Rovida E - Search Results

1

Molecular chaperones as therapeutic targets to counteract proteostasis defects.

Cattaneo M, Dominici R, Cardano M, Diaferia G, Rovida E, Biunno I. Cattaneo M, et al. Among authors: rovida e. J Cell Physiol. 2012 Mar;227(3):1226-34. doi: 10.1002/jcp.22856. J Cell Physiol. 2012. PMID: 21618531 Review.

2

Identification of two novel frameshift mutations in the KCNJ11 gene in two Italian patients affected by Congenital Hyperinsulinism of Infancy.

Biagiotti L, Proverbio MC, Bosio L, Gervasi F, Rovida E, Cerioni V, Bove M, Valin PS, Albarello L, Zamproni I, Grassi S, Doglioni C, Mora S, Chiumello G, Biunno I. Biagiotti L, et al. Among authors: rovida e. Exp Mol Pathol. 2007 Aug;83(1):59-64. doi: 10.1016/j.yexmp.2006.11.006. Epub 2007 Jan 17. Exp Mol Pathol. 2007. PMID: 17316607

3

BRCA1 point mutations in premenopausal breast cancer patients from Central Sudan.

Biunno I, Aceto G, Awadelkarim KD, Morgano A, Elhaj A, Eltayeb EA, Abuidris DO, Elwali NE, Spinelli C, De Blasio P, Rovida E, Mariani-Costantini R. Biunno I, et al. Among authors: rovida e. Fam Cancer. 2014 Sep;13(3):437-44. doi: 10.1007/s10689-014-9717-4. Fam Cancer. 2014. PMID: 24729269

4

Cloning of a gene encoding a DNase I-like endonuclease in the human Xq28 region.

Pergolizzi R, Appierto V, Bosetti A, DeBellis GL, Rovida E, Biunno I. Pergolizzi R, et al. Among authors: rovida e. Gene. 1996 Feb 12;168(2):267-70. doi: 10.1016/0378-1119(95)00741-5. Gene. 1996. PMID: 8654957

5

Molecular characterization of a novel endonuclease (Xib) and possible involvement in lysosomal glycogen storage disorders.

Malferrari G, Mazza U, Tresoldi C, Rovida E, Nissim M, Mirabella M, Servidei S, Biunno I. Malferrari G, et al. Among authors: rovida e. Exp Mol Pathol. 1999 Jun;66(2):123-30. doi: 10.1006/exmp.1999.2254. Exp Mol Pathol. 1999. PMID: 10409440

6

Pathogenic mechanism and modeling of neuroferritinopathy.

Cozzi A, Santambrogio P, Ripamonti M, Rovida E, Levi S. Cozzi A, et al. Among authors: rovida e. Cell Mol Life Sci. 2021 Apr;78(7):3355-3367. doi: 10.1007/s00018-020-03747-w. Epub 2021 Jan 13. Cell Mol Life Sci. 2021. PMID: 33439270 Free PMC article. Review.

7

Study of FTMT and ABCA4 genes in a patient affected by age-related macular degeneration: identification and analysis of new mutations.

Stenirri S, Santambrogio P, Setaccioli M, Erba BG, Pia Manitto M, Rovida E, Ferrari M, Levi S, Cremonesi L. Stenirri S, et al. Among authors: rovida e. Clin Chem Lab Med. 2012 Jan 9;50(6):1021-9. doi: 10.1515/cclm-2011-0854. Clin Chem Lab Med. 2012. PMID: 22706241

8

Identification and computationally-based structural interpretation of naturally occurring variants of human protein C.

Rovida E, Merati G, D'Ursi P, Zanardelli S, Marino F, Fontana G, Castaman G, Faioni EM. Rovida E, et al. Hum Mutat. 2007 Apr;28(4):345-55. doi: 10.1002/humu.20445. Hum Mutat. 2007. PMID: 17152060

9

The role of the L-chain in ferritin iron incorporation. Studies of homo and heteropolymers.

Levi S, Santambrogio P, Cozzi A, Rovida E, Corsi B, Tamborini E, Spada S, Albertini A, Arosio P. Levi S, et al. Among authors: rovida e. J Mol Biol. 1994 May 20;238(5):649-54. doi: 10.1006/jmbi.1994.1325. J Mol Biol. 1994. PMID: 8182740

10

ProCMD: a database and 3D web resource for protein C mutants.

D'Ursi P, Marino F, Caprera A, Milanesi L, Faioni EM, Rovida E. D'Ursi P, et al. Among authors: rovida e. BMC Bioinformatics. 2007 Mar 8;8 Suppl 1(Suppl 1):S11. doi: 10.1186/1471-2105-8-S1-S11. BMC Bioinformatics. 2007. PMID: 17430555 Free PMC article.

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