[HTML][HTML] A long ncRNA links copy number variation to a polycomb/trithorax epigenetic switch in FSHD muscular dystrophy

DS Cabianca, V Casa, B Bodega, A Xynos, E Ginelli… - Cell, 2012 - cell.com
Repetitive sequences account for more than 50% of the human genome. Facioscapulohumeral
muscular dystrophy (FSHD) is an autosomal-dominant disease associated with reduction …

Influence of intermediate and uninterrupted FMR1 CGG expansions in premature ovarian failure manifestation

…, D Toniolo, F Ornaghi, W Vegetti, E Ginelli… - Human …, 2006 - academic.oup.com
BACKGROUND: Studies attempting to precisely define the range of fragile mental retardation
1 (FMR1) expansions and its inf luence in premature ovarian failure (POF) manifestation …

Alternative splicing of the histone demethylase LSD1/KDM1 contributes to the modulation of neurite morphogenesis in the mammalian nervous system

…, F Forneris, E Toffolo, C Verpelli, E Ginelli… - Journal of …, 2010 - Soc Neuroscience
A variety of chromatin remodeling complexes are thought to orchestrate transcriptional programs
that lead neuronal precursors from earliest commitment to terminal differentiation. Here …

Association between idiopathic premature ovarian failure and fragile X premutation

…, G Testa, PG Crosignani, E Ginelli… - Human …, 2000 - academic.oup.com
A total of 106 women affected by premature ovarian failure (POF) were evaluated for fragile
X (FRAXA) premutation. The POF patients were classified as having a familial condition (33 …

Mutation analysis of two candidate genes for premature ovarian failure, DACH2 and POF1B

…, L Dalpra, PG Crosignani, E Ginelli… - Human …, 2004 - academic.oup.com
BACKGROUND: Balanced X;autosome translocations interrupting the ‘critical region’ of the
long arm of the human X chromosome are often associated with premature ovarian failure (…

Mutation analysis of the inhibin alpha gene in a cohort of Italian women affected by ovarian failure

…, MG Tibiletti, L Dalpra, E Ginelli - Human …, 2002 - academic.oup.com
BACKGROUND: Premature ovarian failure (POF) is a secondary hypergonadotrophic
amenorrhoea affecting 1–3% of females, whose aetiology is almost unknown. However, inhibin …

Molecular definition of Xq common-deleted region in patients affected by premature ovarian failure

…, D Furlan, N Villa, W Vegetti, P Crosignani, E Ginelli… - Human Genetics, 2000 - Springer
High-resolution cytogenetic analysis of a large number of women with premature ovarian
failure (POF) identified six patients carrying different Xq chromosome rearrangements. The …

[HTML][HTML] Remodeling of the chromatin structure of the facioscapulohumeral muscular dystrophy (FSHD) locus and upregulation of FSHD-related gene 1 (FRG1) …

…, A Marozzi, S Mueller, E Battaglioli, E Ginelli - BMC biology, 2009 - Springer
… software (Genomatix, Munich, Germany) and identified one CarG box (the DNA binding site
of the YY1 protein) at position -371 from the transcriptional start site (+1), and two flanking E-…

Isolation and characterization of mouse and guinea pig satellite deoxyribonucleic acids

G Corneo, E Ginelli, C Soave, G Bernardi - Biochemistry, 1968 - ACS Publications
… 2% formaldehyde (e and e'). The peak on the left in each tracing except e' corresponds to the
… The peak on the right in the tracing e' corresponds to mouse satellite DNA (p = 1.690 g/ml) …

Repeated sequences in human DNA

G Corneo, E Ginelli, E Polli - Journal of Molecular Biology, 1970 - Elsevier
… DNA I (Cornea, Ginelli & Polli, 1968) and particularly satellite DNA II, isolated in the present
work, are similar in their reassocialtion properties to mouse satel1it.e DNA (Waring & B&ten, …