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Institution

University of Zagreb

EducationZagreb, Grad Zagreb, Croatia
About: University of Zagreb is a education organization based out in Zagreb, Grad Zagreb, Croatia. It is known for research contribution in the topics: Population & European union. The organization has 21769 authors who have published 50267 publications receiving 783239 citations. The organization is also known as: Zagreb University & Sveučilište u Zagrebu.


Papers
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Journal ArticleDOI
Petar Jandrić1, Petar Jandrić2, David Hayes, Ian Truelove3, Paul Levinson4, Peter Mayo5, Thomas Ryberg6, Lilia D. Monzó7, Quaylan Allen7, Paul Alexander Stewart8, Paul R. Carr9, Liz Jackson10, Susan Bridges10, Carlos Escaño11, Dennis Grauslund12, Julia Mañero11, Happiness Onesmo Lukoko13, Peter Bryant14, Ana Fuentes-Martinez15, Andrew Gibbons16, Sean Sturm17, Jennifer Rose18, Mohamed Muhibu Chuma13, Eva Biličić1, Sarah Pfohl19, Ulrika Gustafsson20, Janine Aldous Arantes21, Janine Aldous Arantes22, Derek R. Ford23, Jimmy Ezekiel Kihwele24, Peter Mozelius25, Juha Suoranta, Lucija Jurjević1, Matija Jurčević1, Anne Steketee7, Jones Irwin26, E. Jayne White27, Jacob Davidsen6, Jimmy Jaldemark25, Sandra Abegglen28, Tom R. Burns29, Sandra Sinfield29, James D. Kirylo30, Ivana Batarelo Kokić31, Georgina Stewart16, Glenn Rikowski32, Line Lisberg Christensen6, Sonja Arndt33, Olli Pyyhtinen, Charles Reitz34, Mikkel Lodahl, Niklas Humble25, Rachel Buchanan22, Daniella J. Forster22, Pallavi Kishore35, Jānis John Ozoliņš36, Jānis John Ozoliņš37, Navreeti Sharma35, Shreya Urvashi38, Harry G. Nejad35, Nina Hood17, Marek Tesar17, Yang Wang13, Jake Wright39, James Benedict Brown20, Paul Prinsloo40, Kulpreet Kaur35, Mousumi Mukherjee41, Rene Novak42, Richa Shukla35, Stephanie Hollings13, Ulla Konnerup6, Madhav Mallya35, Anthony Olorundare43, Charlotte Achieng-Evensen7, Abey P. Philip44, Moses Kayode Hazzan45, Kevin Stockbridge7, Blessing Funmi Komolafe46, Blessing Funmi Komolafe47, Ogunyemi Folasade Bolanle13, Michael Hogan48, Bridgette Redder, Sahar D. Sattarzadeh23, Michael Jopling2, Suzanne SooHoo7, Nesta Devine16, Sarah Hayes2 
07 Aug 2020
TL;DR: A collection of 84 author's testimonies and workspace photographs between 18 March and 5 May 2020 was published by as discussed by the authors, with the purpose of collecting the author's workspace photographs and their testimonies.
Abstract: A collection of 84 author's testimonies and workspace photographs between 18 March and 5 May 2020

134 citations

Journal ArticleDOI
TL;DR: Preliminary data indicate that polymer-coated mucoadhesive liposomes are able to carry sufficient amount of drug and to remain attached to the intestinal mucosa for a sufficient period of time to enable prolonged absorption of entrapped drug.
Abstract: Objective: Development of liposomal mucoadhesive drug delivery system, which is able to improve the bioavailability of poorly absorbed oral drugs by prolonging their gastric and intestinal residence time, through facilitating the intimate contact of the delivery system with the absorption membrane. Materials and methods: Liposomes containing model drug atenolol were prepared by the modified ethanol injection method. Liposomes containing atenolol were coated by different mucoadhesive polymers, for example, chitosan, Carbopol 974P, Eudragit L100, and Eudragit S100, to optimize the choice of coating material. The delivery systems were tested for their in vitro mucoadhesiveness. Results: Liposomes prepared by the ethanol injection method were of satisfactory size (around 100 nm, before coating). Through the coating of liposomes in the presence of unentrapped material, the entrapment efficiency for drug was increased. In vitro mucoadhesive test confirmed the mucoadhesive properties of the coated layer for all tested polymers; however, Eudragit S100-coated liposomes were superior to other coating materials. Discussion: Eudragit coating appeared to be an optimal polymer choice. These preliminary data indicate that polymer-coated mucoadhesive liposomes are able to carry sufficient amount of drug and to remain attached to the intestinal mucosa for a sufficient period of time to enable prolonged absorption of entrapped drug. Conclusion: While keeping in mind that the in vivo conditions may vary with the in vitro ones, we may recommend the system described in our work for possible oral delivery of peptides and phytochemicals.

