11 research outputs found
Infection of Semen-Producing Organs by SIV during the Acute and Chronic Stages of the Disease
- Author
- A Brogi
- A Cheret
- A Filippini
- A Lafeuillade
- A Miyake
- A Rivenson
- A Tachet
- AA Kiessling
- AJ Quayle
- AL Puaux
- Anna Le Tortorec
- Anne Maillard
- Anne-Pascale Satie
- AZ Decrion
- B Leynaert
- B Ling
- B Muciaccia
- BA Araneo
- BA Bladergroen
- Bernard Jégou
- BP Setchell
- C Graziosi
- C Solas
- CD Pilcher
- CJ Miller
- D Posada
- D Swofford
- DB Hales
- DH Castrillon
- DJ Anderson
- DJ Anderson
- DM Smith
- E Terasawa
- E Vicenzi
- E Vivier
- EL Delwart
- FM Hecht
- G Paulis
- GJ Nuovo
- H Thiebot
- H Wolff
- H Wolff
- H Zhang
- HM Behre
- Hélène Denis
- I Karlsson
- IW Nasr
- J Eron
- J Fantini
- J Ghosn
- J Nilsson
- J Pudney
- J Pudney
- JD Nicopoullos
- JD Thompson
- JK Pullium
- JL Greenier
- JN Krieger
- JW Streilein
- K Abel
- K Abel
- K Benlhassan-Chahour
- K Kedzierska
- Karim Mannioui
- KH Mayer
- KL Kroodsma
- L Bujan
- L Bujan
- L Chakrabarti
- LE Davis
- LH Hu
- LH Ping
- LJ Miller
- M Bomsel
- M Da Silva
- M El-Dermiry
- M Markowitz
- M Moniuszko
- M Naito
- M Shehu-Xhilaga
- MJ Wawer
- MK O'Bryan
- MM Shevchuk
- N Dejucq
- N Dejucq-Rainsford
- N Garrido
- Nathalie Dejucq-Rainsford
- NL Haigwood
- O Benveniste
- O Delezay
- P De Cesaris
- P Gupta
- P Pollanen
- Peter Sommer
- Pierre Roques
- PL Vernazza
- R Hofmann-Lehmann
- RA Byrn
- RB Alexander
- RC Eyre
- RM Anderson
- RM Grant
- Roger Le Grand
- RW Coombs
- RW Coombs
- S Paranjpe
- S Willey
- SC Shiboski
- SI Staprans
- SJ Little
- SK Pillai
- Sylvanne Daniels
- T Bourlet
- T Zhu
- V Dioszeghy
- V Roulet
- V Roulet
- W Suarez-Pinzon
- X Liu
- Z Dai
- Publication venue
- Public Library of Science
- Publication date
- 01/01/2008
- Field of study
International audienceBACKGROUND: Although indirect evidence suggests the male genital tract as a possible source of persistent HIV shedding in semen during antiretroviral therapy, this phenomenon is poorly understood due to the difficulty of sampling semen-producing organs in HIV+ asymptomatic individuals. METHODOLOGY/PRINCIPAL FINDINGS: Using a range of molecular and cell biological techniques, this study investigates SIV infection within reproductive organs of macaques during the acute and chronic stages of the disease. We demonstrate for the first time the presence of SIV in the testes, epididymides, prostate and seminal vesicles as early as 14 days post-inoculation. This infection persists throughout the chronic stage and positively correlates with blood viremia. The prostate and seminal vesicles appear to be the most efficiently infected reproductive organs, followed by the epididymides and testes. Within the male genital tract, mostly T lymphocytes and a small number of germ cells harbour SIV antigens and RNA. In contrast to the other organs studied, the testis does not display an immune response to the infection. Testosteronemia is transiently increased during the early phase of the infection but spermatogenesis remains unaffected. CONCLUSIONS/SIGNIFICANCE: The present study reveals that SIV infection of the macaque male genital tract is an early event and that semen-producing organs display differential infection levels and immune responses. These results help elucidate the origin of HIV in semen and constitute an essential base to improving the design of antiretroviral therapies to eradicate virus from semen
Fusarium: more than a node or a foot-shaped basal cell
- Author
- Abdel-Azeem M. A.
- Abdollahzadeh J.
- Abdolrasouli Alireza
- Akulov A.
- Alberts Johanna F.
- Araújo João P.M.
- Ariyawansa Hiran A.S.
- Bakhshi Mounes
- Ben Hadj Amor A.
- Bensch Konstanze
- Bezerra J. D. P.
- Boekhout T.
- Cai L.
- Carbia Mauricio
- Cardinali Gianluigi
- Castañeda-Ruiz R. F.
- Celis-Ramírez Adriana Marcela
- Chaturvedi Vishnu
- Chaverri Priscila
- Collémare Jérôme
- Croll Daniel
- Crous P. W.
- Câmara M. P. S.
- Damm Ulrike
- Decock Cony A.
- Ezekiel Chibundu N.
- Fan X. L.
- Fernández Norma Beatriz
- Frisvad Jens Christian
- Gaya Ester
- Gené J.
- González Cristian D.
- Gramaje David
- Groenewald J.Z.
- Grube Martin
- Guarnaccia V.
- Guarro J.
- Guevara-Suarez Marcela I.
- Gupta Vijai Kumar
- Haddaji A.
- Haelewaters Danny
- Hagen Ferry
- Hansen Karen
- Hashimoto A.
- Hernández-Restrepo Margarita
- Hirooka Y.
- Houbraken Jos A. M. P.
- Hubka Vít
- Hyde K.D.
- Iturriaga Teresa M.
- Jeewon Rajesh
- Johnston Peter R.
- Jurjević Željko
- Karaltı İskender
- Kema Gerrit H. J.
- Korsten L.
- Kuramae Eiko Eurya
- Kušan Ivana
- Labuda Román
- Lamprecht Sandra Christina
- Lawrence Daniel P.
- Lechat Christian
- Lee Hyangburm
- Li Hongye
- Litovka Yulia A.
- Lombard L.
- Maharachchikumbura Sajeewa S. N.
- Marín-Felix Yasmina
- Matio Kemkuignou B.
- Matočec Neven
- McTaggart Alistair R.
- Merwe N. A. van der
- Messias Rodrigues Anderson
- Mlčoch Patrik
- Mugnai Laura
- Nakashima Chiharu
- Nilsson R. H.
- Noumeur Sara Raouia
- Pavlov Igor N.
- Peralta M. P.
- Phillips Alan J. L.
- Pitt John I.
- Ploch Sebastian
- Polizzi Giancarlo
- Quaedvlieg William
- Rajeshkumar Kunhiraman C.
- Restrepo Silvia
- Rhaïem Azza
- Robert J.
- Robert Vincent A. R. G.
- Rossman Amy Y.
- Salgado-Salazar Catalina
- Samson Robert A.
- Sandoval-Denis M.
- Santos Ariana C. S.
- Schroers H. J.
- Seifert K. A.
- Shivas Roger G.
- Souza-Motta C. M.
- Stadler Marc
- Summerbell Richard C.
- Sun G. Y.
- Swart Wijnand J.
- Szöke Szániszló
- Tan Yupei
- Taylor Joanne E.
- Taylor John W.
- Taylor P. W. J.
- Thines Marco
- Verkley Gerard J. M.
- Vieira Tiago Patricia
- Vieira Willie A. S.
- Visagie C. M.
- Vizzini Alfredo
- Vries Ronald P. de
- Váczy Kálmán Zoltán
- Weir Bevan S.
- Wiele Nathalie van de
- Wijayawardene Nalin N.
- Xia J. W.
- Yilmaz N.
- Yurkov Andrey M.
- Yáñez-Morales María de Jesús
- Zamora Juan Carlos
- Zare Rasoul
- Zhang C. L.
