Novelli G - Search Results

1

Gene expression profile study in CFTR mutated bronchial cell lines.

Gambardella S, Biancolella M, D'Apice MR, Amati F, Sangiuolo F, Farcomeni A, Chillemi G, Bueno S, Desideri A, Novelli G. Gambardella S, et al. Among authors: novelli g. Clin Exp Med. 2006 Dec;6(4):157-65. doi: 10.1007/s10238-006-0116-5. Clin Exp Med. 2006. PMID: 17191107

2

Polymerase chain reaction in the detection of mRNA transcripts from the slow skeletal troponin T (TNNT1) gene in myotonic dystrophy and normal muscle.

Novelli G, Gennarelli M, Zelano G, Sangiuolo F, Lo Cicero S, Samson F, Dallapiccola B. Novelli G, et al. Cell Biochem Funct. 1992 Dec;10(4):251-6. doi: 10.1002/cbf.290100407. Cell Biochem Funct. 1992. PMID: 1473264

3

[The correlation between the genotype and the clinical expression of cystic fibrosis].

Lucidi V, Novelli G, Castro M, Sangiuolo F, Papadatou B, Ferretti F, Orrù M, Dallapiccola B. Lucidi V, et al. Among authors: novelli g. Pediatr Med Chir. 1992 Sep-Oct;14(5):513-5. Pediatr Med Chir. 1992. PMID: 1488308 Italian.

4

The cystic fibrosis delta F508 mutation in the Albanian population.

Novelli G, Sangiuolo F, Mokini V, Cikuli M, Piazza A, Dallapiccola B. Novelli G, et al. Am J Hum Genet. 1992 Apr;50(4):875-6. Am J Hum Genet. 1992. PMID: 1550133 Free PMC article. No abstract available.

5

A serine-to-arginine (AGT-to-CGT) mutation in codon 549 of the CFTR gene in an Italian patient with severe cystic fibrosis.

Sangiuolo F, Novelli G, Murru S, Dallapiccola B. Sangiuolo F, et al. Among authors: novelli g. Genomics. 1991 Apr;9(4):788-9. doi: 10.1016/0888-7543(91)90380-w. Genomics. 1991. PMID: 1903761 No abstract available.

6

The search for south European cystic fibrosis mutations: identification of two new mutations, four variants, and intronic sequences.

Gasparini P, Nunes V, Savoia A, Dognini M, Morral N, Gaona A, Bonizzato A, Chillon M, Sangiuolo F, Novelli G, et al. Gasparini P, et al. Among authors: novelli g. Genomics. 1991 May;10(1):193-200. doi: 10.1016/0888-7543(91)90500-e. Genomics. 1991. PMID: 2045102

7

Polymorphic DNA haplotypes and delta F508 deletion in 212 Italian CF families.

Novelli G, Gasparini P, Savoia A, Pignatti PF, Sangiuolo F, Dallapiccola B. Novelli G, et al. Hum Genet. 1990 Sep;85(4):420-1. doi: 10.1007/BF02428291. Hum Genet. 1990. PMID: 2210757

8

Molecular characterization of a frameshift mutation in exon 19 of the CFTR gene.

Sangiuolo F, Lo Cicero S, Maceratesi P, Quattrucci S, Novelli G, Dallapiccola B. Sangiuolo F, et al. Among authors: novelli g. Hum Mutat. 1993;2(5):422-4. doi: 10.1002/humu.1380020517. Hum Mutat. 1993. PMID: 7504970 No abstract available.

9

The up-to-date molecular genetics of cystic fibrosis.

Novelli G, Sangiuolo F, Maceratesi P, Dallapiccola B. Novelli G, et al. Biomed Pharmacother. 1994;48(10):455-63. doi: 10.1016/0753-3322(94)90006-x. Biomed Pharmacother. 1994. PMID: 7532022 Review. No abstract available.

10

Analysis of the elastin gene in 60 patients with clinical diagnosis of Williams syndrome.

Mari A, Amati F, Mingarelli R, Giannotti A, Sebastio G, Colloridi V, Novelli G, Dallapiccola B. Mari A, et al. Among authors: novelli g. Hum Genet. 1995 Oct;96(4):444-8. doi: 10.1007/BF00191804. Hum Genet. 1995. PMID: 7557968

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