71 research outputs found
Uncoupling of IL-6 signaling and LC3-associated phagocytosis drives immunoparalysis during sepsis
- Author
- Publication venue
- 'Elsevier BV'
- Publication date
- 01/01/2021
- Field of study
Contains fulltext :
238107.pdf (Publisherâs version ) (Closed access)Immune deactivation of phagocytes is a central event in the pathogenesis of sepsis. Herein, we identify a master regulatory role of IL-6 signaling on LC3-associated phagocytosis (LAP) and reveal that uncoupling of these two processes during sepsis induces immunoparalysis in monocytes/macrophages. In particular, we demonstrate that activation of LAP by the human fungal pathogen Aspergillus fumigatus depends on ERK1/2-mediated phosphorylation of p47phox subunit of NADPH oxidase. Physiologically, autocrine IL-6/JAK2/Ninein axis orchestrates microtubule organization and dynamics regulating ERK recruitment to the phagosome and LC3(+) phagosome (LAPosome) formation. In sepsis, loss of IL-6 signaling specifically abrogates microtubule-mediated trafficking of ERK, leading to defective activation of LAP and impaired killing of bacterial and fungal pathogens by monocytes/macrophages, which can be selectively restored by IL-6 supplementation. Our work uncovers a molecular pathway linking IL-6 signaling with LAP and provides insight into the mechanisms underlying immunoparalysis in sepsis
Dynamic Phenotypic Clustering in Noisy Ecosystems
- Author
- A Blarer
- A Gonzalez
- A Pernthaler
- A-M Neutel
- AJ McKane
- BT Grenfell
- CM Jessup
- CM Mutshinda
- CR Allen
- CS Holling
- D Simberloff
- D Tilman
- D Tilman
- D Tilman
- DA Vasseur
- DA Vasseur
- DS Wilson
- DS Wilson
- E Beninca
- E Ranta
- E Ranta
- E Ranta
- E Ranta
- ER Pianka
- F Azam
- G Bell
- I Akoumianaki
- I Akoumianaki
- I Volkov
- J Green
- J Ripa
- J Ripa
- JE Houlahan
- JG Skellam
- JH Brown
- JL Klug
- JP Aparicio
- JT Wootton
- JV Greenman
- JV Greenman
- JV Greenman
- KC Abbott
- KJ Haynes
- L Becks
- L Ruokolainen
- M Doebeli
- M Egas
- M Loreau
- M Scheffer
- M Westoby
- MB Bonsall
- Morten Ernebjerg
- MW Cadotte
- N Shoresh
- O Leimar
- OL Petchey
- P Abrams
- P SzabĂł
- P Yodzis
- PAP Moran
- R Lande
- R Levins
- RA Armstrong
- RC Lewontin
- RC MacLean
- RL Tate III
- RM May
- RM May
- RM May
- RM Nisbet
- RM Nisbet
- Roy Kishony
- S Aikio
- SA Frank
- SA Levin
- SJ Pirt
- SP Hubbell
- T Butler
- T Gouhier
- TK Stead
- V Dakos
- Van Savage
- VM Savage
- Publication venue
- Public Library of Science
- Publication date
- 01/01/2011
- Field of study
In natural ecosystems, hundreds of species typically share the same environment and are connected by a dense network of interactions such as predation or competition for resources. Much is known about how fixed ecological niches can determine species abundances in such systems, but far less attention has been paid to patterns of abundances in randomly varying environments. Here, we study this question in a simple model of competition between many species in a patchy ecosystem with randomly fluctuating environmental conditions. Paradoxically, we find that introducing noise can actually induce ordered patterns of abundance-fluctuations, leading to a distinct periodic variation in the correlations between species as a function of the phenotypic distance between them; here, difference in growth rate. This is further accompanied by the formation of discrete, dynamic clusters of abundant species along this otherwise continuous phenotypic axis. These ordered patterns depend on the collective behavior of many species; they disappear when only individual or pairs of species are considered in isolation. We show that they arise from a balance between the tendency of shared environmental noise to synchronize species abundances and the tendency for competition among species to make them fluctuate out of step. Our results demonstrate that in highly interconnected ecosystems, noise can act as an ordering force, dynamically generating ecological patterns even in environments lacking explicit niches
