400 research outputs found
La sécrétion de la protéine tau : mécanisme de propagation de la pathologie de tau dans la maladie d’Alzheimer
- Author
- Publication venue
- Publication date
- 01/04/2016
- Field of study
Dans la maladie d’Alzheimer, il existe deux marqueurs histopathologiques : les plaques amyloïdes composées de la protéine amyloïde-bêta et les enchevêtrements neurofibrillaires (NFTs) composés de la protéine tau agrégée. Dans le cerveau, la propagation de la pathologie de tau est observée le long des circuits neuronaux connectés synaptiquement, selon une séquence de stades, caractérisés par le Docteur Braak en 1991. Chez les patients, le degré de démence corrèle avec le nombre de NFTs. Ces derniers apparaissent dans des régions précises du cerveau et se propagent, de manière prédictible, le long des projections neuronales à des stades plus tardifs de la pathologie. Il reste à éclaircir la manière dont les NFTs se propagent dans les différentes régions du cerveau.
Dans notre laboratoire, nous avons émis l’hypothèse que la propagation de tau pourrait se produire par un processus de transmission de cellule à cellule. Ainsi, la protéine tau serait tout d’abord sécrétée par un neurone, puis endocytée par un neurone adjacent. Nos travaux de recherche se sont concentrés sur la sécrétion de la protéine tau.
Dans une première étape, nous avons démontré l’existence de la sécrétion active de tau dans l’espace extracellulaire, en utilisant des modèles in vitro de cellules non neuronales et neuronales. Par la suite, nous avons caractérisé les formes de protéines tau sécrétées. Enfin dans un dernier temps, nous avons exploré les voies de sécrétion de la protéine tau ainsi que les mécanismes régulant ce phénomène. Nous avons réussi à moduler la sécrétion de tau en reproduisant plusieurs insultes observées dans la maladie d’Alzheimer. Nos recherches nous ont permis d’identifier l’appareil de Golgi comme étant une organelle dont la fragmentation augmente la sécrétion de la protéine tau. A la lumière de cette découverte, nous avons été capable de moduler la sécrétion de tau en ciblant spécifiquement l’activité de cdk5 et l’expression de rab1A contrôlant la morphologie du Golgi. Ainsi, nous avons réussi à diminuer significativement la sécrétion de la protéine tau.
Nos travaux de recherche proposent de nouvelles cibles thérapeutiques pour la maladie d’Alzheimer, visant à diminuer la propagation de la pathologie de tau par de nouveaux mécanismes cellulaires.In Alzheimer’s disease, the amyloid plaques and the neurofibrillary tangles composed of misfolded aggregated tau protein are the two hallmarks of the pathology. In the brain, the propagation of tau pathology was observed along the neuronal circuits. Described by Doctor Braak in 1991, the appearence of the neurofibrillary tangles was predictable in the brain and correlated with the degree of cognitive deficits. Its remains unclear how tau pathology spreads in the brain.
In our laboratory, we made the hypothesis that the propagation could occur by cell-to-cell transmission. This implies that NFTs would propagate in the brain by the release of misfolded tau aggregates from an affected neuron followed by its uptake in neighboring neurons. My thesis focuses on the mechanism of tau secretion. Firstly, we demonstrated that tau was actively secreted in the extracellular space by non neuronal cells and primary neurons. Then, we characterized the tau secreted forms. Finally, we explored the secretory pathways and the mechanisms leading to tau secretion. We were able to modulate tau secretion by mimicking specific insults observed in Alzheimer disease. Our research led us to identify the Golgi apparatus as a major contributor to tau secretion. Concomitant with this, modulation of cdk5 pathway and rab1A expression, which are known to affect the Golgi morphology, altered significantly tau secretion.
Our research provides new therapeutic strategies for Alzheimer’s disease, targeting tau secretion to reduce the propagation of tau pathology by new cellular mecanisms
G3BP1 promotes stress-induced RNA granule interactions to preserve polyadenylated mRNA
- Author
- Publication venue
- 'Rockefeller University Press'
- Publication date
- 06/04/2015
- Field of study
G3BP1, a target of TDP-43, is required for normal stress granule (SG) assembly, but the functional consequences of failed SG assembly remain unknown. Here, using both transformed cell lines and primary neurons, we investigated the functional impact of this disruption in SG dynamics. While stress-induced translational repression and recruitment of key SG proteins was undisturbed, depletion of G3BP1 or its upstream regulator TDP-43 disturbed normal interactions between SGs and processing bodies (PBs). This was concomitant with decreased SG size, reduced SG–PB docking, and impaired preservation of polyadenylated mRNA. Reintroduction of G3BP1 alone was sufficient to rescue all of these phenotypes, indicating that G3BP1 is essential for normal SG–PB interactions and SG function
Midbrain organoids with an SNCA gene triplication model key features of synucleinopathy
- Author
- Abdian Narges
- Beitel Lenore K
- Cai Eddie
- Chen Carol X -Q
- Deneault Eric
- Durcan Thomas M
- Fon Edward A
- Karamchandani Jason
- Kunath Tilo
- Lépine Paula
- Mathur Meghna
- Maussion Gilles
- Mohamed Nguyen-Vi
- Nami Harris
- Nicouleau Michael
- Ramamurthy Janani
- Singh Dolt Karamjit
- Sirois Julien
- Soubannier Vincent
- Stratton Jo Anne
- Tabatabaei Mahdieh
- Thomas Rhalena A
- Wen Dingke
- Publication venue
- 'Oxford University Press (OUP)'
- Publication date
- 25/09/2021
- Field of study
Hyperphosphorylation and Cleavage at D421 Enhance Tau Secretion
- Author
- A de Calignon
- A de Calignon
- A Madeira
- AM Nicholson
- B Borroni
- B Fevrier
- C Gomes
- C Thery
- C-A Maurage
- D Simon
- DM Barten
- DP Hanger
- E Vanmechelen
- G Carmel
- GV Johnson
- H Braak
- H Hampel
- H Hampel
- H Hampel
- H Hampel
- H Hampel
- HJ Lee
- I Alafuzoff
- J Bertrand
- J Lauckner
- J Mandell
- J Saraste
- JB Helms
- Jessica Rivest-McGraw
- Johanne Bertrand
- JS Yoo
- K Blennow
- K Buerger
- K Buerger
- K Gousset
- K Ishiguro
- L Bierer
- L Liu
- LM Shaw
- M Diaz-Hernandez
- M Morris
- M Tanudji
- M Urushitani
- Mark R. Cookson
- Michel Lauzon
- Nguyen-Vi Mohamed
- Nicole Leclerc
- P Arriagada
- R Kohnken
- R Rissman
- S Perreault
- S Ponnambalam
- S Saman
- T Kimura
- V Lee
- Vanessa Plouffe
- W Kim
- W Kim
- W Nickel
- Publication venue
- Public Library of Science
- Publication date
- 15/05/2012
- Field of study
It is well established that tau pathology propagates in a predictable manner in Alzheimer’s disease (AD). Moreover, tau accumulates in the cerebrospinal fluid (CSF) of AD’s patients. The mechanisms underlying the propagation of tau pathology and its accumulation in the CSF remain to be elucidated. Recent studies have reported that human tau was secreted by neurons and non-neuronal cells when it was overexpressed indicating that tau secretion could contribute to the spreading of tau pathology in the brain and could lead to its accumulation in the CSF. In the present study, we showed that the overexpression of human tau resulted in its secretion by Hela cells. The main form of tau secreted by these cells was cleaved at the C-terminal. Surprisingly, secreted tau was dephosphorylated at several sites in comparison to intracellular tau which presented a strong immunoreactivity to all phospho-dependent antibodies tested. Our data also revealed that phosphorylation and cleavage of tau favored its secretion by Hela cells. Indeed, the mimicking of phosphorylation at 12 sites known to be phosphorylated in AD enhanced tau secretion. A mutant form of tau truncated at D421, the preferential cleavage site of caspase-3, was also significantly more secreted than wild-type tau. Taken together, our results indicate that hyperphosphorylation and cleavage of tau by favoring its secretion could contribute to the propagation of tau pathology in the brain and its accumulation in the CSF
Design and baseline characteristics of the finerenone in reducing cardiovascular mortality and morbidity in diabetic kidney disease trial
- Author
- Abdel-Rahman Emaad
- Abhayaratna Walter
- Abramof Ness Rosane
- Acosta Idalia
- Adams Atoya
- Adawi Faiad
- Adler Sharon
- Ahmed Fayzal
- Aizenberg Diego
- Ajani Dilawar
- Al-Karadsheh Amer
- Albota Adrian
- Alferi Dino
- Alicic Radica
- Alla Sreedhara
- Allison D
- Almeida Edgar
- Alpizar Salazar Melchor
- Amer Joseph
- Amod Aslam
- Andrawis Nabil
- Antonio Bossi Carlo
- Antsiferov Mikhail
- Antunes Daniela
- Araki Hideo
- Arango Clara
- Arcos Edgar
- Arif Ahmed
- Arif Imrozia
- Arkhipov Mikhail
- Armaly Zaher
- Aroca Gustavo
- Asprusten Emil
- Atar Shaul
- Avila Pardo Sandro
- Awad Ahmed
- Axthelm Christoph
- Azizad Masoud
- Azizah Aziz Nor
- B Brouwer C
- Babikova Jana
- Babkin Andrey
- Badak Ozer
- Bahrami Michael
- Bajcsi Dora
- Baker John
- Bala Cornelia
- Ballesteros Rosa
- Bansal Shweta
- Barag Steven
- Barakzoy Ahmad
- Baranov Vitaliy
- Barbarash Olga
- Barbonta Hortensia
- Barney Mark
- Barre Paul
- Barrera Sandra
- Barreto Carlos
- Barreto Germ\ue1n
- Bartolacci In\ue9s
- Bashir Khalid
- Bashkin Amir
- Bastidas Adrian Miriam
