336 research outputs found
Reduced microvascular density in omental biopsies of children with chronic kidney disease
- Author
- A Adair
- A Edwards-Richards
- A Shimizu
- AE Rizzardi
- AK Bonamy
- AK Singh
- Anja Lingnau
- AR Pries
- AR Pries
- AS Go
- Axel Schneider
- B Schaefer
- Bernd Lahrmann
- Betti Schaefer
- Bruno Ranchin
- C Korn
- C Maric-Bilkan
- C Sabanayagam
- Christian Freise
- CJ Lockhart
- Claus Peter Schmitt
- D Collins
- D Fliser
- D Franke
- DH Kang
- Dorothea Burkhardt
- ED Tran
- F Baffert
- F Feihl
- F Stam
- G Mayer
- Gema Ariceta
- GJ Schwartz
- GS Di Marco
- Hamoud Nasser
- IB Lobov
- J Jacobi
- J Tornig
- Jaap A. Joles
- JF Carroll
- K Amann
- K Amann
- K Amann
- L Eklund
- M Baumann
- M Flisinski
- M Norman
- Maria Bartosova
- Michal Malina
- MJ Sarnak
- N Kobayashi
- Niels Grabe
- OH Thang
- P Brambilla
- Peter Sallay
- Petra Degenhardt
- PO Bonetti
- QL Ooi
- R Deva
- R Vanholder
- RA Gottlieb
- RC Shroff
- RC Shroff
- Rimante Cerkauskiene
- S David
- SC Nussenzweig
- TB Drueke
- TJ Anderson
- Uwe Querfeld
- YC Tsai
- YJ Hsu
- Publication venue
- 'Public Library of Science (PLoS)'
- Publication date
- 01/01/2016
- Field of study
Endothelial dysfunction is an early manifestation of cardiovascular disease (CVD) and consistently observed in patients with chronic kidney disease (CKD). We hypothesized that CKD is associated with systemic damage to the microcirculation, preceding macrovascular pathology. To assess the degree of "uremic microangiopathy", we have measured microvascular density in biopsies of the omentum of children with CKD.Omental tissue was collected from 32 healthy children (0-18 years) undergoing elective abdominal surgery and from 23 age-matched cases with stage 5 CKD at the time of catheter insertion for initiation of peritoneal dialysis. Biopsies were analyzed by independent observers using either a manual or an automated imaging system for the assessment of microvascular density. Quantitative immunohistochemistry was performed for markers of autophagy and apoptosis, and for the abundance of the angiogenesis-regulating proteins VEGF-A, VEGF-R2, Angpt1 and Angpt2.Microvascular density was significantly reduced in uremic children compared to healthy controls, both by manual imaging with a digital microscope (median surface area 0.61% vs. 0.95%, p<0.0021 and by automated quantification (total microvascular surface area 0.89% vs. 1.17% p = 0.01). Density measured by manual imaging was significantly associated with age, height, weight and body surface area in CKD patients and healthy controls. In multivariate analysis, age and serum creatinine level were the only independent, significant predictors of microvascular density (r2 = 0.73). There was no immunohistochemical evidence for apoptosis or autophagy. Quantitative staining showed similar expression levels of the angiogenesis regulators VEGF-A, VEGF-receptor 2 and Angpt1 (p = 0.11), but Angpt2 was significantly lower in CKD children (p = 0.01).Microvascular density is profoundly reduced in omental biopsies of children with stage 5 CKD and associated with diminished Angpt2 signaling. Microvascular rarefaction could be an early systemic manifestation of CKD-induced cardiovascular disease
mKikGR, a Monomeric Photoswitchable Fluorescent Protein
- Author
- A Miyawaki
- A Sawano
- Anna B. Kochaniak
- Antoine M. van Oijen
- Atsushi Miyawaki
- C Flors
- C Geisler
- DM Chudakov
- DM Chudakov
- DM Chudakov
- E Betzig
- GH Patterson
- GS Baird
- H Mizuno
- H Shroff
- H Tsutsui
- Hidekazu Tsutsui
- I Hayashi
- J Lippincott-Schwartz
- J Wiedenmann
- J Zhang
- K Nienhaus
- KA Lukyanov
- M Cotlet
- MJ Rust
- NG Gurskaya
- PS Dittrich
- R Ando
- R Ando
- R Heim
- RC Cadwell
- RE Thompson
- RY Tsien
- S Habuchi
- S Habuchi
- S Habuchi
- Satoshi Habuchi
- Shuguang Zhang
- ST Hess
- VV Verkhusha
- Publication venue
- Public Library of Science
- Publication date
- 01/01/2008
- Field of study
The recent demonstration and utilization of fluorescent proteins whose fluorescence can be switched on and off has greatly expanded the toolkit of molecular and cell biology. These photoswitchable proteins have facilitated the characterization of specifically tagged molecular species in the cell and have enabled fluorescence imaging of intracellular structures with a resolution far below the classical diffraction limit of light. Applications are limited, however, by the fast photobleaching, slow photoswitching, and oligomerization typical for photoswitchable proteins currently available. Here, we report the molecular cloning and spectroscopic characterization of mKikGR, a monomeric version of the previously reported KikGR that displays high photostability and switching rates. Furthermore, we present single-molecule imaging experiments that demonstrate that individual mKikGR proteins can be localized with a precision of better than 10 nanometers, suggesting their suitability for super-resolution imaging
Microcalcifications in breast cancer: novel insights into the molecular mechanism and functional consequence of mammary mineralisation.
