Zobrazeno 1 - 10
of 36
pro vyhledávání: '"Abdul Aziz Mohamed Yusoff"'
Autor:
Siti Nazihahasma Hassan, Abdul Aziz Mohamed Yusoff, Zamzuri Idris, Norhanani Mohd Redzwan, Farizan Ahmad
Publikováno v:
Future Journal of Pharmaceutical Sciences, Vol 10, Iss 1, Pp 1-9 (2024)
Abstract Background Nutrient stress (NS), one of the hallmarks of the tumour microenvironment, can render cancer cells tolerant to cytotoxicity. Fibroblasts, on the other hand, have cancer cell-like traits, such as plasticity and resiliency. Hence, t
Externí odkaz:
https://doaj.org/article/3348baa3291340848c54e8cccff22d52
Autor:
Siti Muslihah Ab Radzak, Siti Zulaikha Nashwa Mohd Khair, Zamzuri Idris, Wan Muhamad Amir Wan Ahmad, Azim Patar, Abdul Aziz Mohamed Yusoff
Publikováno v:
Eurasian Journal of Medicine, Vol 56, Iss 1, Pp 7-14 (2024)
Background: Investigating the role of mitochondrial DNA (mtDNA) alterations and their impact on brain tumor progression remains a significant focus in cancer research. The research aimed to explore the specific contributions of mtDNA copy number chan
Externí odkaz:
https://doaj.org/article/c7013a8c5f6241d58ed72b97b4fd4295
Autor:
Mutaz Jamal Al-Khreisat, Nor Hayati Ismail, Abedelmalek Tabnjh, Faezahtul Arbaeyah Hussain, Abdul Aziz Mohamed Yusoff, Muhammad Farid Johan, Md Asiful Islam
Publikováno v:
Diagnostics, Vol 13, Iss 12, p 2068 (2023)
Burkitt lymphoma (BL) is a form of B-cell malignancy that progresses aggressively and is most often seen in children. While Epstein–Barr virus (EBV) is a double-stranded DNA virus that has been linked to a variety of cancers, it can transform B lym
Externí odkaz:
https://doaj.org/article/03553835ba0941ecb3bd1ce2904ea50f
Autor:
Nur Atikah Zakaria, Rosnah Bahar, Wan Zaidah Abdullah, Abdul Aziz Mohamed Yusoff, Shaharum Shamsuddin, Ridhwan Abdul Wahab, Muhammad Farid Johan
Publikováno v:
Frontiers in Pediatrics, Vol 10 (2022)
Thalassemias are monogenic hematologic diseases that are classified as α- or β-thalassemia according to its quantitative abnormalities of adult α- or β-globin chains. β-thalassemia has widely spread throughout the world especially in Mediterrane
Externí odkaz:
https://doaj.org/article/4abf11e7cb924a9cbb0f7c3358ee8115
Autor:
Siti Zulaikha Nashwa Mohd Khair, Abdul Salim Ismail, Zunaina Embong, Abdul Aziz Mohamed Yusoff
Publikováno v:
Journal of Ophthalmic & Vision Research, Vol 14, Iss 2, Pp 171-178 (2019)
Purpose: To determine the mutational analyses of familial exudative vitreoretinopathy (FEVR)-causing genes in Malay patients with retinopathy of prematurity (ROP) to obtain preliminary data for gene alterations in the Malay community. Methods: A comp
Externí odkaz:
https://doaj.org/article/e6bb46499db747debfa9dce774a755c5
Autor:
Abdul Aziz Mohamed Yusoff, Wan Salihah Wan Abdullah, Siti Zulaikha Nashwa Mohd Khair, Siti Muslihah Abd Radzak
Publikováno v:
Oncology Reviews, Vol 13, Iss 1 (2019)
Mitochondria are cellular machines essential for energy production. The biogenesis of mitochondria is a highly complex and it depends on the coordination of the nuclear and mitochondrial genome. Mitochondrial DNA (mtDNA) mutations and deletions are s
Externí odkaz:
https://doaj.org/article/19b9195e74aa44d19183903c944d2ac5
Autor:
Nur Atikah Zakaria, Md Asiful Islam, Wan Zaidah Abdullah, Rosnah Bahar, Abdul Aziz Mohamed Yusoff, Ridhwan Abdul Wahab, Shaharum Shamsuddin, Muhammad Farid Johan
Publikováno v:
Biomolecules, Vol 11, Iss 5, p 755 (2021)
Thalassemia, an inherited quantitative globin disorder, consists of two types, α– and β–thalassemia. β–thalassemia is a heterogeneous disease that can be asymptomatic, mild, or even severe. Considerable research has focused on investigating
Externí odkaz:
https://doaj.org/article/77857f8e357349df896c322d6cde0f72
Publikováno v:
Biomedical Research and Therapy. 9:5375-5383
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ef924aed6d6026343a0193e5045a67ab
https://doi.org/10.15419/bmrat.v9i10.775
https://doi.org/10.15419/bmrat.v9i10.775
Autor:
Siti Nazihahasma Hassan, Abdul Aziz Mohamed Yusoff, Zamzuri Idris, Norhanani Mohd Redzwan, Farizan Ahmad
Publikováno v:
Fundamental & Clinical Pharmacology.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::44c3d6e667e0c2224cc750d11564e1c6
https://doi.org/10.1111/fcp.12900
https://doi.org/10.1111/fcp.12900
Autor:
Jing Yit Pua, Ang Lee, Vienna Zi Wei Khor, Thanaseelan Pushpanathan, Abdul Aziz Mohamed Yusoff, Zamzuri Idris, Azim Patar
Publikováno v:
Asian Journal of Medicine and Biomedicine. 6:61-63
The discovery of isocitrate dehydrogenase isoform 1 (IDH1) mutation as a key molecular marker has resulted in a change in glial tumour classification [1]. IDH1 mutations are commonly in gliomas, particularly in low-grade gliomas and secondary gliobla
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d7293d1a4df4187be7618b7c86776f95
https://doi.org/10.37231/ajmb.2022.6.s1.528
https://doi.org/10.37231/ajmb.2022.6.s1.528