Interactions Between Laminin Receptor and the Cytoskeleton During Translation and Cell Motility
- Author
- A Vedeler
- AJ Ridley
- B Hugle
- BH Toh
- C Hundt
- C Thepparit
- CL Ford
- D Auth
- D Hamill
- D Pineiro
- D Pineiro
- DA Lauffenburger
- DA Ornelles
- Daniel Meruelo
- E Ardini
- E Lazarides
- F Basolo
- FA van den Brule
- G Pelosi
- GV Ludwig
- H Lesot
- HL Malinoff
- J Hesketh
- J Scheiman
- J Scheiman
- J Yannariello-Brown
- JE Hesketh
- JJ Wolosewick
- JV Small
- K Mafune
- Kelly V. Jamieson
- KS Wang
- KS Wang
- KV Jamieson
- KV Jamieson
- Lisa Venticinque
- M Cervera
- M Demianova
- M Osborn
- Maddy Parsons
- MB Goldberg
- N Kondoh
- NC Rao
- P Traub
- PH Tio
- R Lenk
- RD Goldman
- RL Cody
- S Brown
- S Buto
- S Ferrari
- S Gauczynski
- S Kim
- S Menard
- SD Chuong
- SR Gross
- SS Brown
- T Akoumianaki
- T Susantad
- TD Pollard
- TH Landowski
- TJ Mitchison
- UM Wewer
- V Berno
- WJ van Venrooij
- WT Loging
- X Sanjuan
- Y Kaneda
- Publication venue
- Public Library of Science
- Publication date
- 07/01/2011
- Field of study
Human laminin receptor acts as both a component of the 40S ribosomal subunit to mediate cellular translation and as a cell surface receptor that interacts with components of the extracellular matrix. Due to its role as the cell surface receptor for several viruses and its overexpression in several types of cancer, laminin receptor is a pathologically significant protein. Previous studies have determined that ribosomes are associated with components of the cytoskeleton, however the specific ribosomal component(s) responsible has not been determined. Our studies show that laminin receptor binds directly to tubulin. Through the use of siRNA and cytoskeletal inhibitors we demonstrate that laminin receptor acts as a tethering protein, holding the ribosome to tubulin, which is integral to cellular translation. Our studies also show that laminin receptor is capable of binding directly to actin. Through the use of siRNA and cytoskeletal inhibitors we have shown that this laminin receptor-actin interaction is critical for cell migration. These data indicate that interactions between laminin receptor and the cytoskeleton are vital in mediating two processes that are intimately linked to cancer, cellular translation and migration
Is prolonged infusion of piperacillin/tazobactam and meropenem in critically ill patients associated with improved pharmacokinetic/pharmacodynamic and patient outcomes? An observation from the Defining Antibiotic Levels in Intensive care unit patients (DALI) cohort
- Author
- Abdul-Aziz M. H.
- Adembri C.
- Afonso E.
- Afonso S.
- Akoumianaki E.
- Akova M.
- Albanese J.
- Aloizos S.
- Alvarez-Lerma F.
- Anthopoulos G.
- Antipa E.
- Antoniadou E.
- Arribas A. M.
- Arvaniti K.
- Baldesi O.
- Balla M.
- Baptista J. P.
- Bardolet N.
- Bassetti M.
- Bekos V.
- Berry W.
- Blasco M. A.
- Brett S.
- Cardoso T.
- Castillo C.
- Catalan M.
- Chaintoutis C.
- Choutas G.
- Chytas I.
- Clouva-Molyvdas F. -M.
- Colon D.
- Constantin J. M.
- Cortegiani A.
- Crespo R. Z.
- Dapper I.
- De Backer D. D.
- De Crop L. D.
