95 research outputs found
The activating mutation R201C in GNAS promotes intestinal tumourigenesis in Apc(Min/+) mice through activation of Wnt and ERK1/2 MAPK pathways.
- Author
- A Horvath
- A Horvath
- A Plagge
- BE Hayward
- C H Wilson
- CA Landis
- CA Stratakis
- CE Eberhart
- CJ Chen
- CN Johnstone
- D J Adams
- DB Levy
- F Luo
- F Luo
- F Palos-Paz
- F Radtke
- GA Orner
- GC Yang
- GF Taboada
- H Nishihara
- H Su
- HE Abud
- HE MacMahon
- I Nishisho
- JA McCubrey
- JA Rudolph
- JA Wilkins
- JL Bos
- JM Kirk
- KJ Livak
- KM Haigis
- LD Wood
- LK Su
- LS Kirschner
- LS Weinstein
- LS Weinstein
- M Barbacid
- M Brink
- M Conti
- M J Arends
- MC Fragoso
- MC Fragoso
- MD Castellone
- MD Houslay
- MM Taketo
- MT Collins
- N Kalfa
- OJ Sansom
- OM Sieber
- PJ Stork
- R E McIntyre
- R Happle
- RH Giles
- T Sjoblom
- T Zhang
- V Kotoula
- WF Dietrich
- Y Araki
- Publication venue
- Oncogene
- Publication date
- 12/08/2010
- Field of study
Somatically acquired, activating mutations of GNAS, the gene encoding the stimulatory G-protein Gsalpha subunit, have been identified in kidney, thyroid, pituitary, leydig cell, adrenocortical and, more recently, in colorectal tumours, suggesting that mutations such as R201C may be oncogenic in these tissues. To study the role of GNAS in intestinal tumourigenesis, we placed GNAS R201C under the control of the A33-antigen promoter (Gpa33), which is almost exclusively expressed in the intestines. The GNAS R201C mutation has been shown to result in the constitutive activation of Gsalpha and adenylate cyclase and to lead to the autonomous synthesis of cyclic adenosine monophosphate (cAMP). Gpa33(tm1(GnasR201C)Wtsi/+) mice showed significantly elevated cAMP levels and a compensatory upregulation of cAMP-specific phosphodiesterases in the intestinal epithelium. GNAS R201C alone was not sufficient to induce tumourigenesis by 12 months, but there was a significant increase in adenoma formation when Gpa33(tm1(GnasR201C)Wtsi/+) mice were bred onto an Apc(Min/+) background. GNAS R201C expression was associated with elevated expression of Wnt and extracellular signal-regulated kinase 1/2 mitogen-activated protein kinase (ERK1/2 MAPK) pathway target genes, increased phosphorylation of ERK1/2 MAPK and increased immunostaining for the proliferation marker Ki67. Furthermore, the effects of GNAS R201C on the Wnt pathway were additive to the inactivation of Apc. Our data strongly suggest that activating mutations of GNAS cooperate with inactivation of APC and are likely to contribute to colorectal tumourigenesis
The efficacy and safety of prokinetic agents in critically ill patients receiving enteral nutrition: a systematic review and meta-analysis of randomized trials.
- Author
- A Acosta
- A Dive
- A Dive
- A Dive
- Andrew Rhodes
- B Hu
- C Booth
- C Johannes
- C Jooste
- C Kao
- D Craven
- D Goldhill
- D Guelon
- D Heiselman
- D Heyland
- D Heyland
- D Heyland
- D Heyland
- D Moher
- D Yavagal
- Derek C. Angus
- F Moore
- Fayez Alshamsi
- G Lanfranchi
- G Zaloga
- H Mentec
- H Parkman
- H Paz
- J Alverdy
- J Barbey
- J Berne
- J Higgins
- J Higgins
- J Malagelada
- J Montejo
- J Pinilla
- J Reignier
- K Kudsk
- K Whatley
- Kim Lewis
- Laura Evans
- Lauralyn Mcintyre
- M Barclay
- M Chapman
- M Egger
- M Nassaj
- M Tarling
- M Tryba
- N Nguyen
- N Nguyen
- N Nguyen
- O Hu
- O Petring
- P Griffith
- R Calcroft
- R DerSimonian
- R Heading
- R MacLaren
- R MacLaren
- R MacLaren
- R MacLaren
- R Schoenenberger
- S Adam
- S Kalliafas
- S McClave
- S McClave
- Saleh Almenawer
- T Nursal
- T Weihrauch
- W Alhazzani
- Waleed Alhazzani
- Zuhoor Alqahtani
- Publication venue
- 'Springer Science and Business Media LLC'
- Publication date
- 01/01/2016
- Field of study
