157 research outputs found
Natural killer cells attenuate cytomegalovirus-induced hearing loss in mice
- Author
- A Honeycutt
- AA Scalzo
- AA Scalzo
- AH Park
- AH Park
- AH Park
- Albert H. Park
- Ali A. Almishaal
- Anne Zhang
- B Polic
- BA Parikh
- CA Biron
- CC Morton
- Elaine Hillas
- FR Pass
- H Arase
- HR Smith
- HT Reyburn
- I Bubic
- I Kosugi
- JF Bukowski
- Jun Yang
- K Ikuta
- KB Fowler
- KB Fowler
- KB Fowler
- KR Stratton
- L Hao
- L Song
- Liting Chen
- Matthew A. Firpo
- ML Engman
- N Terrazzini
- PD Mathur
- Pranav D. Mathur
- R Gazit
- RD Bradford
- Robert F. Kalejta
- S Jonjic
- SD Grosse
- SJ Schachtele
- TP Cheng
- TP Cheng
- V Bekiaris
- V Prod'homme
- Wayne M. Yokoyama
- X Li
- Y Gan
- Y Wang
- Yong Wang
- Publication venue
- Digital Commons@Becker
- Publication date
- 01/01/2017
- Field of study
<div><p>Congenital cytomegalovirus (CMV) infection is the most common non-hereditary cause of sensorineural hearing loss (SNHL) yet the mechanisms of hearing loss remain obscure. Natural Killer (NK) cells play a critical role in regulating murine CMV infection via NK cell recognition of the Ly49H cell surface receptor of the viral-encoded m157 ligand expressed at the infected cell surface. This Ly49H NK receptor/m157 ligand interaction has been found to mediate host resistance to CMV in the spleen, and lung, but is much less effective in the liver, so it is not known if this interaction is important in the context of SNHL. Using a murine model for CMV-induced labyrinthitis, we have demonstrated that the Ly49H/m157 interaction mediates host resistance in the temporal bone. BALB/c mice, which lack functional Ly49H, inoculated with mCMV at post-natal day 3 developed profound hearing loss and significant outer hair cell loss by 28 days of life. In contrast, C57BL/6 mice, competent for the Ly49H/m157 interaction, had minimal hearing loss and attenuated outer hair cell loss with the same mCMV dose. Administration of Ly49H blocking antibody or inoculation with a mCMV viral strain deleted for the m157 gene rendered the previously resistant C57BL/6 mouse strain susceptible to hearing loss to a similar extent as the BALB/c mouse strain indicating a direct role of the Ly49H/m157 interaction in mCMV-dependent hearing loss. Additionally, NK cell recruitment to sites of infection was evident in the temporal bone of inoculated susceptible mouse strains. These results demonstrate participation of NK cells in protection from CMV-induced labyrinthitis and SNHL in mice.</p></div
Peroxiredoxin 3 Is a Redox-Dependent Target of Thiostrepton in Malignant Mesothelioma Cells
- Author
- A Basu
- A Shukla
- AG Cox
- AG Cox
- AG Cox
- AJ Moore
- Arti Shukla
- AS Tsao
- B Pandit
- B Pandit
- B Qiao
- BM Burgering
- BN Perry
- Brian Cunniff
- Brooke Mossman
- CE Wenner
- D Trachootham
- DF Calvisi
- DS Widmer
- E Gemenetzidis
- EL Greer
- FR Reale
- GA Gusarova
- GT Hanson
- GT Wondrak
- Harvey Pass
- HI Pass
- HJ Park
- HJ Park
- J Laoukili
- J Laoukili
- J Laoukili
- J Millour
- J Nordberg
- J Zielonka
- Jack Arbiser
- JE Klaunig
- JM Kwok
- JM Kwok
- JR Knight
- JR Lohman
- K Kahlos
- K Kim
- K Kundu
- Kelsey Preston
- Kheng Newick
- KK Brown
- KK Ho
- L Fried
- L Serrander
- M Halasi
- ML Chiu
- ML Major
- Nicholas Heintz
- NS Hegde
- Paul Held
- PJ Chua
- PM Burch
- R Docampo
- R Reliene
- RA Stahel
- RB Hamanaka
- RE Francis
- RY Ma
- S Qiao
- SK Radhakrishnan
- SL Bausch
- SS Myatt
- Sumitra Deb
- TJ Phalen
- UB McGovern
- UG Bhat
- UG Bhat
- VL Kinnula
- W Korver
- W Korver
- WC Burhans
- WH Koppenol
- X Sun
- X Zhang
- YM Janssen-Heininger
- Z Yuan
- Publication venue
- Public Library of Science
- Publication date
- 25/06/2012
- Field of study
Thiostrepton (TS) is a thiazole antibiotic that inhibits expression of FOXM1, an oncogenic transcription factor required for cell cycle progression and resistance to oncogene-induced oxidative stress. The mechanism of action of TS is unclear and strategies that enhance TS activity will improve its therapeutic potential. Analysis of human tumor specimens showed FOXM1 is broadly expressed in malignant mesothelioma (MM), an intractable tumor associated with asbestos exposure. The mechanism of action of TS was investigated in a cell culture model of human MM. As for other tumor cell types, TS inhibited expression of FOXM1 in MM cells in a dose-dependent manner. Suppression of FOXM1 expression and coincidental activation of ERK1/2 by