Sfoglia per Autore
FMR1 PREMUTATION AND PREMATURE OVARIAN FAILURE
2007 N. Locatelli, A. D’Ambrosio, B. Bodega, S. Bione, D. Toniolo, E. Ginelli, A. Marozzi
Molecular and functional characterization of BMP15 variants associated with secondary amenorrhea and Premature Ovarian Failure (POF)
2008 R. Rossetti, E. Di Pasquale, A. Marozzi, S. Bione, P. Beck-Peccoz, L. Persani
Molecular and functional characterization of BMP15 variants associated with secondary amenorrhea and premature ovarian failure (POF)
2008 R. Rossetti, E. Di Pasquale, A. Marozzi, S. Bione, P.L.M. Beck Peccoz, L. Persani
Intra-chromosomal looping within FSHD locus provides the epigenitic link between D4Z4 array and FRG1 gene expression
2008 B. Bodega, G.A. DI CAPUA, S. Cheli, F. Grasser, S. Mueller, A. Marozzi, E. Battaglioli, E. Ginelli
Genetic aspects of female reproduction
2008 J. Collins, K. Diedrich, S. Franks, J.P. Geraedts, P.A. Jacobs, B. Karges, S. Kennedy, A. Marozzi, L. Regan, D.T. Baird, P.G. Crosignani, P. Devroey, E. Diczfalusy, J.L. Evers, B.C. Fauser, L. Fraser, L. Gianaroli, A. Glasier, I. Liebaer, G. Ragni, A. Sunde, B. Tarlatzis, A. Van Steirteghem, ESHRE Capri Workshop Group
In Vitro Molecular And Functional Studies Of Bmp15 Mutations Associated With Premature Ovarian Failure
2008 R. Rossetti, A. Marozzi, S. Bione, E. Di Pasquale, P. Beck-Peccoz, L. Persani
Molecular characterization of premature ovarian failure associated with FMR1 premutation
2008 N. Locatelli, K. Camelin, B. Bodega, S. Bione, D. Toniolo, C. Santoro, E. Ginelli, A. Marozzi
Polycomb complex shapes the higher order of D4Z4 chromatin structure during differentiation of normal and FSHD muscle stem cells
2008 B. Bodega, S. Brunelli, F. Grasser, N. Locatelli, R. Meneveri, A. Marozzi, S. Mueller, E. Battaglioli, E. Ginelli
Candidate gene analyses in Caucasian patients with Primary Ovarian Insufficiency (POI)
2009 R. Rossetti, C. Cacciatore, A. Marozzi, D. Cordella, S. Bione, S. Cannavo, D. Bernard, T. Cole, J. Clayton Smith, P. Beck-Peccoz, L. Persani
SCREENING OF SIX CANDIDATE GENES FOR PRIMARY OVARIAN INSUFFICIENCY (POI) IN A LARGE CAUCASIAN FEMALE POPULATION
2009 R. Rossetti, C. Cacciatore, A. Marozzi, D. Cordella, P. Beck-Peccoz, L. Persani, N. Italiano per lo studio dei Difetti Ovarici
A large-scale association study to assess the impact of known variants of the human INHA gene on premature ovarian failure
2009 T. Corre, J. Schuettler, S. Bione, A. Marozzi, L. Persani, R. Rossetti, F. Torricelli, I. Giotti, P. Vogt, D. Toniolo, I. Network for the study of Ovarian Dysfunctions
BMP15 mutations associated with primary ovarian insufficiency cause a defective production of bioactive protein
2009 R. Rossetti, E. Di Pasquale, A. Marozzi, S. Bione, D. Toniolo, P. Grammatico, L. M. Nelson, P. Beck-Peccoz, L. Persani
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. Bodega, G. Di Capua, F. Grasser, S. Cheli, S. Brunelli, M. Mora, R. Meneveri, A. Marozzi, S. Mueller, E. Battaglioli, E. Ginelli
Dissecting the role of FMR1 mRNA in the molecular FXPOI pathogenesis
2010 N. Locatelli, V. Padovano, M. Cavaletto, C. Caslini, C. Santoro, G. Pietrini, E. Ginelli, A. Marozzi
Cytogenetics of premature ovarian failure : an investigation on 269 affected women
2011 S. Baronchelli, D. Conconi, E. Panzeri, A. Bentivegna, S. Redaelli, S. Lissoni, F. Saccheri, N. Villa, F. Crosti, E. Sala, E. Martinoli, M. Volontè, A. Marozzi, L. Dalprà
Investigating the role of X chromosome breakpoints in premature ovarian failure
2012 S. Baronchelli, N. Villa, S. Redaelli, S. Lissoni, F. Saccheri, E. Panzeri, D. Conconi, A. Bentivegna, F. Crosti, E. Sala, F. Bertola, A. Marozzi, A. Pedicini, M. Ventruto, M.A. Police, L. Dalprà
L’ereditarietà dei caratteri complessi
2014 L. Amicone, C. Cicchini, F. Citarella, M. Colombi, S. Crovella, A. Marozzi, A. Melis, P. Riva, C. Ross, B. Porfirio, A. Turco, B. Varriale
Identification of genetic factors associated with neural tube defects
2014 V. Massa, G. Soldà, L. Avagliano, G. Fazio, G. Cazzaniga, G. Bulfamante, A. Marozzi, F. Cotelli, A. Pistocchi, A. Gallina
Identification of rare CNVs involving genes acting in oocyte maturation and differentiation in a cohort of patients affected by Primary Ovarian Insufficiency
2014 I. Bestetti, C. Castronovo, M. Crippa, R. Rossetti, A. Pistocchi, C. Caslini, C. Sala, D. Toniollo, L. Persani, A. Marozzi, P. Finelli
Molecular understanding of the FMR1 premutation and fragile X-associated premature ovarian failure
2014 C. Caslini, A. Crespi, G. Pietrini, A. Marozzi
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