Siti Aishah Sulaiman
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View article: Long Noncoding RNAs TYMSOS, VASH1-AS1, and LINC01001 Expressions as Biomarkers of β-thalassaemia Severity Among the Malaysian Patients
Long Noncoding RNAs TYMSOS, VASH1-AS1, and LINC01001 Expressions as Biomarkers of β-thalassaemia Severity Among the Malaysian Patients Open
BACKGROUND: β-thalassaemia has heterogeneous disease severities ranging from mild to trait, and major. Long noncoding RNAs (lncRNAs) are known to regulate microRNAs (miRNAs) and genes, possibly modifying the disease phenotypes. However, li…
View article: Economic evaluation of quantitative point-of-care testing versus spectrophotometric assay for population screening of glucose-6-phosphate dehydrogenase deficiency in Malaysia: A time-driven activity-based cost analysis
Economic evaluation of quantitative point-of-care testing versus spectrophotometric assay for population screening of glucose-6-phosphate dehydrogenase deficiency in Malaysia: A time-driven activity-based cost analysis Open
Background: Glucose-6-phosphate dehydrogenase deficiency (G6PDd) is a common genetic disorder that can lead to life-threatening complications, including acute hemolytic anemia. Effective screening using advanced technology, such as point-o…
View article: G6PD deficiency in Malaysia’s Proto-Malay Orang Asli indigenous population: A molecular and epidemiological study
G6PD deficiency in Malaysia’s Proto-Malay Orang Asli indigenous population: A molecular and epidemiological study Open
Glucose-6-phosphate dehydrogenase deficiency (G6PDd) is one of the most common genetic disorders worldwide and remains highly prevalent in malaria-endemic regions. Individuals with G6PDd are at risk of severe complications, including acute…
View article: Gene co-expression module study identifies key genes and pathways underpinning hypercholesterolemia-induced atherosclerosis development
Gene co-expression module study identifies key genes and pathways underpinning hypercholesterolemia-induced atherosclerosis development Open
Background Familial hypercholesterolemia (FH) is a significant risk factor for atherosclerosis due to elevated levels of low-density lipoprotein (LDL) cholesterol in arterial walls. This study aimed to determine the key genes involved in t…
View article: Analysis of The Low-Density Lipoprotein Receptor (LDLR) Gene Among Family Hypercholesterolemia (FH) Patients in Malaysia: A Case Study
Analysis of The Low-Density Lipoprotein Receptor (LDLR) Gene Among Family Hypercholesterolemia (FH) Patients in Malaysia: A Case Study Open
Hiperkolesterolemia Familial (FH) adalah penyakit metabolisme lipoprotein yang menyebabkan peningkatan paras lipoprotein berketumpatan rendah (LDL-C) dalam darah sejak lahir. FH diwarisi secara autosomal dominan melalui mutasi gen LDLR, AP…
View article: Genetics of type 2 diabetes (T2D) in Malaysia: a review
Genetics of type 2 diabetes (T2D) in Malaysia: a review Open
Type 2 diabetes (T2D) is a significant public health concern in Malaysia, with rising prevalence across its multi-ethnic population. Genetic predisposition plays a key role in the development of T2D, but studies focusing on Malaysian popul…
View article: Genetic screening of malay familial hypercholesterolemia patient for LDLRAP1/PCSK9/APOB mutations via whole exome sequencing
Genetic screening of malay familial hypercholesterolemia patient for LDLRAP1/PCSK9/APOB mutations via whole exome sequencing Open
Background Familial Hypercholesterolemia (FH) is a hereditary lipid disorder with an autosomal dominant genetic inheritance, characterized by high low-density lipoprotein cholesterol (LDL-C) levels and premature atherosclerosis. An elevate…
View article: Study on the Potential of MARDI Specialty Rice for the Production of Local Parboiled Rice
Study on the Potential of MARDI Specialty Rice for the Production of Local Parboiled Rice Open
Producing specialty rice varieties with unique qualities is an essential research focus at MARDI. Additionally, producing parboiled rice from local specialty varieties adds value to the rice industry. This study evaluated two local special…
View article: Fabrication and surface modification of direct growth graphene FET for DNA mutation-detection
Fabrication and surface modification of direct growth graphene FET for DNA mutation-detection Open
View article: Whole Exome Sequencing of a Rare Disease, Mullerian Agenesis and Anorectal Anomaly: A Case Report
Whole Exome Sequencing of a Rare Disease, Mullerian Agenesis and Anorectal Anomaly: A Case Report Open