- Bautista Albert
- Bautista Jose
- Bech Jesper
- Beddhu Srinivasan
- Beltr\ue1n L\uf3pez Nelly
- Ben Chetrit Sydney
- Benitez Diego
- Benjamin Sabrina
- Berar Yanay Noa
- Berenji Ramin
- Bertram Pitt
- Bertsch John
- Besada Diego
- Bhana Sindeep
- Bhargava Anuj
- Bilz Stefan
- Birkenfeld Andreas
- Birriel Jose
- Bittar Julio
- Blanco Guillermo
- Bleich David
- Boletis Ioannis
- Bondarets Iryna
- Bonora Enzo
- Bornfreund Jonathan
- Boshnyashka Radostina
- Botelho Roberto
- Botero Rodrigo
- Botsyurko Volodymyr
- Bouarich Hanane
- Brada Michal
- Brandao Ilidio
- Brar Harjeet
- Braun Hermann
- Brezina Jiri
- Brian Susan
- Brietzke Stephen
- Brito Claudia
- Bruchfeld Annette
- Bruno Giorda Carlo
- Brusco Osvaldo
- Bu Ruifang
- Bucek Petr
- Buganova Ingrid
- Burgner Anna
- Busch Klaus
- Busch Robert
- Butrymowicz Patrycja
- C Bakker R
- C\ue1rdenas Tatiana
- Caceaune Elena
- Cai Hanqing
- Calabr\uf2 Paolo
- Calero Francesca
- Canadas Rafael
- Canani Luis
- Caramori Maria
- Cardona Jose
- Cariou Bertrand
- Carlo Maggi Davide
- Carlos Palma Juan
- Carlos Prieto Juan
- Carlson Brian
- Carpio Jose
- Carvalho Rui
- Case Christopher
- Castro Cristina
- Catindig Elizabeth
- Catrinoiu Doina
- Cayli Murat
- Cereto Castro Fernando
- Cerqueira Maria
- Chahin Mariano
- Chang Chiz-Tzung
- Chantrel Fran\ue7ois
- Chen Dejun
- Chen Nan
- Chen Qinkai
- Cheng Jinluo
- Chernikova Viktoriia
- Chernin Gil
- Chernyavskaya Elena
- Chew Wong Alfredo
- Christina Nowack
- Chuang Lee-Ming
- Chung ChoonHee
- Ciechanowski Kazimierz
- Cieslik Grazyna
- Cigarr\ue1n Guldris Secundino
- Cimino Roberto
- Clavel Sylvaine
- Clodi Martin
- Cobos Jorge
- Colman Peter
- Colquhoun David
- Constantin Ciprian
- Contzen Christel
- Conway James
- Coronel Julian
- Cortes-Maisonet Gregorio
- Cortes-Maisonet Gregorio
- Cournoyer Serge
- Crawford Veronica
- Cristina Gregorini Maria
- Cruz Humberto
- Cruzado Garrit Josep
- Cure Carlos
- Curiac Dan
- Cutfield Rick
- Dandillaya Ramprasad
- Dang Cuong
- Danos Peter
- Darawsha Mahmud
- de \uc1lvaro Fernando
- de Paula Rogerio
- Deerochanawong Chaicharn
- Degenhardt Stefan
- Demko Arkadiy
- Derwahl Karl
- Dhanireddy Soni
- Din Zia
- Distiller Larry
- Dixon Bradley
- Dolores Mart\uednez Esteban M\uaa
- Donath Marc
- Donets Oleksandra
- Dong Junwu
- Dong Youping
- Doshi Ankur
- Doubel Peter
- Dreval Alexander
- Drexel Heinz
- Du Yuming
- Dumas Richard
- Dumitrescu Adriana
- Dunn Peter
- Dur\ue1n Carlos
- Duyck Francis
- Dzupina Andrej
- E Costa Fernando Teixeira
- Ebenbichler Christoph
- Ebisui Osamu
- Edelsberger Tomas
- Edin Anton
- Eduardo Figueiredo Carlos
- Eduardo Salles Joao
- Efrati Shai
- Ekinci Elif
- El Shahawy Mahfouz
- El-Shahawy Mohammed
- Elbert Alicia
- Elias Mazen
- Eliaschewitz Freddy
- Eliasson Ken
- Emdin Michele
- Engelen Wendy
- Eren Necmi
- Eriksen Erik
- Ermakova Polina
- Escalada San Mart\uedn Javier
- Escobedo de la Pe\uf1a Jorge
- Esteves Cesar
- Eugenia Canziani Maria
- Eustace Joe
- Evans John
- Faber Jens
- Fadda George
- Fang Sum Chee
- Fang Yi
- Fangh\ue4nel Salm\uf3n Guillermo
- Farah Ghassan
- Farber Evgeny
- Farooq Umar
- Fauvel Jean-Pierre
- Fernando Roland
- Fiaccadori Enrico
- Fikry Sameh
- Fink Raymond
- Finnes Trine
- Fiorina Paolo
- First Brian
- Fitz-Patrick David
- Flack John
- Fliesser-G\uf6rzer Evelyn
- Fluck Patrick
- Fogelfeld Leon
- Fonseca Vivian
- Forti Adriana
- Franek Edward
- Frank Malin
- Frias Juan
- Fujita Naruhiro
- Furuya Ryuichi
- Fushtey Ivan
- G Lieverse A
- Galcer\ue1n Josep
- Gallouj Karim
- Galphin Claude
- Galyavich Albert
- Gansevoort Ron
- Garc\ueda Hern\ue1ndez Pedro
- Garc\ueda Luis
- Garcia-Mayol Luis
- Gaysina Leyla
- Gelersztein Elizabeth
- George L Bakris
- Georgiev Dimitar
- Gerasimos Filippatos
- Giebel Thomas
- Gillard Pieter
- Giorgio Battaglia Giovanni
- Gislason Gunnar
- Glandt Mariela
- Goldstein Gary
- Goluch Richard
- Gonz\ue1lez Albarr\ue1n Olga
- Gonz\ue1lez G\ue1lvez Guillermo
- Gonz\ue1lez Gonz\ue1lez Jos\ue9
- Gonz\ue1lez Fernando
- Gonzalez Edgar
- Gonzalez-Abreu Francisco
- Gordeev Ivan
- Gore Ashwini
- Gouet Didier
- Grachova Mariia
- Grant David
- Grossman Ehud
- Guan Tianjun
- Guerci Bruno
- Guerrot Dominique
- Guia Jose
- Gul Ibrahim
- Gulakova Drahomira
- Gumprecht Janusz
- Guo Weiying
- Guron Gregor
- Gushterova Valentina
- Guti\ue9rrez Ochoa Ramiro
- Guzm\ue1n Gustavo
- H Boonstra A
- H\uf8ivik Hans
- Habwe Violet
- Hagemeier Robert
- Hagenow Andreas
- Halabi Majdi
- Haller Hermann
- Halpern Stephen
- Hamamoto Yoshiyuki
- Hamasaki Akihiro
- Hamet Pavel
- Hamilton Maxine
- Hammoud Jamal
- Handelsman Stuart
- Hangaard J\uf8rgen
- Hanna Fahmy
- Hanusch Ursula
