786 research outputs found
Voxel-wise comparisons of cellular microstructure and diffusion-MRI in mouse hippocampus using 3D Bridging of Optically-clear histology with Neuroimaging Data (3D-BOND)
- Author
- A Erturk
- A Labate
- A Seehaus
- AC Silva
- AR Khan
- B Jeurissen
- B Yang
- B Zhang
- C Errico
- D Rueckert
- D Wu
- DK Jones
- EA Susaki
- EB Hutchinson
- EH Chang
- F Sepehrband
- F Trojsi
- G Xu
- H Hama
- H Zhang
- HU Dodt
- IP Bruce
- J Mollink
- JA Wells
- JD Tournier
- JV Manjon
- JV Manjon
- JV Manjon
- K Becker
- K Chung
- K Schilling
- K Singh
- L Feng
- M Aggarwal
- M Goubran
- M Jenkinson
- MA Jacobs
- MD Budde
- MT Ke
- N Renier
- R Tomer
- RC Mandl
- SP Lee
- T Blumenfeld-Katzir
- TB Dyrby
- TM Nir
- Publication venue
- 'Springer Science and Business Media LLC'
- Publication date
- 01/03/2018
- Field of study
A key challenge in medical imaging is determining a precise correspondence between image properties and tissue microstructure. This comparison is hindered by disparate scales and resolutions between medical imaging and histology. We present a new technique, 3D Bridging of Optically-clear histology with Neuroimaging Data (3D-BOND), for registering medical images with 3D histology to overcome these limitations. Ex vivo 120 × 120 × 200 μm resolution diffusion-MRI (dMRI) data was acquired at 7 T from adult C57Bl/6 mouse hippocampus. Tissue was then optically cleared using CLARITY and stained with cellular markers and confocal microscopy used to produce high-resolution images of the 3D-tissue microstructure. For each sample, a dense array of hippocampal landmarks was used to drive registration between upsampled dMRI data and the corresponding confocal images. The cell population in each MRI voxel was determined within hippocampal subregions and compared to MRI-derived metrics. 3D-BOND provided robust voxel-wise, cellular correlates of dMRI data. CA1 pyramidal and dentate gyrus granular layers had significantly different mean diffusivity (p > 0.001), which was related to microstructural features. Overall, mean and radial diffusivity correlated with cell and axon density and fractional anisotropy with astrocyte density, while apparent fibre density correlated negatively with axon density. Astrocytes, axons and blood vessels correlated to tensor orientation
Cytokinesis in bloodstream stage Trypanosoma brucei requires a family of katanins and spastin
- Author
- A Baines
- A Errico
- A Hemphill
- A Karabay
- A Roll-Mecak
- A Roll-Mecak
- A Schneider
- A Schneider
- A Woods
- B Lacroix
- B Wickstead
- C Benz
- C Hertz-Fowler
- C Lu
- C Vedrenne
- Caroline Clucas
- Corinna Benz
- D Buster
- D Spitznagel
- D Zhang
- D Zhang
- Dan Zilberstein
- DJ LaCount
- DR Robinson
- E Detmer
- E Panteris
- E Wirtz
- EE Dymek
- FJ Ahmad
- FJ McNally
- FJ McNally
- G Burkard
- GR Forsythe
- H Sudo
- H Sudo
- H Sudo
- HH Lee
- HP Price
- J Guizetti
- J Van den Abbeele
- JA Garcia-Salcedo
- JA Schiel
- JC Munday
- JD Diaz-Valencia
- Jeremy C. Mottram
- JJ Hartman
- JJ Hartman
- JT Ma
- JW Connell
- K Gull
- K McNally
- K Toyo-oka
- KJ Evans
- KP Mcnally
- KP McNally
- KP Mcnally
- KR Matthews
- KY Chan
- L Kohl
- L Qiang
- L Rindisbacher
- M Agromayor
- M Casanova
- M Srayko
- MQ Rasi
- MR Dow
- N Balaban
- N Balaban
- N Sharma
- P Bastin
- Q Meng
- R Sasse
- R Sharma
- S Biebinger
- S Kelly
- S Monnerat
- S Olego-Fernandez
- S Redmond
- S Vaughan
- SG Lillico
