Projects per year
Personal profile
Biography
Tamar works in the School of Biological Sciences in the Faculty of Science at Monash University as a Research Fellow.
Network
Recent external collaboration on country level. Dive into details by clicking on the dots.
Projects 2016 2022
Elucidating a novel mechanism for coping with harmful mutations
Australian Research Council (ARC)
1/02/19 → 31/01/22
Project: Research
Investigation of Therapies for Nemaline Myopathy
Association Francaise contre les Myopathies (French Muscular Dystrophy Association)
1/08/16 → 31/07/18
Project: Research
Evaluating therapies to improve muscle function in nemaline myopathy
Muscular Dystrophy Association
1/02/16 → 31/01/19
Project: Research
Research Output 2007 2019
Cellular rescue in a zebrafish model of congenital muscular dystrophy type 1A
Hall, T., Wood, A., Ehrlich, O. V., Li, M., Sonntag, C., Cole, N. J., Huttner, I. G., Sztal, T. & Currie, P., 12 Oct 2019, (Accepted/In press) In : Npj Regenerative Medicine. 4, p. 1-13 21.Research output: Contribution to journal › Article › Research › peer-review
Open Access
File
Correspondence between behavioural, physiological and anatomical measurements of visual function in inhibitory-neuron-ablated zebrafish
Xie, J., Goodbourn, P., Bui, B. V., Sztal, T. & Jusuf, P. R., 2019, In : Investigative Ophthalmology and Visual Science. 60, 14, p. 4681-4690 10 p.Research output: Contribution to journal › Article › Research › peer-review
Open Access
File
KBTBD13 is an Actin-Binding Protein that Modulates Muscle Kinetics. Journal of Clinical Investigation
de Winter, J. M., Molenaar, J. P., Yuen, M., van der Pijl, R., Shen, S., Conijn, S., van de Locht, M., Willigenburg, M., Bogaards, S. J. P., van Kleef, E. S. B., Lassche, S., Persson, M., Rassier, D. E., Sztal, T. E., Ruparelia, A. A., Oorschot, V., Ramm, G., Hall, T. E., Xiong, Z., Johnson, C. N. & 21 others, , 15 Aug 2019, (Accepted/In press) In : Journal of Clinical Investigation.Research output: Contribution to journal › Article › Research › peer-review
7
Citations
(Scopus)
Genetic compensation triggered by actin mutation prevents the muscle damage caused by loss of actin protein
Sztal, T. E., McKaige, E. A., Williams, C., Ruparelia, A. A. & Bryson-Richardson, R. J., 1 Feb 2018, In : PLoS Genetics. 14, 2, 15 p., e1007212.Research output: Contribution to journal › Article › Research › peer-review
Open Access
File
4
Citations
(Scopus)
L-tyrosine supplementation does not ameliorate skeletal muscle dysfunction in zebrafish and mouse models of dominant skeletal muscle α-actin nemaline myopathy
Messineo, A., Gineste, C., Sztal, T. E., McNamara, E., Vilmen, C., Ogier, A., Hahne, D., Bendahan, D., Laing, N., Bryson-Richardson, R. J., Gondin, J. & Nowak, K. J., 2018, In : Scientific Reports. 8, 1, p. 1-12 12 p., 11490.Research output: Contribution to journal › Article › Research › peer-review
Open Access
File