Pirooz Ebrahimi

ORCID: 0000-0002-8612-4893
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About
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Research Areas
  • Pancreatic function and diabetes
  • Lipoproteins and Cardiovascular Health
  • Health and Well-being Studies
  • RNA modifications and cancer
  • Trace Elements in Health
  • Heavy Metal Exposure and Toxicity
  • Cancer-related molecular mechanisms research
  • Diverse Scientific Research in Ukraine
  • Neurogenesis and neuroplasticity mechanisms
  • Multiple Sclerosis Research Studies
  • IL-33, ST2, and ILC Pathways
  • Ophthalmology and Visual Health Research
  • Hormonal Regulation and Hypertension
  • Parasitic Infections and Diagnostics
  • Mesenchymal stem cell research
  • Aluminum toxicity and tolerance in plants and animals
  • Genetics and Neurodevelopmental Disorders
  • Inflammasome and immune disorders
  • Regulation of Appetite and Obesity
  • Antiplatelet Therapy and Cardiovascular Diseases
  • Listeria monocytogenes in Food Safety
  • Cancer Genomics and Diagnostics
  • Nerve injury and regeneration
  • Bone Metabolism and Diseases
  • Ear Surgery and Otitis Media

University of Calabria
2022-2023

Tehran University of Medical Sciences
2023

Universal Scientific Education and Research Network
2019-2021

Jordan Hospital
2021

Sapienza University of Rome
2017-2018

Iran University of Medical Sciences
2018

Islamic Azad University Medical Branch of Tehran
2011

Maturity-onset diabetes of the young (MODY), an autosomal dominant disease, is frequently misdiagnosed as type 1 or 2 diabetes. Molecular diagnosis essential to distinguish them. This study was done investigate prevalence MODY subtypes and patients' clinical characteristics.A total 43 out 230 individuals with were selected based on age >6 months, family history diabetes, absence marked obesity, measurable C-peptide. Next-generation direct SANGER sequencing performed screen MODY-related...

10.1515/jpem-2022-0390 article EN Journal of Pediatric Endocrinology and Metabolism 2022-09-14

This research resulted in the identification and submission of a novel RUNX2 gene mutation affected members studied pedigree. Mutation screening is an effective method for early diagnosis CCD individuals.

10.1002/ccr3.2825 article EN Clinical Case Reports 2020-04-03

This study aimed to consider the expression of Nrf2, NLRP3 and caspase 1 genes, as well oxidative stress, protective role N-acetyl cysteine (NAC) in liver rats treated with cadmium (Cd). Male were randomly divided into five groups including G1 (control), G2 (single dose Cd), G3 (continuous G4 Cd + NAC), G5 NAC). Levels malondialdehyde (MDA) total antioxidant capacity (TAC) measured. Expression genes was considered using RT-PCR. NAC treatments significantly improved TAC, but decreased MDA...

10.5620/eaht.2021024 article EN cc-by-nc Environmental Analysis Health and Toxicology 2021-10-29

Abstract Introduction: Angiotensin Converting Enzyme or ACE is an exopeptidase that causes the conversion of angiotensin I to II, vasoconstriction, and aldosterone secretion. gene polymorphism (I/D) more enzyme activity increases risk coronary artery disease CAD. Aims: To examine role Gene Polymorphisms by Stent Types (Biomime, Supraflex, Xience) has been investigated in patients who underwent angioplasty this study. Material & Methods: Patients in-stent restenosis group (ISR + ) (N=53)...

10.21203/rs.3.rs-2803200/v1 preprint EN cc-by Research Square (Research Square) 2023-04-19

Introduction: Toxoplasma gondii (T. gondii) is distributed worldwide and infects most species. The serious incidence severe or fatal injury caused by T. infection clearly indicates the necessity for event of a vaccine. current study goals were to evaluate serological applications gondiirhoptry protein 1 (ROP1) antigen. Materials methods: We created polymer vaccine using eukaryotic plasmid, pROP1. Purification one-step metal affinity chromatography allowed recovery milligram amounts purified...

10.29252/jbrms.4.3.39 article EN cc-by Journal of Basic Research in Medical Sciences 2017-06-01
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