- SH Park
- T Sherwin
- T Sherwin
- T Sherwin
- Tansy C. Hammarton
- TC Hammarton
- TC Hammarton
- TC Hammarton
- TC Hammarton
- W Yu
- WQ Yu
- Z Li
- Z Li
- Publication venue
- 'Public Library of Science (PLoS)'
- Publication date
- 01/01/2012
- Field of study
Microtubule severing enzymes regulate microtubule dynamics in a wide range of organisms and are implicated in important cell cycle processes such as mitotic spindle assembly and disassembly, chromosome movement and cytokinesis. Here we explore the function of several microtubule severing enzyme homologues, the katanins (KAT80, KAT60a, KAT60b and KAT60c), spastin (SPA) and fidgetin (FID) in the bloodstream stage of the African trypanosome parasite, Trypanosoma brucei. The trypanosome cytoskeleton is microtubule based and remains assembled throughout the cell cycle, necessitating its remodelling during cytokinesis. Using RNA interference to deplete individual proteins, we show that the trypanosome katanin and spastin homologues are non-redundant and essential for bloodstream form proliferation. Further, cell cycle analysis revealed that these proteins play essential but discrete roles in cytokinesis. The KAT60 proteins each appear to be important during the early stages of cytokinesis, while downregulation of KAT80 specifically inhibited furrow ingression and SPA depletion prevented completion of abscission. In contrast, RNA interference of FID did not result in any discernible effects. We propose that the stable microtubule cytoskeleton of T. brucei necessitates the coordinated action of a family of katanins and spastin to bring about the cytoskeletal remodelling necessary to complete cell divisio
Omalizumab efficacy in cases of chronic spontaneous urticaria is not explained by the inhibition of sera activity in effector cells
- Author
- A Eggel
- A Fusari
- A Kaplan
- A Navines-Ferrer
- A Valero
- AP Kaplan
- AP Kaplan
- B Wedi
- BL Gruber
- C Bindslev-Jensen
- CE Grattan
- D Alvarez-Errico
- D MacGlashan Jr.
- DW MacGlashan Jr.
- E Serrano-Candelas
- F Bossi
- GN Konstantinou
- HJ Hoffmann
- I Jauregui
- J Gericke
- JA Bernstein
- JA Boyce
- JM Harris
- KH Waibel
- KM Yasnowsky
- LA Beck
- LF Pennington
- LJ Tong
- M Ferrer
- M Ferrer
- M Ferrer
- M Hide
- M Maurer
- MA Chan
- ML Sanz
- O Guzelbey
- O Noga
- R Skiepko
- S Altrichter
- T Zuberbier
- TW Chang
- U Bullerkotte
- Publication venue
- 'Springer Science and Business Media LLC'
- Publication date
- 30/04/2018
- Field of study
Omalizumab (OmAb) is a humanized anti-IgE antibody approved for the treatment of chronic spontaneous urticaria (CSU). OmAb's mechanism of action is known to include actions on free IgE and on pre-bound IgE. However, OmAb is equally and rapidly effective against autoimmune and non-autoimmune urticaria where IgE involvement is not clear, suggesting the involvement of additional mechanisms of action. In this study, we sought to investigate the ability of OmAb to inhibit mast cell and basophil degranulation induced by sera from CSU patients. For this purpose, we performed a comparison between the in vitro incubation of sera from CSU patients treated with OmAb and the in vivo administration of OmAb in a clinical trial. We found that OmAb added in vitro to sera from CSU patients did not modify the ability of the sera to induce cell degranulation. Similarly, the sera from patients treated with OmAb in the context of the clinical trial who had a good clinical outcome maintained the capacity to activate mast cells and basophils. Thus, we conclude that the beneficial activity of OmAb does not correlate with the ability of patient sera to induce cell degranulation