- Publication venue
- 'Elsevier BV'
- Publication date
- 24/02/2022
- Field of study
Recent publications have argued that there are potentially serious consequences for researchers in recognising distinct genera in the terminal fusarioid clade of the family Nectriaceae. Thus, an alternate hypothesis, namely a very broad concept of the genus Fusarium was proposed. In doing so, however, a significant body of data that supports distinct genera in Nectriaceae based on morphology, biology, and phylogeny is disregarded. A DNA phylogeny based on 19 orthologous protein-coding genes was presented to support a very broad concept of Fusarium at the F1 node in Nectriaceae. Here, we demonstrate that re-analyses of this dataset show that all 19 genes support the F3 node that represents Fusarium sensu stricto as defined by F. sambucinum (sexual morph synonym Gibberella pulicaris). The backbone of the phylogeny is resolved by the concatenated alignment, but only six of the 19 genes fully support the F1 node, representing the broad circumscription of Fusarium. Furthermore, a re-analysis of the concatenated dataset revealed alternate topologies in different phylogenetic algorithms, highlighting the deep divergence and unresolved placement of various Nectriaceae lineages proposed as members of Fusarium. Species of Fusarium s. str. are characterised by Gibberella sexual morphs, asexual morphs with thin- or thick-walled macroconidia that have variously shaped apical and basal cells, and trichothecene mycotoxin production, which separates them from other fusarioid genera. Here we show that the Wollenweber concept of Fusarium presently accounts for 20 segregate genera with clear-cut synapomorphic traits, and that fusarioid macroconidia represent a character that has been gained or lost multiple times throughout Nectriaceae. Thus, the very broad circumscription of Fusarium is blurry and without apparent synapomorphies, and does not include all genera with fusarium-like macroconidia, which are spread throughout Nectriaceae (e.g., Cosmosporella, Macroconia, Microcera). In this study four new genera are introduced, along with 18 new species and 16 new combinations. These names convey information about relationships, morphology, and ecological preference that would otherwise be lost in a broader definition of Fusarium. To assist users to correctly identify fusarioid genera and species, we introduce a new online identification database, Fusarioid-ID, accessible at www.fusarium.org. The database comprises partial sequences from multiple genes commonly used to identify fusarioid taxa (act1, CaM, his3, rpb1, rpb2, tef1, tub2, ITS, and LSU). In this paper, we also present a nomenclator of names that have been introduced in Fusarium up to January 2021 as well as their current status, types, and diagnostic DNA barcode data. In this study, researchers from 46 countries, representing taxonomists, plant pathologists, medical mycologists, quarantine officials, regulatory agencies, and students, strongly support the application and use of a more precisely delimited Fusarium (= Gibberella) concept to accommodate taxa from the robust monophyletic node F3 on the basis of a well-defined and unique combination of morphological and biochemical features. This F3 node includes, among others, species of the F. fujikuroi, F. incarnatum-equiseti, F. oxysporum, and F. sambucinum species complexes, but not species of Bisifusarium [F. dimerum species complex (SC)], Cyanonectria (F. buxicola SC), Geejayessia (F. staphyleae SC), Neocosmospora (F. solani SC) or Rectifusarium (F. ventricosum SC). The present study represents the first step to generating a new online monograph of Fusarium and allied fusarioid genera (www.fusarium.org)
Association of a Total Cholesterol Polygenic Score with Cholesterol Levels and Pathological Biomarkers across the Alzheimer’s Disease Spectrum
- Author
- Publication venue
- 'MDPI AG'
- Publication date
- 17/11/2021
- Field of study
Midlife hypercholesterolemia is a well-known risk factor for sporadic Alzheimer’s disease (AD), and like AD, it is highly influenced by genetics with heritability estimates of 32–63%. We thus hypothesized that genetics underlying peripheral blood total cholesterol (TC) levels could influence the risk of developing AD. We created a weighted polygenic score (TC-PGS) using summary data from a meta-analysis of TC genome-wide association studies for evaluation in three independent AD-related cohorts spanning pre-clinical, clinical, and pathophysiologically proved AD. APOE-ε4 variant was purposely included in the analysis as it represents an already well-established genetic risk factor for both AD and circulating TC. We could vastly improve the performance of the score when considering p-value thresholds for inclusion in the score, sex, and statin use. This optimized score (p-value threshold of 1 × 10−6 for inclusion in the score) explained 18.2% of the variance in TC levels in statin free females compared to 6.9% in the entire sample and improved prediction of hypercholesterolemia (receiver operator characteristics analysis revealed area under the curve increase from 70.8% to 80.5%). The TC-PGS was further evaluated for association with AD risk and pathology. We found no association between the TC-PGS and either of the AD hallmark pathologies, assessed by cerebrospinal fluid levels of Aβ-42, p-Tau, and t-Tau, and 18F-NAV4694 and 18F-AV-1451 positron emission tomography. Similarly, we found no association with the risk of developing amyloid pathology or becoming cognitively impaired in individuals with amyloid pathology
Studies of neutron-induced light-ion production with the MEDLEY facility
- Author
- Publication venue
- 'EDP Sciences'
- Publication date
- 01/01/2007
- Field of study
International audienceThe growing interest in applications involving high-energy neutrons (E > 20 MeV) demands high-quality experimental data on neutron-induced reactions. Such data have been measured with the MEDLEY setup at the The Svedberg Laboratory (TSL), Uppsala, Sweden. It has been used to measure differential cross sections for elastic nd scattering and double-differential cross sections for light-ion production (A ≤ 4) with targets ranging from C to U and at incident neutron energies around 96MeV. We summarize the experimental results obtained so far and compared with theoretical reaction model calculations. A new method for correcting charged-particle spectra for thick target effects has been used for data obtained with the MEDLEY facility. The new quasi-monoenergetic neutron beam facility of TSL offers the possibility to extend these measurements up to neutron energies of 175MeV. In January 2007, the neutron beam facility at TSL has been equipped with improved shielding and pre-collimator to reduce the background observed with MEDLEY during the first experimental campaigns at 175MeV to an acceptable level. We present the current status of the MEDLEY facility after the shielding upgrade. We summarize also our ongoing projects including both measurements of light-ion production at 175MeV from C to U targets and fission studies of U-238 in the energy region of 11 to 175MeV
SCANDAL - a facility for elastic neutron scattering studies in the 50-130 MeV range
- Author
- Ataç A.
- Bergenwall B.
- Blideanu V.
- Blomgren J.
- Dangtip S.
- Elmgren K.
- Eudes P.
- Haddad Ferid
- Herpers U.
- Johansson C.
- Jonsson O.
- Kerveno M.
- Kirchner T.
- Klug J.
- Le Brun C.
- Lebrun C.
- Lecolley F.R.
- Lecolley J.F.
- Louvel M.
- Marie Nathalie
- Michel R.
- Nadel-Turonski P.
- Neumann S.
- Nilsson L.
- Oberstedt A.
- Olsson N.
- Pomp S.
- Rahm J.
- Renberg P.-U.
- Ringbom A.
- Schweitzer C.
- Slypen I.
- Smirnov A.N.
- Stuttgé L.
- Tippawan U.
- Tovesson F.
- V. Prokofiev A.
- Varignon C.
- Publication venue
- 'Elsevier BV'
- Publication date
- 01/01/2002
- Field of study
A facility for detection of scattered neutrons in the energy interval 50–130 MeV, SCAttered Nucleon Detection AssembLy (SCANDAL), has recently been installed at the 20–180 MeV neutron beam facility of The Svedberg Laboratory, Uppsala. It is primarily intended for studies of elastic neutron scattering, but can be used for (n,p) and (n,d) reaction experiments as well. The performance of the spectrometer is illustrated in measurements of the (n,p) and (n,n) reactions on 1H and 12C. In addition, the neutron beam facility is described in some detail
Ripened Dairy Products Differentially Affect Hepatic Lipid Content and Adipose Tissue Oxidative Stress Markers in Obese and Type 2 Diabetic Mice
- Author
- Acheson K. J.
- Amandine Everard
- Backhed F.
- Bertoni G.
- Brun P.
- Callon C.
- Cani P. D.
- Cani P. D.
- Cani P. D.
- Choi H. K.
- Dandona P.
- Dewulf E. M.
- Duparc T.
- Folch J.
- Frid A. H.
- Fumeron F.
- Furukawa S.
- Gentile C. L.
- Geurts L.
- Guessous I.
- LeBlanc M. J.
- Levy J. R.
- Lucie Geurts
- Nathalie M. Delzenne
- Neyrinck A. M.
- Neyrinck A. M.
- Nilsson M.
- Pachikian B. D.
- Pascale le Ruyet
- Patrice D. Cani
- Pereira M. A.
- Petersen K. F.
- Polichetti E.
- Rebolledo O. R.
- Roden M.
- Samuel V. T.
- Sohet F. M.
- Sohet F. M.
- Stefan N.
- Wat E.
- Yecies J. L.
