Overview
Availability
- Associate Professor Tony Huynh is:
- Available for supervision
Research interests
-
Type 1 Diabetes
Diabetes technology and immunotherapy
-
Steroidogenesis
Measurement and quantification of various steroids
-
Newborn Screening
Congenital hypothyroidism and congenital adrenal hyperplasia
Works
Search Professor Tony Huynh’s works on UQ eSpace
2013
Journal Article
Effects of Dantrolene therapy on disease phenotype in Dystrophin deficient mdx mice
Quinn, James L., Huynh, Tony, Uaesoontrachoon, Kitipong, Tatem, Kathleen, Phadke, Aditi, Van der Meulen, Jack H., Yu, Qing and Nagaraju, Kannaboyina (2013). Effects of Dantrolene therapy on disease phenotype in Dystrophin deficient mdx mice. PLoS Currents (NOV). doi: 10.1371/currents.md.e246cf493a7edb1669f42fb735936b46
2013
Journal Article
VBP15, a novel anti-inflammatory and membrane-stabilizer, improves muscular dystrophy without side effects
Heier, Christopher R., Damsker, Jesse M., Yu, Qing, Dillingham, Blythe C., Huynh, Tony, Van der Meulen, Jack H., Sali, Arpana, Miller, Brittany K., Phadke, Aditi, Scheffer, Luana, Quinn, James, Tatem, Kathleen, Jordan, Sarah, Dadgar, Sherry, Rodriguez, Olga C., Albanese, Chris, Calhoun, Michael, Gordish-Dressman, Heather, Jaiswal, Jyoti K., Connor, Edward M., Mccall, John M., Hoffman, Eric P., Reeves, Eric K. M. and Nagaraju, Kanneboyina (2013). VBP15, a novel anti-inflammatory and membrane-stabilizer, improves muscular dystrophy without side effects. EMBO Molecular Medicine, 5 (10), 1569-1585. doi: 10.1002/emmm.201302621
2013
Journal Article
The effects of MyD88 deficiency on disease phenotype in dysferlin-deficient A/J mice: Role of endogenous TLR ligands
Uaesoontrachoon, Kitipong, Cha, Hee-Jae, Ampong, Beryl, Sali, Arpana, Vandermeulen, Jack, Wei, Benjamin, Creeden, Brittany, Huynh, Tony, Quinn, James, Tatem, Kathleen, Rayavarapu, Sree, Hoffman, Eric P. and Nagaraju, Kanneboyina (2013). The effects of MyD88 deficiency on disease phenotype in dysferlin-deficient A/J mice: Role of endogenous TLR ligands. Journal of Pathology, 231 (2), 199-209. doi: 10.1002/path.4207
2009
Journal Article
Benefit of early commencement of growth hormone therapy in children with Prader-Willi syndrome
Nyunt, O., Harris, M., Hughes, I., Huynh, T., Davies, P. S. W. and Cotterill, A. M. (2009). Benefit of early commencement of growth hormone therapy in children with Prader-Willi syndrome. Journal of Pediatric Endocrinology and Metabolism, 22 (12), 1151-1158. doi: 10.1515/JPEM.2009.22.12.1151
2009
Journal Article
Investigating maturity onset diabetes of the young
Nyunt, Ohn, Wu, Joyce Y, McGown, Ivan N, Harris, Mark, Huynh, Tony, Leong, Gary M, Cowley, David M and Cotterill, Andrew M (2009). Investigating maturity onset diabetes of the young. Clinical Biochemist Reviews, 30 (2), 67-74.
2009
Journal Article
The clinical and biochemical spectrum of congenital adrenal hyperplasia secondary to 21-hydroxylase deficiency
Huynh, Tony, McGown, Ivan, Cowley, David, Nyunt, Ohn, Leong, Gary M., Harris, Mark and Cotterill, Andrew M. (2009). The clinical and biochemical spectrum of congenital adrenal hyperplasia secondary to 21-hydroxylase deficiency. Clinical Biochemist Reviews, 30 (2), 75-86.
2009
Conference Publication
A selective glucocorticoid receptor modulator improves muscle function in a mouse model for Duchenne muscular dystrophy
Huynh, Tony, Trebbin, Andrea, Cowley, David, Bowling, Francis, Leong, Gary M., Cotterill, Andrew M., Harris, Mark, De Bosscher, Karolien, Haegeman, Guy and Hoey, Andrew J. (2009). A selective glucocorticoid receptor modulator improves muscle function in a mouse model for Duchenne muscular dystrophy. BASEL: KARGER.
2009
Journal Article
The association between ketoacidosis and 25(OH)-vitamin D-3 levels at presentation in children with type 1 diabetes mellitus
Huynh, Tony, Greer, Ristan M., Nyunt, Ohn, Bowling, Francis, Cowley, David, Leong, Gary M., Cotterill, Andrew M. and Harris, Mark (2009). The association between ketoacidosis and 25(OH)-vitamin D-3 levels at presentation in children with type 1 diabetes mellitus. Pediatric Diabetes, 10 (1), 38-43. doi: 10.1111/j.1399-5448.2008.00439.x
2009
Journal Article
A novel V185DfsX4 mutation of the AAAS gene in a 2-year-old boy with Triple A Syndrome
Cotterill, A. M., Cowley, D., Harris, M., Huynh, T., Leong, G. M., McGown, I. and Nyunt, O. (2009). A novel V185DfsX4 mutation of the AAAS gene in a 2-year-old boy with Triple A Syndrome. Clinical Pediatric Endocrinology, 18 (2), 73-75. doi: 10.1297/cpe.18.73
2009
Conference Publication
Congenital adrenal hyperplasia genotyping strategy using MLPA and DNA sequencing: an Australian cohort
Huynh, Tony, McGown, Ivan, Cowley, David, Harris, Mark, Leong, Gary M. and Cotterill, Andrew M. (2009). Congenital adrenal hyperplasia genotyping strategy using MLPA and DNA sequencing: an Australian cohort. BASEL: KARGER.
2008
Conference Publication
Hyperinsulinism of infancy associated with a novel paternally inherited alteration in the KCNJ11 gene
Cotterill, A. M., Cowley, D., Dahiya, R., Greer, R. M., Harris, M., Huynh, T., Leong, G., McGown, I., Nyunt, O., Venter, D. J. and Walker, R. (2008). Hyperinsulinism of infancy associated with a novel paternally inherited alteration in the KCNJ11 gene. Australasian Paediatric Endocrine Group Annual Scientific Meeting, Canberra, ACT, Australia, 17-19 November 2008.
Funding
Current funding
Supervision
Availability
- Associate Professor Tony Huynh is:
- Available for supervision
Looking for a supervisor? Read our advice on how to choose a supervisor.
Media
Enquiries
For media enquiries about Associate Professor Tony Huynh's areas of expertise, story ideas and help finding experts, contact our Media team: