Toffolatti L - Search Results

1

Multiple exon skipping and RNA circularisation contribute to the severe phenotypic expression of exon 5 dystrophin deletion.

Gualandi F, Trabanelli C, Rimessi P, Calzolari E, Toffolatti L, Patarnello T, Kunz G, Muntoni F, Ferlini A. Gualandi F, et al. Among authors: toffolatti l. J Med Genet. 2003 Aug;40(8):e100. doi: 10.1136/jmg.40.8.e100. J Med Genet. 2003. PMID: 12920092 Free PMC article. No abstract available.

2

Genomic definition of a pure intronic dystrophin deletion responsible for an XLDC splicing mutation: in vitro mimicking and antisense modulation of the splicing abnormality.

Gualandi F, Rimessi P, Cardazzo B, Toffolatti L, Dunckley MG, Calzolari E, Patarnello T, Muntoni F, Ferlini A. Gualandi F, et al. Among authors: toffolatti l. Gene. 2003 Jun 5;311:25-33. doi: 10.1016/s0378-1119(03)00527-4. Gene. 2003. PMID: 12853135

3

Analysis of 22 deletion breakpoints in dystrophin intron 49.

Nobile C, Toffolatti L, Rizzi F, Simionati B, Nigro V, Cardazzo B, Patarnello T, Valle G, Danieli GA. Nobile C, et al. Among authors: toffolatti l. Hum Genet. 2002 May;110(5):418-21. doi: 10.1007/s00439-002-0721-7. Epub 2002 Apr 9. Hum Genet. 2002. PMID: 12073011

4

Investigating the mechanism of chromosomal deletion: characterization of 39 deletion breakpoints in introns 47 and 48 of the human dystrophin gene.

Toffolatti L, Cardazzo B, Nobile C, Danieli GA, Gualandi F, Muntoni F, Abbs S, Zanetti P, Angelini C, Ferlini A, Fanin M, Patarnello T. Toffolatti L, et al. Genomics. 2002 Nov;80(5):523-30. Genomics. 2002. PMID: 12408970

5

Tempo and mode of evolution of a primate-specific retrotransposon belonging to the LINE 1 family.

Cardazzo B, Bargelloni L, Toffolatti L, Rimessi P, Ferlini A, Patarnello T. Cardazzo B, et al. Among authors: toffolatti l. J Mol Evol. 2003;57 Suppl 1:S268-76. doi: 10.1007/s00239-003-0036-x. J Mol Evol. 2003. PMID: 15008424

6

Intervening sequences in paralogous genes: a comparative genomic approach to study the evolution of X chromosome introns.

Cardazzo B, Bargelloni L, Toffolatti L, Patarnello T. Cardazzo B, et al. Among authors: toffolatti l. Mol Biol Evol. 2003 Dec;20(12):2034-41. doi: 10.1093/molbev/msg213. Epub 2003 Aug 29. Mol Biol Evol. 2003. PMID: 12949145

7

Expression analysis of androgen-responsive genes in the prostate of veal calves treated with anabolic hormones.

Toffolatti L, Rosa Gastaldo L, Patarnello T, Romualdi C, Merlanti R, Montesissa C, Poppi L, Castagnaro M, Bargelloni L. Toffolatti L, et al. Domest Anim Endocrinol. 2006 Jan;30(1):38-55. doi: 10.1016/j.domaniend.2005.05.008. Epub 2005 Jun 28. Domest Anim Endocrinol. 2006. PMID: 16023321

8

A possible missense mutation detected in the dystrophin gene by Double-Strand Conformation Analysis (DSCA).

Saad FA, Vita G, Toffolatti L, Danieli GA. Saad FA, et al. Among authors: toffolatti l. Neuromuscul Disord. 1994 Jul;4(4):335-41. doi: 10.1016/0960-8966(94)90069-8. Neuromuscul Disord. 1994. PMID: 7981590

9

MYCN expression in human rhabdomyosarcoma cell lines and tumour samples.

Toffolatti L, Frascella E, Ninfo V, Gambini C, Forni M, Carli M, Rosolen A. Toffolatti L, et al. J Pathol. 2002 Apr;196(4):450-8. doi: 10.1002/path.1068. J Pathol. 2002. PMID: 11920742

10

Concomitant amplification and expression of PAX7-FKHR and MYCN in a human rhabdomyosarcoma cell line carrying a cryptic t(1;13)(p36;q14).

Frascella E, Lenzini E, Schafer BW, Brecevic L, Dorigo E, Toffolatti L, Nanni P, De Giovanni C, Rosolen A. Frascella E, et al. Among authors: toffolatti l. Cancer Genet Cytogenet. 2000 Sep;121(2):139-45. doi: 10.1016/s0165-4608(00)00258-2. Cancer Genet Cytogenet. 2000. PMID: 11063797

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

47 results

Search Page

Filters