- Publication venue
- 'American Chemical Society (ACS)'
- Publication date
- Field of study
Aberrant activation of TCL1A promotes stem cell expansion in clonal haematopoiesis
- Author
- Abecasis Goncalo R
- Albert Christine
- Arnett Donna K
- Barnes Kathleen C
- Becker Lewis C
- Belk Julia A
- Bick Alexander G
- Bis Joshua C
- Blackwell Thomas W
- Blangero John
- Boerwinkle Eric
- Bouzid Hind
- Bowden Donald W
- Brody Jennifer A
- Broome Jai G
- Burugula Bala Bharathi
- Cade Brian E
- Chami Nathalie
- Chen Yii-Der Ida
- Cho Michael H
- Correa Adolfo
- Curran Joanne E
- Custer Brian S
- Cutler Michael J
- Daniel Bence
- Darbar Dawood
- de Andrade Mariza
- DeMeo Dawn L
- Desai Pinkal
- Duggirala Ravindranath
- Fornage Myriam
- Freedman Barry I
- Gao Yan
- Gopakumar Jayakrishnan
- Gu C. Charles
- Guo Xiuqing
- He Jiang
- Heckbert Susan R
- Hou Lifang
- Irvin Marguerite R
- Jahn Nikolaus
- Jaiswal Siddhartha
- Johnsen Jill M
- Johnson Andrew D
- Kane John P
- Kang Hyun M
- Kaplan Robert
- Kardia Sharon L. R
- Kenny Eimear E
- Kitzman Jacob O
- Knight Stacey
- Konkle Barbara A
- Kooperberg Charles
- Kääb Stefan
- Laurie Cecelia A
- Lee Wen-Jane
- Lewis Joshua P
- Lloyd-Jones Donald M
- Loos Ruth J. F
- Luna Sofia E
- Ly Nghi
- Mack Taralynn M
- Manson JoAnn E
- Marcus Gregory M
- Mathias Rasika A
- McGarvey Stephen
- Melander Olle
- Miao Zhuang
- Mitchell Shaneice R
- Muhlestein J. Brent
- Natarajan Pradeep
- Nilsson Peter M
- O\u27Connell Jeffrey R
- Palmer Nicholette D
- Peyser Patricia A
- Prothro Katherine P
- Psaty Bruce M
- Pullinger Clive R
- Qiao Dandi
- Raffield Laura M
- Redline Susan
- Reiner Alexander P
- Rich Stephen S
- Rienstra Michiel
- Roden Dan M
- Rotter Jerome I
- Satpathy Ansuman T
- Shoemaker M. Benjamin
- Shuldiner Alan R
- Silverman Edwin K
- Sinner Moritz F
- Smith Albert V
- Smith J. Gustav
- Smith Nicholas L
- Taylor Kent D
- Tiwari Hemant
- Tracy Russell P
- Uddin Md Mesbah
- Van der Harst Pim
- Vasan Ramachandran S
- von Falkenhausen Aenne S
- Weinstock Joshua S
- Wheeler Marsha M
- Whitsel Eric A
- Wiggins Kerri L
- Williams Keoki L
- Xiao Shujie
- Yanek Lisa R
- Yang Mao
- Yun Jeong H
- Zhou Ying
- Publication venue
- Henry Ford Health Scholarly Commons
- Publication date
- 01/04/2023
- Field of study
Mutations in a diverse set of driver genes increase the fitness of haematopoietic stem cells (HSCs), leading to clonal haematopoiesis(1). These lesions are precursors for blood cancers(2-6), but the basis of their fitness advantage remains largely unknown, partly owing to a paucity of large cohorts in which the clonal expansion rate has been assessed by longitudinal sampling. Here, to circumvent this limitation, we developed a method to infer the expansion rate from data from a single time point. We applied this method to 5,071 people with clonal haematopoiesis. A genome-wide association study revealed that a common inherited polymorphism in the TCL1A promoter was associated with a slower expansion rate in clonal haematopoiesis overall, but the effect varied by driver gene. Those carrying this protective allele exhibited markedly reduced growth rates or prevalence of clones with driver mutations in TET2, ASXL1, SF3B1 and SRSF2, but this effect was not seen in clones with driver mutations in DNMT3A. TCL1A was not expressed in normal or DNMT3A-mutated HSCs, but the introduction of mutations in TET2 or ASXL1 led to the expression of TCL1A protein and the expansion of HSCs in vitro. The protective allele restricted TCL1A expression and expansion of mutant HSCs, as did experimental knockdown of TCL1A expression. Forced expression of TCL1A promoted the expansion of human HSCs in vitro and mouse HSCs in vivo. Our results indicate that the fitness advantage of several commonly mutated driver genes in clonal haematopoiesis may be mediated by TCL1A activation
Erratum to: Guidelines for the use and interpretation of assays for monitoring autophagy (3rd edition) (Autophagy, 12, 1, 1-222, 10.1080/15548627.2015.1100356
- Author
- Abdelmohsen Kotb
- Abe Akihisa
- Abedin Md Joynal
- Abeliovich Hagai
- Adachi Hiroaki
- Adams Christopher M.
- Adams Peter D.
- Adeli Khosrow
- Adhihetty Peter J.
- Adler Sharon G.
- Agam Galila
- Agarwal Rajesh
- Aghi Manish K.
- Agnello Maria
- Agostinis Patrizia
- Aguilar Patricia V.
- Aguirre-Ghiso Julio
- Airoldi Edoardo M.
- Ait-Si-Ali Slimane
- Akematsu Takahiko
- Akporiaye Emmanuel T.
- Al-Rubeai Mohamed
- Albaiceta Guillermo M.
- Albanese Chris
- Albani Diego
- Albert Matthew L.
- Aldudo Jesus
- Algül Hana
- Alirezaei Mehrdad
- Alloza Iraide
- Almasan Alexandru
- Almonte-Beceril Maylin
- Alnemri Emad S.
- Alonso Covadonga
- Altan-Bonnet Nihal
- Altieri Dario C.
- Alvarez Silvia
- Alvarez-Erviti Lydia
- Alves Sandro
- Amadoro Giuseppina
- Amano Atsuo
- Amantini Consuelo
- Ambrosio Santiago
- Amelio Ivano
- Amer Amal O.
- Amessou Mohamed
- Amon Angelika
- An Zhenyi
- Anania Frank A.
- Andersen Stig U.
- Andley Usha P.
- Andreadi Catherine K.
- Andrieu-Abadie Nathalie
- Anel Alberto
- Ann David K.
- Anoopkumar-Dukie Shailendra
- Antonioli Manuela
- Aoki Hiroshi
- Apostolova Nadezda
- Aquila Saveria
- Aquilano Katia
- Araki Koichi
- Arama Eli
- Aranda Agustin
- Araya Jun
- Arcaro Alexandre
- Arias Esperanza
- Arimoto Hirokazu
- Ariosa Aileen R.
- Armstrong Jane L.
- Arnould Thierry
- Arozena Abraham Acevedo
- Arsov Ivica
- Asanuma Katsuhiko
- Askanas Valerie
- Asselin Eric
- Atarashi Ryuichiro
- Atherton Sally S.
- Atkin Julie D.
- Attardi Laura D.
- Auberger Patrick
- Auburger Georg
- Aurelian Laure
- Autelli Riccardo
- Avagliano Laura
- Avantaggiati Maria Laura
- Avrahami Limor
- Awale Suresh
- Azad Neelam
- Bachetti Tiziana
- Backer Jonathan M.
- Bae Dong-Hun
- Bae Jae-Sung
- Bae Ok-Nam
- Bae Soo Han
- Baehrecke Eric H.
- Baek Seung-Hoon
- Baghdiguian Stephen
- Bagniewska-Zadworna Agnieszka
- Bai Hua
- Bai Jie
- Bai Xue-Yuan
- Bailly Yannick
- Balaji Kithiganahalli Narayanaswamy
- Balduini Walter
- Ballabio Andrea
- Balzan Rena
- Banerjee Rajkumar
- Bao Haijun
- Barbato Daniele Lettieri
- Barbeau Benoit
- Barrachina Maria D.
- Barreiro Esther
- Bartel Bonnie
- Bartolomé Alberto
- Bassham Diane C.
- Bassi Maria Teresa
- Bast Robert C.
- Basu Alakananda
- Batista Maria Teresa
- Batoko Henri
- Battino Maurizio
- Bauckman Kyle
- Baumgarner Bradley L.
- Bayer K. Ulrich
- Beale Rupert
- Beaulieu Jean-François
- Beck George R.
- Becker Christoph
- Beckham J. David
- Bednarski Patrick J.
- Begley Thomas J.
- Behl Christian
- Behrends Christian
- Behrens Georg M. N.
- Behrns Kevin E.
- Bejarano Eloy
- Belaid Amine
- Belleudi Francesca
- Berchem Guy
- Bergamaschi Daniele
- Bergami Matteo
- Berkhout Ben
- Berliocchi Laura
- Bernard Amélie
- Bernard Monique
- Bernassola Francesca
- Bertolotti Anne
- Bess Amanda S.
- Besteiro Sébastien
- Bettuzzi Saverio
- Bhalla Savita
- Bhattacharyya Shalmoli
- Bhutia Sujit K.
- Biagosch Caroline
- Bianchi Michele Wolfe
- Biard-Piechaczyk Martine
- Billes Viktor
- Bincoletto Claudia
- Bingol Baris
- Bird Sara W.
- Bitoun Marc
- Bjedov Ivana
- Blackstone Craig
- Blanc Lionel
- Blanco Guillermo A.
- Blomhoff Heidi Kiil
- Boada-Romero Emilio
- Boes Marianne
- Boesze-Battaglia Kathleen
- Boise Lawrence H.
- Bolino Alessandra
- Boman Andrea
- Bonaldo Paolo
- Bordi Matteo
- Bosch Jürgen
- Botana Luis M.
- Botti Joelle
- Bou German
- Bouchecareilh Marion
- Boucher Marie-Josée
- Bouché Marina
- Boulton Michael E.
- Bouret Sebastien G.
- Boya Patricia
- Boyer-Guittaut Michaël
- Bozhkov Peter V.
- Brady Nathan
- Braga Vania M. M.
- Brancolini Claudio
- Braus Gerhard H.
- Bravosan-Pedro José M.
- Brennan Lisa A.
- Bresnick Emery H.
- Brest Patrick
- Bridges Dave
- Bringer Marie-Agnès
- Brini Marisa
- Brito Glauber C.
- Brodin Bertha
- Brookes Paul S.
- Brown Eric J.
- Brown Karen
- Broxmeyer Hal E.
- Bruhat Alain
- Brum Patricia Chakur
- Brumell John H.
