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Results: 1 to 20 of 29

1.

An integrated genomic-transcriptomic approach supports a role for the proto-oncogene BCL3 in atherosclerosis.

Marchetti G, Girelli D, Zerbinati C, Lunghi B, Friso S, Meneghetti S, Coen M, Gagliano T, Guastella G, Bochaton-Piallat ML, Pizzolo F, Mascoli F, Malerba G, Bovolenta M, Ferracin M, Olivieri O, Bernardi F, Martinelli N.

Thromb Haemost. 2014 Nov 6;113(3). [Epub ahead of print]

PMID:
25374339
[PubMed - as supplied by publisher]
2.

The DMD locus harbours multiple long non-coding RNAs which orchestrate and control transcription of muscle dystrophin mRNA isoforms.

Bovolenta M, Erriquez D, Valli E, Brioschi S, Scotton C, Neri M, Falzarano MS, Gherardi S, Fabris M, Rimessi P, Gualandi F, Perini G, Ferlini A.

PLoS One. 2012;7(9):e45328. doi: 10.1371/journal.pone.0045328. Epub 2012 Sep 21.

PMID:
23028937
[PubMed - indexed for MEDLINE]
Free PMC Article
3.

Antisense-induced messenger depletion corrects a COL6A2 dominant mutation in Ullrich myopathy.

Gualandi F, Manzati E, Sabatelli P, Passarelli C, Bovolenta M, Pellegrini C, Perrone D, Squarzoni S, Pegoraro E, Bonaldo P, Ferlini A.

Hum Gene Ther. 2012 Dec;23(12):1313-8. doi: 10.1089/hum.2012.109. Epub 2012 Nov 6.

PMID:
22992134
[PubMed - indexed for MEDLINE]
Free PMC Article
4.

Genetic characterization in symptomatic female DMD carriers: lack of relationship between X-inactivation, transcriptional DMD allele balancing and phenotype.

Brioschi S, Gualandi F, Scotton C, Armaroli A, Bovolenta M, Falzarano MS, Sabatelli P, Selvatici R, D'Amico A, Pane M, Ricci G, Siciliano G, Tedeschi S, Pini A, Vercelli L, De Grandis D, Mercuri E, Bertini E, Merlini L, Mongini T, Ferlini A.

BMC Med Genet. 2012 Aug 16;13:73.

PMID:
22894145
[PubMed - indexed for MEDLINE]
Free PMC Article
5.

The absence of dystrophin brain isoform expression in healthy human heart ventricles explains the pathogenesis of 5' X-linked dilated cardiomyopathy.

Neri M, Valli E, Alfano G, Bovolenta M, Spitali P, Rapezzi C, Muntoni F, Banfi S, Perini G, Gualandi F, Ferlini A.

BMC Med Genet. 2012 Mar 28;13:20. doi: 10.1186/1471-2350-13-20.

PMID:
22455600
[PubMed - indexed for MEDLINE]
Free PMC Article
6.

Rapid, comprehensive analysis of the dystrophin transcript by a custom micro-fluidic exome array.

Bovolenta M, Scotton C, Falzarano MS, Gualandi F, Ferlini A.

Hum Mutat. 2012 Mar;33(3):572-81. doi: 10.1002/humu.22017. Epub 2012 Jan 25.

PMID:
22223181
[PubMed - indexed for MEDLINE]
7.

Macrophages: a minimally invasive tool for monitoring collagen VI myopathies.

Gualandi F, Curci R, Sabatelli P, Martoni E, Bovolenta M, Maraldi MN, Merlini L, Ferlini AA.

Muscle Nerve. 2011 Jul;44(1):80-4. doi: 10.1002/mus.21999. Epub 2011 Apr 12.

PMID:
21488057
[PubMed - indexed for MEDLINE]
8.

Antisense modulation of both exonic and intronic splicing motifs induces skipping of a DMD pseudo-exon responsible for x-linked dilated cardiomyopathy.

Rimessi P, Fabris M, Bovolenta M, Bassi E, Falzarano S, Gualandi F, Rapezzi C, Coccolo F, Perrone D, Medici A, Ferlini A.

Hum Gene Ther. 2010 Sep;21(9):1137-46. doi: 10.1089/hum.2010.010.

PMID:
20486769
[PubMed - indexed for MEDLINE]
9.

Custom CGH array profiling of copy number variations (CNVs) on chromosome 6p21.32 (HLA locus) in patients with venous malformations associated with multiple sclerosis.

Ferlini A, Bovolenta M, Neri M, Gualandi F, Balboni A, Yuryev A, Salvi F, Gemmati D, Liboni A, Zamboni P.

BMC Med Genet. 2010 Apr 28;11:64. doi: 10.1186/1471-2350-11-64.

PMID:
20426824
[PubMed - indexed for MEDLINE]
Free PMC Article
10.

Identification of a deep intronic mutation in the COL6A2 gene by a novel custom oligonucleotide CGH array designed to explore allelic and genetic heterogeneity in collagen VI-related myopathies.

Bovolenta M, Neri M, Martoni E, Urciuolo A, Sabatelli P, Fabris M, Grumati P, Mercuri E, Bertini E, Merlini L, Bonaldo P, Ferlini A, Gualandi F.

