9 research outputs found
Lapatinib and Poziotinib Overcome ABCB1-Mediated Paclitaxel Resistance in Ovarian Cancer
- Author
- Publication venue
- UKnowledge
- Publication date
- 04/08/2021
- Field of study
Conventional frontline treatment for ovarian cancer consists of successive chemotherapy cycles of paclitaxel and platinum. Despite the initial favorable responses for most patients, chemotherapy resistance frequently leads to recurrent or refractory disease. New treatment strategies that circumvent or prevent mechanisms of resistance are needed to improve ovarian cancer therapy. We established in vitro paclitaxel-resistant ovarian cancer cell line and organoid models. Gene expression differences in resistant and sensitive lines were analyzed by RNA sequencing. We manipulated candidate genes associated with paclitaxel resistance using siRNA or small molecule inhibitors, and then screened the cells for paclitaxel sensitivity using cell viability assays. We used the Bliss independence model to evaluate the anti-proliferative synergy for drug combinations. ABCB1 expression was upregulated in paclitaxel-resistant TOV-21G (q \u3c 1x10-300), OVCAR3 (q = 7.4x10-156) and novel ovarian tumor organoid (p = 2.4x10-4) models. Previous reports have shown some tyrosine kinase inhibitors can inhibit ABCB1 function. We tested a panel of tyrosine kinase inhibitors for the ability to sensitize resistant ABCB1-overexpressing ovarian cancer cell lines to paclitaxel. We observed synergy when we combined poziotinib or lapatinib with paclitaxel in resistant TOV-21G and OVCAR3 cells. Silencing ABCB1 expression in paclitaxel-resistant TOV-21G and OVCAR3 cells reduced paclitaxel IC50 by 20.7 and 6.2-fold, respectively. Furthermore, we demonstrated direct inhibition of paclitaxel-induced ABCB1 transporter activity by both lapatinib and poziotinib. In conclusion, lapatinib and poziotinib combined with paclitaxel synergizes to inhibit the proliferation of ABCB1-overexpressing ovarian cancer cells in vitro. The addition of FDA-approved lapatinib to second-line paclitaxel therapy is a promising strategy for patients with recurrent ovarian cancer
Significance of Pelvic Fluid Observed during Ovarian Cancer Screening with Transvaginal Sonogram
- Author
- Baldwin-Branch Lauren A.
- Davis Caeli
- DeSimone Christopher P.
- Dietrich Charles S., III
- Dietrich Hayley
- Erol Lindsay
- Ferrell Emily Lenk
- Gallion Holly H.
- Gorski Justin W.
- Hutchcraft Megan L.
- McDowell Anthony B.
- Miller Rachel W.
- Pavlik Edward J.
- Per Nicholas J.
- Riggs McKayla J.
- Ueland Frederick R.
- van Nagell John R., Jr.
- Publication venue
- UKnowledge
- Publication date
- 01/01/2022
- Field of study
The primary objective was to examine the role of pelvic fluid observed during transvaginal ultrasonography (TVS) in identifying ovarian malignancy. A single-institution, observational study was conducted within the University of Kentucky Ovarian Cancer Screening trial from January 1987 to September 2019. We analyzed true-positive (TP), false-positive (FP), true-negative (TN), and false-negative (FN) groups for the presence of pelvic fluid during screening encounters. Measured outcomes were the presence and duration of fluid over successive screening encounters. Of the 48,925 women surveyed, 2001 (4.1%) had pelvic fluid present during a TVS exam. The odds ratio (OR) of detecting fluid in the comparison group (TN screen; OR = 1) significantly differed from that of the FP cases (benign pathology; OR: 13.4; 95% confidence interval (CI): 9.1â19.8), the TP cases with a low malignant potential (LMP; OR: 28; 95% CI: 26.5â29.5), TP ovarian cancer cases (OR: 50.4; 95% CI: 27.2â93.2), and FN ovarian cancer cases (OR: 59.3; 95% CI: 19.7â178.1). The mean duration that pelvic fluid was present for women with TN screens was 2.2 ± 0.05 encounters, lasting 38.7 ± 1.3 months. In an asymptomatic screening population, free fluid identified in TVS exams was more associated with ovarian malignancy than in the control group or benign ovarian tumors. While pelvic free fluid may not solely discriminate malignancy from non-malignancy, it appears to be clinically relevant and warrants thoughtful consideration
Calibration of the CMS hadron calorimeters using proton-proton collision data at root s=13 TeV
- Author
- Aarrestad Thea Klaeboe
- Abbaneo Duccio
- Abbiendi Giovanni
- Abbrescia Marcello
- Abdullin Salavat
- Abercrombie Daniel
- Acharya Himal
- Acosta Darin
- Acosta John Gabriel
- Adam Wolfgang
- Adamov George
- Adams Mark Raymond
- Adams Todd
- Adzic Petar
- Afanasiev Serguei
- Agapitos Antonis
- Agarwal Garvita
- Aggleton Robin
- Agram Jean-Laurent
- Aguilar-Benitez Manuel
- Agyel D.