TS were abrogated by pre-incubation of cells with the antioxidant N-acetyl-L-cysteine (NAC), indicating its mechanism of action in MM cells is redox-dependent. Examination of the mitochondrial thioredoxin reductase 2 (TR2)-thioredoxin 2 (TRX2)-peroxiredoxin 3 (PRX3) antioxidant network revealed that TS modifies the electrophoretic mobility of PRX3. Incubation of recombinant human PRX3 with TS in vitro also resulted in PRX3 with altered electrophoretic mobility. The cellular and recombinant species of modified PRX3 were resistant to dithiothreitol and SDS and suppressed by NAC, indicating that TS covalently adducts cysteine residues in PRX3. Reduction of endogenous mitochondrial TRX2 levels by the cationic triphenylmethane gentian violet (GV) promoted modification of PRX3 by TS and significantly enhanced its cytotoxic activity. Our results indicate TS covalently adducts PRX3, thereby disabling a major mitochondrial antioxidant network that counters chronic mitochondrial oxidative stress. Redox-active compounds like GV that modify the TR2/TRX2 network may significantly enhance the efficacy of TS, thereby providing a combinatorial approach for exploiting redox-dependent perturbations in mitochondrial function as a therapeutic approach in mesothelioma
Seropositivity to Cytomegalovirus, Inflammation, All-Cause and Cardiovascular Disease-Related Mortality in the United States
- Author
- A Bajpai
- A Wikby
- A Wikby
- A Wikby
- Adrian Hernandez
- AE Aiello
- AE Aiello
- AG Bertoni
- Allison E. Aiello
- AM Simanek
- Amanda M. Simanek
- Ambarish Dutta
- B Galobardes
- B Reinhardt
- C Bason
- C Lunardi
- D Chan
- David Melzer
- E Guetta
- E Hsich
- EC Costalonga
- ES Mocarski Jr
- ET Roberts
- EW Gunter
- FA Colugnati
- FJ Nieto
- FR Stassen
- FR Stassen
- G Pawelec
- G Rose
- GC Wang
- GD Almeida
- GK Singh
- Graham Pawelec
- H Kuper
- HN Schmaltz
- J Olsson
- J Zhu
- JA Tice
- JB Dowd
- JB Muhlestein
- Jennifer Beam Dowd
- JL Melnick
- JL Melnick
- K Berencsi
- K Prasad
- K Rask
- KJ Rothman
- KS Krabbe
- L Arcavi
- L Harkins
- LJ Albert
- LP He
- M Samanta
- M Smieja
- MA Mendall
- MC van Dam-Mieras
- MG Hendrix
- N Sathiakumar
- PD Smith
- PD Sorlie
- PM Ridker
- PM Ridker
- RF Pass
- RJ ooney
- S Blankenberg
- S Chidrawar
- SA Staras
- SE Epstein
- SE Epstein
- SE Epstein
- SG Hansen
- SR Hadrup
- T Knosel
- TA Lee
- TB Harris
- TE Strandberg
- VL Shavers
- W Britt
- WR Lin
- Publication venue
- Public Library of Science
- Publication date
- 01/02/2011
- Field of study
Studies have suggested that CMV infection may influence cardiovascular disease (CVD) risk and mortality. However, there have been no large-scale examinations of these relationships among demographically diverse populations. The inflammatory marker C-reactive protein (CRP) is also linked with CVD outcomes and mortality and may play an important role in the pathway between CMV and mortality. We utilized a U.S. nationally representative study to examine whether CMV infection is associated with all-cause and CVD-related mortality. We also assessed whether CRP level mediated or modified these relationships., 2006 (N = 14153) in the National Health and Nutrition Examination Survey (NHANES) III (1988–1994). Cox proportional hazard models were used to estimate hazard ratios (HR) and 95% confidence intervals (CI) for all-cause and CVD-related mortality by CMV serostatus. After adjusting for multiple confounders, CMV seropositivity remained statistically significantly associated with all-cause mortality (HR 1.19, 95% CI: 1.01, 1.41). The association between CMV and CVD-related mortality did not achieve statistical significance after confounder adjustment. CRP did not mediate these associations. However, CMV seropositive individuals with high CRP levels showed a 30.1% higher risk for all-cause mortality and 29.5% higher risk for CVD-related mortality compared to CMV seropositive individuals with low CRP levels.CMV was associated with a significant increased risk for all-cause mortality and CMV seropositive subjects who also had high CRP levels were at substantially higher risk for both for all-cause and CVD-related mortality than subjects with low CRP levels. Future work should target the mechanisms by which CMV infection and low-level inflammation interact to yield significant impact on mortality
Global patient outcomes after elective surgery: prospective cohort study in 27 low-, middle- and high-income countries.
