61 research outputs found
Malignant inflammation in cutaneous T-cell lymphoma: a hostile takeover
- Author
- A Antonelli
- A Ciree
- A Mishra
- A Pileri
- A Rabenhorst
- A Sors
- A Ungewickell
- A Vacca
- A Willerslev-Olsen
- A Willerslev-Olsen
- A Woetmann
- AC Hsi
- AC Silva Almeida da
- AG Bais
- AH Diwan
- AH Rook
- AH Rook
- AH Rook
- Anders Woetmann
- B Belloni
- B Lauenborg
- BO Dulmage
- BR Vowels
- C Brender
- C Gunther
- C Thode
- CL Berger
- CL Berger
- CM Jackow
- CP Tensen
- D Abeni
- D Lu
- D Peng
- E Contassot
- E Guenova
- E Netchiporouk
- E Papadavid
- EJ Kim
- Erik Langhoff
- F Sallusto
- GS Wood
- H Echchakir
- H Fujita
- H Ohmatsu
- H Suga
- H Yu
- IH Pedersen
- IV Litvinov
- IV Litvinov
- IV Litvinov
- IV Litvinov
- Ivan V. Litvinov
- J Choi
- J Richmond
- JD Bouaziz
- JJ Campbell
- JJ Scarisbrick
- JJ Scarisbrick
- JS Chung
- JZ Qin
- K Asadullah
- K Asadullah
- K Asadullah
- K Ferenczi
- K Kantekure
- K Ohta
- K Subbaramaiah
- K Wolk
- KF Izban
- KL Kopp
- KL Kopp
- KL Kopp
- KR Suchin
- L Bao
- L Chen
- L Fontao
- L Wang
- Lars Iversen
- Lise M. Lindahl
- LJ Geskin
- LY McGirt
- M Bagot
- M Duvic
- M Duvic
- M Duvic
- M Ito
- M Kasprzycka
- M Marzec
- M Nebozhyn
- M Nielsen
- M Sugaya
- M Sugaya
- M Tosolini
- M Tuzova
- M Wysocka
- M Wysocka
- MA Ionescu
- Mariusz A. Wasik
- ME Kadin
- MH Vermeer
- ML De
- MS Kester van
- MT Cheah
- N Accart
- N Franck
- N Nagarsheth
- Niels Odum
- Nigel P. Mongan
- NS Agar
- O Zoi-Toli
- P Gaur
- P Kalinski
- PI Axelrod
- Q Zhang
- Q Zhang
- Q Zhang
- R Doom van
- R Doom van
- R Doom van
- R Dummer
- R Talpur
- R Willemze
- RA Wilcox
- RA Wilcox
- RA Wilcox
- RM Abraham
- RT Hoppe
- S Ehrentraut
- S Esmailzadeh
- S Fredholm
- S Furudate
- S Hahtola
- S Ikeda
- S Munir
- S Nakahata
- S Samimi
- SA Islam
- SK Bromley
- T Kakinuma
- T Kallinich
- T Krejsgaard
- T Krejsgaard
- T Krejsgaard
- T Krejsgaard
- T Krejsgaard
- T Krejsgaard
- T Miyagaki
- T Miyagaki
- T Miyagaki
- T Miyagaki
- T Miyagaki
- T Nagasawa
- ThorbjĂžrn Krejsgaard
- U Dobbeling
- V Blaschke
- V Kodelja
- V Nguyen
- VE Johnson
- VH Sommer
- VN Kristensen
- W Si
- WJ Woollard
- X Ma
- X Ni
- X Ni
- X Wu
- Y Fujita
- Y Komohara
- Y Lou
- Y Tokura
- YB Kural
- YH Kim
- Publication venue
- 'Springer Science and Business Media LLC'
- Publication date
- 01/01/2016
- Field of study
Cutaneous T-cell lymphomas (CTCL) are characterized by the presence of chronically inflamed skin lesions containing malignant T cells. Early disease presents as limited skin patches or plaques and exhibits an indolent behavior. For many patients, the disease never progresses beyond this stage, but in approximately one third of patients, the disease becomes progressive, and the skin lesions start to expand and evolve. Eventually, overt tumors develop and the malignant T cells may disseminate to the blood, lymph nodes, bone marrow, and visceral organs, often with a fatal outcome. The transition from early indolent to progressive and advanced disease is accompanied by a significant shift in the nature of the tumor-associated inflammation. This shift does not appear to be an epiphenomenon but rather a critical step in disease progression. Emerging evidence supports that the malignant T cells take control of the inflammatory environment, suppressing cellular immunity and anti-tumor responses while promoting a chronic inflammatory milieu that fuels their own expansion. Here, we review the inflammatory changes associated with disease progression in CTCL and point to their wider relevance in other cancer contexts. We further define the term "malignant inflammation" as a pro-tumorigenic inflammatory environment orchestrated by the tumor cells and discuss some of the mechanisms driving the development of malignant inflammation in CTCL