- Ahmad Ashfaq
- Ahmad Muhammad
- Ahmad Muhammad
- Ahuja Sudha
- Akbiyik Melike
- Akchurin Nural
- Akgun Bora
- 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
- Alvarez Gonzalez Barbara
- Alverson George
- Alves FĂĄbio LĂșcio
- Alves Gilvan
- Aly Reham
- Alyari Maral
- Amapane Nicola
- Ambrogi Federico
- Amendola Chiara
- Amin Nick
- Amsler Claude
- Anagnostou Georgios
- Anagul S.
- Anderson Dustin
- Andrea Jeremy
- Andreev Vladimir
- Andreev Yuri
- Andrews Michael Benjamin
- Androsov Konstantin
- Antchev Georgy
- Antunovic Zeljko
- Apanasevich Leonard
- Apollinari Giorgio
- Apresyan Artur
- Apyan Aram
- Araujo Mariana
- Arcaro Daniel
- Arcidiacono Roberta
- Arenton Michael Wayne
- Argiro Stefano
- Arneodo Michele
- Asavapibhop Burin
- Asawatangtrakuldee Chayanit
- Asenov Patrick
- Askew Andrew
- Asmuss Paul
- Assran Yasser
- Atakisi Ismail Okan
- Ather Mohsan Waseem
- Attikis Alexandros
- Auffray Etiennette
- Aushev Tagir
- Autermann Christian
- Auzinger Georg
- Avati Valentina
- Avery Paul
- Avila Carlos
- Ayala Edy
- 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 Drew
- Baechler Joachim
- Bagliesi Giuseppe
- Bahinipati Seema
- Baillon Paul
- Bainbridge Robert
- Bakas Georgios
- Bakhshiansohi Hamed
- Bakirci Mustafa Numan
- Baldenegro Barrera Cristian
- Ball Austin
- Ball Fionn
- Ban Yong
- Band Reyer
- Banerjee Sudeshna
- Banerjee Sunanda
- Bansal Sunil
- Barbagli Giuseppe
- Barberis Emanuela
- Bargassa Pedrame
- Baringer Philip
- Barker Anthony
- Barnes Virgil E
- Barney David
- Barnyakov Alexander
- Baron Owen
- Barria Patrizia
- Barrio Luna Mar
- Bartek Rachel
- Barth Christian
- Bartosik Nazar
- BartĂłk MĂĄrton
- Baselga Marta
- Bastos Diogo
- Bat Ayse
- Battilana Carlo
- Baty Austin
- Bauerdick Lothar AT
- Baur Sebastian
- Bayshev Igor
- Bean Alice
- Beauceron Stephanie
- Beaudette Florian
- Beernaert Kelly
- Beghin Diego
- Behera Prafulla Kumar
- Behnke Olaf
- Behrens Ulf
- Bein Samuel
- Belchior Batista Das Chagas Ewerton
- Belforte Stefano
- Bell Ken W
- Bellan Riccardo
- Belloni Alberto
- Belyaev Alexander
- Belyaev Andrey
- Benaglia Andrea
- Benato Lisa
- Bencze Gyorgy
- Bendavid Joshua
- Benecke Anna
- Benelli Gabriele
- Beni Noemi
- Benitez Jose F
- Benussi Luigi
- Benvenuti Alberto
- Beretvas Andrew
- Bergauer Thomas
- Berger Pirmin
- Berger Thomas
- Beri Suman Bala
- BermĂșdez MartĂnez Armando
- Bernardes Cesar Augusto
- Bernet Colin
- Berry Douglas
- Berryhill Jeffrey
- Bertacchi Valerio
- Bertsche David
- Besancon Marc
- Beschi Andrea
- Betts Russell Richard
- Bhal Eshwen
- Bhandari Rohan
- Bhardwaj Ashutosh
- Bhardwaj Rishika
- Bharti Monika
- Bhat Muzamil Ahmad
- Bhat Pushpalatha C
- Bhatnagar Vipin
- Bhattacharya Rajarshi
- Bhattacharya Saptaparna
- Bhattacharya Satyaki
- Bhattacharya Soham
- Bhawandeep Bhawandeep
- Bheesette Srinidhi
- Bhopatkar Vallary
- Bhowmik Debabrata
- Bhowmik Sandeep
- Bhyun Ji Hwan
- Bi Ran
- Bialkowska Helena
- Bianchini Lorenzo
- Bianco Michele
- Bianco Stefano
- Biasini Maurizio
- Biino Cristina
- Bilei Gian Mario
- Bilican F.
