Novelli G - Search Results

1

Different prelamin A forms accumulate in human fibroblasts: a study in experimental models and progeria.

Dominici S, Fiori V, Magnani M, Schena E, Capanni C, Camozzi D, D'Apice MR, Le Dour C, Auclair M, Caron M, Novelli G, Vigouroux C, Maraldi NM, Lattanzi G. Dominici S, et al. Among authors: novelli g. Eur J Histochem. 2009 Jan-Mar;53(1):43-52. doi: 10.4081/ejh.2009.43. Eur J Histochem. 2009. PMID: 19351612 Free article.

2

Hexokinase in human chorionic villi.

Magnani M, Novelli G, Stocchi V. Magnani M, et al. Among authors: novelli g. Early Hum Dev. 1985 Jul;11(2):149-56. doi: 10.1016/0378-3782(85)90102-1. Early Hum Dev. 1985. PMID: 3875479

3

The strange case of the "lumper" lamin A/C gene and human premature ageing.

Novelli G, D'Apice MR. Novelli G, et al. Trends Mol Med. 2003 Sep;9(9):370-5. doi: 10.1016/s1471-4914(03)00162-x. Trends Mol Med. 2003. PMID: 13129702 Review.

4

Biochemical characterization of two GALK1 mutations in patients with galactokinase deficiency.

Sangiuolo F, Magnani M, Stambolian D, Novelli G. Sangiuolo F, et al. Among authors: novelli g. Hum Mutat. 2004 Apr;23(4):396. doi: 10.1002/humu.9223. Hum Mutat. 2004. PMID: 15024738

5

Paternal origin of LMNA mutations in Hutchinson-Gilford progeria.

D'Apice MR, Tenconi R, Mammi I, van den Ende J, Novelli G. D'Apice MR, et al. Among authors: novelli g. Clin Genet. 2004 Jan;65(1):52-4. doi: 10.1111/j..2004.00181.x. Clin Genet. 2004. PMID: 15032975 No abstract available.

6

Analysis of TNF-alpha promoter polymorphisms in the susceptibility to beryllium hypersensitivity.

Dotti C, D'Apice MR, Rogliani P, Novelli G, Saltini C, Amicosante M. Dotti C, et al. Among authors: novelli g. Sarcoidosis Vasc Diffuse Lung Dis. 2004 Mar;21(1):29-34. doi: 10.1007/s11083-004-9308-3. Sarcoidosis Vasc Diffuse Lung Dis. 2004. PMID: 15127972

7

Toward the pharmacogenomics of cystic fibrosis--an update.

Sangiuolo F, D'Apice MR, Gambardella S, Di Daniele N, Novelli G. Sangiuolo F, et al. Among authors: novelli g. Pharmacogenomics. 2004 Oct;5(7):861-78. doi: 10.1517/14622416.5.7.861. Pharmacogenomics. 2004. PMID: 15469408 Review.

8

Gene expression profiling of fibroblasts from a human progeroid disease (mandibuloacral dysplasia, MAD #248370) through cDNA microarrays.

Amati F, Biancolella M, D'Apice MR, Gambardella S, Mango R, Sbraccia P, D'Adamo M, Margiotti K, Nardone A, Lewis M, Novelli G. Amati F, et al. Among authors: novelli g. Gene Expr. 2004;12(1):39-47. doi: 10.3727/000000004783992189. Gene Expr. 2004. PMID: 15473259 Free PMC article.

9

Somatic and gonadal mosaicism in Hutchinson-Gilford progeria.

Wuyts W, Biervliet M, Reyniers E, D'Apice MR, Novelli G, Storm K. Wuyts W, et al. Among authors: novelli g. Am J Med Genet A. 2005 May 15;135(1):66-8. doi: 10.1002/ajmg.a.30663. Am J Med Genet A. 2005. PMID: 15793835

10

Altered pre-lamin A processing is a common mechanism leading to lipodystrophy.

Capanni C, Mattioli E, Columbaro M, Lucarelli E, Parnaik VK, Novelli G, Wehnert M, Cenni V, Maraldi NM, Squarzoni S, Lattanzi G. Capanni C, et al. Among authors: novelli g. Hum Mol Genet. 2005 Jun 1;14(11):1489-502. doi: 10.1093/hmg/ddi158. Epub 2005 Apr 20. Hum Mol Genet. 2005. PMID: 15843404

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