- Brunetti-Pierri Nicola
- Bryson-Richardson Robert J.
- Buch Shilpa
- Buchan Alastair M.
- Budak Hikmet
- Bulavin Dmitry V.
- Bultman Scott J.
- Bultynck Geert
- Bumbasirevic Vladimir
- Burelle Yan
- Burke Robert E.
- Burmeister Margit
- Bánhegyi Gábor
- Bédard Pierre-André
- Bénard Giovanni
- Böckler Stefan
- Bütikofer Peter
- Caberlotto Laura
- Cadwell Ken
- Cahova Monika
- Cai Dongsheng
- Cai Jingjing
- Cai Qian
- Calatayud Sara
- Camougrand Nadine
- Campagne Menno van Lookeren
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- Vogl Dan T.
- Voitsekhovskaja Olga V.
- von Haefen Clarissa
- von Schwarzenberg Karin
- Voth Daniel E.
- Vouret-Craviari Valérie
- Vuori Kristina
- Vyas Jatin M.
- Váchová Libuše
- Véscovi Eleonora García
- Waeber Christian
- Walker Cheryl Lyn
- Walker Mark J.
- Walter Jochen
- Wan Lei
- Wan Xiangbo
- Wang Bo
- Wang Caihong
- Wang Chao-Yung
- Wang Chengshu
- Wang Chenran
- Wang Chuangui
- Wang Dong
- Wang Fen
- Wang Fuxin
- Wang Guanghui
- Wang Hai-Jie
- Wang Haichao
- Wang Hong-Gang
- Wang Hongmin
- Wang Horng-Dar
- Wang Jing
- Wang Junjun
- Wang Mei
- Wang Mei-Qing
- Wang Pei-Yu
- Wang Peng
- Wang Richard C.
- Wang Shuo
- Wang Ting-Fang
- Wang Xian
- Wang Xiao-Jia
- Wang Xiao-Wei
- Wang Xin
- Wang Xuejun
- Wang Yan
- Wang Yanming
- Wang Ying
- Wang Ying-Jan
- Wang Yipeng
- Wang Yu
- Wang Yu Tian
- Wang Yuqing
- Wang Zhi-Nong
- Wappner Pablo
- Ward Carl
- Ward Diane McVey
- Warnes Gary
- Watada Hirotaka
- Watanabe Yoshihisa
- Watase Kei
- Weaver Timothy E.
- Weekes Colin D.
- Wei Jiwu
- Weide Thomas
- Weihl Conrad C.
- Weindl Günther
- Weis Simone Nardin
- Wen Longping
- Wen Xin
- Wen Yunfei
- Westermann Benedikt
- Weyand Cornelia M.
- White Anthony R.
- White Eileen
- Whitton J. Lindsay
- Whitworth Alexander J.
- Wiels Joëlle
- Wild Franziska
- Wildenberg Manon E.
- Wileman Tom
- Wilkinson Deepti Srinivas
- Wilkinson Simon
- Willbold Dieter
- Williams Chris
- Williams Katherine
- Williamson Peter R.
- Winklhofer Konstanze F.
- Witkin Steven S.
- Wohlgemuth Stephanie E.
- Wollert Thomas
- Wolvetang Ernst J.
- Wong Esther
- Wong G. William
- Wong Richard W.
- Wong Vincent Kam Wai
- Woodcock Elizabeth A.
- Wright Karen L.
- Wu Chunlai
- Wu Defeng
- Wu Gen Sheng
- Wu Jian
- Wu Junfang
- Wu Mian
- Wu Min
- Wu Shengzhou
- Wu William K. K.
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- Xia Gui-Xian
- Xia Tian
- Xia Weiliang
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- Xiao Hengyi
- Xiao Jian
- Xiao Shi
- Xiao Wuhan
- Xie Chuan-Ming
- Xie Zhiping
- Xie Zhonglin
- Xilouri Maria
- Xiong Yuyan
- Xu Chuanshan
- Xu Congfeng
- Xu Feng
- Xu Haoxing
- Xu Hongwei
- Xu Jian
- Xu Jianzhen
- Xu Jinxian
- Xu Liang
- Xu Xiaolei
- Xu Yangqing
- Xu Ye
- Xu Zhi-Xiang
- Xu Ziheng
- Xue Yu
- Yamada Takahiro
- Yamamoto Ai
- Yamanaka Koji
- Yamashina Shunhei
- Yamashiro Shigeko
- Yan Bing
- Yan Bo
- Yan Xianghua
- Yan Zhen
- Yanagi Yasuo
- Yang Dun-Sheng
- Yang Jin-Ming
- Yang Liu
- Yang Minghua
- Yang Pei-Ming
- Yang Peixin
- Yang Qian
- Yang Wannian
- Yang Wei Yuan
- Yang Xuesong
- Yang Yi
- Yang Ying
- Yang Zhifen
- Yang Zhihong
- Yao Meng-Chao
- Yao Pamela J.
- Yao Xiaofeng
- Yao Zhenyu
- Yao Zhiyuan
- Yasui Linda S.
- Ye Mingxiang
- Yedvobnick Barry
- Yeganeh Behzad
- Yeh Elizabeth S.
- Yeyati Patricia L.
- Yi Fan
- Yi Long
- Yin Xiao-Ming
- Yip Calvin K.
- Yoo Yeong-Min
- Yoo Young Hyun
- Yoon Seung-Yong
- Yoshida Ken-Ichi
- Yoshimori Tamotsu
- Young Ken H.
- Yu Huixin
- Yu Jane J.
- Yu Jin-Tai
- Yu Jun
- Yu Li
- Yu W. Haung
- Yu Xiao-Fang
- Yu Zhengping
- Yuan Junying
- Yuan Zhi-Min
- Yue Beatrice Y. J. T.
- Yue Jianbo
- Yue Zhenyu
- Zacks David N.
- Zacksenhaus Eldad
- Zaffaroni Nadia
- Zaglia Tania
- Zakeri Zahra
- Zecchini Vincent
- Zeng Jinsheng
- Zeng Min
- Zeng Qi
- Zervos Antonis S.
- Zhang Donna D.
- Zhang Fan
- Zhang Guo
- Zhang Guo-Chang
- Zhang Hao
- Zhang Hong
- Zhang Hongbing
- Zhang Jian
- Zhang Jiangwei
- Zhang Jianhua
- Zhang Jing-Pu
- Zhang Li
- Zhang Lin
- Zhang Long
- Zhang Ming-Yong
- Zhang Xiangnan
- Zhang Xu Dong
- Zhang Yan
- Zhang Yang
- Zhang Yanjin
- Zhang Yingmei
- Zhang Yunjiao
- Zhao Mei
- Zhao Wei-Li
- Zhao Xiaonan
- Zhao Yan G.
- Zhao Ying
- Zhao Yongchao
- Zhao Yu-Xia
- Zhao Zhendong
- Zhao Zhizhuang J.
- Zheng Dexian
- Zheng Xi-Long
- Zheng Xiaoxiang
- Zhivotovsky Boris
- Zhong Qing
- Zhou Guang-Zhou
- Zhou Guofei
- Zhou Huiping
- Zhou Shu-Feng
- Zhou Xu-Jie
- Zhu Hongxin
- Zhu Hua
- Zhu Wei-Guo
- Zhu Wenhua
- Zhu Xiao-Feng
- Zhu Yuhua
- Zhuang Shi-Mei
- Zhuang Xiaohong
- Ziparo Elio
- Zois Christos E.
- Zoladek Teresa
- Zong Wei-Xing
- Zorzano Antonio
- Zughaier Susu M.
- Publication venue
- 'Informa UK Limited'
- Publication date
- 01/01/2016
- Field of study
non present
Guidelines for the use and interpretation of assays for monitoring autophagy (3rd edition)
- Author
- Abdelmohsen Kotb
- Abe Akihisa
- Abedin Md Joynal
- Abeliovich Hagai
- Adachi Hiroaki
- Adams Christopher M.
- Adams Peter D.
- Adeli Khosrow
- Adhihetty Peter J.
- Adler Sharon G.
- Agam Galila
- Agarwal Rajesh
- Aghi Manish K.
- Agnello Maria
- Agostinis Patrizia
- Aguilar Patricia V.
- Aguirre-Ghiso Julio
- Airoldi Edoardo M.
- Ait-Si-Ali Slimane
- Akematsu Takahiko
- Akporiaye Emmanuel T.
- Al-Rubeai Mohamed
- Albaiceta Guillermo M.
- Albanese Chris
- Albani Diego
- Albert Matthew L.
- Aldudo Jesus
- Alguel Hana
- Alirezaei Mehrdad
- Alloza Iraide
- Almasan Alexandru
- Almonte-Beceril Maylin
- Alnemri Emad S.
- Alonso Covadonga
- Altan-Bonnet Nihal
- Altieri Dario C.
- Alvarez Silvia
- Alvarez-Erviti Lydia
- Alves Sandro
- Amadoro Giuseppina
- Amano Atsuo
- Amantini Consuelo
- Ambrosio Santiago
- Amelio Ivano
- Amer Amal O.
- Amessou Mohamed
- Amon Angelika
- An Zhenyi
- Ana Gonzalez-Polo Rosa
- Anania Frank A.
