369 research outputs found
LRRK2 is a negative regulator of <em>Mycobacterium tuberculosis</em> phagosome maturation in macrophages
- Author
- Publication venue
- Wiley - VCH Verlag
- Publication date
- 01/01/2018
- Field of study
\ua9 2018 EMBO. Mutations in the leucine-rich repeat kinase 2 (LRRK2) are associated with Parkinson\u27s disease, chronic inflammation and mycobacterial infections. Although there is evidence supporting the idea that LRRK2 has an immune function, the cellular function of this kinase is still largely unknown. By using genetic, pharmacological and proteomics approaches, we show that LRRK2 kinase activity negatively regulates phagosome maturation via the recruitment of the Class III phosphatidylinositol-3 kinase complex and Rubicon to the phagosome in macrophages. Moreover, inhibition of LRRK2 kinase activity in mouse and human macrophages enhanced Mycobacterium tuberculosis phagosome maturation and mycobacterial control independently of autophagy. In vivo, LRRK2 deficiency in mice resulted in a significant decrease in M. tuberculosis burdens early during the infection. Collectively, our findings provide a molecular mechanism explaining genetic evidence linking LRRK2 to mycobacterial diseases and establish an LRRK2-dependent cellular pathway that controls M. tuberculosis replication by regulating phagosome maturation
Application of the Phenomenex EZ:faastâą amino acid analysis kit for rapid gas-chromatographic determination of concentrations of plasma tryptophan and its brain uptake competitors
- Author
- Publication venue
- Springer Vienna
- Publication date
- 01/01/2007
- Field of study
The Phenomenex EZ:faastâą amino acid analysis kit is available for gas (GC) or liquid (LC) chromatographic analysis of amino acids (AA) using mass spectrometry (MS) and other GC detectors. We used it for rapid GC determination of plasma tryptophan, its brain uptake competitors (Val, Leu, Ile, Phe and Tyr) and many other amino acids. Based on solid-phase extraction, this fast method enables one person to process two plasma samples in 8â10 min and six samples in âŒ15 min up to GC injection and a 7-min GC run per plasma sample. Using a Perkin-Elmer Clarus 500 GC, a Total Chrome software, a flame-ionisation detector (FID) and norvaline as internal standard, we used this method to analyse âŒ1,000 plasma samples from normal subjects undergoing acute tryptophan depletion and loading tests. The limit of detection for most amino acids is 1 nmol/ml (1 ΌM) and in many cases less. With manual injection, coefficients of variation for the above six amino acids were 1.5â6.2% (intra-assay) and 3.8â9.7% (inter-assay). This simple, rapid and elegant method will be valuable to the amino acid analyst and researcher, as it can save much manpower time and meet urgent emergency requests and the demands of a high-throughput laboratory
Search for new phenomena in final states with an energetic jet and large missing transverse momentum in pp collisions at â s = 8 TeV with the ATLAS detector
- Author
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- Tsukerman II
- Tsulaia V
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- Tsybychev D
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- Tudorache A
- Tudorache V
- Tulbure TT
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- Turchikhin S
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- Valentinetti S
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- Vallier A
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- Van Vulpen I
- Vanadia M
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- Vandenbroucke M
- Vandewall ER
- Vaniachine A
- Vannicola D
- Vari R
- Varnes EW
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- Varouchas D
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- Vasile ME
- Vasquez GA
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- Vazquez CJB
- Vazquez JGP
- Veatch J
- Vecchio V
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- Veloce LM
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- Vermeulen JC
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- Vetterli MC
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- Vukotic I
- Wagner P
- Wagner W
- Wagner-Kuhr J
- Wahdan S
- Wahlberg H
- Walbrecht VM
- Walder J