- Author
- Ab Majid MA
- Ab Rahman AS
- Ab Rahman R
- Abayasinghe C
- Abbott T
- Abdullah NH
- Abdur-Rahman L
- Abeloos J
- Abernethy C
- Abidin UN
- Abrunhosa A
- Absar M
- Adam S
- Adams D
- Adams G
- Adamson M
- Adekola O
- Adelaja Y
- Ademola A
- Adenekan A
- Adenike O
- Adeolu AA
- Adetoye A
- Adewale B
- Adigun T
- Adolfsson A
- Aflori L
- Africander C
- Afshari A
- Agarwal V
- Agodirin O
- Aguero Vera M
- Aguzzoli C
- Ahmad A
- Ahmad N
- Ahmad T
- Ahmad T
- Ahmad Y
- Ahmed A
- Ahmed J
- Ai Y
- Aignatoaie M
- Aimoniotou-Georgiou E
- Akanmu O
- Akerman N
- Akinwale M
- Akring I
- Al 'Amri K
- Al Anizi M
- Al hussaini S
- Al-Soudaine Y
- Aladin H
- Alagbe-Briggs O
- Alaman Laguarda G
- Albaj S
- Alcock D
- Alcock L
- Aldecoa C
- Aldecoa C
- Aleixo FB
- Alexander H
- Alexander M
- Alexander-Sefre F
- Alherz F
- Ali H
- Ali M
- Ali S
- Alias A
- Alias AH
- Alias RLR
- Alit MA
- Allen S
- Allen SJ
- Allison J
- Alloj C
- Allorto NL
- Allsop J
- Almeida W
- Alonso E
- Alphonsus C
- Alvares D
- Alves MJ
- Amador JCB
- Ameer Y
- Amendola CP
- Ami N
- Amstrup-Hansen L
- Anagnou A
- Andersen C
- Anderson C
- Anderson C
- Anderson F
- Anderson P
- Andreadaki E
- Andreou A
- Andreou P
- Andrew A
- Andrews E
- Angermair S
- Angus K
- Anillo V
- Antal O
- Antill P
- Antoniadou E
- Antonina W
- Apagaki E
- Apostolou K
- Applewhaite C
- Aquino LPG
- Ar P
- Arawwawala D
- Ardern D
- Argue R
- Arkalaki E
- Armaganidis A
- Armstrong J
- Armstrong R
- Arnaoutoglou C
- Arnaoutoglou E
- Arnold G
- Arrandale L
- Arrich J
- Arrigo M
- Arshad H
- Arshad MA
- Arumugam S
- Arustei M
- Arvaniti K
- Arya A
- Arya S
- Asimakos A
- Asudo F
- Athanasakis E
- Atiku M
- Attrill E
- Attwood C
- Auer P
- Avidan M
- Avila Sanchez FJ
- Avila EJD
- Avis J
- Awad H
- Axioti E
- Ayyaz H
- Azam UAA
- Azambuja P
- Azevedo C
- Aziz FZ
- Baas P
- Baghirzada L
- Bai H-P
- Bai Y
- Baillie S
- Baines D
- Baio TH
- Bairaktari A
- Baker G
- Baker K-A
- Baker P
- Balain B
- Balaji P
- Balajonda N
- Balanescu A
- Balasubramaniam M
- Baldisserotto S
- Baldwin J
- Baldwin M
- Balfoussia D
- Bali C
- Bandeira ME
- Banerjee R
- Bankewitz C
- Banner-Goodspeed V
- Bao Q
- Barcraft-Barnes H
- Barneto L
- Barnett A
- Baroselli A
- Barraclough J
- Barras J-P
- Barrett S
- Barrett WJ
- Basanth S
- Batchelor N
- Bateman B
- Bates A
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- Batista HD
- Bauchmuller K
- Bauer M
- Baumgarten G
- Baxter L
- Beaton C
- Beattie S
- Beavis V
- Bechan S
- Bejia T
- Belciu I
- Belda MT
- Bell G
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- Bellandi M
- Bello J
- Beloeil H
- Belskiy V
- Ben-Menachem E
- Benavent P
- Benevento A
- Bengeri S
- Bennett C
- Bennett M
- Bennett R
- Bennett V
- Bentley C
- Beretta L
- Berg A
- Bergin C
- Bernard A
- Berntsen E
- Bertram W
- Bester D
- Bester M
- Bettega F
- Bettinelli A
- Bhardwaj N
- Bhatia K
- Bhula C
- Bi Y
- Biais M
- Biccard BM
- Bidd H
- Bidgoli J
- Biffen A
- Bignami E
- Bilolikar A
- Bin Mustapha MT
- Birch J
- Bishop DG
- Biyase T
- Bizios C
- Blackwell C
- Blackwood D
- Blaj M
- Blakemore SP
- Bland M
- Blunt M
- Blyth K
- Bocchino S
- Bodansky D
- Bodger P
- Boer C
- Boereboom C
- Boggiano V
- Bogner G
- Bolaji B
- Bolton D
- Boone M
- Boschi L
- Boshier P
- Botes M
- Botis I
- Bottini C
- Bottrill F
- Bouchez S
- Boulton K
- Bouris V
- Bourner L
- Boutsikos G
- Bouwman A
- Bouwman RA
- Bowrey S
- Boxall L
- Boyd C
- Bradburn M
- Bradley J
- Branagan G
- Branco T
- Brand B
- Brandsborg B
- Breitenstein S
- Brennan A
- Brennan E
- Brenner L
- Brincat M
- Briscoe R
- Bristogiannis S
- Brooke J
- Brookes J
- Brookes M
- Brooks C
- Broomby R
- Brotto AF
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- Brunete T
- Brunswicker A
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- Buckley S
- Buerkle C
- Buhre W
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- Builu PM
- Buise M
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- Burns K
- Burrows L
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- Burston B
- Burtenshaw A
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- Cabezuelo E
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- Cawthorn L
- Cernea DD
- Chaddock M