- Author
- A Bellahcene
- A Bellahcene
- A Gericke
- A Hernandez-Santana
- A Lochter
- A Shioi
- A Yavorskyy
- AJ Evans
- AL Boskey
- AM Simao
- AS Haka
- BK Seo
- BL Eckhardt
- C Maniatopoulos
- C Peacock
- CJ Aslakson
- CM Büsing
- CM Giachelli
- CM Giachelli
- DGA Nelson
- DR Chen
- E Mansson
- E Thurfjell
- EA McSherry
- ES Tomlinson
- G McMahon
- GK Hunter
- GS Stein
- H Murer
- H Orimo
- J Chen
- J H Harmey
- JB Lian
- JJ James
- JN VanHouten
- KA Lomashvili
- L Frappart
- L Frappart
- L Hughes
- L Tabar
- M Gulsun
- M Keykhosravani
- M Lelekakis
- M P Morgan
- MJ Coelho
- MJ Radi
- MM Cooke
- MP Morgan
- PH Rolland
- R Baker
- R F Cox
- R Robison
- RC Shroff
- S Hofvind
- S Ramdass
- SS Virk
- T Kirsch
- T Standal
- TA Owen
- TC Holme
- W Jahnen-Dechent
- WN Addison
- X Wang
- Publication venue
- e-publications@RCSI
- Publication date
- 10/01/2012
- Field of study
BACKGROUND: Mammographic microcalcifications represent one of the most reliable features of nonpalpable breast cancer yet remain largely unexplored and poorly understood.
METHODS: We report a novel model to investigate the in vitro mineralisation potential of a panel of mammary cell lines. Primary mammary tumours were produced by implanting tumourigenic cells into the mammary fat pads of female BALB/c mice.
RESULTS: Hydroxyapatite (HA) was deposited only by the tumourigenic cell lines, indicating mineralisation potential may be associated with cell phenotype in this in vitro model. We propose a mechanism for mammary mineralisation, which suggests that the balance between enhancers and inhibitors of physiological mineralisation are disrupted. Inhibition of alkaline phosphatase and phosphate transport prevented mineralisation, demonstrating that mineralisation is an active cell-mediated process. Hydroxyapatite was found to enhance in vitro tumour cell migration, while calcium oxalate had no effect, highlighting potential consequences of calcium deposition. In addition, HA was also deposited in primary mammary tumours produced by implanting the tumourigenic cells into the mammary fat pads of female BALB/c mice.
CONCLUSION: This work indicates that formation of mammary HA is a cell-specific regulated process, which creates an osteomimetic niche potentially enhancing breast tumour progression. Our findings point to the cells mineralisation potential and the microenvironment regulating it, as a significant feature of breast tumour development
Patient, tumor, and healthcare factors associated with regional variability in lung cancer survival: a Spanish high‑resolution population‑based study
- Author
- A Micheli
- A Redondo-Sendino
- AG Sacher
- C Aggarwal
- C Allemani
- C. García
- CM Tammemagi
- D Salmerón
- D. Petrova
- E-R Salomaa
- E. Bayo
- E. Salamanca-Fernández
- GS Shroff
- H Skuladottir
- I Corazziari
- J Galceran
- J. Expósito
- J. Tallón
- JB Fu
- JJ Sánchez-Cruz
- JP Wisnivesky
- L Xie
- LA Torre
- LM Woods
- LT Nordquist
- M Lembicz
- M Mun
- M Sant
- M. A. Luque-Fernandez
- M. L. Fajardo
- M. Rodríguez-Barranco
- M. Sant
- M.-J. Sánchez
- MCS Wong
- MD Chirlaque
- ME Charlson
- MJ Viñas Casasola
- MP Perme
- N Nishinarita
- P Leyn De
- P. Minicozzi
- PW Dickman
- R Angelis De
- R Moore
- S Francisci
- S Gandini
- StataCorp
- V Groot De
- WA Fry
- WM Alberts
- Y Tsunezuka
- Y.-L. Chang-Chan
- YK Tan
- Publication venue
- 'Springer Science and Business Media LLC'
- Publication date
- 19/10/2018
- Field of study
Purpose
The third most frequently diagnosed cancer in Europe in 2018 was lung cancer; it is also the leading cause of cancer death in Europe. We studied patient and tumor characteristics, and patterns of healthcare provision explaining regional variability in lung cancer survival in southern Spain.
