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Protein synthesis levels are increased in a subset of individuals with fragile X syndrome.

Jacquemont S, Pacini L, Jønch AE, Cencelli G, Rozenberg I, He Y, D'Andrea L, Pedini G, Eldeeb M, Willemsen R, Gasparini F, Tassone F, Hagerman R, Gomez-Mancilla B, Bagni C.

Hum Mol Genet. 2018 Aug 9. doi: 10.1093/hmg/ddy291. [Epub ahead of print] No abstract available.


Protein synthesis levels are increased in a subset of individuals with fragile X syndrome.

Jacquemont S, Pacini L, Jønch AE, Cencelli G, Rozenberg I, He Y, D'Andrea L, Pedini G, Eldeeb M, Willemsen R, Gasparini F, Tassone F, Hagerman R, Gomez-Mancilla B, Bagni C.

Hum Mol Genet. 2018 Jun 15;27(12):2039-2051. doi: 10.1093/hmg/ddy099.


Editorial overview: Neurobiology of disease (2018).

Bagni C, Kreitzer AC.

Curr Opin Neurobiol. 2018 Feb;48:iv-vi. doi: 10.1016/j.conb.2018.01.005. Epub 2018 Jan 30. No abstract available.


Gender Equality from a European Perspective: Myth and Reality.

Salinas PC, Bagni C.

Neuron. 2017 Nov 15;96(4):721-729. doi: 10.1016/j.neuron.2017.10.002.


The fragile X mental retardation protein regulates tumor invasiveness-related pathways in melanoma cells.

Zalfa F, Panasiti V, Carotti S, Zingariello M, Perrone G, Sancillo L, Pacini L, Luciani F, Roberti V, D'Amico S, Coppola R, Abate SO, Rana RA, De Luca A, Fiers M, Melocchi V, Bianchi F, Farace MG, Achsel T, Marine JC, Morini S, Bagni C.

Cell Death Dis. 2017 Nov 16;8(11):e3169. doi: 10.1038/cddis.2017.521.


Reducing eIF4E-eIF4G interactions restores the balance between protein synthesis and actin dynamics in fragile X syndrome model mice.

Santini E, Huynh TN, Longo F, Koo SY, Mojica E, D'Andrea L, Bagni C, Klann E.

Sci Signal. 2017 Nov 7;10(504). pii: eaan0665. doi: 10.1126/scisignal.aan0665.


Arc Requires PSD95 for Assembly into Postsynaptic Complexes Involved with Neural Dysfunction and Intelligence.

Fernández E, Collins MO, Frank RAW, Zhu F, Kopanitsa MV, Nithianantharajah J, Lemprière SA, Fricker D, Elsegood KA, McLaughlin CL, Croning MDR, Mclean C, Armstrong JD, Hill WD, Deary IJ, Cencelli G, Bagni C, Fromer M, Purcell SM, Pocklington AJ, Choudhary JS, Komiyama NH, Grant SGN.

Cell Rep. 2017 Oct 17;21(3):679-691. doi: 10.1016/j.celrep.2017.09.045.


New insights into the metastatic behavior after breast cancer surgery, according to well-established clinicopathological variables and molecular subtypes.

Buonomo OC, Caredda E, Portarena I, Vanni G, Orlandi A, Bagni C, Petrella G, Palombi L, Orsaria P.

PLoS One. 2017 Sep 18;12(9):e0184680. doi: 10.1371/journal.pone.0184680. eCollection 2017.


Cognitive Dysfunctions in Intellectual Disabilities: The Contributions of the Ras-MAPK and PI3K-AKT-mTOR Pathways.

Borrie SC, Brems H, Legius E, Bagni C.

Annu Rev Genomics Hum Genet. 2017 Aug 31;18:115-142. doi: 10.1146/annurev-genom-091416-035332. Review.


The non-coding RNA BC1 regulates experience-dependent structural plasticity and learning.