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- Chan HMH
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- Chan P
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- Chan YL
- Chande S
- Chandler B
- Chandra S
- Chandrasekharan S
- Chang YH
- Chaniotaki F
- Charitos E
- Charlalampidoy A
- Charles R
- Chatterjee D
- Chatterjee J
- Chatzimichali CA
- Chau S
- Chazova E
- Cheah C
- Cheah S
- Cheeseman M
- Cheing Y
- Chen C
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- Chen F
- Chen H
- Chen J
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- Chen L
- Chen L
- Chen L-L
- Chen P
- Chen Q
- Chen R
- Chen S
- Chen S
- Chen S
- Chen Y
- Chen Y
- Chen Y
- Chen Y
- Chen Z
- Cheng B
- Cheng KH
- Cheng Z
- Cheong E
- Cherian R
- Cherrett V
- Chetty RR
- Chew M
- Chhabra A
- Chicken D-W
- Chilinciuc I
- Chin II
- Chirkut S
- Chisbert Cuenca V
- Chlorou D
- Choi H-MD
- Choi S
- Chow L
- Christian R
- Christiansen IC
- Christmas N
- Christodoulidis G
- Christodoulopoulou T
- Christofaki M
- Christoforidis D
- Chronis C
- Chu HM
- Chu S
- Chua P
- Chukkambotla S
- Chung CKE
- Cifra E
- Ciobanu C
- Ciobotaru OR
- Cirstea E
- Clark R
- Clarkson A
- Clarkson R
- Claxton A
- Clemmons K
- Cloro LM
- Clyde A
- Cobzaru I
- Codita A
- Colangelo A
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- Comptaer N
- Conde C
- Conradie A
- Constantin K
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- Cooper L
- Cooper L
- Cooper M
- Cooper R
- Cooper S
- Copaciu E
- Cope J
- Copetti E
- Copley E
- Copotoiu SM
- Coppens M
- Corneci D
- Cornell J
- Cornish J
- Correia da Silva RFM
- Corti D
- Costanzo E
- Costelloe H
- Cotter R
- Cotterell S
- Cotterill D
- Coughlan E
- Coulter I
- Coulter S
- Coutinho F
- Cowton A
- Cox H
- Cozar OI
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- Craven R
- Craw N
- Craw S
- Creary T
- Cripps H
- Critchley R
- Cronje L
- Cruickshank R
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- Cueva A
- Cunha P
- Curley G
- Currow H
- Czepanski C
- Czeslick E
- D'Andrea R
- da Costa Fischer BF
- Dafnios N
- Dai H
- Dai Q
- Dai Q
- Dai SY
- Daikou P
- Dalamagka M
- Dalampini E
- Dali-Kemmery L
- Dalton E
- Damant R
- Daniel C
- Daniel GD
- Daniel H
- Daniel H
- Daniel S
- Dankl D
- Darko J
- Darwish S
- Das S
- Dasrath A
- Datson A
- Daubeny T
- Daugaard M
- Davari M
- Dave T
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- Davies K
- Davies L
- Davies Z
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- Davis F
- Davis S
- Daya B
- De Andres Ibanez JA
- de Araujo DM
- De Baerdemaeker L
- de Beer J
- de Boer HD
- De Bruyne A
- de Campos Ferreira MF
- de Fretes J
- de Gasperi J
- De Hert S
- De Jongh K
- De Kegel D
- De Meyer JN
- De Oliveira MC
- de Rudnicki S
- de Swardt M
- de Vasconcellos K
- de Villiers M
- de Wet J
- Deacon M
- Deblaere I
- Dedemadi G
- Deen T
- Deepak S
- Deighton K
- Deja M
- Delgado Garcia DR
- Delgado Navarro C
- Della Rocca G
- Dempsey G
- Dempster A
- den Hoedt M
- Denham S
- Dent K
- Dermitzaki D
- Desbordes J
- Despotidis V
- Diaconescu C
- Dias F
- Dias S
- Dickson J
- Ditai J
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- do Nascimento Junior P
- Dobson G
- Docherty P
- Dodiyi-Manuel A
- Dodsworth K
- Dolan R
- Dong B
- Donohue R
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- Douglas J
- Doumos R
- Downes C
- Doyle D
- Dragnea D
- Dragoescu NA
- Drake M
- Drimala M
- Drinkwater Z
- Drummond L
- Du F
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- Du X
- Duarte C
- Dube NZ
- Duca A
- Dudgeon L
- Dudson R
- Duenser M
- Dumitrascu CO
- Dumitrescu A
- Dunay A
- Dunk N
- Durant E
- Durodola A
- Dursin AN
- Durst A
- Duttchen K
- Dutu M
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- Dylst D
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- Dzulkipli N
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- Edwards J
- Edwards M
- Edwards M
- Efthymiadi A
- Egan T
- Eggleston C
- Eichwalder A
- Eikman J
- Ekelund K
- el Manser D
- El-Sayed A
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- Elgasim M
- Ellis J
- Ellis K
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- Endersby S
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- Epodoi J
