Pignatti PF - Search Results

1

A tetranucleotide repeat polymorphism in the cystic fibrosis gene.

Gasparini P, Dognini M, Bonizzato A, Pignatti PF, Morral N, Estivill X. Gasparini P, et al. Among authors: pignatti pf. Hum Genet. 1991 Apr;86(6):625. doi: 10.1007/BF00201556. Hum Genet. 1991. PMID: 1709137 No abstract available.

2

Restriction site generating-polymerase chain reaction (RG-PCR) for the probeless detection of hidden genetic variation: application to the study of some common cystic fibrosis mutations.

Gasparini P, Bonizzato A, Dognini M, Pignatti PF. Gasparini P, et al. Among authors: pignatti pf. Mol Cell Probes. 1992 Feb;6(1):1-7. doi: 10.1016/0890-8508(92)90064-5. Mol Cell Probes. 1992. PMID: 1347644

3

A frameshift mutation (2869insG) in the second transmembrane domain of the CFTR gene: identification, regional distribution, and clinical presentation.

Nunes V, Bonizzato A, Gaona A, Dognini M, Chillón M, Casals T, Pignatti PF, Novelli G, Estivill X, Gasparini P. Nunes V, et al. Among authors: pignatti pf. Am J Hum Genet. 1992 May;50(5):1140-2. Am J Hum Genet. 1992. PMID: 1373935 Free PMC article. No abstract available.

4

Nine cystic fibrosis patients homozygous for the CFTR nonsense mutation R1162X have mild or moderate lung disease.

Gasparini P, Borgo G, Mastella G, Bonizzato A, Dognini M, Pignatti PF. Gasparini P, et al. Among authors: pignatti pf. J Med Genet. 1992 Aug;29(8):558-62. doi: 10.1136/jmg.29.8.558. J Med Genet. 1992. PMID: 1381442 Free PMC article.

5

A new approach for identifying non-pathogenic mutations. An analysis of the cystic fibrosis transmembrane regulator gene in normal individuals.

Bombieri C, Giorgi S, Carles S, de Cid R, Belpinati F, Tandoi C, Pallares-Ruiz N, Lazaro C, Ciminelli BM, Romey MC, Casals T, Pompei F, Gandini G, Claustres M, Estivill X, Pignatti PF, Modiano G. Bombieri C, et al. Among authors: pignatti pf. Hum Genet. 2000 Feb;106(2):172-8. doi: 10.1007/s004390051025. Hum Genet. 2000. PMID: 10746558 Free article.

6

Analysis of the entire coding region of the cystic fibrosis transmembrane regulator gene in idiopathic pancreatitis.

Castellani C, Gomez Lira M, Frulloni L, Delmarco A, Marzari M, Bonizzato A, Cavallini G, Pignatti P, Mastella G. Castellani C, et al. Hum Mutat. 2001 Aug;18(2):166. doi: 10.1002/humu.1172. Hum Mutat. 2001. PMID: 11462247

7

Forensic applications of molecular genetic analysis: an Italian collaborative study on paternity testing by the determination of variable number of tandem repeat DNA polymorphisms.

Gasparini P, Mandich P, Novelli G, Bellone E, Sangiuolo F, De Stefano F, Potenza L, Trabetti E, Marigo M, Pignatti PF, et al. Gasparini P, et al. Among authors: pignatti pf. Hum Hered. 1991;41(3):174-81. doi: 10.1159/000153997. Hum Hered. 1991. PMID: 1937491

8

The cystic fibrosis gene is not likely to be involved in chronic obstructive pulmonary disease.

Gasparini P, Savoia A, Luisetti M, Peona V, Pignatti PF. Gasparini P, et al. Among authors: pignatti pf. Am J Respir Cell Mol Biol. 1990 Mar;2(3):297-9. doi: 10.1165/ajrcmb/2.3.297. Am J Respir Cell Mol Biol. 1990. PMID: 1968751

9

Frequency distribution of the alleles of several variable number of tandem repeat DNA polymorphisms in the Italian population.

Gasparini P, Trabetti E, Savoia A, Marigo M, Pignatti PF. Gasparini P, et al. Among authors: pignatti pf. Hum Hered. 1990;40(2):61-8. doi: 10.1159/000153907. Hum Hered. 1990. PMID: 1970803

10

Regional distribution of cystic fibrosis linked DNA haplotypes in Italy, a collaborative study.

Gasparini P, Cappello N, Dallapiccola B, Devoto M, Estivill X, Ferrari M, Leoni G, Novelli G, Piazza A, Pignatti PF, et al. Gasparini P, et al. Among authors: pignatti pf. Gene Geogr. 1990 Apr;4(1):53-64. Gene Geogr. 1990. PMID: 1980604

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