Khoo Boon Yin

Dr. Khoo Boon Yin


Research Focus & Metrics

Academic Career Length

19Years (2008-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

View All Publications
30 October 2014 in BMC Complementary and Alternative Medicine
Verified
Journal Article
Open access
PDF file
IAItem Atangwho
Item Atangwho
KYKhoo Boon Yin
Khoo Boon Yin
MUMuhammad Ihtisham Umar
Muhammad Ihtisham Umar
MAMariam Ahmad
Mariam Ahmad
MAMohd Zaini Asmawi
Mohd Zaini Asmawi
This study evaluated the impact of Vernonia amygdalina (VA) on the transcription of key enzymes involved in cellular modulation of glucose in streptozotocin-induced diabetic rats in a bid to understand the possible anti-diabetic mechanism of VA.

27 June 2008 in Biochemical and Biophysical Research Communications
Verified
Journal Article
Closed access
KYKhoo Boon Yin
Khoo Boon Yin
NNNazalan Najimudin
Nazalan Najimudin
TMTengku Sifzizul Tengku Muhammad
Tengku Sifzizul Tengku Muhammad

11 January 2016 in Cytotechnology
Verified
Journal Article
Closed access
PDF file
KNKalpanah Nadarajan
Kalpanah Nadarajan
PBPrabha Balaram
Prabha Balaram
KYKhoo Boon Yin
Khoo Boon Yin

24 June 2013 in BMC Infectious Diseases
Verified
Journal Article
Open access
PDF file
AAAtefeh Amerizadeh
Atefeh Amerizadeh
KYKhoo Boon Yin
Khoo Boon Yin
ATAi Ying Teh
Ai Ying Teh
MGMajid Golkar
Majid Golkar
IKIzzati Zahidah Abdul Karim
Izzati Zahidah Abdul Karim
RNRahmah Noordin
Rahmah Noordin
Background: Toxoplasma gondii is an obligate intracellular zoonotic parasite of the phylum Apicomplexa which infects a wide range of warm-blooded animals, including humans. In this study in-vivo induced antigens of this parasite was investigated using in-vivo induced antigen technology (IVIAT) and pooled sera from patients with serological evidence of acute infection. Methods: The pooled sera was first pre-absorbed against three different preparations of antigens from in-vitro-grown cells of each T. gondii and E. coli XL1-Blue MRF’, subsequently it was used to screen T. gondii cDNA phage expression library. Positive clones from each group were subjected to quantitative real-time PCR expression analysis on mRNA of in-vivo and in-vitro grown parasites. Results: A total of 29 reactive clones from each IgM and IgG immunoscreenings were found to have high homology to T. gondii genes. Quantitative real-time PCR expression analysis showed that 20 IgM-detected genes and 11 IgG-detected genes were up-regulated in-vivo relative to their expression levels in-vitro. These included genes encoding micronemes, sterol-regulatory element binding protein site, SRS34A, MIC2-associated protein M2AP, nucleoredoxin, protein phosphatase 2C and several hypothetical proteins. A hypothetical protein (GenBank accession no. 7899266) detected by IgG had the highest in-vivo over in-vitro fold change of 499.86; while another up-regulated hypothetical protein (GenBank accession no. 7898829) recognized by IgM showed high sensitivity (90%) and moderate specificity (70%) in detecting T. gondii antibodies when tested with 20 individual serum samples. Conclusion: The highly up-regulated genes and the corresponding proteins, in particular the hypothetical proteins, may be useful in further studies on understanding the disease pathogenesis and as potential vaccine candidates.