- Walker R
- Walker SD
- Walkowiak W
- Wallangen V
- Wang AM
- Wang AZ
- Wang C
- Wang F
- Wang H
- Wang J
- Wang P
- Wang Q
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- Wang R-J
- Wang SM
- Wang W
- Wang WT
- Wang WX
- Wang Y
- Wang Z
- Wanotayaroj C
- Warburton A
- Ward CP
- Wardrope DR
- Warrack N
- Washbrook A
- Watson AT
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- Waugh BM
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- Weber SM
- Weidberg AR
- Weingarten J
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- Werner MD
- Wessels M
- Weston TD
- Whalen K
- Whallon NL
- Wharton AM
- White A
- White AS
- White MJ
- Whiteson D
- Whitmore BW
- Wiedenmann W
- Wiel C
- Wielers M
- Wieseotte N
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- Wiik-Fuchs LAM
- Wilkens HG
- Wilkins LJ
- Williams HH
- Williams S
- Willis C
- Willocq S
- Wingerter-Seez I
- Winkels E
- Winklmeier F
- Winston OJ
- Winter BT
- Wittgen M
- Wobisch M
- Wolf A
- Wolf TMH
- Wolff R
- Wolker R
- Wollrath J
- Wolter MW
- Wolters H
- Wong VWS
- Woods NL
- Worm SD
- Wosiek BK
- Wozniak KW
- Wraight K
- Wu SL
- Wu X
- Wu Y
- Wyatt TR
- Wynne BM
- Xella S
- Xi Z
- Xia L
- Xiao X
- Xiotidis I
- Xu D
- Xu H
- Xu L
- Xu T
- Xu W
- Xu Z
- Yabsley B
- Yacoob S
- Yajima K
- Yallup DP
- Yamaguchi N
- Yamaguchi Y
- Yamamoto A
- Yamatani M
- Yamazaki T
- Yamazaki Y
- Yan Z
- Yang HJ
- Yang HT
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- Yang X
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- Yao W-M
- Yap YC
- Yasu Y
- Yatsenko E
- Ye H
- Ye J
- Ye S
- Yeletskikh I
- Yexley MR
- Yigitbasi E
- Yildiz HD
- Yorita K
- Yoshihara K
- Young C
- Young CJS
- Yu J
- Yuan R
- Yue X
- Zaazoua M
- Zabinski B
- Zacharis G
- Zaffaroni E
- Zahreddine J
- Zaitsev AM
- Zakareishvili T
- Zakharchuk N
- Zambito S
- Zanzi D
- Zaripovas DR
- Zeissner S
- Zeitnitz C
- Zemaityte G
- Zeng JC
- Zenin O
- Zenis T
- Zerwas D
- Zgubic M
- Zhang B
- Zhang DF
- Zhang G
- Zhang H
- Zhang J
- Zhang L
- Zhang M
- Zhang R
- Zhang S
- Zhang X
- Zhang Y
- Zhang Z
- Zhao P
- Zhao Z
- Zhemchugov A
- Zheng Z
- Zhong D
- Zhou B
- Zhou C
- Zhou M
- Zhou MS
- 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 N
- Zimmermann S
- Zinonos Z
- Ziolkowski M
- Zivkovic L
- Zobernig G
- Zoccoli A
- Zoch K
- Zorbas TG
- Zou R
- Zu Theenhausen HM
- Zwalinski L
- Publication venue
- 'Springer Science and Business Media LLC'
- Publication date
- 01/01/2015
- Field of study
Results of a search for new phenomena in final states with an energetic jet and large missing transverse momentum are reported. The search uses 20.3 fbâ1 of â s = 8 TeV data collected in 2012 with the ATLAS detector at the LHC. Events are required to have at least one jet with pT > 120 GeV and no leptons. Nine signal regions are considered with increasing missing transverse momentum requirements between Emiss T > 150 GeV and Emiss T > 700 GeV. Good agreement is observed between the number of events in data and Standard Model expectations. The results are translated into exclusion limits on models with either large extra spatial dimensions, pair production of weakly interacting dark matter candidates, or production of very light gravitinos in a gauge-mediated supersymmetric model. In addition, limits on the production of an invisibly decaying Higgs-like boson leading to similar topologies in the final state are presente
Extracellular DNA Chelates Cations and Induces Antibiotic Resistance in Pseudomonas aeruginosa Biofilms
- Author
- A Brooun
- A Folkesson
- A Smyth
- AL Goodman
- AL Smith
- AL Spoering
- AS Bayer
- BD Corbin
- BD Hoyle
- C Prigent-Combaret
- C Ranasinha
- C Ryder
- C Vuong
- CB Whitchurch
- CB Whitchurch
- CL Darnell
- CU Riedel
- D Davies
- DG Davies
- E Drenkard
- E Drenkard
- EA Cowley
- EA Groisman
- EL Macfarlane
- EL Macfarlane
- GA O'Toole
- H Ceri
- H Kumon
- Heidi Mulcahy
- I Keren
- I Ventre
- J Lam
- JA Haagensen
- JA Lesley
- JB McPhee
- JB McPhee
- JC Nickel
- JD Vrany
- JL Kadurugamuwa
- JR Govan
- JR Govan
- JR Govan
- JS Webb
- JW Costerton
- JW Costerton
- K Hilpert
- Laetitia Charron-Mazenod
- LB Soong
- LR Prost
- M Allesen-Holm
- M Shigeta
- MD Parkins
- Michael S. Gilmore
- ML Zaharik
- MR Parsek
- N Martin-Orozco
- P Gilbert
- PA Suci
- PK Singh