- Bilin Bugra
- Bilki Burak
- Bin Anuar Afiq Aizuddin
- Bisello Dario
- Bitioukov Sergei
- Blekman Freya
- Blinov Vladimir
- Blobel Volker
- Bloch Daniel
- Bloch Philippe
- Bloom Kenneth
- Bluj Michal
- Blumenfeld Barry
- Boccali Tommaso
- Bocci Andrea
- Bodek Arie
- Boimska Bozena
- Boletti Alessio
- Bologna Simone
- Bols Emil SĂžrensen
- Bonacorsi Daniele
- Bonchev Miroslav
- Bondu Olivier
- Boos Edouard
- Boran Fatma
- Borchsh Vladislav
- Boren Samuel
- 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
- Bowen James
- Bozzo Marco
- Bragagnolo Alberto
- Braghieri Alessandro
- Braibant-Giacomelli Sylvie
- Brainerd Christopher
- Brandstetter Johannes
- Brandt Stephanie
- Branson James G
- Bravo Cameron
- Breedon Richard
- Breeze Shane
- Brew Christopher
- Brigljevic Vuko
- Brinkerhoff Andrew
- Brivio Francesco
- Brochero Cifuentes Javier Andres
- Brom Jean-Marie
- Brondolin Erica
- Brooke James John
- Brown Robert M
- Brun Hugues
- Bruno Giacomo
- Brzhechko Danyyl
- Bucci Rachael
- Buccilli Andrew
- Buchanan James
- Buchmuller Oliver
- Bueghly James
- Bundock Aaron
- Bunin Pavel
- Bunkowski Karol
- Buontempo Salvatore
- Burkett Kevin
- Burkle Bjorn
- Burns Douglas
- Burt Kira
- Busson Philippe
- Busza Wit
- Butler Joel Nathan
- Butler Philip H
- Butz Erik
- Bylinkin Alexander
- Bylsma Ben
- Byszuk Adrian
- Cabrera Andrés
- Cabrillo Iban Jose
- Cadamuro Luca
- Caillol CĂ©cile
- Cakir Altan
- Calabria Cesare
- Calderon De La Barca Sanchez Manuel
- Calderon Alicia
- Cali Ivan Amos
- Call Kenneth
- Calligaris Luigi
- 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
- Caratelli Alessandro
- Cardini Andrea
- Carlin Roberto
- Carlsmith Duncan
- Carnes Andrew
- 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
- Ceccarelli Rudy
- Ceci Sasa
- Celik Ali
- Cepeda Maria
- Cerati Giuseppe Benedetto
- Cerci Salim
- Cerminara Gianluca
- Cerrada Marcos
- Cerri Olmo
- Chabert Eric Christian
- Chadeeva Marina
- Chang Paoti
- Chang Philip
- Chanon Nicolas
- Chao Yuan
- Chaparro Sierra Luisa Fernanda
- Chapon Emilien
- Charlot Claude
- Chatterjee Kalyanmoy
- Chatterjee Rajdeep Mohan
- Chatterjee Suman
- Chauhan Shubhanshu
- Chauhan Sushil
- Chaves Jorge
- Chawla Ridhi
- Chazin Quero Barbara
- Checchia Paolo
- Chekhovsky Vladimir
- Chen Geng
- Chen Guo-Ming
- Chen He-Sheng
- Chen Kai-Feng
- Chen Mingshui
- Chen Po-Hsun
- Chen Xuan
- Chen Yuan
- Chenarani Shirin
- Cheng Tongguang
- Cheng Yangyang
- Cherepanov Vladimir
- Chernyavskaya Nadezda
- Chertok Maxwell
- Cheung Harry
- Chhibra Simranjit Singh
- Chiarito Brandon
- Chierici Roberto
- Chinellato Jose
- Chlebana Frank
- Cho Sungwoong
- Choi Junho
- Choi Suyong
- Choi Young-Il
- Chou John Paul
- Choudhary Brajesh C
- Choudhury Somnath
- Chtchipounov Leonid
- Chu Jennifer
- Chudasama Ruchi
- Chwalek Thorsten
- Ciangottini Diego
- Cieri Davide
- Ciesielski Robert
- Ciocca Claudia
- Ciocci Maria Agnese
- Cipriani Marco
- Ciriolo Vincenzo
- Cirkovic Predrag
- Citron Matthew
- Cittolin Sergio
- Ciulli Vitaliano
- Civinini Carlo
- Claes Daniel R
- Clare Robert
- Clarida Warren
- Clement Emyr
- Clerbaux Barbara
- CMS Collaboration
- Cockerill David JA
- Cocoros Alice
- Codispoti Giuseppe
- Coelho Eduardo
- Colaleo Anna
- Cole Joanne
- Colino Nicanor
- Collard Caroline
- Colling David
- Cometti Simona
- Connor Patrick
- Consuegra RodrĂguez Sandra
- Contardo Didier
- Conte Eric
- Contreras-Campana Christian
- Conway John
- Conway Rylan
- Cooper Seth
- Cooperstein Stephane
- Cornelis Tom
- Correia Silva Gilson
- Cosby Christopher
- Cossutti Fabio
- Costa Marco
- Costa Salvatore
- Coubez Xavier
- Couderc Fabrice
- Coughlan John A
- Cousins Robert
- Covarelli Roberto
- Cox Bradley
- Cox Peter Timothy
- Creanza Donato
- Cremonesi Matteo
- Cristella Leonardo
- Csanad Mate
- Csorgo Tamas Ferenc
- Cucciati Giacomo
- Cuevas Javier
- Cuffiani Marco
- Cumalat John Perry
- Cummings Grace
- Curry David
- Cussans David
- Cutts David
- Czellar Sandor
- D'Alessandro Raffaello
- D'Alfonso Mariarosaria
- D'Enterria David
- D'Hondt Jorgen
- 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
- Daskalakis Georgios
- Dasu Sridhara