BACKGROUND: Intolerance to enteral nutrition is common in critically ill adults, and may result in significant morbidity including ileus, abdominal distension, vomiting and potential aspiration events. Prokinetic agents are prescribed to improve gastric emptying. However, the efficacy and safety of these agents in critically ill patients is not well-defined. Therefore, we conducted a systematic review and meta-analysis to determine the efficacy and safety of prokinetic agents in critically ill patients. METHODS: We searched MEDLINE, EMBASE, and Cochrane Library from inception up to January 2016. Eligible studies included randomized controlled trials (RCTs) of critically ill adults assigned to receive a prokinetic agent or placebo, and that reported relevant clinical outcomes. Two independent reviewers screened potentially eligible articles, selected eligible studies, and abstracted pertinent data. We calculated pooled relative risk (RR) for dichotomous outcomes and mean difference for continuous outcomes, with the corresponding 95 % confidence interval (CI). We assessed risk of bias using Cochrane risk of bias tool, and the quality of evidence using grading of recommendations assessment, development, and evaluation (GRADE) methodology. RESULTS: Thirteen RCTs (enrolling 1341 patients) met our inclusion criteria. Prokinetic agents significantly reduced feeding intolerance (RR 0.73, 95 % CI 0.55, 0.97; P = 0.03; moderate certainty), which translated to 17.3 % (95 % CI 5, 26.8 %) absolute reduction in feeding intolerance. Prokinetics also reduced the risk of developing high gastric residual volumes (RR 0.69; 95 % CI 0.52, 0.91; P = 0.009; moderate quality) and increased the success of post-pyloric feeding tube placement (RR 1.60, 95 % CI 1.17, 2.21; P = 0.004; moderate quality). There was no significant improvement in the risk of vomiting, diarrhea, intensive care unit (ICU) length of stay or mortality. Prokinetic agents also did not significantly increase the rate of diarrhea. CONCLUSION: There is moderate-quality evidence that prokinetic agents reduce feeding intolerance in critically ill patients compared to placebo or no intervention. However, the impact on other clinical outcomes such as pneumonia, mortality, and ICU length of stay is unclear
A gravitational-wave standard siren measurement of the Hubble constant
- Author
- Abbott
- Abbott
- Abbott
- Abbott
- Abdalla
- Acernese
- Ackley
- Adams
- Adams
- Addesso
- Adhikari
- Adya
- Affeldt
- Afrough
- Agarwal
- Agathos
- Agatsuma
- Aggarwal
- Aguiar
- Aiello
- Ain
- Ajith
- Alexander
- Allam
- Allen
- Allen
- Allocca
- Altin
- Amato
- Ananyeva
- Anderson
- Anderson
- Angelova
- Annis
- Antier
- Appert
- Arai
- Araya
- Arcavi Iair
- Areeda
- Arnaud
- Arun
- Ascenzi
- Ashton
- Ast
- Aston
- Astone
- Atallah
- Aufmuth
- Aulbert
- AultONeal
- Austin
- Avila-Alvarez
- Babak
- Bacon
- Bader
- Bae
- Baker
- Balanutsa
- Balbinot
- Baldaccini
- Ballardin
- Ballmer
- Banagiri
- Barayoga
- Barclay
- Barish
- Barker
- Barkett
- Barone
- Barr
- Barsotti
- Barsuglia
- Barta
- Bartlett
- Bartos
- Bassiri
- Basti
- Batch
- Bawaj
- Bayley
- Bazzan
- Bechtol
- Beer
- Bejger
- Belahcene
- Bell
- Benoit-Lévy
- Berger
- Berger
- Bergmann
- Bero
- Berry
- Bersanetti
- Bertin
- Bertolini
- Betzwieser
- Bhagwat
- Bhandare
- Bilenko
- Billingsley
- Billman
- Birch
- Birney
- Birnholtz
- Biscans
- Biscoveanu
- Bisht
- Bitossi
- Biwer
- Bizouard
- Blackburn
- Blackman
- Blair
- Blair
- Blair
- Blanchard
- Bloemen
- Bock
- Bode
- Boer
- Bogaert
- Bohe
- Bondu
- Bonilla
- Bonnand
- Boom
- Bork
- Boschi
- Bose
- Bossie
- Bouffanais
- Bozzi
- Bradaschia
- Brady
- Branchesi
- Brau
- Briant
- Bridle
- Brillet
- Brinkmann
- Brisson
- Brockill
- Broida
- Brooks
- Brooks
- Brout
- Brown
- Brown
- Brunett
