Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Maged Barakat"'
Autor:
Mohamed T. Abd El-Rahim, Nahla A. Hussein, Amr E. El-Hakim, Yasser E. Shahein, Ragaa R. Hamed, Maged Barakat
Publikováno v:
International Journal of Biological Macromolecules. 47:614-622
Immunoscreening of a cDNA expression library of the Rhipicephalus (Boophilus) annulatus tick with purified rabbit anti-R annulatus salivary glands antigens polyclonal antibodies led to the identification of a 661bp sequence. The sequence includes an
Autor:
Manal F. Ismail, Maged Barakat, Zakareya Elkhayat, Naglaa Kholoussi, Jackleen Raafat, Hala G. Elnady
Publikováno v:
Journal of Biochemical and Molecular Toxicology. 24:343-350
Apoptosis is the primary mechanism through which most chemotherapeutic agents induce tumor cell death. The purpose of this study was to monitor the expression of pro- and anti-apoptotic proteins CD(95) , Bcl-2, as well as copper and zinc levels in th
Publikováno v:
Journal of Diabetes and its Complications. 23:199-208
Wersternized diet, containing high fat diet intake combined with high consumption of softdrinks, is accused with the emerge of modern epidemic obesity and diabesity. Therefore, we aimed to study the effect of this diet combination on the homeostasis
Publikováno v:
Journal of Pineal Research. 33:87-94
The brain normally derives most of its energy from the aerobic oxidation of glucose and therefore it must be nourished with a rich supply of both glucose and oxygen. Interference with the blood supply, such as in ischemia, could shift the brain to se
Publikováno v:
Clinical Laboratory. 59
BACKGROUND A new, sensitive, noninvasive method for the detection of urothelial carcinomas of the bladder would open new possibilities in both the diagnosis and follow up of patients. METHODS Voided urine specimens were collected from patients with h
Autor:
Maged Barakat, Maha M. Kobesiy, Ahmed El Kotoury, Mona L. Essawi, Manal F. Ismail, Hanan H. Afifi
Publikováno v:
Journal of the Formosan Medical Association, Vol 112, Iss 11, Pp 707-712 (2013)
Background/Purpose Noonan syndrome (NS) is inherited as an autosomal dominant disorder with dysmorphic facies, short stature, and cardiac defects, which can be caused by missense mutations in the protein tyrosine phosphatase nonreceptor type 11 ( PTP
Publikováno v:
Journal of pineal research. 33(2)
The brain normally derives most of its energy from the aerobic oxidation of glucose and therefore it must be nourished with a rich supply of both glucose and oxygen. Interference with the blood supply, such as in ischemia, could shift the brain to se