Zobrazeno 1 - 10
of 72
pro vyhledávání: '"Olfat SHAKER"'
Autor:
Moustafa Ali Saad, Hala Ibrahem El Gendy, Ahmed Hatem Laymouna, Olfat Shaker, Mervat Essam Behiry
Publikováno v:
Egyptian Journal of Medical Human Genetics, Vol 25, Iss 1, Pp 1-8 (2024)
Abstract Background Behcet's syndrome (BS) is a variable-vessel vasculitis characterized by hyperactive innate immunity. The nuclear factor kappa B (NFKB) pathway is involved in the regulation of inflammatory responses including innate and adaptive i
Externí odkaz:
https://doaj.org/article/728374bc66fe447fb55b7c9a954a2139
Publikováno v:
Türk Patoloji Dergisi, Vol 40, Iss 3, Pp 149-161 (2024)
Objective: A few studies indicate that human papillomavirus (HPV) induces aberrant expression of microRNAs (miRNAs) and correlate this with p16INK4a in oral dysplasia (OD) and oral squamous cell carcinoma (OSCC). Therefore, this study aimed to evalua
Externí odkaz:
https://doaj.org/article/531eca4e274c48f0bc73133163311365
Publikováno v:
BMC Oral Health, Vol 24, Iss 1, Pp 1-6 (2024)
Abstract Background The scientific community has been particularly interested in oral squamous cell carcinoma (OSCC) because of the cancer’s extremely high incidence and fatality rates worldwide. It has been proposed that paxillin is involved in ce
Externí odkaz:
https://doaj.org/article/1bf977543d454fb38cdb1afb82a386c9
Autor:
Salma Mohamed Mostafa, Ibrahim Elebrashy, Hemmat El Haddad, Olfat Shaker, Naglaa Abdel Razek, Ahmed Fayed
Publikováno v:
Diabetology & Metabolic Syndrome, Vol 16, Iss 1, Pp 1-9 (2024)
Abstract Background Patients with Type 2 diabetes mellitus (T2DM) have decreased bone health. We aimed to investigate serum levels of bone turnover markers (BTMs) (markers of bone formation and bone resorption) and bone mineral density (BMD) at three
Externí odkaz:
https://doaj.org/article/e070aa3d1de4479a821574700da5c81a
Autor:
Dalia A. Gaber, Mohamed Shokr, Olfat Shaker, Kamelia Ahmed Zaki, Haidy Samir Khalil, Amany M. Wahb
Publikováno v:
Scientific Reports, Vol 14, Iss 1, Pp 1-13 (2024)
Abstract The expression of ACE2 is linked to disease severity in COVID-19 patients. The ACE2 receptor gene polymorphisms are considered determinants for SARS-CoV-2 infection and its outcome. In our study, serum ACE2 and its genetic variant S19P rs736
Externí odkaz:
https://doaj.org/article/d7b43410739b4662b4f70496585e2efd
Autor:
Mostafa Abdelsamie, Fat’heya Zahran, Amal A. Hussine, Olfat Shaker, Abdulaziz Mohsen Al-mahallawi
Publikováno v:
BMC Oral Health, Vol 23, Iss 1, Pp 1-11 (2023)
Abstract Background Oral lichen planus (OLP) is a chronic mucocutaneous immunologically mediated condition that has a great adverse effect on oral functions. Corticosteroids are still the first drugs of choice used in the treatment of OLP; however, t
Externí odkaz:
https://doaj.org/article/d8cf22e00ea44f8498ac4f5b3fe9d88e
Publikováno v:
Biochemistry and Biophysics Reports, Vol 36, Iss , Pp 101562- (2023)
Downregulating Angiotensin Converting Enzyme2 (ACE2) expression may be a shared mechanism for RNA viruses. Aim: Evaluate the expressions of ACE2 effectors: the long non-coding RNA ‘MALAT-1’, the micro-RNA ‘miR-200c-3p’ and the histone deacety
Externí odkaz:
https://doaj.org/article/471ca53fb8444f76a5b068c2db409d9a
Autor:
Amani Ali, Hamed Osman, Azza Zaki, Olfat Shaker, Asma Elsayed, Mostafa Abdelwahed, Rehab Mohammed
Publikováno v:
Iranian Journal of Basic Medical Sciences, Vol 25, Iss 12, Pp 1487-1497 (2022)
Objective(s): The prevalence of chronic kidney disease in diabetics is progressively increasing with an increased risk of fatal complications. Materials and Methods: Sixty male albino rats were used in the study, and type 2 diabetes mellitus were ind
Externí odkaz:
https://doaj.org/article/4cd33c5521d54cedad194eeb8eeb0a20
Publikováno v:
Future Science OA, Vol 8, Iss 10 (2022)
Aim: To investigate the expression profile and diagnostic potentials of serum miR-92a, 134, and 375 in acute ischemic stroke (AIS) patients. Materials & methods: Serum miRs-92a, 134, and 375 expression profiles were estimated by qRT-PCR for 70 AIS pa
Externí odkaz:
https://doaj.org/article/8239ee07e2eb4729adcbd2d8fd4bf9bf
Autor:
Gehan Abdel-Fattah Hegazy, Olfat Shaker, Omnia Aly, Hanan Hassan Zaki, Mohamed R Herzalla, Ahmed Fathy Gomaa, Safaa Sayed, Maysa M Haroon
Publikováno v:
Indian Journal of Rheumatology, Vol 16, Iss 2, Pp 152-158 (2021)
Background: Rheumatoid arthritis (RA) is a relatively common autoimmune disease in which genetic risk factors are well defined. Genetic studies are promising in exploring the long noncoding ribonucleic acids (lncRNAs): growth arrest-specific 5 (GAS5)
Externí odkaz:
https://doaj.org/article/6faf0dd4d525405797ec537efa77ca9b