Zobrazeno 1 - 10
of 33
pro vyhledávání: '"Mohamed M, Zedan"'
Autor:
Mohamed M. Zedan, Ali Sobh, Alshimaa Magdy, Mai S. Korkor, Zeinab R. Attia, Nada Khaled, Yousra Sadeq, Ahmed Hazem El-Nagdy, Ahmed E. Taha, Mohamed Ahmed Noureldin, Mohamed Taman, Doaa Mosad Mosa, Marwa H. Elnagdy
Publikováno v:
Pediatric Rheumatology Online Journal, Vol 22, Iss 1, Pp 1-11 (2024)
Abstract Background Measurement of the circulating levels of long-non-coding RNAs (lncRNAs) in lupus nephritis (LN) patients could dramatically explore more insights about the disease pathogenesis. Hence, we aimed to quantify the level of expression
Externí odkaz:
https://doaj.org/article/965048697e8e4f1fbe2eb6961400a9df
Autor:
Ahmed M. El-Refaey, Ayman Z. Elsamanoudy, Zakarya Elmorsy, Eman Gaber, Amr Sarhan, Aymman Hammad, Mohamed M. Zedan, Ashraf Bakr
Publikováno v:
Saudi Journal of Kidney Diseases and Transplantation, Vol 32, Iss 6, Pp 1615-1627 (2021)
Idiopathic nephrotic syndrome (NS) is one of the most common primary glomerular diseases in children. In this study, we investigate the association of single-nucleotide polymorphisms of nephrin gene and glucocorticoid receptor gene (NR3C1) and suscep
Externí odkaz:
https://doaj.org/article/e33ab12596a54f819837468cc02ff856
Publikováno v:
Egyptian Journal of Chest Disease and Tuberculosis, Vol 70, Iss 2, Pp 208-214 (2021)
Background Asthma is known to be a heterogeneous disease that forms a problem in asthma management. Symptom-based asthma phenotyping with endotyping of the proposed phenotype is a trial to solve this problem. Asthma phenotypes and endotypes facilitat
Externí odkaz:
https://doaj.org/article/0adf4a786edc474f894e02023fcf038e
Autor:
Riham Eid, Ashraf Bakr, Atef Elmougy, Mohamed M Zedan, Nahla A Allam, Amr Sarhan, Ayman Hammad, Ahmed M El-Refaey, Nashwa Hamdy
Publikováno v:
Saudi Journal of Kidney Diseases and Transplantation, Vol 31, Iss 6, Pp 1376-1387 (2020)
Hemolytic-uremic syndrome (HUS) is a leading cause of childhood acute kidney injury (AKI) worldwide, with its postdiarrheal (D+HUS) form being the most common. Scarce data are available regarding D+HUS epidemiology from developing countries. This stu
Externí odkaz:
https://doaj.org/article/e36e690c02d5460dbf66accefdb7cca0
Autor:
Zeinab R. Attia, Mohamed M. Zedan, Thuraya M. Mutawi, Entsar A. Saad, Rania A. Abd El Azeem, Mohamed A. El Basuni
Publikováno v:
Children, Vol 9, Iss 9, p 1271 (2022)
Permanent systemic inflammation is a defining feature of systemic lupus erythematosus (SLE), which affects multiple organs. Gelatinase B/matrix metalloproteinase-9 (MMP-9) is an essential protease investigated in inflammation that has been linked to
Externí odkaz:
https://doaj.org/article/3095f4b2c5c143c899a97fb87f9206f4
Publikováno v:
Biomarkers in Medicine. 15:1669-1680
Aim: To demonstrate whether sCD14 and CD14 (rs2569190 A/G and rs2569191 C/T) genetic variants are associated with systemic lupus erythematosus (SLE) risk, for the first time, in Egyptian pediatrics and adolescents. Materials & methods: sCD14 concentr
Autor:
Mohamed M. Zedan, Ahmed K. Mansour, Ashraf A. Bakr, Mohamed A. Sobh, Hesam Khodadadi, Evila Lopes Salles, Abdulmohsin Alhashim, Babak Baban, Olga Golubnitschaja, Ahmed A. Elmarakby
Publikováno v:
International Journal of Molecular Sciences, Vol 23, Iss 344, p 344 (2022)
International Journal of Molecular Sciences
International Journal of Molecular Sciences; Volume 23; Issue 1; Pages: 344
International Journal of Molecular Sciences
International Journal of Molecular Sciences; Volume 23; Issue 1; Pages: 344
Glomerular endothelial injury and effectiveness of glomerular endothelial repair play a crucial role in the progression of glomerulonephritis. Although the potent immune suppressive everolimus is increasingly used in renal transplant patients, advers
Deoxyribonuclease I (DNase I) is a potential endonuclease enzyme implicated in several immune diseases such as SLE. The objective of this study was to investigate the influence of rs1053874 A/G DNase I polymorphism on SLE susceptibility and to study
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::424ddd9e0292d4e226f269d019fd8839
https://doi.org/10.21203/rs.3.rs-1727269/v1
https://doi.org/10.21203/rs.3.rs-1727269/v1
Autor:
Mohamed M Zedan, Mamdouh R. El-Sawi, Thuraya M Mutawi, Andrea Gaedigk, Raida S. Yahya, Mahmoud M Zakria
Publikováno v:
Pharmacogenomics. 22:323-334
Aim: This study investigated major allelic variants of CYP2D6, CYP3A4 and CYP3A5 in Egyptians, an Arabic population for which there is little information regarding these important pharmacogenes. Patients & methods: CYP2D6*2, *4, *5, *10, *41 and gene
Publikováno v:
Clinical Biochemistry. 88:37-42
Background Systemic lupus erythematosus (SLE) is a chronic autoimmune disease associated with increased oxidative stress that participates in immune dysregulation, and injury resulting in loss of immune tolerance and increased auto-antibody productio