Methods
A population-based cohort study included all 1196 incident first invasive primary lung cancer (C33–C34 according to ICD-10) cases diagnosed between 2010 and 2011 with follow-up until April 2015. Data were drawn from local population-based cancer registries and patients’ hospital medical records from all public and private hospitals from two regions in southern Spain.
Results
There was evidence of regional differences in lung cancer late diagnosis (58% stage IV in Granada vs. 65% in Huelva, p value < 0.001). Among patients with stage I, only 67% received surgery compared with 0.6% of patients with stage IV. Patients treated with a combination of radiotherapy, chemotherapy, and surgery had a 2-year mortality risk reduction of 94% compared with patients who did not receive any treatment (excess mortality risk 0.06; 95% CI 0.02–0.16). Geographical differences in survival were observed between the two regions: 35% vs. 26% at 1-year since diagnosis.
Conclusions
The observed geographic differences in survival between regions are due in part to the late cancer diagnosis which determines the use of less effective therapeutic options. Results from our study justify the need for promoting lung cancer early detection strategies and the harmonization of the best practice in lung cancer management and treatment.Maria Jose Sanchez Perez is supported by the Andalusian Department of Health: Research, Development, and Innovation Office project grant PI-0152/2017. Miguel Angel Luque-Fernandez is supported by the Spanish National Institute of Health, Carlos III Miguel Servet I Investigator Award (CP17/00206)
Eating disorders: the current status of molecular genetic research
- Author
- A Dempfle
- A Frisch
- A Hinney
- A Hinney
- A Hinney
- A Hinney
- A Hinney
- A Hinney
- A Hinney
- A Hinney
- A Hinney
- A Hinney
- A Hinney
- A Karwautz
- A Kipman
- A Ziegler
- AJ Holland
- AJ Holland
- AJ Walley
- American Psychiatric Association (APA)
- Anke Hinney
- AS Kaplan
- AW Bergen
- AW Bergen
- B Devlin
- B Nacmias
- B Xu
- C Dong
- C Lopez
- C Vaisse
- C Vaisse
- CG Fairburn
- CG Fairburn
- CM Bulik
- CM Bulik
- CM Bulik
- CM Bulik
- CM Bulik
- D Sundaramurthy
- DA Campbell
- DA Collier
- DC Jimerson
- DD Di Bella
- DE Grice
- E Michaelovsky
- E Mikołajczyk
- E Nisoli
- EE Walters
- EE Walters
- EH Young
- ES Gershon
- F Fumeron
- F Geller
- F Rybakowski
- F Rybakowski
- G Hasler
- G Thorleifsson
- GS Yeo
- H Frieling
- H Frieling
- H Frieling
- H Shroff
- I Gottesman
- IS Farooqi
- J Flint
- J Frey
- J Hager
- J Hebebrand
- J Hebebrand
- J Hebebrand
- J Hebebrand
- J Hebebrand
- J Hebebrand
- J Holliday
- J Little
- J Ott
- JC Halford
- JE Blundell
- JH Moore
- JL Treasure
- JM Mercader
- JM Mercader
- Johannes Hebebrand
- K Holtkamp
- KA Gendall
- KL Klump
- KL Klump
- KL Klump
- KL Klump
- KM Brown
- L Bruins-Slot
- M Dmitrzak-Weglarz
- M Gabrovsek
- M Haluzík
- M Koronyo-Hamaoui
- M Misra
- M Ribases
- M Ribasés
- M Ribasés
- M Ribasés
- M Strober
- M Strober
- MA Enoch
- MC Slof-Op ‘t Landt
- MJ Khoury
- MM Swarbrick
- N Lauzurica
- N Matejek
- N Nishiguchi
- N Potoczna
- NB Freimer
- ND Quinton
- NH Golden
- P Boutin
- P Gorwood
- P Gorwood
- P Gorwood
- P Monteleone
- R Bachner-Melman
- R Branson
- RA Price
- RD Levitan
- RD Levitan
- RE Urwin
- RE Urwin
- RJ Wurtman
- RM Dardennes
- RS Ahima
- S Cichon
- S Ehrlich
- S Friedel
- S Grinspoon
- S Herpertz
- S Matsushita
- S Saito
- S Sorbi
- SA Bacanu
- SE Mazzeo
- SM Wilksch
- Susann Scherag
- T Ando
- T Vink
- TD Brewerton
- TD Müller
- TM Frayling
- V Di Marzo
- V Haas
- V Ricca
- VC Barry
- W Kaye
- WH Kaye
- WH Kaye
- WH Kaye
- WH Kaye
- WH Kaye
