188 research outputs found
A Novel Role for PECAM-1 (CD31) in Regulating Haematopoietic Progenitor Cell Compartmentalization between the Peripheral Blood and Bone Marrow
- Author
- A Peled
- AJ Wagers
- AM Glodek
- B Heissig
- C Voermans
- Christopher D. Buckley
- CT Hua
- D Graesser
- D Zicha
- DE Jackson
- DE Wright
- DI Leavesley
- E Ferrero
- Emma J. Ross
- Ewan A. Ross
- FC Yang
- G Bazzoni
- G de Haan
- GA McQuibban
- GE Rainger
- Gerard Nash
- H Geiger
- HE Broxmeyer
- HG Kopp
- I Nelissen
- I Petit
- IB Mazo
- IL Weissman
- IN Bird
- JL Christensen
- JM Enciso
- Jon Frampton
- K Akashi
- K Hattori
- K Sagawa
- KA Reedquist
- KL Yong
- M Lenter
- M Maas
- MA Goodell
- MF de Bruijn
- MJ Kiel
- MX Wong
- N Ilan
- N Ilan
- Neena Kalia
- NJ Pumphrey
- NT Luu
- PJ Newman
- PJ Newman
- S Lee
- Sian Lax
- SK Nilsson
- SM Watt
- ST Avecilla
- Steve P. Watson
- Stuart Egginton
- Sylvie Freeman
- T Papayannopoulou
- T Sugiyama
- Tarvinder S. Dhanjal
- Tie Zheng Hou
- TS Dhanjal
- V Ling
- WA Slieker
- Willliam F. Wade
- Y Katayama
- Y Nakamura
- Y Wu
- Yan Zhao
- Z Ahmed
- Zubair Ahmed
- Publication venue
- Public Library of Science
- Publication date
- 01/06/2008
- Field of study
Although the expression of PECAM-1 (CD31) on vascular and haematopoietic cells within the bone marrow microenvironment has been recognized for some time, its physiological role within this niche remains unexplored. In this study we show that PECAM-1 influences steady state hematopoietic stem cell (HSC) progenitor numbers in the peripheral blood but not the bone marrow compartment. PECAM-1−/− mice have higher levels of HSC progenitors in the blood compared to their littermate controls. We show that PECAM-1 is required on both progenitors and bone marrow vascular cells in order for efficient transition between the blood and bone marrow to occur. We have identified key roles for PECAM-1 in both the regulation of HSC migration to the chemokine CXCL12, as well as maintaining levels of the matrix degrading enzyme MMP-9 in the bone marrow vascular niche. Using intravital microscopy and adoptive transfer of either wild type (WT) or PECAM-1−/− bone marrow precursors, we demonstrate that the increase in HSC progenitors in the blood is due in part to a reduced ability to migrate from blood to the bone marrow vascular niche. These findings suggest a novel role for PECAM-1 as a regulator of resting homeostatic progenitor cell numbers in the bloo
Feebly-interacting particles: FIPs 2022 Workshop Report
- Author
- Antel C
- Battaglieri M
- Beacham J
- Boehm C
- Buchmüller O
- Calore F
- Carenza P
- Chauhan B
- Cladè P
- Coloma P
- Crivelli P
- Dandoy V
- Darmé L
- De Roeck A
- Deppisch FF
- Dey B
- Drewes M
- Echenard B
- Flambaum VV
- Foldenauer P
- Gatti C
- Giannotti M
- Golutvin A
- Gonzalez-Garcia MC
- Gori S
- Goudzovski E
- Granelli A
- Grote H
- Guellati-Khelifa S
- Hajer J
- Harris P
- Hearty C
- Heuchel D
- Hostert M
- Junius S
- Kahlhoefer F
- Klaric J
- Kling F
- Klose P
- Knolle J
- Kopp J
- Kwon O
- Lanfranchi G
- Lantwin O
- Li L
- Lindner A
- Lopez-Pavon J
- Marocco J
- Martin JW
- Middleton S
- Milstead S
- Oceano I
- O’Hare CAJ
- Paoloni A
- Pascoli S
- Petcov ST
- Pospelov M
- Pöttgen R
- Raggi M
- Ripellino G
- Samsonov IB
- Sandner S
- Shelton J
- Song N
- Stadnik YV
- Sun C
- Söldner-Rembold S
- Tastet JL
- Toro N
- Tran N
- Trevisani N
- Ulmer S
- Urrea S
- Velghe B
- Wallisch B
- Wong YYY
- Zorbilmez C
- Zurek K
- Publication venue