- De Pascale G. D.
- De Rosa F. G.
- De Waele J. J.
- Dimopoulos G.
- Dugernier T.
- Dulhunty J.
- Dupont H.
- Ebm C.
- Esperatti M.
- Feijoo N.
- Fernado J.
- Fernandez F.
- Fernandez J. L.
- Fildisis G.
- Galvan B.
- Garde P. M.
- Garro P.
- Gavala A.
- Giannakou M.
- Giarratano A.
- Giasnetsova T.
- Gkiokas G.
- Goncalves-Pereira J.
- Gonzalo G.
- Gordon A.
- Gracia-Arnillas M. P.
- Gritsi-Gerogianni N.
- Jaber S.
- Joannes-Boyau O.
- Jorens P.
- Kalatzi T.
- Kalogirou M.
- Kapogiannis S.
- Karatzas S.
- Kaukonen K. -M.
- Komnos A.
- Kompoti M.
- Koukoubani T.
- Koulenti D.
- Kouliatsis G.
- Koulouras V.
- Koutsoukou A.
- Kydona C.
- Kyriakopoulou M.
- Laskou M.
- Lasocki S.
- Lathyris D.
- Lefrant J. -Y.
- Lei K.
- Lilitsis E.
- Lipman J.
- Lopez M. J.
- Mahjoub Y.
- Malledant Y.
- Malliotakis P.
- Marco Ranieri V.
- Martin C.
- Mastromauro I.
- Matamis D.
- McKenzie C.
- Meyer E.
- Michalia M.
- Molin A.
- Montagnani L.
- Montalto F.
- Montejo J. C.
- Montravers P.
- Moran C.
- Myrianthefs P.
- Nakos G.
- Nikolakopoulos F.
- Nikolaou H.
- Nogal F. D.
- Orban C.
- Ostermann M.
- Ots E.
- Ozveren A.
- Papanikolaou M.
- Paraforou T.
- Paul S.
- Payen J. C.
- Pelosi P.
- Petrochilou K.
- Pettila V.
- Pottecher J.
- Prieto I.
- Psychogiou V.
- Raineri S. M.
- Rantis T.
- Rello J.
- Rhodes A.
- Ribas A. M.
- Roberts J. A.
- Rovira A.
- Ruano L.
- Rubulotta F.
- Sandroni C.
- Sebastian R.
- Sertaridou E.
- Smith J.
- Soldatou O.
- Soultati I.
- Spapen H.
- Spiropoulou K.
- Spring A.
- Starr T.
- Stotz M.
- Strano M. T.
- Strouvalis I.
- Taccone F. S.
- Teja J. L.
- Templeton M.
- Theodorou V.
- Torres A.
- Urbino R.
- Velasco M. M. M.
- Vidaur L.
- Villa G.
- Wallis S. C.
- Wauters J.
- Xristodoulou A.
- Zafeiridis T.
