Zobrazeno 1 - 10
of 42
pro vyhledávání: '"Ezalia, Esa"'
Autor:
Nur Aisyah Aziz, Nurul Hidayah Musa, Melina Mathews, Komalah Thevii Rajenderan, Faidatul Syazlin Abdul Hamid, Syahzuwan Hassan, Syahira Lazira Omar, Wan Nurul Afiqha Binti Wan Yusoff, Melanie Ling Binti Mohd Din, Nurul Amira Binti Jamaludin, Wan Rohani Wan Taib, Ezalia Esa, Norafiza Mohd Yasin
Publikováno v:
Human Genome Variation, Vol 11, Iss 1, Pp 1-4 (2024)
Abstract Hemoglobin (Hb) Vancleave (NM_000518.5:c.431 A > T; dbSNP: rs33918338) is an extremely rare structural hemoglobin variant worldwide, and studies are limited. This report describes the case of a 16-year-old male patient who presented with sec
Externí odkaz:
https://doaj.org/article/3c36a899bc754a71bd972baef08a6509
Autor:
Zahidah Abu Seman, Fadly Ahid, Nor Rizan Kamaluddin, Ermi Neiza Mohd Sahid, Ezalia Esa, Siti Shahrum Muhamed Said, Norazlina Azman, Wan Khairull Dhalila Wan Mat, Julia Abdullah, Nurul Aqilah Ali, Mohd Khairul Nizam Mohd Khalid, Yuslina Mat Yusoff
Publikováno v:
BMC Research Notes, Vol 17, Iss 1, Pp 1-8 (2024)
Abstract Objective Mutational analysis of BCR::ABL1 kinase domain (KD) is a crucial component of clinical decision algorithms for chronic myeloid leukemia (CML) patients with failure or warning responses to tyrosine kinase inhibitor (TKI) therapy. Th
Externí odkaz:
https://doaj.org/article/ec23452a481e4309b0f21ac9bb3102d4
Autor:
Ezalia Esa, Ahmad Sabry Mohamad, Roszymah Hamzah, Faidatul Syazlin Abdul Hamid, Nur Aisyah Aziz, Veena Sevaratnam, Jameela Sathar, Guo Chen, Norafiza Mohd Yasin
Publikováno v:
eJHaem, Vol 4, Iss 4, Pp 940-948 (2023)
Abstract Haemoglobin (Hb) G‐Makassar is a rare Hb variant. It presents a diagnostic challenge as it imitates sickle Hb (Hb S) in standard electrophoresis and high‐performance liquid chromatography assays requiring DNA analysis to confirm diagnosi
Externí odkaz:
https://doaj.org/article/b43e13c9ad3e447b8414029b066c9f17
Autor:
Hannah Taufiq, Kamal Shaik Fakiruddin, Umaiya Muzaffar, Moon Nian Lim, Syahnaz Rusli, Nor Rizan Kamaluddin, Ezalia Esa, Syahril Abdullah
Publikováno v:
Therapeutic Advances in Respiratory Disease, Vol 17 (2023)
Background: In coronavirus disease 2019 (COVID-19) patients, elevated levels of inflammatory cytokines from over stimulation of immune cells have become a concern due to the potential outburst of cytokine storm that damages the tissues and organs, es
Externí odkaz:
https://doaj.org/article/a816202719444f5b8acef107a06a16d0
Autor:
Norafiza Mohd Yasin, Faidatul Syazlin Abdul Hamid, Syahzuwan Hassan, Yuslina Mat Yusoff, Ermi Neiza Mohd Sahid, Ezalia Esa
Publikováno v:
Diagnostics, Vol 13, Iss 20, p 3286 (2023)
Malaysia is a multicultural and multiethnic country comprising numerous ethnic groups. From the total population of 32.7 million, Malays form the bulk of the Bumiputera in Malaysia comprise about 69.9%, followed by Chinese 22.8%, Indian 6.6%, and oth
Externí odkaz:
https://doaj.org/article/12c6a652de9548e4949be687191efd09
Autor:
Stella Tamana, Maria Xenophontos, Anna Minaidou, Coralea Stephanou, Cornelis L Harteveld, Celeste Bento, Joanne Traeger-Synodinos, Irene Fylaktou, Norafiza Mohd Yasin, Faidatul Syazlin Abdul Hamid, Ezalia Esa, Hashim Halim-Fikri, Bin Alwi Zilfalil, Andrea C Kakouri, ClinGen Hemoglobinopathy Variant Curation Expert Panel, Marina Kleanthous, Petros Kountouris
Publikováno v:
eLife, Vol 11 (2022)
Haemoglobinopathies are the commonest monogenic diseases worldwide and are caused by variants in the globin gene clusters. With over 2400 variants detected to date, their interpretation using the American College of Medical Genetics and Genomics (ACM
Externí odkaz:
https://doaj.org/article/685e2a791891446ba71327c90bbdab61
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:
Norafiza Mohd Yasin, Faidatul Syazlin Abdul Hamid, Syahzuwan Hassan, Aziee Sudin, Haiyuni Yassim, Ermi Neiza Mohd Sahid, Yuslina Mat Yusoff, Ezalia Esa, Mohamed Saleem
Publikováno v:
Frontiers in Pediatrics, Vol 10 (2022)
AbstractWe report the haematological parameters and molecular characterization of beta zero (β°) South East Asia (SEA) deletion in the HBB gene cluster with unusually high levels of Hb F compared to a classical heterozygous beta zero (β°)-thalass
Externí odkaz:
https://doaj.org/article/09be1a71f55542b2ac7c7f3e16beb90e
Autor:
Nur Atiqah Haizum Abdullah, Nur Qisya Afifah Veronica Sainik, Ezalia Esa, Nur Afrina Muhamad Hendri, Muhamad Rusdi Ahmad Rusmili, Wayne C. Hodgson, Mohd Farooq Shaikh, Iekhsan Othman
Publikováno v:
Frontiers in Pharmacology, Vol 13 (2022)
Oxidative stress is one of the factors involved in the pathogenesis of several neurodegenerative diseases. It has been reported that a secretory phospholipase A2 known as A2-EPTX-NSm1a has lower cytotoxicity in neuronal cells compared to its crude Na
Externí odkaz:
https://doaj.org/article/908fd2b370bd4d568979e33f6b63e847
Autor:
Nur-Aisyah Aziz, Wan-Rohani Wan Taib, Nur-Khairunnisa Kharolazaman, Imilia Ismail, Hamid Ali Nagi Al-Jamal, Nadiah Wan-Arfah Wan Abdul Jamil, Ezalia Esa, Hishamshah Ibrahim
Publikováno v:
Scientific Reports, Vol 11, Iss 1, Pp 1-6 (2021)
Abstract This study sought to determine the potential role of HBB haplotypes to predict beta-thalassemia in the Malaysian population. A total of 543 archived samples were selected for this study. Five tagging SNPs in the beta-globin gene (HBB; NG_000
Externí odkaz:
https://doaj.org/article/b6f83b202f7944819ba8a21e16708e7e