- Buchanan
- Buckley
- Buckley-Geer
- Budnev
- Buikema
- Bulik
- Bulten
- Buonanno
- Burke
- Buskulic
- Butler
- Buy
- Byer
- Bécsy
- Cabero
- Cadonati
- Cagnoli
- Cahillane
- Calderón Bustillo
- Callister
- Calloni
- Camp
- Canepa
- Canizares
- Cannon
- Cano
- Cao
- Cao
- Capano
- Capocasa
- Carbognani
- Caride
- Carnero Rosell
- Carney
- Carrasco Kind
- Carretero
- Casanueva Diaz
- Casentini
- Castander
- Caudill
- Cavaglià
- Cavalier
- Cavalieri
- Cella
- Cepeda
- Cerdá-Durán
- Cerretani
- Cesarini
- Chamberlin
- Chan
- Chao
- Charlton
- Chase
- Chassande-Mottin
- Chatterjee
- Chatziioannou
- Cheeseboro
- Chen
- Chen
- Chen
- Cheng
- Chia
- Chincarini
- Chiummo
- Chmiel
- Cho
- Cho
- Chornock
- Chow
- Christensen
- Chu
- Chua
- Chua
- Chung
- Chung
- Ciani
- Ciolfi
- Cirelli
- Cirone
- Clara
- Clark
- Clearwater
- Cleva
- Cocchieri
- Coccia
- Cohadon
- Cohen
- Colla
- Collette
- Cominsky
- Constancio
- Conti
- Cook
- Cooper
- Copperwheat
- Corban
- Corbitt
- Cordero-Carrión
- Corley
- Cornish
- Corsi
- Cortese
- Costa
- Coughlin
- Coughlin
- Coulon
- Coulter
- Countryman
- Couvares
- Covas
- Cowan
- Coward
- Cowart
- Cowperthwaite
- Coyne
- Coyne
- Creighton
- Creighton
- Cripe
- Crowder
- Cullen
- Cumming
- Cunha
- Cunningham
- Cuoco
- D'Andrea
- D'Antonio
- Da Costa
- Da Silva Costa
- Dal Canton
- Danilishin
- Danzmann
- Dasgupta
- Datrier
- Dattilo
- Dave
- Davier
- Davis
- Davis
- Daw
- Day
- De Laurentis
- De Pietri
- De Rosa
- De Rossi
- De Ugarte-Postigo
- De Varona
- De
- DeBra
- Degallaix
- Del Pozzo
- Deléglise
- Demos
- Denker
- Dent
- DePoy
- Dergachev
- DeRosa
- Desai
- DeSalvo
- Devenson
- Dhurandhar
- Di Fiore
- Di Giovanni
- Di Girolamo
- Di Lieto
- Di Pace
- Di Palma
- Di Renzo
- Diehl
- Dietrich
- Doctor
- Dolique
- Donovan
- Dooley
- Doravari
- Dorrington
- Douglas
- Dovale Álvarez
- Downes
- Drago
- Dreissigacker
- Driggers
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- Drout
- Du
- Ducrot
- Dupej
- Durret
- Dwyer
- Dálya
- Díaz
- Edo
- Edwards
- Effler
- Eftekhari
- Eggenstein
- Ehrens
- Eichholz
- Eikenberry
- Eisenstein
- Essick
- Estevez
- Estrada
- Etienne
- Etzel
- Evans
- Evans
- Evans
- Factourovich
- Fafone
- Fair
- Fairhurst
- Fan
- Farinon
- Farr
- Farr
- Fauchon-Jones
- Favata
- Fays
- Fee
- Fehrmann
- Feicht
- Fejer
- Fernandez
- Fernandez-Galiana
- Ferrante
- Ferreira
- Ferrini
- Fidecaro
- Finley
- Finstad
- Fiori
- Fiorucci
- Fishbach
- Fisher
- Fitz-Axen
- Flaminio
- Flaugher
- Fletcher
- Foley
- Fong
- Fong
- Font
- Forsyth
- Forsyth
- Fosalba
- Fournier
- Frasca
- Frasconi
- Frei
- Freise
- Frey
- Frey
- Frieman
- Fries
- Fritschel
- Frolov
- Fryer
- Fulda
- Fyffe
- Fynbo
- Gabbard
- Gadre
- Gaebel
- Gair
- Gammaitoni
- Ganija
- Gaonkar
- Garcia-Quiros
- García-Bellido
- Garufi
- Gateley
- Gaudio
- Gaur
- Gayathri
- Gaztanaga
- Gehrels
- Gemme
- Genin
- Gennai
- George
- George
- Gerdes
- Gergely
- Germain
- Ghonge
- Ghosh
- Ghosh Abhirup
- Ghosh Archisman
- Giaime
- Giannantonio
- Giardina
- Giazotto
- Gill
- Gill
- Glover
- Goetz
- Goetz
- Goldstein
- Gomes
- Goncharov
- Gonzalez Castro
- González
- González-Fernández
- Gopakumar
- Gorbovskoy
- Gorbunov
- Gorodetsky
- Gossan
- Gosselin
- Gouaty
- Grado
- Graef
- Granata
- Grant
- Gras
- Gray
- Greco
- Green
- Greiner
- Gress
- Gretarsson
- Groot
- Grote
- Gruen
- Gruendl
- Grunewald
- Gruning
- Guidi
- Guo
- Gupta
- Gupta
- Gushwa
- Gustafson
- Gustafson
- Gutierrez
- Haislip
- Halim
- Hall
- Hall
- Hamilton
- Hammond
- Haney
- Hanke
- Hanks
- Hanna
- Hanna
- Hannam
- Hannuksela
- Hanson
- Hardwick
- Harms
- Harry
- Harry
- Hart
- Hartley
- Hartley
- Haster
- Haughian
- Healy
- Heidmann
- Heintze
- Heitmann
- Hello
- Hemming
- Hendry
- Heng
- Hennig
- Heptonstall
- Herner
- Heurs
- Hild
- Hinderer
