54 research outputs found
Abstracts of presentations on plant protection issues at the fifth international Mango Symposium Abstracts of presentations on plant protection issues at the Xth international congress of Virology: September 1-6, 1996 Dan Panorama Hotel, Tel Aviv, Israel August 11-16, 1996 Binyanei haoma, Jerusalem, Israel
- Author
- Abd El Ghaffar M.
- Abo El Nasr M.
- Abo-Zeid A.
- Abou Haidar M.
- Ackerman M.
- Adamia R.
- Ahlquist P.
- Ahlquist Paul
- Al-Kaff N.
- Alberto Otto Paulo
- Aleman M.
- Allam E.
- Alonso J.
- Alvarez J.
- AmbrĂłs S.
- Amvam R.
- Antignus Y.
- Artes L.
- Artes L.
- Atabekov J.
- Atissime K.
- Augustyniak J.
- Axmann A.
- Bacalangco N.
- Balardshishvili N.
- Balazs Ervin
- Bally Ian
- Balsalobre J.
- BalĂĄzs Ervin
- Bao Y.
- Barak R.
- Barrios M.
- BarĂłn M.
- Bateson M.
- Bateson M.
- Batlle A.
- Bauer U.
- Baulcombe D.
- Baulcombe David
- Baumstark T.
- Bautista M.
- Baybikov T.
- Beachy R.
- Beetham P.
- Bel P.
- Bellés J.
- Benscher D.
- Berger P.
- Bernal J.
- Bertens Peter
- Berzins V.
- Bishnoi S.
- Biyiti L.
- Blaine L.
- Boccardo G.
- Bol J.
- Bonfiglioli R.
- Bortoletto N.
- BoscĂĄn de M. Nancy
- Bostros Bastawros Mikhail
- Bouchet P.
- Braithwaite Kathryn
- Briddon R.
- Brunt A.
- Bujarski Jozef
- Bunk Hans-Jörk
- BurgyĂĄn J.
- BurgyĂĄn JĂłzsef
- BĂłsquez E.
- BĂŒchen-Osmond C.
- Candresse T.
- Canto T.
- Carrére Isabelle
- Carter S.
- Casper R.
- Cassidy Pour
- Cecchini E.
- Chaleeprom W.
- Chamberlain D.
- Chang B.
- Chanishvili T.
- Chen J.
- Coates L.
- Cohen S.
- Colls A.
- Conejero V.
- Cook G.
- Cooke A.
- Covey S.
- Covey S.
- Crescenzi A.
- d'Aquilio M.
- d'Aquino L.
- Dafalla G.
- Dahal Ganesh
- Dale J.
- Dale J.
- Dallwitz M.
- Dalmay T.
- Damame S.
- DarĂČs J.
- Dasgupta Indranil
- Davidson A.
- Dawson W.
- Dean J.
- Derrick P.
- Desvignes J.
- Diaz de LeĂłn F.
- Ding X.
- Dorokhov Y.
- Druka A.
- Druka Arnis
- Dugdale B.
- Dunez J.
- DĂez J.
- El Afifi Soheir
- El-Dougdoug K.
- El-Shamy M.
- Elisabeth Johansen I.
- English David
- Eskarous J.
- Esparza S.
- Falik E.
- Farungsang N.
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- Fauquet C.
- Fauquet Claude
- Fayos J.
- Felden Brice
- Feldhoff A.
- Fels A.
- Feng Zhu
- Figlerowicz Marek
- Fischer R.
- Flasinski S.
- Flasinski Stanislaw
- Flores R.
- Freeman S.
- Fuchs Y.
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- Garcia M.
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- Geri C.
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- Godoy Freddy
- Goldbach Rob
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- Gosbee M.
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- Grdzelishvili V.
- Greenwood Aaron
- Grieco F.
- Gronenborn B.
- Gross H.
- Gumedzoe M.
- Guyatt K.
- GĂłra A.
- Haas B.
- Hadidi A.
- Hajimorad M.
- Hammond R.
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- Havelda Z.
- Hay Jo
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- Henderson J.
- Henkel J.
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- Holmes Rowland
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- Hulanicka D.
- Hull R.
- Hull Roger
- Irwin J.
