Dallapiccola B - Search Results

1

Evaluation of a DHPLC-based assay for rapid detection of RET germline mutations in Italian patients with medullary thyroid carcinoma.

Torrente I, Arturi F, D'Aloiso L, Colosimo A, De Luca A, Ferretti E, Russo D, Chiefari E, Scarpelli D, Bisceglia M, Dallapiccola B, Filetti S. Torrente I, et al. Among authors: dallapiccola b. J Endocrinol Invest. 2004 Feb;27(2):111-6. doi: 10.1007/BF03346254. J Endocrinol Invest. 2004. PMID: 15129804

2

Plasmid DNA and low-frequency electromagnetic fields.

D'Agruma L, Colosimo A, Angeloni U, Novelli G, Dallapiccola B. D'Agruma L, et al. Among authors: dallapiccola b. Biomed Pharmacother. 1993;47(2-3):101-5. doi: 10.1016/0753-3322(93)90298-y. Biomed Pharmacother. 1993. PMID: 8218948

3

Detection of eight beta-thalassemia mutations using a DNA enzyme immunoassay.

Colosimo A, Novelli G, Cavicchini A, Dallapiccola B. Colosimo A, et al. Among authors: dallapiccola b. Int J Clin Lab Res. 1996;26(2):136-9. doi: 10.1007/BF02592357. Int J Clin Lab Res. 1996. PMID: 8856368

4

Two new missense mutations (A105T and C110G) in the norrin gene in two Italian families with Norrie disease and familial exudative vitreoretinopathy.

Torrente I, Mangino M, Gennarelli M, Novelli G, Giannotti A, Vadalà P, Dallapiccola B. Torrente I, et al. Among authors: dallapiccola b. Am J Med Genet. 1997 Oct 17;72(2):242-4. doi: 10.1002/(sici)1096-8628(19971017)72:2<242::aid-ajmg23>3.0.co;2-m. Am J Med Genet. 1997. PMID: 9382152 No abstract available.

5

First-trimester prenatal diagnosis of Ellis-van Creveld syndrome using linked microsatellite markers.

Torrente I, Mangino M, De Luca A, Mingarelli R, Gennarelli M, Giannotti A, Novelli G, Dallapiccola B. Torrente I, et al. Among authors: dallapiccola b. Prenat Diagn. 1998 May;18(5):504-6. Prenat Diagn. 1998. PMID: 9621386

6

From genetic research into clinical practice.

Dallapiccola B, Torrente I, Mingarelli R, Novelli G. Dallapiccola B, et al. Acta Genet Med Gemellol (Roma). 1997;46(3):139-46. doi: 10.1017/s0001566000000556. Acta Genet Med Gemellol (Roma). 1997. PMID: 9645231

7

A novel mutation (R271X) in the myotubularin gene causes a severe miotubular myopathy.

De Luca A, Torrente I, Mangino M, Bertini E, Dallapiccola B, Novelli G. De Luca A, et al. Among authors: dallapiccola b. Hum Hered. 1999 Jan;49(1):59-60. doi: 10.1159/000022843. Hum Hered. 1999. PMID: 9858861

8

A single-nucleotide polymorphism in the human bone morphogenetic protein-4 (BMP 4) gene.

Mangino M, Torrente I, De Luca A, Sanchez O, Dallapiccola B, Novelli G. Mangino M, et al. Among authors: dallapiccola b. J Hum Genet. 1999;44(1):76-7. doi: 10.1007/s100380050113. J Hum Genet. 1999. PMID: 9929985

9

Simple version of "megaprimer" PCR for site-directed mutagenesis.

Colosimo A, Xu Z, Novelli G, Dallapiccola B, Gruenert DC. Colosimo A, et al. Among authors: dallapiccola b. Biotechniques. 1999 May;26(5):870-3. doi: 10.2144/99265bm15. Biotechniques. 1999. PMID: 10337479 Free article. No abstract available.

10

Gene transfection efficiency of tracheal epithelial cells by DC-chol-DOPE/DNA complexes.

Colosimo A, Serafino A, Sangiuolo F, Di Sario S, Bruscia E, Amicucci P, Novelli G, Dallapiccola B, Mossa G. Colosimo A, et al. Among authors: dallapiccola b. Biochim Biophys Acta. 1999 Jul 15;1419(2):186-94. doi: 10.1016/s0005-2736(99)00067-x. Biochim Biophys Acta. 1999. PMID: 10407070 Free article.

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