- Hjorth
- Hoak
- Hofman
- Holt
- Holz
- Honscheid
- Hopkins
- Horst
- Hosseinzadeh Griffin
- Hough
- Houston
- Howell
- Howell D. Andrew
- Hreibi
- Hu
- Huerta
- Huet
- Hughey
- Husa
- Huterer
- Huttner
- Huynh-Dinh
- Indik
- Inta
- Intini
- Irwin
- Isa
- Isac
- Isi
- Iyer
- Izumi
- Jacqmin
- Jain
- James
- Jani
- Jaranowski
- Jawahar
- Jeltema
- Jiménez-Forteza
- Johnson
- Johnson
- Jones
- Jones
- Jonker
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- Junker
- Kalaghatgi
- Kalogera
- Kamai
- Kandhasamy
- Kang
- Kanner
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- Karvinen
- Kasen
- Kasen
- Kasprzack
- Katolik
- Katsavounidis
- Katzman
- Kaufer
- Kawabe
- Keitel
- Kemball
- Kennedy
- Kent
- Kent
- Kessler
- Key
- Khalili
- Khan
- Khan
- Khan
- Khazanov
- Kijbunchoo
- Kilpatrick
- Kim
- Kim
- Kim
- Kim
- Kim
- Kim Chunglee
- Kimbrell
- King
- King
- Kinley-Hanlon
- Kirchhoff
- Kissel
- Kleybolte
- Klimenko
- Knowles
- Koch
- Koehlenbeck
- Koley
- Kondrashov
- Kontos
- Kornilov
- Korobko
- Korth
- Kouprianov
- Kowalska
- Kozak
- Krause
- Kringel
- Krishnan
- Kron
- Krämer
- Królak
- Kuehn
- Kuehn
- Kuhlmann
- Kumar
- Kumar
- Kumar
- Kuo
- Kuropatkin
- Kutynia
- Kwang
- Kéfélian
- Lackey
- Lahav
- Lai
- Landry
- Lang
- Lange
- Lantz
- Lanza
- Lartaux-Vollard
- Lasky
- Laxen
- Lazzarini
- Lazzaro
- Leaci
- Leavey
- Lee
- Lee
- Lee
- Lee
- Lee
- Lehmann
- Lenon
- Leonardi
- Leroy
- Letendre
- Levan
- Levato
- Levin
- Li
- Li
- Lima
- Lin
- Linker
- Lipunov
- Littenberg
- Liu
- Liu
- Lo
- Lockerbie
- London
- Lopes
- Lord
- Lorenzini
- Loriette
- Lormand
- Losurdo
- Lough
- Lourenço
- Lousto
- Lovelace
- Lumaca
- Lundgren
- Lyman
- Lynch
- Lück
- Ma
- Macas
- Macfoy
- Machenschalk
- MacInnis
- Macleod
- Madore
- Magaña Hernandez
- Magaña Zertuche
- Magaña-Sandoval
- Magee
- Maia
- Majorana
- Maksimovic
- Man
- Mandel
- Mandic
- Mangano
- Mansell
- Manske
- Mantovani
- March
- Marchesoni
- Margutti
- Marion
- Markakis
- Markosyan
- Markowitz
- Maros
- Marquina
- Marriner
- Marshall
- Martelli
- Martellini
- Martin
- Martin
- Martynov
- Mason
- Massera
- Masserot
- Massinger
- Masso-Reid
- Mastrogiovanni
- Matas
- Matheson
- Matichard
- Matone
- Mavalvala
- Mazumder
- McCarthy
- McClelland
- McCormick
- McCuller
- McCully Curtis
- McGuire
- McIntyre
- McIver
- McMahon
- McManus
- McNeill
- McRae
- McWilliams
- Meacher
- Meadors
- Medina
- Mehmet
- Meidam
- Mejuto-Villa
- Melatos
- Mendell
- Mercer
- Merilh
- Merzougui
- Meshkov
- Messenger
- Messick
- Metzdorff
- Metzger
- Meyers
- Miao
- Michel
- Middleton
- Mikhailov
- Milano
- Miller
- Miller
- Miller
- Miller
- Millhouse
- Milovich-Goff
- Milvang-Jensen
- Minazzoli
- Minenkov
- Ming
- Miquel
- Mishra
- Mitra
- Mitrofanov
- Mitselmakher
- Mittleman
- Moffa
- Moggi
- Mogushi
- Mohan
- Mohapatra
- Montani
- Moore
- Moraru
- Moreno
- Morriss
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- Mueller
- Muir
- Muir
- Mukherjee
- Mukherjee
- Mukherjee Arunava
- Mukund
- Mullavey
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- Muratore
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- Murray
- Muñiz
- Muñoz
- Márka
- Márka
- Napier
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- Naticchioni
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- Neilsen
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- Nelemans
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- Nguyen
- Nicholl
- Nichols
- Nielsen
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- Nocera
- Nolting
- Nord
- North
- Nugent
- Nuttall
- O'Brien
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- O'Reilly
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- Oberling
- Ogando
- Ogin
- Oh
- Oh
- Ohme
- Okada
- Oliver
- Oppermann
- Oram Richard J.