- Datta Abhisek
- Dauncey Paul
- David Tinoco Mendes Andre
- 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 Mattia Marco
- De Moraes Gregores Eduardo
- De Oliveira Martins Carley
- De Palma Mauro
- De Roeck Albert
- De Souza Lemos Dener
- de TrocĂłniz Jorge F
- De Wit Adinda
- De Wolf Eddi A
- Debbins Paul
- Deelen Nikkie
- Defranchis Matteo Maria
- Deile Mario
- Deiters Konrad
- 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
- Demaria Natale
- Demina Regina
- Demiragli Zeynep
- Demiroglu Zuhal Seyma
- Demiyanov Andrey
- Denegri Daniel
- Depasse Pierre
- Derdzinski Mark
- Dermenev Alexander
- Dev Nabarun
- Devetak Damir
- Dewanjee Ram Krishna
- Dey Sourav
- Dezoort Gage
- Dharmaratna Welathantri GD
- Dhingra Nitish
- Di Crescenzo Antonia
- Di Croce Davide
- Di Florio Adriano
- Di Francesco Agostino
- Di Guida Salvatore
- Di Marco Emanuele
- Di Maria Riccardo
- Di Mattia Alessandro
- Diab Batoul
- Diamantopoulou Magda
- Diemoz Marcella
- Dierlamm Alexander
- Diez Pardos Carmen
- Dildick Sven
- Dilsiz Kamuran
- Dimitrov Anton
- Dimova Tatyana
- Dinardo Mauro Emanuele
- Dini Paolo
- Dissertori GĂŒnther
- Dittmann Jay
- Dittmar Michael
- Dittmer Susan
- Doan Thi Hien
- Dobson Marc
- Dobur Didar
- Dodd Laura
- Dolek Furkan
- Dolen James
- Dominguez Aaron
- DomĂnguez Damiani Daniela
- Donato Silvio
- DonegĂ Mauro
- Dordevic Milos
- Dorfer Christian
- Dorigo Tommaso
- Dorney Brian
- Doroba Krzysztof
- Dosselli Umberto
- Dozen Candan
- Dragicevic Marko
- Dremin Igor
- Dreyer Torben
- Duarte Campderros Jordi
- Duarte Javier
- Dube Sourabh
- Dudenas Vytautas
- Dudko Lev
- Dugad Shashikant
- Duh Yi-ting
- Dulemba Joseph Lynn
- Dumanoglu Isa
- Dupont Niels
- Durgut SĂŒleyman
- Duric Senka
- Durkin Lloyd Stanley
- Dutta Dipanwita
- Dutta Irene
- Dutta Suchandra
- Dutta Valentina
- DĂŒnser Marc
- Ebrahimi Aliakbar
- Eckerlin Guenter
- Ecklund Karl Matthew
- Eckstein Doris
- Eerola Paula
- Ehataht Karl
- Eichhorn Thomas
- El Mamouni Houmani
- El Morabit Karim
- Elgammal Sherif
- Elliott-Peisert Anna
- Elmer Peter
- Elvira Victor Daniel
- Elwood Adam
- Emediato Luiz
- Eminizer Nicholas
- Eno Sarah Catherine
- Epshteyn Vladimir
- Erbacher Robin
- Erdmann Martin
- Erdmann Wolfram
- Erdweg Sören
- Eren Engin
- Erice Carlos
- Erodotou Eleni
- Errico Filippo
- Ershov Alexander
- Erö Janos
- Escalante Del Valle Alberto
- Esch Thomas
- Eskandari Tadavani Esmaeel
- Eskut Eda
- Etesami Seyed Mohsen
- Eusebi Ricardo
- Evangelou Ioannis
- Evans Andrew
- Evdokimov Olga
- Everaerts Pieter
- Eysermans Jan
- Fabbri Fabrizio
- Fabbro Bernard
- Fabozzi Francesco
- Faccioli Pietro
- Fallavollita Francesco
- Fallon Colin
- Falmagne Guillaume
- Faltermann Nils
- Fanfani Alessandra
- Fang Wenxing
- Fangmeier Caleb
- FanĂČ Livio
- Fasanella Daniele
- Faure Jean-Louis
- Favart Laurent
- Fay Jean
- Fedi Giacomo
- Fehling David
- Felcini Marta
- Feld Lutz
- Feng Lei
- Feng Yongbin
- Ferbel Thomas
- Ferencek Dinko
- Ferguson Thomas
- Fernandez Bedoya Cristina
- Fernandez Menendez Javier
- Fernandez Marcos
- Fernåndez Manteca Pedro José
- FernĂĄndez Ramos Juan Pablo
- Ferri Federico
- Ferro Fabrizio
- Field Richard D
- Fienga Francesco
- Finco Linda
- Finger Jr Michael
- Finger Miroslav
- Fiore Luigi
- Fiorendi Sara
- Fiori Francesco
- Fischer Benjamin
- Fischer Robert
- Flacher Henning
- Flechl Martin
- Flix Jose
- Florent Alice
- Flores Chad
- Florez Carlos
- Flowers Sean
- FlĂŒgge GĂŒnter
- Focardi Ettore
- Folgueras Santiago
- Fonseca De Souza Sandro
- Fontaine Jean-Charles
- Fontanesi Elisa
- Ford William T
- Forthomme Laurent
- Foudas Costas
- Fouz Maria Cruz
- Francis Brian
- Franco Sevilla Manuel
- Francois Brieuc
- Frankenthal Andre
- Franzoni Giovanni
- Freed Sarah
- Freeman Jim
- Freer Chad
- Fruehwirth Rudolf
- Fröhlich Alexander
- Fulcher Jonathan
- Funk Garrett
- Funk Wolfgang
- Gadrat SĂ©bastien
- Galanti Mario
- Galati Giuliana
- Galinhas Bruno
- Gallinaro Michele
- Gallo Elisabetta
- Galloni Camilla
- Gandrajula Reddy Pratap
- Gandrakota Abhijith
- Ganjour Serguei
- Gao Xuyang
- Garbers Christoph
- Garcia Fuentes Francisco Ignacio
- Garcia-Bellido Aran
