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O Ainoon
O Ainoon
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引用次数
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年份
Glucose‐6‐phosphate dehydrogenase (G6PD) variants in Malaysian Malays
O Ainoon, YH Yu, AL Amir Muhriz, NY Boo, SK Cheong, NH Hamidah
Human mutation 21 (1), 101-101, 2003
1172003
Polymorphic sites in the African population detected by sequence analysis of the glucose-6-phosphate dehydrogenase gene outline the evolution of the variants A and A-.
TJ Vulliamy, A Othman, M Town, A Nathwani, AG Falusi, PJ Mason, ...
Proceedings of the National Academy of Sciences 88 (19), 8568-8571, 1991
1011991
Semiquantitative screening test for G6PD deficiency detects severe deficiency but misses a substantial proportion of partially-dificient females
O Ainoon, A Alawiyah, YH Yu, SK Cheong, NH Hamidah, NY Boo, ...
Southeast Asian journal of tropical medicine and public health 34 (2), 405-414, 2003
842003
Glucose‐6‐phosphate dehydrogenase (G6PD) variants in Malaysian Chinese
O Ainoon, J Joyce, NY Boo, SK Cheong, ZA Zainal, NH Hamidah
Human Mutation 14 (4), 352-352, 1999
481999
Comparison of detection of glucose-6-phosphate dehydrogenase deficiency using fluorescent spot test, enzyme assay and molecular method for prediction of severe neonatal …
FL Wang, NY Boo, O Ainoon, MK Wong
Singapore medical journal 50 (1), 62-67, 2009
452009
Complete molecular characterisation of glucose-6-phosphate dehydrogenase (G6PD) deficiency in a group of Malaysian Chinese neonates.
O Ainoon, NY Boo, YH Yu, SK Cheong, HN Hamidah, JH Lim
The Malaysian journal of pathology 26 (2), 89-98, 2004
402004
Molecular characteristic of alpha thalassaemia among patients diagnosed in UKM Medical Centre
RZ Azma, O Ainoon, A Hafiza, I Azlin, AR Noor Farisah, S Nor Hidayati, ...
Malays J Pathol 36 (1), 27-32, 2014
302014
G6PD enzyme activity in normal term Malaysian neonates and adults using a OSMMR2000-D kit with Hb normalization
RZ Azma, N Hidayati, NR Farisah, NH Hamidah, O Ainoon
Southeast Asian journal of tropical medicine and public health 41 (4), 982, 2010
302010
Homozygous variant of UGT1A1 gene mutation and severe neonatal hyperbilirubinemia
NY Boo, FL Wong, MK Wang, A Othman
Pediatrics International 51 (4), 488-493, 2009
292009
Assessment of P-gp and MRP1 activities using MultiDrugQuant™ Assay Kit: a preliminary study of correlation between protein expressions and its functional activities in newly …
N Hamidah
Malays J Pathol 30, 87-93, 2008
242008
Prevalence of iron deficiency anaemia and thalassaemia trait among undergraduate medical students
RZ Azma, O Ainoon, I Azlin, H Hamenuddin, NA Hadi, WK Tatt, ...
Clinica Terapeutica 163 (4), 287, 2012
232012
In vitro expression of erythropoietin by transfected human mesenchymal stromal cells
PL Mok, SK Cheong, CF Leong, A Othman
Cytotherapy 10 (2), 116-124, 2008
232008
Risk factors associated with unconjugated neonatal hyperbilirubinemia in Malaysian neonates
F Wong, NY Boo, A Othman
Journal of tropical pediatrics 59 (4), 280-285, 2013
222013
Ex vivo expanded SSEA-4+ human limbal stromal cells are multipotent and do not express other embryonic stem cell markers
MN Lim, NH Hussin, A Othman, T Umapathy, P Baharuddin, R Jamal, ...
Molecular Vision 18, 1289, 2012
212012
Flow cytometric analysis of intracellular myeloperoxidase distinguishes lymphocytes, monocytes and granulocytes
H Unit
211998
Extended and stable gene expression via nucleofection of MIDGE construct into adult human marrow mesenchymal stromal cells
PL Mok, SK Cheong, CF Leong, KH Chua, O Ainoon
Cytotechnology 64, 203-216, 2012
202012
Variants of organic anion transporter polypeptide 2 gene are not risk factors associated with severe neonatal hyperbilirubinemia
FL Wong, NY Boo, O Ainoon, MK Wang
Malays J Pathol 31 (2), 99-104, 2009
202009
Prevalence of uridine glucuronosyl transferase 1A1 (UGT1A1) mutations in Malay neonates with severe jaundice
I Azlin, FL Wong, M Ezham, A Hafiza, O Ainoon
Malays J Pathol 33 (2), 95-100, 2011
182011
Thalassaemia in Malaysia: a strategy for prevention.
O Ainoon, SK Cheong
The Malaysian journal of pathology 16 (1), 23-27, 1994
151994
Co-inheritance of compound heterozygous Hb Constant Spring and a single--α 3.7 gene deletion with heterozygous δβ thalassaemia: A diagnostic challenge.
RZ Azma, A Othman, N Azman, H Alauddin, A Ithnin, N Yusof, NF Razak, ...
Malaysian Journal of Pathology 34 (1), 2012
122012
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