- 'Springer Science and Business Media LLC'
- Publication date
- 11/12/2023
- Field of study
Particle physics today faces the challenge of explaining the mystery of dark matter, the origin of matter over anti-matter in the Universe, the origin of the neutrino masses, the apparent fine-tuning of the electro-weak scale, and many other aspects of fundamental physics. Perhaps the most striking frontier to emerge in the search for answers involves new physics at mass scales comparable to familiar matter, below the GeV-scale, or even radically below, down to sub-eV scales, and with very feeble interaction strength. New theoretical ideas to address dark matter and other fundamental questions predict such feebly interacting particles (FIPs) at these scales, and indeed, existing data provide numerous hints for such possibility. A vibrant experimental program to discover such physics is under way, guided by a systematic theoretical approach firmly grounded on the underlying principles of the Standard Model. This document represents the report of the FIPs 2022 workshop, held at CERN between the 17 and 21 October 2022 and aims to give an overview of these efforts, their motivations, and the decadal goals that animate the community involved in the search for FIPs
Solitary median maxillary central incisor (SMMCI) syndrome
- Author
- A Verloes
- AK Holm
- AR Simon
- B Boudailliez
- BD Vanzieleghem
- BW Small
- ChA Righini
- DC Scott
- DJ Aughton
- E Mass
- E Mofson
- E Roessler
- E Tavin
- EB Rappaport
- ED Fulstow
- EY Chan
- F Cole
- F Parentin
- FP Santoro
- FS Lo
- G Captier
- H Arlis
- H Hattori
- HG Artman
- HS Heussler
- I Buntinx
- I Kjaer
- I Kjaer
- IB Kjellin
- J Suss
- JA Golden
- JK Huang
- JK Huang
- JL Rubenstein
- JP Fryns
- JR Hayward
- K Youko
- KB Becktor
- L Garavelli
- L Nanni
- LM Dolan
- M Harrison
- M Marini
- M Masuno
- M Miura
- M Muenke
- M Vanelli
- ML Hunter
- MM Cohen Jr
- MM Cohen Jr
- MM Cohen Jr
- OM Yassin
- P Fleming
- PJ Walker
- PR Parker
- RK Hall
- RK Hall
- RK Wesley
- RM Liberfarb
- RM Winter
- Roger K Hall
- RS Tubbs
- S Bamba
- S Oberoi
- SA Berry
- SA Berry
- SA Royal
- SC Maréchaux
- SG Frints
- SG Kocsis
- SM Matthai
- T Van Den Abbeele
- U Hehr
- U Moog
- W Bacon
- W Kopp
- Publication venue
- BioMed Central
- Publication date
- 01/04/2006
- Field of study
Solitary median maxillary central incisor syndrome (SMMCI) is a complex disorder consisting of multiple, mainly midline defects of development resulting from unknown factor(s) operating in utero about the 35th–38th day(s) from conception. It is estimated to occur in 1:50,000 live births. Aetiology is uncertain. Missense mutation in the SHH gene (I111F) at 7q36 may be associated with SMMCI. The SMMCI tooth differs from the normal central incisor, in that the crown form is symmetric; it develops and erupts precisely in the midline of the maxillary dental arch in both primary and permanent dentitions. Congenital nasal malformation (choanal atresia, midnasal stenosis or congenital pyriform aperture stenosis) is positively associated with SMMCI. The presence of an SMMCI tooth can predict associated anomalies and in particular the serious anomaly holoprosencephaly. Common congenital anomalies associated with SMMCI are: severe to mild intellectual disability, congenital heart disease, cleft lip and/or palate and less frequently, microcephaly, hypopituitarism, hypotelorism, convergent strabismus, oesophageal and duodenal atresia, cervical hemivertebrae, cervical