Zobrazeno 1 - 10
of 19
pro vyhledávání: '"Gilane M. Sabry"'
Publikováno v:
Heliyon, Vol 6, Iss 2, Pp e03341- (2020)
Osteoporosis is a skeletal degenerative disease characterised by abnormal bone turnover with scant bone formation and overabundant bone resorption. The present approach was intended to address the potency of nanohydroxyapatite (nHA), chitosan/hydroxy
Externí odkaz:
https://doaj.org/article/6091e1b9b3934645bf0b8dc497e54785
Autor:
Abdel-Rahman N. Zekri, Abeer A. Bahnasy, Fatma elzahraa M. Shoeab, Waleed S. Mohamed, Dina H. El-Dahshan, Fahmey T. Ali, Gilane M. Sabry, Nairajana Dasgupta, Sayed S. Daoud
Publikováno v:
Journal of Advanced Research, Vol 5, Iss 1, Pp 27-40 (2014)
We studied promoter methylation (PM) of 11 genes in Peripheral Blood Lymphocytes (PBLs) and tissues of hepatitis C virus (HCV) associated hepatocellular carcinoma (HCC) and chronic hepatitis (CH) Egyptian patients. The present study included 31 HCC w
Externí odkaz:
https://doaj.org/article/c5bbe48190274ca5ae955b950f287564
Autor:
Gilane M. Sabry, Rania S. Salah, Hanaa H. Ahmed, Somia H. Abd-Allah, Wagdy K. B. Khalil, Ahmed A. Abd-Rabou, Rasha E. Hassan
Publikováno v:
RESEARCH JOURNAL OF PHARMACY AND TECHNOLOGY. 14:1255-1266
Autor:
Nehal S. Abouhashem, Rasha E. Hassan, Somia H. Abd-Allah, Gilane M. Sabry, Rehab E. Selim, Wagdy K. B. Khalil, Hanaa H. Ahmed
Publikováno v:
Applied Biochemistry and Biotechnology. 189:284-304
Acute kidney injury (AKI) is a rapid loss of renal function. It has high mortality rates. Still, renal replacement therapy is considered the best solution for recovering AKI. This opens a line of thought to develop an alternative therapy for it witho
Publikováno v:
Heliyon, Vol 6, Iss 2, Pp e03341-(2020)
Heliyon
Heliyon
Osteoporosis is a skeletal degenerative disease characterised by abnormal bone turnover with scant bone formation and overabundant bone resorption. The present approach was intended to address the potency of nanohydroxyapatite (nHA), chitosan/hydroxy
Autor:
Nicolas Etique, Gilane M. Sabry, Hamid Morjani, Bertrand Brassart, Roselyne Garnotel, Rasha E. Hassan, Pierre Jeannesson, Ahmed Mohsen, Philippe Collery, Didier Desmaële
Publikováno v:
Metallomics
Metallomics, Royal Society of Chemistry, 2017, 9 (8), pp.1176-1184. ⟨10.1039/c7mt00049a⟩
Metallomics, Royal Society of Chemistry, 2017, 9 (8), pp.1176-1184. ⟨10.1039/c7mt00049a⟩
International audience; In this study, we investigated the effect of [N-(5-chloro-2-hydroxyphenyl)-l-aspartato] chlorogallate (GS2), a new water soluble gallium complex, on cell invasion and on the expression and activity of matrix metalloproteinases
Autor:
Pierre Jeannesson, Ahmed Mohsen, Hamid Morjani, Philippe Collery, Didier Desmaële, A. M. Badawi, Charles Saby, Gilane M. Sabry, Rasha E. Hassan
Publikováno v:
JBIC Journal of Biological Inorganic Chemistry. 21:837-849
Two water soluble gallium complexes described as [Ga(III)LCl], where L is the deprotonated form of N-2-hydroxybenzyl aspartic acid derivatives, were synthesized and characterized by (1)H NMR, (13)C NMR, FT-IR, mass spectrometry, and elemental analysi
Autor:
Hala M. Ghanem, Ghada A. Abdallah, Hanan H. Shehata, Nevine M. Abd-Elfattah, Hanaa El-Tayeb Nasser, Gilane M. Sabry
Publikováno v:
American Journal of Biochemistry and Biotechnology. 10:281-294
Oxidative stress has been implicated in the pathogenesis of Chronic Obstructive Pulmonary Disease (COPD), due to its effect on proinflammatory gene transcription. Oxidants/antioxidants imbalance is responsible for disease development. The study was d
Autor:
Nairajana Dasgupta, Gilane M. Sabry, Fatma elzahraa M. Shoeab, Abeer A. Bahnasy, Dina H. El-Dahshan, Waleed S. Mohamed, Sayed S. Daoud, Abdel-Rahman N. Zekri, Fahmey T. Ali
Publikováno v:
Journal of Advanced Research
Journal of Advanced Research, Vol 5, Iss 1, Pp 27-40 (2014)
Journal of Advanced Research, Vol 5, Iss 1, Pp 27-40 (2014)
We studied promoter methylation (PM) of 11 genes in Peripheral Blood Lymphocytes (PBLs) and tissues of hepatitis C virus (HCV) associated hepatocellular carcinoma (HCC) and chronic hepatitis (CH) Egyptian patients. The present study included 31 HCC w
Autor:
Abdel-Monem A. Abdalla, Gilane M. Sabry, Nagwa Abdel-Meguid, Tahany M. Maharem, Ragaa R. Hamed, Rasha A. Guneidy
Publikováno v:
Research in Developmental Disabilities. 32:1470-1482
Down syndrome (DS) is the phenotypic manifestation of trisomy 21. Our study was concerned with the characterization and purification of glutathione S-transferase enzyme (GST) from normal and Down syndrome (DS) erythrocytes to illustrate the differenc