Meav-Lang J Lay
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Meav-Lang J Lay has a total of 6 co-authors. Here are the top co-authors by number of shared publications:
- Anne-Louise Ponsonby
The Florey Institute of Neuroscience and Mental Health, The University of Melbourne, Parkville, Australia
1 shared publication - Dominic E. Dwyer
Department of Virology, Centre for Infectious Diseases and Microbiology Laboratory Services, ICPMR, Westmead Hospital, Westmead, NSW 2145, Australia
1 shared publication - Janette Taylor
Virology Department, Centre For Infectious Diseases & Microbiology Laboratory Services, Institute of Clinical Pathology & Medical Research, Institute Road, Westmead Hospital, Westmead 2145, New South Wales, Australia
1 shared publication - Mala Ratnamohan
Virology Department, Centre For Infectious Diseases & Microbiology Laboratory Services, Institute of Clinical Pathology & Medical Research, Institute Road, Westmead Hospital, Westmead 2145, New South Wales, Australia
1 shared publication - Robyn Marjorie Lucas
National Centre for Epidemiology and Population Health, Australian National University, Canberra, Australia
1 shared publication the Ausimmune Investigator Group (AIG)
1 shared publication
Latest Publications
- Open Access
- 22 September 2010
- Published by Springer Nature in Virology Journal
- Vol. 7 (1) , 252
Measurement of Epstein-Barr virus DNA load using a novel quantification standard containing two EBV DNA targets and SYBR Green I dye
Reactivation of Epstein-Barr virus (EBV) infection may cause serious, life-threatening complications in immunocompromised individuals. EBV DNA is often detected in EBV-associated disease states, with viral load believed to be a reflection of virus activity. Two separate real-time quantitative polymerase chain reaction (QPCR) assays using SYBR Green I dye and a single quantification standard containing two EBV genes, Epstein-Barr nuclear antigen-1 (EBNA-1) and BamHI fragment H rightward open reading frame-1 (BHRF-1), were developed to detect and measure absolute EBV DNA load in patients with various EBV-associated diseases. EBV DNA loads and viral capsid antigen (VCA) IgG antibody titres were also quantified on a population sample.
- 22 September 2010
- Published by Springer Nature in Virology Journal
- Vol. 7 (1) , 252
Open AccessMeasurement of Epstein-Barr virus DNA load using a novel quantification standard containing two EBV DNA targets and SYBR Green I dye
Reactivation of Epstein-Barr virus (EBV) infection may cause serious, life-threatening complications in immunocompromised individuals. EBV DNA is often detected in EBV-associated disease states, with viral load believed to be a reflection of virus activity. Two separate real-time quantitative polymerase chain reaction (QPCR) assays using SYBR Green I dye and a single quantification standard containing two EBV genes, Epstein-Barr nuclear antigen-1 (EBNA-1) and BamHI fragment H rightward open reading frame-1 (BHRF-1), were developed to detect and measure absolute EBV DNA load in patients with various EBV-associated diseases. EBV DNA loads and viral capsid antigen (VCA) IgG antibody titres were also quantified on a population sample.