Mullerian agenesis or Mayer-Rokitansky-Kuster-Hauser Syndrome (MRKH) Type-II is a congenital defect in the Mullerian duct that results in the absence of a uterus in women. The aetiology of this syndrome is unknown and has been considered a…
View article: Development of DNA-Based Lateral Flow Assay for Detection of LDLR Gene Mutation for Familial Hypercholesterolemia
Development of DNA-Based Lateral Flow Assay for Detection of LDLR Gene Mutation for Familial Hypercholesterolemia Open
Background: The techniques for detecting single nucleotide polymorphisms (SNP) require lengthy and complex experimental procedures and expensive instruments that may only be available in some laboratories. Thus, a deoxyribonucleic acid (DN…
View article: Comprehensive Analysis of microRNA Methylation Profiles and Determination of Their Functional Significance in Colorectal Cancer: A Study Protocol
Comprehensive Analysis of microRNA Methylation Profiles and Determination of Their Functional Significance in Colorectal Cancer: A Study Protocol Open
Colorectal cancer (CRC) is a leading cause of cancer-associated fatalities globally. Despite the notable progress in diagnostics and patient care, challenges persist in areas such as early detection, prognostic variable identification, met…
View article: Geometrical Characterisation of TiO2-rGO Field-Effect Transistor as a Platform for Biosensing Applications
Geometrical Characterisation of TiO2-rGO Field-Effect Transistor as a Platform for Biosensing Applications Open
The performance of the graphene-based field-effect transistor (FET) as a biosensor is based on the output drain current (Id). In this work, the signal-to-noise ratio (SNR) was investigated to obtain a high-performance device that produces …
View article: Evaluation of Physical Quality Characterization MRQ 107 Parboil Rice Production Using Selected Parameter
Evaluation of Physical Quality Characterization MRQ 107 Parboil Rice Production Using Selected Parameter Open
Rice (Oryza sativa L.) is a significant source of nourishment in most Asian countries since it is a primary source of carbohydrates, micronutrients (Fe and Zn) and vitamins, offering broad prospects for food and nutritional security. MARDI…
View article: Population screening for glucose-6-phosphate dehydrogenase deficiency using quantitative point-of-care tests: a systematic review
Population screening for glucose-6-phosphate dehydrogenase deficiency using quantitative point-of-care tests: a systematic review Open
Background: Glucose-6-phosphate dehydrogenase (G6PD) deficiency is an X-linked hereditary disorder and a global public health concern that is most prevalent in malaria-endemic regions including Asia, Africa, and the Mediterranean. G6PD-def…
View article: Hypercholesterolemia in the Malaysian Cohort Participants: Genetic and Non-Genetic Risk Factors
Hypercholesterolemia in the Malaysian Cohort Participants: Genetic and Non-Genetic Risk Factors Open
Hypercholesterolemia was prevalent in 44.9% of The Malaysian Cohort participants, of which 51% were Malay. This study aimed to identify the variants involved in hypercholesterolemia among Malays and to determine the association between gen…
View article: Genetic Polymorphisms and Diversity in Nonalcoholic Fatty Liver Disease (NAFLD): A Mini Review
Genetic Polymorphisms and Diversity in Nonalcoholic Fatty Liver Disease (NAFLD): A Mini Review Open
Nonalcoholic fatty liver disease (NAFLD) is a common liver disease with a wide spectrum of liver conditions ranging from hepatic steatosis to nonalcoholic steatohepatitis (NASH), fibrosis, cirrhosis, and hepatocellular carcinoma. The preva…
View article: Editorial: Genetic and molecular diversity in Parkinson's disease
Editorial: Genetic and molecular diversity in Parkinson's disease Open
EDITORIAL article Front. Aging Neurosci., 16 December 2022Sec. Parkinson’s Disease and Aging-related Movement Disorders Volume 14 - 2022 | https://doi.org/10.3389/fnagi.2022.1094914
View article: Immunomodulatory effects of extracellular vesicles in glioblastoma
Immunomodulatory effects of extracellular vesicles in glioblastoma Open
Glioblastoma (GB) is a type of brain cancer that can be considered aggressive. Glioblastoma treatment has significant challenges due to the immune privilege site of the brain and the presentation of an immunosuppressive tumor microenvironm…
View article: COVID-19 in Malaysia: exposure assessment and prevention practices among healthcare workers at a teaching hospital
COVID-19 in Malaysia: exposure assessment and prevention practices among healthcare workers at a teaching hospital Open