- Eskildsen KZ
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- Everingham K
- Ewe R
- Ezekiel E
- Ezike H
- Fagerlund MJ
- Faina L
- Falk E
- Fan H
- Fan L
- Fan Y
- Fanfani LC
- Faponle F
- Faria e Maia D
- Faria F
- Farid N
- Farina Z
- Farrell H
- Farrow M
- Fasina O
- Fatungase OM
- Faulds M
- Fei Y
- Fellinger P
- Feng Y
- Fengas L
- Fergey L
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- Fernandez S
- Ferrando C
- Filipescu D
- Filippopoulos A
- Finch A
- Fiorentza K
- Fischbach N
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- Fleisher LA
- Flores Risco S
- Flores AAA
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- Foley J
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- Foord D
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- Foot J
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- Forsans E
- Forstner K
- Foster R
- Foubert L
- Fouracres A
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- Fowler C
- Fraga JM
- Fragandreas G
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- Franklin J
- Franks R
- Frantzeskos G
- Freeman D
- Freeman V
- Freethy A
- Freitas K
- Freschini A
- Freschini D
- Frewer N
- Fritsch G
- Frost V
- Fu K
- Fu S
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- Fuentes I
- Fulton G
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- Furrer M
- Furtado Paiva AA
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- Gardikou VV
- Gardiner M
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- Garg S
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- Gastaldi C
- Gatke MR
- Gatta A
- Gaudin C
- Gavril L
- Gbolahan O
- Ge X
- Geddoa B
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- Geldenhuys J
- Geng W
- Georgakakis G
- George R
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- Georgopoulou E
- Gercek Y
- Germann R
- Geromarkaki E
- Ghafar FNIA
- Ghignone F
- Ghosh A
- Ghushe N
- Giancarlo L
- Giannaki C
- Gibson-Lapsley H
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- Giles J
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- Gille J
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- Gilmour F
- Gkini K-P
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- Glasgow E
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- Granum SN
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- Greaves R
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- 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
Pan-cancer analysis of whole genomes
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- The ICGC/TCGA Pan-Cancer Analysis of Whole Genomes Consortium View Correspondence (jump link)
- Thiessen
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- Zhang
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- Zhang
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- Zhang H. b
- Zhao
- Zheng
- Zhou
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- Zhu
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- zi zj
- zm Jayaseelan
- Zou
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- Ó. A. th
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- Publication venue
- Publication date
- 11/12/2019
- Field of study
Cancer is driven by genetic change, and the advent of massively parallel sequencing has enabled systematic documentation of this variation at the whole-genome scale(1-3). Here we report the integrative analysis of 2,658 whole-cancer genomes and their matching normal tissues across 38 tumour types from the Pan-Cancer Analysis of Whole Genomes (PCAWG) Consortium of the International Cancer Genome Consortium (ICGC) and The Cancer Genome Atlas (TCGA). We describe the generation of the PCAWG resource, facilitated by international data sharing using compute clouds. On average, cancer genomes contained 4-5 driver mutations when combining coding and non-coding genomic elements; however, in around 5% of cases no drivers were identified, suggesting that cancer driver discovery is not yet complete. Chromothripsis, in which many clustered structural variants arise in a single catastrophic event, is frequently an early event in tumour evolution; in acral melanoma, for example, these events precede