134 citations

Journal ArticleDOI
Massimo Sartelli, Dieter G. Weber1, Etienne Ruppé2, Matteo Bassetti3  +169 moreInstitutions (114)
TL;DR: The AGORA (Antimicrobials: A Global Alliance for Optimizing their Rational Use in Intra-Abdominal Infections) project as discussed by the authors is an international task force from 79 different countries has joined this project by sharing a document on the rational use of antimicrobial therapy for patients with IAIs.
Abstract: Intra-abdominal infections (IAI) are an important cause of morbidity and are frequently associated with poor prognosis, particularly in high-risk patients. The cornerstones in the management of complicated IAIs are timely effective source control with appropriate antimicrobial therapy. Empiric antimicrobial therapy is important in the management of intra-abdominal infections and must be broad enough to cover all likely organisms because inappropriate initial antimicrobial therapy is associated with poor patient outcomes and the development of bacterial resistance. The overuse of antimicrobials is widely accepted as a major driver of some emerging infections (such as C. difficile), the selection of resistant pathogens in individual patients, and for the continued development of antimicrobial resistance globally. The growing emergence of multi-drug resistant organisms and the limited development of new agents available to counteract them have caused an impending crisis with alarming implications, especially with regards to Gram-negative bacteria. An international task force from 79 different countries has joined this project by sharing a document on the rational use of antimicrobials for patients with IAIs. The project has been termed AGORA (Antimicrobials: A Global Alliance for Optimizing their Rational Use in Intra-Abdominal Infections). The authors hope that AGORA, involving many of the world's leading experts, can actively raise awareness in health workers and can improve prescribing behavior in treating IAIs.

134 citations

Journal ArticleDOI
TL;DR: It is shown the systemic administration of low levels of TSH increases bone volume and improves bone microarchitecture and strength in aged OVX rats, suggesting TSH directly affects bone remodeling in vivo.
Abstract: We show the systemic administration of low levels of TSH increases bone volume and improves bone microarchitecture and strength in aged OVX rats. TSH's actions are mediated by its inhibitory effects on RANKL-induced osteoclast formation and bone resorption coupled with stimulatory effects on osteoblast differentiation and bone formation, suggesting TSH directly affects bone remodeling in vivo. Introduction Thyroid-stimulating hormone (TSH) receptor haploinsufficient mice with normal circulating thyroid hormone levels have reduced bone mass, suggesting that TSH directly affects bone remodeling. We examined whether systemic TSH administration restored bone volume in aged ovariectomized (OVX) rats and influenced osteoclast formation and osteoblast differentiation in vitro. Materials and methods Sprague-Dawley rats were OVX at 6 months, and TSH therapy was started immediately after surgery (prevention mode; n = 80) or 7 mo later (restoration mode; n = 152). Hind limbs and lumbar spine BMD was measured at 2- or 4-wk intervals in vivo and ex vivo on termination at 8-16 wk. Long bones were subjected to microCT, histomorphometric, and biomechanical analyses. The direct effect of TSH was examined in osteoclast and osteoblast progenitor cultures and established rat osteosarcoma-derived osteoblastic cells. Data were analyzed by ANOVA Dunnett test. Results In the prevention mode, low doses (0.1 and 0.3 microg) of native rat TSH prevented the progressive bone loss, and importantly, did not increase serum triiodothyroxine (T3) and thyroxine (T4) levels in aged OVX rats. In restoration mode, animals receiving 0.1 and 0.3 microg TSH had increased BMD (10-11%), trabecular bone volume (100-130%), trabecular number (25-40%), trabecular thickness (45-60%), cortical thickness (5-16%), mineral apposition and bone formation rate (200-300%), and enhanced mechanical strength of the femur (51-60%) compared with control OVX rats. In vitro studies suggest that TSH's action is mediated by its inhibitory effects on RANKL-induced osteoclast formation, as shown in hematopoietic stem cells cultivated from TSH-treated OVX rats. TSH also stimulates osteoblast differentiation, as shown by effects on alkaline phosphatase activity, osteocalcin expression, and mineralization rate. Conclusions These results show for the first time that systemically administered TSH prevents bone loss and restores bone mass in aged OVX rats through both antiresorptive and anabolic effects on bone remodeling.

134 citations

Journal ArticleDOI
A. Adare1, S. Afanasiev2, C. A. Aidala3, C. A. Aidala4  +520 moreInstitutions (63)
TL;DR: In this article, the PHENIX experiment at RHIC has measured the centrality dependence of the direct photon yield from Au+Au collisions at sNN−−−√=200 GeV down to pT=0.4 GeV/c.
Abstract: The PHENIX experiment at RHIC has measured the centrality dependence of the direct photon yield from Au+Au collisions at sNN−−−√=200 GeV down to pT=0.4 GeV/c. Photons are detected via photon conversions to e+e− pairs and an improved technique is applied that minimizes the systematic uncertainties that usually limit direct photon measurements, in particular at low pT. We find an excess of direct photons above the Ncoll-scaled yield measured in p+p collisions. This excess yield is well described by an exponential distribution with an inverse slope of about 240MeV/c in the pT range 0.6–2.0 GeV/c. While the shape of the pT distribution is independent of centrality within the experimental uncertainties, the yield increases rapidly with increasing centrality, scaling approximately with Nαpart, where α=1.38±0.03(stat)±0.07(syst).

134 citations


Authors

Showing all 22096 results

NameH-indexPapersCitations
Harry Campbell150897115457
Joseph R. Ecker14838194860
Igor Rudan142658103659
Nikola Godinovic1381469100018
Ivica Puljak134143697548
Damir Lelas133135493354
Željko Ivezić12934484365
Piotr Ponikowski120762131682
Marin Soljacic11776451444
Ivan Dikic10735952088
Ozren Polasek10243652674
Mordechai Segev9972940073
Srdan Verstovsek96104538936
Segev BenZvi9548232127
Mirko Planinic9446731957
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Performance
Metrics
No. of papers from the Institution in previous years
YearPapers
2023119
2022529
20213,277
20203,360
20193,176
20183,042