Targeting ATXN2 Using Antisense Oligonucleotides as a Treatment for Spinocerebellar Ataxia Type 2 (SCA2)

被引:0
|
作者
Scoles, Daniel [4 ]
Schneider, Matthew [4 ]
Meera, Pratap [3 ]
Figueroa, Karla [4 ]
Hung, Gene [1 ]
Rigo, Frank [2 ]
Bennett, Frank [2 ]
Otis, Thomas [3 ]
Pulst, Stefan [4 ]
机构
[1] ISIS Pharmaceut, 2280 Faraday Ave, Carlsbad, CA 92008 USA
[2] Isis Pharmaceut Inc, Carlsbad, CA USA
[3] Univ Calif Los Angeles, Los Angeles, CA USA
[4] Univ Utah, Salt Lake City, UT USA
关键词
D O I
暂无
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
S30.007
引用
收藏
页数:2
相关论文
共 50 条
  • [41] Factors associated with ATXN2 CAG/CAA repeat intergenerational instability in Spinocerebellar ataxia type 2
    Almaguer-Mederos, L. E.
    Mesa, J. M. L.
    Gonzalez-Zaldivar, Y.
    Almaguer-Gotay, D.
    Cuello-Almarales, D.
    Aguilera-Rodriguez, R.
    Falcon, N. S.
    Gispert, S.
    Auburger, G.
    Velazquez-Perez, L.
    CLINICAL GENETICS, 2018, 94 (3-4) : 346 - 350
  • [42] Spinocerebellar ataxia 2 (SCA2): morphometric analyses in 11 autopsies
    Estrada, R
    Galarraga, J
    Orozco, G
    Nodarse, A
    Auburger, G
    ACTA NEUROPATHOLOGICA, 1999, 97 (03) : 306 - 310
  • [43] Spinocerebellar ataxia 2 (SCA2): morphometric analyses in 11 autopsies
    R. Estrada
    Joaquín Galarraga
    Guillermo Orozco
    Alberto Nodarse
    Georg Auburger
    Acta Neuropathologica, 1999, 97 : 306 - 310
  • [44] Unexpanded and intermediate CAG polymorphisms at the SCA2 locus (ATXN2) in the Cuban population: evidence about the origin of expanded SCA2 alleles
    Miguel Laffita-Mesa, Jose
    Velazquez-Perez, Luis C.
    Santos Falcon, Nieves
    Cruz-Marino, Tania
    Gonzalez Zaldivar, Yanetza
    Vazquez Mojena, Yaimee
    Almaguer-Gotay, Dennis
    Almaguer Mederos, Luis Enrique
    Rodriguez Labrada, Roberto
    EUROPEAN JOURNAL OF HUMAN GENETICS, 2012, 20 (01) : 41 - 49
  • [45] Unexpanded and intermediate CAG polymorphisms at the SCA2 locus (ATXN2) in the Cuban population: evidence about the origin of expanded SCA2 alleles
    José Miguel Laffita-Mesa
    Luis C Velázquez-Pérez
    Nieves Santos Falcón
    Tania Cruz-Mariño
    Yanetza González Zaldívar
    Yaimee Vázquez Mojena
    Dennis Almaguer-Gotay
    Luis Enrique Almaguer Mederos
    Roberto Rodríguez Labrada
    European Journal of Human Genetics, 2012, 20 : 41 - 49
  • [46] A largest case series study of spinocerebellar ataxia type 2(SCA2) from India: Do SCA2 clinical subtypes exists?
    Srivastava, A. K.
    Sonakar, A. K.
    Shakya, S.
    Suroliya, V.
    Takkar, A.
    Ahmad, I.
    Singh, R. K.
    Singh, I.
    Vibha, D.
    Shukla, G.
    Goyal, V.
    Prasad, K.
    Garg, A.
    Faruq, M.
    MOVEMENT DISORDERS, 2016, 31 : S345 - S345
  • [47] MODIFIERS OF AGE AT ONSET IN SPINOCEREBELLAR ATAXIA TYPE 2(SCA2): CAG LENGTH OF OTHER SCA LOCI DO NOT INFLUENCE AGE AT ONSET IN SCA2
    Singh, R.
    Sonakar, A. K.
    Srivastava, A. K.
    Faruq, M.
    PARKINSONISM & RELATED DISORDERS, 2018, 46 : E61 - E62
  • [48] The spinocerebellar ataxia type 2 (SCA2) phenotype includes typical Parkinson's disease
    Gwinn-Hardy, K
    Farrer, M
    Chen, JY
    Liu, HC
    Liu, TY
    Boss, MA
    Koroshetz, W
    Waters, C
    Singleton, A
    Hardy, J
    NEUROLOGY, 2000, 54 (07) : A265 - A265
  • [49] Common Origin of Pure and Interrupted Repeat Expansions in Spinocerebellar Ataxia Type 2 (SCA2)
    Ramos, Eliana Marisa
    Martins, Sandra
    Alonso, Isabel
    Emmel, Vanessa E.
    Saraiva-Pereira, Maria Luiza
    Jardim, Laura Bannach
    Coutinho, Paula
    Sequeiros, Jorge
    Silveira, Isabel
    AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS, 2010, 153B (02) : 524 - 531
  • [50] Amyotrophic lateral sclerosis and spinocerebellar ataxia type 2 in a family with full CAG repeat expansions of ATXN2
    Tazen, S.
    Figueroa, K.
    Kwan, J. Y.
    Goldman, J.
    Hunt, A.
    Sampson, J.
    Gutmann, L.
    Pulst, S.
    Mitsumoto, H.
    Kuo, S. H.
    MOVEMENT DISORDERS, 2013, 28 : S241 - S242