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of 31
pro vyhledávání: '"Iman Ehsan"'
Autor:
Ashique Al Hoque, Debasmita Dutta, Brahamacharry Paul, Leena Kumari, Iman Ehsan, Moumita Dhara, Biswajit Mukherjee, Mohiuddin Quadir, Benny Abraham Kaipparettu, Soumik Laha, Shantanu Ganguly
Publikováno v:
Cancer Nanotechnology, Vol 14, Iss 1, Pp 1-34 (2023)
Abstract Prostate cancer (PCa) is one of the fatal illnesses among males globally. PCa-treatment does not include radiotherapy. Chemotherapy eventually causes drug resistance, disease recurrence, metastatic advancement, multi-organ failure, and death
Externí odkaz:
https://doaj.org/article/d0d8145a49bf41a89be3af69103b9019
Akademický článek
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Akademický článek
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Autor:
Abdel-Meguid, Iman Ehsan, Abdel-Salam, Ekram, Latif, Doaa M Abdel, Korraa, Soheir, Ismaiel, Amal
Publikováno v:
In Egyptian Journal of Medical Human Genetics January 2013 14(1):49-53
Autor:
Walaa Fakher, Dina El-Tabie, Nihal Mohamed El-Refaie, Iman Ehsan Abdel-Meguid, Radwa Ezzat Amin, Hala Ahmed El-Gindy
Publikováno v:
Journal of Child Science. 11:e233-e239
Introduction Down syndrome (DS) is the most common chromosomal disorder. It is accompanied by several comorbidities, which could lead to severe morbidity and mortality. Congenital heart disease (CHD) is one of the most commonly described condition. O
Autor:
Hoda M Abd El-Ghany, Iman Ehsan Abdel Meguid, Rabab El Hawary, Safa Meshaal, Iman Taha Lafy Shimila, Eman Roshdy Radwan
Publikováno v:
Laboratory medicine. 53(4)
Objective Recurrent infection in Down syndrome (DS) has been previously documented; the potential role of platelets and neutrophil-platelet interaction has not been addressed in previous studies. Patients and Methods Using flow cytometry, we evaluate
Autor:
Zeinab, Nour, Kariman, El-Hamamsy, Iman, Ehsan, Lobna, Fawaz, Olfat, Shaker, Dalia, Mossallam, Hala, ElGindy
Publikováno v:
Rep Biochem Mol Biol
BACKGROUND: Sepsis is one of the most common causes of multiorgan failure. Sepsis requires the presence of infection with a resultant systemic inflammatory state. Organ dysfunction occurs from the combination of the two processes. Sepsis is the main
Autor:
Nihal AlMenabawy, Hebatallah M Hassaan, Manal Ramadan, Iman Ehsan Abdel Meguid, Hala Ahmed El Gindy, Christian Beetz, Laila Selim
Publikováno v:
Mitochondrion. 65
Mitochondrial DNA (mtDNA) depletion syndromes (MDS) are a heterogeneous group of rare autosomal recessive genetic disorders characterized by a decrease in the number of mtDNA copies inside the organ involved. There are three distinct forms of MDS inc
Autor:
Iman Ehsan, Leena Kumari, Ramkrishna Sen, Ashique Al Hoque, Biswajit Mukherjee, Alankar Mukherjee, Prasanta Ghosh, Sanchari Bhattacharya
Publikováno v:
Journal of Drug Delivery Science and Technology. 75:103689
Autor:
Yasir Faraz Abbasi, Ashique Al Hoque, Md Abdullah Al Maruf, Kazi Asraf Ali, Sneha Anand, Rajan Annie Mariya, Soumyabrata Banerjee, Muhammad Nazmul Baqui, Hriday Bera, Manas R. Biswal, Apala Chakraborty, Manas Chakraborty, Pranabesh Chakraborty, Samrat Chakraborty, Shreyasi Chakraborty, Bappaditya Chatterjee, Bhaskar Das, Surajit Das, Arnab De, Sanjay Dey, Moumita Dhara, Debasmita Dutta, Dishari Dutta, Lopamudra Dutta, Iman Ehsan, Anurag Kumar Gautam, Prasanta Ghosh, Xiong Guo, Md Saquib Hasnain, Chowdhury Mobaswar Hossain, Jagadeesh Induru, Sougata Jana, Tarak Nath Khatua, Sylvia N. Kłodzińska, Pranesh Kumar, Leena Kumari, Amit Kundu, Buddhadev Layek, Arpan Mahanty, Sabyasachi Maiti, Siddhartha Maity, Sanchita Mandal, Sreejan Manna, Priyanka Maurya, Nidhi Mishra, Laboni Mondal, N.S. Hari Narayana Moorthy, Biswajit Mukherjee, Amit Kumar Nayak, Hanne Mørck Nielsen, Dilipkumar Pal, Kushal Pal, Raviraj Pal, Poonam Parashar, Jwala Patel, G.P. Rajalekshmy, P.S. Rajinikanth, Manisheeta Ray, M.R. Rekha, Pradyot Kumar Roy, Sudipta Saha, Ratan Sahoo, Amalesh Samanta, Shubhini A. Saraf, Srimanta Sarkar, Soma Sengupta, Zahra Shariatinia, Neelu Singh, Samipta Singh, Kevin Sneed, Archana Bharti Sonkar, Sreya Suresh, Riddhi Vichare
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1776d7a87ffeeabf87dc6eef50607e2d
https://doi.org/10.1016/b978-0-12-820874-8.09991-7
https://doi.org/10.1016/b978-0-12-820874-8.09991-7