Pieretti M - Search Results

1

Alu-primed polymerase chain reaction for regional assignment of 110 yeast artificial chromosome clones from the human X chromosome: identification of clones associated with a disease locus.

Nelson DL, Ballabio A, Victoria MF, Pieretti M, Bies RD, Gibbs RA, Maley JA, Chinault AC, Webster TD, Caskey CT. Nelson DL, et al. Among authors: pieretti m. Proc Natl Acad Sci U S A. 1991 Jul 15;88(14):6157-61. doi: 10.1073/pnas.88.14.6157. Proc Natl Acad Sci U S A. 1991. PMID: 2068096 Free PMC article.

2

The sulfatase gene family: cross-species PCR cloning using the MOPAC technique.

Grompe M, Pieretti M, Caskey CT, Ballabio A. Grompe M, et al. Among authors: pieretti m. Genomics. 1992 Apr;12(4):755-60. doi: 10.1016/0888-7543(92)90306-d. Genomics. 1992. PMID: 1572648

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. Among authors: pieretti m. Genomics. 1992 Jul;13(3):594-600. doi: 10.1016/0888-7543(92)90129-g. Genomics. 1992. PMID: 1322353

4

Rapid assembly of lambda phage contigs within YAC clones.

Pieretti M, Tonlorenzi R, Ballabio A. Pieretti M, et al. Nucleic Acids Res. 1991 May 25;19(10):2795-6. doi: 10.1093/nar/19.10.2795. Nucleic Acids Res. 1991. PMID: 1828295 Free PMC article.

5

Absence of expression of the FMR-1 gene in fragile X syndrome.

Pieretti M, Zhang FP, Fu YH, Warren ST, Oostra BA, Caskey CT, Nelson DL. Pieretti M, et al. Cell. 1991 Aug 23;66(4):817-22. doi: 10.1016/0092-8674(91)90125-i. Cell. 1991. PMID: 1878973

6

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: pieretti m. Cell. 1991 May 31;65(5):905-14. doi: 10.1016/0092-8674(91)90397-h. Cell. 1991. PMID: 1710175

7

A gene deleted in Kallmann's syndrome shares homology with neural cell adhesion and axonal path-finding molecules.

Franco B, Guioli S, Pragliola A, Incerti B, Bardoni B, Tonlorenzi R, Carrozzo R, Maestrini E, Pieretti M, Taillon-Miller P, Brown CJ, Willard HF, Lawrence C, Graziella Persico M, Camerino G, Ballabio A. Franco B, et al. Among authors: pieretti m. Nature. 1991 Oct 10;353(6344):529-36. doi: 10.1038/353529a0. Nature. 1991. PMID: 1922361

8

DNA methylation represses FMR-1 transcription in fragile X syndrome.

Sutcliffe JS, Nelson DL, Zhang F, Pieretti M, Caskey CT, Saxe D, Warren ST. Sutcliffe JS, et al. Among authors: pieretti m. Hum Mol Genet. 1992 Sep;1(6):397-400. doi: 10.1093/hmg/1.6.397. Hum Mol Genet. 1992. PMID: 1301913

9

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: pieretti m. Cell. 1991 Dec 20;67(6):1047-58. doi: 10.1016/0092-8674(91)90283-5. Cell. 1991. PMID: 1760838

10

Multiple primer pairs polymerase chain reaction for the detection of human papillomavirus types.

Anceschi MM, Falcinelli C, Pieretti M, Cosmi EV. Anceschi MM, et al. Among authors: pieretti m. J Virol Methods. 1990 Apr;28(1):59-65. doi: 10.1016/0166-0934(90)90087-v. J Virol Methods. 1990. PMID: 2161420

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