- GarcĂa Alonso Andrea
- Garg Rocky Bala
- Garutti Erika
- Gary J William
- Gascon Susan
- Gasparini Fabrizio
- Gasparini Ugo
- Gastler Daniel
- Gavrilenko Mikhail
- 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
- GiljanoviÄ Duje
- Gill Karl
- Gilmore Jason
- Girgis Semiray
- Givernaud Alain
- Glege Frank
- Gleyzer Sergei V
- Gninenko Sergei
- Go Yeonju
- Godinovic Nikola
- Goerlach Ulrich
- Goh Junghwan
- Gokbulut Gul
- Gola Mohit
- Goldenzweig Pablo
- 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
- Gonzalez Suarez Rebeca
- Gonzalez Daniel
- GonzĂĄlez FernĂĄndez Juan Rodrigo
- GonzĂĄlez HernĂĄndez Carlos Felipe
- Gorbunov Ilya
- Gottmann Artur
- Gottschalk Erik
- Gouskos Loukas
- Gouzevitch Maxime
- Govoni Pietro
- Goy Lopez Silvia
- Gozzelino Andrea
- Grab Christoph
- Grados Luyando Juan Manuel
- Grandi Claudio
- Granier de Cassagnac Raphael
- Gras Philippe
- Grassi Tullio
- Gray Lindsey
- Grebenyuk Anastasia
- Green Dan
- Greene Senta
- Gribushin Andrey
- Grippo Maria Teresa
- Gritsan Andrei
- Grohsjean Alexander
- Gruchala Marek
- Grunewald Martin
- Grynyov Boris
- Grzanka Leszek
- GrĂŒnendahl Stefan
- Guchait Monoranjan
- Guiducci Luigi
- Guilbaud Maxime
- Guler Yalcin
- Gulhan Doga
- Gunnellini Paolo
- Gunter Thoth
- Gupta Rajat
- Gurpinar guler Emine
- Gurrola Alfredo
- Gutay Laszlo
- Guthoff Moritz
- Guts Sergey
- Gutsche Oliver
- Guzzi Luca
- Gyun Dooyeon
- GĂłmez Espinosa Tirso Alejandro
- GĂłrski Maciej
- GĂŒlmez Erhan
- Ha Seungkyu
- Haddad Yacine
- Hadjiiska Roumyana
- Hadley Mary
- Hadley Nicholas John
- Hagopian Sharon
- Hagopian Vasken
- Hahn Kristan Allan
- Haj Ahmad Wael
- Hajdu Csaba
- Hakala John
- Halkiadakis Eva
- Hall Geoffrey
- Haller Johannes
- Hamel de Monchenault Gautier
- Han Jiyeon
- Hangal Dhanush Anil
- Hanlon Jim
- Hansen Peter
- Hanson Gail
- Haranko Mykyta
- Harb Ali
- Hardenbrook Joshua
- Harder Kristian
- Harper Sam
- Harr Robert
- Harrendorf Marco Alexander
- 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
- Haytmyradov Maksat
- Hazen Eric
- He He
- Heath Greg P
- Heath Helen F
- Hebbeker Thomas
- Heering Arjan Hendrix
- Hegde Vinay
- Hegeman Jeroen
- Heidegger Constantin
- HeikkilÀ Jaana Kristiina
- Heindl Maximilian
- Heintz Ulrich
- Heller Ryan
- Henderson Conor
- Hensel Carsten
- Heredia-De La Cruz Ivan
- Hernandez Jose M
- Herndon Matthew
- Hervé Alain
- Higginbotham Samuel
- Hildreth Michael
- Hill Christopher
- Hiltbrand Joshua
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- Ălvarez FernĂĄndez Adrian
- Ăzçelik Ăzlem
- Publication venue
- Publication date
- 01/01/2019
- Field of study
Methods are presented for calibrating the hadron calorimeter system of theCMSetector at the LHC. The hadron calorimeters of the CMS experiment are sampling calorimeters of brass and scintillator, and are in the form of one central detector and two endcaps. These calorimeters cover pseudorapidities vertical bar eta vertical bar ee data. The energy scale of the outer calorimeters has been determined with test beam data and is confirmed through data with high transverse momentum jets. In this paper, we present the details of the calibration methods and accuracy.Peer reviewe
Pathways to Myocardial Hypertrophy
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- 'Springer Science and Business Media LLC'
- Publication date
- Field of study
Pharmacokinetics and Pharmacodynamics of Antiretrovirals in the Central Nervous System
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- Field of study
Evolocumab and clinical outcomes in patients with cardiovascular disease
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- Venegas Carrillo La
- Verheye S
- Vertes G
- Veze I
- Vida Gutierrez M
- Vidotti Mh
- Viigimaa M
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- Vikman S
- Vinanska D
- Vintila Mm
- Violante Ortiz Rm
- Vishnevsky A
- Visman A
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- Voevoda M
- Vogel Dr
- Volkov V
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- von Hodenberg E
- Vora K
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- Wang D
- Wang Huei
- Wang J
- Wasserman Scott M.
