The world's first wiki where authorship really matters (Nature Genetics, 2008). Due credit and reputation for authors. Imagine a global collaborative knowledge base for original thoughts. Search thousands of articles and collaborate with scientists around the globe.

wikigene or wiki gene protein drug chemical gene disease author authorship tracking collaborative publishing evolutionary knowledge reputation system wiki2.0 global collaboration genes proteins drugs chemicals diseases compound
Hoffmann, R. A wiki for the life sciences where authorship matters. Nature Genetics (2008)
 
MeSH Review

Trinucleotide Repeat Expansion

 
 
Welcome! If you are familiar with the subject of this article, you can contribute to this open access knowledge base by deleting incorrect information, restructuring or completely rewriting any text. Read more.
 

Disease relevance of Trinucleotide Repeat Expansion

 

High impact information on Trinucleotide Repeat Expansion

 

Biological context of Trinucleotide Repeat Expansion

 

Gene context of Trinucleotide Repeat Expansion

References

  1. Elevated levels of FMR1 mRNA in carrier males: a new mechanism of involvement in the fragile-X syndrome. Tassone, F., Hagerman, R.J., Taylor, A.K., Gane, L.W., Godfrey, T.E., Hagerman, P.J. Am. J. Hum. Genet. (2000) [Pubmed]
  2. Ataxin-2 and huntingtin interact with endophilin-A complexes to function in plastin-associated pathways. Ralser, M., Nonhoff, U., Albrecht, M., Lengauer, T., Wanker, E.E., Lehrach, H., Krobitsch, S. Hum. Mol. Genet. (2005) [Pubmed]
  3. Autonomic dysfunction in Machado-Joseph disease. Yeh, T.H., Lu, C.S., Chou, Y.H., Chong, C.C., Wu, T., Han, N.H., Chen, R.S. Arch. Neurol. (2005) [Pubmed]
  4. Preliminary evidence of genetic anticipation in Graves' disease. Brix, T.H., Petersen, H.C., Iachine, I., Hegedüs, L. Thyroid (2003) [Pubmed]
  5. Decreased expression of DMPK: correlation with CTG repeat expansion and fibre type composition in myotonic dystrophy type 1. Salvatori, S., Fanin, M., Trevisan, C.P., Furlan, S., Reddy, S., Nagy, J.I., Angelini, C. Neurol. Sci. (2005) [Pubmed]
  6. FRA10B structure reveals common elements in repeat expansion and chromosomal fragile site genesis. Hewett, D.R., Handt, O., Hobson, L., Mangelsdorf, M., Eyre, H.J., Baker, E., Sutherland, G.R., Schuffenhauer, S., Mao, J.I., Richards, R.I. Mol. Cell (1998) [Pubmed]
  7. Regional and cellular expression of the dentatorubral-pallidoluysian atrophy gene in brains of normal and affected individuals. Nishiyama, K., Nakamura, K., Murayama, S., Yamada, M., Kanazawa, I. Ann. Neurol. (1997) [Pubmed]
  8. Huntington's disease gene: regional and cellular expression in brain of normal and affected individuals. Landwehrmeyer, G.B., McNeil, S.M., Dure, L.S., Ge, P., Aizawa, H., Huang, Q., Ambrose, C.M., Duyao, M.P., Bird, E.D., Bonilla, E. Ann. Neurol. (1995) [Pubmed]
  9. Single-stranded DNA binding proteins isolated from mouse brain recognize specific trinucleotide repeat sequences in vitro. Yano-Yanagisawa, H., Li, Y., Wang, H., Kohwi, Y. Nucleic Acids Res. (1995) [Pubmed]
  10. Autosomal dominant chorea-acanthocytosis with polyglutamine-containing neuronal inclusions. Walker, R.H., Morgello, S., Davidoff-Feldman, B., Melnick, A., Walsh, M.J., Shashidharan, P., Brin, M.F. Neurology (2002) [Pubmed]
  11. Detection of radiation and cyclophosphamide-induced mutations in individual mouse sperm at a human expanded trinucleotide repeat locus transgene. Zhang, Y., Monckton, D.G., Siciliano, M.J., Connor, T.H., Meistrich, M.L. Mutat. Res. (2002) [Pubmed]
  12. Nonrandom X inactivation and selection of fragile X full mutation in fetal fibroblasts. Sun, Y.J., Baumer, A. Am. J. Med. Genet. (1999) [Pubmed]
  13. Ophthalmological findings in patients with spinocerebellar ataxia type 1 are not correlated with neurological anticipation. Abe, T., Abe, K., Tsuda, T., Itoyama, Y., Tamai, M. Graefes Arch. Clin. Exp. Ophthalmol. (2001) [Pubmed]
  14. Huntington's disease. Gusella, J.F., MacDonald, M.E. Semin. Cell Biol. (1995) [Pubmed]
  15. Structure and expression of the Huntington's disease gene: evidence against simple inactivation due to an expanded CAG repeat. Ambrose, C.M., Duyao, M.P., Barnes, G., Bates, G.P., Lin, C.S., Srinidhi, J., Baxendale, S., Hummerich, H., Lehrach, H., Altherr, M. Somat. Cell Mol. Genet. (1994) [Pubmed]
  16. Detection of expanded CAG repeats in bipolar affective disorder using the repeat expansion detection (RED) method. Lindblad, K., Nylander, P.O., De bruyn, A., Sourey, D., Zander, C., Engström, C., Holmgren, G., Hudson, T., Chotai, J., Mendlewicz, J. Neurobiol. Dis. (1995) [Pubmed]
  17. Anterior cingulate cortical transplantation in transgenic Huntington's disease mice. van Dellen, A., Deacon, R., York, D., Blakemore, C., Hannan, A.J. Brain Res. Bull. (2001) [Pubmed]
  18. Clinical and electrophysiological features in Chinese patients with Kennedy's disease. Hui, A.C., Cheung, P.T., Tang, A.S., Fu, M., Wong, L., Kay, R. Clinical neurology and neurosurgery. (2004) [Pubmed]
 
WikiGenes - Universities