Zobrazeno 1 - 10
of 70
pro vyhledávání: '"Enrico Ginelli"'
Autor:
Veronica Colangelo, Stéphanie François, Giulia Soldà, Raffaella Picco, Francesca Roma, Enrico Ginelli, Raffaella Meneveri
Publikováno v:
PLoS ONE, Vol 9, Iss 10, p e108411 (2014)
Emerging evidence has demonstrated that miRNA sequences can regulate skeletal myogenesis by controlling the process of myoblast proliferation and differentiation. However, at present a deep analysis of miRNA expression in control and FSHD myoblasts d
Externí odkaz:
https://doaj.org/article/604697306aac4d28affe125b4df585c3
Autor:
Stefania Cheli, Stephanie François, Beatrice Bodega, Francesco Ferrari, Elena Tenedini, Enrica Roncaglia, Sergio Ferrari, Enrico Ginelli, Raffaella Meneveri
Publikováno v:
PLoS ONE, Vol 6, Iss 6, p e20966 (2011)
Determine global gene dysregulation affecting 4q-linked (FSHD-1) and non 4q-linked (FSHD-2) cells during early stages of myogenic differentiation. This approach has been never applied to FSHD pathogenesis.By in vitro differentiation of FSHD-1 and FSH
Externí odkaz:
https://doaj.org/article/fa573f8e39e14b8c8a769b5d6e5ed012
Autor:
Beatrice Bodega, Alexandros Xynos, Enrico Ginelli, Valentina Casa, Yujiro Tanaka, Daphne S. Cabianca, Davide Gabellini
Publikováno v:
Cell
Summary Repetitive sequences account for more than 50% of the human genome. Facioscapulohumeral muscular dystrophy (FSHD) is an autosomal-dominant disease associated with reduction in the copy number of the D4Z4 repeat mapping to 4q35. By an unknown
Autor:
Cristiana Lavazza, Paolo Picozzi, Beatrice Bodega, Anna Marozzi, Carmelo Carlo-Stella, Enrico Ginelli, Elena Rossi
Publikováno v:
ResearcherID
Scopus-Elsevier
Scopus-Elsevier
The constitutive over-expression of the retinol dehydrogenase 10 (RDH10) gene, involved in retinoic acid (RA) biosynthesis, produced in HepG2 cells a significant antiproliferative response, but not signs of apoptosis. An indirect assay based on the C
Autor:
Anna Marozzi, Beatrice Bodega, Enrico Ginelli, Maria Francesca Cardone, Mariano Rocchi, Raffaella Meneveri
Publikováno v:
Genomics. 88(5):564-571
In Macaca mulatta, the single rDNA array is flanked by a patchwork of sequences including subregions of human Yp11.2, 4q35.2, and 10p15.3. This composite DNA region is characterized by unique or low-copy sequences, resembling a potentially transcribe
Autor:
Donatella Barisani, Marta Sabbadini, Giuseppe Miserocchi, Raffaella Meneveri, Anna Marozzi, Enrico Ginelli, Elena Conforti
Publikováno v:
Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease. 1638(2):149-156
To investigate the molecular events taking place during the development of hydraulic interstitial edema, we analyzed by microarray and conventional molecular techniques the variation of gene expression in lung from rabbits treated with slow-rate sali
Autor:
Nicoletta Archidiacono, A. Rollier, I. Piccini, Raffaella Meneveri, L. Carbone, Enrico Ginelli, Anna Marozzi, L. Ballarati
Publikováno v:
Gene. 296:21-27
We have investigated the evolutionary history of the 4q35 paralogous region, and of a sub-family of interspersed LSau repeats. In HSA, 4q35 duplications were localized at 1q12, 3p12.3, 4q35, 10q26, 20cen, whereas duplicons and interspersed LSau repea
Autor:
Giulia Soldà, Veronica Colangelo, Stephanie François, Francesca Roma, Raffaella Meneveri, Enrico Ginelli, Raffaella Picco
Publikováno v:
PLoS ONE
PLoS ONE, Vol 9, Iss 10, p e108411 (2014)
PLoS ONE, Vol 9, Iss 10, p e108411 (2014)
Emerging evidence has demonstrated that miRNA sequences can regulate skeletal myogenesis by controlling the process of myoblast proliferation and differentiation. However, at present a deep analysis of miRNA expression in control and FSHD myoblasts d
Autor:
Leda Dalprà, Maria Grazia Tibiletti, Nicoletta Villa, Anna Marozzi, Raffaella Meneveri, Walter Vegetti, E. Manfredini, Enrico Ginelli, Pier Giorgio Crosignani, Daniela Furlan
Publikováno v:
Scopus-Elsevier
High-resolution cytogenetic analysis of a large number of women with premature ovarian failure (POF) identified six patients carrying different Xq chromosome rearrangements. The patients (one familial and five sporadic cases) were negative for Turner
Autor:
Ivana Magnani, C. Bassi, Anna Marozzi, A. Ventura, Raffaella Meneveri, Nicoletta Sacchi, Enrico Ginelli, Mariano Rocchi, Salvatore Saccone
Publikováno v:
Gene. 256:43-50
We have isolated and characterised one PAC clone (dJ233C1) containing a linkage between alphoid and non-alphoid DNA. The non-alphoid DNA was found to map at the pericentromeric region of chromosome 20, both on p and q sides, and to contain homologies