- Ishiguro Akiro
- Ishikawa M.
- Ivanov K.
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- Janda M.
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- Janzen D.
- Jeske Holger
- Johnson A.
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- Joyce D.
- Kalvatchev Z.
- Karagöz Ali
- Karim M.
- Kasdorf G.
- Kavanagh Tony
- Kearney C.
- Keinan A.
- Keller K.
- Kerbel C.
- Kheyr-Pour A.
- Kierzek A.
- Kikkert M.
- Kim C.
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- Kobiler I.
- Kolaskar A.
- Kormelink R.
- Krczal G.
- KrĂŒger D.
- Kubelkova D.
- Kuo T.
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- Kuznetsov Yuri
- Lachman O.
- Lamaty G.
- Laux I.
- Leclerc Denis
- Lecoq H.
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- Lekkerkerker Annemarie
- Liangyi Kang
- Liao Y.
- Licis N.
- Lin N.
- Lin Na-Sheng
- Lisa V.
- Lizado M.
- Lohuis H.
- Lomonossoff G.
- Lot H.
- Lucia Duarte Ana
- Luis M.
- LĂĄzara J.
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- Maiss E.
- Malavasi Aldo
- Malcuit Isabelle
- Malkin Alexander
- Martelli G.
- Martin M.
- Martins A.
- Masalkar S.
- Maymon M.
- McPherson Alexander
- Meehan Brian
- Meiri Eti
- Meng A.
- Merits A.
- Miller Eric
- Miller M.
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- Minafra A.
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- Morag A.
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- Moyer J.
- Mumcuoglu M.
- Muñoz C.
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- Nagel Julianne
- Nagy Peter
- Nagy Tibor
- Naik P.
- Nelson R.
- Nemchinov L.
- Nuss D.
- O'Hare Tim
- Obligado A.
- Ofek G.
- Ohshima K.
- Okada Y.
- Omer H.
- Omer O.
- Orosz LĂĄszlĂł
- Owens R.
- Paduch-Cichal E.
- Palkovics LĂĄszlĂł
- PallĂĄs V.
- Palmenberg A.
- Palukaitis P.
- Papp PĂ©ter
- Pawlowicz J.
- Pearlsman M.
- Pesis E.
- Peters D.
- Peña J.
- Phillips S.
- Piazzolla P.
- Pietersen G.
- Pilartz Marcel
- Pinkas Y.
- Ploetz R.
- Po Tien
- Poliyka H.
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- Price B.
- Proll D.
- Prusky D.
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- Puurand Ă.
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- Qiu G.
- Qiu W.
- Rabenstein F.
- Rabinstein F.
- Raccah B.
- Ragozzino A.
- Rahontei J.
- Restrepo-Hartwig M.
- Restrepo-Hartwig Maria
- Reusken Chantal
- Reved R.
- Revers F.
- Rey M.
- Rezler A.
- Ribeiro I.
- Richert-Pöggeler K.
- Riesner D.
- Rishi Narayan
- RodrCarlos C.
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- Rossetto C.
- Roth I.
- Rybicki E.
- Saaiman W.
- Saarma M.
- Sabino J.
- Sadowy E.
- Sako N.
- Saldarelli P.
- Salm S.
- Sano Teruo
- Sanz A.
- Sariol-Carbelo Carlos
- Sarkar S.
- Savenkov E.
- Schaffer B.
- Schiebel R.
- Schiebel W.
- Schlesinger M.
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- Schröder A.
- Scott S.
- Senchugova N.
- Serra M.
- Sgro J.
- Shaklay M.
- Shaw J.
- Shepherd R.
- Shiel P.
- Shohat B.
- Shohat M.
- Shun Ding Xin
- Singer S.
- Singh Gajendra
- Skrzeczkowska S.
- Smirnyagina Ekaterina
- Smith Grant
- Smith H.
- Soares N.
- Solovyev A.
- Sonone A.
- Sorri O.
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- Spak J.
- Spall V.
- Spieker R.
- Staub U.
- Steger G.
- Stein-Margolina V.
- Stevens M.
- Symons R.
- Szittya György
- SĂĄlanki Katalin
- SĂĄnchez-Pina M.