- Hao Chuanming
- Harcsa Eleonora
- Hart Randolph
- Hartman Israel
- Hasalova Zapletalova Jitka
- Hasnul Halimi Bin Wan Hasan Wan
- Hasslacher Christoph
- Hatazaki Masahiro
- Hatunic Mensud
- Hatziagelaki Erifili
- Hayashi Terumasa
- Heigerick Glenn
- Heitor Susana
- Hellberg Olof
- Hellgren Margareta
- Henein Sam
- Hern\ue1ndez Jaras Julio
- Hern\ue1ndez Eric
- Hernandez German
- Hernandez-Cassis Carlos
- Herrera Carlos
- Higashi Takayuki
- Hirohata Yoshihide
- Hissa Miguel
- Hoffmann Michal
- Hola Olga
- Holian John
- Honkasalo Mikko
- Honkasalo Mikko
- Horacek Thomas
- Horinouchi Shuji
- Hornova Lucie
- Houdova Jana
- Hougardy Jean-Michel
- Hrmova Helena
- Humaloja Kari
- Hung Cheng-Chieh
- Hwang YouCheol
- Ibarra Jaime
- Ibern\uf3n Meritxell
- Imoto Hirofumi
- Inagaki Akemi
- Inagaki Masayuki
- Ioannidis Ioannis
- Ipatko Irina
- Iranmanesh Ali
- Irizar Santana Sa\ufal
- Isayeva Anna
- Ishii Masao
- Ishiko Tamayo
- Jackson Timothy
- Jain Mahendra
- Jamerson Kenneth
- Jansen van Rensburg Dirkie
- Jaramillo Carlos
- Jaramillo Nicol\ue1s
- Jaroslaw Pacyk Grzegorz
- Jiang Fangfang
- Jiang Ju-Ying
- Jiang Sheng
- Jinnouchi Hideaki
- Johnson Karen
- Joshi Mukesh
- Joshi Shaifali
- Juhl Claus
- Juli\ue1n Segura de la Morena Jos\ue9
- Jungmair Wolfgang
- Kahal Hassan
- Kalashnikova Marina
- Kalathil Dhanya
- Kalina Akos
- Kanai Hidetoshi
- Kananen Kristiina
- Kanda Daisuke
- Kanehara Hideo
- Kang JunGoo
- Kantola Ilkka
- Karasek David
- Karlsson Thomas
- Kashima Masayuki
- Kato Kiyoe
- Katsuki Takeshi
- Kattah William
- Kawamitsu Katsunori
- Kawasaki Satsuki
- Kayali Zeid
- Kaye William
- Kazup Szilvia
- Kelly Allan
- Keltai Katalin
- Khalimov Yuriy
- Khan Bobby
- Khan Muhammad
- Khanh Tran
- Kharait Sourabh
- Kikuchi Fumi
- Kikuchi Hidetoshi
- Kilvert Anne
- Kim HyeSoon
- Kim InJoo
- Kim JaeHyeon
- Kim SinGon
- Kirschner Robert
- Kiss Julianna
- Klein Alexandre
- Klimontov Vadim
- Kloos Christof
- Klyuchkova Neli
- Kobalava Zhanna
- Kobayashi Kunihisa
- Koch Stanley
- Koch Thorsten
- Kocyigit Ismail
- Kogut Dmytro
- Koide Junko
- Koistinen Arvo
- Komisarenko Julia
- Kooy Adriaan
- Kopecka Sarka
- Kopyt Nelson
- Korff Gary
- Korsoff Pirkko
- Kosachunhanan Natapong
- Kosmacheva Elena
- Kotzker Wayne
- Kounadi Theodora
- Kovacs Laszlo
- Kovar Richard
- Kovesdy Csaba
- Koziolova Natalya
- Kr\ufcger Thilo
- Krarup Thure
- Kravchun Nonna
- Krcova Eva
- Krebs Jeremy
- Kreit Camil
- Krekels Marielle
- Kriauciuniene Dovile
- Krishna Arvind
- Kronfli Saeed
- Krzykowska Jolanta
- Kuang Jian
- Kubota Miyuki
- Kuchar Jiri
- Kumbasar Abdulbaki
- Kurnatowska Ilona
- Kusano Yoshiro
- Kutejova Vlasta
- Kvitkova Lyudmila
- Kyriakidou Christina
- L Penne E
- L\uf3pez M\uf3nica
- L\uf6ndahl Magnus
- La Manna Gaetano
- Lahtela Jorma
- Laimer Markus
- Lakha Deepak
- Lamboy Beata
- Landa Katarzyna
- Larnefeldt Hans
- Lasiene Jurate
- Lazcano Soto Jos\ue9
- LE Meur Yannick
- Lee ByungWan
- Lee Chien-Te
- Lee Keung
- Lee Paul
- Lee WooJe
- Lei Minxiang
- Leite Jr Maurilo
- LeJeune Derek
- Lemus Brenda
- Lerman Sam
- Levashov Sergey
- Li Dongmei
- Li Hongmei
- Li Jingmei
- Li Ling
- Li Yan
- Li Yuxiu
- Li Zhonghe
- Li\ue9vano Manuel
- Liberman Alberto
- Liberty Idit
- Libis Roman
- Lim Soo
- Lindhardt Morten
- Lindholm Carl-Johan
- Linfert Douglas
- Literati-Nagy Botond
- Liu Fang
- Liu Jian
- Liu Yinghong
- Liu Yuantao
- Liu Zhihong
- Liutkus Joanne
- Long Gang
- Loong Loh Chek
- Lora Henry
- Lu Guoyuan
- Lu Weiping
- Lu Yibing
- Lubanda Hana
- Lucheva Mariya
- Ludvik Bernhard
- Luigi Cavalot Franco
- Luis M Ruilope
- Lurie Alexander
- M Barendregt J N
- M van Leendert Ruud J
- M\ue9ndez Machado Gustavo
- M\ufcller Joachim
- Ma Jianhua
- MacIsaac Richard
- Maddukuri Geetha
- Madero Rovalo Magdalena
- Madore Francois
- Madrzejewski Adam
- Madsbad Sten
- Madziarska Katarzyna
- Maeda Hajime
- Maffei Laura
- Magno Alexander
- Maia Lilia
- Makriniotou Ioanna
- Maletz Louis
- Malyar Kateryna
- Malykh Natalia
- Malyutina Sofya
- Mandayam Sreedhar
- Mandviwala Mustafa
- Mankovsky Borys
- Mann Mah Peak
- Manova Petya
- Mar\ueda Pascual Izuel Jos\ue9
- Marasaev Vyacheslav
- Mareev Vyacheslav
- Maria Veronelli Anna
- Markell Mariana
- Mart\uednez Deben Francisco
- Martin Earl
- Martinho Valdemar
- Martins Judith
- Martynenko Vladimir
- Martynyuk Liliya
- Maslyanko Vitaliy
- Matos Pedro
- Matsubayashi Sunao
- Matsumoto Kazunari
- Matsuo Yasuto
- Matsuoka Naoki
- Matyasek Ivo
- Mayfield Ronald
- Mazur Stanislaw
- Mazza Giuseppe
- Mbogua Caroline
- McCafferty Kieran
- McFarlane Philip
- McMullen Dierdre
- Mediavilla Juan
- Medina Marcelo
- Meisner Carl
- Melo Pedro
- Merai Imad
