Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Amal M.H. Mackawy"'
Publikováno v:
Egyptian Journal of Medical Human Genetics, Vol 16, Iss 4, Pp 333-341 (2015)
Hepatitis C virus (HCV) has been associated with high prevalence of steatosis and fibrosis. The impact of single-nucleotide polymorphisms (SNP) of patatin-like phospholipase domain-containing protein 3 (PNPLA3) on the development of steatosis and fib
Externí odkaz:
https://doaj.org/article/681e32b8b27d4ae3b21195279f69a228
Publikováno v:
Biotechnology and Applied Biochemistry. 66:634-642
Early diagnosis of non-small cell lung cancer (NSCLC) is essential for patient treatment and prognosis. Long noncoding RNA (lncRNA) have potential roles in tumor initiation and differentiation. The objective of this study was to investigate whether t
Autor:
Amal M.H. Mackawy, Ebtesam M. Ibrahim, Jehan El‐Gendy, Amal S. El-Shal, Abeer A. Saeed, Mai M. Hasan, Eman M. A. Abdelghany
Publikováno v:
Journal of cellular biochemistryREFERENCES. 121(2)
Background Chronic hyperglycemia is linked to either subfertility or infertility among diabetic males. Pioglitazone is one of the thiazolidinediones (TZDs) drugs that are selective peroxisome proliferator-activated receptor (PPAR-γ agonists used for
Publikováno v:
Meta Gene
Background Diabetic nephropathy (DN) is a chronic microangiopathic complication of type 2 diabetes mellitus (DM).Vascular endothelial dysfunction resulting from impaired nitric oxide synthase (NOS) activity in the vascular endothelial cells has been
Publikováno v:
Meta Gene
Background To date the published data concerning the possible interplay between vitamin D (VitD) and Vit D receptor (VDR) gene polymorphism with the immune/inflammatory mediators in type 2 diabetes mellitus (DM) is insufficient. Some of the immune no
Publikováno v:
Meta Gene. 21:100584
The DNA repair gene polymorphisms are supposed to boost the tumorigenesis and prognosis of cancers. The X-ray repair complementing defective repair in Chinese hamster cells 3 (XRCC3) gene has a pivotal role in the DNA repair process which if mutated
Publikováno v:
Egyptian Journal of Medical Human Genetics. 13:291-299
Hepatitis C virus (HCV) infection is a global health problem in Egypt and causes different liver disease spectrum. Evidence indicates that angiotensin I converting enzyme (ACE) gene polymorphism may play a role in determining disease progression. We
Publikováno v:
Mansoura Journal of Forensic Medicine and Clinical Toxicology. 18:97-111
Patients undergoing hemodialysis are exposed to medical devices containing di-ethylhexyl phthalate(DEHP). There is an ongoing discussion about the risks of DEHP exposure for the general population aswell as for specific subgroups in various medical s
Objectives: Vitamin D deficiency is a global health problem, its role as an immune modulator has been recently emphasized. The evidence is increasingly pointing towards vitamin D significant role in reducing the incidence of autoimmune diseases. Howe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d6a76fe2ba50ee4ef62b33799241f0f0
https://europepmc.org/articles/PMC3921055/
https://europepmc.org/articles/PMC3921055/
Publikováno v:
Global Journal of Health Science. 3
Background: A common C677T mutation of methylenetetrahydrofolate reductase (MTHFR) gene is reported to be associated with hyperhomocysteinemia a risk for atherosclerotic vascular diseases and ischemic stroke (IS). Aim: To clarify the possible role of