BMC Med Genet. 2010 Mar 19;11:44. doi: 10.1186/1471-2350-11-44.

PMID:
20302629
[PubMed - indexed for MEDLINE]
Free PMC Article
11.

Prenatal diagnosis of Duchenne muscular dystrophy by comparative genomic hybridization.

Bovolenta M, Rimessi P, Dolcini B, Ravani A, Ferlini A, Gualandi F.

Clin Genet. 2010 May;77(5):503-6. doi: 10.1111/j.1399-0004.2009.01340.x. Epub 2009 Dec 10. No abstract available.

PMID:
20002456
[PubMed - indexed for MEDLINE]
12.

Autosomal recessive Bethlem myopathy.

Gualandi F, Urciuolo A, Martoni E, Sabatelli P, Squarzoni S, Bovolenta M, Messina S, Mercuri E, Franchella A, Ferlini A, Bonaldo P, Merlini L.

Neurology. 2009 Dec 1;73(22):1883-91. doi: 10.1212/WNL.0b013e3181c3fd2a.

PMID:
19949035
[PubMed - indexed for MEDLINE]
13.

Exon skipping-mediated dystrophin reading frame restoration for small mutations.

Spitali P, Rimessi P, Fabris M, Perrone D, Falzarano S, Bovolenta M, Trabanelli C, Mari L, Bassi E, Tuffery S, Gualandi F, Maraldi NM, Sabatelli-Giraud P, Medici A, Merlini L, Ferlini A.

Hum Mutat. 2009 Nov;30(11):1527-34. doi: 10.1002/humu.21092.

PMID:
19760747
[PubMed - indexed for MEDLINE]
14.

Identification and characterization of novel collagen VI non-canonical splicing mutations causing Ullrich congenital muscular dystrophy.

Martoni E, Urciuolo A, Sabatelli P, Fabris M, Bovolenta M, Neri M, Grumati P, D'Amico A, Pane M, Mercuri E, Bertini E, Merlini L, Bonaldo P, Ferlini A, Gualandi F.

Hum Mutat. 2009 May;30(5):E662-72. doi: 10.1002/humu.21022.

PMID:
19309692
[PubMed - indexed for MEDLINE]
15.

Cationic PMMA nanoparticles bind and deliver antisense oligoribonucleotides allowing restoration of dystrophin expression in the mdx mouse.

Rimessi P, Sabatelli P, Fabris M, Braghetta P, Bassi E, Spitali P, Vattemi G, Tomelleri G, Mari L, Perrone D, Medici A, Neri M, Bovolenta M, Martoni E, Maraldi NM, Gualandi F, Merlini L, Ballestri M, Tondelli L, Sparnacci K, Bonaldo P, Caputo A, Laus M, Ferlini A.

Mol Ther. 2009 May;17(5):820-7. doi: 10.1038/mt.2009.8. Epub 2009 Feb 24.

PMID:
19240694
[PubMed - indexed for MEDLINE]
Free PMC Article
16.

A novel custom high density-comparative genomic hybridization array detects common rearrangements as well as deep intronic mutations in dystrophinopathies.

Bovolenta M, Neri M, Fini S, Fabris M, Trabanelli C, Venturoli A, Martoni E, Bassi E, Spitali P, Brioschi S, Falzarano MS, Rimessi P, Ciccone R, Ashton E, McCauley J, Yau S, Abbs S, Muntoni F, Merlini L, Gualandi F, Ferlini A.

BMC Genomics. 2008 Nov 28;9:572. doi: 10.1186/1471-2164-9-572.

PMID:
19040728
[PubMed - indexed for MEDLINE]
Free PMC Article
17.

Transcriptional behavior of DMD gene duplications in DMD/BMD males.

Gualandi F, Neri M, Bovolenta M, Martoni E, Rimessi P, Fini S, Spitali P, Fabris M, Pane M, Angelini C, Mora M, Morandi L, Mongini T, Bertini E, Ricci E, Vattemi G, Mercuri E, Merlini L, Ferlini A.

Hum Mutat. 2009 Feb;30(2):E310-9. doi: 10.1002/humu.20881.

PMID:
18853462
[PubMed - indexed for MEDLINE]
18.

PLC-beta2 monitors the drug-induced release of differentiation blockade in tumoral myeloid precursors.

Brugnoli F, Bovolenta M, Benedusi M, Miscia S, Capitani S, Bertagnolo V.

J Cell Biochem. 2006 May 1;98(1):160-73.

PMID:
16408290
[PubMed - indexed for MEDLINE]
19.

The evolution of the atheromatous plaque: ultrastructural evidence.

Aleotti A, Boldrini P, Bovolenta MR, Cervellati F, Martines G.

J Submicrosc Cytol Pathol. 2005 Apr;37(1):53-7.

PMID:
16136728
[PubMed - indexed for MEDLINE]
20.

A simple and efficient highly enantioselective synthesis of alpha-ionone and alpha-damascone.

Bovolenta M, Castronovo F, VadalĂ  A, Zanoni G, Vidari G.

J Org Chem. 2004 Dec 10;69(25):8959-62.

PMID:
15575784
[PubMed - indexed for MEDLINE]

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