Generalized epilepsy with febrile seizure plus (GEFS+) spectrum: Novel de novo mutation of SCN1A detected in a Malaysian patient

por Tan, Emmilia H., Yusoff, Abdul Aziz M., Abdullah, Jafri M., Razak, Salmi A.
Publicado 2012

The Uprising of Mitochondrial DNA Biomarker in Cancer

por Mohd Khair, Siti Zulaikha Nashwa, Abd Radzak, Siti Muslihah, Mohamed Yusoff, Abdul Aziz
Publicado 2021

Research highlights on contributions of mitochondrial DNA microsatellite instability in solid cancers – an overview

por Yusoff, Abdul Aziz Mohamed, Radzak, Siti Muslihah Abd, Khair, Siti Zulaikha Nashwa Mohd
Publicado 2022

Detection of FZD4, LRP5 and TSPAN12 Genes Variants in Malay Premature Babies with Retinopathy of Prematurity

por Mohd Khair, Siti Zulaikha Nashwa, Ismail, Abdul Salim, Embong, Zunaina, Mohamed Yusoff, Abdul Aziz
Publicado 2019

Association of The IDH1 C.395G>A (R132H) Mutation with Histological Type in Malay Brain Tumors

por Yusoff, Abdul Aziz Mohamed, Zulfakhar, Fatin Najwa, Sul’ain, Mohd Dasuki, Idris, Zamzuri, Abdullah, Jafri Malin
Publicado 2016

Roles of EphA2 Receptor in Angiogenesis Signaling Pathway of Glioblastoma Multiforme

por Baharuddin, Wan Noor Ainun, Yusoff, Abdul Aziz Mohamed, Abdullah, Jafri Malin, Osman, Zul Faizuddin, Ahmad, Farizan
Publicado 2018

A comprehensive overview of mitochondrial DNA 4977-bp deletion in cancer studies

por Yusoff, Abdul Aziz Mohamed, Abdullah, Wan Salihah Wan, Khair, Siti Zulaikha Nashwa Mohd, Radzak, Siti Muslihah Abd
Publicado 2019

Prevalence of mitochondrial DNA common deletion in patients with gliomas and meningiomas: A first report from a Malaysian study group

por Mohamed Yusoff, Abdul Aziz, Mohd Khair, Siti Zulaikha Nashwa, Abd Radzak, Siti Muslihah, Idris, Zamzuri, Lee, Hsin-Chen
Publicado 2020

Insights regarding mitochondrial DNA copy number alterations in human cancer

por Abd Radzak, Siti Muslihah, Mohd Khair, Siti Zulaikha Nashwa, Ahmad, Farizan, Patar, Azim, Idris, Zamzuri, Yusoff, Abdul Aziz Mohamed
Publicado 2022

Characterisation of Primary Human Hippocampal Astrocyte Cell Culture Following Exposure to Hypoxia

por Nor Nazli, Nurul Atikah, Muthuraju, Sangu, Ahmad, Farizan, Mohamed Yusoff, Abdul Aziz, Jaafar, Hasnan, Shamsuddin, Shaharum, Abdullah, Jafri Malin
Publicado 2023

Genetic Manipulation Strategies for β-Thalassemia: A Review

por Zakaria, Nur Atikah, Bahar, Rosnah, Abdullah, Wan Zaidah, Mohamed Yusoff, Abdul Aziz, Shamsuddin, Shaharum, Abdul Wahab, Ridhwan, Johan, Muhammad Farid
Publicado 2022

Mitochondrial 10398A>G NADH-Dehydrogenase Subunit 3 of Complex I Is Frequently Altered in Intra-Axial Brain Tumors in Malaysia

por Mohamed Yusoff, Abdul Aziz, Zulfakhar, Fatin Najwa, Mohd Khair, Siti Zulaikha Nashwa, Wan Abdullah, Wan Salihah, Abdullah, Jafri Malin, Idris, Zamzuri
Publicado 2018

Trkb-IP3 Pathway Mediating Neuroprotection in Rat Hippocampal Neuronal Cell Culture Following Induction of Kainic Acid

por Chong, Pei Nei, Sangu, Muthuraju, Huat, Tee Jong, Reza, Faruque, Begum, Tahamina, Yusoff, Abdul Aziz Mohamed, Jaafar, Hasnan, Abdullah, Jafri Malin
Publicado 2018

Worldwide Prevalence of Epstein–Barr Virus in Patients with Burkitt Lymphoma: A Systematic Review and Meta-Analysis

por Al-Khreisat, Mutaz Jamal, Ismail, Nor Hayati, Tabnjh, Abedelmalek, Hussain, Faezahtul Arbaeyah, Mohamed Yusoff, Abdul Aziz, Johan, Muhammad Farid, Islam, Md Asiful
Publicado 2023

Epigenetic Insights and Potential Modifiers as Therapeutic Targets in β–Thalassemia

por Zakaria, Nur Atikah, Islam, Md Asiful, Abdullah, Wan Zaidah, Bahar, Rosnah, Mohamed Yusoff, Abdul Aziz, Abdul Wahab, Ridhwan, Shamsuddin, Shaharum, Johan, Muhammad Farid
Publicado 2021

Detection of somatic mutations in the mitochondrial DNA control region D-loop in brain tumors: The first report in Malaysian patients

por Mohamed Yusoff, Abdul Aziz, Mohd Nasir, Khairol Naaim, Haris, Khalilah, Mohd Khair, Siti Zulaikha Nashwa, Abdul Ghani, Abdul Rahman Izaini, Idris, Zamzuri, Abdullah, Jafri Malin
Publicado 2017

Overexpression of human mitochondrial valyl tRNA synthetase can partially restore levels of cognate mt-tRNA(Val) carrying the pathogenic C25U mutation

por Rorbach, Joanna, Yusoff, Abdul Aziz, Tuppen, Helen, Abg-Kamaludin, Dyg P., Chrzanowska-Lightowlers, Zofia M.A., Taylor, Robert W., Turnbull, Douglass M., McFarland, Robert, Lightowlers, Robert N.
Publicado 2008