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Page 1
Oligodendrocytes in Development, Myelin Generation and Beyond.
Cells. 2019 Nov 12;8(11):1424. doi: 10.3390/cells8111424.
Cells. 2019.
PMID: 31726662
Free PMC article.
Review.
The Synaptic and Neuronal Functions of the X-Linked Intellectual Disability Protein Interleukin-1 Receptor Accessory Protein Like 1 (IL1RAPL1).
Montani C, Gritti L, Beretta S, Verpelli C, Sala C.
Montani C, et al. Among authors: gritti l.
Dev Neurobiol. 2019 Jan;79(1):85-95. doi: 10.1002/dneu.22657. Epub 2018 Dec 21.
Dev Neurobiol. 2019.
PMID: 30548231
Review.
Item in Clipboard
Eukaryotic Elongation Factor 2 Kinase a Pharmacological Target to Regulate Protein Translation Dysfunction in Neurological Diseases.
Beretta S, Gritti L, Verpelli C, Sala C.
Beretta S, et al. Among authors: gritti l.
Neuroscience. 2020 Oct 1;445:42-49. doi: 10.1016/j.neuroscience.2020.02.015. Epub 2020 Feb 21.
Neuroscience. 2020.
PMID: 32088293
Review.
Item in Clipboard
The X-Linked Intellectual Disability Protein IL1RAPL1 Regulates Dendrite Complexity.
Montani C, Ramos-Brossier M, Ponzoni L, Gritti L, Cwetsch AW, Braida D, Saillour Y, Terragni B, Mantegazza M, Sala M, Verpelli C, Billuart P, Sala C.
Montani C, et al. Among authors: gritti l.
J Neurosci. 2017 Jul 12;37(28):6606-6627. doi: 10.1523/JNEUROSCI.3775-16.2017. Epub 2017 Jun 2.
J Neurosci. 2017.
PMID: 28576939
Free PMC article.
Item in Clipboard
Modelling genetic mosaicism of neurodevelopmental disorders in vivo by a Cre-amplifying fluorescent reporter.
Trovato F, Parra R, Pracucci E, Landi S, Cozzolino O, Nardi G, Cruciani F, Pillai V, Mosti L, Cwetsch AW, Cancedda L, Gritti L, Sala C, Verpelli C, Maset A, Lodovichi C, Ratto GM.
Trovato F, et al. Among authors: gritti l.
Nat Commun. 2020 Dec 3;11(1):6194. doi: 10.1038/s41467-020-19864-w.
Nat Commun. 2020.
PMID: 33273479
Free PMC article.
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Rescuing epileptic and behavioral alterations in a Dravet syndrome mouse model by inhibiting eukaryotic elongation factor 2 kinase (eEF2K).
Beretta S, Gritti L, Ponzoni L, Scalmani P, Mantegazza M, Sala M, Verpelli C, Sala C.
Beretta S, et al. Among authors: gritti l.
Mol Autism. 2022 Jan 3;13(1):1. doi: 10.1186/s13229-021-00484-0.
Mol Autism. 2022.
PMID: 34980259
Free PMC article.
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Novel IL1RAPL1 mutations associated with intellectual disability impair synaptogenesis.
Ramos-Brossier M, Montani C, Lebrun N, Gritti L, Martin C, Seminatore-Nole C, Toussaint A, Moreno S, Poirier K, Dorseuil O, Chelly J, Hackett A, Gecz J, Bieth E, Faudet A, Heron D, Frank Kooy R, Loeys B, Humeau Y, Sala C, Billuart P.
Ramos-Brossier M, et al. Among authors: gritti l.
Hum Mol Genet. 2015 Feb 15;24(4):1106-18. doi: 10.1093/hmg/ddu523. Epub 2014 Oct 9.
Hum Mol Genet. 2015.
PMID: 25305082
Free PMC article.
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