- Publication venue
- 'Oxford University Press (OUP)'
- Publication date
- 01/01/2016
- Field of study
Objectives:We utilized the database of the Defining Antibiotic Levels in Intensive care unit patients (DALI) study to statistically compare the pharmacokinetic/pharmacodynamic and clinical outcomes between prolonged-infusion and intermittent-bolus dosing of piperacillin/tazobactam and meropenem in critically ill patients using inclusion criteria similar to those used in previous prospective studies.Methods: This was a post hoc analysis of a prospective, multicentre pharmacokinetic point-prevalence study (DALI), which recruited a large cohort of critically ill patients from 68 ICUs across 10 countries.Results: Of the 211 patients receiving piperacillin/tazobactam and meropenem in the DALI study, 182 met inclusion criteria. Overall, 89.0% (162/182) of patients achieved the most conservative target of 50% fT(> MIC) (time over which unbound or free drug concentration remains above the MIC). Decreasing creatinine clearance and the use of prolonged infusion significantly increased the PTA for most pharmacokinetic/pharmacodynamic targets. In the subgroup of patients who had respiratory infection, patients receiving beta-lactams via prolonged infusion demonstrated significantly better 30 day survival when compared with intermittent-bolus patients [86.2% (25/29) versus 56.7% (17/30); P=0.012]. Additionally, in patients with a SOFA score of >= 9, administration by prolonged infusion compared with intermittent-bolus dosing demonstrated significantly better clinical cure [73.3% (11/15) versus 35.0% (7/20); P=0.035] and survival rates [73.3% (11/15) versus 25.0% (5/20); P=0.025].Conclusions: Analysis of this large dataset has provided additional data on the niche benefits of administration of piperacillin/tazobactam and meropenem by prolonged infusion in critically ill patients, particularly for patients with respiratory infections
Distinct Functional Roles of ÎČ-Tubulin Isotypes in Microtubule Arrays of Tetrahymena thermophila, a Model Single-Celled Organism
- Author
- AM Ferris
- Andrew Pelling
- C Dingwall
- C Fulton
- C Walss-Bass
- CD Malone
- Cristina Miceli
- D Wloga
- D Wloga
- Daniela Sparvoli
- E Joachimiak
- E Nogales
- E Nogales
- E Orias
- EC Raff
- EC Raff
- ES Cole
- F Chiappori
- F Marziale
- H. William Detrich
- HA Snaith
- HV Goodson
- HV Goodson
- J Duan
- J Gaertig
- J Gaertig
- J Gaertig
- J Gaertig
- J Gaertig
- J Löwe
- J Wolfe
- JA Eisen
- JB Tucker
- JD Thompson
- JJ Smith
- JR LaFountain Jr
- K Fujiu
- K Fujiu
- K Kamath
- KE McGrath
- KM Karrer
- KM Tyler
- L Xia
- L Xia
- LJ Leandro-Garcia
- M Iwamoto
- M Kavallaris
- MA MartĂ-Renom
- MA Tischfield
- MC Yao
- MC Yao
- MC Yao
- MG Nielsen
- MG Nielsen
- MG Nielsen
- NE Williams
- P Maddox
- P Seve
- PA Joe
- Patrizia Ballarini
- PG McKean
- PP Gan
- R Bhattacharya
- R Bhattacharya
- R Thazhath
- RD Allen
- RF Ludueña
- RS Coyne
- S Barchetta
- S Pucciarelli
- S Pucciarelli
- Sabrina Barchetta
- Sandra Pucciarelli
- SF Bakhoum
- T Akoumianaki
- Ting Yu
- U Eichenlaub-Ritter
- UK Laemmli
- W Miao
- Y Shang
- YF Inclan
- Publication venue
- Public Library of Science
- Publication date
- 01/01/2012
- Field of study
<div><h3>Background</h3><p>The multi-tubulin hypothesis proposes that each tubulin isotype performs a unique role, or subset of roles, in the universe of microtubule function(s). To test this hypothesis, we are investigating the functions of the recently discovered, noncanonical ÎČ-like tubulins (BLTs) of the ciliate, <em>Tetrahymena thermophila</em>. <em>Tetrahymena</em> forms 17 distinct microtubular structures whose assembly had been thought to be based on single α- and ÎČ-isotypes. However, completion of the macronuclear genome sequence of <em>Tetrahymena</em> demonstrated that this ciliate possessed a ÎČ-tubulin multigene family: two synonymous genes (<em>BTU1</em> and <em>BTU2</em>) encode the canonical ÎČ-tubulin, BTU2, and six genes (<em>BLT1-6</em>) yield five divergent ÎČ-tubulin isotypes. In this report, we examine the structural features and functions of two of the BLTs (BLT1 and BLT4) and compare them to those of BTU2.</p> <h3>Methodology/Principal Findings</h3><p>With respect to BTU2, BLT1 and BLT4 had multiple sequence substitutions in their GTP-binding sites, in their interaction surfaces, and in their microtubule-targeting motifs, which together suggest that they have specialized functions. To assess the roles of these tubulins <em>in vivo</em>, we transformed <em>Tetrahymena</em> with expression vectors that direct the synthesis of GFP-tagged versions of the isotypes. We show that GFP-BLT1 and GFP-BLT4 were not detectable in somatic cilia and basal bodies, whereas GFP-BTU2 strongly labeled these structures. During cell division, GFP-BLT1 and GFP-BLT4, but not GFP-BTU2, were incorporated into the microtubule arrays of the macronucleus and into the mitotic apparatus of the micronucleus. GFP-BLT1 also participated in formation of the microtubules of the meiotic apparatus of the micronucleus during conjugation. Partitioning of the isotypes between nuclear and ciliary microtubules was confirmed biochemically.</p> <h3>Conclusion/Significance</h3><p>We conclude that <em>Tetrahymena</em> uses a family of distinct ÎČ-tubulin isotypes to construct subsets of functionally different microtubules, a result that provides strong support for the multi-tubulin hypothesis.</p> </div
Guidelines for the use and interpretation of assays for monitoring autophagy (4th edition)
- Author
- A. -G. Wu
- A. C. Ma
- A. K. Au
- Abdel-Aziz A. K.
