Botta A - Search Results

1

Altered Ca2+ homeostasis and endoplasmic reticulum stress in myotonic dystrophy type 1 muscle cells.

Botta A, Malena A, Loro E, Del Moro G, Suman M, Pantic B, Szabadkai G, Vergani L. Botta A, et al. Genes (Basel). 2013 Jun 4;4(2):275-92. doi: 10.3390/genes4020275. Genes (Basel). 2013. PMID: 24705164 Free PMC article.

2

The CTG repeat expansion size correlates with the splicing defects observed in muscles from myotonic dystrophy type 1 patients.

Botta A, Rinaldi F, Catalli C, Vergani L, Bonifazi E, Romeo V, Loro E, Viola A, Angelini C, Novelli G. Botta A, et al. J Med Genet. 2008 Oct;45(10):639-46. doi: 10.1136/jmg.2008.058909. Epub 2008 Jul 8. J Med Genet. 2008. PMID: 18611984

3

Normal myogenesis and increased apoptosis in myotonic dystrophy type-1 muscle cells.

Loro E, Rinaldi F, Malena A, Masiero E, Novelli G, Angelini C, Romeo V, Sandri M, Botta A, Vergani L. Loro E, et al. Among authors: botta a. Cell Death Differ. 2010 Aug;17(8):1315-24. doi: 10.1038/cdd.2010.33. Epub 2010 Apr 30. Cell Death Differ. 2010. PMID: 20431600

4

Overexpression of microRNA-206 in the skeletal muscle from myotonic dystrophy type 1 patients.

Gambardella S, Rinaldi F, Lepore SM, Viola A, Loro E, Angelini C, Vergani L, Novelli G, Botta A. Gambardella S, et al. Among authors: botta a. J Transl Med. 2010 May 20;8:48. doi: 10.1186/1479-5876-8-48. J Transl Med. 2010. PMID: 20487562 Free PMC article.

5

Aberrant splicing and expression of the non muscle myosin heavy-chain gene MYH14 in DM1 muscle tissues.

Rinaldi F, Terracciano C, Pisani V, Massa R, Loro E, Vergani L, Di Girolamo S, Angelini C, Gourdon G, Novelli G, Botta A. Rinaldi F, et al. Among authors: botta a. Neurobiol Dis. 2012 Jan;45(1):264-71. doi: 10.1016/j.nbd.2011.08.010. Epub 2011 Aug 18. Neurobiol Dis. 2012. PMID: 21872659 Free article.

6

MBNL142 and MBNL143 gene isoforms, overexpressed in DM1-patient muscle, encode for nuclear proteins interacting with Src family kinases.

Botta A, Malena A, Tibaldi E, Rocchi L, Loro E, Pena E, Cenci L, Ambrosi E, Bellocchi MC, Pagano MA, Novelli G, Rossi G, Monaco HL, Gianazza E, Pantic B, Romeo V, Marin O, Brunati AM, Vergani L. Botta A, et al. Cell Death Dis. 2013 Aug 15;4(8):e770. doi: 10.1038/cddis.2013.291. Cell Death Dis. 2013. PMID: 23949219 Free PMC article.

7

Reliable and versatile immortal muscle cell models from healthy and myotonic dystrophy type 1 primary human myoblasts.

Pantic B, Borgia D, Giunco S, Malena A, Kiyono T, Salvatori S, De Rossi A, Giardina E, Sangiuolo F, Pegoraro E, Vergani L, Botta A. Pantic B, et al. Among authors: botta a. Exp Cell Res. 2016 Mar 1;342(1):39-51. doi: 10.1016/j.yexcr.2016.02.013. Epub 2016 Feb 19. Exp Cell Res. 2016. PMID: 26905645

8

Riboflavin-Responsive and -Non-responsive Mutations in FAD Synthase Cause Multiple Acyl-CoA Dehydrogenase and Combined Respiratory-Chain Deficiency.

Olsen RKJ, Koňaříková E, Giancaspero TA, Mosegaard S, Boczonadi V, Mataković L, Veauville-Merllié A, Terrile C, Schwarzmayr T, Haack TB, Auranen M, Leone P, Galluccio M, Imbard A, Gutierrez-Rios P, Palmfeldt J, Graf E, Vianey-Saban C, Oppenheim M, Schiff M, Pichard S, Rigal O, Pyle A, Chinnery PF, Konstantopoulou V, Möslinger D, Feichtinger RG, Talim B, Topaloglu H, Coskun T, Gucer S, Botta A, Pegoraro E, Malena A, Vergani L, Mazzà D, Zollino M, Ghezzi D, Acquaviva C, Tyni T, Boneh A, Meitinger T, Strom TM, Gregersen N, Mayr JA, Horvath R, Barile M, Prokisch H. Olsen RKJ, et al. Among authors: botta a. Am J Hum Genet. 2016 Jun 2;98(6):1130-1145. doi: 10.1016/j.ajhg.2016.04.006. Am J Hum Genet. 2016. PMID: 27259049 Free PMC article.

9

Effect of the [CCTG]n repeat expansion on ZNF9 expression in myotonic dystrophy type II (DM2).

Botta A, Caldarola S, Vallo L, Bonifazi E, Fruci D, Gullotta F, Massa R, Novelli G, Loreni F. Botta A, et al. Biochim Biophys Acta. 2006 Mar;1762(3):329-34. doi: 10.1016/j.bbadis.2005.11.004. Epub 2005 Dec 6. Biochim Biophys Acta. 2006. PMID: 16376058 Free article.

10

Gene expression analysis in myotonic dystrophy: indications for a common molecular pathogenic pathway in DM1 and DM2.

Botta A, Vallo L, Rinaldi F, Bonifazi E, Amati F, Biancolella M, Gambardella S, Mancinelli E, Angelini C, Meola G, Novelli G. Botta A, et al. Gene Expr. 2007;13(6):339-51. doi: 10.3727/000000006781510705. Gene Expr. 2007. PMID: 17708420 Free PMC article.

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