Transfusion-transmitted infections
- Author
- A Kitchen
- A Manns
- A Ohagen
- A Pineda
- A Plentz
- A Saito-Ito
- A Sanchez-Quijano
- A Yoshikawa
- AC Ghani
- AD Kitchen
- AH Diwan
- AH Peden
- American Association of Blood Banks
- B Custer
- B Weber
- B Weber
- B Zavizion
- B Zavizion
- C Niederhauser
- C Velati
- CA Llewelyn
- CD Hillyer
- CDC
- CDC
- CF Hogman
- CG Schuttler
- CG Wu
- Christian Brander
- CJ Liu
- CK Lee
- CP Engelfriet
- CP McDonald
- CP McDonald
- CR Seed
- CT Fang
- CT Korves
- D de Korte
- D Kumar
- D Prati
- DA Leiby
- DA Leiby
- DA Leiby
- Damiano Castelli
- DF Roucoux
- DM Knowles
- E Boxall
- E Brojer
- E Delwart
- E Purdy
- E Tabor
- EC Vamvakas
- EL Murphy
- EL Murphy
- EL Snyder
- F Alkassab
- F Corbin 3rd
- F Knutson
- FA Proietti
- Florian Bihl
- Francesco Marincola
- G Andreu
- G Kinde
- GA Ortolano
- GA Schmunis
- GM Busch
- H Yugi
- HW Reesink
- I Cacciola
- J Akiba
- J Blumel
- J Coste
- J Debeir
- J McCullough
- J Pillonel
- JA Aznar
- JC Faber
- JC Faber
- JM Jongerius
- JP Allain
- JP Pelletier
- K Matsubayashi
- K Soldan
- K Soldan
- LD Fast
- LH Gould
- LJ Cardo
- LJ Cardo
- LN Pealer
- LR Petersen
- M Alvarez do Barrio
- M Chassaigne
- M Frey-Wettstein
- M Goldman
- M Mungai
- M Pittman
- MA Blajchman
- MA Blajchman
- MA Blajchman
- MA Blajchman
- ME Brecher
- ME Brecher
- ME Brecher
- MG McEntegart
- MH Koppelman
- MH Koppelman
- MJ Jeon
- MP Busch
- MP Busch
- MR Visconti
- MT Niu
- N Hunter
- N Regamey
- O Silvie
- P Gowland
- P Hellstern
- PE Hewitt
- PF Coleman
- PH Ruane
- PL Chiodini
- R Biswas
- R Offergeld
- RJ Benjamin
- Roger Y Dodd
- RP Goodrich
- RP Goodrich
- RY Dodd
- RY Dodd
- S Kleinman
- S Laperche
- S Levicnik-Stezinar
- S Murphy
- S Zhong
- SC Dollard
- SJ Wagner
- SJ Wagner
- SL Stramer
- SL Stramer
- SL Stramer
- T Mather
- T Nishizawa
- UF Koenigbauer
- W Hladik
- WC Van Voorhis
- WE Hitzler
- Y Tanaka
- Publication venue
- BioMed Central
- Publication date
- 01/06/2007
- Field of study
Although the risk of transfusion-transmitted infections today is lower than ever, the supply of safe blood products remains subject to contamination with known and yet to be identified human pathogens. Only continuous improvement and implementation of donor selection, sensitive screening tests and effective inactivation procedures can ensure the elimination, or at least reduction, of the risk of acquiring transfusion transmitted infections. In addition, ongoing education and up-to-date information regarding infectious agents that are potentially transmitted via blood components is necessary to promote the reporting of adverse events, an important component of transfusion transmitted disease surveillance. Thus, the collaboration of all parties involved in transfusion medicine, including national haemovigilance systems, is crucial for protecting a secure blood product supply from known and emerging blood-borne pathogens
Guidelines for the use and interpretation of assays for monitoring autophagy (4th edition)1.