Chromatin remodelling factor SMARCD2 regulates transcriptional networks controlling differentiation of neutrophil granulocytes
- Author
- A Alajem
- A Khanna-Gupta
- A Komiyama
- A Rau
- AD Friedman
- Alejandro A Schäffer
- AR Quinlan
- Asbjørg Stray-Pedersen
- BG Wilson
- BR Cairns
- C Hall
- C Liongue
- Christian Mertes
- Christoph Klein
- Christoph Ziegenhain
- CT Griffin
- D Croft
- D Kotlarz
- D Álvarez-Errico
- Daniel Petersheim
- Eckhard Wolf
- Ehsan Bahrami
- EO Glocker
- F Ellett
- FJ Sedlazeck
- FM Cernilogar
- G Bohn
- Graham J Lieschke
- H Cedar
- H Hu
- H Li
- H Li
- H Lickert
- Hans-Peter Horny
- Heinrich Schmidt
- HF Lin
- HT Huang
- IL de la Serna
- J Breton-Gorius
- J Harrow
- J Krosl
- J Krumsiek
- J Lekstrom-Himes
- J Shi
- JA Dahl
- JA Gagnon
- JA Lekstrom-Himes
- Jacek Puchałka
- JD Buenrostro
- JI Gallin
- Julien Gagneur
- LJ Zhu
- M Adli
- M Buscarlet
- M Koike
- M Koulnis
- M Lawrence
- M Lek
- M Milacic
- M Tanaka
- Maik Dahlhoff
- Marlon R Schneider
- Maximilian Witzel
- ME Newman
- Meino Rohlfs
- MI Love
- Miguel R Abboud
- MY Tolstorukov
- N Iriyama
- ND Meeker
- P Krawitz
- P Shannon
- PB Rahl
- Peter D Arkwright
- Peter M Krawitz
- R Yamanaka
- RF Wynn
- S Picelli
- SA Renshaw
- SH Orkin
- T Gkikopoulos
- T Hamada
- T Wada
- Tomas Racek
- V Jojic
- V Madan
- VA Cruickshank
- Vahid Pazhakh
- VR Ramirez-Carrozzi
- W Verbeek
- Wolfgang Enard
- Y Liao
- Y Liu
- Yanxin Fan
- Publication venue
- 'Springer Science and Business Media LLC'
- Publication date
- 01/05/2017
- Field of study
Decreased Striatal RGS2 Expression Is Neuroprotective in Huntington's Disease (HD) and Exemplifies a Compensatory Aspect of HD-Induced Gene Regulation
- Author
- A Hodges
- A Kuhn
- A Wyttenbach
- B Zucker
- BL Apostol
- BS Spektor
- CT Chu
- D Spano
- E Roze
- EA Thomas
- EC Stack
- EM Snyder
- F Errico
- FC Nucifora Jr
- H Runne
- J Han
- JA Bibb
- JC Lievens
- JR Crittenden
- K Obrietan
- K Wennerberg
- KL Sugars
- KL Sugars
- LS Bernstein
- M DiFiglia
- M Hetman
- M Inoue-Mochita
- MA Ariano
- N Rudinskiy
- Ozgun Gokce
- P Maher
- P Vargiu
- PA Desplats
- R Joseph
- R Kotter
- R Luthi-Carter
- R Luthi-Carter
- R Luthi-Carter
- R Luthi-Carter
- R Truant
- RJ Ferrante
- Ruth Luthi-Carter
- S Gines
- S Paul
- S Paul
- S Salim
- S Sinnarajah
- S Subramaniam
- S Zheng
- SP Heximer
- SP Heximer
- SW Davies
- T Anger
- T Ingi
- Tamara Seredenina
- Xiao-Jiang Li
- Y Song
- Publication venue
- Public Library of Science
- Publication date
- 01/01/2011
- Field of study
The molecular phenotype of Huntington's disease (HD) is known to comprise highly reproducible changes in gene expression involving striatal signaling genes. Here we test whether individual changes in striatal gene expression are capable of mitigating HD-related neurotoxicity.We used protein-encoding and shRNA-expressing lentiviral vectors to evaluate the effects of RGS2, RASD2, STEP and NNAT downregulation in HD. Of these four genes, only RGS2 and RASD2 modified mutant htt fragment toxicity in cultured rat primary striatal neurons. In both cases, disease modulation was in the opposite of the predicted direction: whereas decreased expression of RGS2 and RASD2 was