- PS Stewart
- RB Fick Jr
- RE Hancock
- RE Hancock
- RE Hancock
- RK Ernst
- RS Baltimore
- S Baconnais
- S Lewenza
- S Lewenza
- S Lewenza
- S Moreau-Marquis
- S Rajan
- S Shak
- SD Aaron
- Shawn Lewenza
- SL Kuchma
- SM Kirov
- SM Moskowitz
- SR Schooling
- T Murata
- TF Mah
- TI Nicas
- V Brinkmann
- WE Regelmann
- Z Qin
- Publication venue
- Public Library of Science
- Publication date
- 01/11/2008
- Field of study
Biofilms are surface-adhered bacterial communities encased in an extracellular matrix composed of DNA, bacterial polysaccharides and proteins, which are up to 1000-fold more antibiotic resistant than planktonic cultures. To date, extracellular DNA has been shown to function as a structural support to maintain Pseudomonas aeruginosa biofilm architecture. Here we show that DNA is a multifaceted component of P. aeruginosa biofilms. At physiologically relevant concentrations, extracellular DNA has antimicrobial activity, causing cell lysis by chelating cations that stabilize lipopolysaccharide (LPS) and the outer membrane (OM). DNA-mediated killing occurred within minutes, as a result of perturbation of both the outer and inner membrane (IM) and the release of cytoplasmic contents, including genomic DNA. Sub-inhibitory concentrations of DNA created a cation-limited environment that resulted in induction of the PhoPQ- and PmrAB-regulated cationic antimicrobial peptide resistance operon PA3552âPA3559 in P. aeruginosa. Furthermore, DNA-induced expression of this operon resulted in up to 2560-fold increased resistance to cationic antimicrobial peptides and 640-fold increased resistance to aminoglycosides, but had no effect on ÎČ-lactam and fluoroquinolone resistance. Thus, the presence of extracellular DNA in the biofilm matrix contributes to cation gradients, genomic DNA release and inducible antibiotic resistance. DNA-rich environments, including biofilms and other infection sites like the CF lung, are likely the in vivo environments where extracellular pathogens such as P. aeruginosa encounter cation limitation
Global analysis of estrogen receptor beta binding to breast cancer cell genome reveals an extensive interplay with estrogen receptor alpha for target gene regulation
- Author
- A Hurtado
- A Licznar
- AI Saeed
- Alessandro Weisz
- B Van Steensel
- BD Adams
- BS Katzenellenbogen
- C Ambrosino
- C Frezza
- C Scafoglio
- C Vyhlidal
- C Williams
- C Zhao
- C Zhao
- CM Klinge
- CY Lin
- D Behrens
- E Portales-Casamar
- EC Chang
- ER Mardis
- G Di Leva
- G Lazennec
- G Maillot
- G Nassa
- GA Blobel
- Gary P Schroth
- Giorgio Giurato
- Giovanni Nassa
- H Al-Nakhle
- H Granok
- H Sugiura
- IM Bonapace
- J Chen
- J Frasor
- J Frasor
- J Matthews
- J Matthews
- JM Hall
- JQ Chen
- JS Carroll
- JW Simpkins
- K Cartharius
- K Pettersson
- K Pettersson
- K Weigelt
- KA Mattingly
- KH Fritzemeier
- L Bermont
- L Castellano
- L Cicatiello
- L Cicatiello
- L Cicatiello
- L Mao
- L Massaad-Massade
- Lorenzo Ferraro
- Luigi Cicatiello
- M Ravo
- Margherita Mutarelli
- Maria Francesca Papa
- Maria Ravo
- Maria Rosaria De Filippo
- MJ Fullwood
- MK Lindberg
- MV Iorio
- MV Iorio
- N Heldring
- NC Andrews
- NS Wickramasinghe
- OI Vivar
- Oli MV Grober
- Ornella Paris
- P Bhat-Nakshatri
- P Ordonez-Moran
- P Pace
- P Webb
- Q Felty
- RM Kuhn
- Roberta Tarallo
- S Aulmann
- S Bauer
- S Caporali
- S Mahony
- S Paruthiyil
- S Safe
- S Saji
- SH Yang
- Shujun Luo
- SJ Ho Sui
- SM Cowley
- T Buterin
- TH Charn
- TL Bailey
- Vladimir Benes
- X Li
- Y Leung
- Y Liu
- Y Zhang
- Z Bai
- Publication venue
- BioMed Central
- Publication date
- 01/01/2011
- Field of study
Background: Estrogen receptors alpha (ERa) and beta (ERb) are transcription factors (TFs) that mediate estrogen signaling and define the hormone-responsive phenotype of breast cancer (BC). The two receptors can be found co-expressed and play specific, often opposite, roles, with ERb being able to modulate the effects of ERa on gene transcription and cell proliferation. ERb is frequently lost in BC, where its presence generally correlates with a better prognosis of the disease. The identification of the genomic targets of ERb in hormone-responsive BC cells is thus a critical step to elucidate the roles of this receptor in estrogen signaling and tumor cell biology.
