Ferrari M - Search Results

1

Molecular diagnosis of genetic diseases.

Ferrari M, Cremonesi L, Carrera P, Bonini PA. Ferrari M, et al. Clin Biochem. 1996 Jun;29(3):201-8. doi: 10.1016/0009-9120(95)02022-e. Clin Biochem. 1996. PMID: 8740505 Review. No abstract available.

2

Simultaneous detection of delta F508, G542X, N1303K and 1717-1G-->A mutations in cystic fibrosis by capillary electrophoresis in polymer networks.

Gelfi C, Righetti PG, Magnani C, Cremonesi L, Ferrari M. Gelfi C, et al. Among authors: ferrari m. Clin Chim Acta. 1994 Sep;229(1-2):181-9. doi: 10.1016/0009-8981(94)90240-2. Clin Chim Acta. 1994. PMID: 7527312 No abstract available.

3

Search for mutations in pancreatic sufficient cystic fibrosis Italian patients: detection of 90% of molecular defects and identification of three novel mutations.

Brancolini V, Cremonesi L, Belloni E, Pappalardo E, Bordoni R, Seia M, Russo S, Padoan R, Giunta A, Ferrari M. Brancolini V, et al. Among authors: ferrari m. Hum Genet. 1995 Sep;96(3):312-8. doi: 10.1007/BF00210414. Hum Genet. 1995. PMID: 7544319

4

A nonsense mutation (Gln-673-Term) in exon 17 of the human dystrophin gene detected by heteroduplex analysis.

Barbieri AM, Soriani N, Tubiello GM, Ferrari M, Carrera P. Barbieri AM, et al. Among authors: ferrari m. Hum Genet. 1995 Sep;96(3):343-4. doi: 10.1007/BF00210420. Hum Genet. 1995. PMID: 7649554

5

Informativity of intragenic microsatellites for carrier detection and prenatal diagnosis of cystic fibrosis in the Italian population.

Magnani C, Cremonesi L, Belloni E, Ferrari M, Seia M, Russo MP, Devoto M, Ronchetto P, Romeo G. Magnani C, et al. Among authors: ferrari m. Clin Genet. 1994 Mar;45(3):135-9. doi: 10.1111/j.1399-0004.1994.tb04010.x. Clin Genet. 1994. PMID: 7913006

6

Substitution of Leu for Pro-193 in the insulin receptor in a patient with a genetic form of severe insulin resistance.

Carrera P, Cordera R, Ferrari M, Cremonesi L, Taramelli R, Andraghetti G, Carducci C, Dozio N, Pozza G, Taylor SI, et al. Carrera P, et al. Among authors: ferrari m. Hum Mol Genet. 1993 Sep;2(9):1437-41. doi: 10.1093/hmg/2.9.1437. Hum Mol Genet. 1993. PMID: 8242067

7

Mutational analysis of muscle and brain specific promoter regions of dystrophin gene in DMD/BMD Italian patients by denaturing gradient gel electrophoresis (DGGE).

Tubiello G, Carrera P, Soriani N, Morandi L, Ferrari M. Tubiello G, et al. Among authors: ferrari m. Mol Cell Probes. 1995 Dec;9(6):441-6. doi: 10.1006/mcpr.1995.0067. Mol Cell Probes. 1995. PMID: 8808315

8

Seven novel additional small mutations and a new alternative splicing in the human dystrophin gene detected by heteroduplex analysis and restricted RT-PCR heteroduplex analysis of illegitimate transcripts.

Barbieri AM, Soriani N, Ferlini A, Michelato A, Ferrari M, Carrera P. Barbieri AM, et al. Among authors: ferrari m. Eur J Hum Genet. 1996;4(3):183-7. doi: 10.1159/000472193. Eur J Hum Genet. 1996. PMID: 8840119

9

Genotype-phenotype correlation in cystic fibrosis patients.

Ferrari M, Cremonesi L. Ferrari M, et al. Ann Biol Clin (Paris). 1996;54(6):235-41. Ann Biol Clin (Paris). 1996. PMID: 8949420 Review.

10

Double-gradient DGGE for optimized detection of DNA point mutations.

Cremonesi L, Firpo S, Ferrari M, Righetti PG, Gelfi C. Cremonesi L, et al. Among authors: ferrari m. Biotechniques. 1997 Feb;22(2):326-30. doi: 10.2144/97222rr01. Biotechniques. 1997. PMID: 9043706 Free article.

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