Ratti A - Search Results

1

RNA-binding proteins and RNA metabolism: a new scenario in the pathogenesis of Amyotrophic lateral sclerosis.

Colombrita C, Onesto E, Tiloca C, Ticozzi N, Silani V, Ratti A. Colombrita C, et al. Among authors: ratti a. Arch Ital Biol. 2011 Mar;149(1):83-99. doi: 10.4449/aib.v149i1.1261. Arch Ital Biol. 2011. PMID: 21412718 Review.

2

Identification of multiple transcribed sequences from the spinal muscular atrophy region of human chromosome 5.

Pizzuti A, Colosimo A, Ratti A, Capon F, Gennarelli M, Silani V, Ghezzi C, Lo Cicero S, Calabrese G, Palka G, et al. Pizzuti A, et al. Among authors: ratti a. Biochem Biophys Res Commun. 1995 Jan 5;206(1):294-301. doi: 10.1006/bbrc.1995.1041. Biochem Biophys Res Commun. 1995. PMID: 7818533

3

Human homologue sequences to the Drosophila dishevelled segment-polarity gene are deleted in the DiGeorge syndrome.

Pizzuti A, Novelli G, Mari A, Ratti A, Colosimo A, Amati F, Penso D, Sangiuolo F, Calabrese G, Palka G, Silani V, Gennarelli M, Mingarelli R, Scarlato G, Scambler P, Dallapiccola B. Pizzuti A, et al. Among authors: ratti a. Am J Hum Genet. 1996 Apr;58(4):722-9. Am J Hum Genet. 1996. PMID: 8644734 Free PMC article.

4

UFD1L, a developmentally expressed ubiquitination gene, is deleted in CATCH 22 syndrome.

Pizzuti A, Novelli G, Ratti A, Amati F, Mari A, Calabrese G, Nicolis S, Silani V, Marino B, Scarlato G, Ottolenghi S, Dallapiccola B. Pizzuti A, et al. Among authors: ratti a. Hum Mol Genet. 1997 Feb;6(2):259-65. doi: 10.1093/hmg/6.2.259. Hum Mol Genet. 1997. PMID: 9063746

5

Immunomagnetic isolation of human developing motor neurons.

Silani V, Brioschi A, Braga M, Ciammola A, Zhou FC, Bonifati C, Ratti A, Pizzuti A, Buscaglia M, Scarlato G. Silani V, et al. Among authors: ratti a. Neuroreport. 1998 Apr 20;9(6):1143-7. doi: 10.1097/00001756-199804200-00034. Neuroreport. 1998. PMID: 9601683

6

Isolation and characterization of a novel transcript embedded within HIRA, a gene deleted in DiGeorge syndrome.

Pizzuti A, Novelli G, Ratti A, Amati F, Bordoni R, Mandich P, Bellone E, Conti E, Bengala M, Mari A, Silani V, Dallapiccola B. Pizzuti A, et al. Among authors: ratti a. Mol Genet Metab. 1999 Jul;67(3):227-35. doi: 10.1006/mgme.1999.2868. Mol Genet Metab. 1999. PMID: 10381330

7

Stem cells in the treatment of amyotrophic lateral sclerosis (ALS).

Silani V, Fogh I, Ratti A, Sassone J, Ciammola A, Cova L. Silani V, et al. Among authors: ratti a. Amyotroph Lateral Scler Other Motor Neuron Disord. 2002 Dec;3(4):173-81. doi: 10.1080/146608202760839001. Amyotroph Lateral Scler Other Motor Neuron Disord. 2002. PMID: 12710505 Review.

8

Stem cell therapy for neurodegenerative diseases: the issue of transdifferentiation.

Cova L, Ratti A, Volta M, Fogh I, Cardin V, Corbo M, Silani V. Cova L, et al. Among authors: ratti a. Stem Cells Dev. 2004 Feb;13(1):121-31. doi: 10.1089/154732804773099326. Stem Cells Dev. 2004. PMID: 15068700 Review.

9

A role for the ELAV RNA-binding proteins in neural stem cells: stabilization of Msi1 mRNA.

Ratti A, Fallini C, Cova L, Fantozzi R, Calzarossa C, Zennaro E, Pascale A, Quattrone A, Silani V. Ratti A, et al. J Cell Sci. 2006 Apr 1;119(Pt 7):1442-52. doi: 10.1242/jcs.02852. J Cell Sci. 2006. PMID: 16554442 Free article.

10

Identification of new ANG gene mutations in a large cohort of Italian patients with amyotrophic lateral sclerosis.

Gellera C, Colombrita C, Ticozzi N, Castellotti B, Bragato C, Ratti A, Taroni F, Silani V. Gellera C, et al. Among authors: ratti a. Neurogenetics. 2008 Feb;9(1):33-40. doi: 10.1007/s10048-007-0111-3. Epub 2007 Dec 18. Neurogenetics. 2008. PMID: 18087731

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