Results: Expression of full-length ERb in hormone-responsive, ERa-positive MCF-7 cells resulted in a marked reduction in cell proliferation in response to estrogen and marked effects on the cell transcriptome. By ChIP-Seq we identified 9702 ERb and 6024 ERa binding sites in estrogen-stimulated cells, comprising sites occupied by either ERb, ERa or both ER subtypes. A search for TF binding matrices revealed that the majority of the binding sites identified comprise one or more Estrogen Response Element and the remaining show binding matrixes for other TFs known to mediate ER interaction with chromatin by tethering, including AP2, E2F and SP1. Of 921 genes differentially regulated by estrogen in ERb+ vs ERb- cells, 424 showed one or more ERb site within 10 kb. These putative primary ERb target genes control cell proliferation, death, differentiation, motility and adhesion, signal transduction and transcription, key cellular processes that might explain the biological and clinical phenotype of tumors expressing this ER subtype. ERb binding in close proximity of several miRNA genes and in the mitochondrial genome, suggests the possible involvement of this receptor in small non-coding RNA biogenesis and mitochondrial genome functions.
Conclusions: Results indicate that the vast majority of the genomic targets of ERb can bind also ERa, suggesting that the overall action of ERb on the genome of hormone-responsive BC cells depends mainly on the relative concentration of both ERs in the cell
The nuclear receptor ERÎČ engages AGO2 in regulation of gene transcription, RNA splicing and RISC loading
- Author
- A Bardin
- A Clocchiatti
- A Heger
- A Medina-Rivera
- A Rueda
- AE Damdimopoulos
- AG Beristain
- AK Siraj
- Alessandro Weisz
- Angela Cordella
- Annamaria Salvati
- AR Quinlan
- B Huang
- B Langmead
- BA Janowski
- BD Adams
- Biancamaria Pierri
- C Ambrosino
- C Carissimi
- C Dravis
- C Forster
- C Stellato
- C Thomas
- C Trapnell
- C Trapnell
- C Williams
- C Zhao
- CJ Watson
- Concetta Ambrosino
- CT Quang
- CY Lin
- D Carter
- D Fumagalli
- D Schmidt
- DH Kim
- DN Dago
- EC Chang
- F Cirillo
- F Zambelli
- Francesca Rizzo
- G Hutvagner
- G Korkmaz
- G Meister
- G Nassa
- G Nassa
- G St Laurent
- GB Jang
- Giorgio Giurato
- Giovanna Marchese
- Giovanni Cimmino
- Giovanni Nassa
- Giuseppina Bruno
- H Sudo
- H Zang
- H Zuo
- HS Elsarraj
- I Bado
- J Hock
- J Hock
- J Liu
- JA Vizcaino
- JD Keene
- JH Krege
- JM Taliaferro
- JS Menet
- JY Ip
- K Cartharius
- KR Covington
- KV Morris
- L Hodges-Gallagher
- L Yang
- LB Watkin
- LC Murphy
- Luca Ricciardi
- Luciano Milanesi
- M Allo
- M Ameyar-Zazoua
- M Benhamed
- M Fan
- M Madeira
- M Pathan
- MA Ashaie
- Maria Ravo
- MH Liu
- MI Love
- MJ Cowley
- MJ Fullwood
- N Dey
- N Moshkovich
- N Zatula
- O Paris
- OI Vivar
- OM Grober
- P Machanick
- P Maruvada
- P Shannon
- R Das
- R Leeuw de
- R Panero
- R Tarallo
- RB Lanz
- RJ Bourgo
- RK Kalathur
- Roberta Tarallo
- RT Dorsam
- S Anders
- S Anders
- S Cho
- S Heinz
- S Jauliac
- SJ Holwerda
- SJ Zardawi
- SK Ghosh
- SY Kwon
- T Svingen
- T Ye
- TA Rand
- Teresa Rocco
- Tuula A. Nyman
- TW Chen
- U Golebiewska
- Valerio Gigantino
- X Wang
- Y Chen
- Y Kakihara
- Y Zhang
- YK Leung
- YL Khodor
- Z Ning
- Z Ye
- Publication venue
- 'Springer Science and Business Media LLC'
- Publication date
- Field of study
The desmosome and pemphigus
- Author
- A Al-Amoudi
- A Asimaki
- A Baroni
- A Bruin de
- A Chrostek
- A Heuser
- A Kljuic
- A Lanza
- A Lyell
- A Rampazzo
- A Sakuntabhai
- A Schmidt
