Connection

TETSUO ASHIZAWA to Repetitive Sequences, Nucleic Acid

This is a "connection" page, showing publications TETSUO ASHIZAWA has written about Repetitive Sequences, Nucleic Acid.
  1. How much expansion to be diseased?: toward repeat size and myotonic dystrophy type 2. Neurology. 2009 Feb 10; 72(6):484-5.
    View in: PubMed
    Score: 0.282
  2. Somatic and germline instability of the ATTCT repeat in spinocerebellar ataxia type 10. Am J Hum Genet. 2004 Jun; 74(6):1216-24.
    View in: PubMed
    Score: 0.203
  3. Large expansion of the ATTCT pentanucleotide repeat in spinocerebellar ataxia type 10. Nat Genet. 2000 Oct; 26(2):191-4.
    View in: PubMed
    Score: 0.158
  4. CAG repeat size and clinical presentation in Huntington's disease. Neurology. 1994 Jun; 44(6):1137-43.
    View in: PubMed
    Score: 0.102
  5. Characteristics of intergenerational contractions of the CTG repeat in myotonic dystrophy. Am J Hum Genet. 1994 Mar; 54(3):414-23.
    View in: PubMed
    Score: 0.100
  6. Effects of the sex of myotonic dystrophy patients on the unstable triplet repeat in their affected offspring. Neurology. 1994 Jan; 44(1):120-2.
    View in: PubMed
    Score: 0.099
  7. Somatic instability of CTG repeat in myotonic dystrophy. Neurology. 1993 Dec; 43(12):2674-8.
    View in: PubMed
    Score: 0.098
  8. Anticipation in myotonic dystrophy. II. Complex relationships between clinical findings and structure of the GCT repeat. Neurology. 1992 Oct; 42(10):1877-83.
    View in: PubMed
    Score: 0.091
  9. 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: 0.077
  10. Recent progress in spinocerebellar ataxia type-10 (SCA10). Cerebellum. 2005; 4(1):37-42.
    View in: PubMed
    Score: 0.053
  11. Clinical features and ATTCT repeat expansion in spinocerebellar ataxia type 10. Arch Neurol. 2002 Aug; 59(8):1285-90.
    View in: PubMed
    Score: 0.045
  12. Polymerase chain reaction amplification of expanded ATTCT repeat in spinocerebellar ataxia type 10. Ann Neurol. 2002 Feb; 51(2):271-2.
    View in: PubMed
    Score: 0.043
  13. The GAA triplet-repeat expansion in Friedreich ataxia interferes with transcription and may be associated with an unusual DNA structure. Am J Hum Genet. 1998 Jan; 62(1):111-21.
    View in: PubMed
    Score: 0.033
  14. Cardiac involvement in a large kindred with myotonic dystrophy. Quantitative assessment and relation to size of CTG repeat expansion. JAMA. 1995 Sep 13; 274(10):813-9.
    View in: PubMed
    Score: 0.028
  15. De novo myotonic dystrophy mutation in a Nigerian kindred. Am J Hum Genet. 1995 May; 56(5):1067-74.
    View in: PubMed
    Score: 0.027
  16. An unstable triplet repeat in a gene related to myotonic muscular dystrophy. Science. 1992 Mar 06; 255(5049):1256-8.
    View in: PubMed
    Score: 0.022
  17. Huntington's Disease-like 2 (HDL2) in North America and Japan. Ann Neurol. 2004 Nov; 56(5):670-4.
    View in: PubMed
    Score: 0.013
  18. Spinocerebellar ataxia type 10 in the French population. Ann Neurol. 2002 Mar; 51(3):408-9.
    View in: PubMed
    Score: 0.011
  19. Effect of myotonic dystrophy trinucleotide repeat expansion on DMPK transcription and processing. Genomics. 1995 Jul 01; 28(1):1-14.
    View in: PubMed
    Score: 0.007
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.