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محمد على ابراهيم محمد على

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Curriculum Vitae

Mohamed Ali Ibrahim Mohamed ally

Faculty Science - Department Biochemistry Department

Scientific degrees

BSc In NULL, [2010]
MSc In NULL, [2014]
(Biological studies on liver cells derived from the liver cells derived from stem cells moderation)
PhD In NULL, [2019]

الحالة الوظيفية الحالية :

قائم بالعمل

Academic Jobs

معيد : 24/10/2010
Doctor Assisant : 16/2/2014
Doctor : 25/6/2019

Publications

1 - Hepatocyte derived from Rat Bone Marrow Mesenchymal Stem Cells (2013).

2 - Improvement of Renal Failure Using Wharton’s Jelly Derived Mesenchymal Stem Cells (2018).

3 - Three-dimensional bioprinting for organ bioengineering: promise and pitfalls (2018).

4 - A Photo‐Crosslinkable Kidney ECM‐Derived Bioink Accelerates Renal Tissue Formation (2019).

5 - Sustained release of stromal cell–derived factor-1 alpha from silk fibroin microfiber promotes urethral reconstruction in rabbits (2020).

6 - Possible mechanisms for the renoprotective action of adipose-derived mesenchymal stem cells with CD44 targeted hyaluronic acid against renal ischemia (2021).

7 - Preparation, spectroscopic, characterizations and biological studies of new charge transfer complexes formed between fluconazole drug with various acceptors (2021).

8 - 3D BIOPRINTED RENAL TISSUE CONSTRUCTS USING A NOVEL KIDNEY ECM-DERIVED BIOINK (2020).

9 - 3D Bioprinting of Human Kidney Construct: A Step Towards Solid Organ Printing (2017).

10 - Preparation, spectroscopic characterizations and biological studies of a new charge transfer complex formed between fluconazole drug with various acceptors (2021).

11 - Design, spectroscopic, structural characterization, and biological studies for new complexes via charge transfer interaction of ciprofloxacin drug with π acceptors (2022).

12 - Identification of Epigenetic Interactions between miRNA and Gene Expression as Potential Prognostic Markers in Bladder Cancer (2022).

13 - Hepatoprotective Effects of Hyaluronic Acid-Preconditioned Bone Marrow Mesenchymal Stem Cells against Liver Toxicity via the Inhibition of Apoptosis and the Wnt/β-Catenin Signaling Pathway (2023).

Research Area