Tulli S[au] - Search Results

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2018	1
2019	1
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Page 1

The mechanism of degeneration of striatal neuronal subtypes in Huntington disease.

Rikani AA, Choudhry Z, Choudhry AM, Rizvi N, Ikram H, Mobassarah NJ, Tulli S. Rikani AA, et al. Among authors: tulli s. Ann Neurosci. 2014 Jul;21(3):112-4. doi: 10.5214/ans.0972.7531.210308. Ann Neurosci. 2014. PMID: 25206077 Free PMC article. Review.

m-AAA and i-AAA complexes coordinate to regulate OMA1, the stress-activated supervisor of mitochondrial dynamics.

Consolato F, Maltecca F, Tulli S, Sambri I, Casari G. Consolato F, et al. Among authors: tulli s. J Cell Sci. 2018 Apr 9;131(7):jcs213546. doi: 10.1242/jcs.213546. J Cell Sci. 2018. PMID: 29545505

Pathogenic variants in the AFG3L2 proteolytic domain cause SCA28 through haploinsufficiency and proteostatic stress-driven OMA1 activation.

Tulli S, Del Bondio A, Baderna V, Mazza D, Codazzi F, Pierson TM, Ambrosi A, Nolte D, Goizet C, Toro C, Baets J, Deconinck T, DeJonghe P, Mandich P, Casari G, Maltecca F. Tulli S, et al. J Med Genet. 2019 Aug;56(8):499-511. doi: 10.1136/jmedgenet-2018-105766. Epub 2019 Mar 25. J Med Genet. 2019. PMID: 30910913 Free PMC article.

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