- Ormiston
- Ortega
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- Ossokine
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- Pace
- Page
- Page
- Pai
- Pai
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- Palamos
- Palashov
- Palazzi
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- Pan
- Pan Howard
- Pan Huang-Wei
- Pang
- Pang
- Pankow
- Pannarale
- Pant
- Paoletti
- Paoli
- Papa
- Parida
- Parker
- Pascucci
- Pasqualetti
- Passaquieti
- Passuello
- Patil
- Patricelli
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- Pearlstone
- Pedraza
- Pedurand
- Pekowsky
- Pele
- Penn
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- Perley
- Perreca
- Perri
- Pfeiffer
- Phelps
- Pian
- Piccinni
- Pichot
- Piergiovanni
- Pierro
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- Pinard
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- Piro
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- Plazas
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- Poggiani
- Popolizio
- Porter
- Post
- Powell
- Poznanski Dovi
- Prasad
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- Predoi
- Prestegard
- Prijatelj
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- Prodi
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- Puncken
- Punturo
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- Pürrer
- Qi
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- Quintero
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- Raab
- Rabeling
- Radkins
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- Raja
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- Read
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- Rei
- Reichart
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- Reitze
- Ren
- Rest
- Reyes
- Ricci
- Ricker
- Rieger
- Riles
- Rizzo
- Robertson
- Robie
- Robinet
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- Rolland
- Rollins
- Roma
- Romano
- Romano
- Romel
- Romer
- Romie
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- Rosińska
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- Rosswog
- Rowan
- Rowlinson
- Ruggi
- Rutins
- Ryan
- Rykoff
- Rüdiger
- Sachdev
- Sadecki
- Sadeghian
- Saffe
- Sakellariadou
- Sako
- Salconi
- Saleem
- Salemi
- Samajdar
- Sammut
- Sampson
- Sanchez
- Sanchez
- Sanchez
- Sanchis-Gual
- Sand
- Sandberg
- Sanders
- Sassolas
- Sathyaprakash
- Saulson
- Sauseda
- Sauter
- Savage
- Sawadsky
- Scarpine
- Schale
- Scheel
- Scheuer
- Schlegel
- Schmidt
- Schmidt
- Schnabel
- Schofield
- Schreiber
- Schubnell
- Schuette
- Schulte
- Schulze
- Schutz
- Schwalbe
- Schönbeck
- Scolnic
- Scott
- Scott
- Secco
- Seidel
- Sellers
- Sengupta
- Sentenac
- Sequino
- Sergeev
- Serra-Ricart
- Sevilla-Noarbe
- Shaddock
- Shaffer
- Shah
- Shahriar
- Shaner
- Shao
- Shapiro
- Shappee
- Shawhan
- Sheperd
- Shoemaker
- Shoemaker
- Siebert
- Siellez
- Siemens
- Sieniawska
- Sigg
- Silva
- Simon
- Singer
- Singh
- Singhal
- Sintes
- Slagmolen
- Smith
- Smith
- Smith
- Smith
- Smith
- Smith
- Soares-Santos
- Sobreira
- Somala
- Son
- Sonnenberg
- Sorazu
- Sorrentino
- Souradeep
- Spencer
- Srivastava
- Staats
- Staley
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- Steer
- Steinke
- Steinlechner
- Steinlechner
- Steinmeyer
- Stevenson
- Stone
- Stops
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- Strigin
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- Sturani
- Stuver
- Suchyta
- Summerscales
- Sun
- Sunil
- Suresh
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- Swinkels
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- Taylor
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- Tiwari
- Tiwari
- Tokmakov
- Toland
- Tonelli
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- Vikram
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- Vinciguerra
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- Vo
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- Vyatchanin
- Wade
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- Walker
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- Wang
- Wang
- Wang
- Wang
- Ward
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- Was
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- Watson
- Weaver
- Wei
- Weinert
- Weinstein
- Weiss
- Weller
- Wen
- Wessel
- Wester
- Westerweck
- Westphal
- Wette
- Weßels
- Whelan
- Whitcomb
- Whiting
- Whittle
- Wiersema
- Wilken
- Williams
- Williams
- Williams
- Williamson
- Willis
- Willke
- Wimmer
- Winkler
- Wipf
- Wittel
- Woan
- Woehler
- Wofford
- Wong
- Worden
- Wright
- Wu
- Wysocki
- Xiao
- Yamamoto
- Yancey
- Yang
- Yang
- Yanny
- Yap
- Yazback
- Yu Hang
- Yu Haocun
- Yurkov
- Yvert
- Zadrozny
- Zanolin
- Zelenova
- Zendri
- Zenteno
- Zevin
- Zhang
- Zhang
- Zhang
- Zhang
- Zhang
- Zhao
- Zhou
- Zhou
- Zhu
- Zhu
- Zimmerman
- Zucker
- Zweizig
- Publication venue
- Publication date
- 01/01/2017
- Field of study
