Agrawal, P., T. Ganesh, D. Oliva, and A. W. Mohamed,
"S-shaped and v-shaped gaining-sharing knowledge-based algorithm for feature selection",
Applied Intelligence, vol. 52, issue 1: Springer US New York, pp. 81-112, 2022.
Abstractn/a
Alkafafy, M. E., S. M. Sayed, S. A. El-Shazly, M. M. Ahmed, K. M. Shoghy, and R. F. Rashed,
"S100 EXPRESSION IN THE EPIDIDYMIS OF DROMEDARY CAMEL DURING BREEDING AND NONBREEDING SEASONS: IMMUNOHISTOCHEMICAL AND MOLECULAR STUDIES ",
Journal of Camel Practice and Research, vol. 25, issue 1, pp. 37-43, 2018.
Ismail, H. M. S., P. J. Hurd, M. I. M. Khalil, T. Kouzarides, A. Bannister, and I. Gout,
"S6 kinase 2 is bound to chromatin-nuclear matrix cellular fractions and is able to phosphorylate histone H3 at threonine 45 in vitro and in vivo.",
Journal of cellular biochemistry, vol. 115, issue 6, pp. 1048-62, 2014 Jun.
AbstractThe activity of S6 kinases (S6K) is highly induced in cancer cells highlighting an essential role in carcinogenesis. The S6K family has two members: S6K1 and S6K2 which bear common as well as distinct features. In an attempt to identify S6K2 unique sequence features compared to S6K1, we applied extensive bioinformatic analysis and motif search approaches. Interestingly, we identified 14 unique protein signatures which are present in proteins directly connected to chromatin and/or involved in transcription regulation. Using chromatin binding assay, we biochemically showed that S6K2 is bound to chromatin as well as nuclear matrix cellular fractions in HEK293 cells. The presence of S6K2 in chromatin fractions raised the possibility that it may be in close proximity to a number of chromatin substrates. For that, we then searched for S6K phosphorylation consensus sites RXRXXT/S in mammalian proteins using the SWISS-PROT database. Interestingly, we identified some potential phosphorylation sites in histone H3 (Thr45). Using in vitro kinase assays and siRNA-based knockdown strategy; we confirmed that S6K2 but not S6K1 or AKT is essential for histone H3-Thr45 phosphorylation in HEK293 cells. Furthermore, we show that the nuclear localisation sequence in the S6K2 C-terminus is essential for this modification. We have found that, H3-Thr45 phosphorylation correlates to S6K activation in response to mitogens and TPA-induced cell differentiation of leukaemic cell lines U937, HL60 and THP1. Overall, we demonstrate that S6K2 is a novel kinase that can phosphorylate histone H3 at position Thr45, which may play a role during cell proliferation and/or differentiation.
Said, M., M. El-Beshlawy, M. E. Raziky, N. Zayed, W. El-Akel, Y. Saad, and M. Mabrouk,
"Sa1057 The Impact of Normal Liver Transaminases on Hepatic Fibrosis and Response to HCV Treatment: A Cohort Egyptian Study of 4277 Patients",
Gastroenterology, vol. 142, no. 5: WB Saunders, pp. S–957, 2012.
Abstractn/a
Selim, S., M. M. Y. Madany, A. M. Reyad, B. F. Alowaiesh, N. Hagagy, M. M. Al-Sanea, S. S. Alsharari, and H. AbdElgawad,
"Saccharomonospora actinobacterium alleviates phytotoxic hazards of tungsten nanoparticles on legumes’ growth and osmotic status",
Journal of Environmental Chemical Engineering, vol. 9, issue 6: Elsevier, pp. 106395, 2021.
Abstractn/a
Abdel-Tawwab, M., R. H. Khalil, N. A. Younis, T. A. M. A. Selema, A. H. Saad, S. O. M. El-Werwary, A. H. Gouda, A. M. Soliman, S. H. H. Shady, and M. N. Monie,
"Saccharomyces cerevisiae supplemented diets mitigate the effects of waterborne cadmium toxicity on gilthead seabream (Sparus aurata L.): growth performance, haemato-biochemical, stress biomarkers, and histopathological investigations",
Veterinary Research Communications, vol. 48, issue 1, pp. 69-84, 2024.