associated with the HD condition, restoring expression enhanced degeneration of striatal cells. Conversely, silencing of RGS2 or RASD2 enhanced disease-related changes in gene expression and resulted in significant neuroprotection. These results indicate that RGS2 and RASD2 downregulation comprises a compensatory response that allows neurons to better tolerate huntingtin toxicity. Assessment of the possible mechanism of RGS2-mediated neuroprotection showed that RGS2 downregulation enhanced ERK activation. These results establish a novel link between the inhibition of RGS2 and neuroprotective modulation of ERK activity.Our findings both identify RGS2 downregulation as a novel compensatory response in HD neurons and suggest that RGS2 inhibition might be considered as an innovative target for neuroprotective drug development
Evidence for Top Quark Production in Nucleus-Nucleus Collisions
- Author
- Aarrestad TK
- Aarup Petersen H
- Abbaneo D
- Abbiendi G
- Abbrescia M
- Abdullin S
- Abercrombie D
- Acharya H
- Acosta D
- Acosta JG
- Adam W
- Adams E
- Adams MR
- Adams T
- Adloff C
- Adzic P
- Afanasiev S
- Agapitos A
- Agarwal G
- Aggleton R
- Agram J-L
- Aguilar-Benitez M
- Ahmad A
- Ahmad M
- Ahmed A
- Ahuja S
- Akbiyik M
- Akchurin N
- Akgun B
- Akpinar A
- Albajar C
- Albergo S
- Albert A
- Albrow M
- Alcaraz Maestre J
- Aldaya Martin M
- Aldá Júnior WL
- Aleksandrov A
- Alexander J
- Alhusseini M
- Alimena J
- Alison J
- Allen B
- Almond J
- Alvarez Gonzalez B
- Alverson G
- Alves GA
- Aly R
- Alyari M
- Amapane N
- Ambrogi F
- Amendola C
- Amin N
- Amram O
- Amsler C
- Anagnostou G
- Anderson D
- Andrea J
- Andreev V
- Andreev Y
- Andrews MB
- Androsov K
- Ang L
- Antchev G
- Antunovic Z
- Apanasevich L
- Apollinari G
- Appelt E
- Apresyan A
- Apyan A
- Araujo M
- Arcaro D
- Arcidiacono R
- Arenton MW
- Argiro S
- Arneodo M
- Aruta C
- Asavapibhop B
- Asawatangtrakuldee C
- Asenov P
- Asghar MI
- Asilar E
- Askew A
- Asmuss P
- Atakisi IO
- Atanasov I
- Ather MW
- Attikis A
- Auffray E
- Aushev T
- Auzinger G
- Avati V
- Avery P
- Avila C
- Awan MIM
- Ayala E
- Aydogmus Sen F
- Azarkin M
- Azhgirey I
- Aziz T
- Azzi P
- Azzurri P
- Baarmand MM
- Babaev A
- Babounikau I
- Bacchetta N
- Bachiller I
- Bachtis M
- Backhaus M
- Baden A
- Baechler J
- Bagliesi G
- Bahinipati S
- Baillon P
- Bainbridge R
- Bakas G
- Bakhshiansohi H
- Baldenegro Barrera C
- Ball AH
- Ban Y
- Band R
- Banerjee S
- Banerjee S
- Bansal S
- Barbagli G
- Barberis E
- Bargassa P
- Baringer P
- Barnes VE
- Barney D
- Baron O
- Barrio Luna M
- Bartek R
- Bartosik N
- Bartók M
- Baselga M
- Baskakov A
- Bastos D
- Battilana C
- Baty A
- Bauerdick LAT
- Baur S
- Baxter S
- Bayshev I
- Bean A
- Beauceron S
- Beaudette F
- Becerril Gonzalez H
- Bechtel J
- Beghin D
- Behera PK
- Behera SC
- Behnke O
- Bein S
- Belchior Batista Das Chagas E
- Belforte S
- Bell KW
- Bellan R
- Belloni A
- Bellora A
- Belyaev A
- Belyaev A
- Benaglia A
- Benato L
- Bencze G
- Bendavid J
- Benecke A
- Benelli G
- Beni N
- Benitez JF
- Benussi L
- Beretvas A
- Bergauer T
- Berger P
- Berger T
- Beri SB
- Bermúdez Martínez A
- Bernardes CA
- Bernet C
- Berry D
- Berryhill J
- Bertacchi V
- Besancon M
- Beschi A
- Bhal E
- Bhandari R
- Bhardwaj A
- Bharti M
- Bhat MA
- Bhat PC
- Bhatnagar V
- Bhattacharya R
- Bhattacharya S
- Bhattacharya S
- Bhattacharya S
- Bheesette S
- Bhowmik D
- Bhowmik S
- Bhyun JH
- Bi R
