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Items: 17

1.

Attenuation of neuro-inflammation improves survival and neurodegeneration in a mouse model of severe neonatal hyperbilirubinemia.

Vodret S, Bortolussi G, Iaconcig A, Martinelli E, Tiribelli C, Muro AF.

Brain Behav Immun. 2018 May;70:166-178. doi: 10.1016/j.bbi.2018.02.011. Epub 2018 Feb 16.

PMID:
29458193
2.

Repeated AAV-mediated gene transfer by serotype switching enables long-lasting therapeutic levels of hUgt1a1 enzyme in a mouse model of Crigler-Najjar Syndrome Type I.

Bočkor L, Bortolussi G, Iaconcig A, Chiaruttini G, Tiribelli C, Giacca M, Benvenuti F, Zentilin L, Muro AF.

Gene Ther. 2017 Oct;24(10):649-660. doi: 10.1038/gt.2017.75. Epub 2017 Aug 14.

PMID:
28805798
3.

Promoterless gene targeting without nucleases rescues lethality of a Crigler-Najjar syndrome mouse model.

Porro F, Bortolussi G, Barzel A, De Caneva A, Iaconcig A, Vodret S, Zentilin L, Kay MA, Muro AF.

EMBO Mol Med. 2017 Oct;9(10):1346-1355. doi: 10.15252/emmm.201707601.

4.

Modulation of bilirubin neurotoxicity by the Abcb1 transporter in the Ugt1-/- lethal mouse model of neonatal hyperbilirubinemia.

Bockor L, Bortolussi G, Vodret S, Iaconcig A, Jašprová J, Zelenka J, Vitek L, Tiribelli C, Muro AF.

Hum Mol Genet. 2017 Jan 1;26(1):145-157. doi: 10.1093/hmg/ddw375.

PMID:
28025333
5.

TDP-43 regulates β-adducin (Add2) transcript stability.

Costessi L, Porro F, Iaconcig A, Muro AF.

RNA Biol. 2014;11(10):1280-90. doi: 10.1080/15476286.2014.996081.

6.

Characterization of the distal polyadenylation site of the ß-adducin (Add2) pre-mRNA.

Costessi L, Porro F, Iaconcig A, Nedeljkovic M, Muro AF.

PLoS One. 2013;8(3):e58879. doi: 10.1371/journal.pone.0058879. Epub 2013 Mar 15.

7.

Long-distance regulation of Add2 pre-mRNA3'end processing.

Nedeljkovic M, Costessi L, Iaconcig A, Porro F, Muro AF.

RNA Biol. 2013 Apr;10(4):516-27. doi: 10.4161/rna.23855. Epub 2013 Feb 14.

8.

Identification of 3' gene ends using transcriptional and genomic conservation across vertebrates.

Morgan M, Iaconcig A, Muro AF.

BMC Genomics. 2012 Dec 18;13:708. doi: 10.1186/1471-2164-13-708.

9.

CPEB2, CPEB3 and CPEB4 are coordinately regulated by miRNAs recognizing conserved binding sites in paralog positions of their 3'-UTRs.

Morgan M, Iaconcig A, Muro AF.

Nucleic Acids Res. 2010 Nov;38(21):7698-710. doi: 10.1093/nar/gkq635. Epub 2010 Jul 25.

10.

beta-adducin (Add2) KO mice show synaptic plasticity, motor coordination and behavioral deficits accompanied by changes in the expression and phosphorylation levels of the alpha- and gamma-adducin subunits.

Porro F, Rosato-Siri M, Leone E, Costessi L, Iaconcig A, Tongiorgi E, Muro AF.

Genes Brain Behav. 2010 Feb;9(1):84-96. doi: 10.1111/j.1601-183X.2009.00537.x. Epub 2009 Sep 22.

11.

A major fraction of fibronectin present in the extracellular matrix of tissues is plasma-derived.

Moretti FA, Chauhan AK, Iaconcig A, Porro F, Baralle FE, Muro AF.

J Biol Chem. 2007 Sep 21;282(38):28057-62. Epub 2007 Jul 19.

12.

Unexpected rescue of alpha-synuclein and multimerin1 deletion in C57BL/6JOlaHsd mice by beta-adducin knockout.

Gajović S, Mitrecić D, Augustincić L, Iaconcig A, Muro AF.

Transgenic Res. 2006 Apr;15(2):255-9.

PMID:
16604465
13.

Impaired motor coordination in mice lacking the EDA exon of the fibronectin gene.

Chauhan AK, Moretti FA, Iaconcig A, Baralle FE, Muro AF.

Behav Brain Res. 2005 Jun 3;161(1):31-8. Epub 2005 Apr 12.

PMID:
15904707
14.

RNA folding affects the recruitment of SR proteins by mouse and human polypurinic enhancer elements in the fibronectin EDA exon.

Buratti E, Muro AF, Giombi M, Gherbassi D, Iaconcig A, Baralle FE.

Mol Cell Biol. 2004 Feb;24(3):1387-400.

16.

Regulated splicing of the fibronectin EDA exon is essential for proper skin wound healing and normal lifespan.

Muro AF, Chauhan AK, Gajovic S, Iaconcig A, Porro F, Stanta G, Baralle FE.

J Cell Biol. 2003 Jul 7;162(1):149-60.

17.

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