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pro vyhledávání: '"Patrizia Calandra1"'
Autor:
Patrizia Calandra1, Nicoletta Rossi 1, Richard J. L. F. Lemmers 2, Emanuela Teveroni 1, Mauro Monforte 3, Enzo Ricci 3, Fabiola Moretti 1, Silvère M. van der Maarel 2, Giancarlo Deidda 1.
Publikováno v:
FSH Society Facioscapulohumeral Muscular Dystrophy [FSHD] 2018 International Research Congress & Research Planning Meetings, las vegas NV USA, June 8-9, 2018
info:cnr-pdr/source/autori:Patrizia Calandra1, Nicoletta Rossi 1, Richard J. L. F. Lemmers 2, Emanuela Teveroni 1, Mauro Monforte 3, Enzo Ricci 3, Fabiola Moretti 1, Silvère M. van der Maarel 2, Giancarlo Deidda 1./congresso_nome:FSH Society Facioscapulohumeral Muscular Dystrophy [FSHD] 2018 International Research Congress & Research Planning Meetings/congresso_luogo:las vegas NV USA/congresso_data:June 8-9, 2018/anno:2018/pagina_da:/pagina_a:/intervallo_pagine
info:cnr-pdr/source/autori:Patrizia Calandra1, Nicoletta Rossi 1, Richard J. L. F. Lemmers 2, Emanuela Teveroni 1, Mauro Monforte 3, Enzo Ricci 3, Fabiola Moretti 1, Silvère M. van der Maarel 2, Giancarlo Deidda 1./congresso_nome:FSH Society Facioscapulohumeral Muscular Dystrophy [FSHD] 2018 International Research Congress & Research Planning Meetings/congresso_luogo:las vegas NV USA/congresso_data:June 8-9, 2018/anno:2018/pagina_da:/pagina_a:/intervallo_pagine
FSHD forms are associated to D4Z4 DNA hypomethylation on 4qA allelic chromosomes. These epigenetic changes provide a transcriptionally permissive chromatin environment leading to the production of a pathogenic protein DUX4. We have shown that the epi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=cnr_________::88df7498b43115eeb5bbac0a82a9402f
http://www.cnr.it/prodotto/i/395753
http://www.cnr.it/prodotto/i/395753
Autor:
Emanuela Teveroni1, 2, Marsha Pellegrino1, Sabrina Sacconi3, 4, Patrizia Calandra1, Isabella Cascino1, Stefano Farioli-Vecchioli1, Roberta Morosetti5, Giorgio Tasca6, Enzo Ricci5, Giuliana Galluzzi1, Alfredo Pontecorvi2, Marco Crescenzi8, Giancarlo Deidda1, Fabiola Moretti1, 9
Publikováno v:
FSH Society Facioscapulohumeral Muscular Dystrophy [FSHD] 2016 International Research Consortium & Research Planning Meetings, Boston MA, USA, 10-11 November 2016
info:cnr-pdr/source/autori:Emanuela Teveroni1,2, Marsha Pellegrino1, Sabrina Sacconi3,4, Patrizia Calandra1, Isabella Cascino1, Stefano Farioli-Vecchioli1, Roberta Morosetti5, Giorgio Tasca6, Enzo Ricci5, Giuliana Galluzzi1, Alfredo Pontecorvi2, Marco Crescenzi8, Giancarlo Deidda1#, Fabiola Moretti1,9#/congresso_nome:FSH Society Facioscapulohumeral Muscular Dystrophy [FSHD] 2016 International Research Consortium & Research Planning Meetings/congresso_luogo:Boston MA, USA/congresso_data:10-11 November 2016/anno:2016/pagina_da:/pagina_a:/intervallo_pagine
info:cnr-pdr/source/autori:Emanuela Teveroni1,2, Marsha Pellegrino1, Sabrina Sacconi3,4, Patrizia Calandra1, Isabella Cascino1, Stefano Farioli-Vecchioli1, Roberta Morosetti5, Giorgio Tasca6, Enzo Ricci5, Giuliana Galluzzi1, Alfredo Pontecorvi2, Marco Crescenzi8, Giancarlo Deidda1#, Fabiola Moretti1,9#/congresso_nome:FSH Society Facioscapulohumeral Muscular Dystrophy [FSHD] 2016 International Research Consortium & Research Planning Meetings/congresso_luogo:Boston MA, USA/congresso_data:10-11 November 2016/anno:2016/pagina_da:/pagina_a:/intervallo_pagine
Facioscapulohumeral muscular dystrophy (FSHD) is characterized by extreme variability in symptoms with females being less severely affected than males and presenting a higher proportion of asymptomatic carriers. Gender factors involved in the disease
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=cnr_________::dc65d9590183f1a3939a061bdeb0db1f
http://www.cnr.it/prodotto/i/363483
http://www.cnr.it/prodotto/i/363483