- Bialkowska H
- Bianchini L
- Bianco M
- Bianco S
- Biasini M
- Biino C
- Bilei GM
- Bilin B
- Bilki B
- Bin Anuar AA
- Bisello D
- Black K
- Blekman F
- Blinov V
- Bloch D
- Bloch P
- Bloom K
- Bluj M
- Blumenfeld B
- Boccali T
- Bocci A
- Bodek A
- Boimska B
- Boletti A
- Bologna S
- Bols ES
- Bonacorsi D
- Bonanomi M
- Bonchev M
- Bonomally S
- Boos E
- Boran F
- Borchsh V
- Borg J
- Borgonovi L
- Bornheim A
- Borras K
- Bortignon P
- Bose T
- Bossini E
- Botta C
- Botta V
- Boudoul G
- Bouhali O
- Bourgatte G
- Bourilkov D
- Bozzo M
- Bragagnolo A
- Braghieri A
- Braibant-Giacomelli S
- Brainerd C
- Brandt S
- Branson JG
- Bravo C
- Breedon R
- Breeze S
- Brew C
- Brigljevic V
- Brinkerhoff A
- Brivio F
- Brochero Cifuentes JA
- Brom J-M
- Brondolin E
- Brooke JJ
- Brown RM
- Brunner D
- Bruno G
- Brzhechko D
- Brücken E
- Bucci R
- Buccilli A
- Buchanan J
- Buchmuller O
- Bueghly J
- Bundock A
- Bunkowski K
- Buontempo S
- Burkett K
- Burkle B
- Burns D
- Burt K
- Bury F
- Busson P
- Busza W
- Butalla S
- Butler JN
- Butler PH
- Butz E
- Bylinkin A
- Bylsma B
- Byszuk A
- Cabrera A
- Cabrillo IJ
- Cadamuro L
- Caillol C
- Cakir A
- Calabria C
- Calandri A
- Calderon De La Barca Sanchez M
- Calderon A
- Cali IA
- Call K
- Calligaris L
- Calzaferri S
- Camen C
- Caminada L
- Campagnari C
- Campanini R
- Campbell A
- Camporesi T
- Candelise V
- Canelli MF
- Canepa A
- Cankocak K
- Capiluppi P
- Cappati A
- Caputo C
- Caraway B
- Cardini A
- Cardwell B
- Carle A
- Carlin R
- Carrera Jarrin E
- Carrillo Montoya CA
- Carrillo Moreno S
- Cartiglia N
- Carvalho Antunes De Oliveira A
- Carvalho W
- Casarsa M
- Caspart R
- Cassese A
- Castaldi R
- Castaneda Hernandez A
- Castilla-Valdez H
- Castro A
- Cavallari F
- Cavallo FR
- Cavallo N
- Cavanaugh R
- Ceard L
- Ceccarelli R
- Cepaitis V
- Cepeda M
- Cerati GB
- Cerci S
- Cerminara G
- Cerrada M
- Cerri O
- Cetorelli F
- Chabert EC
- Chahal GS
- Chang P
- Chang P
- Chanon N
- Chao Y
- Chapon E
- Charaf O
- Charlot C
- Chatterjee RM
- Chatterjee S
- Chauhan S
- Chauhan S
- Chawla R
- Chazin Quero B
- Checchia P
- Chekhovsky V
- Chen C
- Chen G
- Chen GM
- Chen HS
- Chen KF
- Chen M
- Chen PH
- Chen X
- Chen Y
- Chen Y
- Chen Z
- Chenarani S
- Cheng T
- Cheng Y
- Cherepanov V
- Chernyavskaya N
- Chertok M
- Cheung HWK
- Chhibra SS
- Chiarito B
- Chierici R
- Chinellato J
- Chistov R
- Chlebana F
- Cho S
- Choi J
- Choi S
- Choi Y
- Chou JP
- Choudhary BC
- Choudhury S
- Chu J
- Chudasama R
- Chwalek T
- Ciangottini D
- Ciocca C
- Ciocci MA
- Cipriani M
- Ciriolo V
- Cirkovic P
- Citron M
- Cittolin S
- Ciulli V
- Civinini C
- Claes DR
- Clare R
- Clement E
- Clerbaux B
- CMS Collaboration
- Cockerill DJA
- Coelho E
- Colaleo A
- Cole JE
- Colino N
- Collard C
- Colling D
- Cometti S
- Connor P
- Consuegra Rodríguez S
- Contardo D
- Conway J
- Conway R
- Cooper SI
- Cooperstein S
- Corcodilos L
- Cornelis T
- Correia Silva G
- Cosby C
- Cossutti F
- Costa M
- Costa S
- Coubez X
- Couderc F
- Cousins R
- Covarelli R
- Cox B
- Cox PT
- Cranshaw DJ
- Creanza D
- Cremonesi M
- Cristella L
- Csanad M
- Csorgo T
- Cuevas J
- Cuffiani M
- Cumalat JP
- Cummings G
- Cussans D
- Cutts D
- Czellar S
- D'Alessandro R
- D'Alfonso M
- D'Enterria D
- D'Hondt J
- Da Costa EM
- Da Rold A
- Da Silveira GG
- Dabrowski A
- Daci N
- Dalchenko M
- Dallavalle GM
- Damarseckin S
- Damgov J
- Danilov M
- Danilov V
- Daponte V
- Darwish MR
