Search Results - "Ismail, Endom"
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Prevalence and molecular heterogeneity of glucose-6-phosphate dehydrogenase (G6PD) deficiency in the Senoi Malaysian Orang Asli population
Published in PloS one (12-12-2023)“…Glucose-6-phosphate dehydrogenase (G6PD) deficiency is an X-linked genetic disorder characterized by reduced G6PD enzyme levels in the blood. This condition is…”
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Journal Article -
2
3'-UTR variations and G6PD deficiency
Published in Journal of human genetics (01-04-2013)“…The combination of two silent mutations, c.1311C>T in exon 11 and IVS11 T93C (glucose-6-phosphate dehydrogenase (G6PD) 1311T/93C), with unknown mechanism, have…”
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Journal Article -
3
Population screening for glucose-6-phosphate dehydrogenase deficiency using quantitative point-of-care tests: a systematic review
Published in Frontiers in genetics (14-06-2023)“…Glucose-6-phosphate dehydrogenase (G6PD) deficiency is an X-linked hereditary disorder and a global public health concern that is most prevalent in…”
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4
The Clinical Significance of Interleukin-1 Receptor Antagonist +2018 Polymorphism in Rheumatoid Arthritis
Published in PloS one (22-04-2016)“…Interleukin-1 receptor antagonist (IL-1Ra) acts as an inhibitor of IL-1; which is one of the culprit cytokines in rheumatoid arthritis (RA). Although +2018…”
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5
The first Malay database toward the ethnic-specific target molecular variation
Published in BMC research notes (30-04-2015)“…The Malaysian Node of the Human Variome Project (MyHVP) is one of the eighteen official Human Variome Project (HVP) country-specific nodes. Since its inception…”
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6
Fine-scale population structure of Malays in Peninsular Malaysia and Singapore and implications for association studies
Published in Human genomics (22-07-2015)“…Fine scale population structure of Malays - the major population in Malaysia, has not been well studied. This may have important implications for both…”
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Journal Article -
7
Prevalence and molecular heterogeneity of glucose-6-phosphate dehydrogenase
Published in PloS one (12-12-2023)“…Glucose-6-phosphate dehydrogenase (G6PD) deficiency is an X-linked genetic disorder characterized by reduced G6PD enzyme levels in the blood. This condition is…”
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Journal Article -
8
Molecular Characterisation of α‐ and β‐Thalassaemia among Indigenous Senoi Orang Asli Communities in Peninsular Malaysia
Published in Annals of human genetics (01-09-2017)“…Summary Thalassaemia is a public health problem in Malaysia, with each ethnic group having their own common mutations. However, there is a lack on data on the…”
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Journal Article -
9
The population genomic landscape of human genetic structure, admixture history and local adaptation in Peninsular Malaysia
Published in Human genetics (01-09-2014)“…Peninsular Malaysia is a strategic region which might have played an important role in the initial peopling and subsequent human migrations in Asia. However,…”
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10
Molecular Characterisation of [alpha]- and [beta]-Thalassaemia among Indigenous Senoi Orang Asli Communities in Peninsular Malaysia
Published in Annals of human genetics (01-09-2017)“…Summary Thalassaemia is a public health problem in Malaysia, with each ethnic group having their own common mutations. However, there is a lack on data on the…”
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Journal Article -
11
Suppression of carbonyl reductase expression enhances malignant behaviour in uterine cervical squamous cell carcinoma: Carbonyl reductase predicts prognosis and lymph node metastasis
Published in Cancer letters (01-12-2011)“…Highlights ► We investigated the clinical significance of CR in uterine cervical SCC tissues. ► We examined how CR affects cancer cell behaviour in vitro . ►…”
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12
A Unique Interaction of IVS-I-1 (G>A) (HBA2: c.95+1G>A) with Hb Adana (HBA2: c.179G>A) Presenting as Transfusion-Dependent α-Thalassemia
Published in Hemoglobin (04-07-2018)“…Nondeletional α-globin mutations are known to cause more serious clinical effects than deletional ones. A rare IVS-I-1 (G>A) (HBA2: c.95+1G>A) donor splice…”
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13
Multiplex amplification refractory mutation system (MARMS) for the detection of β-globin gene mutations among the transfusion-dependent β-thalassemia Malay patients in Kelantan, Northeast of Peninsular Malaysia
Published in American journal of blood research (01-01-2014)“…The aim of this study was to adapt MARMS with some modifications to detect beta mutation in our cohort of thalassemia patients. We focused only on…”
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Journal Article -
14
Carbonyl reductase : A novel metastasis-modulating function
Published in Cancer research (Chicago, Ill.) (01-03-2000)“…To explore reasons for differences in the malignancy of tumors, we have compared two cell lines derived from a mouse lung adenocarcinoma cell line that differ…”
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Journal Article -
15
Gene expression contributing to the metastatic phenotype
Published 01-01-2003“…Metastasis is a complex multistage process, involving changes in the expression of various genes, including oncogenes and tumour suppressor genes. As a…”
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Dissertation