On 17 August 2017, the Advanced LIGO 1 and Virgo 2 detectors observed the gravitational-wave event GW170817-a strong signal from the merger of a binary neutron-star system 3 . Less than two seconds after the merger, a γ-ray burst (GRB 170817A) was detected within a region of the sky consistent with the LIGO-Virgo-derived location of the gravitational-wave source 4-6 . This sky region was subsequently observed by optical astronomy facilities 7 , resulting in the identification 8-13 of an optical transient signal within about ten arcseconds of the galaxy NGC 4993. This detection of GW170817 in both gravitational waves and electromagnetic waves represents the first 'multi-messenger' astronomical observation. Such observations enable GW170817 to be used as a 'standard siren' 14-18 (meaning that the absolute distance to the source can be determined directly from the gravitational-wave measurements) to measure the Hubble constant. This quantity represents the local expansion rate of the Universe, sets the overall scale of the Universe and is of fundamental importance to cosmology. Here we report a measurement of the Hubble constant that combines the distance to the source inferred purely from the gravitational-wave signal with the recession velocity inferred from measurements of the redshift using the electromagnetic data. In contrast to previous measurements, ours does not require the use of a cosmic 'distance ladder' 19 : the gravitational-wave analysis can be used to estimate the luminosity distance out to cosmological scales directly, without the use of intermediate astronomical distance measurements. We determine the Hubble constant to be about 70 kilometres per second per megaparsec. This value is consistent with existing measurements 20,21 , while being completely independent of them. Additional standard siren measurements from future gravitationalwave sources will enable the Hubble constant to be constrained to high precision
Global patient outcomes after elective surgery: prospective cohort study in 27 low-, middle- and high-income countries.
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- Ab Rahman AS
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- Zonneveldt H
- Zou X
- Zoulamoglou M
- Zsisku L
- Publication venue
- 'Oxford University Press (OUP)'
- Publication date
- 01/01/2016
- Field of study
BACKGROUND: As global initiatives increase patient access to surgical treatments, there remains a need to understand the adverse effects of surgery and define appropriate levels of perioperative care. METHODS: We designed a prospective international 7-day cohort study of outcomes following elective adult inpatient surgery in 27 countries. The primary outcome was in-hospital complications. Secondary outcomes were death following a complication (failure to rescue) and death in hospital. Process measures were admission to critical care immediately after surgery or to treat a complication and duration of hospital stay. A single definition of critical care was used for all countries. RESULTS: A total of 474 hospitals in 19 high-, 7 middle- and 1 low-income country were included in the primary analysis. Data included 44 814 patients with a median hospital stay of 4 (range 2-7) days. A total of 7508 patients (16.8%) developed one or more postoperative complication and 207 died (0.5%). The overall mortality among patients who developed complications was 2.8%. Mortality following complications ranged from 2.4% for pulmonary embolism to 43.9% for cardiac arrest. A total of 4360 (9.7%) patients were admitted to a critical care unit as routine immediately after surgery, of whom 2198 (50.4%) developed a complication, with 105 (2.4%) deaths. A total of 1233 patients (16.4%) were admitted to a critical care unit to treat complications, with 119 (9.7%) deaths. Despite lower baseline risk, outcomes were similar in low- and middle-income compared with high-income countries. CONCLUSIONS: Poor patient outcomes are common after inpatient surgery. Global initiatives to increase access to surgical treatments should also address the need for safe perioperative care. STUDY REGISTRATION: ISRCTN5181700
Multi-messenger observations of a binary neutron star merger
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- Pankow C
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- Pant BC
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- Pekeur NW
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- Piccinni OJ
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- Pierro V
- Pignata G
- Pike S
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- Piran T
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- Piranomonte S
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- Piro AL
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- Publication date
- 01/01/2017
- Field of study