dermoid, hypothyroidism, scoliosis, absent kidney, micropenis and ambiguous genitalia. Short stature is present in half the children. Diagnosis should be made by eight months of age, but can be made at birth and even prenatally at 18–22 weeks from the routine mid-trimester ultrasound scan. Management depends upon the individual anomalies present. Choanal stenosis requires emergency surgical treatment. Short stature may require growth hormone therapy. SMMCI tooth itself is mainly an aesthetic problem, which is ideally managed by combined orthodontic, prosthodontic and oral surgical treatment; alternatively, it can be left untreated
Methods for the guideline-based development of quality indicators--a systematic review
- Author
- A Advani
- A Donabedian
- A Hutchinson
- AHCPR
- AHRQ
- AM Hardy
- AQUA-Institut
- B Sens
- BD Frijling
- BJ LaClair
- CE Desch
- Center for Reviews and Dissemination
- CH MacLean
- CJ Wang
- DA Bergman
- DC Hadorn
- DS Lee
- E Blozik
- E Van Den Boogaard
- EA McGlynn
- EA McGlynn
- EJ Kongnyuy
- Eva Blozik
- FF Duffy
- FI Burge
- H Wollersheim
- HM Hearnshaw
- HM Krumholz
- HS Hermanides
- I Draskovic
- IB Kopp
- J Mainz
- J Mainz
- J Mainz
- J Yazdany
- JA Schouten
- JA Spertus
- JD Scinto
- JR Sugarman
- JV Tu
- K Light
- KN Lohr
- L Martirosyan
- LT van Hulst
- M Ouwens
- MA Radtke
- Martin Scherer
- MJ Nijkrake
- MM Ouwens
- MN Marshall
- NA Estes III
- P Giesen
- PA James
- R Baker
- RF Redberg
- RH Brook
- RH Brook
- RH Brook
- RH Brook
- RJ Thomas
- RM Califf
- RO Bonow
- RPMG Hermens
- SA Forbes
- SM Campbell
- SM Campbell
- SM Campbell
- SM Mourad
- T Kötter
- Thomas Kötter
- WE Golden
- WJ Graham
- ÄZQ (Ärztliches Zentrum für Qualität in der Medizin)
- Publication venue
- BioMed Central
- Publication date
- 01/01/2012
- Field of study
<p>Abstract</p> <p>Background</p> <p>Quality indicators (QIs) are used in many healthcare settings to measure, compare, and improve quality of care. For the efficient development of high-quality QIs, rigorous, approved, and evidence-based development methods are needed. Clinical practice guidelines are a suitable source to derive QIs from, but no gold standard for guideline-based QI development exists. This review aims to identify, describe, and compare methodological approaches to guideline-based QI development.</p> <p>Methods</p> <p>We systematically searched medical literature databases (Medline, EMBASE, and CINAHL) and grey literature. Two researchers selected publications reporting methodological approaches to guideline-based QI development. In order to describe and compare methodological approaches used in these publications, we extracted detailed information on common steps of guideline-based QI development (topic selection, guideline selection, extraction of recommendations, QI selection, practice test, and implementation) to predesigned extraction tables.</p> <p>Results</p> <p>From 8,697 hits in the database search and several grey literature documents, we selected 48 relevant references. The studies were of heterogeneous type and quality. We found no randomized controlled trial or other studies comparing the ability of different methodological approaches to guideline-based development to generate high-quality QIs. The relevant publications featured a wide variety of methodological approaches to guideline-based QI development, especially regarding guideline selection and extraction of recommendations. Only a few studies reported patient involvement.</p> <p>Conclusions</p> <p>Further research is needed to determine which elements of the methodological approaches identified, described, and compared in this review are best suited to constitute a gold standard for guideline-based QI development. For this research, we provide a comprehensive groundwork.</p