- Mesbah Rafik
- Meyer Jill
- Mich\ue1n Alfredo
- Mileder Margit
- Min Cho Young
- Mindrescu Nicoleta
- Minh Nui Nguyen
- Minkova Dotska
- Minton Stephen
- Mirasol Roberto
- Mistodie Cristina
- Mitha Essack
- Miyaoka Hiroaki
- Mkrtumyan Ashot
- Mo Zhaohui
- Mocherla Bharat
- Mohamad Masni
- Mohd Ali Norhaliza
- Mohd Izani Wan Mohamed Wan
- Mokrejsova Magdalena
- Molina Dora
- Mong Bee Yong
- Monier Arnaud
- Montero Manuel
- Moranne Olivier
- Morita Takeshi
- Mosenzon Ofri
- Moustafa Moustafa
- Murao Satoshi
- Myshanych Halyna
- Myung Yu Jae
- Nadkarni Salil
- Nagy Laszlo
- Najme Khir Rizmy
- Nakayama Mikihiro
- Nakazawa Jun
- Nakhle Samer
- Napora Piotr
- Navarro Jesus
- Navickas Antanas
- Nechaeva Galina
- Negrisanu Gabriela
- Nelson Craig
- Neudorfer Peter
- Nevarez Ruiz Luis
- Neyra Nilda
- Ngoc Nguyen Boi
- Nguyen Son Pham
- Nica Romanita
- Nicol Philip
- Nicole Mentenich
- Nielsen Joan
- Nieminen Sakari
- Nieminen Tuomo
- Nikolaev Konstantin
- Nimer Assy
- Nina Petunina
- Nirmalaraj Kingsley
- Nischik Ruth
- Niu Jianying
- Nolasco Fernando
- Nomiyama Takashi
- Nonchev Boyan
- Noori Ebrahim
- Noritake Masayuki
- Noronha Irene
- Norwood Paul
- Nowicki Michal
- Numrungroad Visal
- Nur Fatnoon Nik Ahmad Nik
- Nyirati Gabor
- O Donovan Richard
- O Keefe Dennis
- O Meara Yvonne
- Ochodnicka Zuzana
- Ocicka-Kozakiewicz Anna
- Odugbesan A
- Ogiwara Takayuki
- Oguz Aytekin
- Ohashi Hiroshi
- Okamoto Hideki
- Okenka Libor
- Oliver David
- Onaca Adriana
- Oparil Suzanne
- Osonoi Takeshi
- Ozdogan Oner
- P\ue9rez Manghi Federico
- Packham David
- Palyutin Shamil
- Pamugas Glenda
- Pang Ip Tai
- Pani Antonello
- Paoli-Bruno Jorge
- Paolino Bruno
- Papadopoulou Dorothea
- Papagianni Aikaterini
- Pape Alexia
- Paschoalin Nathalia
- Paschoalin Raphael
- Pascual Santos Julio
- Passadakis Ploumis
- Patel Rajesh
- Patel Rakesh
- Paulweber Bernhard
- Paveliu Silvia
- Pech\ue8re-Bertschi Antoinette
- Pecoits Filho Roberto
- Pedersen-Bjergaard Pedersen-Bjergaard Ulrik
- Peixoto Aldo
- Peng Ai
- Pereira Amalia
- Pereira Marcio
- Pererva Larysa
- Pergola Pablo
- Perico Norberto
- Pertseva Nataliia
- Peter Kolkhof
- Peterson Sean
- Petro Gizella
- Pettis Karlton
- Pf\ufctzner Andreas
- Phi Kon Sui
- Phuong Tran Lan
- Piatti PierMarco
- Pichmanova Mariyana
- Pimenov Leonid
- Pintilei Ella
- Pisani Antonio
- Pisoni Roberto
- Pistrosch Frank
- Poch Esteban
- Podgorski Gracjan
- Polaina Rusillo Manuel
- Ponduchi Mirela
- Pongchaiyakul Chatlert
- Ponzani Paola
- Pop Lavinia
- Popa Amorin
- Popeil Larry
- Popescu Alexandrina
- Portes Evandro
- Posada Jorge
- Poulsen Per
- Prabhakar Sharma
- Prager Rudolf
- Prakova Zhulieta
- Prazny Martin
- Precoma Dalton
- Prei f Wolfgang
- Prischl Friedrich
- Pumprla Jiri
- R Winkelmann Bernhard
- Radulian Gabriela
- Radzeviciene Lina
- Raina Rupesh
- Rajiv Agarwal
- Ramanathan Kodangudi
- Ramos L\uf3pez Gabriel
- Ramos-Gonez Luis
- Rangelov Rangel
- Ranjith Naresh
- Rashkov Rosen
- Rasmussen Ole
- Rastogi Anjay
- Ratnasingam Jeyakantha
- Rayner Brian
- Rea Rosangela
- Rechkova Elena
- Red\uf3n Josep
- Reddan Donal
- Rein-Hedin Erik
- Reisin Efrain
- Rendell Marc
- Rewerska Barbara
- Reyes Eliana
- Rheeder Paul
- Ricardo Colomar Javier
- Rice Sam
- Riella Miguel
- Rinke Andrea
- Risberg Knut
- Rocco Michael
- Rocke Jan
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- Roger Simon
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- Romero Carmen
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- Rose Ludger
- Ross Dennis
- Rossing Peter
- Rothman Jeffrey
- Roussel Ronan
- Roy-Chaudhury Prabir
- Rudofsky Gottfried
- Rudolph Lance
- Ruhullah Yusuf
- Rump Lars
- Ruoff Gary
- Rusicka Teresa
- Ruxer Jan
- Rymar Oksana
- Ryu Jeffrey
- S\ue1nchez Juan Carlos
- S\ue1nchez Gregorio
- Saavedra Victor
- Sadeharju Karita
- Sahani Mandeep
- Sahin Idris
- Salda\uf1a Mendoza Arturo
- Samuels Garfield
- San Tan Ru
- Sanabria Hugo
- Sanchez William
- Santamar\ueda Olmo Rafael
- Santorelli Gennaro
- Santoro Domenico
- Sardinov Ruslan
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- Sarvan Mohamed
- Sasaki Nobuhiro
- Satirapoj Bancha
- Sauque Reyna Leobardo
- Saxena Sanjeev
- Sch\uf6ll Norbert
- Sch\uf6nherr Hans-Robert
- Sch\ufcrholz Thomas
- Scheen Andr\ue9
- Schernthaner Gerit-Holger
- Schettler Volker
- Schiefke Ingolf
- Schlichthaar Heike
- Schneider Karoly
- Schousboe Karoline
- Schr\uf6ppel Bernd
- Schwartz Daniel
- Schwartz Doron
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- Scott Russell
- Seco Gilberto
- Seeber Mary
- Sekigami Taiji
- Sels\ue5s Hilde
- Semenova Olga
- Serhiyenko Oleksandr
