Zobrazeno 1 - 10
of 24
pro vyhledávání: '"Piera Trionfini"'
Autor:
Luca Perico, Marta Todeschini, Federica Casiraghi, Marilena Mister, Anna Pezzotta, Tobia Peracchi, Susanna Tomasoni, Piera Trionfini, Ariela Benigni, Giuseppe Remuzzi
Publikováno v:
Frontiers in Immunology, Vol 14 (2023)
We examined the immune response in subjects previously infected with SARS-CoV2 and infection-naïve 9 months after primary 2-dose COVID-19 mRNA vaccination and 3 months after the booster dose in a longitudinal cohort of healthcare workers. Nine month
Externí odkaz:
https://doaj.org/article/c6dd1c6048334328923fb6f16ace37a3
Autor:
Luca Perico, Marina Morigi, Anna Pezzotta, Daniela Corna, Valerio Brizi, Sara Conti, Cristina Zanchi, Fabio Sangalli, Piera Trionfini, Sara Buttò, Christodoulos Xinaris, Susanna Tomasoni, Carlamaria Zoja, Giuseppe Remuzzi, Ariela Benigni, Barbara Imberti
Publikováno v:
Scientific Reports, Vol 11, Iss 1, Pp 1-18 (2021)
Abstract Abnormal kidney development leads to lower nephron number, predisposing to renal diseases in adulthood. In embryonic kidneys, nephron endowment is dictated by the availability of nephron progenitors, whose self-renewal and differentiation re
Externí odkaz:
https://doaj.org/article/348d577fe4874089875fa592c84cadd5
Autor:
Piera Trionfini, Elena Romano, Marco Varinelli, Lorena Longaretti, Paola Rizzo, Roberta Giampietro, Annalina Caroli, Sistiana Aiello, Marta Todeschini, Federica Casiraghi, Giuseppe Remuzzi, Ariela Benigni, Susanna Tomasoni
Publikováno v:
International Journal of Molecular Sciences, Vol 24, Iss 14, p 11810 (2023)
Induced pluripotent stem cells (iPSC) have huge potential as cell therapy for various diseases, given their potential for unlimited self-renewal and capability to differentiate into a wide range of cell types. Although autologous iPSCs represents the
Externí odkaz:
https://doaj.org/article/e5678163ce1a4b1fb661134be7459673
Publikováno v:
Stem Cell Research, Vol 57, Iss , Pp 102580- (2021)
Human induced pluripotent stem cells (iPSCs) have great promise in regenerative medicine. However, several limitations, including immune-incompatibility, have raised concerns regarding their clinical application. Recent studies have shown that human
Externí odkaz:
https://doaj.org/article/831fefabf399488f847c57f65799c790
Publikováno v:
Stem Cell Research, Vol 47, Iss , Pp 101881- (2020)
Autosomal dominant polycystic kidney disease (ADPKD) is the most common hereditary kidney disease, characterised by the development of multiple fluid-filled cysts in the kidneys and other organs. PKD1 and PKD2 are the two major causative genes encodi
Externí odkaz:
https://doaj.org/article/8b150a7e28904e458dc1b52042b27ef4
Publikováno v:
Stem Cell Research, Vol 42, Iss , Pp - (2020)
Autosomal dominant polycystic kidney disease (ADPKD) is the most prevalent inherited renal disease, characterized by multiple cysts that can lead to kidney failure resulting in end-stage renal disease. ADPKD is mainly caused by mutations in either th
Externí odkaz:
https://doaj.org/article/58ed6469b4ac464d870a597e20d67090
Autor:
Lorena Longaretti, Piera Trionfini, Valerio Brizi, Christodoulos Xinaris, Caterina Mele, Matteo Breno, Elena Romano, Roberta Giampietro, Giuseppe Remuzzi, Ariela Benigni, Susanna Tomasoni
Publikováno v:
Biomedicines, Vol 9, Iss 12, p 1808 (2021)
No effective treatments are available for familial steroid-resistant Focal Segmental Glomerulosclerosis (FSGS), characterized by proteinuria due to ultrastructural abnormalities in glomerular podocytes. Here, we studied a private PAX2 mutation identi
Externí odkaz:
https://doaj.org/article/08aef8f4506544499d69db0102459812
Autor:
Susanna Tomasoni, Caterina Mele, Piera Trionfini, Roberta Giampietro, Valerio Brizi, Lorena Longaretti, Giuseppe Remuzzi, Ariela Benigni, Matteo Breno, Christodoulos Xinaris, Elena Romano
Publikováno v:
Biomedicines; Volume 9; Issue 12; Pages: 1808
Biomedicines
Biomedicines, Vol 9, Iss 1808, p 1808 (2021)
Biomedicines
Biomedicines, Vol 9, Iss 1808, p 1808 (2021)
No effective treatments are available for familial steroid-resistant Focal Segmental Glomerulosclerosis (FSGS), characterized by proteinuria due to ultrastructural abnormalities in glomerular podocytes. Here, we studied a private PAX2 mutation identi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8b100a0ccbc268dc79e583449da21e8a
Publikováno v:
Stem Cell Research, Vol 57, Iss, Pp 102580-(2021)
Stem Cell Research
Stem Cell Research
Human induced pluripotent stem cells (iPSCs) have great promise in regenerative medicine. However, several limitations, including immune-incompatibility, have raised concerns regarding their clinical application. Recent studies have shown that human
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b949cd97d0aee5a7ea619c6ae79d18cd
http://www.sciencedirect.com/science/article/pii/S187350612100427X
http://www.sciencedirect.com/science/article/pii/S187350612100427X
Publikováno v:
Stem Cell Research, Vol 47, Iss, Pp 101881-(2020)
Autosomal dominant polycystic kidney disease (ADPKD) is the most common hereditary kidney disease, characterised by the development of multiple fluid-filled cysts in the kidneys and other organs. PKD1 and PKD2 are the two major causative genes encodi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5f491b8621124902f403fba178e3ab81
http://www.sciencedirect.com/science/article/pii/S1873506120301823
http://www.sciencedirect.com/science/article/pii/S1873506120301823