- WH Kaye
- World Health Organization
- Z Siegfried
- Publication venue
- Springer-Verlag
- Publication date
- 01/01/2009
- Field of study
Anorexia nervosa (AN) and bulimia nervosa (BN) are complex disorders characterized by disordered eating behavior where the patient’s attitude towards weight and shape, as well as their perception of body shape, are disturbed. Formal genetic studies on twins and families suggested a substantial genetic influence for AN and BN. Candidate gene studies have initially focused on the serotonergic and other central neurotransmitter systems and on genes involved in body weight regulation. Hardly any of the positive findings achieved in these studies were unequivocally confirmed or substantiated in meta-analyses. This might be due to too small sample sizes and thus low power and/or the genes underlying eating disorders have not yet been analyzed. However, some studies that also used subphenotypes (e.g., restricting type of AN) led to more specific results; however, confirmation is as yet mostly lacking. Systematic genome-wide linkage scans based on families with at least two individuals with an eating disorder (AN or BN) revealed initial linkage regions on chromosomes 1, 3 and 4 (AN) and 10p (BN). Analyses on candidate genes in the chromosome 1 linkage region led to the (as yet unconfirmed) identification of certain variants associated with AN. Genome-wide association studies are under way and will presumably help to identify genes and pathways involved in these eating disorders. The elucidation of the molecular mechanisms underlying eating disorders might improve therapeutic approaches
Muon reconstruction and identification efficiency in ATLAS using the full Run 2 pp collision data set at \sqrt{s}=13 TeV
- Author
- Aad G
- Abbott B
- Abbott DC
- Abeling K
- Abhayasinghe DK
- Abidi SH
- AbouZeid OS
- Abraham NL
- Abramowicz H
- Abreu H
- Abud AA
- Abulaiti Y
- Acharya BS
- Achkar B
- Adam L
- Adamczyk L
- Adamek L
- Adelman J
- Adiguzel A
- Adorni S
- Adye T
- Affolder AA
- Afik Y
- Agapopoulou C
- Agaras MN
- Aggarwal A
- Agheorghiesei C
- Aguilar-Saavedra JA
- Agullo PM
- Ahmad A
- Ahmadov F
- Ahmed WS
- Ahnen JV
- Ai X
- Aielli G
- Akatsuka S
- Akbiyik M
- Akesson TPA
- Akilli E
- Akimov AV
- Alberghi GL
- Albert J
- Alderweireldt S
- Aleksa M
- Aleksandrov IN
- Alexa C
- Alexopoulos T
- Alfonsi A
- Alfonsi F
- Alhroob M
- Ali B
- Ali S
- Aliev M
- Alimonti G
- Allaire C
- Allbrooke BMM
- Allen BW
- Allport PP
- Aloisio A
- Alonso F
- Alpigiani C
- Alves FLL
- Alviggi MG
- Ambler A
- Ambroz L
- Amelung C
- Amidei D
- Amoroso S
- Amrouche CS
- An F
- Anastopoulos C
- Andari N
- Andeen T
- Anders JK
- Andrean SY
- Andreazza A
- Andrei V
- Anelli CR
- Angelidakis S
- Angerami A
- Anisenkov AV
- Annovi A
- Antel C
- Anthony MT
- Antipov E
- Antonelli M
- Antrim DJA
- Anulli F
- Aoki M
- Aparo MA
- Aranda CP
- Aranzabal N
- Araya ST
- Arcangeletti C
- Arce ATH
- Arguin J-F
- Argyropoulos S
- Arling J-H
- Armbruster AJ
- Armstrong A
- Arnaez O
- Arnold H
- Artoni G
- Asada H
- Asai K
- Asai S
- Asawatavonvanich T
- Asbah NA
- Asimakopoulou EM
- Asquith L
- Assahsah J
- Assamagan K
- Astalos R
- Astigarraga MEP
- Atkin RJ
- Atkinson M
- Atlay NB
- Atmani H
- Atmasiddha PA
- Augsten K
- Austrup VA
- Avolio G
- Ayoub MK
- Azuelos G
- Babal D
- Bachacou H
- Bachas K
- Backman F
- Bagnaia P
- Bahilo JJL
- Bahrasemani H
- Bailey AJ
- Bailey VR
- Baines JT
- Bakalis C
- Baker OK
- Bakker PJ
- Bakos E
- Balaji S
- Balasubramanian R
- Baldin EM
- Balek P
- Balli F
- Balunas WK
- Balz J
- Banas E
- Bandieramonte M
- Bandyopadhyay A
- Banerjee S
- Barak L
- Barbe WM
