Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Reham, Sameh"'
Publikováno v:
Middle East Journal of Cancer, Vol 15, Iss 4, Pp 289-296 (2024)
Background: Triple-negative breast cancer (TNBC) is characterized by a poor prognosis. Consequently, the current research aims to identify new therapeutic targets for TNBC patients. Trichorhinophalangeal syndrome type 1 (TRPS1), a novel GATA transcri
Externí odkaz:
https://doaj.org/article/da71bd9508b0499cbf962f1a9082f2c5
Autor:
Samia, Hussein, Ahmed El Shabrawy, Lasheen, Amr A, Abdelrahman, Amira S, Al-Karamany, Reham, Sameh, Ahmed, Algazeery
Publikováno v:
Asian Pacific Journal of Cancer Prevention. 23:1761-1768
Ovarian cancer is the fifth leading cause of cancer-related deaths among women worldwide. Unfortunately, early detection tests are relatively lacking. Diagnosis in the late stages of the disease carries a poor prognosis.To evaluate the relationship b
Autor:
Lobna A. Abdelaziz, Hayam E. Rashed, Reham Sameh, Eman A. Elsebai, Shireen S. Muhammad, Nashwa Nawar, Mohamed I. Abdelhamid
Publikováno v:
Revista de Senología y Patología Mamaria. 34:200-207
Introduction Immune system plays an important role in behavior of cancer. Breast cancer and its stroma display high levels of immune-cell infiltrates (tumor-infiltrating lymphocytes TILs). Programmed cell death-ligand 1 (PD-L1) is one key inhibitor m
Autor:
Reham Sameh, Mohamed Fawzy Ramadan, Naglaa A. Mostafa, Khaled Abdelwahab, Samar M. Abdel-Raouf
Publikováno v:
Journal of histotechnology. 45(1)
Enhancer of zeste homolog 2 (EZH2) and AT-rich interactive domain 1A (ARID1A) expression in urothelial carcinoma (UC) has not been well studied. ARID1A is a novel tumor suppressor gene coding for a chromatin remodeling protein that is mutated in urin
Autor:
Ahmad Embaby, Reham Sameh, Samia Hussein, Sherin Elshorbagy, Norhan A. Sabbah, Haitham Mohamed, Tarek Khamis, Huda F. Ebian
Publikováno v:
Cancer biomarkers : section A of Disease markers. 32(3)
BACKGROUND: Both Fms-like tyrosine kinase 3-internal tandem duplication (FLT3-ITD) and Additional Sex Comb-like 1 (ASXL1) mutations are frequent and early genetic alteration events in acute myeloid leukemia (AML) patients. These genetic alterations m