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Mostrati risultati da 1 a 20 di 41
Titolo Data di pubblicazione Autori Tipo File Abstract
Mutations in the coding region of the FOXL2 gene are not a major cause of idiopathic premature ovarian failure 2004 B. BodegaP.G. CrosignaniE. GinelliA. Marozzi + Article (author) -
Identification of new variants of GDF9 gene in large cohort of women with Premature Ovarian Failure 2006 R. RossettiE. Di PasqualeB. Bodega­P. Beck-PeccozA. MarozziL. Persani + Conference Object -
Identification of new variants of human BMP15 gene in a large cohort of women with premature ovarian failure 2006 E. Di PasqualeR. RossettiA. MarozziB. BodegaP. Beck-PeccozL. Persani + Article (author) -
Influence of intermediate and uninterrupted FMR1 CGG expansions in premature ovarian failure manifestation 2006 B. BodegaE. GinelliA. Marozzi + Article (author) -
The boundary of macaque rDNA is constituted by low-copy sequences conserved during evolution 2006 B. BodegaA. MarozziE. Ginelli + Article (author) -
Forced Expression of RDH10 Gene Retards Growth of HepG2 Cells 2007 B. BodegaC. LavazzaC. Carlo-StellaA. MarozziE. Ginelli + Article (author) -
DISSECTING THE GENETIC BASIS AND MOLECULAR MECHANISMS OF PREMATURE OVARIAN FAILURE 2007 A. MarozziB. BodegaN. Locatelli + Conference Object -
Evolutionary genomic remodelling of the human 4q subtelomere (4q35.2) 2007 B. BodegaE. BattaglioliA. MarozziP.V. RivaE. Ginelli + Article (author) -
FMR1 PREMUTATION AND PREMATURE OVARIAN FAILURE 2007 N. LocatelliB. BodegaE. GinelliA. Marozzi + Conference Object -
Intra-chromosomal looping within FSHD locus provides the epigenitic link between D4Z4 array and FRG1 gene expression 2008 B. BodegaDI CAPUA, GABRIELLA ALEJANDRAS. CheliA. MarozziE. BattaglioliE. Ginelli + Conference Object -
Polycomb complex shapes the higher order of D4Z4 chromatin structure during differentiation of normal and FSHD muscle stem cells 2008 B. BodegaN. LocatelliA. MarozziE. Battaglioli + Article (author) -
Molecular characterization of premature ovarian failure associated with FMR1 premutation 2008 LOCATELLI, NADIAB. BodegaE. GinelliA. Marozzi + Article (author) -
Remodeling of the chromatin structure of the facioscapulohumeral muscular dystrophy (FSHD) locus and upregulation of FSHD-related gene 1 (FRG1) expression during human myogenic differentiation 2009 B. BodegaG. Di CapuaS. CheliA. MarozziE. BattaglioliE. Ginelli + Article (author) -
Chromatin regulated interchange between polycomb repressive complex 2 (PRC2)-Ezh2 and PRC2-Ezh1 complexes controls myogenin activation in skeletal muscle cells 2011 BODEGA, BEATRICED. Pasini + Article (author) -
A long ncRNA links copy number variation to a polycomb/trithorax epigenetic switch in FSHD muscular dystrophy 2012 B. BodegaE. Ginelli + Article (author) -
Evolutionary history of linked D4Z4 and Beta satellite clusters at the FSHD locus (4q35) 2012 M. GiussaniB. BodegaE. Ginelli + Article (author) -
Repetitive elements dynamics in cell identity programming, maintenance and disease 2014 Bodega B. + Article (author) -
A promoter-level mammalian expression atlas 2014 Bodega B. + Article (author) -
Lamin A/C sustains PcG protein architecture, maintaining transcriptional repression at target genes 2015 Bodega B. + Article (author) -
Transcribed enhancers lead waves of coordinated transcription in transitioning mammalian cells 2015 Bodega B.Sato H. + Article (author) -
Mostrati risultati da 1 a 20 di 41
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