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- Abdel-Aziz AK
- Abdelfatah S
- Abdellatif M
- Abdoli A
- Abel S
- Abeliovich H
- Abildgaard MH
- Abudu YP
- Acevedo-Arozena A
- Adamopoulos IE
- Adeli K
- Adolph TE
- Adornetto A
- Aflaki E
- Agam G
- Agarwal A
- Aggarwal BB
- Agnello M
- Agostinis P
- Agrewala JN
- Agrotis A
- Aguilar PV
- Ahmad ST
- Ahmed ZM
- Ahumada-Castro U
- Aits S
- Aizawa S
- Akkoc Y
- Akoumianaki T
- Akpinar HA
- Al-Abd AM
- Al-Akra L
- Al-Gharaibeh A
- Alaoui-Jamali MA
- Alberti S
- Alcocer-GĂłmez E
- Alessandri C
- Ali M
- Alim Al-Bari MA
- Aliwaini S
- Alizadeh J
- Almacellas E
- Almasan A
- Alonso A
- Alonso GD
- Altan-Bonnet N
- Altieri DC
- Alves da Costa C
- Alves S
- Alzaharna MM
- Amadio M
- Amantini C
- Amaral C
- Ambrosio S
- Amer AO
- Ammanathan V
- An Z
- Andersen SU
- Andrabi SA
- Andrade-Silva M
- Andres AM
- Angelini S
- Ann D
- Anozie UC
- Ansari MY
- Antas P
- Antebi A
- AntĂłn Z
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- AraĂșjo WL
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- Ălvarez ĂMC
- Ăvalos Y
- Ănal G
- ĂstĂŒn S
- ÄoliÄ M
- ÄokiÄ J
- Ćœerovnik E
- Publication venue
- 'Informa UK Limited'
- Publication date
- 01/01/2021
- Field of study
In 2008, we published the first set of guidelines for standardizing research in autophagy. Since then, this topic has received increasing attention, and many scientists have entered the field. Our knowledge base and relevant new technologies have also been expanding. Thus, it is important to formulate on a regular basis updated guidelines for monitoring autophagy in different organisms. Despite numerous reviews, there continues to be confusion regarding acceptable methods to evaluate autophagy, especially in multicellular eukaryotes. Here, we present a set of guidelines for investigators to select and interpret methods to examine autophagy and related processes, and for reviewers to provide realistic and reasonable critiques of reports that are focused on these processes. These guidelines are not meant to be a dogmatic set of rules, because the appropriateness of any assay largely depends on the question being asked and the system being used. Moreover, no individual assay is perfect for every situation, calling for the use of multiple techniques to properly monitor autophagy in each experimental setting. Finally, several core components of the autophagy machinery have been implicated in distinct autophagic processes (canonical and noncanonical autophagy), implying that genetic approaches to block autophagy should rely on targeting two or more autophagy-related genes that ideally participate in distinct steps of the pathway. Along similar lines, because multiple proteins involved in autophagy also regulate other cellular pathways including apoptosis, not all of them can be used as a specific marker for bona fide autophagic responses. Here, we critically discuss current methods of assessing autophagy and the information they can, or cannot, provide. Our ultimate goal is to encourage intellectual and technical innovation in the field
Effect of high-fat diets on body composition, lipid metabolism and insulin sensitivity, and the role of exercise on these parameters
- Author
- A.H. Lancha Junior
- Awad AB
- Binkoski AE
- Boss A
