Vitiello L - Search Results

1

Loss-of-function mutation of the GPR40 gene associates with abnormal stimulated insulin secretion by acting on intracellular calcium mobilization.

Vettor R, Granzotto M, De Stefani D, Trevellin E, Rossato M, Farina MG, Milan G, Pilon C, Nigro A, Federspil G, Vigneri R, Vitiello L, Rizzuto R, Baratta R, Frittitta L. Vettor R, et al. Among authors: vitiello l. J Clin Endocrinol Metab. 2008 Sep;93(9):3541-50. doi: 10.1210/jc.2007-2680. Epub 2008 Jun 26. J Clin Endocrinol Metab. 2008. PMID: 18583466

2

Fine analysis of the short arm of chromosome 1 in sporadic and familial pheochromocytoma.

Opocher G, Schiavi F, Vettori A, Pampinella F, Vitiello L, Calderan A, Vianello B, Murgia A, Martella M, Taccaliti A, Mantero F, Mostacciuolo ML. Opocher G, et al. Among authors: vitiello l. Clin Endocrinol (Oxf). 2003 Dec;59(6):707-15. doi: 10.1046/j.1365-2265.2003.01910.x. Clin Endocrinol (Oxf). 2003. PMID: 14974911

3

The glucose-dependent insulinotropic polypeptide receptor is overexpressed amongst GNAS1 mutation-negative somatotropinomas and drives growth hormone (GH)-promoter activity in GH3 cells.

Occhi G, Losa M, Albiger N, Trivellin G, Regazzo D, Scanarini M, Monteserin-Garcia JL, Fröhlich B, Ferasin S, Terreni MR, Fassina A, Vitiello L, Stalla G, Mantero F, Scaroni C. Occhi G, et al. Among authors: vitiello l. J Neuroendocrinol. 2011 Jul;23(7):641-9. doi: 10.1111/j.1365-2826.2011.02155.x. J Neuroendocrinol. 2011. PMID: 21554434

4

Analysis of differential lipofection efficiency in primary and established myoblasts.

Pampinella F, Lechardeur D, Zanetti E, MacLachlan I, Benharouga M, Lukacs GL, Vitiello L. Pampinella F, et al. Among authors: vitiello l. Mol Ther. 2002 Feb;5(2):161-9. doi: 10.1006/mthe.2002.0528. Mol Ther. 2002. PMID: 11829523 Free article.

5

A novel loss-of-function LGI1 mutation linked to autosomal dominant lateral temporal epilepsy.

Striano P, de Falco A, Diani E, Bovo G, Furlan S, Vitiello L, Pinardi F, Striano S, Michelucci R, de Falco FA, Nobile C. Striano P, et al. Among authors: vitiello l. Arch Neurol. 2008 Jul;65(7):939-42. doi: 10.1001/archneur.65.7.939. Arch Neurol. 2008. PMID: 18625862

6

Dystrophin-positive fibers in Duchenne dystrophy: origin and correlation to clinical course.

Fanin M, Danieli GA, Cadaldini M, Miorin M, Vitiello L, Angelini C. Fanin M, et al. Among authors: vitiello l. Muscle Nerve. 1995 Oct;18(10):1115-20. doi: 10.1002/mus.880181007. Muscle Nerve. 1995. PMID: 7659105

7

Transfection of cultured myoblasts in high serum concentration with DODAC:DOPE liposomes.

Vitiello L, Bockhold K, Joshi PB, Worton RG. Vitiello L, et al. Gene Ther. 1998 Oct;5(10):1306-13. doi: 10.1038/sj.gt.3300729. Gene Ther. 1998. PMID: 9930335

8

Macrophage-secreted factors enhance the in vitro expansion of DMD muscle precursor cells while preserving their myogenic potential.

Malerba A, Pasut A, Frigo M, De Coppi P, Baroni MD, Vitiello L. Malerba A, et al. Among authors: vitiello l. Neurol Res. 2010 Feb;32(1):55-62. doi: 10.1179/174313209X380865. Epub 2008 Dec 23. Neurol Res. 2010. PMID: 19108751

9

Three-dimensional porous scaffold allows long-term wild-type cell delivery in dystrophic muscle.

Carnio S, Serena E, Rossi CA, De Coppi P, Elvassore N, Vitiello L. Carnio S, et al. Among authors: vitiello l. J Tissue Eng Regen Med. 2011 Jan;5(1):1-10. doi: 10.1002/term.282. J Tissue Eng Regen Med. 2011. PMID: 20607681

10

A 3' consensus splice mutation in the human dystrophin gene detected by a screening for intra-exonic deletions.

Saad FA, Vitiello L, Merlini L, Mostacciuolo ML, Oliviero S, Danieli GA. Saad FA, et al. Among authors: vitiello l. Hum Mol Genet. 1992 Aug;1(5):345-6. doi: 10.1093/hmg/1.5.345. Hum Mol Genet. 1992. PMID: 1303213 No abstract available.

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