Ferrari M - Search Results

1

A new polymorphism in exon 14 of the dystrophin gene detected by RT-PCR and DGGE.

Barbieri AM, Soriani N, Ferrari M, Carrera P. Barbieri AM, et al. Among authors: ferrari m. Mol Cell Probes. 1997 Apr;11(2):161-2. doi: 10.1006/mcpr.1996.0092. Mol Cell Probes. 1997. PMID: 9160332 No abstract available.

2

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

3

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

4

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

5

Capillary zone electrophoresis in polymer networks of polymerase chain reaction-amplified oligonucleotides: the case of congenital adrenal hyperplasia.

Gelfi C, Orsi A, Righetti PG, Zanussi M, Carrera P, Ferrari M. Gelfi C, et al. Among authors: ferrari m. J Chromatogr B Biomed Appl. 1994 Jul 1;657(1):201-5. doi: 10.1016/0378-4347(94)80088-x. J Chromatogr B Biomed Appl. 1994. PMID: 7952069

6

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.

7

Rapid detection of 21-hydroxylase deficiency mutations by allele-specific in vitro amplification and capillary zone electrophoresis.

Carrera P, Barbieri AM, Ferrari M, Righetti PG, Perego M, Gelfi C. Carrera P, et al. Among authors: ferrari m. Clin Chem. 1997 Nov;43(11):2121-7. Clin Chem. 1997. PMID: 9365397

8

Detection of rifampin resistance in Mycobacterium tuberculosis by double gradient-denaturing gradient gel electrophoresis.

Scarpellini P, Braglia S, Carrera P, Cedri M, Cichero P, Colombo A, Crucianelli R, Gori A, Ferrari M, Lazzarin A. Scarpellini P, et al. Among authors: ferrari m. Antimicrob Agents Chemother. 1999 Oct;43(10):2550-4. doi: 10.1128/AAC.43.10.2550. Antimicrob Agents Chemother. 1999. PMID: 10508043 Free PMC article.

9

Double-gradient denaturing gradient gel electrophoresis assay for identification of L-ferritin iron-responsive element mutations responsible for hereditary hyperferritinemia-cataract syndrome: identification of the new mutation C14G.

Cremonesi L, Fumagalli A, Soriani N, Ferrari M, Levi S, Belloli S, Ruggeri G, Arosio P. Cremonesi L, et al. Among authors: ferrari m. Clin Chem. 2001 Mar;47(3):491-7. Clin Chem. 2001. PMID: 11238302

10

Mutational scanning of the ABCR gene with double-gradient denaturing-gradient gel electrophoresis (DG-DGGE) in Italian Stargardt disease patients.

Fumagalli A, Ferrari M, Soriani N, Gessi A, Foglieni B, Martina E, Manitto MP, Brancato R, Dean M, Allikmets R, Cremonesi L. Fumagalli A, et al. Among authors: ferrari m. Hum Genet. 2001 Sep;109(3):326-38. doi: 10.1007/s004390100583. Hum Genet. 2001. PMID: 11702214

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