- Barberio EL
- Barberis D
- Barbero M
- Barbour G
- Barillari T
- Barisits M-S
- Barkeloo J
- Barklow T
- Barnea R
- Barnett BM
- Barnett RM
- Barnovska-Blenessy Z
- Baroncelli A
- Barone G
- Barr AJ
- Barreiro F
- Barron U
- Barsov S
- Bartels F
- Bartoldus R
- Bartolini G
- Barton AE
- Bartos P
- Basalaev A
- Basan A
- Bassalat A
- Basso MJ
- Bates RL
- Batlamous S
- Batley JR
- Batool B
- Battaglia M
- Bauce M
- Bauer F
- Bauer P
- Bawa HS
- Bayirli A
- Beacham JB
- Beau T
- Beauchemin PH
- Becherer F
- Bechtle P
- Beck HC
- Beck HP
- Becker K
- Becot C
- Beddall A
- Beddall AJ
- Bednyakov VA
- Bedognetti M
- Bee CP
- Beermann TA
- Begalli M
- Begel M
- Behera A
- Behr JK
- Beisiegel F
- Belfkir M
- Bell AS
- Bella G
- Bella LA
- Bellagamba L
- Bellerive A
- Bellos P
- Beloborodov K
- Belotskiy K
- Belyaev NL
- Benchekroun D
- Benekos N
- Benhammou Y
- Benjamin DP
- Benoit M
- Bensinger JR
- Bentvelsen S
- Beresford L
- Beretta M
- Berge D
- Berger N
- Bergmann B
- Bergsten LJ
- Beringer J
- Berlendis S
- Berlingen JM
- Bernardi G
- Bernius C
- Bernlochner FU
- Berry T
- Berta P
- Berthold A
- Bertram IA
- Besson N
- Bethke S
- Betti A
- Bevan AJ
- Beyer J
- Bhatta S
- Bhattacharya DS
- Bhattarai P
- Bhopatkar VS
- Bi R
- Bianchi RM
- Biebel O
- Biedermann D
- Bielski R
- Bierwagen K
- Biesuz NV
- Biglietti M
- Billoud TRV
- Bindi M
- Bingul A
- Bini C
- Biondi S
- Birch-sykes CJ
- Birman M
- Bisanz T
- Biswal JP
- Biswas D
- Bitadze A
- Bittrich C
- Bjorke K
- Blazek T
- Bloch I
- Blocker C
- Blue A
- Blumenschein U
- Bobbink GJ
- Bobrovnikov VS
- Bocchetta SS
- Boeriu OEV
- Bogavac D
- Bogdanchikov AG
- Bohm C
- Boisvert V
- Bokan P
- Bolanos GR
- Bold T
- Bolz AE
- Bomben M
- Bona M
- Bonilla JS
- Boonekamp M
- Booth CD
- Borbely AG
- Borecka-Bielska HM
- Borgna LS
- Borisov A
- Borissov G
- Bortoletto D
- Bosca SR
- Boscherini D
- Bosman M
- Bostanabad MG
- Bouaouda K
- Boudreau J
- Bouhova-Thacker EV
- Boumediene D
- Bourdarios CA
- Boveia A
- Boyd J
- Boye D
- Boyko IR
- Bozson AJ
- Bracinik J
- Brahimi N
- Brandt G
- Brandt O
- Braren F
- Brau B
- Brau JE
- Brendlinger K
- Brener R
- Brenner L
- Brenner R
- Bressler S
- Bret MC
- Brickwedde B
- Briglin DL
- Britton D
- Britzger D
- Brock I
- Brock R
- Brooijmans G
- Brooks WK
- Brost E
- Brueers B
- Bruncko D
- Bruni A
- Bruni G
- Bruschi M
- Bruscino N
- Bryngemark L
- Buanes T
- Buat Q
- Buchholz P
- Buckley AG
- Budagov IA
- Buescher V
- Bugge MK
- Bulekov O
- Bullard BA
- Burch TJ
- Burdin S
- Burgard CD
- Burger AM
- Burghgrave B
- Burr JTP
- Burton CD
- Burzynski JC
- Buschmann E
- Bussey PJ
- Butler JM
- Buttar CM
- Butterworth JM
- Butti P
- Buttinger W
- Buzatu A
- Buzykaev AR
- Bylund OB
- Cabras G
- Caforio D
- Cai H
- Cairo VMM
- Cakir IT
- Cakir O
- Calace N
- Calafiura P
- Calderini G
- Calfayan P
- Callea G
- Caloba LP
- Caltabiano A
- Calvet D
- Calvet S
- Calvet TP
- Calvetti M
- Camarda S
- Camarri P
- Camelia EA
- Camerlingo MT
- Cameron D
- Camincher C
- Campana S
- Campanelli M
- Camplani A
- Canale V
- Canesse A
- Cantero J
- Cao T
- Cao Y
- Capriles FGD
- Capua M
- Cardarelli R
- Cardillo F
- Carducci G
- Carli I
- Carli T
- Carlino G
- Carlson BT
- Carlson EM
- Carminati L
- Carney RMD
- Caron S
- Carquin E
- Carra S
- Carratta G
- Carter JWS
- Carter TM
- Casado MP
- Casha AF
- Castiglia EG
- Castillo FL
- Castillo LRF
- Castro NF
- Catinaccio A
- Catmore JR
- Cattai A
- Cavaliere V
- Cavasinni V
- Celebi E
- Celli F
- Cerny K
- Cerqueira AS
- Cerri A
- Cerrito L
- Cerutti F
- Cervelli A
- Cetin SA
- Chadi Z
- Chakraborty D
- Chan J
- Chan WS
- Chan WY
- Chapman JD
- Chargeishvili B
- Charlton DG