- Abdelfatah S.
- Abdellatif M.
- Abdoli A.
- Abel S.
- Abeliovich H.
- Abildgaard M. H.
- Abudu Y. P.
- Acevedo-Arozena A.
- Adamopoulos I. E.
- Adeli K.
- Adolph T. E.
- Adornetto A.
- Aflaki E.
- Agam G.
- Agarwal A.
- Aggarwal B. B.
- Agnello M.
- Agostinis P.
- Agrewala J. N.
- Agrotis A.
- Aguilar P. V.
- Ahmad S. T.
- Ahmed Z. M.
- Ahumada-Castro U.
- Aits S.
- Aizawa S.
- Akkoc Y.
- Akoumianaki T.
- Akpinar H. A.
- Al-Abd A. M.
- Al-Akra L.
- Al-Gharaibeh A.
- Alaoui-Jamali M. A.
- Alberti S.
- Alcocer-Gomez E.
- Alessandri C.
- Ali M.
- Alim Al-Bari M. A.
- Aliwaini S.
- Alizadeh J.
- Almacellas E.
- Almasan A.
- Alonso A.
- Alonso G. D.
- Altan-Bonnet N.
- Altieri D. C.
- Alvarez E. M. C.
- Alves da Costa C.
- Alves S.
- Alzaharna M. M.
- Amadio M.
- Amantini C.
- Amaral C.
- Ambrosio S.
- Amer A. O.
- Ammanathan V.
- An Z.
- Andersen S. U.
- Andrabi S. A.
- Andrade-Silva M.
- Andres A. M.
- Angelini S.
- Ann D.
- Anozie U. C.
- Ansari M. Y.
- Antas P.
- Antebi A.
- Anton Z.
- Anwar T.
- Apetoh L.
- Apostolova N.
- Araki T.
- Araki Y.
- Arasaki K.
- Araujo W. L.
- Araya J.
- Arden C.
- Arevalo M. -A.
- Arguelles S.
- Arias E.
- Arikkath J.
- Arimoto H.
- Ariosa A. R.
- Armstrong-James D.
- Arnaune-Pelloquin L.
- Aroca A.
- Arroyo D. S.
- Arsov I.
- Artero R.
- Asaro D. M. L.
- Aschner M.
- Ashrafizadeh M.
- Ashur-Fabian O.
- Atanasov A. G.
- Auberger P.
- Auner H. W.
- Aurelian L.
- Autelli R.
- Avagliano L.
- Avalos Y.
- Aveic S.
- Aveleira C. A.
- Avin-Wittenberg T.
- Aydin Y.
- Ayton S.
- Ayyadevara S.
- Azzopardi M.
- B. C. B. Ko
- Baba M.
- Backer J. M.
- Backues S. K.
- Bae D. -H.
- Bae O. -N.
