Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Ilaria Olivieri"'
Autor:
Endre Sebestyén, Fabrizia Marullo, Federica Lucini, Cristiano Petrini, Andrea Bianchi, Sara Valsoni, Ilaria Olivieri, Laura Antonelli, Francesco Gregoretti, Gennaro Oliva, Francesco Ferrari, Chiara Lanzuolo
Publikováno v:
Nature Communications, Vol 11, Iss 1, Pp 1-16 (2020)
Hutchinson-Gilford progeria syndrome is a genetic disease where an aberrant form of Lamin A disrupts chromatin by interfering with lamina associated domains. Here, the authors present the SAMMY-seq, a method for genome-wide characterization of hetero
Externí odkaz:
https://doaj.org/article/2551c3f1e7794b139aa2db7812391766
Autor:
Ilaria Olivieri
Publikováno v:
Storicamente, Vol 6, Iss 1 (2010)
The documentation of an infanticide trial, which took place in 1889 in Modena, allowed the reconstruction of the social setting for the judicial proceedings of a young woman accused of a crime that throughout the 19th century underwent a radical lega
Externí odkaz:
https://doaj.org/article/d46b75c6c0e64693baf97a1b638233c8
Autor:
Cristiano Petrini, Chiara Lanzuolo, Gennaro Oliva, Endre Sebestyén, Federica Lucini, Sara Valsoni, Francesco Ferrari, Louis Antonelli, Andrea Bianchi, Francesco Gregoretti, Fabrizia Marullo, Ilaria Olivieri
Publikováno v:
Nature Communications
Nature Communications, Vol 11, Iss 1, Pp 1-16 (2020)
Nature communications 11 (2020): 6274. doi:10.1038/s41467-020-20048-9
info:cnr-pdr/source/autori:Sebestyen E, Marullo F, Lucini F, Petrini C, Bianchi A, Valsoni S, Olivieri I, Antonelli L, Gregoretti F, Oliva G, Ferrari F, Lanzuolo C./titolo:SAMMY-seq reveals early alteration of heterochromatin and deregulation of bivalent genes in Hutchinson-Gilford Progeria Syndrome/doi:10.1038%2Fs41467-020-20048-9/rivista:Nature communications/anno:2020/pagina_da:6274/pagina_a:/intervallo_pagine:6274/volume:11
Nature Communications, Vol 11, Iss 1, Pp 1-16 (2020)
Nature communications 11 (2020): 6274. doi:10.1038/s41467-020-20048-9
info:cnr-pdr/source/autori:Sebestyen E, Marullo F, Lucini F, Petrini C, Bianchi A, Valsoni S, Olivieri I, Antonelli L, Gregoretti F, Oliva G, Ferrari F, Lanzuolo C./titolo:SAMMY-seq reveals early alteration of heterochromatin and deregulation of bivalent genes in Hutchinson-Gilford Progeria Syndrome/doi:10.1038%2Fs41467-020-20048-9/rivista:Nature communications/anno:2020/pagina_da:6274/pagina_a:/intervallo_pagine:6274/volume:11
Hutchinson-Gilford progeria syndrome is a genetic disease caused by an aberrant form of Lamin A resulting in chromatin structure disruption, in particular by interfering with lamina associated domains. Early molecular alterations involved in chromati
Autor:
Cristiano Petrini, Fabrizia Marullo, Sara Valsoni, Federica Lucini, Louis Antonelli, Francesco Ferrari, Ilaria Olivieri, Andrea Bianchi, Francesco Gregoretti, Chiara Lanzuolo, Endre Sebestyén, Gennaro Oliva
Hutchinson-Gilford progeria syndrome (HGPS) is characterized by the progressive accumulation of progerin, an aberrant form of Lamin A. This leads to chromatin structure disruption, in particular by interfering with Lamina Associated Domains. Although
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9b7ad8f27a9ed632d285583806b91a73
Autor:
Roberta Battini, Manuela Casarano, G. Rossi, R. Di Pietro, Giovanni Cioni, Ilaria Olivieri, Giuseppina Sgandurra
Publikováno v:
Developmental Medicine & Child Neurology. 58:22-26
Autor:
Valentina Menici, Roberta Battini, Ilaria Olivieri, Giovanni Cioni, Simona Lucibello, Chiara Velli, Manuela Casarano, Francesca Sini, Giuseppina Sgandurra, Domenico M. Romeo, Roberta Di Pietro
Publikováno v:
European Journal of Physical and Rehabilitation Medicine. 54
BACKGROUND Movement Disorder-Childhood Rating Scales (MD-CRS) have been designed in two forms (0-3 and 4-18 years) to accurately evaluate various movement disorders in children. AIM The aim of this study is to evaluate the MD-CRS reliability when use
Publikováno v:
Developmental Medicine & Child Neurology
Autor:
Giuseppina Sgandurra, Giovanni Cioni, Roberta Battini, Domenico M. Romeo, Ilaria Olivieri, Roberta Di Pietro, Manuela Casarano
Background The Movement Disorder-Childhood Rating Scale represents a new tool for assessment of movement disorders during developmental age. In this study, we evaluated a cohort of 68 patients affected by various types of movement disorders and treat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b572ce11fbc86977a46247021891f877
http://hdl.handle.net/11568/761727
http://hdl.handle.net/11568/761727
Autor:
Roberta Di Pietro, Ilaria Olivieri, Manuela Casarano, Eugenio Mercuri, Domenico M. Romeo, Roberta Battini, Giuseppina Sgandurra, Giovanni Cioni
Publikováno v:
European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society. 18(6)
Background Movement Disorder-Childhood Rating Scale (MD-CRS) is a new tool for assessment of movement disorders during developmental age. Aim In this study we evaluated a cohort of 47 patients affected by dyskinetic cerebral palsy and treated with an