Non-classical forms of pemphigus: pemphigus herpetiformis, IgA pemphigus, paraneoplastic pemphigus and IgG/IgA pemphigus
- Author
- Adriana Maria Porro
- Amagai M
- Amagai M
- Amagai M
- Amagai M
- Amagai M
- Anhalt GJ
- Anhalt GJ
- Arranz D
- Asahina A
- Barrance VP
- Beutner EH
- Borradori L
- Bruckner AL
- Bull RH
- Buxton RS
- Camisa C
- Chan LS
- Chan LS
- Chorzelski TP
- Chorzelski TP
- Cozzani E
- Cunha PR
- Czernik A
- DeMento FJ
- Duarte IB
- Durham A
- Düker I
- Emmerson RW
- Fang Y
- Feng SY
- Fernandes IC
- Floden CH
- Fullerton SH
- Gengoux P
- Gooptu C
- Gruss C
- Hashimoto T
- Hashimoto T
- Hashimoto T
- Hashimoto T
- Hashimoto T
- Hashimoto T
- Hashimoto T
- Heng A
- Hertl M
- Hodak E
- Horn TD
- Hosoda S
- Howell SM
- Huff JC
- Huhn KM
- Iida K
- Ingber A
- Inui S
- Ishii K
- Ishii N
- Jablonska S
- Kaplan I
- Kimyai-Asadi A
- Kitajima Y
- Kopp T
- Kowalewski C
- Kozlowska A
- Kubo A
- Kubota Y
- Laura de Sena Nogueira Maehara
- Lebeau S
- Leger S
- Leithauser LA
- Liu Q
- Livia de Vasconcelos Nasser Caetano
- Lu Y
- Lutz ME
- Maciejowska E
- Maldonado F
- Marinovic B
- Martel P
- Maruyama H
- Marzano AV
- Mentink LF
- Micali G
- Miida H
- Milvia Maria dos Santos Enokihara
- Mimouni D
- Mimouni D
- Miura T
- Miyagawa S
- Miyagawa S
- Morita E
- Morizane S
- Moutran R
- Müller R
- Nakajima K
- Nakashima H
- Nguyen VT
- Nishikawa T
- Nousari HC
- Nousari HC
- O'Toole EA
- Ohata C
- Ohyama B
- Oiso N
- Palleschi GM
- Patrício P
- Prado R
- Qian SX
- Robinson ND
- Ruiz-Genao DP
- Sanchez-Palacios C
- Santi CG
- Santiago-et-Sánchez-Mateos D
- Schepens I
- Seah PP
- Sklavounou A
- Sneddon I
- Sneddon IB
- Szturz P
- Tagami H
- Taintor AR
- Tajima M
- Tateishi C
- Tsuruta D
- Verdier-Sevrain S
- Wakahara M
- Wallach D
- Wallach D
- Wang J
- Wang J
- Weston WL
- Yasuda H
- Zaraa I
- Zaraa I
- Zhu X
- Zimmermann J
- Publication venue
- 'FapUNIFESP (SciELO)'
- Publication date
- 01/01/2014
- Field of study
The pemphigus group comprises the autoimmune intraepidermal blistering diseases classically divided into two major types: pemphigus vulgaris and pemphigus foliaceous. Pemphigus herpetiformis, IgA pemphigus, paraneoplastic pemphigus and IgG/IgA pemphigus are rarer forms that present some clinical, histological and immunopathological characteristics that are different from the classical types. These are reviewed in this article. Future research may help definitively to locate the position of these forms in the pemphigus group, especially with regard to pemphigus herpetiformis and the IgG/ IgA pemphigus.Universidade Federal de São Paulo (UNIFESP), Escola Paulista de Medicina (EPM) Dermatology DepartmentUniversidade Federal de São Paulo (UNIFESP), Escola Paulista de Medicina (EPM) Dermatology and Pathology DepartmentsUNIFESP, EPM, Dermatology DepartmentUNIFESP, EPM, Dermatology and Pathology DepartmentsSciEL
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
- Abercrombie D
- Acharya H
- Acosta D
- Acosta JG
- Adam W
- Adams E
- Adams MR
- Adams T
- Adloff C
- Adzic P
- Agapitos A
- Agarwal G
- Aggleton R
- Agram J-L
- Aguilar-Benitez M
- Ahmad A
- Ahmad M
- Ahmed A
- Ahuja S
- Aime C
- 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
