Spinocerebellar ataxia:Epigenetic and cell model studies of SCA type 8

Spinocerebellar ataxia:Epigenetic and cell model studies of SCA type 8

碩士 === 國立臺灣師範大學 === 生命科學研究所 === 97 === Abstract Spinocerebellar ataxia type 8 (SCA8) involves the expression of an expanded CTG/CAG combined repeats from opposite strands producing CUG expansion transcripts (ATXN8OS) and a polyglutamine expansion protein (ATXN8). SCA8 disease does not show complete...

Full description

Bibliographic Details
Main Authors:	Ghin-Chueh Lee, 李金玨
Other Authors:	Guey-Jen Lee-Chen
Format:	Others
Language:	zh-TW
Published:	2009
Online Access:	http://ndltd.ncl.edu.tw/handle/uzwm3b

Similar Items

Electronystagmography findings in spinocerebellar ataxia type 3 (SCA3) and type 2 (SCA2)
by: Bianca Simone Zeigelboim, et al.
Published: (2011-10-01)

Spinocerebellar ataxia 36 (SCA36): “Costa da Morte ataxia”
by: M. Arias, et al.
Published: (2017-07-01)

Insight Into Spinocerebellar Ataxia Type 31 (SCA31) From Drosophila Model
by: Taro Ishiguro, et al.
Published: (2021-05-01)

Disrupted Calcium Signaling in Animal Models of Human Spinocerebellar Ataxia (SCA)
by: Francesca Prestori, et al.
Published: (2019-12-01)

Multimodal neurophysiological study of SCA2 and SCA3 autosomal dominant hereditary spinocerebellar ataxias
by: S. Álvarez-Paradelo, et al.
Published: (2011-01-01)

Clinical and genetic analysis of spinocerebellar ataxia type 7 (SCA7) in Zambian families
by: Masharip Atadzhanov, et al.
Published: (2017-11-01)

Genetic and Molecular analysis of the Spinocerebellar ataxia type 7 (SCA7) disease gene
by: Jonasson, Jenni
Published: (2000)

Ancestral origin of the ATTCT repeat expansion in spinocerebellar ataxia type 10 (SCA10).
by: Teresa Almeida, et al.
Published: (2009-01-01)

Inheritance patterns of ATCCT repeat interruptions in spinocerebellar ataxia type 10 (SCA10) expansions.
by: Ivette Landrian, et al.
Published: (2017-01-01)

The Ins and Outs of a Polyglutamine Neurodegenerative Disease: Spinocerebellar Ataxia Type 1 (SCA1)
by: Harry T. Orr
Published: (2000-06-01)

Collaborative Efforts for Spinocerebellar Ataxia Research in the United States: CRC-SCA and READISCA
by: Chih-Chun Lin, et al.
Published: (2020-08-01)

Spinocerebellar ataxias: Genetic testing of SCA2、SCA14 and interaction analysis between expanded SCA17 TBP and HMGB1
by: Hsiang-Ming Chen, et al.
Published: (2007)

Analysis of spinocerebellar ataxia type 8 gene expression and establishment of spinocerebellar type 8 in vitro and in vivo models
by: Wei Lun Chen, et al.
Published: (2006)

Ataxin-7 SUMOylation and its functional consequences in the spinocerebellar ataxia type 7 (SCA7) pathophysiology
by: Marinello, Martina
Published: (2014)

Spinocerebellar ataxia type 15 (sca15) maps to 3p24.2-3pter:
by: Melanie A Knight, et al.
Published: (2003-07-01)

Frequency of KCNC3 DNA variants as causes of spinocerebellar ataxia 13 (SCA13).
by: Karla P Figueroa, et al.
Published: (2011-03-01)

Incidentalome in Neurogenetics: Pathogenic Variant of NSD1 in a Patient With Spinocerebellar Ataxia (SCA)
by: Harvy Velasco, et al.
Published: (2018-03-01)

