Rossi V - Search Results

1

A 2.6 Mb deletion of 6q24.3-25.1 in a patient with growth failure, cardiac septal defect, thin upperlip and asymmetric dysmorphic ears.

Caselli R, Mencarelli MA, Papa FT, Uliana V, Schiavone S, Strambi M, Pescucci C, Ariani F, Rossi V, Longo I, Meloni I, Renieri A, Mari F. Caselli R, et al. Among authors: rossi v. Eur J Med Genet. 2007 Jul-Aug;50(4):315-21. doi: 10.1016/j.ejmg.2007.03.003. Epub 2007 Apr 14. Eur J Med Genet. 2007. PMID: 17512813

2

MECP2 gene mutation analysis in the British and Italian Rett Syndrome patients: hot spot map of the most recurrent mutations and bioinformatic analysis of a new MECP2 conserved region.

Vacca M, Filippini F, Budillon A, Rossi V, Della Ragione F, De Bonis ML, Mercadante G, Manzati E, Gualandi F, Bigoni S, Trabanelli C, Pini G, Calzolari E, Ferlini A, Meloni I, Hayek G, Zappella M, Renieri A, D'Urso M, D'Esposito M, Macdonald F, Kerr A, Dhanjal S, Hulten M. Vacca M, et al. Among authors: rossi v. Brain Dev. 2001 Dec;23 Suppl 1:S246-50. doi: 10.1016/s0387-7604(01)00343-6. Brain Dev. 2001. PMID: 11738884

3

Mutation analysis of the MECP2 gene in British and Italian Rett syndrome females.

Vacca M, Filippini F, Budillon A, Rossi V, Mercadante G, Manzati E, Gualandi F, Bigoni S, Trabanelli C, Pini G, Calzolari E, Ferlini A, Meloni I, Hayek G, Zappella M, Renieri A, D'Urso M, D'Esposito M, MacDonald F, Kerr A, Dhanjal S, Hultén M. Vacca M, et al. Among authors: rossi v. J Mol Med (Berl). 2001;78(11):648-55. doi: 10.1007/s001090000155. J Mol Med (Berl). 2001. PMID: 11269512

4

Mutation in human desmoplakin domain binding to plakoglobin causes a dominant form of arrhythmogenic right ventricular cardiomyopathy.

Rampazzo A, Nava A, Malacrida S, Beffagna G, Bauce B, Rossi V, Zimbello R, Simionati B, Basso C, Thiene G, Towbin JA, Danieli GA. Rampazzo A, et al. Among authors: rossi v. Am J Hum Genet. 2002 Nov;71(5):1200-6. doi: 10.1086/344208. Epub 2002 Oct 8. Am J Hum Genet. 2002. PMID: 12373648 Free PMC article.

5

VAMP subfamilies identified by specific R-SNARE motifs.

Rossi V, Picco R, Vacca M, D'Esposito M, D'Urso M, Galli T, Filippini F. Rossi V, et al. Biol Cell. 2004 May;96(4):251-6. doi: 10.1016/j.biolcel.2003.12.009. Biol Cell. 2004. PMID: 15145528 Review.

6

Alternative splicing of the human gene SYBL1 modulates protein domain architecture of Longin VAMP7/TI-VAMP, showing both non-SNARE and synaptobrevin-like isoforms.

Vacca M, Albania L, Della Ragione F, Carpi A, Rossi V, Strazzullo M, De Franceschi N, Rossetto O, Filippini F, D'Esposito M. Vacca M, et al. Among authors: rossi v. BMC Mol Biol. 2011 May 24;12:26. doi: 10.1186/1471-2199-12-26. BMC Mol Biol. 2011. PMID: 21609427 Free PMC article.

7

Longins: a new evolutionary conserved VAMP family sharing a novel SNARE domain.

Filippini F, Rossi V, Galli T, Budillon A, D'Urso M, D'Esposito M. Filippini F, et al. Among authors: rossi v. Trends Biochem Sci. 2001 Jul;26(7):407-9. doi: 10.1016/s0968-0004(01)01861-8. Trends Biochem Sci. 2001. PMID: 11440841

8

Longins and their longin domains: regulated SNAREs and multifunctional SNARE regulators.

Rossi V, Banfield DK, Vacca M, Dietrich LE, Ungermann C, D'Esposito M, Galli T, Filippini F. Rossi V, et al. Trends Biochem Sci. 2004 Dec;29(12):682-8. doi: 10.1016/j.tibs.2004.10.002. Trends Biochem Sci. 2004. PMID: 15544955 Review.

9

Comparative analysis of plant genomes allows the definition of the "Phytolongins": a novel non-SNARE longin domain protein family.

Vedovato M, Rossi V, Dacks JB, Filippini F. Vedovato M, et al. Among authors: rossi v. BMC Genomics. 2009 Nov 4;10:510. doi: 10.1186/1471-2164-10-510. BMC Genomics. 2009. PMID: 19889231 Free PMC article.

10

Comparative proteome bioinformatics: identification of a whole complement of putative protein tyrosine kinases in the model flowering plant Arabidopsis thaliana.

Carpi A, Di Maira G, Vedovato M, Rossi V, Naccari T, Floriduz M, Terzi M, Filippini F. Carpi A, et al. Among authors: rossi v. Proteomics. 2002 Nov;2(11):1494-503. doi: 10.1002/1615-9861(200211)2:11<1494::AID-PROT1494>3.0.CO;2-#. Proteomics. 2002. PMID: 12442249

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