- Das P
- Das S
- Dasgupta A
- Dash D
- Daskalakis G
- Dasu S
- Datta A
- Dauncey P
- David A
- David P
- Davies G
- Davignon O
- De Barbaro P
- De Boer W
- De Bruyn I
- De Castro Manzano P
- De Clercq J
- De Cosa A
- De Filippis N
- De Guio F
- De Iorio A
- De Jesus Damiao D
- De La Cruz B
- De La Cruz-Burelo E
- De Lentdecker G
- De Leo K
- De Palma M
- De Roeck A
- De Trocóniz JF
- De Wit A
- De Wolf EA
- Deelen N
- Defranchis MM
- Deile M
- Dejardin M
- Del Burgo R
- Del Re D
- Delaere C
- Delannoy AG
- Delannoy H
- Delcourt M
- Delgado Peris A
- Delgado A
- Dell'Orso R
- Della Negra M
- Della Ricca G
- Demaria N
- Demina R
- Demiragli Z
- Demiroglu ZS
- Denegri D
- Depasse P
- Derdzinski M
- Dermenev A
- Dev N
- Dewanjee RK
- Dezoort G
- Dharmaratna WGD
- Dhingra N
- Di Croce D
- Di Domenico MR
- Di Florio A
- Di Francesco A
- Di Marco E
- Di Maria R
- Di Mattia A
- Di Pilato A
- Diab B
- Diamantopoulou M
- Diaz D
- Didukh L
- Diemoz M
- Dierlamm A
- Dildick S
- Dilsiz K
- Dimitrov A
- Dimova T
- Dinardo ME
- Dini P
- Diotalevi T
- Dissertori G
- Dittmann J
- Dittmar M
- Dittmer S
- Dobson M
- Dobur D
- Dodd L
- Dogra S
- Dolek F
- Dolen J
- Dominguez A
- Domínguez Damiani D
- Donato S
- Donegà M
- Donertas IS
- Dordevic M
- Dorfer C
- Dorigo T
- Dorney B
- Doroba K
- Dorsett A
- Dosselli U
- Dozen C
- Dragicevic M
- Dremin I
- Dreyer T
- Duarte Campderros J
- Duarte J
- Dube S
- Dudko L
- Dugad S
- Duh YT
- Dulemba JL
- Dumanoglu I
- Dupont N
- Durgut S
- Duric S
- Durkin LS
- Dutta D
- Dutta I
- Dutta S
- Dutta V
- Dziwok C
- Dünser M
- Ebrahimi A
- Eckerlin G
- Ecklund KM
- Eckstein D
- Eerola P
- Ehataht K
- Eichhorn T
- El Mamouni H
- El Morabit K
- Eliseev D
- Elkafrawy T
- Elliott-Peisert A
- Ellis KV
- Elmer P
- Elmetenawee W
- Elvira VD
- Elwood A
- Eminizer M
- Emriskova N
- Eno SC
- Epshteyn V
- Erbacher R
- Erdmann M
- Erdmann W
- Erice C
- Erodotou E
- Errico F
- Ershov A
- Erö J
- Escalante Del Valle A
- Eskut E
- Estevez Banos LI
- Etesami SM
- Eusebi R
- Evangelou I
- Evans A
- Evdokimov O
- Everaerts P
- Eysermans J
- Fabbri F
- Fabozzi F
- Faccioli P
- Fackeldey P
- Fallavollita F
- Fallon C
- Falmagne G
- Faltermann N
- Fanfani A
- Fang W
- Fangmeier C
- Fanò L
- Fasanella D
- Faure JL
- Favart L
- Fay J
- Fedi G
- Feindt F
- Felcini M
- Feld L
- Feng Y
- Ferbel T
- Ferencek D
- Ferguson T
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- Álvarez Fernández A
- Özçelik Ö
- Publication venue
- Publication date
- 01/01/2019
- Field of study
Peer reviewe
Search for dark matter produced in association with a single top quark or a top quark pair in proton-proton collisions at s=13 TeV
- Author
- Aarrestad TK
- Abbaneo D
- Abbiendi G
- Abbrescia M
- Abdullah WAT Wan
- Abdullin S
- Abdulsalam A
- Abercrombie D
- Abu Zeid S
- Ackert A
- Acosta D
- Acosta JG
- Adam W
- Adams MR
- Adams T
- Adzic P
- Afanasiev S
- Agapitos A
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- Aggleton R
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- Ahmad A
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- Ahmad M
- Ahmed I
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- Aleksandrov A
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- Alhusseini M
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- Alvarez JD Ruiz
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- Publication venue
- Publication date
- 01/01/2019