On 2017 August 17 a binary neutron star coalescence candidate (later designated GW170817) with merger time 12:41:04 UTC was observed through gravitational waves by the Advanced LIGO and Advanced Virgo detectors. The Fermi Gamma-ray Burst Monitor independently detected a gamma-ray burst (GRB 170817A) with a time delay of ~1.7 s with respect to the merger time. From the gravitational-wave signal, the source was initially localized to a sky region of 31 deg2 at a luminosity distance of 40+8-8 Mpc and with component masses consistent with neutron stars. The component masses were later measured to be in the range 0.86 to 2.26 Mo. An extensive observing campaign was launched across the electromagnetic spectrum leading to the discovery of a bright optical transient (SSS17a, now with the IAU identification of AT 2017gfo) in NGC 4993 (at ~40 Mpc) less than 11 hours after the merger by the One- Meter, Two Hemisphere (1M2H) team using the 1 m Swope Telescope. The optical transient was independently detected by multiple teams within an hour. Subsequent observations targeted the object and its environment. Early ultraviolet observations revealed a blue transient that faded within 48 hours. Optical and infrared observations showed a redward evolution over ~10 days. Following early non-detections, X-ray and radio emission were discovered at the transient’s position ~9 and ~16 days, respectively, after the merger. Both the X-ray and radio emission likely arise from a physical process that is distinct from the one that generates the UV/optical/near-infrared emission. No ultra-high-energy gamma-rays and no neutrino candidates consistent with the source were found in follow-up searches. These observations support the hypothesis that GW170817 was produced by the merger of two neutron stars in NGC4993 followed by a short gamma-ray burst (GRB 170817A) and a kilonova/macronova powered by the radioactive decay of r-process nuclei synthesized in the ejecta
Comparative effectiveness and safety of non-vitamin K antagonists for atrial fibrillation in clinical practice: GLORIA-AF Registry
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- Publication venue
- Publication date
- 01/01/2022
- Field of study
Background and purpose: Prospectively collected data comparing the safety and effectiveness of individual non-vitamin K antagonists (NOACs) are lacking. Our objective was to directly compare the effectiveness and safety of NOACs in patients with newly diagnosed atrial fibrillation (AF). Methods: In GLORIA-AF, a large, prospective, global registry program, consecutive patients with newly diagnosed AF were followed for 3 years. The comparative analyses for (1) dabigatran vs rivaroxaban or apixaban and (2) rivaroxaban vs apixaban were performed on propensity score (PS)-matched patient sets. Proportional hazards regression was used to estimate hazard ratios (HRs) for outcomes of interest. Results: The GLORIA-AF Phase III registry enrolled 21,300 patients between January 2014 and December 2016. Of these, 3839 were prescribed dabigatran, 4015 rivaroxaban and 4505 apixaban, with median ages of 71.0, 71.0, and 73.0 years, respectively. In the PS-matched set, the adjusted HRs and 95% confidence intervals (CIs) for dabigatran vs rivaroxaban were, for stroke: 1.27 (0.79–2.03), major bleeding 0.59 (0.40–0.88), myocardial infarction 0.68 (0.40–1.16), and all-cause death 0.86 (0.67–1.10). For the comparison of dabigatran vs apixaban, in the PS-matched set, the adjusted HRs were, for stroke 1.16 (0.76–1.78), myocardial infarction 0.84 (0.48–1.46), major bleeding 0.98 (0.63–1.52) and all-cause death 1.01 (0.79–1.29). For the comparison of rivaroxaban vs apixaban, in the PS-matched set, the adjusted HRs were, for stroke 0.78 (0.52–1.19), myocardial infarction 0.96 (0.63–1.45), major bleeding 1.54 (1.14–2.08), and all-cause death 0.97 (0.80–1.19). Conclusions: Patients treated with dabigatran had a 41% lower risk of major bleeding compared with rivaroxaban, but similar risks of stroke, MI, and death. Relative to apixaban, patients treated with dabigatran had similar risks of stroke, major bleeding, MI, and death. Rivaroxaban relative to apixaban had increased risk for major bleeding, but similar risks for stroke, MI, and death. Registration: URL: https://www.clinicaltrials.gov. Unique identifiers: NCT01468701, NCT01671007. Date of registration: September 2013
Comparative effectiveness and safety of non-vitamin K antagonists for atrial fibrillation in clinical practice: GLORIA-AF Registry
- Author
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- Publication venue
- 'Springer Science and Business Media LLC'
- Publication date
- 01/01/2022
- Field of study
Anticoagulant selection in relation to the SAMe-TT2R2 score in patients with atrial fibrillation. the GLORIA-AF registry
- Author
- Abban D. W.
- Abdul N.
- Abud A. M.
- Adams F.
- Addala S.
- Adragao P.
- Ageno W.
- Aggarwal R.
- Agosti S.
- Agostoni P.
- Aguilar F.
- Aguinaga L.
- Ahmed J.
- Aiello A.
- Ainsworth P.
- Aiub J. R.
- Al-Dallow R.
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- Aldrete Velasco J. A.
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- Andrawis N.
- Angela Koh S. M.
- Anna omaszuk-Kazberuk
- Annoni G.
- Ansalone G.
- Ariani M. K.
- Arias J. C.
- Armero S.
- Arora C.
- Asensi J. O.
- Aslam M. S.
- Asselman M.
- Audouin P.
- Augenbraun C.
- Aydin S.
- Ayryanova I.
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- Badings E.
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- Wang M.
- Wang N.
- Wang T.
- Wang X.
- Warner A. L.
- Watanabe K.
- Wei J.
- Weimar C.
- Weiner S.
- Weinrich R.
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- Wylie J. J.
- Xu X.
- Xu Y.
- Yamanoue H.
- Yamashita T.
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- Yao J.
- Yeh K. -H.
- Yin W. H.
- Yotov Y.
- Zahn R.
- Zanetti F. L.
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- Zeuthen E. L.
- Zhang D.
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- Zhao Z.
- Zheng Y.
- Zhou J.
- Zimmermann S.