- A Schmidt
- A Shimizu
- A Shimizu
- A Sonnenberg
- AB Jaffe
- AI Chernyavsky
- AI Chernyavsky
- AI Chernyavsky
- AI Chernyavsky
- AJ Merritt
- AJ North
- AM Farrell
- AP Kowalczyk
- AP Kowalczyk
- AP Kowalczyk
- AP Kowalczyk
- AP Kowalczyk
- AR Ahmed
- AS Payne
- AS Payne
- B Gerull
- B Hammerling
- B Holthofer
- B Pelacho
- B Rock
- B Rock
- B Santiago-Josefat
- BD Angst
- BM Schaefer
- C Baykal
- C Bierkamp
- C Bierkamp
- C Esaki
- C Feliciani
- C Feliciani
- C Kolly
- C Marcozzi
- C Mertens
- C Mertens
- C Mertens
- C Sitaru
- C Tselepis
- CA Gaudry
- CC Calkins
- CC Calkins
- CJ Skerrow
- CM Borrmann
- CM Cowley
- CM Veldman
- D Brennan
- D Geum
- DC Swartzendruber
- DE Gutstein
- DE Kelly
- DK Armstrong
- DR Garrod
- DW Fawcett
- DW Fawcett
- E Garcia-Gras
- E Muller
- E Schmidt
- E Shu
- EA Bornslaeger
- EA Bornslaeger
- EA Smith
- EE Norgett
- EH Beutner
- EJ Muller
- F Iraji
- F Nollet
- FT Kolligs
- G Gorbsky
- G Izumi
- G McKoy
- GF Odland
- GF Wilgram
- GF Wilgram
- GI Gallicano
- GI Gallicano
- GJ Anhalt
- GJ Anhalt
- GJ Giudice
- GK Menon
- H Aberle
- H Bazzi
- H Hennings
- H Mueller
- H Shimizu
- H Wan
- H Wu
- HJ Choi
- HM Sheu
- HW Heid
- I Sanchez-Carpintero
- I Shimanovich
- I Zagorodniuk
- IA King
- ID Burdett
- J Arnemann
- J Arnemann
- J Arredondo
- J Dhitavat
- J Dhitavat
- J Guay
- J Koeser
- J Rodriguez
- J Waschke
- J Waschke
- J Waschke
- J Weiske
- JA McGrath
- JA McGrath
- JC Bystryn
- JC Bystryn
- JC Bystryn
- JC Jones
- JC Jones
- JE Collins
- Jens Waschke
- JH Lorch
- JJ Bech-Serra
- JJ Jefferson
- JK Wahl
- JK Wahl III
- JP Tintelen van
- JR McMillan
- JR Schiltz
- JR Stanley
- JR Stanley
- K Akat
- K Bhol
- K Hashimoto
- K Ishii
- K Ishii
- K Osada
- K Pilichou
- K Rosen
- K Tsunoda
- K Yoshida
- KB Yancey
- KC Miranda
- KE Harman
- KJ Green
- KJ Green
- KS Grossmann
- L Eshkind
- L Koulu
- L Lo Muzio
- L Rickman
- L Shapiro
- L Williamson
- L Williamson
- LA Bazley
- LA Diaz
- LM Godsel
- M Amagai
- M Amagai
- M Amagai
- M Amagai
- M Amagai
- M Amagai
- M Amagai
- M Amagai
- M Amagai
- M Amagai
- M Amagai
- M Amagai
- M Amagai
- M Chidgey
- M Frusic-Zlotkin
- M Frusic-Zlotkin
- M Fukata
- M Hatzfeld
- M Hatzfeld
- M Hatzfeld
- M Hertl
- M Mathur
- M Milingou
- M Overduin
- M Pasdar
- M Pasdar
- M Pasdar
- M Puviani
- M Sato
- M Schmelz
- M Schmelz
- M Schmelz
- M Schmelz
- M Seishima
- M Seishima
- M Seishima
- M Sekiguchi
- MA Schwarz
- MC Udey
- MD Kottke
- MD Perng
- ME Melish
- MF Jonkman
- MG Farquhar
- MG Mahoney
- MG Mahoney
- MJ Hardman
- MJ Jamora
- MK Hacker-Foegen
- MR Namazi
- MW Wendeler
- N Akhtar
- N Cirillo
- N Cirillo
- N Cirillo
- N Cirillo
- N Cirillo
- N Cirillo
- NA Chitaev
- NA Chitaev
- NJ Korman
- NS McNutt
- NV Whittock
- NV Whittock
- NV Whittock
- O Maeda
- O Memar
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- P Berkowitz
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- P Berkowitz
- P Berkowitz
- P Cowin
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- P Hu
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- PJ Koch
- PJ Koch
- PJ Koch
- PJ Koch
- PM Elias
- PZ Anastasiadis
- R Benndorf
- R Caldelari
- R Gniadecki
- R Moll
- R Moll
- R Muller
- R Muller
- R Ruiz-Velasco
- R Windoffer
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- RL Dusek
- RL Dusek
- RM Farb
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- RW Eyre
- RW Eyre
- S Alema
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- S Bonne
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- S Getsios
