Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Nihal Salah Ibrahim"'
Publikováno v:
Journal of Microbiology, Immunology and Infection, Vol 50, Iss 5, Pp 565-569 (2017)
Background/Purpose: Human parvovirus B-19 (PB-19) is a cause of hemolysis, red blood cell aplasia, and severe conditions in patients with sickle cell anemia, but the molecular mechanisms of the infection are still insufficiently understood. This stud
Externí odkaz:
https://doaj.org/article/6f4749ece8484ad999364da1ae66ec15
Autor:
Nihal Salah Ibrahim, Manal Mohamed Makhlouf, Gehan Hamed Shahin, Mona Kamal Elghamrawy, Nehad Mohammed Hussein
Publikováno v:
Experimental and molecular pathology. 128
Sickle cell disease (SCD) is an inherited genetic disorders of hemoglobin that causes multisystem morbidity. The pathophysiology of SCD is complex and includes HbS polymerization/sickling, hemolysis, endothelial dysfunction and inflammation. Chemokin
Autor:
Alaa Gad, Manal Mohamed Makhlouf, Nihal Salah Ibrahim, Zainab Ali El-Saadany, Asmaa Salama, Mona Salah Al-Din Hamdy
Publikováno v:
Tumori Journal. 103:268-271
Background and aimsThe p73 gene has different isoforms with opposing anti- and pro-apoptotic functions. The pro-apoptotic activities are inhibited by overexpression of the dominant ΔNp73 isoform. The aim of this study was to detect the expression of
Autor:
Nihal Salah Ibrahim, Mohamed Menesy
Publikováno v:
Comparative Clinical Pathology. 25:375-380
Hepatitis C virus (HCV) infection is a significant global health problem. Elevated hepatic iron concentration has often been found in patients with chronic hepatitis C, and this excess iron increases oxidative stress, which can accelerate the progres
Autor:
Somaia Mohammed Mousa, Hoda Sadek, Amany A. Abou-Elalla, Gehad Atef, Ilham Youssry, Nihal Salah Ibrahim
Publikováno v:
Fetal and pediatric pathology. 36(3)
Development of inhibitors against Factor VIII (FVIII) in hemophilia A patients is a serious complication of therapy. Many cytokines, including interleukin-10 (IL10), may affect inhibitor development; however, literature data are not sufficient to pro
Publikováno v:
Journal of Microbiology, Immunology and Infection, Vol 50, Iss 5, Pp 565-569 (2017)
Background/Purpose: Human parvovirus B-19 (PB-19) is a cause of hemolysis, red blood cell aplasia, and severe conditions in patients with sickle cell anemia, but the molecular mechanisms of the infection are still insufficiently understood. This stud