Introduction: During the second wave of the coronavirus disease 19 (COVID-19) pandemic, Malaysia reported several COVID-19 clusters related to healthcare workers. Thus, addressing and understanding the risk of exposure in healthcare worker…
View article: Nonalcoholic Fatty Liver Disease (NAFLD): Pathogenesis and Noninvasive Diagnosis
Nonalcoholic Fatty Liver Disease (NAFLD): Pathogenesis and Noninvasive Diagnosis Open
The global prevalence of nonalcoholic fatty liver disease (NAFLD) or metabolic associated fatty liver disease (MAFLD), as it is now known, has gradually increased. NAFLD is a disease with a spectrum of stages ranging from simple fatty live…
View article: The Role of Oxidative Stress in Suicidal Behaviour Among Bipolar Patients: A Cross-Sectional Study in a Malaysian Sample
The Role of Oxidative Stress in Suicidal Behaviour Among Bipolar Patients: A Cross-Sectional Study in a Malaysian Sample Open
Background: Oxidative stress markers are found to be linked with depression and suicide attempts in bipolar disorder (BD), although the role of DNA damage as a marker of suicidal ideation and attempt has yet to be determined. We aim to inv…
View article: Noncoding RNAs Interactions in Hepatic Stellate Cells during Hepatic Fibrosis
Noncoding RNAs Interactions in Hepatic Stellate Cells during Hepatic Fibrosis Open
Hepatic fibrosis is a reversible wound healing process following liver injury. Although this process is necessary for maintaining liver integrity, severe excessive extracellular matrix accumulation (ECM) could lead to permanent scar format…
View article: ANALYSIS OF BLOOD LNCRNA EXPRESSION PROFILES IN TYPE 2 DIABETES INDIVIDUALS WITH DYSLIPIDEMIA
ANALYSIS OF BLOOD LNCRNA EXPRESSION PROFILES IN TYPE 2 DIABETES INDIVIDUALS WITH DYSLIPIDEMIA Open
INTRODUCTION Long noncoding RNAs (lncRNAs) are large RNA transcripts present in the blood without protein-coding capacity, with specific expression profiles for type 2 diabetes (T2D) and other conditions such as dyslipidemia (DLP). The obj…
View article: Long Non-Coding RNAs (lncRNAs) in Cardiovascular Disease Complication of Type 2 Diabetes
Long Non-Coding RNAs (lncRNAs) in Cardiovascular Disease Complication of Type 2 Diabetes Open
The discovery of non-coding RNAs (ncRNAs) has opened a new paradigm to use ncRNAs as biomarkers to detect disease progression. Long non-coding RNAs (lncRNA) have garnered the most attention due to their specific cell-origin and their exist…
View article: Extracellular Vesicles in the Development of the Non-Alcoholic Fatty Liver Disease: An Update
Extracellular Vesicles in the Development of the Non-Alcoholic Fatty Liver Disease: An Update Open
Non-alcoholic fatty liver disease (NAFLD) is a broad spectrum of liver damage disease from a simple fatty liver (steatosis) to more severe liver conditions such as non-alcoholic steatohepatitis (NASH), fibrosis, and cirrhosis. Extracellula…
View article: Interactions Among Non-Coding RNAs in Diabetic Nephropathy
Interactions Among Non-Coding RNAs in Diabetic Nephropathy Open
Diabetic Nephropathy (DN) is the most common cause of End-stage renal disease (ESRD). Although various treatments and diagnosis applications are available, DN remains a clinical and economic burden. Recent findings showed that noncoding RN…
View article: Advancement in the diagnosis of mitochondrial diseases
Advancement in the diagnosis of mitochondrial diseases Open
Mitochondrial diseases are multi-systemic, heterogeneous groups of diseases that are associated with various neuromuscular problems, cardiovascular disorders, metabolic syndrome, cancer, and obesity. Mitochondrial diseases are due to mutat…
View article: Regulatory Non-coding RNAs Network in Non-alcoholic Fatty Liver Disease
Regulatory Non-coding RNAs Network in Non-alcoholic Fatty Liver Disease Open
Non-alcoholic fatty liver disease (NAFLD) spectrum comprises simple steatosis and non-alcoholic steatohepatitis (NASH) that can lead to fibrosis and cirrhosis. The patients usually have no history of excessive alcohol consumption and other…
View article: MUTATIONAL PROFILES OF F8 AND F9 IN A COHORT OF HAEMOPHILIA A AND HAEMOPHILIA B PATIENTS IN THE MULTI-ETHNIC MALAYSIAN POPULATION
MUTATIONAL PROFILES OF F8 AND F9 IN A COHORT OF HAEMOPHILIA A AND HAEMOPHILIA B PATIENTS IN THE MULTI-ETHNIC MALAYSIAN POPULATION Open
Background: Haemophilia A (HA) and Haemophilia B (HB) are X-linked blood disorders that are caused by various mutations in the factor VIII (F8) and factor IX (F9) genes respectively. Identification of mutations is essential as some of the …