Cookies on this website

We use cookies to ensure that we give you the best experience on our website. If you click 'Accept all cookies' we'll assume that you are happy to receive all cookies and you won't see this message again. If you click 'Reject all non-essential cookies' only necessary cookies providing core functionality such as security, network management, and accessibility will be enabled. Click 'Find out more' for information on how to change your cookie settings.

Search results (15)

« Back to Publications

Neurodegeneration in SCA14 is associated with increased PKCγ kinase activity, mislocalization and aggregation.

Wong MMK. et al, (2018), Acta Neuropathol Commun, 6

A Simplified Method for Generating Purkinje Cells from Human-Induced Pluripotent Stem Cells.

Watson LM. et al, (2018), Cerebellum, 17, 419 - 427

Dominant Mutations in GRM1 Cause Spinocerebellar Ataxia Type 44.

Watson LM. et al, (2017), Am J Hum Genet, 101

Dominant Mutations in GRM1 Cause Spinocerebellar Ataxia Type 44.

Watson LM. et al, (2017), Am J Hum Genet, 101

Dominant Mutations in GRM1 Cause Spinocerebellar Ataxia Type 44.

Watson LM. et al, (2017), Am J Hum Genet, 101, 451 - 458

Recent advances in modelling of cerebellar ataxia using induced pluripotent stem cells.

Wong MMK. et al, (2017), J Neurol Neuromedicine, 2, 11 - 15

Spinocerebellar ataxia type 7 in South Africa: Epidemiology, pathogenesis and therapy.

Watson L. et al, (2016), S Afr Med J, 106, S107 - S109

Induced pluripotent stem cell technology for modelling and therapy of cerebellar ataxia.

Watson LM. et al, (2015), Open Biol, 5

Corrigendum: Cross-talking noncoding RNAs contribute to cell-specific neurodegeneration in SCA7.

Tan JY. et al, (2015), Nat Struct Mol Biol, 22

Allele-specific silencing of mutant Ataxin-7 in SCA7 patient-derived fibroblasts.

Scholefield J. et al, (2014), Eur J Hum Genet, 22, 1369 - 1375

Allele-specific silencing of mutant Ataxin-7 in SCA7 patient-derived fibroblasts

Scholefield J. et al, (2014), European journal of human genetics : EJHG, 22, 1369 - 1375

Cross-talking noncoding RNAs contribute to cell-specific neurodegeneration in SCA7.

Tan JY. et al, (2014), Nat Struct Mol Biol, 21, 955 - 961

Inherited polyglutamine spinocerebellar ataxias in South Africa.

Smith DC. et al, (2012), S Afr Med J, 102, 683 - 686

RNA therapy for polyglutamine neurodegenerative diseases.

Watson LM. and Wood MJA., (2012), Expert reviews in molecular medicine, 14

Polyglutamine disease: from pathogenesis to therapy.

Watson LM. et al, (2012), S Afr Med J, 102, 481 - 484