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- Serusclat Pierre
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- Shahid Nauman
- Shanik Michael
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- Shi Bingyin
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- Shibata Hirotaka
- Shinoda Junji
- Shu Daniel
- Siebert Heidi
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- Silva Gil
- Simon Judit
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- Smelser James
- Smirnov Ivan
- Smith Mark
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- Smuts Nine
- Sobajima Hiroshi
- Soe Kyaw
- Sokolova Liubov
- Solache Ortiz Gustavo
- Soln\uf8r Leidulv
- Solomon Richard
- Solovev Oleg
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- Soufer Joseph
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- Strack Georg
- Strand Jorma
- Strey Christopher
- Strongin Leonid
- Stryzhak Vasyl
- Su Qing
- Suarez Rosa
- Subramanian Bala
- Sue Kirkman M
- Sugitatsu Kazuya
- Sugiura Toshiyuki
- Sugiyama Toru
- Sulosaari Sakari
- Sun Zhuxing
- Suranyi Michael
- Suzuki Daisuke
- Suzuki Masaaki
- Swift Pauline
- Szerlip Harold
- Szilagyi Iosif
- Szocs Albert
- T Luik P
- T\ue4schner Heidrun
- Tagarev Zhivko
- Tamirisa Aparna
- Tanaka Asami
- Tanaka Seiichi
- Tang Shuifu
- Tanque Maribel
- Tarng Der-Cherng
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- Temelkova-Kurktschieva Theodora
- Temizhan Ahmet
- Tengmark Bengt-Olov
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- Thorup Frode
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- Tobe Sheldon
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- Tong Nanwei
- Tonolo Giancarlo
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- Toursarkissian Nicole
- Tran Tuan-Huy
- Treger Richard
- Trevisan Roberto
- Trokis J
- Troya Maribel
- Trujillo Freddy
- Trullenque Gretel
- Tsch\uf6pe Diethelm
- Tsoukas George
- Tsunematsu Izumi
- Tu Shih-Te
- Turcu Liana
- Turk Thomas
- Tytus Richard
- Ujihara Makoto
- Ukhanova Olga
- Ulmer Achim
- Umpierrez Guillermo
- Urbach Daniel
- Urbach Dorothea
- Urbanaviciene Egle
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- Urina Miguel
- Ustundag Sedat
- Vacaru Georgeta
- Valdes Martin
- Valdez Ortiz Rafael
- Valika Shujauddin
- Vallejos Augusto
- van Buren M
- van den Born Bert-Jan
- van der Giet Markus
- VAN Gaal Luc
- VAN Hoang Lam
- van Zyl Louis
- Vanbelleghem Hilde
- Vandeleur James
- Varleta Paola
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- Vasileva Svetla
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- Vi\uf1es Gloria
- Vijayaraman Arutchelvam
- Vila Lobos Ana
- Villagordoa Mesa Juan
- Villegas Iv\ue1n
- Vitou Louise
- Vlad Adrian
- Vlasenko Maryna
- Vorokhobina Natalya
- Wainstein Julio
- Wainstein Julio
- Walsh Michael
- Wan Ronald Ma Ching
- Wang Hao
- Wang Jianqin
- Wang Li
- Wang Lihua
- Wang Xinjun
- Wanner Christoph
- Wasilewska Katarzyna
- Wassermann Alfredo
- Wei Jiali
- Weisnagel Stanley
- Weissman Peter
- Whaley-Connell Adam
- Wierusz-Wysocka Bogna
- Wilderman Igor
- Winston Jonathan
- Wise Jonathan
- Wittert Gary
- Wnetrzak-Michalska Renata
- Wong Yuk-Ki
- Wu Chaoqing
- Wu Mai-Szu
- Wu Ming-Ju
- Wu Tianfeng
- Wudi Krisztina
- Wuerzner Gregoire
- Wynne Katie-Jane
- Xing Changying
- Xiong Fei
- Xu Ning
- Xu Xudong
- Yagil Yoram
- Yajima Ken
- Yakhontov Davyd
- Yale Jean-Francois
- Yamada Daishiro
- Yamada Masayo
- Yamagata Kazuo
- Yamakawa Fumiko
- Yamakawa Ken
- Yamasaki Yoshimitsu
- Yambe Yuko
- Yanai Hidekatsu
- Yang Jinkui
- Yasuda Tetsuyuki
- Yenicerioglu Yavuz
- Yeung Vincent
- Yilmaz Huseyin
- Yin Aiping
- Yoncheva-Mihaylova Mariana
- Young Park Cheol
- Yuan Lee Li
- Yupanqui Hern\ue1n
- Yuryev Michael
- Zakharova Elena
- Zalevskaya Alsu
- Zanozina Olga
- Zaoui Philippe
- Zeig Steven
- Zeng Longyi
- Zhang Hao
- Zhang Yanlin
- Zhang Ying
- Zhao Zhiquan
- Zhdanova Elena
- Zheng Hongguang
- Zhong Ling
- Zhong Liyong
- Zhu Dalong
- Zhukova Larisa
- Zilahi Zsolt
- Zsom Marianna
- Zukermann Robert
- Zykova Tatyana
- Publication venue
- 'S. Karger AG'
- Publication date
- 01/01/2019
- Field of study
Background: Among people with diabetes, those with kidney disease have exceptionally high rates of cardiovascular (CV) morbidity and mortality and progression of their underlying kidney disease. Finerenone is a novel, nonsteroidal, selective mineralocorticoid receptor antagonist that has shown to reduce albuminuria in type 2 diabetes (T2D) patients with chronic kidney disease (CKD) while revealing only a low risk of hyperkalemia. However, the effect of finerenone on CV and renal outcomes has not yet been investigated in long-term trials.
