Dr. Essam M. Abdelalim is a scientist at the Qatar Biomedical Research Institute (QBRI) and an assistant professor at the College of Science and Engineering (CSE) and the College of Health and Life Sciences (CHLS). He received his PhD in Medical Science from Shiga University of Medical Science, Japan. At CHLS, Dr. Abdelalim is coordinating the “Stem Cell Biology” course and also teaches several courses, and supervises several masters and PhD students. Since April 2014, Dr. Abdelalim has been leading the diabetes stem cell research at QBRI.
He has been awarded multiple NPRP grants and QBRI Internal Research grants to study diabetes and pancreatic beta-cell differentiation. He has established strong collaborations in the field of diabetes with key scientists and clinicians from different institutions inside Qatar, including Hamad Medical Corporation (HMC), Sidra Medicine, Weill Cornell Medicine-Qatar (WCM-Q), and Carnegie Mellon University in Qatar (CMUQ). He also plays a key role in the collaboration between Harvard Stem Cell Institute (HSCI) and QBRI/HBKU and he is leading the first collaborative project between HSCI and QBRI.
College of Health and Life Science (CHLS), Hamad Bin Khalifa University (HBKU), Qatar Foundation, Qatar.
Nov. 2018 - PresentCollege of Life Science and Engineering (CSE), Hamad Bin Khalifa University (HBKU), Qatar Foundation, Qatar.
July 2015 - Sept. 2018Qatar Biomedical Research Institute (QBRI), HBKU, Qatar Foundation, Qatar.
April 2014 - PresentCytology & Histology Dep., Fac. of Veterinary Medicine, Suez Canal University, Egypt (on leave of absence).
Nov. 2014 - PresentStem Cell and Regenerative Medicine Center, QBRI, Qatar Foundation, Qatar.
Sep. 2013 - Mar. 2014Molecular Neuroscience Research Center (MNRC), Shiga University of Medical Science, Japan.
Mar. 2012- Apr. 2016Japan Society for Promotion of Science (JSPS), Ministry of Education. MNRC, Shiga University of Medical Science, Japan.
Aug. 2009 - Aug. 2011Cytology & Histology Dep., Faculty of Veterinary Medicine, Suez Canal University, Egypt.
Jun. 2009 - Nov. 2014Molecular Neuroscience Research Center (MNRC), Shiga University of Medical Science, Japan.
Nov. 2008 - Apr. 2009Cytology & Histology Dep., Faculty of Veterinary Medicine, Suez Canal University, Egypt.
Oct. 2002 - Jun. 2009Cytology & Histology Department, Faculty of Veterinary Medicine, Suez Canal University, Egypt.
Dec. 1999 - Oct. 2002Graduate School of Medicine, Shiga University of Medical Science, Japan.
2009Cytology and Histology Dep., Faculty of Veterinary Medicine, Suez Canal University, Egypt.
2002Faculty of Veterinary Medicine, Suez Canal University, Egypt.
1998Aberrant development of pancreatic beta cells derived from human iPSCs with FOXA2 deficiency. Cell Death & Disease, in press.
2021Modeling different types of diabetes using human pluripotent stem cells. Cellular and Molecular Life Sciences, in press.
2020NKX6.1 transcription factor: A crucial regulator of pancreatic β-cell development, identity, and proliferation. Stem Cell Research & Therapy, 2020 Oct 29;11(1):459.
2020Potential application of mesenchymal stem cells and their exosomes in lung injury: an emerging therapeutic option for COVID-19 patients. Stem Cell Research & Therapy, 2020, 2020 Oct 15;11(1):437.
2020PDX1-/NKX6.1+ progenitors derived from human pluripotent stem cells as a novel source of insulin-secreting cells. Diabetes Metab Res Rev. 2020 Aug 28;e3400.
2020Generation of two human iPSC lines from patients with maturity-onset diabetes of the young type 2 (MODY2) and permanent neonatal diabetes due to mutations in the GCK gene. Stem Cell Research, 2020 Oct; 48:101991.
2020Keratinocytes derived from patient-specific induced pluripotent stem cells recapitulate the genetic signature of psoriasis disease. Stem Cells and Development, 2020 Apr 1;29(7):383-400.
2020Scalable Generation of Mesenchymal Stem Cells and Adipocytes from Human Pluripotent Stem Cells. Cells, 9(3), 710.
2020Derivation of a human induced pluripotent stem cell line (QBRIi007-A) from a patient carrying a homozygous intronic mutation (c.613-7T>G) in the SLC2A2 gene. Stem Cell Research, 2020 Feb 24;44:101736.
2020Stem cell therapy for diabetes: beta cells versus pancreatic progenitors. Cells, 9 (2): pii: E283.
2020Generation of a human induced pluripotent stem cell line (QBRIi009-A) from a patient with a heterozygous deletion of FOXA2. Stem Cell Research, 42, 101705.
2020Differentiation of human pluripotent stem cells into two distinct NKX6.1 populations of pancreatic progenitors. Stem Cell Research & Therapy, 9(1):83.
2018Enhanced differentiation of human pluripotent stem cells into pancreatic progenitors co-expressing PDX1 and NKX6.1. Stem Cell Research & Therapy, 2018, 9:15.
2018Pathways governing development of stem cell-derived pancreatic β cells: lessons from embryogenesis. Biol Rev Camb Philos Soc. 93(1):364-389.
2018New proteomic insights on the role of NPR-A in regulating self-renewal of embryonic stem cells. Stem Cell Reviews and Reports, 2014 Aug; 10 (4): 561-72.
2014Pluripotent stem cells as a potential tool for disease modelling and cell therapy in diabetes. Stem Cell Reviews and Reports, 10 (3): 327-337.
2014NPR-A regulates self-renewal and pluripotency of embryonic stem cells. Cell Death & Disease, 2: e127.
2011