- SĂ€nger H.
- SĂrensen Karina
- Takida S.
- Taylor K.
- Tepfer Mark
- Thompson M.
- Thomson M.
- Todd Daniel
- Tomori O.
- Trinidad M.
- Turley R.
- Valkonen J.
- van der Vossen E.
- van Kammen Ab
- van Lent Jan
- van Rossum C.
- Vaquero-Martin C.
- Vera A.
- Verchot Jeanmarie
- Verduin B.
- Verver Jan
- Villegas Lucille
- Visarathanonth N.
- Våzquez Aimé
- Wagner M.
- Waisblum A.
- Walder R.
- Ward Colin
- Waskar D.
- Webb D.
- Wegener B.
- Weksler A.
- Wellink Joan
- Wetzel T.
- Wittner Anita
- Wolfs C.
- Wvpijewski K.
- Wysoki M.
- Xicai Yang
- Xu J.
- Xu Z.
- Yedibahoma S.
- Yekutiely O.
- Yin Yie
- Yu. Morozov S.
- Yuichiro W.
- Yule Liu
- Zagorski W.
- Zaifeng Fan
- Zakay-Rones Z.
- Zauberman G.
- Zelenina D.
- Ălö PĂ©ter
- Publication venue
- Publication date
- 18/06/2018
- Field of study
Approaches in biotechnological applications of natural polymers
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- Publication venue
- 'American Institute of Mathematical Sciences (AIMS)'
- Publication date
- 01/01/2016
- Field of study
Natural polymers, such as gums and mucilage, are biocompatible, cheap, easily available and non-toxic materials of native origin. These polymers are increasingly preferred over synthetic materials for industrial applications due to their intrinsic properties, as well as they are considered alternative sources of raw materials since they present characteristics of sustainability, biodegradability and biosafety. As definition, gums and mucilages are polysaccharides or complex carbohydrates consisting of one or more monosaccharides or their derivatives linked in bewildering variety of linkages and structures. Natural gums are considered polysaccharides naturally occurring in varieties of plant seeds and exudates, tree or shrub exudates, seaweed extracts, fungi, bacteria, and animal sources. Water-soluble gums, also known as hydrocolloids, are considered exudates and are pathological products; therefore, they do not form a part of cell wall. On the other hand, mucilages are part of cell and physiological products. It is important to highlight that gums represent the largest amounts of polymer materials derived from plants. Gums have enormously large and broad applications in both food and non-food industries, being commonly used as thickening, binding, emulsifying, suspending, stabilizing agents and matrices for drug release in pharmaceutical and cosmetic industries. In the food industry, their gelling properties and the ability to mold edible films and coatings are extensively studied. The use of gums depends on the intrinsic properties that they provide, often at costs below those of synthetic polymers. For upgrading the value of gums, they are being processed into various forms, including the most recent nanomaterials, for various biotechnological applications. Thus, the main natural polymers including galactomannans, cellulose, chitin, agar, carrageenan, alginate, cashew gum, pectin and starch, in addition to the current researches about them are reviewed in this article.. }To the Conselho Nacional de Desenvolvimento CientfĂico e TecnolĂłgico (CNPq) for fellowships (LCBBC and MGCC) and the Coordenação de Aperfeiçoamento de Pessoal de NvĂel Superior (CAPES) (PBSA). This study was supported by the Portuguese Foundation for Science and Technology (FCT) under the scope of the strategic funding of UID/BIO/04469/2013 unit, the Project RECI/BBB-EBI/0179/2012 (FCOMP-01-0124-FEDER-027462) and COMPETE 2020 (POCI-01-0145-FEDER-006684) (JAT)
Antiinflammatory Therapy with Canakinumab for Atherosclerotic Disease
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- Zielinski M
- Zieve F
- Zineldine A.