- Andersen Stig U.
- Andley Usha P.
- Andreadi Catherine K.
- Andrieu-Abadie Nathalie
- Anel Alberto
- Ann David K.
- Anoopkumar-Dukie Shailendra
- Antonioli Manuela
- Aoki Hiroshi
- Apostolova Nadezda
- Aquila Saveria
- Aquilano Katia
- Araki Koichi
- Arama Eli
- Aranda Agustin
- Araya Jun
- Arcaro Alexandre
- Arias Esperanza
- Arimoto Hirokazu
- Ariosa Aileen R.
- Armstrong Jane L.
- Arnould Thierry
- Arozena Abraham Acevedo
- Arsov Ivica
- Asanuma Katsuhiko
- Askanas Valerie
- Asselin Eric
- Atarashi Ryuichiro
- Atherton Sally S.
- Atkin Julie D.
- Attardi Laura D.
- Auberger Patrick
- Auburger Georg
- Aurelian Laure
- Autelli Riccardo
- Avagliano Laura
- Avantaggiati Maria Laura
- Avrahami Limor
- Awale Suresh
- Azad Neelam
- Bachetti Tiziana
- Backer Jonathan M.
- Bae Dong-Hun
- Bae Jae-Sung
- Bae Ok-Nam
- Bae Soo Han
- Baehrecke Eric H.
- Baek Seung-Hoon
- Baghdiguian Stephen
- Bagniewska-Zadworna Agnieszka
- Bai Hua
- Bai Jie
- Bai Xue-Yuan
- Bailly Yannick
- Balaji Kithiganahalli Narayanaswamy
- Balduini Walter
- Ballabio Andrea
- Balzan Rena
- Banerjee Rajkumar
- Banhegyi Gabor
- Bao Haijun
- Barbato Daniele Lettieri
- Barbeau Benoit
- Barrachina Maria D.
- Barreiro Esther
- Bartel Bonnie
- Bartolome Alberto
- Bassham Diane C.
- Bassi Maria Teresa
- Bast Robert C., Jr.
- Basu Alakananda
- Batista Maria Teresa
- Batoko Henri
- Battino Maurizio
- Bauckman Kyle
- Baumgarner Bradley L.
- Bayer K. Ulrich
- Beale Rupert
- Beaulieu Jean-Francois
- Beck George R., Jr.
- Becker Christoph
- Beckham J. David
- Bedard Pierre-Andre
- Bednarski Patrick J.
- Begley Thomas J.
- Behl Christian
- Behrends Christian
- Behrens Georg M. N.
- Behrns Kevin E.
- Bejarano Eloy
- Belaid Amine
- Belleudi Francesca
- Benard Giovanni
- Berchem Guy
- Bergamaschi Daniele
- Bergami Matteo
- Berkhout Ben
- Berliocchi Laura
- Bernard Amelie
- Bernard Monique
- Bernassola Francesca
- Bertolotti Anne
- Bess Amanda S.
- Besteiro Sebastien
- Bettuzzi Saverio
- Bhalla Savita
- Bhattacharyya Shalmoli
- Bhutia Sujit K.
- Biagosch Caroline
- Bianchi Michele Wolfe
- Biard-Piechaczyk Martine
- Billes Viktor
- Bincoletto Claudia
- Bingol Baris
- Bird Sara W.
- Bitoun Marc
- Bjedov Ivana
- Blackstone Craig
- Blanc Lionel
- Blanco Guillermo A.
- Blomhoff Heidi Kiil
- Boada-Romero Emilio
- Boeckler Stefan
- Boes Marianne
- Boesze-Battaglia Kathleen
- Boise Lawrence H.
- Bolino Alessandra
- Boman Andrea
- Bonaldo Paolo
- Bordi Matteo
- Bosch Jurgen
- Botana Luis M.
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- Bou German
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- Bouchecareilh Marion
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- Boulton Michael E.
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- Bozhkov Peter V.
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- Brancolini Claudio
- Braus Gerhard H.
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- Brennan Lisa A.
- Bresnick Emery H.
- Bressan Queiroz de Figueiredo Regina Celia
- Brest Patrick
- Bridges Dave
- Bringer Marie-Agnes
- Brini Marisa
- Brito Glauber C.
- Brodin Bertha
- Brookes Paul S.
- Brown Eric J.
- Brown Karen
- Broxmeyer Hal E.
- Bruhat Alain
- Brum Patricia Chakur
- Brumell John H.
- Brunetti-Pierri Nicola
- Bryson-Richardson Robert J.
- Buch Shilpa
- Buchan Alastair M.
- Budak Hikmet
- Buetikofer Peter
- Bulavin Dmitry V.
- Bultman Scott J.
- Bultynck Geert
- Bumbasirevic Vladimir
- Burelle Yan
- Burke Robert E.
- Burmeister Margit
- Caberlotto Laura
- Cadwell Ken
- Cahova Monika
- Cai Dongsheng
- Cai Jingjing
- Cai Qian
- Calatayud Sara
- Camougrand Nadine
- Campanella Michelangelo
- Campbell Grant R.
- Campbell Matthew
- Campello Silvia
- Candau Robin
- Caniggia Isabella
- Cantoni Lavinia
- Cao Lizhi
- Caplan Allan B.
- Caraglia Michele
- Cardinali Claudio
- Cardoso Sandra Morais
- Carew Jennifer S.
- Carleton Laura A.
- Carlin Cathleen R.
- Carloni Silvia
- Carlsson Sven R.
- Carmona-Gutierrez Didac
- Carneiro Leticia A. M.
- Carnevali Oliana
- Carra Serena
- Carrier Alice
- Carroll Bernadette
- Casas Caty
- Casas Josefina
- Cassinelli Giuliana
- Castets Perrine
- Castro-Obregon Susana
- Cavallini Gabriella
- Ceccherini Isabella
- Cecconi Francesco
- Cederbaum Arthur I.
- Cena Valentin
- Cenci Simone
- Cerella Claudia
- Cervia Davide
- Cetrullo Silvia
- Chaachouay Hassan
- Chae Han-Jung
- Chagin Andrei S.
- Chai Chee-Yin
- Chakrabarti Gopal
- Chamilos Georgios
- Chan Edmond Y. W.
- Chan Matthew T. V.
- Chandra Dhyan
- Chandra Pallavi
- Chang Chih-Peng
- Chang Raymond Chuen-Chung
- Chang Ta Yuan
- Chatham John C.
- Chatterjee Saurabh
- Chauhan Santosh
- Che Yongsheng
- Cheetham Michael E.
- Cheluvappa Rajkumar
- Chen Chun-Jung
- Chen Gang
- Chen Guang-Chao
- Chen Guoqiang
- Chen Hongzhuan
- Chen Jeff W.
- Chen Jian-Kang
- Chen Min
- Chen Mingzhou
- Chen Peiwen
- Chen Qi
- Chen Quan
- Chen Shang-Der
- Chen Si
- Chen Steve S-L
- Chen Wei
- Chen Wei-Jung
- Chen Wen Qiang
- Chen Wenli
- Chen Xiangmei
- Chen Yau-Hung
- Chen Ye-Guang
- Chen Yin
- Chen Yingyu
- Chen Yongshun
- Chen Yu-Jen
- Chen Yue-Qin
- Chen Yujie
- Chen Zhen
- Chen Zhong
- Cheng Alan
- Cheng Christopher H. K.
- Cheng Hua
- Cheong Heesun
- Cherry Sara
- Chesney Jason
- Cheung Chun Hei Antonio
- Chevet Eric
- Chi Hsiang Cheng
- Chi Sung-Gil
- Chiacchiera Fulvio
- Chiang Hui-Ling
- Chiarelli Roberto
- Chiariello Mario
- Chieppa Marcello
- Chin Lih-Shen
- Chiong Mario
- Chiu Gigi N. C.
- Cho Dong-Hyung
- Cho Ssang-Goo
- Cho William C.
- Cho Yong-Yeon
- Cho Young-Seok
- Choi Augustine M. K.
- Choi Eui-Ju
- Choi Eun-Kyoung
- Choi Jayoung
- Choi Mary E.
- Choi Seung-Il
- Chou Tsui-Fen
- Chouaib Salem
- Choubey Divaker
- Choubey Vinay
- Chow Kuan-Chih
- Chowdhury Kamal
- Chu Charleen T.
- Chuang Tsung-Hsien
- Chun Taehoon
- Chung Hyewon
- Chung Taijoon
- Chung Yuen-Li
- Chwae Yong-Joon
- Cianfanelli Valentina
- Ciarcia Roberto
- Ciechomska Iwona A.
- Ciriolo Maria Rosa
- Cirone Mara
- Claerhout Sofie
- Clague Michael J.
- Claria Joan
- Clarke Peter G. H.
- Clarke Robert
- Clementi Emilio
- Cleyrat Cedric
- Cnop Miriam
- Coccia Eliana M.
- Cocco Tiziana
- Codogno Patrice
- Coers Joern
- Cohen Ezra E. W.
- Colecchia David
- Coletto Luisa
- Coll Nuria S.