- Charman TP
- Chatterjee M
- Chau CC
- Che S
- Chekanov S
- Chekulaev SV
- Chelkov GA
- Chen B
- Chen C
- Chen CH
- Chen H
- Chen H
- Chen J
- Chen J
- Chen J
- Chen S
- Chen SJ
- Chen X
- Chen Y
- Chen Y-H
- Cheng HC
- Cheng HJ
- Cheplakov A
- Cheremushkina E
- Cheu E
- Cheung K
- Chevalerias TJA
- Chevalier L
- Chiarella V
- Chiarelli G
- Chiodini G
- Chisholm AS
- Chitan A
- Chiu I
- Chiu YH
- Chizhov MV
- Choi K
- Chomont AR
- Chou Y
- Chow YS
- Christopher LD
- Chu MC
- Chu X
- Chudoba J
- Chwastowski JJ
- Chytka L
- Cieri D
- Ciesla KM
- Cindro V
- Cioara IA
- Ciocio A
- Cirotto F
- Citron ZH
- Citterio M
- Ciubotaru DA
- Ciungu BM
- Clark A
- Clark PJ
- Clawson SE
- Clement C
- Coadou Y
- Cobal M
- Coccaro A
- Cochran J
- Codina EP
- Cohen H
- Coimbra AEC
- Cole B
- Colijn AP
- Collot J
- Connell SH
- Connelly IA
- Constantinescu S
- Conventi F
- Cooper-Sarkar AM
- Cormier F
- Cormier KJR
- Cornell SD
- Corpe LD
- Corradi M
- Correia AMH
- Corrigan EE
- Corriveau F
- Costa MJ
- Costanza F
- Costanzo D
- Coutinho YA
- Cowan G
- Cowley JW
- Crane J
- Cranmer K
- Creager RA
- Crepe-Renaudin S
- Crescioli F
- Cristinziani M
- Croft V
- Crosetti G
- Cueto A
- Cui H
- Cukierman AR
- Cunningham WR
- Czekierda S
- Czodrowski P
- Czurylo MM
- D'amen G
- D'Amico V
- D'Auria S
- D'Eramo L
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- Zhao Z
- Zhemchugov A
- Zheng Z
- Zhong D
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- Zhou H
- Zhou M
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- Zhulanov V
- Zieminska D
- Zimine NI
- Zimmermann S
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- Ziolkowski M
- Zivkovic L
- Zobernig G
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- Zorbas TG
- Zou R
- Zwalinski L
- Publication venue
- 'Springer Fachmedien Wiesbaden GmbH'
- Publication date
- 01/01/2021
- Field of study
This article documents the muon reconstruction and identification efficiency obtained by the ATLAS experiment for 139 \hbox {fb}^{-1} of pp collision data at \sqrt{s}=13 TeV collected between 2015 and 2018 during Run 2 of the LHC. The increased instantaneous luminosity delivered by the LHC over this period required a reoptimisation of the criteria for the identification of prompt muons. Improved and newly developed algorithms were deployed to preserve high muon identification efficiency with a low misidentification rate and good momentum resolution. The availability of large samples of Z\rightarrow \mu \mu and J/\psi \rightarrow \mu \mu decays, and the minimisation of systematic uncertainties, allows the efficiencies of criteria for muon identification, primary vertex association, and isolation to be measured with an accuracy at the per-mille level in the bulk of the phase space, and up to the percent level in complex kinematic configurations. Excellent performance is achieved over a range of transverse momenta from 3 GeV to several hundred GeV, and across the full muon detector acceptance of |\eta |<2.7
Measurements of W+W−+ ≥ 1 jet production cross-sections in pp collisions at s = 13 TeV with the ATLAS detector
- Author
- Aad G
- Abbott B
- Abbott DC
- Abed Abud A
- Abeling K
- Abhayasinghe DK
- Abidi SH
- AbouZeid OS
- Abraham NL
- Abramowicz H
- Abreu H
- Abulaiti Y
- Abusleme Hoffman AC
- Acharya BS
- Achkar B
- Adam Bourdarios C
- Adam L
- Adamczyk L
- Adamek L
- Adelman J
- Adiguzel A
- Adorni S
- Adye T
- Affolder AA
- Afik Y
- Agapopoulou C
- Agaras MN
- Aggarwal A
- Agheorghiesei C
- Aguilar-Saavedra JA
- Ahmad A
- Ahmadov F
- Ahmed WS
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- Zhemchugov A
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- Zhulanov V