Patients and Methods: The Finerenone in Reducing CV Mortality and Morbidity in Diabetic Kidney Disease (FIGARO-DKD) trial aims to assess the efficacy and safety of finerenone compared to placebo at reducing clinically important CV and renal outcomes in T2D patients with CKD. FIGARO-DKD is a randomized, double-blind, placebo-controlled, parallel-group, event-driven trial running in 47 countries with an expected duration of approximately 6 years. FIGARO-DKD randomized 7,437 patients with an estimated glomerular filtration rate >= 25 mL/min/1.73 m(2) and albuminuria (urinary albumin-to-creatinine ratio >= 30 to <= 5,000 mg/g). The study has at least 90% power to detect a 20% reduction in the risk of the primary outcome (overall two-sided significance level alpha = 0.05), the composite of time to first occurrence of CV death, nonfatal myocardial infarction, nonfatal stroke, or hospitalization for heart failure.
Conclusions: FIGARO-DKD will determine whether an optimally treated cohort of T2D patients with CKD at high risk of CV and renal events will experience cardiorenal benefits with the addition of finerenone to their treatment regimen.
Trial Registration: EudraCT number: 2015-000950-39; ClinicalTrials.gov identifier: NCT02545049
Operation and performance of the ATLAS Tile Calorimeter in Run 1
- Author
- Aaboud M
- Aad G
- Abbott B
- Abdallah J
- Abdinov O
- Abeloos B
- Abhayasinghe DK
- Abidi SH
- Abouelfadl 
- AbouZeid OS
- Abraham NL
- Abramowicz H
- Abreu H
- Abulaiti Y
- Acharya BS
- Adachi S
- Adamczyk L
- Adelman J
- Adersberger M
- Adiguzel A
- Adye T
- Affolder AA
- Afik Y
- Agheorghiesei C
- Aguilar-Saavedra JA
- Ahmadov F
- Aielli G
- Akatsuka S
- Akerstedt H
- Akilli E
- Akimov AV
- Alberghi GL
- Albert J
- Albicocco P
- Alconada Verzini MJ
- Alderweireldt S
- Aleksa M
- Aleksandrov IN
- Alexa C
- Alexander G
- Alexopoulos T
- Alhroob M
- Ali B
- Alimonti G
- Alison J
- Alkire SP
- Allaire C
- Allbrooke BMM
- Allen BW
- Allport PP
- Aloisio A
- Alonso A
- Alonso F
- Alpigiani C
- Alshehri AA
- Alstaty MI
- Alvarez 
- Alviggi MG
- Amadio BT
- Amaral Coutinho Y
- Ambroz L
- Amelung C
- Amidei D
- Amor 
- Amoroso S
- Amrouche CS
- Anastopoulos C
- Ancu LS
- Andari N
- Andeen T
- Anders CF
- Anders JK
- Anderson KJ
- Andreazza A
- Andrei V
- Anelli CR
- Angelidakis S
- Angelozzi I
- Angerami A
- Anisenkov AV
- Annovi A
- Antel C
- Anthony MT
- Antonelli M
- Antrim DJA
- Anulli F
- Aoki M
- Aperio Bella L
- Arabidze G
- Arai Y
- Araque JP
- Araujo Ferraz V
- Arce ATH
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- Arduh FA
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- Armbruster AJ
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- Baca MJ
- Bachacou H
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- Bailey AJ
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- Baldin EM
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- Balunas WK
- Balz J
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- Bauer F
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- Bussey P
- Butler JM
- Buttar CM
- Butterworth JM
- Butti P
- Buttinger W
- Buzatu A
- Buzykaev AR
- Bührer F
- Büscher D
- Büscher V
- Cabras G
- Cabrera Urbán S
- Caforio D
- Cai H
- Cairo VMM
- Cakir I
- Cakir O
- Calace N
- Calafiura P
- Calandri A
- Calderini G
- Calfayan P
- Callea G
- Caloba LP
- Calvente Lopez S
- Calvet D
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- Capeans Garrido MDM
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- Casado MP
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- Chan WS
- Chan YL
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- Charlton DG
- Chau CC
- Chavez Barajas CA
- Che S
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- Cherkaoui El Moursli R
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- Christodoulou V
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- Conventi F
- Cooper-Sarkar AM
- Cormier F
- Cormier KJR
- Corradi M
- Correia AM
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- Costa MJ
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- Dumitriu AE
- Duncan AK
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- Ecker KM
- Edgar RC
- Eifert T
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- El Kacimi M
- El Kosseifi R
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- Ellert M
- Ellinghaus F
- Elliot AA
- Ellis N
- Elmsheuser J
- Elsing M
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- Zur 
- Zwalinski L
- Ženiš T
- Živković L
- Publication venue
- 'Springer Science and Business Media LLC'
- Publication date
- 01/01/2018
- Field of study
The Tile Calorimeter is the hadron calorimeter covering the central region of the ATLAS experiment at the Large Hadron Collider. Approximately 10,000 photomultipliers collect light from scintillating tiles acting as the active material sandwiched between slabs of steel absorber. This paper gives an overview of the calorimeter’s performance during the years 2008–2012 using cosmic-ray muon events and proton–proton collision data at centre-of-mass energies of 7 and 8TeV with a total integrated luminosity of nearly 30 fb−1. The signal reconstruction methods, calibration systems as well as the detector operation status are presented. The energy and time calibration methods performed excellently, resulting in good stability of the calorimeter response under varying conditions during the LHC Run 1. Finally, the Tile Calorimeter response to isolated muons and hadrons as well as to jets from proton–proton collisions is presented. The results demonstrate excellent performance in accord with specifications mentioned in the Technical Design Report
Combined measurement of differential and total cross sections in the H → γγ and the H → ZZ* → 4ℓ decay channels at s=13 TeV with the ATLAS detector
- Author
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- Aad G
- Abbott B
- Abdinov O
- Abeloos B
- Abhayasinghe DK
- Abidi SH
- Abouzeid OS
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- Abramowicz H
- Abreu H
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- Acharya BS
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- Adamczyk L
- Adelman J
- Adersberger M
- Adiguzel A
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- Akilli E
- Akimov AV
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- Alconada Verzini MJ
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- Aleksa M
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- Allbrooke BMM
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- Zwalinski L
- Álvarez Piqueras D
- Åkesson TPA
- Šfiligoj T
- Ženiš T
- Živković L
- Publication venue
- Elsevier
- Publication date
- 01/01/2018
- Field of study
