Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Madelaine C. Tym"'
Autor:
Maxinne Watchon, Luan Luu, Katherine J. Robinson, Kristy C. Yuan, Alana De Luca, Hannah J. Suddull, Madelaine C. Tym, Gilles J. Guillemin, Nicholas J. Cole, Garth A. Nicholson, Roger S. Chung, Albert Lee, Angela S. Laird
Publikováno v:
Molecular Brain, Vol 14, Iss 1, Pp 1-16 (2021)
Abstract Machado-Joseph disease (MJD, also known as spinocerebellar ataxia type 3) is a fatal neurodegenerative disease that impairs control and coordination of movement. Here we tested whether treatment with the histone deacetylase inhibitor sodium
Externí odkaz:
https://doaj.org/article/c4c31cfe9850482096f4f4f803675be2
Autor:
Katherine J. Robinson, Madelaine C. Tym, Alison Hogan, Maxinne Watchon, Kristy C. Yuan, Stuart K. Plenderleith, Emily K. Don, Angela S. Laird
Publikováno v:
Disease Models & Mechanisms, Vol 14, Iss 10 (2021)
Spinocerebellar ataxia 3 (SCA3, also known as Machado–Joseph disease) is a neurodegenerative disease caused by inheritance of a CAG repeat expansion within the ATXN3 gene, resulting in polyglutamine (polyQ) repeat expansion within the ataxin-3 prot
Externí odkaz:
https://doaj.org/article/58a28b3fec1546bcae968ee506d3ac17
Autor:
Caitlin W. Lucas, Kristy C. Yuan, Julie D. Atkin, Madelaine C. Tym, Ian P. Blair, Maxinne Watchon, Hamideh Shahheydari, Alison L. Hogan, Katherine J. Robinson, Garth A. Nicholson, Emily K. Don, Claire Winnick, Angela S. Laird, Nicholas J. Cole
Publikováno v:
Zebrafish
Amyotrophic lateral sclerosis (ALS) is a fatal neurodegenerative disease characterized by progressive loss of motor neurons. ALS can be modeled in zebrafish (Danio rerio) through the expression of human ALS-causing genes, such as superoxide dismutase
Autor:
Emily K. Don, Kristy C. Yuan, Maxinne Watchon, Stuart K. Plenderleith, Madelaine C. Tym, Alison L. Hogan, Angela S. Laird, Katherine J. Robinson
Spinocerebellar ataxia-3 (SCA3, also known as Machado Joseph Disease), is a neurodegenerative disease caused by inheritance of aATXN3gene containing a CAG repeat expansion, resulting in presence of a polyglutamine (polyQ) repeat expansion within the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::41643f6e1e991ca6e8063f58ce3b1571
https://doi.org/10.1101/2021.03.09.434364
https://doi.org/10.1101/2021.03.09.434364
Autor:
Roger S. Chung, Hannah J. Suddull, Angela S. Laird, Madelaine C. Tym, Luan Luu, Maxinne Watchon, Katherine J. Robinson, Albert Lee, Kristy C. Yuan, Nicholas J. Cole, Gilles J. Guillemin, Alana De Luca, Garth A. Nicholson
Machado-Joseph disease (MJD, also known as spinocerebellar ataxia-3) is a fatal neurodegenerative disease that impairs control and coordination of movement. Here we tested whether treatment with the histone deacetylase inhibitor sodium valproate (SV)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ebe52e814f4dccde843cc0a1d42fa833
https://doi.org/10.1101/2021.03.08.434343
https://doi.org/10.1101/2021.03.08.434343