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- Zinonos Z
- Ziolkowski M
- Zoccoli A
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- Zwalinski L
- Åkesson TPA
- Öncel ÖO
- Ženiš T
- Živković L
- Publication venue
- 'Springer Science and Business Media LLC'
- Publication date
- 01/06/2021
- Field of study
Fiducial and differential cross-section measurements of W+W− production in
association with at least one hadronic jet are presented. These measurements are sensitive
to the properties of electroweak-boson self-interactions and provide a test of perturbative
quantum chromodynamics and the electroweak theory. The analysis is performed using
proton-proton collision data collected at p
s = 13TeV with the ATLAS experiment, corresponding
to an integrated luminosity of 139 fb−1. Events are selected with exactly one oppositely
charged electron-muon pair and at least one hadronic jet with a transverse momentum
of pT > 30 GeV and a pseudorapidity of |�| < 4.5. After subtracting the background
contributions and correcting for detector effects, the jet-inclusive W+W−+ � 1 jet fiducial
cross-section and W+W−+ jets differential cross-sections with respect to several kinematic
variables are measured. These measurements include leptonic quantities, such as the lepton
transverse momenta and the transverse mass of the W+W− system, as well as jet-related
observables such as the leading jet transverse momentum and the jet multiplicity. Limits on
anomalous triple-gauge-boson couplings are obtained in a phase space where interference
between the Standard Model amplitude and the anomalous amplitude is enhanced
Measurements of differential cross-sections in top-quark pair events with a high transverse momentum top quark and limits on beyond the Standard Model contributions to top-quark pair production with the ATLAS detector at √s = 13 TeV
- Author
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- Abbott B
- Abbott DC
- Abeling K
- Abhayasinghe DK
- Abidi SH
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- Zhemchugov A
- Zheng Z
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- Zieminska D
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- Publication venue
- 'Springer Science and Business Media LLC'
- Publication date
- 01/01/2022
- Field of study
Cross-section measurements of top-quark pair production where the hadronically decaying top quark has transverse momentum greater than 355 GeV and the other top quark decays into ℓνb are presented using 139 fb−1 of data collected by the ATLAS experiment during proton-proton collisions at the LHC. The fiducial cross-section at s = 13 TeV is measured to be σ = 1.267 ± 0.005 ± 0.053 pb, where the uncertainties reflect the limited number of data events and the systematic uncertainties, giving a total uncertainty of 4.2%. The cross-section is measured differentially as a function of variables characterising the tt¯ system and additional radiation in the events. The results are compared with various Monte Carlo generators, including comparisons where the generators are reweighted to match a parton-level calculation at next-to-next-to-leading order. The reweighting improves the agreement between data and theory. The measured distribution of the top-quark transverse momentum is used to search for new physics in the context of the effective field theory framework. No significant deviation from the Standard Model is observed and limits are set on the Wilson coefficients of the dimension-six operators OtG and Otq(8), where the limits on the latter are the most stringent to date. [Figure not available: see fulltext.]
