De Stefano ME - Search Results

1

UPR activation specifically modulates glutamate neurotransmission in the cerebellum of a mouse model of autism.

Trobiani L, Favaloro FL, Di Castro MA, Di Mattia M, Cariello M, Miranda E, Canterini S, De Stefano ME, Comoletti D, Limatola C, De Jaco A. Trobiani L, et al. Among authors: de stefano me, de jaco a. Neurobiol Dis. 2018 Dec;120:139-150. doi: 10.1016/j.nbd.2018.08.026. Epub 2018 Sep 7. Neurobiol Dis. 2018. PMID: 30201312

2

Lack of dystrophin functionally affects α3β2/β4-nicotinic acethylcholine receptors in sympathetic neurons of dystrophic mdx mice.

Di Angelantonio S, De Stefano ME, Piccioni A, Lombardi L, Gotti C, Paggi P. Di Angelantonio S, et al. Among authors: de stefano me. Neurobiol Dis. 2011 Feb;41(2):528-37. doi: 10.1016/j.nbd.2010.10.024. Epub 2010 Nov 5. Neurobiol Dis. 2011. PMID: 21056666

3

Shortened primary cilium length and dysregulated Sonic hedgehog signaling in Niemann-Pick C1 disease.

Canterini S, Dragotto J, Dardis A, Zampieri S, De Stefano ME, Mangia F, Erickson RP, Fiorenza MT. Canterini S, et al. Among authors: de stefano me. Hum Mol Genet. 2017 Jun 15;26(12):2277-2289. doi: 10.1093/hmg/ddx118. Hum Mol Genet. 2017. PMID: 28379564

4

Synaptic alterations as a neurodevelopmental trait of Duchenne muscular dystrophy.

De Stefano ME, Ferretti V, Mozzetta C. De Stefano ME, et al. Neurobiol Dis. 2022 Jun 15;168:105718. doi: 10.1016/j.nbd.2022.105718. Epub 2022 Apr 4. Neurobiol Dis. 2022. PMID: 35390481 Free article. Review.

5

Muscle Damage in Dystrophic mdx Mice Is Influenced by the Activity of Ca²⁺-Activated K_Ca3.1 Channels.

Morotti M, Garofalo S, Cocozza G, Antonangeli F, Bianconi V, Mozzetta C, De Stefano ME, Capitani R, Wulff H, Limatola C, Catalano M, Grassi F. Morotti M, et al. Among authors: de stefano me. Life (Basel). 2022 Apr 5;12(4):538. doi: 10.3390/life12040538. Life (Basel). 2022. PMID: 35455028 Free PMC article.

6

Lack of dystrophin leads to the selective loss of superior cervical ganglion neurons projecting to muscular targets in genetically dystrophic mdx mice.

De Stefano ME, Leone L, Lombardi L, Paggi P. De Stefano ME, et al. Neurobiol Dis. 2005 Dec;20(3):929-42. doi: 10.1016/j.nbd.2005.06.006. Epub 2005 Jul 14. Neurobiol Dis. 2005. PMID: 16023353

7

Components of the NGF signaling complex are altered in mdx mouse superior cervical ganglion and its target organs.

Lombardi L, De Stefano ME, Paggi P. Lombardi L, et al. Among authors: de stefano me. Neurobiol Dis. 2008 Dec;32(3):402-11. doi: 10.1016/j.nbd.2008.07.021. Epub 2008 Aug 7. Neurobiol Dis. 2008. PMID: 18725298

8

M2 muscarinic receptor activation regulates Schwann cell differentiation and myelin organization.

Uggenti C, De Stefano ME, Costantino M, Loreti S, Pisano A, Avallone B, Talora C, Magnaghi V, Tata AM. Uggenti C, et al. Among authors: de stefano me. Dev Neurobiol. 2014 Jul;74(7):676-91. doi: 10.1002/dneu.22161. Epub 2014 Jan 9. Dev Neurobiol. 2014. PMID: 24403178

9

The multifaceted role of metalloproteinases in physiological and pathological conditions in embryonic and adult brains.

De Stefano ME, Herrero MT. De Stefano ME, et al. Prog Neurobiol. 2017 Aug;155:36-56. doi: 10.1016/j.pneurobio.2016.08.002. Epub 2016 Aug 13. Prog Neurobiol. 2017. PMID: 27530222 Review.

10

Dystrophin Is Required for the Proper Timing in Retinal Histogenesis: A Thorough Investigation on the mdx Mouse Model of Duchenne Muscular Dystrophy.

Persiconi I, Cosmi F, Guadagno NA, Lupo G, De Stefano ME. Persiconi I, et al. Among authors: de stefano me. Front Neurosci. 2020 Aug 31;14:760. doi: 10.3389/fnins.2020.00760. eCollection 2020. Front Neurosci. 2020. PMID: 32982660 Free PMC article.

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