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Institution

Dow University of Health Sciences

EducationKarachi, Pakistan
About: Dow University of Health Sciences is a education organization based out in Karachi, Pakistan. It is known for research contribution in the topics: Population & Medicine. The organization has 3073 authors who have published 3187 publications receiving 30199 citations.


Papers
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Journal ArticleDOI
Gregory A. Roth1, Gregory A. Roth2, Degu Abate3, Kalkidan Hassen Abate4  +1025 moreInstitutions (333)
TL;DR: Non-communicable diseases comprised the greatest fraction of deaths, contributing to 73·4% (95% uncertainty interval [UI] 72·5–74·1) of total deaths in 2017, while communicable, maternal, neonatal, and nutritional causes accounted for 18·6% (17·9–19·6), and injuries 8·0% (7·7–8·2).

5,211 citations

Journal ArticleDOI
Jeffrey D. Stanaway1, Ashkan Afshin1, Emmanuela Gakidou1, Stephen S Lim1  +1050 moreInstitutions (346)
TL;DR: This study estimated levels and trends in exposure, attributable deaths, and attributable disability-adjusted life-years (DALYs) by age group, sex, year, and location for 84 behavioural, environmental and occupational, and metabolic risks or groups of risks from 1990 to 2017 and explored the relationship between development and risk exposure.

2,910 citations

Journal ArticleDOI
TL;DR: This review increases the understanding of tumor treatment with the promising use of nanotechnology by covering the description of selected tumors, including breast, lungs, colorectal and pancreatic tumors, and applications of relative nanocarriers in these tumors.
Abstract: Nanotechnology has recently gained increased attention for its capability to effectively diagnose and treat various tumors. Nanocarriers have been used to circumvent the problems associated with conventional antitumor drug delivery systems, including their nonspecificity, severe side effects, burst release and damaging the normal cells. Nanocarriers improve the bioavailability and therapeutic efficiency of antitumor drugs, while providing preferential accumulation at the target site. A number of nanocarriers have been developed; however, only a few of them are clinically approved for the delivery of antitumor drugs for their intended actions at the targeted sites. The present review is divided into three main parts: first part presents introduction of various nanocarriers and their relevance in the delivery of anticancer drugs, second part encompasses targeting mechanisms and surface functionalization on nanocarriers and third part covers the description of selected tumors, including breast, lungs, colorectal and pancreatic tumors, and applications of relative nanocarriers in these tumors. This review increases the understanding of tumor treatment with the promising use of nanotechnology.

841 citations

Journal ArticleDOI
Oliver Kepp1, Laura Senovilla1, Ilio Vitale, Erika Vacchelli1, Sandy Adjemian2, Patrizia Agostinis3, Lionel Apetoh4, Fernando Aranda1, Vincenzo Barnaba5, Norma Bloy1, Laura Bracci6, Karine Breckpot7, David Brough8, Aitziber Buqué1, Maria G. Castro9, Mara Cirone5, María Isabel Colombo10, Isabelle Cremer11, Sandra Demaria12, Luciana Dini13, Aristides G. Eliopoulos14, Alberto Faggioni5, Silvia C. Formenti12, Jitka Fucikova15, Lucia Gabriele6, Udo S. Gaipl16, Jérôme Galon11, Abhishek D. Garg3, François Ghiringhelli4, Nathalia A. Giese17, Zong Sheng Guo18, Akseli Hemminki19, Martin Herrmann16, James W. Hodge20, Stefan Holdenrieder21, Jamie Honeychurch8, Hong-Min Hu22, Xing Huang1, Timothy M Illidge8, Koji Kono23, Mladen Korbelik, Dmitri V. Krysko24, Sherene Loi, Pedro R. Lowenstein9, Enrico Lugli25, Yuting Ma1, Frank Madeo26, Angelo A. Manfredi, Isabelle Martins27, Domenico Mavilio25, Laurie Menger28, Nicolò Merendino29, Michael Michaud1, Grégoire Mignot, Karen L. Mossman30, Gabriele Multhoff31, Rudolf Oehler32, Fabio Palombo5, Theocharis Panaretakis33, Jonathan Pol1, Enrico Proietti6, Jean-Ehrland Ricci34, Chiara Riganti35, Patrizia Rovere-Querini, Anna Rubartelli, Antonella Sistigu, Mark J. Smyth36, Juergen Sonnemann, Radek Spisek15, John Stagg37, Abdul Qader Sukkurwala38, Eric Tartour39, Andrew Thorburn40, Stephen H. Thorne18, Peter Vandenabeele24, Francesca Velotti29, Samuel T Workenhe30, Haining Yang41, Wei-Xing Zong42, Laurence Zitvogel1, Guido Kroemer43, Lorenzo Galluzzi43 
TL;DR: Strategies conceived to detect surrogate markers of ICD in vitro and to screen large chemical libraries for putative I CD inducers are outlined, based on a high-content, high-throughput platform that was recently developed.
Abstract: Apoptotic cells have long been considered as intrinsically tolerogenic or unable to elicit immune responses specific for dead cell-associated antigens. However, multiple stimuli can trigger a functionally peculiar type of apoptotic demise that does not go unnoticed by the adaptive arm of the immune system, which we named "immunogenic cell death" (ICD). ICD is preceded or accompanied by the emission of a series of immunostimulatory damage-associated molecular patterns (DAMPs) in a precise spatiotemporal configuration. Several anticancer agents that have been successfully employed in the clinic for decades, including various chemotherapeutics and radiotherapy, can elicit ICD. Moreover, defects in the components that underlie the capacity of the immune system to perceive cell death as immunogenic negatively influence disease outcome among cancer patients treated with ICD inducers. Thus, ICD has profound clinical and therapeutic implications. Unfortunately, the gold-standard approach to detect ICD relies on vaccination experiments involving immunocompetent murine models and syngeneic cancer cells, an approach that is incompatible with large screening campaigns. Here, we outline strategies conceived to detect surrogate markers of ICD in vitro and to screen large chemical libraries for putative ICD inducers, based on a high-content, high-throughput platform that we recently developed. Such a platform allows for the detection of multiple DAMPs, like cell surface-exposed calreticulin, extracellular ATP and high mobility group box 1 (HMGB1), and/or the processes that underlie their emission, such as endoplasmic reticulum stress, autophagy and necrotic plasma membrane permeabilization. We surmise that this technology will facilitate the development of next-generation anticancer regimens, which kill malignant cells and simultaneously convert them into a cancer-specific therapeutic vaccine.

665 citations


Authors

Showing all 3089 results

NameH-indexPapersCitations
Danish Saleheen8621360659
Muhammad Usman61120324848
Pooja Khatri5427613834
Jay Singh513018655
Muhammad Jamil444148021
Asif Rasheed386924698
Sarah P. Young31923138
Fariha Hasan301415803
Nazeer Khan28823377
Muhammad Shahzeb Khan241508186
Muhammad Naeem221892104
M. Saeed Arayne221151497
Irbaz Bin Riaz221232028
Tariq Jamal Siddiqi22617618
Syed Ali21721610
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Performance
Metrics
No. of papers from the Institution in previous years
YearPapers
20236
202230
2021457
2020506
2019398
2018354