Zobrazeno 1 - 10
of 79
pro vyhledávání: '"Zefarina Zulkafli"'
Autor:
Muhamad Aidil Zahidin, Noor Haslina Mohd Noor, Muhammad Farid Johan, Abu Dzarr Abdullah, Zefarina Zulkafli, Hisham Atan Edinur
Publikováno v:
Scientific Data, Vol 11, Iss 1, Pp 1-6 (2024)
Abstract The human mannose-binding lectin (MBL) gene encodes a polymorphic protein that plays a crucial role in the innate immune response. Human MBL deficiency is associated with immunodeficiencies, and its variants have been linked to autoimmune an
Externí odkaz:
https://doaj.org/article/e1d9858d68504a64becd68e7d6834cf2
Autor:
Nur Ain Azman, Zefarina Zulkafli, Nur Salwani Bakar, Mat Ghani Siti Nor Assyuhada, Siti Nur Nabeela A’ifah Mohammad
Publikováno v:
Egyptian Journal of Medical Human Genetics, Vol 25, Iss 1, Pp 1-8 (2024)
Abstract Background Iron deficiency contributes for over half of all anaemia cases, especially among women and children. Iron deficiency anaemia remains a serious public health concern worldwide. The aim of this study is to determine the association
Externí odkaz:
https://doaj.org/article/473279cad68c4ab4baad438441aab206
Autor:
Marini Ramli, Nik Fatma Fairuz Nik Mohd Hasan, Majdan Ramli, Wan Suriana Wan Ab Rahman, Mohd Nazri Hassan, Noor Haslina Mohd Noor, Shafini Mohamed Yusoff, Salfarina Iberahim, Rosnah Bahar, Zefarina Zulkafli
Publikováno v:
Oman Medical Journal, Vol 38, Iss 3, Pp e507-e507 (2023)
Objectives: Hemoglobin constant spring (Hb CS) is a point mutational defect associated with α thalassemia. The aims of this study were to compare the hematological profiles between different Hb CS genotypes and to estimate the range for Zone 2 peak
Externí odkaz:
https://doaj.org/article/d99d5d9ebfbf477fb99b4170560ba5e5
Autor:
Mat Ghani Siti Nor Assyuhada, Zefarina Zulkafli, Noor Haslina Mohd Noor, Siddhartha Pati, Zulhisyam Abdul Kari, Mahmoud A.O. Dawood, Geoffrey Keith Chambers, Hisham Atan Edinur
Publikováno v:
Journal of King Saud University: Science, Vol 35, Iss 4, Pp 102593- (2023)
Population genetic data collected from variable regions in human genome have been extensively used for studying human origins and migration patterns, estimating the probative value of DNA evidence and in disease association studies. Here, we illustra
Externí odkaz:
https://doaj.org/article/6454ac41e98b485099a8c686120fe4b0
Autor:
Yousef Saeed Mohammad Abu Za'ror, Zefarina Zulkafli, Laith Naser Al-Eitan, Lina Elsalem, Belal Abdelaziz Al-Husein, Maryam Azlan
Publikováno v:
Biomedical and Biotechnology Research Journal, Vol 6, Iss 4, Pp 563-568 (2022)
Background: Currently, the high expression of fetal hemoglobin (HbF) in sickle cell disease is treated by hydroxyurea (HU). However, potential adverse effect regarding the use of HU is a major concern. Therefore, the search for an alternative therape
Externí odkaz:
https://doaj.org/article/7295e6ae5e96448882ece79c3559647a
Autor:
Salfarina Iberahim, Noor Haslina Mohd Noor, Mohd Nazri Hassan, Rosnah Bahar, Shafini Mohdmed Yusoff, Marini Ramli, Wan Suriana Wan Abdul Rahman, Zefarina Zulkafli, Marne Abdullah, Ho Sook Fong, Tengku Muzaffar Tengku Mohamed Shihabudin, Hisham Atan Edinur, Norul Hajar Che Ghazali
Publikováno v:
Asian Journal of Transfusion Science, Vol 16, Iss 2, Pp 276-279 (2022)
The Diego (Di) blood group system comprises 22 antigens located on the band 3 protein, most of which are low-prevalence antigens. The majority of antibodies to Diego system antigens were of clinically insignificant; however anti-Dia, -Dib, -Wra, -ELO
Externí odkaz:
https://doaj.org/article/1a48b57f90a941ae9ac52923c9ea758f
Autor:
Yousef Saeed Mohammad Abu Za'ror, Siti Nor Assyuhada Mat Ghani, Nur Salwani Bakar, Zefarina Zulkafli, Maryam Azlan
Publikováno v:
Journal of Applied Hematology, Vol 13, Iss 4, Pp 183-191 (2022)
BACKGROUND: Anemia is one of the most common conditions in women during pregnancy. Fetal hemoglobin (HbF) levels are usually 3.2%) and normal HbA2 level (≤3.2%) to detect mutation at b-globin gene cluster. Allelic discrimination for rs1186868, rs93
Externí odkaz:
https://doaj.org/article/cd08dd20e2404236a0630b1ef3356644
Autor:
Divashini Vijian, Wan Suriana Wan Ab Rahman, Kannan Thirumulu Ponnuraj, Zefarina Zulkafli, Rosnah Bahar, Norafiza Yasin, Syahzuwan Hassan, Ezalia Esa
Publikováno v:
Diagnostics, Vol 13, Iss 5, p 894 (2023)
(1) Background: Alpha (α)-thalassaemia is a genetic disorder that affects 5% of the world population. Deletional or nondeletional mutations of one or both HBA1 and HBA2 on chromosome 16 will result in reduced production of α-globin chains, a compon
Externí odkaz:
https://doaj.org/article/ad5c9b5808104310ad78efb95ab36be8
Autor:
Syahzuwan Hassan, Rosnah Bahar, Muhammad Farid Johan, Ezzeddin Kamil Mohamed Hashim, Wan Zaidah Abdullah, Ezalia Esa, Faidatul Syazlin Abdul Hamid, Zefarina Zulkafli
Publikováno v:
Diagnostics, Vol 13, Iss 3, p 373 (2023)
Thalassemia is one of the most heterogeneous diseases, with more than a thousand mutation types recorded worldwide. Molecular diagnosis of thalassemia by conventional PCR-based DNA analysis is time- and resource-consuming owing to the phenotype varia
Externí odkaz:
https://doaj.org/article/15a4501740da4bf7b2782277d15d0e65
Autor:
Noor Nabila Ramli, Salfarina Iberahim, Noor Haslina Mohd Noor, Zefarina Zulkafli, Tengku Muzaffar Tengku Md Shihabuddin, Mohd Hadizie Din, Muhamad Aizat Mohamed Saat, Ahmad Hadif Zaidin Samsudin
Publikováno v:
Diagnostics, Vol 13, Iss 1, p 150 (2023)
Venous thromboembolism (VTE), which encompasses deep venous thrombosis (DVT) and pulmonary embolism (PE), is a major public health concern due to its high incidences of morbidity and mortality. Patients who have experienced trauma with prolonged immo
Externí odkaz:
https://doaj.org/article/c987025eab2142b8b80ac980008b2f54