- Waxman F
- Webel R
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- Weinberg B
- Weinstein D
- Welker J
- Wermuth S
- Westendorp I
- Weyland K
- Whitney R
- Wierzbicka K
- Wilhoit G
- Wilson S
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- Wiseman A
- Witt N
- Wittert G
- Wiviott Stephen D.
- Wnetrzak-Michalska R
- Wollaert B
- Wood Sk
- Wozakowska-Kaplon B
- Wozniak I
- Wu C
- Wyatt N
- Wöhrle J
- Xu P
- Xue L
- Yakhontova P
- Yamamoto K
- Yamashita K
- Yan J
- Yang E
- Yang P
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- Yang Y
- Yang Z
- Yao Z
- Yasumura Y
- Yataco A
- Yeh H
- Yena L
- Yeoman G
- Yigit Z
- Yilmaz Mb
- Yokoya K
- Yoshimichi G
- Yotov Y
- Youngman D
- Younis L
- Yuge M
- Zabowka M
- Zahn L
- Zamorano Gomez Jl
- Zarich S
- Zateyshchikov D
- Zdrenghea D
- Zechowicz T
- Zeig S
- Zemanek J
- Zeng X
- Zhang L
- Zhang X
- Zhao S
- Zheng Y
- Zheng Z
- Zhou C
- Zhu Y
- Zhurba S
- Zidkova E
- Zieba B
- Ziegler O
- Zilahi Z
- Zrazhevskiy K
- Ăstergren J
- Publication venue
- 'Massachusetts Medical Society'
- Publication date
- 01/01/2017
- Field of study
BACKGROUND Evolocumab is a monoclonal antibody that inhibits proprotein convertase subtilisin-kexin type 9 (PCSK9) and lowers low-density lipoprotein (LDL) cholesterol levels by approximately 60%. Whether it prevents cardiovascular events is uncertain. METHODS We conducted a randomized, double-blind, placebo-controlled trial involving 27,564 patients with atherosclerotic cardiovascular disease and LDL cholesterol levels of 70 mg per deciliter (1.8 mmol per liter) or higher who were receiving statin therapy. Patients were randomly assigned to receive evolocumab (either 140 mg every 2 weeks or 420 mg monthly) or matching placebo as subcutaneous injections. The primary efficacy end point was the composite of cardiovascular death, myocardial infarction, stroke, hospitalization for unstable angina, or coronary revascularization. The key secondary efficacy end point was the composite of cardiovascular death, myocardial infarction, or stroke. The median duration of follow-up was 2.2 years. RESULTS At 48 weeks, the least-squares mean percentage reduction in LDL cholesterol levels with evolocumab, as compared with placebo, was 59%, from a median baseline value of 92 mg per deciliter (2.4 mmol per liter) to 30 mg per deciliter (0.78 mmol per liter) (P<0.001). Relative to placebo, evolocumab treatment significantly reduced the risk of the primary end point (1344 patients [9.8%] vs. 1563 patients [11.3%]; hazard ratio, 0.85; 95% confidence interval [CI], 0.79 to 0.92; P<0.001) and the key secondary end point (816 [5.9%] vs. 1013 [7.4%]; hazard ratio, 0.80; 95% CI, 0.73 to 0.88; P<0.001). The results were consistent across key subgroups, including the subgroup of patients in the lowest quartile for baseline LDL cholesterol levels (median, 74 mg per deciliter [1.9 mmol per liter]). There was no significant difference between the study groups with regard to adverse events (including new-onset diabetes and neurocognitive events), with the exception of injection-site reactions, which were more common with evolocumab (2.1% vs. 1.6%). CONCLUSIONS In our trial, inhibition of PCSK9 with evolocumab on a background of statin therapy lowered LDL cholesterol levels to a median of 30 mg per deciliter (0.78 mmol per liter) and reduced the risk of cardiovascular events. These findings show that patients with atherosclerotic cardiovascular disease benefit from lowering of LDL cholesterol levels below current targets
Measurements of dose-rate effects in the radiation damage of plastic scintillator tiles using silicon photomultipliers
- Author
- Aarrestad Thea Klaeboe
- Abbaneo Duccio
- Abbiendi Giovanni
- Abbrescia Marcello
- Abdullin Salavat
- Abercrombie Daniel
- Acharya Himal
- Acosta Darin
- Acosta John Gabriel
- Adam Wolfgang
- Adamov George
- Adams Mark Raymond
- Adams Todd
- Adzic Petar
- Afanasiev Serguei
- Agapitos Antonis
- Agarwal Garvita
- Aggleton Robin
- Agram Jean-Laurent
- Aguilar-Benitez Manuel
- Agyel D.