- Colucci-Guyon Emma
- Comincini Sergio
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- Corasaniti Maria Tiziana
- Corazzari Marco
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- Cordero Mario D.
- Corral-Ramos Cristina
- Corti Olga
- Cossarizza Andrea
- Costelli Paola
- Costes Safia
- Costes Safia
- Coto-Montes Ana
- Cottet Sandra
- Couve Eduardo
- Covey Lori R.
- Cowart L. Ashley
- Cox Jeffery S.
- Coxon Fraser P.
- Coyne Carolyn B.
- Cragg Mark S.
- Craven Rolf J.
- Crepaldi Tiziana
- Crespo Jose L.
- Criollo Alfredo
- Crippa Valeria
- Cruz Maria Teresa
- Cuervo Ana Maria
- Cuezva Jose M.
- Cui Taixing
- Cutillas Pedro R.
- Czaja Mark J.
- Czyzyk-Krzeska Maria F.
- D'Amelio Marcello
- D'Orazi Gabriella
- Dagda Ruben K.
- Dahmen Uta
- Dai Chunsun
- Dai Wenjie
- Dai Yun
- Dalby Kevin N.
- Dalmasso Guillaume
- Damme Markus
- Darfeuille-Michaud Arlette
- Dargemont Catherine
- Darley-Usmar Victor M.
- Dasarathy Srinivasan
- Dasgupta Biplab
- Dash Srikanta
- Dass Crispin R.
- Davey Hazel Marie
- Davids Lester M.
- Davila David
- Davis Roger J.
- Dawson Ted M.
- Dawson Valina L.
- Daza Paula
- de Belleroche Jackie
- de Figueiredo Paul
- de la Fuente Jose
- De Martino Luisa
- De Matteis Antonella
- De Meyer Guido
- De Milito Angelo
- De Santi Mauro
- de Souza Wanderley
- De Tata Vincenzo
- De Zio Daniela
- Debnath Jayanta
- Dechant Reinhard
- Decuypere Jean-Paul
- Deegan Shane
- Dehay Benjamin
- Del Bello Barbara
- Del Re Dominic P.
- Delage-Mourroux Regis
- Delbridge Lea M. D.
- Deldicque Louise
- Delorme-Axford Elizabeth
- Deng Yizhen
- Dengjel Joern
- Denizot Melanie
- Dent Paul
- Der Channing J.
- Deretic Vojo
- Derrien Benoit
- Deutsch Eric
- Devarenne Timothy P.
- Devenish Rodney J.
- Di Bartolomeo Sabrina
- Di Daniele Nicola
- Di Domenico Fabio
- Di Nardo Alessia
- Di Paola Simone
- Di Pietro Antonio
- Di Renzo Livia
- DiAntonio Aaron
- Diaz-Araya Guillermo
- Diaz-Laviada Ines
- Diaz-Meco Maria T.
- Diaz-Nido Javier
- Dickey Chad A.
- Dickson Robert C.
- Diederich Marc
- Digard Paul
- Dikic Ivan
- Dinesh-Kumar Savithrama P.
- Ding Chan
- Ding Wen-Xing
- Ding Zufeng
- Dini Luciana
- Distler Joerg H. W.
- Diwan Abhinav
- Djavaheri-Mergny Mojgan
- Dmytruk Kostyantyn
- Dobson Renwick C. J.
- Doetsch Volker
- Dokladny Karol
- Dokudovskaya Svetlana
- Donadelli Massimo
- Dong X. Charlie
- Dong Xiaonan
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- Doran Kelly S.
- Dorn Gerald W., II
- dos Santos Claudia Nunes
- Dosenko Victor
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- Dumit Veronica I.
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- Eichinger Ludwig
- Eisenberg Tobias
- Eisenberg-Lerner Avital
- Eissa N. Tony
- El-Deiry Wafik S.
- El-Khoury Victoria
- Elazar Zvulun
- Eldar-Finkelman Hagit
- Elliott Chris J. H.
- Emanuele Enzo
- Emmenegger Urban
- Engedal Nikolai
- Engelbrecht Anna-Mart
- Engelender Simone
- Enserink Jorrit M.
- Erdmann Ralf
- Erenpreisa Jekaterina
- Eri Rajaraman
- Eriksen Jason L.
- Erman Andreja
- Escalante Ricardo
- Eskelinen Eeva-Liisa
- Espert Lucile
- Esteban-Martinez Lorena
- Esther Perez-Perez Maria
- Evans Thomas J.
- Fabri Mario
- Fabrias Gemma
- Fabrizi Cinzia
- Facchiano Antonio
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- Faggioni Alberto
- Fairlie W. Douglas
- Fan Chunhai
- Fan Daping
- Fan Jie
- Fang Shengyun
- Fanto Manolis
- Fanzani Alessandro
- Farkas Thomas
- Faure Mathias
- Favier Francois B.
- Fearnhead Howard
- Federici Massimo
- Fei Erkang
- Felizardo Tania C.
- Feng Hua
- Feng Yibin
- Feng Yuchen
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- Fernandez Alvaro F.
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- Fernandez-Lopez Arsenio
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- Ferraro Elisabetta
- Ferreira-Halder Carmen Verissima
- Fesus Laszlo
- Feuer Ralph
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- Filippi-Chiela Eduardo C.
- Filomeni Giuseppe
- Fimia Gian Maria
- Fingert John H.
- Finkbeiner Steven
- Finkel Toren
- Fiorito Filomena
- Fisher Paul B.
- Flajolet Marc
- Flamigni Flavio
- Florey Oliver
- Florio Salvatore
- Floto R. Andres
- Folini Marco
- Follo Carlo
- Fon Edward A.
- Fornai Francesco
- Fortunato Franco
- Fraldi Alessandro
- Franco Rodrigo
- Francois Arnaud
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- Freyssenet Damien G.
- Frezza Christian
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- Frigo Daniel E.
- Fu Dongxu
- Fuentes Jose M.
- Fueyo Juan
- Fujitani Yoshio
- Fujiwara Yuuki
- Fujiya Mikihiro
- Fukuda Mitsunori
- Fulda Simone
- Fusco Carmela
- Gabryel Bozena
- Gaestel Matthias
- Gailly Philippe
- Gajewska Malgorzata
- Galadari Sehamuddin
- Galili Gad
- Galindo Inmaculada
- Galindo Maria F.
- Galliciotti Giovanna
- Galluzzi Lorenzo
- Galluzzi Luca
- Galy Vincent
- Gammoh Noor
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- Ganley Ian G.
- Gannage Monique
- Gao Fen-Biao
- Gao Feng
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- Garcia Nannig Lorena
- Garcia-Macia Marina
- Garcia-Ruiz Carmen
- Garg Abhishek D.
- Garg Pramod Kumar
- Gargini Ricardo
- Gassen Nils Christian
- Gatica Damian
- Gatti Evelina
- Gavard Julie
- Gavathiotis Evripidis
- Ge Liang
- Ge Pengfei
- Ge Shengfang
- Gean Po-Wu
- Gelmetti Vania
- Genazzani Armando A.
- Geng Jiefei
- Genschik Pascal
- Gerner Lisa
- Gestwicki Jason E.
- Gewirtz David A.
- Ghavami Saeid
- Ghigo Eric
- Ghosh Debabrata
- Giammarioli Anna Maria
- Giampieri Francesca
- Giampietri Claudia
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- Gibellini Lara
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- Ginet Vanessa
- Giordano Antonio
- Giorgini Flaviano
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- Girardin Stephen E.
- Gispert Suzana
- Giuliano Sandy
- Gladson Candece L.
- Glavic Alvaro
- Gleave Martin
- Godefroy Nelly
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- Gokulan Kuppan
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- Gong Qingqiu
- Gongora Celine
- Gonzalez Carlos B.
- Gonzalez-Alegre Pedro
- Gonzalez-Cabo Pilar
- Goping Ing Swie
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- Gorbunov Nikolai V.
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- Goto-Yamada Shino
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- Yao Xiaofeng
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- Yasui Linda S.
- Ye Mingxiang
- Yedvobnick Barry
- Yeganeh Behzad
- Yeh Elizabeth S.
- Yeyati Patricia L.
- Yi Fan
- Yi Long
- Yin Xiao-Ming
- Yip Calvin K.
- Yoo Yeong-Min
- Yoo Young Hyun
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- Yoshida Ken-Ichi
- Yoshimori Tamotsu
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- Yu Huixin
- Yu Jane J.
- Yu Jin-Tai
- Yu Jun
- Yu Li
- Yu W. Haung
- Yu Xiao-Fang
- Yu Zhengping
- Yuan Junying
- Yuan Zhi-Min
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- Yue Jianbo
- Yue Zhenyu
- Zacks David N.
- Zacksenhaus Eldad
- Zaffaroni Nadia
- Zaglia Tania
- Zakeri Zahra
- Zecchini Vincent
- Zeng Jinsheng
- Zeng Min
- Zeng Qi
- Zervos Antonis S.
- Zhang Donna D.
