Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Grace G Y Lim"'
Autor:
Adeline H. Basil, Joan P. L. Sim, Grace G. Y. Lim, Shuping Lin, Hui Ying Chan, Simone Engelender, Kah-Leong Lim
Publikováno v:
Frontiers in Cellular Neuroscience, Vol 11 (2017)
Afadin 6 (AF-6) is an F-actin binding multidomain-containing scaffolding protein that is known for its function in cell-cell adhesion. Interestingly, besides this well documented role, we recently found that AF-6 is a Parkin-interacting protein that
Externí odkaz:
https://doaj.org/article/866310369a4545c09db1b65b6769adfe
Autor:
Grace G Y Lim, Katherine C M Chew, Xiao-Hui Ng, Adeline Henry-Basil, Roy W X Sim, Jeanne M M Tan, Chou Chai, Kah-Leong Lim
Publikováno v:
PLoS ONE, Vol 8, Iss 9, p e73235 (2013)
Disruption of the ubiquitin-proteasome system, which normally identifies and degrades unwanted intracellular proteins, is thought to underlie neurodegeneration. Supporting this, mutations of Parkin, a ubiquitin ligase, are associated with autosomal r
Externí odkaz:
https://doaj.org/article/341b4e7893d44f2b828ee8f7401a706c
Autor:
Katherine C M Chew, Noriyuki Matsuda, Keiko Saisho, Grace G Y Lim, Chou Chai, Hui-Mei Tan, Keiji Tanaka, Kah-Leong Lim
Publikováno v:
PLoS ONE, Vol 6, Iss 5, p e19720 (2011)
Mutations in the parkin gene, which encodes a ubiquitin ligase (E3), are a major cause of autosomal recessive parkinsonism. Although parkin-mediated ubiquitination was initially linked to protein degradation, accumulating evidence suggests that the e
Externí odkaz:
https://doaj.org/article/4987a5e223204bd09706a72f5e91c936
Autor:
Kah-Leong Lim, Grace G. Y. Lim
Publikováno v:
EMBO reports. 18:864-865
Mitophagy, the selective removal of damaged or excess mitochondria by autophagy, is an important process in cellular homeostasis. The outer mitochondrial membrane (OMM) proteins NIX, BNIP3, FUNDC1, and Bcl2‐L13 recruit ATG8 proteins (LC3/GABARAP) t
Publikováno v:
Autophagy-A Double-Edged Sword-Cell Survival or Death?
Parkinson’s disease (PD) is a prevalent neurodegenerative movement disorder whose occurrence crosses geographic, racial and social boundaries affecting 1-2% of the population above the age of 65 (Dorsey et al., 2007). Clinically, the disease is att
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c8044648066bf34c6a8a051d5915097b
https://doi.org/10.5772/54927
https://doi.org/10.5772/54927
Autor:
Jeanne M.M. Tan, Xiao-Hui Ng, Kah-Leong Lim, Adeline Henry-Basil, Grace G. Y. Lim, Chou Chai, Roy W. X. Sim, Katherine C. M. Chew
Publikováno v:
PLoS ONE
PLoS ONE, Vol 8, Iss 9, p e73235 (2013)
PLoS ONE, Vol 8, Iss 9, p e73235 (2013)
Disruption of the ubiquitin-proteasome system, which normally identifies and degrades unwanted intracellular proteins, is thought to underlie neurodegeneration. Supporting this, mutations of Parkin, a ubiquitin ligase, are associated with autosomal r
Publikováno v:
Etiology and Pathophysiology of Parkinson's Disease
Parkinson’s disease (PD) is the most common neurodegenerative movement disorder affecting millions of predominantly elderly individuals worldwide. Originally described as “The Shaking Palsy” in 1817 by the British physician, James Parkinson, th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1ae48aa571f1f3ceb2897a9d6bcf9356
http://www.intechopen.com/articles/show/title/parkin-and-parkinson-s-disease
http://www.intechopen.com/articles/show/title/parkin-and-parkinson-s-disease
Autor:
Kah-Leong Lim, Grace G. Y. Lim
Publikováno v:
Neurobiology of Disease, Vol 43, Iss 1, Pp 9-16 (2011)
The proteasome, which identifies and destroys unwanted proteins rapidly, plays a vital role in maintaining cellular protein homeostasis. Proteins that are destined for proteasome-mediated degradation are usually tagged with a chain of ubiquitin linke
Autor:
Keiko Saisho, Kah-Leong Lim, Hui-Mei Tan, Noriyuki Matsuda, Keiji Tanaka, Katherine C. M. Chew, Grace G. Y. Lim, Chou Chai
Publikováno v:
PLoS ONE, Vol 6, Iss 5, p e19720 (2011)
PLoS ONE
PLoS ONE
Background Mutations in the parkin gene, which encodes a ubiquitin ligase (E3), are a major cause of autosomal recessive parkinsonism. Although parkin-mediated ubiquitination was initially linked to protein degradation, accumulating evidence suggests
Publikováno v:
Journal of Parkinson's Disease. 2019 Supplement 1, Vol. 9, p1-278. 278p.