- S Hatsell
- S Karpati
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- S Miravet
- S Miyagawa
- S Morioka
- S Pieperhoff
- S Schafer
- S Spaeth
- S Woll
- SA Benitah
- SA Grando
- SA Grando
- SE Syed
- SK Runswick
- SM Troyanovsky
- SM Troyanovsky
- SM Troyanovsky
- SW Yeh
- T Hashimoto
- T Kamei
- T Nagasaka
- T Schuh
- T Shimada
- T Sobolik-Delmaire
- T Yin
- T Yin
- TE Kimura
- TJ Boggon
- TS Stappenbeck
- V Aoki
- V Spindler
- V Vasioukhin
- V Vasioukhin
- VK Salato
- VM Braga
- VM Braga
- VT Nguyen
- VT Nguyen
- VT Nguyen
- VT Nguyen
- VT Nguyen
- W Baumgartner
- W Baumgartner
- W Gusek
- W He
- W Heupel
- WF Lever
- WW Franke
- WW Franke
- WW Franke
- X Chen
- X Ding
- X Wang
- X Wang
- XR Bustelo
- Y Aoyama
- Y Aoyama
- Y Futei
- Y Hanakawa
- Y Hanakawa
- Y Jinbu
- Y Kawasaki
- Y Kitajima
- Y Kitajima
- Y Kitajima
- Y Kitajima
- Y Shirakata
- Y Takahashi
- Y Yamamoto
- Y Yamamoto
- Z Den
- Publication venue
- Springer-Verlag
- Publication date
- 01/01/2008
- Field of study
Desmosomes are patch-like intercellular adhering junctions (âmaculae adherentesâ), which, in concert with the related adherens junctions, provide the mechanical strength to intercellular adhesion. Therefore, it is not surprising that desmosomes are abundant in tissues subjected to significant mechanical stress such as stratified epithelia and myocardium. Desmosomal adhesion is based on the Ca2+-dependent, homo- and heterophilic transinteraction of cadherin-type adhesion molecules. Desmosomal cadherins are anchored to the intermediate filament cytoskeleton by adaptor proteins of the armadillo and plakin families. Desmosomes are dynamic structures subjected to regulation and are therefore targets of signalling pathways, which control their molecular composition and adhesive properties. Moreover, evidence is emerging that desmosomal components themselves take part in outside-in signalling under physiologic and pathologic conditions. Disturbed desmosomal adhesion contributes to the pathogenesis of a number of diseases such as pemphigus, which is caused by autoantibodies against desmosomal cadherins. Beside pemphigus, desmosome-associated diseases are caused by other mechanisms such as genetic defects or bacterial toxins. Because most of these diseases affect the skin, desmosomes are interesting not only for cell biologists who are inspired by their complex structure and molecular composition, but also for clinical physicians who are confronted with patients suffering from severe blistering skin diseases such as pemphigus. To develop disease-specific therapeutic approaches, more insights into the molecular composition and regulation of desmosomes are required
Measurements of Higgs bosons decaying to bottom quarks from vector boson fusion production with the ATLAS experiment at â=13TeV
- Author
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- Ă kesson TPA
- Ăncel ĂO
- ĆœeniĆĄ T
- ĆœivkoviÄ L
- Publication venue
- 'Springer Science and Business Media LLC'
- Publication date
- 23/06/2021
- Field of study
The paper presents a measurement of the Standard Model Higgs Boson decaying to b-quark pairs in the vector boson fusion (VBF) production mode. A sample corresponding to 126 fbâ1 of sâ=13TeV protonâproton collision data, collected with the ATLAS experiment at the Large Hadron Collider, is analyzed utilizing an adversarial neural network for event classification. The signal strength, defined as the ratio of the measured signal yield to that predicted by the Standard Model for VBF Higgs production, is measured to be 0.95+0.38â0.36 , corresponding to an observed (expected) significance of 2.6 (2.8) standard deviations from the background only hypothesis. The results are additionally combined with an analysis of Higgs bosons decaying to b-quarks, produced via VBF in association with a photon