- Field of study
A search has been performed for heavy resonances decaying to ZZ or ZW in 2l2q final states, with two charged leptons (l = e, mu) produced by the decay of a Z boson, and two quarks produced by the decay of a W or Z boson. The analysis is sensitive to resonances with masses in the range from 400 to 4500 GeV. Two categories are defined based on the merged or resolved reconstruction of the hadronically decaying vector boson, optimized for high- and low-mass resonances, respectively. The search is based on data collected during 2016 by the CMS experiment at the LHC in proton-proton collisions with a center-of-mass energy of root s = 13 TeV, corresponding to an integrated luminosity of 35.9 fb(-1). No excess is observed in the data above the standard model background expectation. Upper limits on the production cross section of heavy, narrow spin-1 and spin-2 resonances are derived as a function of the resonance mass, and exclusion limits on the production of W' bosons and bulk graviton particles are calculated in the framework of the heavy vector triplet model and warped extra dimensions, respectively.A search has been performed for heavy resonances decaying to ZZ or ZW in 2l2q final states, with two charged leptons (l = e, mu) produced by the decay of a Z boson, and two quarks produced by the decay of a W or Z boson. The analysis is sensitive to resonances with masses in the range from 400 to 4500 GeV. Two categories are defined based on the merged or resolved reconstruction of the hadronically decaying vector boson, optimized for high- and low-mass resonances, respectively. The search is based on data collected during 2016 by the CMS experiment at the LHC in proton-proton collisions with a center-of-mass energy of root s = 13 TeV, corresponding to an integrated luminosity of 35.9 fb(-1). No excess is observed in the data above the standard model background expectation. Upper limits on the production cross section of heavy, narrow spin-1 and spin-2 resonances are derived as a function of the resonance mass, and exclusion limits on the production of W' bosons and bulk graviton particles are calculated in the framework of the heavy vector triplet model and warped extra dimensions, respectively.A search for dark matter produced in association with top quarks in proton-proton collisions at a center-of-mass energy of 13 TeV is presented. The data set used corresponds to an integrated luminosity of 35.9 fb(-1) recorded with the CMS detector at the LHC. Whereas previous searches for neutral scalar or pseudoscalar mediators considered dark matter production in association with a top quark pair only, this analysis also includes production modes with a single top quark. The results are derived from the combination of multiple selection categories that are defined to target either the single top quark or the top quark pair signature. No significant deviations with respect to the standard model predictions are observed. The results are interpreted in the context of a simplified model in which a scalar or pseudoscalar mediator particle couples to a top quark and subsequently decays into dark matter particles. Scalar and pseudoscalar mediator particles with masses below 290 and 300 GeV, respectively, are excluded at 95% confidence level, assuming a dark matter particle mass of 1 GeV and mediator couplings to fermions and dark matter particles equal to unity.Peer reviewe
Search for Higgs Boson Pair Production in the Four b Quark Final State in Proton-Proton Collisions at root s=13 TeV
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- Álvarez CR
- Özçelik Ö
- Publication venue
- Publication date
- 01/01/2022
- Field of study
Search for strongly interacting massive particles generating trackless jets in proton-proton collisions at s = 13 TeV
- Author
- Aarrestad TK
- Aarup Petersen H
- Abbaneo D
- Abbiendi G
- Abbrescia M
- Abdullin S
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- Zenaiev O
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- Zorbilmez C
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- Österberg K
- Özçelik Ö
- Široký J
- Publication venue
- 'Springer Science and Business Media LLC'
- Publication date
- 01/01/2022
- Field of study
A search for dark matter in the form of strongly interacting massive particles (SIMPs) using the CMS detector at the LHC is presented. The SIMPs would be produced in pairs that manifest themselves as pairs of jets without tracks. The energy fraction of jets carried by charged particles is used as a key discriminator to suppress efficiently the large multijet background, and the remaining background is estimated directly from data. The search is performed using proton-proton collision data corresponding to an integrated luminosity of 16.1 fb - 1 , collected with the CMS detector in 2016. No significant excess of events is observed above the expected background. For the simplified dark matter model under consideration, SIMPs with masses up to 100 GeV are excluded and further sensitivity is explored towards higher masses
Search for an exotic decay of the Higgs boson to a pair of light pseudoscalars in the final state with two bquarks and two tau leptons in proton-proton collisions at root s=13 TeV The CMS Collaboration
- Author
- Aarrestad TK
- Abbaneo D
- Abbiendi G
- Abbrescia M
- Abdalla H
- Abdelalim AA
- Abdullah Wan WAT
- Abdullin S
- Abdulsalam A
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- Publication venue
- Publication date
- 01/01/2018
- Field of study
A search for an exotic decay of the Higgs boson to a pair of light pseudoscalar bosons is performed for the first time in the final state with two b quarks and two tau leptons. The search is motivated in the context of models of physics beyond the standard model (SM), such as two Higgs doublet models extended with a complex scalar singlet (2HDM + S), which include the next-to-minimal supersymmetric SM (NMSSM). The results are based on a data set of proton-proton collisions corresponding to an integrated luminosity of 35.9 fb(-1), accumulated by the CMS experiment at the LHC in 2016 at a center-of-mass energy of 13 TeV. Masses of the pseudoscalar boson between 15 and 60 GeVare probed, and no excess of events above the SM expectation is observed. Upper limits between 3 and 12% are set on the branching fraction B(h -> aa -> 2 tau 2b) assuming the SM production of the Higgs boson. Upper limits are also set on the branching fraction of the Higgs boson to two light pseudoscalar bosons in different 2HDM + S scenarios. Assuming the SM production cross section for the Higgs boson, the upper limit on this quantity is as low as 20% for a mass of the pseudoscalar of 40 GeV in the NMSSM. (C) 2018 The Author(s). Published by Elsevier B.V.Peer reviewe
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