Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Abdullahi Ibrahim Uba"'
Autor:
Nouran M. Fahmy, Shaimaa Fayez, Abdullahi Ibrahim Uba, Mohammad Ali Shariati, Abdullah S. M. Aljohani, Ibrahim M. El-Ashmawy, Gaber El-Saber Batiha, Omayma A. Eldahshan, Abdel Nasser Singab, Gokhan Zengin
Publikováno v:
Plants; Volume 12; Issue 9; Pages: 1785
Species belonging to the Zingiberaceae family are of high nutritional, industrial, and medicinal values. In this study, we investigated the effect of processing steps (fresh vs. dried milled rhizomes) and extraction methodologies (hydrodistillation v
Publikováno v:
Journal of Biomolecular Structure and Dynamics. :1-10
Histone deacetylase (HDAC) 8 has been implicated as a potential therapeutic target in a variety of cancers, neurodegenerative disorders, metabolic dysregulation and autoimmune and inflammatory diseases. Several nonselective HDAC inhibitors have been
Publikováno v:
Journal of Biomolecular Structure and Dynamics. 37:4644-4650
Communicated by Ramaswamy H. Sarma.
Autor:
Kemal Yelekçi, Abdullahi Ibrahim Uba
Tubitak Directorate of Research and Development Resources of Kadir Has University Histone deacetylase (HDAC) 10 has been implicated in the pathology of various cancers and neurodegenerative disorders, making the discovery of novel inhibitors of the i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::36768b405b51b233cae9a395da5432f7
https://hdl.handle.net/20.500.12469/3473
https://hdl.handle.net/20.500.12469/3473
Autor:
Abdullahi Ibrahim Uba, Kemal Yelekçi
Publikováno v:
Journal of biomolecular structuredynamics. 37(14)
Histone deacetylases (HDACs) are implicated in the pathology of various cancers, and their pharmacological blockade has proven to be promising in reversing the malignant phenotypes. However, lack of crystal structures of some of the human HDAC isofor
Autor:
Christina Radicella, Chun Wu, Abdullahi Ibrahim Uba, Siyan Liao, Nicolas Scorese, Haiguang Liu, Carolyn Readmond
Publikováno v:
Life Sciences. 252:117643
Aims Non-peptide ligands of oxytocin receptor (OTR) have promising potentialities as therapeutic agents with improved pharmacological properties. WAY-267,464 is a non-peptide agonist which loses its agonist activity when its resorcinol moiety is meth
Autor:
Kemal Yelekçi, Abdullahi Ibrahim Uba
Publikováno v:
Computational biology and chemistry. 75
Human histone deacetylase 6 (HDAC6) has been shown to play a major role in oncogenic cell transformation via deacetylation of alpha-tubulin making it a viable target of anticancer drug design and development. The crystal structure of HDAC6 catalytic