Novelli G - Search Results

1

In vitro restoration of functional SMN protein in human trophoblast cells affected by spinal muscular atrophy by small fragment homologous replacement.

Sangiuolo F, Filareto A, Spitalieri P, Scaldaferri ML, Mango R, Bruscia E, Citro G, Brunetti E, De Felici M, Novelli G. Sangiuolo F, et al. Among authors: novelli g. Hum Gene Ther. 2005 Jul;16(7):869-80. doi: 10.1089/hum.2005.16.869. Hum Gene Ther. 2005. PMID: 16000068

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

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

4

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.

5

A new method for direct analysis of polymerase chain reaction-amplified human papillomavirus using DNA enzyme immunoassay.

Sangiuolo F, De Santis L, Cavicchini A, Angeloni U, Romanini C, Novelli G, Dallapiccola B. Sangiuolo F, et al. Among authors: novelli g. Int J Clin Lab Res. 1994;24(4):223-6. doi: 10.1007/BF02592468. Int J Clin Lab Res. 1994. PMID: 7894049

6

Isolation and cloning by a polymerase chain reaction of a genomic DNA fragment of the human slow skeletal troponin (TNNT1) gene.

Novelli G, Gennarelli M, Sangiuolo F, D'Agruma L, Lo Cicero S, Melchionda S, Dallapiccola B. Novelli G, et al. Cell Biochem Funct. 1993 Sep;11(3):187-91. doi: 10.1002/cbf.290110306. Cell Biochem Funct. 1993. PMID: 8403232

7

Simultaneous detection of delta F508, G542X, N1303K, G551D, and 1717-1G-->A cystic fibrosis alleles by a multiplex DNA enzyme immunoassay.

Sangiuolo F, Maceratesi P, Mesoraca A, Botta A, Cavicchini A, Novelli G, Dallapiccola B. Sangiuolo F, et al. Among authors: novelli g. Int J Clin Lab Res. 1995;25(3):142-5. doi: 10.1007/BF02592555. Int J Clin Lab Res. 1995. PMID: 8562976

8

Non-invasive early prenatal molecular diagnosis using retrieved transcervical trophoblast cells.

Massari A, Novelli G, Colosimo A, Sangiuolo F, Palka G, Calabrese G, Camurri L, Ghirardini G, Milani G, Giorlandino C, Gazzanelli G, Malatesta M, Romanini C, Dallapiccola B. Massari A, et al. Among authors: novelli g. Hum Genet. 1996 Feb;97(2):150-5. doi: 10.1007/BF02265257. Hum Genet. 1996. PMID: 8566945

9

Deletion analysis of the simple tandem repeat loci physically linked to the spinal muscular atrophy locus.

Capon F, Levato C, Bussaglia E, Lo Cicero S, Tizzano EF, Baiget M, Silani V, Pizzuti A, Novelli G, Dallapiccola B. Capon F, et al. Among authors: novelli g. Hum Mutat. 1996;7(3):198-201. doi: 10.1002/(SICI)1098-1004(1996)7:3<198::AID-HUMU3>3.0.CO;2-7. Hum Mutat. 1996. PMID: 8829652

10

Discordant clinical outcome in type III spinal muscular atrophy sibships showing the same deletion pattern.

Capon F, Levato C, Merlini L, Angelini C, Mostacciuolo ML, Politano L, Novelli G, Dallapiccola B. Capon F, et al. Among authors: novelli g. Neuromuscul Disord. 1996 Aug;6(4):261-4. doi: 10.1016/0960-8966(96)00350-1. Neuromuscul Disord. 1996. PMID: 8887955

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