Connection

TETSUO ASHIZAWA to Ataxin-10

This is a "connection" page, showing publications TETSUO ASHIZAWA has written about Ataxin-10.
Connection Strength

4.219
  1. Extended haplotype with rs41524547-G defines the ancestral origin of SCA10. Hum Mol Genet. 2024 09 03; 33(18):1567-1574.
    View in: PubMed
    Score: 0.924
  2. Clinical and Genetic Evaluation of Spinocerebellar Ataxia Type 10 in 16 Brazilian Families. Cerebellum. 2019 Oct; 18(5):849-854.
    View in: PubMed
    Score: 0.657
  3. Inheritance patterns of ATCCT repeat interruptions in spinocerebellar ataxia type 10 (SCA10) expansions. PLoS One. 2017; 12(4):e0175958.
    View in: PubMed
    Score: 0.554
  4. SMRT Sequencing of Long Tandem Nucleotide Repeats in SCA10 Reveals Unique Insight of Repeat Expansion Structure. PLoS One. 2015; 10(8):e0135906.
    View in: PubMed
    Score: 0.494
  5. The impact of interrupted ATXN10 expansions on clinical findings of spinocerebellar ataxia type 10. J Neurol. 2025 Mar 11; 272(4):261.
    View in: PubMed
    Score: 0.239
  6. ATXN10 Gene Expansions in Mexican Patients with Ataxia Without Epilepsy. Cerebellum. 2025 Jan 16; 24(2):33.
    View in: PubMed
    Score: 0.237
  7. Response to ATXN10 Microsatellite Distribution in a Peruvian Amerindian Population. Cerebellum. 2021 12; 20(6):946-947.
    View in: PubMed
    Score: 0.182
  8. Pulse-Field capillary electrophoresis of repeat-primed PCR amplicons for analysis of large repeats in Spinocerebellar Ataxia Type 10. PLoS One. 2020; 15(3):e0228789.
    View in: PubMed
    Score: 0.169
  9. Bolivian kindred with combined spinocerebellar ataxia types 2 and 10. Acta Neurol Scand. 2015 Aug; 132(2):139-42.
    View in: PubMed
    Score: 0.119
  10. Spinocerebellar ataxia type 10. Handb Clin Neurol. 2012; 103:507-19.
    View in: PubMed
    Score: 0.096
  11. Transgenic mice with SCA10 pentanucleotide repeats show motor phenotype and susceptibility to seizure: a toxic RNA gain-of-function model. J Neurosci Res. 2012 Mar; 90(3):706-14.
    View in: PubMed
    Score: 0.095
  12. Ethnic origin and extrapyramidal signs in an Argentinean spinocerebellar ataxia type 10 family. Neurology. 2007 Jul 10; 69(2):216-8.
    View in: PubMed
    Score: 0.070
  13. The role of ataxin 10 in the pathogenesis of spinocerebellar ataxia type 10. Neurology. 2006 Aug 22; 67(4):607-13.
    View in: PubMed
    Score: 0.066
  14. Ataxin 10 induces neuritogenesis via interaction with G-protein beta2 subunit. J Neurosci Res. 2006 May 15; 83(7):1170-8.
    View in: PubMed
    Score: 0.065
  15. Founder Effects of Spinocerebellar Ataxias in the American Continents and the Caribbean. Cerebellum. 2020 Jun; 19(3):446-458.
    View in: PubMed
    Score: 0.043
  16. Spinocerebellar ataxia type 10 in Peru: the missing link in the Amerindian origin of the disease. J Neurol. 2014 Sep; 261(9):1691-4.
    View in: PubMed
    Score: 0.028
  17. Expansion of the Spinocerebellar ataxia type 10 (SCA10) repeat in a patient with Sioux Native American ancestry. PLoS One. 2013; 8(11):e81342.
    View in: PubMed
    Score: 0.027
  18. Expansions, contractions, and fragility of the spinocerebellar ataxia type 10 pentanucleotide repeat in yeast. Proc Natl Acad Sci U S A. 2011 Feb 15; 108(7):2843-8.
    View in: PubMed
    Score: 0.023
  19. Symptom onset of spinocerebellar ataxia type 10 in pregnancy and puerperium. J Clin Neurosci. 2011 Mar; 18(3):437-8.
    View in: PubMed
    Score: 0.022
  20. Spinocerebellar ataxia type 10: Frequency of epilepsy in a large sample of Brazilian patients. Mov Disord. 2010 Dec 15; 25(16):2875-8.
    View in: PubMed
    Score: 0.022
  21. Inactivation of hnRNP K by expanded intronic AUUCU repeat induces apoptosis via translocation of PKCdelta to mitochondria in spinocerebellar ataxia 10. PLoS Genet. 2010 Jun 10; 6(6):e1000984.
    View in: PubMed
    Score: 0.022
  22. Reduced penetrance in a Brazilian family with spinocerebellar ataxia type 10. Arch Neurol. 2007 Apr; 64(4):591-4.
    View in: PubMed
    Score: 0.017
  23. Reduced penetrance of intermediate size alleles in spinocerebellar ataxia type 10. Neurology. 2006 May 23; 66(10):1602-4.
    View in: PubMed
    Score: 0.016
  24. Interruptions in the expanded ATTCT repeat of spinocerebellar ataxia type 10: repeat purity as a disease modifier? Am J Hum Genet. 2006 Jan; 78(1):125-9.
    View in: PubMed
    Score: 0.016
  25. Clinical phenotype of Brazilian families with spinocerebellar ataxia 10. Neurology. 2004 Oct 26; 63(8):1509-12.
    View in: PubMed
    Score: 0.015
Connection Strength

The connection strength for concepts is the sum of the scores for each matching publication.

Publication scores are based on many factors, including how long ago they were written and whether the person is a first or senior author.