- D. Diwan
- D.F. Coelho
- D.S. Chaves
- Delany C
- Deutch B
- Donnelly JE
- Feskens EJ
- Flachs P
- Flatt JP
- Flatt JP
- Friedman JM
- Goodpaster BH
- Harrington WW
- Hill JO
- J.R. Poortmans
- Jakicic JM
- Jenkins DJ
- Kraegen EW
- L.O. Pereira-Lancha
- Li JJ
- Liao FH
- Lichtenstein AH
- MacLean PS
- Marette A
- Mataix J
- Matsuo T
- Matsuo T
- Montoya MT
- Moraes JC
- Morgado N
- Motawi TM
- Muhlhausler B
- Muoio DM
- Oosterveer MH
- P.L. Campos-Ferraz
- Paniagua JA
- Patsouris D
- Pomplun D
- Prentice AM
- R. Ferraz
- Rogge MM
- Rokling-Andersen MH
- Shimomura Y
- Sial S
- Siri-Tarino PW
- Solomon TP
- Storlien LH
- Storlien LH
- Storlien LH
- Storlien LH
- Stubbs RJ
- Takahashi Y
- Takeuchi H
- Takeuchi H
- Unger RH
- van Dijk SJ
- Vessby B
- Vessby B
- Wajchenberg BL
- Wang H
- Westerterp KR
- Yeop HC
- Zhang Y
- Publication venue
- 'FapUNIFESP (SciELO)'
- Publication date
- Field of study
Volume III DUNE far detector technical coordination
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- Publication venue
- 'IOP Publishing'
- Publication date
- 01/01/2020
- Field of study
The preponderance of matter over antimatter in the early universe, the dynamics of the supernovae that produced the heavy elements necessary for life, and whether protons eventually decayâthese mysteries at the forefront of particle physics and astrophysics are key to understanding the early evolution of our universe, its current state, and its eventual fate. The Deep Underground Neutrino Experiment (DUNE) is an international world-class experiment dedicated to addressing these questions as it searches for leptonic charge-parity symmetry violation, stands ready to capture supernova neutrino bursts, and seeks to observe nucleon decay as a signature of a grand unified theory underlying the standard model. The DUNE far detector technical design report (TDR) describes the DUNE physics program and the technical designs of the single- and dual-phase DUNE liquid argon TPC far detector modules. Volume III of this TDR describes how the activities required to design, construct, fabricate, install, and commission the DUNE far detector modules are organized and managed. This volume details the organizational structures that will carry out and/or oversee the planned far detector activities safely, successfully, on time, and on budget. It presents overviews of the facilities, supporting infrastructure, and detectors for context, and it outlines the project-related functions and methodologies used by the DUNE technical coordination organization, focusing on the areas of integration engineering, technical reviews, quality assurance and control, and safety oversight. Because of its more advanced stage of development, functional examples presented in this volume focus primarily on the single-phase (SP) detector module
Nuchal-type fibroma associated with lipoma and traumatic neuroma
- Publication venue
- 'Wiley'
- Publication date
- Field of study
Nuchal fibroma presenting as two posterior neck masses
- Publication venue
- 'Wiley'
- Publication date
- Field of study
Mitochondrial dysfunction and transactivation of p53-dependent apoptotic genes in BaP-treated human fetal lung fibroblasts
- Publication venue
- 'SAGE Publications'
- Publication date
- Field of study
- âŠ