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Tumour Biology : the Journal of the International Society for Oncodevelopmental Biology and Medicine|October 29, 2015
Evaluation and screening of mRNA S100A genes as serological biomarkers in different stages of bladder cancer in EgyptManal F Ismail, Noha A El Boghdady, Marwa I Shabayek, et al.
Acta Biochimica Polonica|July 29, 2015
Methylenetetrahydrofolate reductase gene polymorphisms in Egyptian Turner Syndrome patientsManal F Ismail, Waheba A Zarouk, Mona O Ruby, et al.
Experimental and Molecular Pathology|August 2, 2015
Molecular biomarkers for prediction of response to treatment and survival in triple negative breast cancer patients from EgyptAbeer Bahnassy, Marwa Mohanad, Manal F Ismail, et al.
Acta Biochimica Polonica|June 18, 2014
Simple molecular diagnostic method for fragile X syndrome in Egyptian patients: pilot studyNagwa A Meguid, Manal F Ismail, Rasha S El-Mahdy, et al.
Journal of Interferon & Cytokine Research : the Official Journal of the International Society for Interferon and Cytokine Research|December 19, 2017
Bidirectional Association Between Psoriasis and Obesity: Benefits and RisksNoha A El-Boghdady, Manal F Ismail, Mahmoud F Abd-Alhameed, et al.
Molecular Medicine Reports|April 1, 2015
Transforming growth factor-β, insulin-like growth factor I/insulin-like growth factor I receptor and vascular endothelial growth factor-A: prognostic and predictive markers in triple-negative and non-triple-negative breast cancerAbeer Bahhnassy, Marwa Mohanad, Sabry Shaarawy, et al.
Journal of the Formosan Medical Association = Taiwan Yi Zhi|November 5, 2013
Mutational analysis of the PTPN11 gene in Egyptian patients with Noonan syndromeMona L Essawi, Manal F Ismail, Hanan H Afifi, et al.
Analytical Biochemistry|September 20, 2020
Determination of certain urinary microRNAs as promising biomarkers in diabetic nephropathy patients using gold nanoparticlesAhmed Ibrahim Nossier, Nagwa Ibrahim Shehata, Suzy Mahmoud Morsy, et al.
American Journal of Medical Genetics. Part A|June 3, 2016
Molecular and phenotypic spectrum of ASPM-related primary microcephaly: Identification of eight novel mutationsMohamed S Abdel-Hamid, Manal F Ismail, Hebatallh A Darwish, et al.
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