- Zirlik A
- Zucchetti C
- Publication venue
- 'Massachusetts Medical Society'
- Publication date
- 01/01/2017
- Field of study
Background: Experimental and clinical data suggest that reducing inflammation without affecting lipid levels may reduce the risk of cardiovascular disease. Yet, the inflammatory hypothesis of atherothrombosis has remained unproved. Methods: We conducted a randomized, double-blind trial of canakinumab, a therapeutic monoclonal antibody targeting interleukin-1ÎČ, involving 10,061 patients with previous myocardial infarction and a high-sensitivity C-reactive protein level of 2 mg or more per liter. The trial compared three doses of canakinumab (50 mg, 150 mg, and 300 mg, administered subcutaneously every 3 months) with placebo. The primary efficacy end point was nonfatal myocardial infarction, nonfatal stroke, or cardiovascular death. RESULTS: At 48 months, the median reduction from baseline in the high-sensitivity C-reactive protein level was 26 percentage points greater in the group that received the 50-mg dose of canakinumab, 37 percentage points greater in the 150-mg group, and 41 percentage points greater in the 300-mg group than in the placebo group. Canakinumab did not reduce lipid levels from baseline. At a median follow-up of 3.7 years, the incidence rate for the primary end point was 4.50 events per 100 person-years in the placebo group, 4.11 events per 100 person-years in the 50-mg group, 3.86 events per 100 person-years in the 150-mg group, and 3.90 events per 100 person-years in the 300-mg group. The hazard ratios as compared with placebo were as follows: in the 50-mg group, 0.93 (95% confidence interval [CI], 0.80 to 1.07; P = 0.30); in the 150-mg group, 0.85 (95% CI, 0.74 to 0.98; P = 0.021); and in the 300-mg group, 0.86 (95% CI, 0.75 to 0.99; P = 0.031). The 150-mg dose, but not the other doses, met the prespecified multiplicity-adjusted threshold for statistical significance for the primary end point and the secondary end point that additionally included hospitalization for unstable angina that led to urgent revascularization (hazard ratio vs. placebo, 0.83; 95% CI, 0.73 to 0.95; P = 0.005). Canakinumab was associated with a higher incidence of fatal infection than was placebo. There was no significant difference in all-cause mortality (hazard ratio for all canakinumab doses vs. placebo, 0.94; 95% CI, 0.83 to 1.06; P = 0.31). Conclusions: Antiinflammatory therapy targeting the interleukin-1ÎČ innate immunity pathway with canakinumab at a dose of 150 mg every 3 months led to a significantly lower rate of recurrent cardiovascular events than placebo, independent of lipid-level lowering. (Funded by Novartis; CANTOS ClinicalTrials.gov number, NCT01327846.
ICAR: endoscopic skullâbase surgery
- Author
- Aaron G
- Aaron GP
- Abergel A
- Abouaf L
- Abrishamkar S
- Acioly MA
- Acioly MA
- Acuna RT
- Adams AS
- Adappa ND
- Aferzon M
- Agaimy A
- Agarwal A
- Aggarwal A
- Agrawal D
- Ahmed OH
- Aihara M
- Akagami R
- Alahmadi H
- Albu S
- Albu S
- Albu S
- Alexander A
- Alimohamadi M
- Almefty R
- Almeida JR
- Almeida JR
- Almeida JR
- Almeida JR
- Almeida JR
- Almeida JR
- Almeida JR
- Almond MC
- Alobaid A
- Alobid I
- Alobid I
- Alos L
- AlQahtani A
- Altay T
- Alvarez FL
- Alves MV
- AlâMamgani A
- AlâMefty O
- AlâSheibani S
- Amano K
- Amdur RJ
- Amelot A
- American Academy of Pediatrics Steering Committee on Quality Improvement and Management
- Amichetti M
- Amin SM
- Amit M
- Amit M
- Amit M
- Ammirati M
- Anari S
- Anderson D
- Anderson RL
- Andrade NA
- Andrews JC
- Anik I
- Ansa B
- Ansari M
- Antonelli AR
- Arafah BM
- Arafah BM
- Arafah BM.
- Arai A
- Arat YO
- Arbolay OL
- Ardehali MM
- Armengot M
- Arnautovic KI
- Arrer E
- Arslan HH
- Aryan HE
- Asano S
- Askoxylakis V
- Astrup J
- Awad AJ
- Awad M
- Azad TD
- Aziz KM
- Babin E
- Bachmann G
- Back L
- Backlund EO.