- Amendola C
- Amin N
- Amram O
- Amsler C
- Anagnostou G
- Andrea J
- Andreev V
- Andreev Y
- Andrews MB
- Androsov K
- 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
- Aspell P
- Atakisi IO
- Atanassov I
- Ather MW
- Attikis A
- Auffray E
- Aushev T
- Auzinger G
- Avati V
- Avery P
- Avila C
- Awais A
- Awan MIM
- Ayala E
- Ayala G
- 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
- Baginyan A
- Bagliesi G
- Bahinipati S
- Baillon P
- Bainbridge R
- Bakas G
- Bakhshiansohi H
- Bakirci MN
- Baldenegro Barrera C
- Ball AH
- Ban Y
- Band R
- Bandyopadhyay H
- 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
- Bastos D
- Battilana C
- Baty A
- Bauer G
- Bauerdick LAT
- Baxter S
- Bayshev I
- Bean A
- Beauceron S
- Beaudette F
- Becerril Gonzalez H
- Bechtel J
- Bedoya CF
- 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
- Berardi V
- Berenguer Antequera J
- Beretvas A
- Bergauer T
- Berger P
- Berger T
- Beri SB
- Bermúdez Martínez A
- Bernardes CA
- Bernet C
- Berretti M
- Berry D
- Berryhill J
- Bertacchi V
- Besancon M
- Beschi A
- Bhal E
- 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
- 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
- Bonham B
- 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
- Bottigli U
- Boudoul G
- Bouhali O
- Bourgatte G
- Bourilkov D
- Bozzo M
- Bragagnolo A
- Braghieri A
- Braibant-Giacomelli S
- Brainerd C
- Brandao Malbouisson H
- Brandt S
- Branson JG
- 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
- Buchot Perraguin A
- Bueghly J
- Bundock A
- Bunkowski K
- Buontempo S
- Burkett K
- Burkhardt H
- Burkle B
- Burt K
- Bury F
- Busson P
- Busza W
- Butalla S
- Butler JN
- Butler PH
- Butz E
- Bylinkin A
- Bylsma B
- Cabrera A
- Cabrillo IJ
- Cadamuro L
- Cafagna FS
- Caillol C
- Cakir A
- 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
- Capeans Garrido M
- 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
- Catanesi MG
- 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
- Chaudhary G
- Chauhan S
- Chauhan S
- Chawla R
- Chazin Quero B
- Checchia P
- Chekhovsky V
- Chen C
- 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
- 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<sup>†</sup>
- 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
- 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
- Csanád M
- Csörgő 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 Leonardis F
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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
Evidence for Top Quark Production in Nucleus-Nucleus Collisions
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- Özçelik Ö
- Publication venue
- Publication date
- 01/01/2019
- Field of study
Peer reviewe
Search for dark matter produced in association with a Higgs boson decaying to a pair of bottom quarks in proton-proton collisions at root s=13TeV
- Author
- Aarrestad TK
- Abbaneo D
- Abbiendi G
- Abbrescia M
- Abdullah WATW
- Abdullin S
- Abercrombie D
- Acharya H
- Acosta D
- Acosta JG
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- Özçelik Ö
- Publication venue
- Publication date
- 01/01/2018
- Field of study