- Ahmad Ashfaq
- Ahmad Muhammad
- Ahmad Muhammad
- Ahuja Sudha
- Akbiyik Melike
- Akchurin Nural
- Akgun Bora
- 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
- Alvarez Gonzalez Barbara
- Alverson George
- Alves FĂĄbio LĂșcio
- Alves Gilvan
- Aly Reham
- Alyari Maral
- Amapane Nicola
- Ambrogi Federico
- Amendola Chiara
- Amin Nick
- Amsler Claude
- Anagnostou Georgios
- Anagul S.
- Anderson Dustin
- Andrea Jeremy
- Andreev Vladimir
- Andreev Yuri
- Andrews Michael Benjamin
- Androsov Konstantin
- Antchev Georgy
- Antunovic Zeljko
- Apanasevich Leonard
- Apollinari Giorgio
- Apresyan Artur
- Apyan Aram
- Araujo Mariana
- Arcaro Daniel
- Arcidiacono Roberta
- Arenton Michael Wayne
- Argiro Stefano
- Arneodo Michele
- Asavapibhop Burin
- Asawatangtrakuldee Chayanit
- Asenov Patrick
- Askew Andrew
- Asmuss Paul
- Assran Yasser
- Atakisi Ismail Okan
- Ather Mohsan Waseem
- Attikis Alexandros
- Auffray Etiennette
- Aushev Tagir
- Autermann Christian
- Auzinger Georg
- Avati Valentina
- Avery Paul
- Avila Carlos
- Ayala Edy
- 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 Drew
- Baechler Joachim
- Bagliesi Giuseppe
- Bahinipati Seema
- Baillon Paul
- Bainbridge Robert
- Bakas Georgios
- Bakhshiansohi Hamed
- Bakirci Mustafa Numan
- Baldenegro Barrera Cristian
- Ball Austin
- Ball Fionn
- Ban Yong
- Band Reyer
- Banerjee Sudeshna
- Banerjee Sunanda
- Bansal Sunil
- Barbagli Giuseppe
- Barberis Emanuela
- Bargassa Pedrame
- Baringer Philip
- Barker Anthony
- Barnes Virgil E
- Barney David
- Barnyakov Alexander
- Baron Owen
- Barria Patrizia
- Barrio Luna Mar
- Bartek Rachel
- Barth Christian
- Bartosik Nazar
- BartĂłk MĂĄrton
- Baselga Marta
- Bastos Diogo
- Bat Ayse
- Battilana Carlo
- Baty Austin
- Bauerdick Lothar AT
- Baur Sebastian
- Bayshev Igor
- Bean Alice
- Beauceron Stephanie
- Beaudette Florian
- Beernaert Kelly
- Beghin Diego
- Behera Prafulla Kumar
- Behnke Olaf
- Behrens Ulf
- 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
- Benvenuti Alberto
- Beretvas Andrew
- Bergauer Thomas
- Berger Pirmin
- Berger Thomas
- Beri Suman Bala
- BermĂșdez MartĂnez Armando
- Bernardes Cesar Augusto
- Bernet Colin
- Berry Douglas
- Berryhill Jeffrey
- Bertacchi Valerio
- Bertsche David
- Besancon Marc
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- Hatakeyama Kenichi
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- Haytmyradov Maksat
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- Tonelli Manganote Edmilson José
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- Yusli Mohd Nizam
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- Zaganidis Nicolas
- Zahid Sema
- Zaleski Shawn
- Zalewski Piotr
- Zanetti Anna
- Zanetti Marco
- Zarubin Anatoli
- Zarucki Mateusz
- Zecchinelli Angelo Giacomo
- Zenaiev Oleksandr
- Zenz Seth Conrad
- Zeuner Wolfram Dietrich
- Zevi Della Porta Giovanni
- 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
- Zielinski Marek
- Zientek Margaret
- Zlebcik Radek
- Zobec Joze
- Zoi Irene
- Zolkapli Zukhaimira
- Zorbakir Ibrahim Soner
- Zorbilmez Caglar
- Zotto Pierluigi
- Zou David
- Zucchetta Alberto
- Zumerle Gianni
- Zuo Xunwu
- Zuolo Davide
- Ălvarez FernĂĄndez Adrian
- Ăzçelik Ăzlem
- Publication venue
- Publication date
- 01/01/2020
- Field of study
Measurements are presented of the reduction of signal output due to radiation damage for plastic scintillator tiles used in the hadron endcap (HE) calorimeter of the CMS detector. The tiles were exposed to particles produced in proton-proton (pp) collisions at the CERN LHC with a center-of-mass energy of 13 TeV, corresponding to a delivered luminosity of 50 fbâ1. The measurements are based on readout channels of the HE that were instrumented with silicon photomultipliers, and are derived using data from several sources: a laser calibration system, a movable radioactive source, as well as hadrons and muons produced in pp collisions. Results from several irradiation campaigns using 60Co sources are also discussed. The damage is presented as a function of dose rate. Within the range of these measurements, for a fixed dose the damage increases with decreasing dose rate
Measurements with silicon photomultipliers of dose-rate effects in the radiation damage of plastic scintillator tiles in the CMS hadron endcap calorimeter
- Author
- Aarrestad Thea Klaeboe
- Abbaneo Duccio
- Abbiendi Giovanni
- Abbrescia Marcello
- Abdullin Salavat
- Abercrombie Daniel
- Acharya Himal
- Acosta Darin
- Acosta John Gabriel
- Adam Wolfgang
- Adamov George
- Adams Mark Raymond
- Adams Todd
- Adzic Petar
- Afanasiev Serguei
- Agapitos Antonis
- Agarwal Garvita
- Aggleton Robin
- Agram Jean-Laurent
- Aguilar-Benitez Manuel
- Agyel D.