Erratum: Measurement of angular and momentum distributions of charged particles within and around jets in Pb + Pb and pp collisions at âsNN = 5.02 TeV with the ATLAS detector [Phys. Rev. C 100 , 064901 (2019)]
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- Abbott B
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- Abhayasinghe Dk
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- Nitsche I
- Nitta T
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- Noguchi Y
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- Novgorodova O
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- Okazaki Y
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- Ponomarenko D
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- Wiik-Fuchs Lam
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- Winkels E
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- Xiotidis I
- Xu D
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- Yexley Mr
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- Zhemchugov A
- Zheng Z
- Zhong D
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- Zorbas Tg
- Zou R
- Zwalinski L
- Publication venue
- American Physical Society
- Publication date
- 01/01/2020
- Field of study
Measurement of the ttÂŻttÂŻ production cross section in pp collisions at âs=13 TeV with the ATLAS detector
- Author
- Aad G
- Abbott B
- Abbott DC
- Abed Abud A
- Abeling K
- Abhayasinghe DK
- Abidi SH
- 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
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- Agarwala J
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- Alberghi GL
- Albert J
- Alconada Verzini MJ
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- Aleksa M
- Aleksandrov IN
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- Ă kesson TPA
- Ăncel ĂO
- ĆœeniĆĄ T
- ĆœivkoviÄ L
- Publication venue
- 'Springer Science and Business Media LLC'
- Publication date
- 16/11/2021
- Field of study
A measurement of four-top-quark production using proton-proton collision data at a centre-of-mass energy of 13 TeV collected by the ATLAS detector at the Large Hadron Collider corresponding to an integrated luminosity of 139 fbâ1 is presented. Events are selected if they contain a single lepton (electron or muon) or an opposite-sign lepton pair, in association with multiple jets. The events are categorised according to the number of jets and how likely these are to contain b-hadrons. A multivariate technique is then used to discriminate between signal and background events. The measured four-top-quark production cross section is found to be 26+17â15 fb, with a corresponding observed (expected) significance of 1.9 (1.0) standard deviations over the background-only hypothesis. The result is combined with the previous measurement performed by the ATLAS Collaboration in the multilepton final state. The combined four-top-quark production cross section is measured to be 24+7â6 fb, with a corresponding observed (expected) signal significance of 4.7 (2.6) standard deviations over the background-only predictions. It is consistent within 2.0 standard deviations with the Standard Model expectation of 12.0 ± 2.4 fb
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