Measurements of sensor radiation damage in the ATLAS inner detector using leakage currents
- Author
- Aad G
- Abbott B
- Abbott DC
- Abeling K
- Abhayasinghe DK
- Abidi SH
- AbouZeid OS
- Abraham NL
- Abramowicz H
- Abreu H
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- Abusleme Hoffman AC
- Acharya BS
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- Wenaus T
- Wendland B
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- Wessels M
- Weston TD
- Whalen K
- Wharton AM
- White A
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- White MJ
- Whiteson D
- Wiedenmann W
- Wiel C
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- Wieseotte N
- Wiglesworth C
- Wiik-Fuchs LAM
- Wilkens HG
- Wilkins LJ
- Williams DM
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- Windischhofer PJ
- Wingerter-Seez I
- Winklmeier F
- Winter BT
- Wittgen M
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- Wolf A
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- Wongel AF
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- Worm SD
- Wosiek BK
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- Xiotidis I
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- Yabsley B
- Yacoob S
- Yallup DP
- Yamaguchi N
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- Yamatani M
- Yamauchi H
- Yamazaki T
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- Yan J
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- Yao W-M
- Yap YC
- Ye H
- Ye J
- Ye S
- Yeletskikh I
- Yexley MR
- Yildiz H Duran
- Yin P
- Yorita K
- Yoshihara K
- Young C
- Young CJS
- Yuan R
- Yue X
- Zaazoua M
- Zabinski B
- Zacharis G
- Zaffaroni E
- Zahreddine J
- Zaitsev AM
- Zakareishvili T
- Zakharchuk N
- Zambito S
- Zanzi D
- Zeissner SV
- Zeitnitz C
- Zemaityte G
- Zeng JC
- Zenin O
- Zenis T
- Zenz S
- Zerradi S
- Zerwas D
- Zhang B
- Zhang DF
- Zhang G
- Zhang J
- Zhang K
- Zhang L
- Zhang L
- Zhang M
- Zhang R
- Zhang S
- Zhang X
- Zhang X
- Zhang Z
- Zhao P
- Zhao Y
- Zhao Z
- Zhemchugov A
- Zheng Z
- Zhong D
- Zhou B
- Zhou C
- Zhou H
- Zhou M
- Zhou N
- Zhou Y
- Zhu C
- Zhu CG
- Zhu H
- Zhu HL
- Zhu J
- Zhu Y
- Zhuang X
- Zhukov K
- Zhulanov V
- Zieminska D
- Zimine NI
- Zimmermann S
- Zinonos Z
- Ziolkowski M
- Zoccoli A
- Zoch K
- Zorbas TG
- Zou R
- Zou W
- Zwalinski L
- Publication venue
- IOP
- Publication date
- 01/01/2021
- Field of study
Non-ionizing energy loss causes bulk damage to the silicon sensors of the ATLAS pixel and strip detectors. This damage has important implications for data-taking operations, charged-particle track reconstruction, detector simulations, and physics analysis. This paper presents simulations and measurements of the leakage current in the ATLAS pixel detector and semiconductor tracker as a function of location in the detector and time, using data collected in Run 1 (2010–2012) and Run 2 (2015–2018) of the Large Hadron Collider. The extracted fluence shows a much stronger |z|-dependence in the innermost layers than is seen in simulation. Furthermore, the overall fluence on the second innermost layer is significantly higher than in simulation, with better agreement in layers at higher radii. These measurements are important for validating the simulation models and can be used in part to justify safety factors for future detector designs and interventions.publishedVersio
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