Julian I. Heng, BSc(Hons), PhD
Affiliations: | 2010-2014 | The Australian Regenerative Medicine Institute, Clayton, Victoria, Australia | |
| 2014-2017 | The Harry Perkins Institute of Medical Research | ||
| 2017- | Sarich Neuroscience Research Institute and Curtin University |
Area:
Neurogenesis, Cell Migration, Fate SpecificationWebsite:
https://staffportal.curtin.edu.au/staff/profile/view/Julian.HengGoogle:
"Julian Heng"Mean distance: 16.61 (cluster 11) | S | N | B | C | P |
Parents
Sign in to add mentor| Francois P. Guillemot | post-doc | 2004-2008 | MRC National Institute for Medical Research |
Children
Sign in to add trainee| Ivan Gladwyn-Ng | grad student | 2011-2014 | Australian Regenerative Medicine Institute |
BETA: Related publications
See more...
Publications
|
You can help our author matching system! If you notice any publications incorrectly attributed to this author, please sign in and mark matches as correct or incorrect. |
| Harris L, Zalucki O, Gobius I, et al. (2018) Correction: Transcriptional regulation of intermediate progenitor cell generation during hippocampal development (doi: 10.1242/dev.140681). Development (Cambridge, England). 145 |
| Harris L, Zalucki O, Clément O, et al. (2018) Neurogenic differentiation by hippocampal neural stem and progenitor cells is biased by NFIX expression. Development (Cambridge, England). 145 |
| Clément O, Hemming IA, Gladwyn-Ng IE, et al. (2018) Correction to: Rp58 and p27kip1 coordinate cell cycle exit and neuronal migration within the embryonic mouse cerebral cortex. Neural Development. 13: 1 |
| Edvardson S, Tian G, Cullen H, et al. (2016) Infantile neurodegenerative disorder associated with mutations in TBCD, an essential gene in the tubulin heterodimer assembly pathway. Human Molecular Genetics. 25: 4635-4648 |
| Harris L, Zalucki O, Gobius I, et al. (2016) Transcriptional regulation of intermediate progenitor cell generation during hippocampal development. Development (Cambridge, England). 143: 4620-4630 |
| Li SS, Qu Z, Haas M, et al. (2016) The HSA21 gene EURL/C21ORF91 controls neurogenesis within the cerebral cortex and is implicated in the pathogenesis of Down Syndrome. Scientific Reports. 6: 29514 |
| Haas MA, Ngo L, Li SS, et al. (2016) De Novo Mutations in DENR Disrupt Neuronal Development and Link Congenital Neurological Disorders to Faulty mRNA Translation Re-initiation. Cell Reports |
| Harris L, Zalucki O, Piper M, et al. (2016) Insights into the Biology and Therapeutic Applications of Neural Stem Cells. Stem Cells International. 2016: 9745315 |
| Berkowicz SR, Featherby TJ, Qu Z, et al. (2016) Brinp1 (-/-) mice exhibit autism-like behaviour, altered memory, hyperactivity and increased parvalbumin-positive cortical interneuron density. Molecular Autism. 7: 22 |
| Gladwyn-Ng I, Huang L, Ngo L, et al. (2016) Bacurd1/Kctd13 and Bacurd2/Tnfaip1 are interacting partners to Rnd proteins which influence the long-term positioning and dendritic maturation of cerebral cortical neurons. Neural Development. 11: 7 |