- Baijal V
- Balaker AE
- Ballah D
- Balzer JR
- Banks CA
- Banu MA
- Banu MA
- Banuchi VE
- Barnes L
- Baser B
- Baskin DS
- Battaglia P
- Battaglia P
- Becker AM
- Beckhardt RN
- Bedi AD
- Bedrosian JC
- Bedrosian JC
- BeerâFurlan A
- BeerâFurlan A
- Beham A
- Bejjani GK
- Bell D
- Bell RB
- Bell RB
- Berdahl JP
- Berhouma M
- Berker M
- Berker M
- Berkmann S
- Berkmann S
- Berkmann S
- BernalâSprekelsen M
- BernalâSprekelsen M
- Bernat AL
- Bertrand B
- Bhasker S
- Bhatti SN
- Bidot S
- Bills DC
- Bishop JA
- Biswas D
- Black PM
- Bleier BS
- Bleier BS
- Bleier BS
- Bleier BS
- Bleier BS
- Bloch C
- Bloch O
- Bly RA
- Boghani Z
- Bohman LE
- Bohman LE
- Bokhari AR
- Boling CC
- Bolzoni Villaret A
- Borg A
- Borghei P
- Boukheris H
- Brackmann DE
- Bradley PJ
- Branston NM
- Brastianos PK
- Bremer JW
- Bresson D
- Briet C
- Briggs RJ
- Brodie HA.
- Brown SM
- Bruchhage KL
- BruckerâDavis F
- Brunworth J
- Buchmann L
- Buerke B
- Bujawansa S
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- Bunin GR
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- Butler S
- Butros SR
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- Caballero N
- CaicedoâGranados E
- Caldarelli M
- Campbell E
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- Publication venue
- Publication date
- 01/07/2019
- Field of study
n/
2013 WSES guidelines for management of intra-abdominal infections
- Author
- A Ayite
- A Basoli
- A Chabok
- A Dwivedi
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- Boris Sakakushev
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- Federico Coccolini
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- Luca Ansaloni
- M Cheng
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- M Sinanan
- M Souli
- M Stapfer
- M Tabbara
- MA Gladman
- MA Malangoni
- Mario Paulo Faro
- Mark Malangoni
- Massimo Sartelli
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- O van Ruler
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- P Ambrosetti
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- R Enns
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- Rafael DĂaz-Nieto
- Rao Ivatury
- Raul Coimbra
- RC Bone
- RE Andersson
- RJ Mason
- RM Urbaniak
- RP Dellinger
- RR Hutchins
- RR Kumar
- S Benoist
- S Biondo
- S Janes
- S Jwo
- S Khan
- S Kriwanek
- S Mulier
- S Nasim
- S Pungpapong
- S Sauerland
- S van den Hazel
- SA Cohen
- Salomone Di Saverio
- Sanjay Gupta
- Sanjay Marwah
- SE Araujo
- SK Rasilainen
- SM Hadad
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- SP Hawser
- SR Menakuru
- SS Sarath Chandra
- ST Edino
- Suk-Kyung Hong
- T Eglinton
- T Herzog
- T Kiviluoto
- T Koperna
- T Lehnert
- T Siddiqui
- T Wild
- Takayuki Irahara
- TH Baron
- TH LĂŒning
- TJ Crofts
- TL Hedrick
- Tomohisa Shoko
- U Guller
- V Banz
- V Donckier
- V Emmi
- V Lohsiriwat
- Victor Kong
- VP Bauer
- Wagih Ghnnam
- Walter Biffl
- WJ Lin
- WS Cobb
- WT Siu
- WW Turner Jr
- WY Lau
- Y Abi-Haidar
- Y Adachi
- Yoram Kluger
- Yunfeng Cui
- Zsolt J Balogh
- Publication venue
- Publication date
- 01/01/2013
- Field of study
Peer reviewe
International Consensus Statement on Rhinology and Allergy: Rhinosinusitis
- Author
- Aanaes K
- Abadie WM
- Abi Najm S
- Abigail P
- Abrahams JJ
- Abrass LJ
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- American Academy of Pediatrics Steering Committee on Quality Improvement and Management (AAP SCQIM)
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- Thamboo A
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- Thamboo A
- Tharakan A
- Theodoraki MN
- Thilsing T
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- Tipirneni KE
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- Zurlo JJ
- Zuskin E
- Äulig J
- Publication venue
- 'Wiley'
- Publication date
- 01/01/2021
- Field of study
Background: The 5 years since the publication of the first International Consensus Statement on Allergy and Rhinology: Rhinosinusitis (ICARâRS) has witnessed foundational progress in our understanding and treatment of rhinologic disease. These advances are reflected within the more than 40 new topics covered within the ICARâRSâ2021 as well as updates to the original 140 topics. This executive summary consolidates the evidenceâbased findings of the document. Methods: ICARâRS presents over 180 topics in the forms of evidenceâbased reviews with recommendations (EBRRs), evidenceâbased reviews, and literature reviews. The highest grade structured recommendations of the EBRR sections are summarized in this executive summary. Results: ICARâRSâ2021 covers 22 topics regarding the medical management of RS, which are grade A/B and are presented in the executive summary. Additionally, 4 topics regarding the surgical management of RS are grade A/B and are presented in the executive summary. Finally, a comprehensive evidenceâbased management algorithm is provided. Conclusion: This ICARâRSâ2021 executive summary provides a compilation of the evidenceâbased recommendations for medical and surgical treatment of the most common forms of RS
Factors Affecting the Virological Response Among Chronic Hepatitis C Virus Patients in Yemen
- Author
- Publication venue
- 'Mary Ann Liebert Inc'
- Publication date
- Field of study
A Novel Ultra-Stable, Monomeric Green Fluorescent Protein For Direct Volumetric Imaging of Whole Organs Using CLARITY
- Publication venue
- 'Springer Science and Business Media LLC'
- Publication date
- 12/01/2018
- Field of study
Recent advances in thick tissue clearing are enabling high resolution, volumetric fluorescence imaging of complex cellular networks. Fluorescent proteins (FPs) such as GFP, however, can be inactivated by the denaturing chemicals used to remove lipids in some tissue clearing methods. Here, we solved the crystal structure of a recently engineered ultra-stable GFP (usGFP) and propose that the two stabilising mutations, Q69L and N164Y, act to improve hydrophobic packing in the core of the protein and facilitate hydrogen bonding networks at the surface, respectively. usGFP was found to dimerise strongly, which is not desirable for some applications. A point mutation at the dimer interface, F223D, generated monomeric usGFP (muGFP). Neurons in whole mouse brains were virally transduced with either EGFP or muGFP and subjected to Clear Lipid-exchanged Acrylamide-hybridized Rigid Imaging/Immunostaining/In situ hybridization-compatible Tissue-hYdrogel (CLARITY) clearing. muGFP fluorescence was retained after CLARITY whereas EGFP fluorescence was highly attenuated, thus demonstrating muGFP is a novel FP suitable for applications where high fluorescence stability and minimal self-association are required
Extramedullary hematopoiesis: A report of two cases
- Author
- Publication venue
- 'Spandidos Publications'
- Publication date
- Field of study
Endogenous Fluorescence Analysis: Preliminary Study Revealing the Potential of this Non-invasive Method to Study Mummified Samples
- Author
- Publication venue
- 'Wiley'
- Publication date
- 01/01/2017
- Field of study
International audienceAutofluorescence analysis allows new insights on human tissue without any dye in a non-invasive way and therefore seems well suited to study historical samples. An optical set-up recorded emitted autofluorescence in 1/spectral and 2/lifetime domains from different samples' regions of interest. The studied samples were a mummified right hand, bog body (Tollund Man) feet and a male Caucasian hand (control sample). Spectral analysis revealed that mummified hand exhibited broad autofluorescence spectra, whereas Tollund Man's feet exhibited a weak single peak with 405-nm excitation wavelength. Control sample spectra are weaker than that of the mummified hand but higher than the Tollund Man's feet. Lifetime measurements indicated the presence of classical endogenous fluorophores on the mummified right hand. The Tollund Man's feet exhibited two patterns of lifetime measurements: healthy zone exhibited lifetime values at four emission wavelengths but skin lesions at only two wavelengths. This first report of mummified samples' autofluorescence analysis suggests the potential of optical analysis for archeologic researc
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