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- Baehrecke E. H.
- Baek A.
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- Bagetta G.
- Bagniewska-Zadworna A.
- Bai H.
- Bai J.
- Bai X.
- Bai Y.
- Bairagi N.
- Baksi S.
- Balazadeh S.
- Balbi T.
- Baldari C. T.
- Balduini W.
- Ballabio A.
- Ballester M.
- Balzan R.
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- Banreti A.
- Bao Y.
- Baptista M. S.
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- Bargiela A.
- Barila D.
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- Barmada S. J.
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- Basu A.
- Batoko H.
- Batten I.
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- Behrens G. M. N.
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- Bejarano E.
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- Benitez B. A.
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- Bhattacharya R.
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- Boeuf P.
- Boland B.
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- Borner C.
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- Bosch J.
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- Botana L. M.
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- Boulanger C. M.
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- Bourdenx M.
- Bourgeois B.
- Bourke N. M.
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- Bozkurt T. O.
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- Byrd A.
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- Campesi I.
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- Caraglia M.
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- Carchman E. H.
- Cardenal-Munoz E.
- Cardenas C.
- Cardenas L.
- Cardoso S. M.
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- Carloni S.
- Carmona-Gutierrez D.
- Carneiro L. A.
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- Carrier A.
- Carrier L.
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- Carter A. B.
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- Cassioli C.
- Castillo E. F.
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- Castillo-Lluva S.
- Castoldi F.
- Castori M.
- Castro A. F.
- Castro-Caldas M.
- Castro-Hernandez J.
- Castro-Obregon S.
- Catz S. D.
- Cavadas C.
- Cavaliere F.
- Cavallini G.
- Cavinato M.
- Cayuela M. L.
- Cebollada Rica P.
- Cecarini V.
- Cecconi F.
- Cechowska-Pasko M.
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- Publication venue
- 'Informa UK Limited'
- Publication date
- 01/01/2021
- Field of study
Guidelines for the use and interpretation of assays for monitoring autophagy (4th edition)1.
- Author
- 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
- Anwar T
- Apetoh L
- Apostolova N
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- Araki Y
- Arasaki K
- Araya J
- AraĂșjo WL
- Arden C
- Arguelles S
- Arias E
- Arikkath J
- Arimoto H
- Ariosa AR
- Armstrong-James D
- Arnauné-Pelloquin L
- Aroca A
- Arroyo DS
- Arsov I
- Artero R
- Arévalo M-A
- Asaro DML
- Aschner M
- Ashrafizadeh M
- Ashur-Fabian O
- Atanasov AG
- Au AK
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- Autelli R
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- Aveic S
- Aveleira CA
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- Conti F
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- Coppens I
- Corasaniti MT
- Cordes N
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- Crack PJ
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- Criollo A
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- Csizmadia T
- Cuadrado A
- Cui B
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- Culetto E
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- Cybulsky AV
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- De Amicis F
