Zobrazeno 1 - 10
of 46
pro vyhledávání: '"Giovanna Priante"'
Autor:
Giovanna Priante, Monica Ceol, Lisa Gianesello, Dario Bizzotto, Paola Braghetta, Lorenzo Arcangelo Calò, Dorella Del Prete, Franca Anglani
Publikováno v:
International Journal of Molecular Sciences, Vol 24, Iss 2, p 1313 (2023)
Dent disease (DD1) is a rare tubulopathy caused by mutations in the CLCN5 gene. Glomerulosclerosis was recently reported in DD1 patients and ClC-5 protein was shown to be expressed in human podocytes. Nephrin and actin cytoskeleton play a key role fo
Externí odkaz:
https://doaj.org/article/571f79d9783945debab86ec5dc9516b5
Autor:
Lisa Gianesello, Jennifer Arroyo, Dorella Del Prete, Giovanna Priante, Monica Ceol, Peter C. Harris, John C. Lieske, Franca Anglani
Publikováno v:
Genes, Vol 12, Iss 10, p 1597 (2021)
Dent disease is a rare X-linked renal tubulopathy due to CLCN5 and OCRL (DD2) mutations. OCRL mutations also cause Lowe syndrome (LS) involving the eyes, brain and kidney. DD2 is frequently described as a mild form of LS because some patients may pre
Externí odkaz:
https://doaj.org/article/70a08cbce6fb4b7c8b3ff0f417fd81b9
Autor:
Lisa Gianesello, Giovanna Priante, Monica Ceol, Claudia M. Radu, Moin A. Saleem, Paolo Simioni, Liliana Terrin, Franca Anglani, Dorella Del Prete
Publikováno v:
Scientific Reports, Vol 7, Iss 1, Pp 1-10 (2017)
Abstract Albumin re-uptake is a receptor-mediated pathway located in renal proximal tubuli. There is increasing evidence of glomerular protein handling by podocytes, but little is known about the mechanism behind this process. In this study, we found
Externí odkaz:
https://doaj.org/article/870c4846e16141b892ddc0d384672106
Autor:
Lisa Gianesello, Monica Ceol, Loris Bertoldi, Liliana Terrin, Giovanna Priante, Luisa Murer, Licia Peruzzi, Mario Giordano, Fabio Paglialonga, Vincenzo Cantaluppi, Claudio Musetti, Giorgio Valle, Dorella Del Prete, Franca Anglani, Dent Disease Italian Network
Publikováno v:
International Journal of Molecular Sciences, Vol 21, Iss 2, p 516 (2020)
Dent disease (DD), an X-linked renal tubulopathy, is mainly caused by loss-of-function mutations in CLCN5 (DD1) and OCRL genes. CLCN5 encodes the ClC-5 antiporter that in proximal tubules (PT) participates in the receptor-mediated endocytosis of low
Externí odkaz:
https://doaj.org/article/67afa56451224320899ba5f0e99a8088
Publikováno v:
International Journal of Molecular Sciences, Vol 20, Iss 14, p 3598 (2019)
Apoptotic cell death is usually a response to the cell’s microenvironment. In the kidney, apoptosis contributes to parenchymal cell loss in the course of acute and chronic renal injury, but does not trigger an inflammatory response. What distinguis
Externí odkaz:
https://doaj.org/article/fc832087c9dd406391e02e57df3eecde
Autor:
Dorella Del Prete, Lisa Gianesello, Alejandro Iotti, Monica Ceol, Giovanna Priante, Hernán Trimarchi
Publikováno v:
Journal of Nephrology. 34:1307-1314
Fabry disease is an X-linked disorder due to mutations in α-galactosidase A, resulting in the accumulation of enzyme substrates and cell malfunction. Kidney involvement is frequent, affecting all native kidney cell types. Podocyte damage results in
Autor:
Monica Ceol, Enrica Tosetto, Dorella Del Prete, Lisa Gianesello, Giovanna Priante, Franca Anglani
Publikováno v:
J Investig Med
ClC-5, the electrogenic chloride/proton exchanger strongly expressed in renal proximal tubules, belongs to the endocytic macromolecular complex responsible for albumin and low-molecular-weight protein uptake. ClC-5 was found to be overexpressed in gl
Autor:
Monica Ceol, John C. Lieske, Peter C. Harris, Jennifer Arroyo, Franca Anglani, Lisa Gianesello, Giovanna Priante, Dorella Del Prete
Publikováno v:
Genes
Genes; Volume 12; Issue 10; Pages: 1597
Genes, Vol 12, Iss 1597, p 1597 (2021)
Genes; Volume 12; Issue 10; Pages: 1597
Genes, Vol 12, Iss 1597, p 1597 (2021)
Dent disease is a rare X-linked renal tubulopathy due to CLCN5 and OCRL (DD2) mutations. OCRL mutations also cause Lowe syndrome (LS) involving the eyes, brain and kidney. DD2 is frequently described as a mild form of LS because some patients may pre
When tissues are damaged, they usually heal. The cellular responses towards healing require the prior recognition that damage has occurred. Apoptotic cell death is usually a response to the cell’s microenvironment. In fact, prolonged cellular stres
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2106694d5f4de12ab7ec197a3de46b0b
https://doi.org/10.9734/bpi/rrab/v10/9825d
https://doi.org/10.9734/bpi/rrab/v10/9825d
Autor:
Giovanna Priante, Dorella Del Prete, Monica Ceol, Lorenzo A. Calò, Lisa Gianesello, Franca Anglani
Publikováno v:
Gene
Proteinuria is a well-known risk factor, not only for renal disorders, but also for several other problems such as cardiovascular diseases and overall mortality. In the kidney, the chloride channel Cl(−)/H(+) exchanger C1C-5 encoded by the CLCN5 ge
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::02d88f3cf969c2877afb6cbb8d348542
http://hdl.handle.net/11577/3336102
http://hdl.handle.net/11577/3336102