most somatic point mutations and affect several cancer-associated genes simultaneously. Cancers with abnormal telomere maintenance often originate from tissues with low replicative activity and show several mechanisms of preventing telomere attrition to critical levels. Common and rare germline variants affect patterns of somatic mutation, including point mutations, structural variants and somatic retrotransposition. A collection of papers from the PCAWG Consortium describes non-coding mutations that drive cancer beyond those in the TERT promoter(4); identifies new signatures of mutational processes that cause base substitutions, small insertions and deletions and structural variation(5,6); analyses timings and patterns of tumour evolution(7); describes the diverse transcriptional consequences of somatic mutation on splicing, expression levels, fusion genes and promoter activity(8,9); and evaluates a range of more-specialized features of cancer genomes(8,10-18).Peer reviewe
Measurement of the inclusive and differential Higgs boson production cross sections in the decay mode to a pair of τ Leptons in pp collisions at sqrt[s]=13 TeV
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- Würthwein F
- Xiang Y
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- Yagil A
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- Yao Y
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- Yi K
- Yigitbasi E
- Yohay R
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- Yuldashev BS
- Yumiceva F
- Yusli MN
- Zabi A
- Zacharopoulou A
- Zahid S
- Zaleski S
- Zalewski P
- Zanetti M
- Zarubin A
- Zarucki M
- Zecchinelli AG
- Zeinali M
- Zeuner WD
- Zghiche A
- Zhang F
- Zhang H
- Zhang J
- Zhang L
- Zhang W
- Zhang Y
- Zhang Y
- Zhang Z
- Zhao J
- Zhizhin I
- Zhokin A
- Zhu DH
- Zhu RY
- Ziemons T
- Zoi I
- Zolkapli Z
- Zorbakir IS
- Zorbilmez C
- Zotto P
- Zotz A
- Zou D
- Zou R
- Zucchetta A
- Zumerle G
- Zuo X
- Zuolo D
- Zygala L
- Álvarez Fernández A
- Özçelik Ö
- Publication venue
- 'American Physical Society (APS)'
- Publication date
- 01/01/2022
- Field of study
Measurements of the inclusive and differential fiducial cross sections of the Higgs boson are presented, using the τ lepton decay channel. The differential cross sections are measured as functions of the Higgs boson transverse momentum, jet multiplicity, and transverse momentum of the leading jet in the event, if any. The analysis is performed using proton-proton collision data collected with the CMS detector at the LHC at a center-of-mass energy of 13 TeV and corresponding to an integrated luminosity of 138 fb^{-1}. These are the first differential measurements of the Higgs boson cross section in the final state of two τ leptons. In final states with a large jet multiplicity or with a Lorentz-boosted Higgs boson, these measurements constitute a significant improvement over measurements performed in other final states
Stimulation of angiogenesis resulting from cooperation between macrophages and MDA-MB-231 breast cancer cells: proposed molecular mechanism and effect of tetrathiomolybdate
- Author
- A Carpenter
- A Mantovani
- A Mantovani
- A Saccani
- A Sica
- AA Von Knethen
- AL Welm
- B Hassouneh
- B Jacobs
- C Bailey
- C Brigati
- Caroline Gest
- CG Colpaert
- Claudine Soria
- D Ribatti
- DA Arenberg
- DA Arenberg
- DA Arenberg
- DA Arenberg
- DF Smith
- DL Foss
- E Blot
- E Gottfried
- EH Helinski
- Emmanuel Blot
- EY Lin
- EY Lin
- F Donate
- F Sallusto
- FO Martinez
- FO Martinez
- FR Greten
- GJ Brewer
- GJ Brewer
- H Haghnegahdar
- H Saji
- H Torisu
- HI Pass
- Hong Li
- J Bohuslav
- JC Juarez
- Jean-Pierre Vannier
- Jeannette Soria
- Jérôme Alexandre
- Linda-Louise Pritchard
- Lionel Cazin
- M Sproull
- Marc Laurent
- MM Remedi
- MP Keane
- N Romani
- N Romani
- NW Lukacs
- P Chomarat
- Q Pan
- RD Leek
- RM Strieter
- RM Strieter
- RM Strieter
- Rémi Varin
- S Gordon
- S Tsutsui
- SA Lowndes
- SF Badylak
- T Hagemann
- T Hagemann
- T Ueno
- Ulrich Joimel
- VL Goodman
- Y Luo
- YY Li
- Publication venue
- 'Springer Science and Business Media LLC'
- Publication date
- Field of study
Preventive and therapeutic challenges in combating Zika virus infection: are we getting any closer?