A combined measurement of differential and inclusive total cross sections of Higgs boson production is performed using 36.1 fb−1 of 13 TeV proton–proton collision data produced by the LHC and recorded by the ATLAS detector in 2015 and 2016. Cross sections are obtained from measured H→γγ and H→ZZ*(→4ℓ event yields, which are combined taking into account detector efficiencies, resolution, acceptances and branching fractions. The total Higgs boson production cross section is measured to be 57.0−5.9 +6.0 (stat.) −3.3 +4.0 (syst.) pb, in agreement with the Standard Model prediction. Differential cross-section measurements are presented for the Higgs boson transverse momentum distribution, Higgs boson rapidity, number of jets produced together with the Higgs boson, and the transverse momentum of the leading jet. The results from the two decay channels are found to be compatible, and their combination agrees with the Standard Model predictions
Search for High-Mass Resonances Decaying to τν in pp Collisions at √s=13 TeV with the ATLAS Detector
- Author
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- Zhemchugov A
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- Zhulanov V
- Zibell A
- Zieminska D
- Zimine NI
- Zimmermann S
- Zinonos Z
- Zinser M
- Ziolkowski M
- Zivkovic L
- Zobernig G
- Zoccoli A
- Zoch K
- Zorbas TG
- Zou R
- Zu Theenhausen H Meyer
- zur Nedden M
- Zwalinski L
- Publication venue
- 'American Physical Society (APS)'
- Publication date
- 01/01/2018
- Field of study
A search for high-mass resonances decaying to τν using proton-proton collisions at √s=13 TeV produced by the Large Hadron Collider is presented. Only τ-lepton decays with hadrons in the final state are considered. The data were recorded with the ATLAS detector and correspond to an integrated luminosity of 36.1 fb−1. No statistically significant excess above the standard model expectation is observed; model-independent upper limits are set on the visible τν production cross section. Heavy W′ bosons with masses less than 3.7 TeV in the sequential standard model and masses less than 2.2–3.8 TeV depending on the coupling in the nonuniversal G(221) model are excluded at the 95% credibility level
Performance of missing transverse momentum reconstruction with the ATLAS detector using proton–proton collisions at √s = 13 TeV
- Author
- Aaboud M
- Aad G
- Abbott B
- Abdinov O
- Abeloos B
- Abhayasinghe DK
- Abidi SH
- AbouZeid OS
- Abraham NL
- Abramowicz H
- Abreu H
- Abulaiti Y
- Acharya BS
- Adachi S
- Adamczyk L
- Adelman J
- Adersberger M
- Adiguzel A
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- Akesson TPA
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- Akimov AV
- Alberghi GL
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- Albicocco P
- Alconada Verzini MJ
- Alderweireldt S
- Aleksa M
- Aleksandrov IN
- Alexa C
- Alexopoulos T
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- Allbrooke BMM
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- Anelli CR
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- Yildiz H Duran
- Yorita K
- Yoshihara K
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- Yuen SPY
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- Zalieckas J
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- Zeiner SV
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- Zemaityte G
- Zeng JC
- Zeng Q
- Zenin O
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- Zerwas D
- Zgubic M
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- Zhang DF
- Zhang F
- Zhang G
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- Zhang Y
- Zhang Z
- Zhao P
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- Zhao Z
- Zhemchugov A
- Zhou B
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- Zhu CG
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- Zhuang X
- Zhukov K
- Zhulanov V
- Zibell A
- Zieminska D
- Zimine NI
- Zimmermann S
- Zinonos Z
- Zinser M
- Ziolkowski M
- Zivkovic L
- Zobernig G
- Zoccoli A
- Zoch K
- Zorbas TG
- Zou R
- Zur Nedden M
- Zwalinski L
- Publication venue
- 'Springer Science and Business Media LLC'
- Publication date
- 01/01/2018
- Field of study
The performance of the missing transverse momentum (EmissT) reconstruction with the ATLAS detector is evaluated using data collected in proton–proton collisions at the LHC at a centre-of-mass energy of 13 TeV in 2015. To reconstruct EmissT, fully calibrated electrons, muons, photons, hadronically decaying τ -leptons, and jets reconstructed from calorimeter energy deposits and charged-particle tracks are used. These are combined with the soft hadronic activity measured by reconstructed charged-particle tracks not associated with the hard objects. Possible double counting of contributions from reconstructed charged-particle tracks from the inner detector, energy deposits in the calorimeter, and reconstructed muons from the muon spectrometer is avoided by applying a signal ambiguity resolution procedure which rejects already used signals when combining the various EmissT contributions. The individual terms as well as the overall reconstructed EmissT are evaluated with various performance metrics for scale (linearity), resolution, and sensitivity to the data-taking conditions. The method developed to determine the systematic uncertainties of the EmissT scale and resolution is discussed. Results are shown based on the full 2015 data sample corresponding to an integrated luminosity of 3.2 fb−1
Measurement of the t¯tZ and t¯tW cross sections in proton-proton collisions at √s=13 TeV with the ATLAS detector
- Author
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- Zhemchugov A
- Zheng Z
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- Zimmermann S
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- Zobernig G
- Zoccoli A
- Zoch K
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- Álvarez Piqueras D
- Åkesson TPA
- Šfiligoj T
- Ženiš T
- Živković L
- Publication venue
- 'American Physical Society (APS)'
- Publication date
- 01/01/2019
- Field of study
A measurement of the associated production of a top-quark pair (t¯t) with a vector boson (W, Z) in proton-proton collisions at a center-of-mass energy of 13 TeV is presented, using 36.1 fb−1 of integrated luminosity collected by the ATLAS detector at the Large Hadron Collider. Events are selected in channels with two same- or opposite-sign leptons (electrons or muons), three leptons or four leptons, and each channel is further divided into multiple regions to maximize the sensitivity of the measurement. The t¯tZ and t¯tW production cross sections are simultaneously measured using a combined fit to all regions. The best-fit values of the production cross sections are σt¯tZ=0.95±0.08stat±0.10syst pb and σt¯tW=0.87±0.13stat±0.14syst pb in agreement with the Standard Model predictions. The measurement of the t¯tZ cross section is used to set constraints on effective field theory operators which modify the t¯tZ vertex
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