- Zhang Fan
- Zhang Guo
- Zhang Guo-Chang
- Zhang Hao
- Zhang Hong
- Zhang Hong
- Zhang Hongbing
- Zhang Jian
- Zhang Jian
- Zhang Jiangwei
- Zhang Jianhua
- Zhang Jing-pu
- Zhang Li
- Zhang Lin
- Zhang Lin
- Zhang Long
- Zhang Ming-Yong
- Zhang Xiangnan
- Zhang Xu Dong
- Zhang Yan
- Zhang Yang
- Zhang Yanjin
- Zhang Yingmei
- Zhang Yunjiao
- Zhao Mei
- Zhao Wei-Li
- Zhao Xiaonan
- Zhao Yan G.
- Zhao Ying
- Zhao Yongchao
- Zhao Yu-Xia
- Zhao Zhendong
- Zhao Zhizhuang J.
- Zheng Dexian
- Zheng Xi-Long
- Zheng Xiaoxiang
- Zhivotovsky Boris
- Zhong Qing
- Zhou Guang-Zhou
- Zhou Guofei
- Zhou Huiping
- Zhou Shu-Feng
- Zhou Xu-Jie
- Zhu Hongxin
- Zhu Hua
- Zhu Wei-Guo
- Zhu Wenhua
- Zhu Xiao-Feng
- Zhu Yuhua
- Zhuang Shi-Mei
- Zhuang Xiaohong
- Ziparo Elio
- Zois Christos E.
- Zoladek Teresa
- Zong Wei-Xing
- Zorzano Antonio
- Zughaier Susu M.
- Publication venue
- Publication date
- 01/01/2016
- Field of study
Stoma-free survival after anastomotic leak following rectal cancer resection: worldwide cohort of 2470 patients
- Author
- Aalbers Arend G.J.
- Abbas Ayman
- Abbood Ali Hashim
- Abdeen Basel
- Abdelaal Ahmed Samir
- Abdullah Nik A.N.
- Abdulwahed Eman
- Abelevich Alexander
- Abujamra Saleh
- Acar Nihan Coşgun
- Afzal Asma
- Agalianos Christos
- Agapov Mikhail N.
- Agostinelli Laura
- Ahmed Nagm Eldin Abu Elnga
- Ahmed Safia
- Aigner Felix
- Akyol Cihangir
- Al-Eryani Fatima
- Al-Juaifari Maytham A.
- Al-Najami Issam
- Alanez-Saavedra Javier
- Albakry Rudaina
- Alhardan Anas
- Alhisi Ahmed Jehad
- Ali Ahmed K.
- Alkady Eithar
- Allmer Caterina
- Alonso Alfredo
- Alrayes Bourhan M.H.
- Alshareea Entisar
- Altomare Donato F.
- Altrabulsi Amani
- Alvarez-Bautista Francisco E.
- Amano Takahiro
- Amelung Femke J.
- Anderin Kajsa
- Annicchiarico Alfredo
- Ansorena Yolanda Saralegui
- Antona Francisco Blanco
- Antonopoulou Maria-Ioanna
- Aprile Alessandra
- Aranda María J. Pizarro
- Aretxabala Izaskun del Hoyo
- Armao Francesca T.
- Arroyo Antonio
- Ashmore Daniel
- Ashoush Fouad M. Bassyouni
- Atak İbrahim
- Atanasov Boyko
- Atici Semra Demirli
- Atienza Paula González
- Avanagh Dara O.
- Avellaneda Nicolas
- Aversano Alessia
- Aybar Ahmet B. CiftciEngin
- Aydin Oguzhan
- Ayoub Kusay
- Azevedo Constanca
- Baatrup Gunnar
- Baban Bayar
- Badiani Sarit
- Bahadoer Renu R.
- Baili Efstratia
- Balalis Dimitrios
- Balci Bengi
- Balik Emre
- Ballabio Michele
- Baloyiannis Ioannis
- Barbero-Valenzuela Alejandro
- Bavikatte Akshay
- Bazaev Andrey
- Belev Nikolay
- Bellato Vittoria
- Beltrán de Heredia Juan P.
- Belvedere Angela
- Benkabbou Amine
- Benčurik Vladimir
- Bernal-Sprekelsen Juan C.
- Berney Christophe
- Bethune Rob M.
- Bhandari Santosh
- Bhat Sameer
- Binder Alf-Dorian
- Biondi Alberto
- Bisagni Pietro
- Bislenghi Gabriele
- Bissett Ian
- Bişgin Tayfun
- Bjorsum-Meyer Thomas
- Blas Juan L.
- Bloemen Johanne G.
- Boerma Evert-Jan G.
- Bonito Alba Correa
- Borda Francisco Javier García
- Borda-Arrizabalaga Nerea
- Bottazzoli Elisa I.
- Boutall Adam
- Bouvy Nicole D.
- Božič Tajda Košir
- Brachini Gioia
- Bradley Nicholas
- Bremers Andreas J.A.
- Buchs Nicolas
- Buchwald Pamela
- Bulut Mehmet Turker
- Burger Jacobus W.A.
- Burghgraef Thijs A.
- Busund Sondre
- Buzzi Gianluca
- Buğra Dursun
- Calabro Marcello
- Calero-Lillo Aránzazu
- Calik Bulent
- Carbone Fabio
- Carreño-Villarreal Guillermo
- Carrie Augusto
- Carvello Michele
- Carvello Michele
- Catena Fausto
- Cengiz Fevzi
- Cerbo Daniele
- Ceretti Andrea P.
- Chandio Ashfaq
- Chaoui Ahmed
- Charalabopoulos Alexandros
- Chaudhri Sanjay
- Chautems Roland
- Chawla Tabish
- Chawla Tabish
- Cholewa Hannia
- Christodoulidis Grigorios
- Chrysos Emmanuel
- Cifuentes-Ródenas José A.
- Cirillo Bruno
- Ciubotaru Cezar
- Ciubotaru Cezar
- Clerici Federico
- Coco Claudio
- Coetzee Emile
- Colak Elif
- Collard Maxime K.
- Colucci Nicola
- Colás-Ruiz Enrique
- Connelly Tara M.
- Consten Esther C.J.
- Consten Esther C.J.
- Corbellini Carlo
- Cotte Eddy
- Creemers Davy M.J.
- Crescentini Giacomo
- D'Agostino Luca
- D'Alimonte Lucrezia
- D'Hoore André
- da Costa Devesa Helena M.
- da Silva Nigel
- Daester Silvio
- Darias Iván Soto
- Darlin Lotten
- Darwich Haitham
- Dattani Mit
- de Andrés Beatriz
- de Gheldere Charles
- de Graaf Eelco J.R.
- de Groot-Van Veen Irene
- de Haan Jael
- de La Cruz Cuadrado Cristina
- de Lacy F. Borja
- de Manzoni Giovanni
- de Nes Lindsey C.F.
- de Paola Gilda
- de Pasqual Carlo A.
- de Simone Belinda D.
- de Vriendt Stefanie
- de Wilt Johannes H.W.
- de Ángelis Nicola
- Deeknah Abdulqudus
- Defoort Barbara
- deGiuli Maurizio
- Dekker Jan-Willem T.
- Delrio Paolo
- Demirkiran Ahmet
- den Boer Frank
- Denost Quentin
- Dewulf Maxime
- di Cosmo Maria A.
- Di Saverio Salomone
- Dimofte Gabriel-Mihail
- Dinaux Anne M.
- Dittrich Luca S.
- Diéguez Beatriz
- Docampo Iria Losada
- Dogan Lutfi
- Doornebosch Pascal G.
- Drozdov Evgeniy S.
- Dudi-Venkata Nagendra N.
- Dursun Ayberk
- Duzgun Ozgul
- Dziakova Jana
- Díez-Alonso Manuel
- Echaniz Garazi Elorza
- Echiguer Sabrillah
- Eduard Galliamov
- Egea Jorge García
- el Muhtaseb Mohammad S.
- El-Massoudi Youssef
- Elhadi Muhammed
- Elshennawy Eslam M.
- Enriquez-Navascués José M.
- Erdinc Kemal
- Eriksen Jacob D.
- Ersryd Amanda L.
- Escartín Jorge
- Espín-Basany Eloy
- Estaire-Gómez Mercedes
- Estefania Diego
- Ewedah Moataz
- Fabbri Nicolo
- Fares Hala
- Farguell Jordi
- Faria Luis Queiroz
- Farnesi Francesca
- Fazzin Marta
- Feo Carlo V.
- Ferenschild Floris T.
- Fernández C.L.
- Fernández-Hevia María
- Fernández-Hurtado Ignacio
- Fernández-Martínez Daniel
- Ferreira Catia
- Ferreira Rita Marques
- Ferrer Rocío
- Filimonov Victor B.
- Filipov Emil
- Fioravanti Emanuela
- Flamey Nicolas
- Florea Sabrina
- Folkesson Joakim
- Foppa Caterina
- Foppa Caterina
- Forgan Tim
- Fowler George E.
- Frasson Matteo
- Frivold Tone
- Frontali Alice
- Fujiwara Hajime
- Futaba Kaori
- Gaard Maria
- Gadan Soran
- Galleano Raffaele
- Gallo Gaetano
- García-Flórez Luis J.
