Ratti A - Search Results

1

High frequency of TARDBP gene mutations in Italian patients with amyotrophic lateral sclerosis.

Corrado L, Ratti A, Gellera C, Buratti E, Castellotti B, Carlomagno Y, Ticozzi N, Mazzini L, Testa L, Taroni F, Baralle FE, Silani V, D'Alfonso S. Corrado L, et al. Among authors: ratti a. Hum Mutat. 2009 Apr;30(4):688-94. doi: 10.1002/humu.20950. Hum Mutat. 2009. PMID: 19224587

2

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.

3

cDNA characterization and chromosomal mapping of two human homologues of the Drosophila dishevelled polarity gene.

Pizzuti A, Amati F, Calabrese G, Mari A, Colosimo A, Silani V, Giardino L, Ratti A, Penso D, Calzà L, Palka G, Scarlato G, Novelli G, Dallapiccola B. Pizzuti A, et al. Among authors: ratti a. Hum Mol Genet. 1996 Jul;5(7):953-8. doi: 10.1093/hmg/5.7.953. Hum Mol Genet. 1996. PMID: 8817329

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

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

6

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.

7

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

8

No association of DPP6 with amyotrophic lateral sclerosis in an Italian population.

Fogh I, D'Alfonso S, Gellera C, Ratti A, Cereda C, Penco S, Corrado L, Sorarù G, Castellotti B, Tiloca C, Gagliardi S, Cozzi L, Lupton MK, Ticozzi N, Mazzini L, Shaw CE, Al-Chalabi A, Powell J, Silani V. Fogh I, et al. Among authors: ratti a. Neurobiol Aging. 2011 May;32(5):966-7. doi: 10.1016/j.neurobiolaging.2009.05.014. Epub 2009 Jun 13. Neurobiol Aging. 2011. PMID: 19525032

9

Analysis of FUS gene mutation in familial amyotrophic lateral sclerosis within an Italian cohort.

Ticozzi N, Silani V, LeClerc AL, Keagle P, Gellera C, Ratti A, Taroni F, Kwiatkowski TJ Jr, McKenna-Yasek DM, Sapp PC, Brown RH Jr, Landers JE. Ticozzi N, et al. Among authors: ratti a. Neurology. 2009 Oct 13;73(15):1180-5. doi: 10.1212/WNL.0b013e3181bbff05. Epub 2009 Sep 9. Neurology. 2009. PMID: 19741215 Free PMC article.

10

TDP-43 is recruited to stress granules in conditions of oxidative insult.

Colombrita C, Zennaro E, Fallini C, Weber M, Sommacal A, Buratti E, Silani V, Ratti A. Colombrita C, et al. Among authors: ratti a. J Neurochem. 2009 Nov;111(4):1051-61. doi: 10.1111/j.1471-4159.2009.06383.x. Epub 2009 Sep 16. J Neurochem. 2009. PMID: 19765185 Free article.

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