmand Marc M
- Babaev Anton
- Babounikau Illia
- Bacchetta Nicola
- Bachiller Irene
- Bachtis Michail
- Backhaus Malte
- Baden Drew
- Bagliesi Giuseppe
- Bahinipati Seema
- Baidali Sergei
- Baillon Paul
- Bainbridge Robert
- Bakas Georgios
- Bakhshiansohi Hamed
- Bakirci Mustafa Numan
- Ball Austin
- Ball Fionn
- Ban Yong
- Band Reyer
- Banerjee Sudeshna
- Banerjee Sunanda
- Bansal Sunil
- Barbagli Giuseppe
- Barberis Emanuela
- Bargassa Pedrame
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- Barker Anthony
- Barnes Virgil E
- Barney David
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- Bechtel Janek
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- Beghin Diego
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- Beirão Da Cruz E Silva Cristóvão
- Belchior Batista Das Chagas Ewerton
- Belforte Stefano
- Bell Ken W
- Bellan Riccardo
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- Belyaev Alexander
- Belyaev Andrey
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- Brom Jean-Marie
- Brommer S.
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- Chernyavskaya Nadezda
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- Choudhury Somnath
- Chu Jennifer
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- de Barbaro Pawel
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- De Palma Mauro
- De Roeck Albert
- de Trocóniz Jorge F
- De Wit Adinda
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- Deelen Nikkie
- Defranchis Matteo Maria
- Deiters Konrad
- Dejardin Marc
- Del Burgo Riccardo
- Del Re Daniele
- Delaere Christophe
- Delannoy Andrés G
- Delannoy Hugo
- Delcourt Martin
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- Delgado Andrea
- Dell'Orso Roberto
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- Zarucki Mateusz
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- Zenaiev Oleksandr
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- Zeuner Wolfram Dietrich
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- Zeyrek Mehmet
- Zghiche Amina
- Zhang Aobo
- Zhang Fengwangdong
- Zhang Huaqiao
- Zhang Jingyu
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- Zhu Ren-Yuan
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- Zolkapli Zukhaimira
- Zorbakir Ibrahim Soner
- Zorbilmez Caglar
- Zotto Pierluigi
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- Zumerle Gianni
- Zuo Xunwu
- Zuolo Davide
- Álvarez Fernández Adrian
- Özçelik Özlem
- Publication venue
- Publication date
- 01/01/2019
- Field of study
An embedding technique is presented to estimate standard model tau tau backgrounds from data with minimal simulation input. In the data, the muons are removed from reconstructed mu mu events and replaced with simulated tau leptons with the same kinematic properties. In this way, a set of hybrid events is obtained that does not rely on simulation except for the decay of the tau leptons. The challenges in describing the underlying event or the production of associated jets in the simulation are avoided. The technique described in this paper was developed for CMS. Its validation and the inherent uncertainties are also discussed. The demonstration of the performance of the technique is based on a sample of proton-proton collisions collected by CMS in 2017 at root s = 13 TeV corresponding to an integrated luminosity of 41.5 fb(-1).Peer reviewe
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