Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Alessia Lo Curto"'
Autor:
Giulia Accardi, Filippa Bono, Giuseppe Cammarata, Anna Aiello, Maria Trinidad Herrero, Riccardo Alessandro, Giuseppa Augello, Ciriaco Carru, Paolo Colomba, Maria Assunta Costa, Immaculata De Vivo, Mattia Emanuela Ligotti, Alessia Lo Curto, Rosa Passantino, Simona Taverna, Carmela Zizzo, Giovanni Duro, Calogero Caruso, Giuseppina Candore
Publikováno v:
Cells, Vol 11, Iss 9, p 1505 (2022)
Human ageing can be characterized by a profile of circulating microRNAs (miRNAs), which are potentially predictors of biological age. They can be used as a biomarker of risk for age-related inflammatory outcomes, and senescent endothelial cells (ECs)
Externí odkaz:
https://doaj.org/article/e2a8357ce87b468abe0283592974a58a
Autor:
Alessia Lo Curto, Simona Taverna, Maria Assunta Costa, Rosa Passantino, Giuseppa Augello, Giorgia Adamo, Anna Aiello, Paolo Colomba, Carmela Zizzo, Marco Zora, Giulia Accardi, Giuseppina Candore, Daniele Francofonte, Tiziana Di Chiara, Riccardo Alessandro, Calogero Caruso, Giovanni Duro, Giuseppe Cammarata
Publikováno v:
Cells, Vol 10, Iss 2, p 356 (2021)
Fabry disease (FD) is a lysosomal storage disorder (LSD) characterized by lysosomal accumulation of glycosphingolipids in a wide variety of cytotypes, including endothelial cells (ECs). FD patients experience a significantly reduced life expectancy c
Externí odkaz:
https://doaj.org/article/dd46536a03144ca6961649a8754ef272
Autor:
Giuseppe Cammarata, Simona Taverna, Alessia Lo Curto, Tiziana Di Chiara, Giovanni Duro, Giuseppina Candore
Publikováno v:
Current pharmaceutical design
(2019).
info:cnr-pdr/source/autori:Giuseppe Cammarata; Giovanni Duro; Tiziana Di Chiara; Alessia Lo Curto; Simona Taverna; Giuseppina Candore./titolo:Circulating miRNAs in Successful and Unsuccessful Aging. A Mini-review/doi:/rivista:Current pharmaceutical design (Print)/anno:2019/pagina_da:/pagina_a:/intervallo_pagine:/volume
(2019).
info:cnr-pdr/source/autori:Giuseppe Cammarata; Giovanni Duro; Tiziana Di Chiara; Alessia Lo Curto; Simona Taverna; Giuseppina Candore./titolo:Circulating miRNAs in Successful and Unsuccessful Aging. A Mini-review/doi:/rivista:Current pharmaceutical design (Print)/anno:2019/pagina_da:/pagina_a:/intervallo_pagine:/volume
Aging is a multifactorial process that affects the organisms at genetic, molecular and cellular levels. This process modifies several tissues with a negative impact on cells physiology, tissues and organs functionality, altering their regeneration ca
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b663eca627b179aff463244357330275
https://doi.org/10.2174/1381612825666191119091644
https://doi.org/10.2174/1381612825666191119091644
Autor:
Anna Aiello, Giulia Accardi, Giuseppina Candore, Riccardo Alessandro, Daniele Francofonte, Carmela Zizzo, Giuseppe Cammarata, Giorgia Adamo, Giovanni Duro, Paolo Colomba, Alessia Lo Curto, Rosa Passantino, Giuseppa Augello, Marco Zora, Tiziana Di Chiara, Calogero Caruso, Maria Assunta Costa, Simona Taverna
Publikováno v:
Cells
Volume 10
Issue 2
Cells, Vol 10, Iss 356, p 356 (2021)
Cells (2021).
info:cnr-pdr/source/autori:Lo Curto A; Taverna S; Costa MA; Passantino R; Augello G; Adamo G; Aiello A ; Colomba P; Zizzo C; Zora M; Accardi G; Candore G; Francofonte D; Di Chiara T; Alessandro R; Caruso C; Duro G; Cammarata G;/titolo:Can Be miR-126-3p a Biomarker of Premature Aging? An Ex Vivo and In Vitro Study in Fabry Disease/doi:/rivista:Cells/anno:2021/pagina_da:/pagina_a:/intervallo_pagine:/volume
Volume 10
Issue 2
Cells, Vol 10, Iss 356, p 356 (2021)
Cells (2021).
info:cnr-pdr/source/autori:Lo Curto A; Taverna S; Costa MA; Passantino R; Augello G; Adamo G; Aiello A ; Colomba P; Zizzo C; Zora M; Accardi G; Candore G; Francofonte D; Di Chiara T; Alessandro R; Caruso C; Duro G; Cammarata G;/titolo:Can Be miR-126-3p a Biomarker of Premature Aging? An Ex Vivo and In Vitro Study in Fabry Disease/doi:/rivista:Cells/anno:2021/pagina_da:/pagina_a:/intervallo_pagine:/volume
Fabry disease (FD) is a lysosomal storage disorder (LSD) characterized by lysosomal accumulation of glycosphingolipids in a wide variety of cytotypes, including endothelial cells (ECs). FD patients experience a significantly reduced life expectancy c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dbb2dfa9a76392130429717a03c3a4b8
Autor:
Serafina Sciarrino, Silvia Vitale, Giuseppe Cammarata, Paolo Colomba, Marco Zora, Emanuela Maria Marsana, Carmela Zizzo, Roberta Olivieri, Simone Scalia, Daniele Francofonte, Chiara Brando, Simona Taverna, Giovanni Duro, Alessia Lo Curto
Publikováno v:
Aging (N.Y.N.Y.) (2020).
info:cnr-pdr/source/autori:Simona Taverna; Giuseppe Cammarata; Paolo Colomba; Serafina Sciarrino; Carmela Zizzo; Daniele Francofonte; Marco Zora; Simone Scalia; Chiara Brando; Alessia Lo Curto; Emanuela Maria Marsana; Roberta Olivieri; Silvia Vitale; Giovanni Duro./titolo:Pompe disease: pathogenesis, molecular genetics and diagnosis/doi:/rivista:Aging (N.Y.N.Y.)/anno:2020/pagina_da:/pagina_a:/intervallo_pagine:/volume
Aging (Albany NY)
info:cnr-pdr/source/autori:Simona Taverna; Giuseppe Cammarata; Paolo Colomba; Serafina Sciarrino; Carmela Zizzo; Daniele Francofonte; Marco Zora; Simone Scalia; Chiara Brando; Alessia Lo Curto; Emanuela Maria Marsana; Roberta Olivieri; Silvia Vitale; Giovanni Duro./titolo:Pompe disease: pathogenesis, molecular genetics and diagnosis/doi:/rivista:Aging (N.Y.N.Y.)/anno:2020/pagina_da:/pagina_a:/intervallo_pagine:/volume
Aging (Albany NY)
Pompe disease (PD) is a rare autosomal recessive disorder caused by mutations in the GAA gene, localized on chromosome 17 and encoding for acid alpha-1,4-glucosidase (GAA). Currently, more than 560 mutations spread throughout GAA gene have been repor
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::858b60d30469953e27bbe2ab47c52fa5
https://publications.cnr.it/doc/426767
https://publications.cnr.it/doc/426767