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- Der CJ
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- Descoteaux A
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- Di Fonzo A
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- Diwan A
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- Dobrinski I
- Dobrovinskaya O
- Dobrowolski R
- Dobson RCJ
- Dokmeci Emre S
- Donadelli M
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- Dubrovska A
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- 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
Novel insights in ICU-acquired respiratory muscle dysfunction: implications for clinical care
- Author
- A Abdellaoui
- A Demoule
- A Demoule
- AD Martin
- AM Schols
- Annemijn H. Jonkman
- B Jonghe De
- BM Bissett
- CS Sassoon
- D Adler
- D Annane
- D Colombo
- D Farmakis
- D Pavlovic
- Diana Jansen
- E Akoumianaki
- E Zanotti
- EC Goligher
- G Bellani
- GS Supinski
- HW Hees van
- HW Hees van
- J Doorduin
- J Doorduin
- J Doorduin
- J Takala
- L Liu
- L Pan
- L Papazian
- Leo M. A. Heunks
- LM Heunks
- M Maddocks
- PE Hooijman
- S Bhasin
- S Jaber
- S Levine
- S Matecki
- SE Cattapan
- SN Hussain
- T Mauri
- WJ Schellekens
- YM Luo
- Publication venue
- 'Springer Science and Business Media LLC'
- Publication date
- Field of study
âAwakeâ extracorporeal membrane oxygenation (ECMO): pathophysiology, technical considerations, and clinical pioneering
- Author
- A Benzing
- A Davies
- A Pesenti
- A Protti
- A Rubino
- AB Froese
- AH Morris
- Alessandro Santini
- Andriy I. Batchinsky
- Antonio Pesenti
- C Frostell
- C Putensen
- CW Hoopes
- CY Ho
- D Camboni
- D Chiumello
- D Hayes Jr
- D Mascheroni
- D Schnell
- D Tanaka
- D Toumpanakis
- D Trenchard
- DA Turner
- DC Abrams
- DG Kiely
- DJ Funk
- DN Hager
- DO Warner
- DP Mason
- E Akoumianaki
- E Spinelli
- EA Phillipson
- G Hedenstierna
- G Lang
- G MacLaren
- G Scano
- GJ Peek
- H Wrigge
- I Inci
- J Duffin
- J Javidfar
- J Javidfar
- J Yu
- JD Hunter
- KJ Rehder
- KM Olsson
- L Gattinoni
- L Gattinoni
- L Gattinoni
- L Gattinoni
- L Kubin
- L Sorbo Del
- Luciano Gattinoni
- M Barnard
- M Bucourt de
- N Latronico
- Nicola Bottino
- NK Burki
- O Wiesner
- P Caironi
- P Morimont
- PE Wright
- R Roncon-Albuquerque Jr
- RD Tallman Jr
- S Field
- S Kluge
- S Lin
- S Ouimet
- SR Hopkins
- Stefania Crotti
- T Fuehner
- T Kolobow
- T Langer
- T Langer
- T Pranikoff
- T Vassilakopoulos
- T Yoshida
- Thomas Langer
- TJ Nuckton
- UH Schmidt
- WD Schweickert
- Publication venue
- 'Springer Science and Business Media LLC'
- Publication date
- Field of study
Diagnostic methods to assess inspiratory and expiratory muscle strength
- Author
- Akoumianaki E
- André Luis Pereira de Albuquerque
- AraĂșjo PR
- Baydur A
- Baydur A
- Beda A
- Black LF
- Black LF
- Boon AJ
- Boussuges A
- Carlos Roberto Ribeiro Carvalho
- Caruso P
- Caruso P
- Chaudri MB
- Chiumello D
- Coelho CM
- Criswell E
- Daube JR
- de Bruin PF
- De Troyer A
- de Troyer A
- Dyspnea
- Elena Prina
- Gottesman E
- HamnegÄard CH
- Houston JG
- Hughes PD
- HĂ©ritier F
- Irwin RS
- Jeferson George Ferreira
- Katagiri M
- Khamiees M
- Koulouris N
- Koulouris N
- Kyroussis D
- Kyroussis D
- Laghi F
- Laporta D
- Laroche CM
- Lerolle N
- Lerolle N
- Leticia Zumpano Cardenas
- Lofaso F
- Luo YM
- Luo YM
- Man WD
- Man WD
- Marcelo Ceneviva Macchione
- Martin AD
- Matamis D
- Mayra Caleffi Pereira
- Merletti R
- Neder JA
- PatrĂcia Fernandes Trevizan
- Pauliane Vieira Santana
- Pedro Caruso
- Polkey MI
- Polkey MI
- Rahn H
- Renata Pletsch
- Rubin DI
- Similowski T
- Stefanutti D
- Steier J
- Stell IM
- Summerhill EM
- Suzuki J
- Testa A
- Truwit JD
- Uldry C
- Uldry C
- Vinicius Iamonti
- Wragg S
- Yang KL
- Publication venue
- 'FapUNIFESP (SciELO)'
- Publication date
- Field of study
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