Crippa V - Search Results

1

BAG3 Pro209 mutants associated with myopathy and neuropathy relocate chaperones of the CASA-complex to aggresomes.

Adriaenssens E, Tedesco B, Mediani L, Asselbergh B, Crippa V, Antoniani F, Carra S, Poletti A, Timmerman V. Adriaenssens E, et al. Among authors: crippa v. Sci Rep. 2020 May 29;10(1):8755. doi: 10.1038/s41598-020-65664-z. Sci Rep. 2020. PMID: 32472079 Free PMC article.

2

Aggregation and proteasome: the case of elongated polyglutamine aggregation in spinal and bulbar muscular atrophy.

Rusmini P, Sau D, Crippa V, Palazzolo I, Simonini F, Onesto E, Martini L, Poletti A. Rusmini P, et al. Among authors: crippa v. Neurobiol Aging. 2007 Jul;28(7):1099-111. doi: 10.1016/j.neurobiolaging.2006.05.015. Epub 2006 Jun 15. Neurobiol Aging. 2007. PMID: 16781019

3

The small heat shock protein B8 (HspB8) promotes autophagic removal of misfolded proteins involved in amyotrophic lateral sclerosis (ALS).

Crippa V, Sau D, Rusmini P, Boncoraglio A, Onesto E, Bolzoni E, Galbiati M, Fontana E, Marino M, Carra S, Bendotti C, De Biasi S, Poletti A. Crippa V, et al. Hum Mol Genet. 2010 Sep 1;19(17):3440-56. doi: 10.1093/hmg/ddq257. Epub 2010 Jun 22. Hum Mol Genet. 2010. PMID: 20570967 Free article.

4

Proteasomal and autophagic degradative activities in spinal and bulbar muscular atrophy.

Rusmini P, Bolzoni E, Crippa V, Onesto E, Sau D, Galbiati M, Piccolella M, Poletti A. Rusmini P, et al. Among authors: crippa v. Neurobiol Dis. 2010 Nov;40(2):361-9. doi: 10.1016/j.nbd.2010.06.016. Epub 2010 Jul 16. Neurobiol Dis. 2010. PMID: 20621188 Review.

5

A role of small heat shock protein B8 (HspB8) in the autophagic removal of misfolded proteins responsible for neurodegenerative diseases.

Crippa V, Carra S, Rusmini P, Sau D, Bolzoni E, Bendotti C, De Biasi S, Poletti A. Crippa V, et al. Autophagy. 2010 Oct;6(7):958-60. doi: 10.4161/auto.6.7.13042. Epub 2010 Oct 16. Autophagy. 2010. PMID: 20699640

6

17-AAG increases autophagic removal of mutant androgen receptor in spinal and bulbar muscular atrophy.

Rusmini P, Simonini F, Crippa V, Bolzoni E, Onesto E, Cagnin M, Sau D, Ferri N, Poletti A. Rusmini P, et al. Among authors: crippa v. Neurobiol Dis. 2011 Jan;41(1):83-95. doi: 10.1016/j.nbd.2010.08.023. Epub 2010 Sep 9. Neurobiol Dis. 2011. PMID: 20816782

7

Dysregulation of axonal transport and motorneuron diseases.

Sau D, Rusmini P, Crippa V, Onesto E, Bolzoni E, Ratti A, Poletti A. Sau D, et al. Among authors: crippa v. Biol Cell. 2011 Feb;103(2):87-107. doi: 10.1042/BC20100093. Biol Cell. 2011. PMID: 21250942 Review.

8

Muscle cells and motoneurons differentially remove mutant SOD1 causing familial amyotrophic lateral sclerosis.

Onesto E, Rusmini P, Crippa V, Ferri N, Zito A, Galbiati M, Poletti A. Onesto E, et al. Among authors: crippa v. J Neurochem. 2011 Jul;118(2):266-80. doi: 10.1111/j.1471-4159.2011.07298.x. Epub 2011 Jun 2. J Neurochem. 2011. PMID: 21554318 Free PMC article.

9

Alteration of protein folding and degradation in motor neuron diseases: Implications and protective functions of small heat shock proteins.

Carra S, Crippa V, Rusmini P, Boncoraglio A, Minoia M, Giorgetti E, Kampinga HH, Poletti A. Carra S, et al. Among authors: crippa v. Prog Neurobiol. 2012 May;97(2):83-100. doi: 10.1016/j.pneurobio.2011.09.009. Epub 2011 Sep 29. Prog Neurobiol. 2012. PMID: 21971574 Review.

10

The anabolic/androgenic steroid nandrolone exacerbates gene expression modifications induced by mutant SOD1 in muscles of mice models of amyotrophic lateral sclerosis.

Galbiati M, Onesto E, Zito A, Crippa V, Rusmini P, Mariotti R, Bentivoglio M, Bendotti C, Poletti A. Galbiati M, et al. Among authors: crippa v. Pharmacol Res. 2012 Feb;65(2):221-30. doi: 10.1016/j.phrs.2011.12.001. Epub 2011 Dec 10. Pharmacol Res. 2012. PMID: 22178654 Free PMC article.

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