Ashizawa T - Search Results

1

Decreased expression of myotonin-protein kinase messenger RNA and protein in adult form of myotonic dystrophy.

Fu YH, Friedman DL, Richards S, Pearlman JA, Gibbs RA, Pizzuti A, Ashizawa T, Perryman MB, Scarlato G, Fenwick RG Jr, et al. Fu YH, et al. Among authors: ashizawa t. Science. 1993 Apr 9;260(5105):235-8. doi: 10.1126/science.8469976. Science. 1993. PMID: 8469976

2

Anticipation in myotonic dystrophy. II. Complex relationships between clinical findings and structure of the GCT repeat.

Ashizawa T, Dubel JR, Dunne PW, Dunne CJ, Fu YH, Pizzuti A, Caskey CT, Boerwinkle E, Perryman MB, Epstein HF, et al. Ashizawa T, et al. Neurology. 1992 Oct;42(10):1877-83. doi: 10.1212/wnl.42.10.1877. Neurology. 1992. PMID: 1407566

3

Phenotypic expression of the myotonic dystrophy gene in monozygotic twins.

Dubel JR, Armstrong RM, Perryman MB, Epstein HF, Ashizawa T. Dubel JR, et al. Among authors: ashizawa t. Neurology. 1992 Sep;42(9):1815-7. doi: 10.1212/wnl.42.9.1815. Neurology. 1992. PMID: 1513473

4

An unstable triplet repeat in a gene related to myotonic muscular dystrophy.

Fu YH, Pizzuti A, Fenwick RG Jr, King J, Rajnarayan S, Dunne PW, Dubel J, Nasser GA, Ashizawa T, de Jong P, et al. Fu YH, et al. Among authors: ashizawa t. Science. 1992 Mar 6;255(5049):1256-8. doi: 10.1126/science.1546326. Science. 1992. PMID: 1546326

5

Diagnostic value of ophthalmologic findings in myotonic dystrophy: comparison with risks calculated by haplotype analysis of closely linked restriction fragment length polymorphisms.

Ashizawa T, Hejtmancik JF, Liu J, Perryman MB, Epstein HF, Koch DD. Ashizawa T, et al. Am J Med Genet. 1992 Jan 1;42(1):55-60. doi: 10.1002/ajmg.1320420113. Am J Med Genet. 1992. PMID: 1364051

6

Anticipation in myotonic dystrophy. I. Statistical verification based on clinical and haplotype findings.

Ashizawa T, Dunne CJ, Dubel JR, Perryman MB, Epstein HF, Boerwinkle E, Hejtmancik JF. Ashizawa T, et al. Neurology. 1992 Oct;42(10):1871-7. doi: 10.1212/wnl.42.10.1871. Neurology. 1992. PMID: 1407565

7

cDNA surveying of specific tissue expression of human chromosome 19 sequences.

Dunne PW, Wang SW, Ashizawa T, Perryman MB, Epstein HF. Dunne PW, et al. Among authors: ashizawa t. Genomics. 1992 Oct;14(2):263-9. doi: 10.1016/s0888-7543(05)80215-0. Genomics. 1992. PMID: 1427842

8

Characteristics of intergenerational contractions of the CTG repeat in myotonic dystrophy.

Ashizawa T, Anvret M, Baiget M, Barceló JM, Brunner H, Cobo AM, Dallapiccola B, Fenwick RG Jr, Grandell U, Harley H, et al. Ashizawa T, et al. Am J Hum Genet. 1994 Mar;54(3):414-23. Am J Hum Genet. 1994. PMID: 8116611 Free PMC article.

9

Characterization of a YAC and cosmid contig containing markers tightly linked to the myotonic dystrophy locus on chromosome 19.

Buxton J, Shelbourne P, Davies J, Jones C, Perryman MB, Ashizawa T, Butler R, Brook D, Shaw D, de Jong P, et al. Buxton J, et al. Among authors: ashizawa t. Genomics. 1992 Jul;13(3):526-31. doi: 10.1016/0888-7543(92)90120-h. Genomics. 1992. PMID: 1639381

10

NcoI and TaqI RFLPs for human M creatine kinase (CKM).

Perryman MB, Hejtmancik JF, Ashizawa T, Armstrong R, Lin SC, Roberts R, Epstein HF. Perryman MB, et al. Among authors: ashizawa t. Nucleic Acids Res. 1988 Sep 12;16(17):8744. doi: 10.1093/nar/16.17.8744. Nucleic Acids Res. 1988. PMID: 2901731 Free PMC article. No abstract available.

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