Zobrazeno 1 - 10
of 17
pro vyhledávání: '"Chad C. Cheetham"'
Autor:
Fumiaki Yokoi, Huan-Xin Chen, Mai Tu Dang, Chad C Cheetham, Susan L Campbell, Steven N Roper, J David Sweatt, Yuqing Li
Publikováno v:
PLoS ONE, Vol 10, Iss 3, p e0120916 (2015)
DYT1 dystonia is an inherited movement disorder caused by mutations in DYT1 (TOR1A), which codes for torsinA. Most of the patients have a trinucleotide deletion (ΔGAG) corresponding to a glutamic acid in the C-terminal region (torsinA(ΔE)). Dyt1 Δ
Externí odkaz:
https://doaj.org/article/f358a7afcaec458fbca1b68aab27d38b
Publikováno v:
PLoS ONE, Vol 8, Iss 8, p e72491 (2013)
DYT1 early-onset generalized torsion dystonia (DYT1 dystonia) is an inherited movement disorder caused by mutations in one allele of DYT1 (TOR1A), coding for torsinA. The most common mutation is a trinucleotide deletion (ΔGAG), which causes a deleti
Externí odkaz:
https://doaj.org/article/e45a2504d9154a959076024f5bb1eaa1
Autor:
Mark P DeAndrade, Li Zhang, Atbin Doroodchi, Fumiaki Yokoi, Chad C Cheetham, Huan-Xin Chen, Steven N Roper, J David Sweatt, Yuqing Li
Publikováno v:
PLoS ONE, Vol 7, Iss 4, p e35518 (2012)
Polymorphisms in BTBD9 have recently been associated with higher risk of restless legs syndrome (RLS), a neurological disorder characterized by uncomfortable sensations in the legs at rest that are relieved by movement. The BTBD9 protein contains a B
Externí odkaz:
https://doaj.org/article/38820f198fbe4df78498e134850cb750
Autor:
Yuqing Li, Amy Trongnetrpunya, J. Michael Wyss, Mark P. DeAndrade, Mingzhou Ding, Chad C. Cheetham, Ning Peng, Fumiaki Yokoi
Publikováno v:
Movement Disorders. 31:1633-1639
Introduction DYT1 dystonia is an autosomal-dominant movement disorder characterized by abnormal, often repetitive, movements and postures. Its hallmark feature is sustained or intermittent contractions of muscles involving co-contractions of antagoni
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e476e454b96af25d726dbaa4ad6800c1
https://doi.org/10.1002/mds.26677
https://doi.org/10.1002/mds.26677
Publikováno v:
Behavioural Brain Research. 226:465-472
DYT1 early-onset generalized torsion dystonia is an inherited movement disorder associated with mutations in DYT1 that codes for torsinA protein. The most common mutation seen in this gene is a trinucleotide deletion of GAG. We previously reported a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::52866ee0f6c93014f73cca9e42a231c4
https://doi.org/10.1016/j.bbr.2011.10.002
https://doi.org/10.1016/j.bbr.2011.10.002
Autor:
Chad C. Cheetham, Huan-Xin Chen, Fumiaki Yokoi, J. David Sweatt, Mai Tu Dang, Steven N. Roper, Susan Campbell, Yuqing Li
Publikováno v:
PLoS ONE
PLoS ONE, Vol 10, Iss 3, p e0120916 (2015)
PLoS ONE, Vol 10, Iss 3, p e0120916 (2015)
DYT1 dystonia is an inherited movement disorder caused by mutations in DYT1 (TOR1A), which codes for torsinA. Most of the patients have a trinucleotide deletion (ΔGAG) corresponding to a glutamic acid in the C-terminal region (torsinAΔE). Dyt1 ΔGA
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a1eba79d243d5bd7f057cbc457f5b62a
http://europepmc.org/articles/PMC4370625
http://europepmc.org/articles/PMC4370625
Autor:
Yokoi, Fumiaki1, Cheetham, Chad C.2,3, Campbell, Susan L.3, Sweatt, J. David3, Li, Yuqing1 yuqing.li@neurology.ufl.edu
Publikováno v:
PLoS ONE. Aug2013, Vol. 8 Issue 8, p1-7. 7p.
Autor:
Lyu, Shangru, Doroodchi, Atbin, Xing, Hong, Sheng, Yi, DeAndrade, Mark P., Yang, Youfeng, Johnson, Tracy L., Clemens, Stefan, Yokoi, Fumiaki, Miller, Michael A., Xiao, Rui, Li, Yuqing
Publikováno v:
Brain Structure & Function; Jul2020, Vol. 225 Issue 6, p1743-1760, 18p
Autor:
Yokoi, Fumiaki1, Yang, Guang2, Li, JinDong2, DeAndrade, Mark P.1, Zhou, Tong2, Li, Yuqing1 yli@uab.edu
Publikováno v:
Journal of Biochemistry. Oct2010, Vol. 148 Issue 4, p459-466. 8p. 3 Graphs.
Autor:
DeAndrade, Mark P., Trongnetrpunya, Amy, Yokoi, Fumiaki, Cheetham, Chad C., Peng, Ning, Wyss, J. Michael, Ding, Mingzhou, Li, Yuqing
Publikováno v:
Movement Disorders; Nov2016, Vol. 31 Issue 11, p1633-1639, 7p