Pizzuti A - Search Results

1

Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndrome.

Verkerk AJ, Pieretti M, Sutcliffe JS, Fu YH, Kuhl DP, Pizzuti A, Reiner O, Richards S, Victoria MF, Zhang FP, et al. Verkerk AJ, et al. Among authors: pizzuti a. Cell. 1991 May 31;65(5):905-14. doi: 10.1016/0092-8674(91)90397-h. Cell. 1991. PMID: 1710175

2

Variation of the CGG repeat at the fragile X site results in genetic instability: resolution of the Sherman paradox.

Fu YH, Kuhl DP, Pizzuti A, Pieretti M, Sutcliffe JS, Richards S, Verkerk AJ, Holden JJ, Fenwick RG Jr, Warren ST, et al. Fu YH, et al. Among authors: pizzuti a. Cell. 1991 Dec 20;67(6):1047-58. doi: 10.1016/0092-8674(91)90283-5. Cell. 1991. PMID: 1760838

3

A transposon-like element in the deletion-prone region of the dystrophin gene.

Pizzuti A, Pieretti M, Fenwick RG, Gibbs RA, Caskey CT. Pizzuti A, et al. Genomics. 1992 Jul;13(3):594-600. doi: 10.1016/0888-7543(92)90129-g. Genomics. 1992. PMID: 1322353

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: pizzuti a. Science. 1992 Mar 6;255(5049):1256-8. doi: 10.1126/science.1546326. Science. 1992. PMID: 1546326

5

Triplet repeat mutations in human disease.

Caskey CT, Pizzuti A, Fu YH, Fenwick RG Jr, Nelson DL. Caskey CT, et al. Among authors: pizzuti a. Science. 1992 May 8;256(5058):784-9. doi: 10.1126/science.1589758. Science. 1992. PMID: 1589758 Review.

6

Relationship between parental trinucleotide GCT repeat length and severity of myotonic dystrophy in offspring.

Redman JB, Fenwick RG Jr, Fu YH, Pizzuti A, Caskey CT. Redman JB, et al. Among authors: pizzuti a. JAMA. 1993 Apr 21;269(15):1960-5. JAMA. 1993. PMID: 8464127

7

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: pizzuti a. Science. 1993 Apr 9;260(5105):235-8. doi: 10.1126/science.8469976. Science. 1993. PMID: 8469976

8

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. Among authors: pizzuti a. Neurology. 1992 Oct;42(10):1877-83. doi: 10.1212/wnl.42.10.1877. Neurology. 1992. PMID: 1407566

9

Pentanucleotide repeat length polymorphism at the human CD4 locus.

Edwards MC, Clemens PR, Tristan M, Pizzuti A, Gibbs RA. Edwards MC, et al. Among authors: pizzuti a. Nucleic Acids Res. 1991 Sep 11;19(17):4791. doi: 10.1093/nar/19.17.4791-a. Nucleic Acids Res. 1991. PMID: 1891380 Free PMC article.

10

Assignment of the gene for a ubiquitin fusion degradation protein (Ufd1l) to mouse chromosome 16B1-B4, syntenic with the Tuple1 gene.

Botta A, Jurecic V, Pizzuti A, Novelli G, Dallapiccola B, Baldini A. Botta A, et al. Among authors: pizzuti a. Cytogenet Cell Genet. 1997;77(3-4):264-5. doi: 10.1159/000134592. Cytogenet Cell Genet. 1997. PMID: 9284932 No abstract available.

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