Briz V, Restivo L, Pasciuto E, Juczewski K, Mercaldo V, Lo AC, Baatsen P, Gounko NV, Borreca A, Girardi T, Luca R, Nys J, Poorthuis RB, Mansvelder HD, Fisone G, Ammassari-Teule M, Arckens L, Krieger P, Meredith R, Bagni C.

Nat Commun. 2017 Aug 17;8(1):293. doi: 10.1038/s41467-017-00311-2.


Absence of the Fragile X Mental Retardation Protein results in defects of RNA editing of neuronal mRNAs in mouse.

Filippini A, Bonini D, Lacoux C, Pacini L, Zingariello M, Sancillo L, Bosisio D, Salvi V, Mingardi J, La Via L, Zalfa F, Bagni C, Barbon A.

RNA Biol. 2017 Nov 2;14(11):1580-1591. doi: 10.1080/15476286.2017.1338232. Epub 2017 Sep 5.


Mitochondrial dysfunction in Autism Spectrum Disorder: clinical features and perspectives.

Hollis F, Kanellopoulos AK, Bagni C.

Curr Opin Neurobiol. 2017 Aug;45:178-187. doi: 10.1016/j.conb.2017.05.018. Epub 2017 Jun 16. Review.


Clinical and Molecular Assessment in a Female with Fragile X Syndrome and Tuberous Sclerosis.

Yrigollen CM, Pacini L, Nobile V, Lozano R, Hagerman RJ, Bagni C, Tassone F.

J Genet Disord Genet Rep. 2016;5(3). pii: 139. doi: 10.4172/2327-5790.1000139. Epub 2016 Jul 15.


Mutant HSPB1 causes loss of translational repression by binding to PCBP1, an RNA binding protein with a possible role in neurodegenerative disease.

Geuens T, De Winter V, Rajan N, Achsel T, Mateiu L, Almeida-Souza L, Asselbergh B, Bouhy D, Auer-Grumbach M, Bagni C, Timmerman V.

Acta Neuropathol Commun. 2017 Jan 11;5(1):5. doi: 10.1186/s40478-016-0407-3.


Impaired GABAergic inhibition in the hippocampus of Fmr1 knockout mice.

Sabanov V, Braat S, D'Andrea L, Willemsen R, Zeidler S, Rooms L, Bagni C, Kooy RF, Balschun D.

Neuropharmacology. 2017 Apr;116:71-81. doi: 10.1016/j.neuropharm.2016.12.010. Epub 2016 Dec 21.


Neurons acetylate their way to migration.

Borrie SC, Bagni C.

EMBO Rep. 2016 Dec;17(12):1674-1676. Epub 2016 Oct 21. No abstract available.


Somatosensory map expansion and altered processing of tactile inputs in a mouse model of fragile X syndrome.

Juczewski K, von Richthofen H, Bagni C, Celikel T, Fisone G, Krieger P.

Neurobiol Dis. 2016 Dec;96:201-215. doi: 10.1016/j.nbd.2016.09.007. Epub 2016 Sep 8.


Cooperativity in RNA-protein interactions: the complex is more than the sum of its partners.

Achsel T, Bagni C.

Curr Opin Neurobiol. 2016 Aug;39:146-51. doi: 10.1016/j.conb.2016.06.007. Epub 2016 Jun 25. Review.


Accumulated common variants in the broader fragile X gene family modulate autistic phenotypes.

Stepniak B, Kästner A, Poggi G, Mitjans M, Begemann M, Hartmann A, Van der Auwera S, Sananbenesi F, Krueger-Burg D, Matuszko G, Brosi C, Homuth G, Völzke H, Benseler F, Bagni C, Fischer U, Dityatev A, Grabe HJ, Rujescu D, Fischer A, Ehrenreich H.

EMBO Mol Med. 2015 Dec;7(12):1565-79. doi: 10.15252/emmm.201505696.


MD and Docking Studies Reveal That the Functional Switch of CYFIP1 is Mediated by a Butterfly-like Motion.

Di Marino D, Chillemi G, De Rubeis S, Tramontano A, Achsel T, Bagni C.

J Chem Theory Comput. 2015 Jul 14;11(7):3401-10. doi: 10.1021/ct500431h.


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