- Ahmad Ashfaq
- Ahmad Muhammad
- Ahmad Muhammad
- Ahuja Sudha
- Akbiyik Melike
- Akchurin Nural
- Akgun Bora
- 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
- Alvarez Gonzalez Barbara
- Alverson George
- Alves FĂĄbio LĂșcio
- Alves Gilvan
- Aly Reham
- Alyari Maral
- Amapane Nicola
- Ambrogi Federico
- Amendola Chiara
- Amin Nick
- Amsler Claude
- Anagnostou Georgios
- Anagul S.
- Anderson Dustin
- Andrea Jeremy
- Andreev Vladimir
- Andreev Yuri
- Andrews Michael Benjamin
- Androsov Konstantin
- Antchev Georgy
- Antunovic Zeljko
- Apanasevich Leonard
- Apollinari Giorgio
- Apresyan Artur
- Apyan Aram
- Araujo Mariana
- Arcaro Daniel
- Arcidiacono Roberta
- Arenton Michael Wayne
- Argiro Stefano
- Arneodo Michele
- Asavapibhop Burin
- Asawatangtrakuldee Chayanit
- Asenov Patrick
- Askew Andrew
- Asmuss Paul
- Assran Yasser
- Atakisi Ismail Okan
- Ather Mohsan Waseem
- Attikis Alexandros
- Auffray Etiennette
- Aushev Tagir
- Autermann Christian Tobias
- Auzinger Georg
- Avati Valentina
- Avery Paul
- Avila Carlos
- Ayala Edy
- Azarkin Maksim
- Azhgirey Igor
- Aziz Tariq
- Azzi Patrizia
- Azzurri Paolo
- Baarmand Marc M.
- Babaev Anton
- Babounikau Illia
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- Backhaus Malte
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- Banerjee Sunanda
- Bansal Sunil
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- Zecchinelli Angelo Giacomo
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- Zevi Della Porta Giovanni
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- Zhu Ren-Yuan
- Zielinski Marek
- Zientek Margaret
- Zlebcik Radek
- Zobec Joze
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- Zolkapli Zukhaimira
- Zorbakir Ibrahim Soner
- Zorbilmez Caglar
- Zotto Pierluigi
- Zou David
- Zucchetta Alberto
- Zumerle Gianni
- Zuo Xunwu
- Zuolo Davide
- Ălvarez FernĂĄndez Adrian
- Ăzçelik Ăzlem
- Publication venue
- 'IOP Publishing'
- Publication date
- 01/01/2020
- Field of study
International audienceMeasurements are presented of the reduction of signal output due to radiation damage for two types of plastic scintillator tiles used in the hadron endcap (HE) calorimeter of the CMS detector. The tiles were exposed to particles produced in proton-proton (pp) collisions at the CERN LHC with a center-of-mass energy of 13 TeV, corresponding to a delivered luminosity of 50 fbâ1. The measurements are based on readout channels of the HE that were instrumented with silicon photomultipliers, and are derived using data from several sources: a laser calibration system, a movable radioactive source, as well as hadrons and muons produced in pp collisions. Results from several irradiation campaigns using 60Co sources are also discussed. The damage is presented as a function of dose rate. Within the range of these measurements, for a fixed dose the damage increases with decreasing dose rate
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- Salzburg Australia
- San Francisco Unified School District
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- Social Services Oahu
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- Stanley J.C.
- State of the County Los Angeles 1987. Los Angeles
- Stavig G.R.
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- Steinberg Laurence
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- U.S. Census Bureau
- U.S. Equal Employment Opportunity Commission
- US. Commission on Civil Rights.
- Uyematsu Amy
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- Waianae Coast Culture and Arts Society
- Waldinger Roger D
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- Publication venue
- 'UCLA American Indian Studies Center'
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