Zobrazeno 1 - 10
of 89
pro vyhledávání: '"Zubaidah, Zakaria"'
Publikováno v:
Journal of Medical Case Reports, Vol 17, Iss 1, Pp 1-7 (2023)
Abstract Background The 18q- deletion syndrome is a rare congenital chromosomal disorder caused by a partial deletion of the long arm of chromosome 18. The diagnosis of a patient with this syndrome relies on the family medical history, physical exami
Externí odkaz:
https://doaj.org/article/20d972eacc62480b92575232b3f0d2ef
Autor:
Yuslina Mat Yusoff, Fadly Ahid, Zahidah Abu Seman, Julia Abdullah, Nor Rizan Kamaluddin, Ezalia Esa, Zubaidah Zakaria
Publikováno v:
Molecular Cytogenetics, Vol 14, Iss 1, Pp 1-13 (2021)
Abstract Background Relapsed acute myeloid leukemia (AML) is associated with the acquisition of additional somatic mutations which are thought to drive phenotypic adaptability, clonal selection and evolution of leukemic clones during treatment. We pe
Externí odkaz:
https://doaj.org/article/95524437b05b40a19d801d7d5300bc44
Autor:
Mathiyazhagan Rengasamy, Gurbind Singh, Noor Atiqah Fakharuzi, Siddikuzzaman, Sudha Balasubramanian, Priyanka Swamynathan, Charan Thej, Gopinath Sasidharan, Pawan Kumar Gupta, Anjan Kumar Das, Ahmad Zuhairi Abd Rahman, Kamal Shaik Fakiruddin, Lim Moon Nian, Zubaidah Zakaria, Anish S. Majumdar
Publikováno v:
Stem Cell Research & Therapy, Vol 8, Iss 1, Pp 1-12 (2017)
Abstract Background Mesenchymal stromal cells (MSCs) from various tissues have shown moderate therapeutic efficacy in reversing liver fibrosis in preclinical models. Here, we compared the relative therapeutic potential of pooled, adult human bone mar
Externí odkaz:
https://doaj.org/article/301918f2e34643b3bbd58aa0a7ecd94e
Autor:
Norashikin Zakaria, Narazah Mohd Yusoff, Zubaidah Zakaria, Darius Widera, Badrul Hisham Yahaya
Publikováno v:
Frontiers in Oncology, Vol 8 (2018)
Cancer stem cells (CSCs) are a subpopulation of cancer cells that play a pivotal role in tumor development, invasion, metastasis, and recurrence. We and others have reported significant involvement of the NF-κB pathway in regulating CSCs of non-smal
Externí odkaz:
https://doaj.org/article/40783993ae014a4199464cea1aad01b7
Autor:
Ezalia Esa, Alifah Nadia Abu Hassan, Yuslina Mat Yusoff, Rashidah Mohamed, Soo-Min Lim, Indhira Subbiah, Ariwibawa Kasmani Mohd Hashim, Peng-Choon Lau, Ahmad Zuhairi Abdul Rahman, Caroline Siew-Ling Ho, Elsa Haniffah Mejia Mohamed, Ehram Jamian, Shamsul Mohd Zain, Yuh Fen Pung, Kian-Meng Chang, Zubaidah Zakaria, Nor Rizan Kamaluddin
Publikováno v:
Genetic Testing and Molecular Biomarkers. 25:199-210
Background: The association between dysregulated microRNAs (miRNAs) and acute myeloid leukemia (AML) is well known. However, our understanding of the regulatory role of miRNAs in the cytogeneticall...
Autor:
Mohammad Masrin Md Zahrin, Yi Shen Wong, Rachel Sing-Kiat Ting, Zubaidah Zakaria, Abu Sufian Ahmad, Jack Siew Yu Wong, Chien Joo Lim, Masita Arip, Jessie Koh Sing Tnay, Shahren Ahmad Zaidi Adruce, Chuo Yew Ting, Yew Fong Lee
Publikováno v:
Transfus Med Hemother
Introduction: Past studies pay little attention to the intention to donate hematopoietic stem cells (HSC) among blood donors. This study investigated the level of and the influence of socio-demographic characteristics, knowledge, attitude, subjective
Autor:
Fadly Ahid, Zahidah Abu Seman, Yuslina Mat Yusoff, Julia Abdullah, Zubaidah Zakaria, Nor Rizan Kamaluddin, Ezalia Esa
Publikováno v:
Molecular Cytogenetics
Molecular Cytogenetics, Vol 14, Iss 1, Pp 1-13 (2021)
Molecular Cytogenetics, Vol 14, Iss 1, Pp 1-13 (2021)
Background Relapsed acute myeloid leukemia (AML) is associated with the acquisition of additional somatic mutations which are thought to drive phenotypic adaptability, clonal selection and evolution of leukemic clones during treatment. We performed h
Autor:
Faidatul Syazlin Abdul Hamid, Rahimah Ahmad, Mohamed Saleem, Nur Aisyah Aziz, Syahira Lazira Omar, Siti Hida Hajira Mohamad Arif, Jameela Sathar, Zubaidah Zakaria
Publikováno v:
Thalassemia Reports, Vol 5, Iss 1 (2015)
We report a novel deletion at the HBA2 presented with Hb H disease in two Malaysian- Chinese patients. The two unrelated probands were diagnosed with Hb H disease in a primary hematological screening for thalassemia. Results from routine molecular an
Externí odkaz:
https://doaj.org/article/78d51f0ff7804a37bef86116fde1317d
Autor:
Chia, Wai Kit, Sharifah, Noor Akmal, Reena, Rahayu Md Zin, Zubaidah, Zakaria, Clarence-Ko, Ching Huat, Rohaizak, Muhammad, Naqiyah, Ibrahim, Srijit, Das, Hisham, Abdullah Nor, Asmiati, Arbi, Rafie, Md Kaslan
Publikováno v:
In Cancer Genetics and Cytogenetics 2010 196(1):7-13
Publikováno v:
Journal of Clinical and Diagnostic Research, Vol 7, Iss 2, Pp 355-357 (2013)
ABSTRACT The premature ovarian failures with underlying chromosomal abnormalities are normally X-linked, although their associations with the autosomal and the Robertsonian translocations are also possible. Here, we are reporting a case of premat
Externí odkaz:
https://doaj.org/article/bb9d841ea26b43e194eddbd3653135c5