- Author
- A Basu
- A Bayer
- A David
- A Mathur
- AA van der Eijk
- AS Richard
- AV Matondang
- B Murgue
- B Pulendran
- B Pulendran
- BJ Blitvich
- C Fourcade
- C Li
- C Morrison
- CF Lin
- CV Ventura
- D Gaucher
- D Meaney-Delman
- DJ Roberts
- E Miller
- EC Gilmore
- EL de Azeredo
- Emily A. Weber
- FR Cugola
- G Calvet
- G Screaton
- GW Dick
- GW Dick
- H El Costa
- H Li
- H Liang
- H Tang
- HJ Willison
- IA Rodenhuis-Zybert
- J Mlakar
- J Reefhuis
- JA Cooper
- JJ Miner
- JM Anaya
- JM Mansuy
- JM Turmel
- K Clyde
- KL Spalding
- L Priyamvada
- L Schuler-Faccini
- LM Araujo
- LM Johansen
- M Dupont-Rouzeyrol
- M Sarno
- M Xu
- MA Johansson
- MC Bonaldo
- MC Magalhaes-Barbosa
- Meera V. Singh
- ML Silva
- MT Alonzo
- NC Bambakidis
- Nicole E. Stirpe
- O Bragina
- O Karimi
- PA Jenum
- PP Garcez
- PR Hutchings
- Q Liang
- R Hamel
- R Machold
- RF Pass
- RS Azevedo
- RS Sellers
- RW Driggers
- S Cauchemez
- S He
- S Honda
- S Nakao
- S Rinaldi
- Sanjay B. Maggirwar
- SC Weaver
- SL Rossi
- T Dos Santos
- T Ishikawa
- T Srichaikul
- TJ Nowakowski
- VA Kostyuchenko
- VB Singh
- Vir B. Singh
- VM Cao-Lormeau
- Y Yamaguchi
- YS Lin
- Publication venue
- 'Springer Science and Business Media LLC'
- Publication date
- Field of study
Search for long-lived particles decaying to leptons with large impact parameter in proton-proton collisions at root s=13 TeV
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- 6z\ue7elik 6.
- \uc1lvarez C. Ram\uf3n
- Aarrestad T. K.
- Abbaneo D.
- Abbiendi G.
- Abbrescia M.
- Abdalla H.
- Abdullah W. A. T. Wan
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- Abercrombie D.
- Abreu A.
- Acharya H.
- Acosta D.
- Ad\ue1n D. P\ue9rez
- Adam W.
- Adamidis K.
- Adams E.
- Adams M. R.
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- Addesa F. M.
- Adloff C.
- Adzic P.
- Afanasiev S.
- Agapitos A.
- Agarwal G.
- Aggleton R.
- Agram J. -L.
- Aguilar-Benitez M.
- Ahmad A.
- Ahmad M.
- Ahmad W. Haj
- Ahmed A.
- Ahuja S.
- Aime\u2018 C.
- Akchurin N.
- Akgun B.
- Akpinar A.
- Albergo S.
- Albert A.
- Albrecht S.
- Albrow M.
- Aleksandrov A.
- Alexander J.
- Alhusseini M.
- Alimena J.
- Alison J.
- Almond J.
- Alonso A. Garc\ueda
- Alpana K.
- Alvarez J. D. Ruiz
- Alverson G.
- Alves G. A.
- Aly R.
- Alyari M.
- Amapane N.
- Amarilo K. Mota
- Ambrozas M.
- Amendola C.
- Amin N.
- Amram O.
- Amsler C.
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- Anagnostou G.
- Anampa K. Hurtado
- Andrea J.
- Andreassi G.
- Andreev V.
- Andreev Yu.
- Andrejkovic J. W.
- Andrews M. B.
- Androsov K.
- Angioni G. L. Pinna
- Anguiano J.
- Antchev G.
- Antequera J. Berenguer
- Anthony D.
- Antunovic Z.
- Anuar A. A. Bin
- Apollinari G.
- Apparu D.
- Appelt E.
- Apresyan A.
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- Arbol P. Martinez Ruiz del
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- Arcidiacono R.
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- Azzurri P.
- B\ue4rtschi P.
- Baarmand M. M.
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- Bachiller I.
- Bachtis M.
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- Baillon P.
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- Band R.
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- Banos L. I. Estevez
- Bansal S.
- Barbagli G.
- Barberis E.
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- Baringer P.
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- Baron O.
- Barrera C. Baldenegro
- Barrera C. Oropeza
- Barria P.
- Bart\uf3k M.
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- Bartosik N.
- Bastos D.
- Battilana C.
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- Bayshev I.
- Bean A.
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- Becerra D. A. Sanz
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- Bedoya Cristina F.
- Beghin D.
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- Behnke O.
- Bein S.
- Belforte S.
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- Belyaev A.
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- Benaglia A.
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- Bendavid J.
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- Bestintzanos I.
- Bethani A.
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- Bhowmik D.
- Bhowmik S.
- Bhyun J. H.
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- Bialkowska H.
- Bianchini L.
- Bianco M.
- Bianco S.
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- Bilin B.
- Bindhu V. K. Muraleedharan Nair
- Bisello D.
- Black K.
- Blekman F.
- Blinov V.
- Bloch D.
- Bloch P.
- Bloom K.
- Bluj M.
- Blumenfeld B.
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- Boldrini G.
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- Wyslouch B.
- Xiang Y.
- Xiao J.
- Xiao M.
- Xiao R.
- Xie S.
- Xie W.
- Yagil A.
- Yalvac M.
- Yan F.
- Yan X.
- Yang S.
- Yang S.
- Yang U. K.
- Yang Y. C.
- Yao Y.
- Yarar H.
- Yates B. R.
- Yazgan E.
- Ye Z.
- Yetkin E. A.
- Yi K.
- Yigitbasi E.
- Yohay R.
- Yoo H. D.