- Gareb Fahed
- Garmanova Tatiana
- Garulli Gianluca
- Gecim Ibrahim E.
- Geitenbeek Ritch
- George Sarah
- Ghazouani Omar
- Ghignone Federico
- Ghmagh Reem
- Gialamas Eleftherios
- Gielis Manuel
- Giuffrida Mario
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- Janssen Paul T.J.
- Jarimba Aldo M. Rodrigues
- Jou-Valencia Daniela
- Julaihi Rokayah
- Jutesten Henrik
- Kacem Montasser
- Kader Rawaz
- Kamer Erdinc
- Kapadia Raj
- Kara Yasin
- Karamanliev Martin
- Karavokyros Ioannis
- Karmi Fahed
- Karsten Tom
- Karydakis Lysandros
- Kaya Tayfun
- Kelly Michael E.
- Keskin Metin
- Ketelaers Stijn H.J.
- Khader Ahmed A.E.
- Khedr Gehan Abd Elatti
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- Konishi Tsuyoshi
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- Kostromitskiy Dmitriy N.
- Kozan Ramazan
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- Kraft Miquel
- Krastev Panche
- Krohn Nina
- Kroon Hidde M.
- Kryzauskas Marius
- Kulle Cemil B.
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- Kusters Miranda
- Kynaston James
- La Terra Antonio
- Lacy Antonio M.
- Lambrechts Anton
- Lamme Bas
- Lamparelli Michael
- Lantone Giuliano
- Lapolla Pierfrancesco
- Lara Juan E. Sánchez
- Larcinese Antonella
- Larkin John O.
- Larkin John O.
- Larsson Per-Anders
- Latkauskas Tadas
- Lauka Lelde
- Leeuwenburgh Marjolein M.
- Lefevre Jérémie H.
- Leijtens Jeroen W.A.
- Leung Edmund
- Leventoğlu Sezai
- Lindqvist Ebba
- Liu Jianliang
- Longhi Marco
- Lopez Jose M. Gil
- Lorenzon Laura
- Lorusso Leonardo
- Losada Manuel
- Lucchi Andrea
- Luncă Sorinel
- Lutfi Hamid
- Lydrup Marie-Louise
- López-Lara Manuel
- López-Rodríguez-Arias Francisco
- Macau Florin
- Machackova Maria
- Maghrebi Houcine
- Majbar Mohammed A.
- Mak Tony Wing-Chung
- Manatakis Dimitrios
- Mansour Ali
- Manzo Carlo A.
- Marchegiani Francesco
- Marcos Elena Bermejo
- Mariani Nicolò M.
- Marinelli Andreas
- Markaryan Daniil G.
- Maroli Annalisa
- Marques Sonia M. Ribeiro
- Martinek Lubomir
- Martins Sonia Fortuna
- Martínez María Labalde
- Martínez-Pinedo Carlos
- Maslyankov Svilen
- Massey Lisa
- Matthiessen Peter
- Mattioni Laura A.
- Matías-García Belén
- McCormick Paul H.
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- Melnikov Andrey A.
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- Mendoza-Moreno Fernando
- Meroni Paola
- Mia Imraan
- Mikalauskas Saulius
- Mingoli Andrea
- Mishra Amitabh
- Mitteregger Martin
- Miu Victor
- Moctezuma-Velázquez Paulina
- Mohamed Abudi
- Mohsine Raouf
- Monib Fatma A.
- Monson John
- Montero José A. Alcázar
- Montroni Isacco
- Morales Bernaldo de Quirós Javier T.
- Morgan Matthew
- Msherghi Ahmed A.
- Mueller Simone
- Mugla Naser
- Mukherjee Tanmoy
- Muratore Andrea
- Muriel Jorge Sancho
- Musters Gijsbert D.
- Muñoz-Collado Salvador
- Muşină Ana-Maria
- Mínguez-Ruiz Germán
- Nair Gavin
- Navarro-Sánchez Antonio
- Neary Peter
- Negoi Ionut
- Negoita Valentina M.
- Nespoli Luca
- Ng Simon Siuman
- Niazi Ammar
- Nichita Vladimir-Ion
- Niemer Quirine
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- Nilsson Karl
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- Pesce Antonio
- Petropolou Thalia
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- Picciariello Arcangelo
- Picone Emanuele
- Pikuniene Ingrida
- Pinto Francisca Lima
- Pire-Abaitua Gerardo
- Pirozzolo Giovanni
- Piyadeoğlu Deniz
- Plastiras Aris
- Pletinckx Pieter
- Polat Fatih
- Polle Sebastiaan W.
- Polydorou Adreas
- Porta Andrea
- Poskus Tomas
- Pratschke Johann
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- Rauf Hareem
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- Recordare Alfonso
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- Roos Daphne
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- Rotholtz Nicolas
- Rottoli Matteo
- Ruiz Hernan
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- Sebastian Boby
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- Seitinger Gerald
- Semiao Miguel
- Septiem Javier García
- Serralta Daniel
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- Shaikh Shafaque
- Shapiro Joël
- Siaw Oliver
- Sibiç Osman
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- Singh Nirbhaibir
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- Staffan Maria
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- Tamini Nicolò
- Tanase Ioan
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- Tantoura Mohammad
- Tanzanu Marta
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- Taverne Sophie B.M.
- Tejedor Patricia
- Teras Juri
- Teras Roland M.
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- Tomasicchio Giovanni
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- Tonchev Pencho
- Toorenvliet Boudewijn R.
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- Tuynmann Jurriaan B.
- Tzovaras George
- Ubels Sander
- Ugolini Giampaolo
- Ulgur Hanife Şeyda
- Uluk Deniz
- Vailas Michail
- Vailati Bruna B.
- van Dalsen Annette D.
- van den Broek Nathalie E.J.
- van den Hengel Berber
- van der Burg Sjirk
- van der Zijden Charlène J.
- van Gerven Pieter
- van Kessel Charlotte S.
- van Praagh Jasper B.
- van Schaik Ted G.
- van Westreenen Hendrik L.
- van Workum Frans
- Vanclooster Patrick
- Vansteenbrugge Louis
- Vasile Mihai
- Venianaki Maria
- Verdaasdonk Emiel G.G.
- Vergara-Fernández Omar
- Vermaas Maarten
- Verstappen Sonja
- Vignotto Chiara
- Villar Óscar García
- Vittori Laura
- Vles Wouter J.
- von Flue Markus
- Voron Thibault
- Vosbeek Noortje
- Vuagniaux Aurelie
- Vázquez Andrea
- Waqar Usama
- Waqar Usama
- Ward Nicholas
- Warden Claire
- Westerterp Marinke
- Wienholts Kiedo
- Wiering Bastiaan
- Wijma Allard G.
- Wildeboer Aurelia C.L.
- Wolthuis Albert
- Wong Michael P.K.
- Woods Kayla
- Xenaki Sofia
- Xynos Evangelos
- Yalkin Omer
- Yanishev Alexey
- Yuksel Osman
- Zabala Jesús Gómez
- Zakaria Andee D.
- Zakaria Zaidi
- Zanini Nicola
- Zanus Giacomo
- Zazo Aya
- Zazo Rama
- Zucchella Martino
- Zukanović Goran
- Zwakman Marije
- Çakir Murat
- Ćosić Jurica
- Šantak Goran
- Šimleša Damir
- Šlenfuktas Vygintas
- Žilinskas Justas
- Publication venue
- Publication date
- 01/12/2023
- Field of study
Background: The optimal treatment of anastomotic leak after rectal cancer resection is unclear. This worldwide cohort study aimed to provide an overview of four treatment strategies applied. Methods: Patients from 216 centres and 45 countries with anastomotic leak after rectal cancer resection between 2014 and 2018 were included. Treatment was categorized as salvage surgery, faecal diversion with passive or active (vacuum) drainage, and no primary/secondary faecal diversion. The primary outcome was 1-year stoma-free survival. In addition, passive and active drainage were compared using propensity score matching (2: 1). Results: Of 2470 evaluable patients, 388 (16.0 per cent) underwent salvage surgery, 1524 (62.0 per cent) passive drainage, 278 (11.0 per cent) active drainage, and 280 (11.0 per cent) had no faecal diversion. One-year stoma-free survival rates were 13.7, 48.3, 48.2, and 65.4 per cent respectively. Propensity score matching resulted in 556 patients with passive and 278 with active drainage. There was no statistically significant difference between these groups in 1-year stoma-free survival (OR 0.95, 95 per cent c.i. 0.66 to 1.33), with a risk difference of -1.1 (95 per cent c.i. -9.0 to 7.0) per cent. After active drainage, more patients required secondary salvage surgery (OR 2.32, 1.49 to 3.59), prolonged hospital admission (an additional 6 (95 per cent c.i. 2 to 10) days), and ICU admission (OR 1.41, 1.02 to 1.94). Mean duration of leak healing did not differ significantly (an additional 12 (-28 to 52) days). Conclusion: Primary salvage surgery or omission of faecal diversion likely correspond to the most severe and least severe leaks respectively. In patients with diverted leaks, stoma-free survival did not differ statistically between passive and active drainage, although the increased risk of secondary salvage surgery and ICU admission suggests residual confounding