Literature DB >> 19147916

Lack of variation of ATTCT pentanucleotide repeats at ATXN10 gene between clinically diagnosed ataxia patients and normal individuals originated from Chinese Han.

Jun-Ling Wang1, Hong Jiang, Shen Zhang, Qian Xu, Ya-Fang Zhou, Shu-Sheng Liao, Lu Shen, Xin-Xiang Yan, Huai-Xu Zhu, Qian Pan, Kun Xia, Bei-Sha Tang.   

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Year:  2008        PMID： 19147916     DOI： 10.1007/s12041-008-0045-z

Source DB:  PubMed          Journal:  J Genet        ISSN： 0022-1333            Impact factor:   1.166


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  18 in total

1.  Spinocerebellar ataxia type 10 is rare in populations other than Mexicans.

Authors:  T Matsuura; L P W Ranum; V Volpini; M Pandolfo; H Sasaki; K Tashiro; K Watase; H Y Zoghbi; T Ashizawa
Journal:  Neurology       Date:  2002-03-26       Impact factor: 9.910

2.  Spinocerebellar ataxia type 10 in the French population.

Authors:  Hiroto Fujigasaki; Sandrine Tardieu; Agnès Camuzat; Giovanni Stevanin; Eric LeGuern; Tohru Matsuura; Tetsuo Ashizawa; Alexandra Dürr; Alexis Brice
Journal:  Ann Neurol       Date:  2002-03       Impact factor: 10.422

3.  FXTAS, SCA10, and SCA17 in American patients with movement disorders.

Authors:  Ana I Seixas; Martin H Maurer; Mark Lin; Colleen Callahan; Alka Ahuja; Tohru Matsuura; Christopher A Ross; Fuki M Hisama; Isabel Silveira; Russell L Margolis
Journal:  Am J Med Genet A       Date:  2005-07-01       Impact factor: 2.802

4.  Clinical phenotype of Brazilian families with spinocerebellar ataxia 10.

Authors:  H A G Teive; B B Roa; S Raskin; P Fang; W O Arruda; Y Correa Neto; R Gao; L C Werneck; T Ashizawa
Journal:  Neurology       Date:  2004-10-26       Impact factor: 9.910

5.  Interruptions in the expanded ATTCT repeat of spinocerebellar ataxia type 10: repeat purity as a disease modifier?

Authors:  Tohru Matsuura; Ping Fang; Christopher E Pearson; Parul Jayakar; Tetsuo Ashizawa; Benjamin B Roa; David L Nelson
Journal:  Am J Hum Genet       Date:  2005-11-15       Impact factor: 11.025

6.  Large expansion of the ATTCT pentanucleotide repeat in spinocerebellar ataxia type 10.

Authors:  T Matsuura; T Yamagata; D L Burgess; A Rasmussen; R P Grewal; K Watase; M Khajavi; A E McCall; C F Davis; L Zu; M Achari; S M Pulst; E Alonso; J L Noebels; D L Nelson; H Y Zoghbi; T Ashizawa
Journal:  Nat Genet       Date:  2000-10       Impact factor: 38.330

Review 7.  Recent progress in spinocerebellar ataxia type-10 (SCA10).

Authors:  Xi Lin; Tetsuo Ashizawa
Journal:  Cerebellum       Date:  2005       Impact factor: 3.847

8.  Mapping of a new autosomal dominant spinocerebellar ataxia to chromosome 22.

Authors:  L Zu; K P Figueroa; R Grewal; S M Pulst
Journal:  Am J Hum Genet       Date:  1999-02       Impact factor: 11.025

9.  Molecular genetics of hereditary spinocerebellar ataxia: mutation analysis of spinocerebellar ataxia genes and CAG/CTG repeat expansion detection in 225 Italian families.

Authors:  Alfredo Brusco; Cinzia Gellera; Claudia Cagnoli; Alessandro Saluto; Alessia Castucci; Chiara Michielotto; Vincenza Fetoni; Caterina Mariotti; Nicola Migone; Stefano Di Donato; Franco Taroni
Journal:  Arch Neurol       Date:  2004-05

Review 10.  Spinocerebellar ataxias: an update.

Authors:  Bing-wen Soong; Henry L Paulson
Journal:  Curr Opin Neurol       Date:  2007-08       Impact factor: 5.710
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  1 in total

1.  Spinocerebellar ataxia type 11 in the Chinese Han population.

Authors:  Qian Xu; Xiaohui Li; Junling Wang; JiPing Yi; Lifang Lei; Lu Shen; Hong Jiang; Kun Xia; Qian Pan; Beisha Tang
Journal:  Neurol Sci       Date:  2009-09-19       Impact factor: 3.307
  1 in total

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