Roles of the Carbonic Anhydrase 8 in Spinocerebellar Ataxia Type 3
by: Yi-Ting Li, et al.
Published: (2015)

Construction of Spinocerebellar Ataxia Type 17 Cellular Models Studies of Spinocerebellar Ataxias in Cellular Models
by: Ya-Chun Yu, et al.
Published: (2005)

RNA gain-of-function in spinocerebellar ataxia type 8.
by: Randy S Daughters, et al.
Published: (2009-08-01)

Molecular Genetic studies of spinocerebellar ataxia type 8
by: I-Cheng Chen, et al.
Published: (2010)

Expansion of the Spinocerebellar ataxia type 10 (SCA10) repeat in a patient with Sioux Native American ancestry.
by: Khalaf Bushara, et al.
Published: (2013-01-01)

Generation of spinocerebellar ataxia type 3 patient-derived induced pluripotent stem cell line SCA3.B11
by: Susanne K. Hansen, et al.
Published: (2016-05-01)

Generation of spinocerebellar ataxia type 3 patient-derived induced pluripotent stem cell line SCA3.A11
by: Susanne K. Hansen, et al.
Published: (2016-05-01)

Genetic testing of spinocerebellar ataxia types 2 and 17 and oxidative stress study of lymphoblastoid cells with SCA17 TBP expansion
by: FL Chen, et al.
Published: (2006)

Molecular diagnosis of spinocerebellar ataxias and studies of pathogenesis of spinocerebellar ataxia type 3 and type 7
by: Hui-Fang Tsai, et al.
Published: (2005)

Spinocerebellar ataxia type 8 : genetic and promoter functional studies
by: Shih-Huan Kao, et al.
Published: (2008)

Epilepsy in spinocerebellar ataxia type 8: a case report
by: Arun Swaminathan
Published: (2019-11-01)

Spinocerebellar ataxia type 17: genetic testing and oxidative stress and cytotoxicity studies using SCA17 lymphoblastoid and HEK-293 cell models
by: Pei-Ying Lin, et al.
Published: (2008)

Spinocerebellar Ataxia
by: J Gordon Millichap
Published: (1988-07-01)

Spinocerebellar ataxias
by: Bryer, Alan
Published: (2017)

Spinocerebellar Ataxias
by: Huda Y. Zoghbi
Published: (2000-10-01)

Spinocerebellar Ataxia
Published: (2012)

Spinocerebellar ataxias Ataxias espinocerebelares
by: Hélio A.G. Teive
Published: (2009-12-01)

Spinocerebellar Ataxia 7: A Report of Unaffected Siblings Who Married into Different SCA 7 Families
by: Fariha Zaheer, et al.
Published: (2014-01-01)

Brain Derived Neurotrophic Factor (BDNF) Delays Onset of Pathogenesis in Transgenic Mouse Model of Spinocerebellar Ataxia Type 1 (SCA1)
by: Aaron Mellesmoen, et al.
Published: (2019-01-01)

Phenotype variability and early onset ataxia symptoms in spinocerebellar ataxia type 7: comparison and correlation with other spinocerebellar ataxias
by: Marcus Vinicius Cristino de Albuquerque, et al.
Published: (2015-01-01)

Generation of an induced pluripotent stem cell line from a patient with spinocerebellar ataxia type 3 (SCA3): HIHCNi002-A
by: Stefanie Nicole Hayer, et al.
Published: (2018-07-01)

Spinocerebellar ataxia 17 (SCA17) pathogenic mechanisms: Chaperones function and misfolding proteins caused by the expanded polyglutamine in TATA-binding protein
by: Li-Ching Lee, et al.
Published: (2009)

Simplified Model of PKCγ Signaling Dysregulation and Cytosol-to-Membrane Translocation Kinetics During Neurodegenerative Spinocerebellar Ataxia Type 14 (SCA14)
by: Naveed Aslam, et al.
Published: (2020-01-01)