- Yoo J.
- Yoon I.
- You Z.
- Yu D.
- Yu G. B.
- Yu I.
- Yu P. r.
- Yu S. S.
- Yuan L.
- Yuan S.
- Yuldashev B. S.
- Yumiceva F.
- Yusli M. N.
- Yzquierdo A. P\ue9rez-Calero
- Zabi A.
- Zacharopoulou A.
- Zahid S.
- Zaleski S.
- Zalewski P.
- Zanetti M.
- Zarubin A.
- Zarucki M.
- Zecchinelli A. G.
- Zeinali M.
- Zeuner W. D.
- Zghiche A.
- Zhang F.
- Zhang H.
- Zhang J.
- Zhang L.
- Zhang W.
- Zhang Y.
- Zhang Y.
- Zhang Y.
- Zhang Z.
- Zhao J.
- Zhizhin I.
- Zhokin A.
- Zhu D. H.
- Zhu R. Y.
- Ziemons T.
- Zoi I.
- Zolkapli Z.
- Zorbakir I. S.
- Zorbilmez C.
- Zotto P.
- Zotz A.
- Zou D.
- Zou R.
- Zucchetta A.
- Zumerle G.
- Zuo X.
- Zuolo D.
- Zygala L.
- Publication venue
- 'Springer Science and Business Media LLC'
- Publication date
- 01/01/2022
- Field of study
A search for new long-lived particles decaying to leptons using proton–proton collision data produced by the CERN LHC at s√=13TeV is presented. Events are selected with two leptons (an electron and a muon, two electrons, or two muons) that both have transverse impact parameter values between 0.01 and 10cm and are not required to form a common vertex. Data used for the analysis were collected with the CMS detector in 2016, 2017, and 2018, and correspond to an integrated luminosity of 118 (113)fb−1 in the ee channel (eμ and μμ channels). The search is designed to be sensitive to a wide range of models with displaced eμ, ee, and μμ final states. The results constrain several well-motivated models involving new long-lived particles that decay to displaced leptons. For some areas of the available phase space, these are the most stringent constraints to date
A new calibration method for charm jet identification validated with proton-proton collision events at √s = 13 TeV
- Author
- Aarrestad TK
- Aarup Petersen H
- Abbaneo D
- Abbiendi G
- Abbrescia M
- Abdalla H
- Abdullin S
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- Yagil A
- Yalvac M
- Yan F
- Yan X
- Yang S
- Yang S
- Yang U
- Yang YC
- Yao Y
- Yarar H
- Yates B
- Yazgan E
- Ye Z
- Yetkin EA
- Yi K
- Yigitbasi E
- Yohay R
- Yoo HD
- Yoo J
- Yoon I
- You Z
- Yu D
- Yu GB
- Yu I
- Yu P-R
- Yu S-S
- Yuan L
- Yuan S
- Yuldashev BS
- Yumiceva F
- Yusli MN
- Zabi A
- Zacharopoulou A
- Zahid S
- Zaleski S
- Zalewski P
- Zanetti M
- Zarubin A
- Zarucki M
- Zecchinelli AG
- Zeinali M
- Zeuner WD
- Zghiche A
- Zhang F
- Zhang H
- Zhang J
- Zhang L
- Zhang S
- Zhang W
- Zhang Y
- Zhang Y
- Zhang Z
- Zhao J
- Zhizhin I
- Zhokin A
- Zhu DH
- Zhu R-Y
- Ziemons T
- Zoi I
- Zolkapli Z
- Zorbakir IS
- Zorbilmez C
- Zotto P
- Zou D
- Zou R
- Zucchetta A
- Zumerle G
- Zuo X
- Zuolo D
- Zygala L
- Álvarez Fernández A
- Özçelik Ö
- Publication venue
- 'IOP Publishing'
- Publication date
- 01/01/2022
- Field of study
ArXiv ePrint: 2111.03027Copyright © 2022 CERN for the benefit of the CMS collaboration. Many measurements at the LHC require efficient identification of heavy-flavour jets, i.e. jets originating from bottom (b) or charm (c) quarks. An overview of the algorithms used to identify c jets is described and a novel method to calibrate them is presented. This new method adjusts the entire distributions of the outputs obtained when the algorithms are applied to jets of different flavours. It is based on an iterative approach exploiting three distinct control regions that are enriched with either b jets, c jets, or light-flavour and gluon jets. Results are presented in the form of correction factors evaluated using proton-proton collision data with an integrated luminosity of 41.5 fb-1 at √s = 13 TeV, collected by the CMS experiment in 2017. The closure of the method is tested by applying the measured correction factors on simulated data sets and checking the agreement between the adjusted simulation and collision data. Furthermore, a validation is performed by testing the method on pseudodata, which emulate various mismodelling conditions. The calibrated results enable the use of the full distributions of heavy-flavour identification algorithm outputs, e.g. as inputs to machine-learning models. Thus, they are expected to increase the sensitivity of future physics analyses.SCOAP
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