Skip to main page content
Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

My NCBI Filters
Text availability
Article attribute
Article type
Publication date

Search Results

2,311 results
Filters applied: . Clear all Results are displayed in a computed author sort order. Results by year timeline is unavailable
Page 1
Amino acid sequences flanking polyglutamine stretches influence their potential for aggregate formation.
Nozaki K, Onodera O, Takano H, Tsuji S. Nozaki K, et al. Neuroreport. 2001 Oct 29;12(15):3357-64. doi: 10.1097/00001756-200110290-00042. Neuroreport. 2001. PMID: 11711886
These results are in agreement with the clinical observation that ages of disease onset in patients with spinocerebellar ataxia type 2 or Huntington's disease are lower than those in patients with DRPLA or Machado-Joseph disease having expanded CAG repeats of the same leng …
These results are in agreement with the clinical observation that ages of disease onset in patients with spinocerebellar ataxia type 2 or Hu …
Molecular genetics of triplet repeats: unstable expansion of triplet repeats as a new mechanism for neurodegenerative diseases.
Tsuji S. Tsuji S. Intern Med. 1997 Jan;36(1):3-8. doi: 10.2169/internalmedicine.36.3. Intern Med. 1997. PMID: 9058092 Review.
Expansion of trinucleotide repeats has been identified as a common mechanism of hereditary neurodegenerative diseases including spinal and bulbar muscular atrophy (SBMA), Huntington's disease, dentatorubral-pallidoluysian atrophy (DRPLA), Machado-Joseph disease (MJD), frag …
Expansion of trinucleotide repeats has been identified as a common mechanism of hereditary neurodegenerative diseases including spinal and b …
A novel long and unstable CAG/CTG trinucleotide repeat on chromosome 17q.
Ikeuchi T, Sanpei K, Takano H, Sasaki H, Tashiro K, Cancel G, Brice A, Bird TD, Schellenberg GD, Pericak-Vance MA, Welsh-Bohmer KA, Clark LN, Wilhelmsen K, Tsuji S. Ikeuchi T, et al. Genomics. 1998 Apr 15;49(2):321-6. doi: 10.1006/geno.1998.5266. Genomics. 1998. PMID: 9598323
The CAG/CTG repeat is highly polymorphic, with a heterozygosity of 85%, and exhibits a bimodal distribution (allele S, 10-26 repeat units, and allele L, 50-92 repeat units). ...
The CAG/CTG repeat is highly polymorphic, with a heterozygosity of 85%, and exhibits a bimodal distribution (allele S, 10-26 repeat u …
Thalamic form of Creutzfeldt-Jakob disease or fatal insomnia? Report of a sporadic case with normal prion protein genotype.
Kawasaki K, Wakabayashi K, Kawakami A, Higuchi M, Kitamoto T, Tsuji S, Takahashi H. Kawasaki K, et al. Acta Neuropathol. 1997 Mar;93(3):317-22. doi: 10.1007/s004010050621. Acta Neuropathol. 1997. PMID: 9083566
Machado-Joseph disease gene products carrying different carboxyl termini.
Goto J, Watanabe M, Ichikawa Y, Yee SB, Ihara N, Endo K, Igarashi S, Takiyama Y, Gaspar C, Maciel P, Tsuji S, Rouleau GA, Kanazawa I. Goto J, et al. Neurosci Res. 1997 Aug;28(4):373-7. doi: 10.1016/s0168-0102(97)00056-4. Neurosci Res. 1997. PMID: 9274833 Review.
Refined genetic location of the chromosome 2p-linked progressive muscular dystrophy gene.
Illarioshkin SN, Ivanova-Smolenskaya IA, Tanaka H, Poleshchuk VV, Markova ED, Tsuji S. Illarioshkin SN, et al. Genomics. 1997 Jun 1;42(2):345-8. doi: 10.1006/geno.1997.4725. Genomics. 1997. PMID: 9192858
2,311 results
Jump to page
Feedback