A search for dark matter produced in association with a Higgs boson decaying to a pair of bottom quarks is performed in proton-proton collisions at a center-of-mass energy of 13 TeV collected with the CMS detector at the LHC. The analyzed data sample corresponds to an integrated luminosity of 35.9 fb(-1). The signal is characterized by a large missing transverse momentum recoiling against a bottom quark-antiquark system that has a large Lorentz boost. The number of events observed in the data is consistent with the standard model background prediction. Results are interpreted in terms of limits both on parameters of the type-2 two-Higgs doublet model extended by an additional light pseudoscalar boson a (2HDM+a) and on parameters of a baryonic Z simplified model. The 2HDM+a model is tested experimentally for the first time. For the baryonic Z model, the presented results constitute the most stringent constraints to date.Peer reviewe
Observation of a New Excited Beauty Strange Baryon Decaying to Ξb- π+π-
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- Yi K
- Yigitbasi E
- Yohay R
- Yoo HD
- Yoo J
- Yoon I
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- Yu I
- Yu PR
- Yu SS
- Yuan L
- Yuan S
- 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
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- Zhao J
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- Zhokin A
- Zhu DH
- Zhu RY
- Ziemons T
- Zientek M
- Zlebcik R
- Zoi I
- Zolkapli Z
- Zorbakir IS
- Zorbilmez C
- Zotto P
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- Zuolo D
- Zygala L
- Álvarez Fernández A
- Özçelik Ö
- Publication venue
- American Physical Society
- Publication date
- 01/01/2021
- Field of study
The Ξb-π+π- invariant mass spectrum is investigated with an event sample of proton-proton collisions at s=13 TeV, collected by the CMS experiment at the LHC in 2016-2018 and corresponding to an integrated luminosity of 140 fb-1. The ground state Ξb- is reconstructed via its decays to J/ψΞ- and J/ψΛK-. A narrow resonance, labeled Ξb(6100)-, is observed at a Ξb-π+π- invariant mass of 6100.3±0.2(stat)±0.1(syst)±0.6(Ξb-) MeV, where the last uncertainty reflects the precision of the Ξb- baryon mass. The upper limit on the Ξb(6100)- natural width is determined to be 1.9 MeV at 95% confidence level. The low Ξb(6100)- signal yield observed in data does not allow a measurement of the quantum numbers of the new state. However, following analogies with the established excited Ξc baryon states, the new Ξb(6100)- resonance and its decay sequence are consistent with the orbitally excited Ξb- baryon, with spin and parity quantum numbers JP=3/2-
Observation of the B-s(0) -> X(3872)phi Decay
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- Publication venue
- Publication date
- 01/01/2020
- Field of study
Using a data sample of proton-proton collisions at root s = 13 TeV, corresponding to an integrated luminosity of 140 fb(-1) collected by the CMS experiment in 2016-2018, the B-s(0) -> X(3872)phi decay is observed. Decays into J/psi pi(+)pi(-) and K+K- are used to reconstruct, respectively, the X(3872) and phi. The ratio of the product of branching fractions B[B-s(0) -> X(3872)phi]B[X(3872) -> J/psi pi(+)pi(-)] to the product B[B-s(0) ->psi(2S)phi]B[psi(2S) -> J/psi pi(+)pi(-)] is measured to be [2.21 +/- 0.29(stat) +/- 0.17(syst)]%. The ratio B[B-s(0) -> X(3872)phi]/B[B-0 -> X(3872)K-0] is found to be consistent with one, while the ratio B[B-s(0) -> X(3872)phi]/B[B+-> X(3872)K+] is two times smaller. This suggests a difference in the production dynamics of the X(3872) in B-0 and B(0)s meson decays compared to B+. The reported observation may shed new light on the nature of the X(3872) particle.Peer reviewe
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