- Zini A.
- Zizzo S.
- Zong W.
- Zukerman L. S.
- Publication venue
- Hellenic Society of Cardiology. Publishing services by Elsevier B.V.
- Publication date
- 01/01/2021
- Field of study
Aim: The SAMe-TT2R2 score helps identify patients with atrial fibrillation (AF) likely to have poor anticoagulation control during anticoagulation with vitamin K antagonists (VKA) and those with scores >2 might be better managed with a target-specific oral anticoagulant (NOAC). We hypothesized that in clinical practice, VKAs may be prescribed less frequently to patients with AF and SAMe-TT2R2 scores >2 than to patients with lower scores. Methods and results: We analyzed the Phase III dataset of the Global Registry on Long-Term Oral Antithrombotic Treatment in Patients with Atrial Fibrillation (GLORIA-AF), a large, global, prospective global registry of patients with newly diagnosed AF and ≥1 stroke risk factor. We compared baseline clinical characteristics and antithrombotic prescriptions to determine the probability of the VKA prescription among anticoagulated patients with the baseline SAMe-TT2R2 score >2 and ≤ 2. Among 17,465 anticoagulated patients with AF, 4,828 (27.6%) patients were prescribed VKA and 12,637 (72.4%) patients an NOAC: 11,884 (68.0%) patients had SAMe-TT2R2 scores 0-2 and 5,581 (32.0%) patients had scores >2. The proportion of patients prescribed VKA was 28.0% among patients with SAMe-TT2R2 scores >2 and 27.5% in those with scores ≤2. Conclusions: The lack of a clear association between the SAMe-TT2R2 score and anticoagulant selection may be attributed to the relative efficacy and safety profiles between NOACs and VKAs as well as to the absence of trial evidence that an SAMe-TT2R2-guided strategy for the selection of the type of anticoagulation in NVAF patients has an impact on clinical outcomes of efficacy and safety. The latter hypothesis is currently being tested in a randomized controlled trial. Clinical trial registration: URL: https://www.clinicaltrials.gov//Unique identifier: NCT01937377, NCT01468701, and NCT01671007
A control oriented strategy of disruption prediction to avoid the configuration collapse of tokamak reactors
- Author
- Abid N.
- Abraham K.
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- Adabonyan O.
- Adrich P.
- Afanasev V.
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- Alderson-Martin M.
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- Alekseev A. G.
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- Zagorski R.
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- Zwingmann W.
- Zychor I.
- Łaszyńska E.
- Publication venue
- country:GB
- Publication date
- 01/01/2024
- Field of study
The objective of thermonuclear fusion consists of producing electricity from the coalescence of light nuclei in high temperature plasmas. The most promising route to fusion envisages the confinement of such plasmas with magnetic fields, whose most studied configuration is the tokamak. Disruptions are catastrophic collapses affecting all tokamak devices and one of the main potential showstoppers on the route to a commercial reactor. In this work we report how, deploying innovative analysis methods on thousands of JET experiments covering the isotopic compositions from hydrogen to full tritium and including the major D-T campaign, the nature of the various forms of collapse is investigated in all phases of the discharges. An original approach to proximity detection has been developed, which allows determining both the probability of and the time interval remaining before an incoming disruption, with adaptive, from scratch, real time compatible techniques. The results indicate that physics based prediction and control tools can be developed, to deploy realistic strategies of disruption avoidance and prevention, meeting the requirements of the next generation of devices.Confining plasma and managing disruptions in tokamak devices is a challenge. Here the authors demonstrate a method predicting and possibly preventing disruptions and macroscopic instabilities in tokamak plasma using data from JET
Overview of JET results for optimising ITER operation
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- Abid N.
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- Publication venue
- International Atomic Energy Agency
- Publication date
- 27/07/2022
- Field of study
The JET 2019–2020 scientific and technological programme exploited the results of years of concerted scientific and engineering work, including the ITER-like wall (ILW: Be wall and W divertor) installed in 2010, improved diagnostic capabilities now fully available, a major neutral beam injection upgrade providing record power in 2019–2020, and tested the technical and procedural preparation for safe operation with tritium. Research along three complementary axes yielded a wealth of new results. Firstly, the JET plasma programme delivered scenarios suitable for high fusion power and alpha particle (α) physics in the coming D–T campaign (DTE2), with record sustained neutron rates, as well as plasmas for clarifying the impact of isotope mass on plasma core, edge and plasma-wall interactions, and for ITER pre-fusion power operation. The efficacy of the newly installed shattered pellet injector for mitigating disruption forces and runaway electrons was demonstrated. Secondly, research on the consequences of long-term exposure to JET-ILW plasma was completed, with emphasis on wall damage and fuel retention, and with analyses of wall materials and dust particles that will help validate assumptions and codes for design and operation of ITER and DEMO. Thirdly, the nuclear technology programme aiming to deliver maximum technological return from operations in D, T and D–T benefited from the highest D–D neutron yield in years, securing results for validating radiation transport and activation codes, and nuclear data for ITER
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