Zobrazeno 1 - 10
of 33
pro vyhledávání: '"R. Graziotto"'
Autor:
Ugo Vertolli, Josef Nachtigal, Augusto Antonello, Ermanno De Paoli Vitali, R. Graziotto, Michele Piva, Riccardo Zagatti, Franca Anglani, Angela D'Angelo, Enrica Tosetto, Carmelo Cascone, Giovanni Gambaro, L. Artifoni, L. Citron, Federico Nalesso, Antonio Lupo, Piero Conz, Roberto Dell'Aquila
Publikováno v:
Journal of Human Genetics. 51:25-30
Dent’s disease (DD) involves nephrocalcinosis, urolithiasis, hypercalciuria, LMW proteinuria, and renal failure in various combinations. Males are affected. It is caused by mutations in the chloride channel CLCN5 gene. It has been suggested that DD
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f288167a68b4a6cbe5ebc1f52315d917
https://doi.org/10.1007/s10038-005-0317-x
https://doi.org/10.1007/s10038-005-0317-x
Autor:
Paolo Scannapieco, Antonella Russo, Roberto Salmaso, Alessandro Negro, Maurizio Onisto, R. Graziotto, Paola Zeilante, Carlo Foresta
Publikováno v:
Experimental Cell Research. 248:620-626
A novel human cDNA sequence has been isolated from human testis cDNA library. This sequence, named PD1, reveals an open reading frame encoding a protein of 520 amino acids. A partial sequence similarity has been found with the RBM gene involved in th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8caff0166b67f629c38d84449c88793e
https://doi.org/10.1006/excr.1999.4449
https://doi.org/10.1006/excr.1999.4449
Autor:
Franca Anglani, Luciana Bonfante, Giuseppe Scaparrotta, Lucrezia Furian, Dorella Del Prete, Marialuisa Valente, Paolo Rigotti, Daniela Vianello, Angela D'Angelo, R. Graziotto, Giovanni Gambaro, Emilia Tiralongo, Monica Ceol
Background/aims In kidney transplants, the renin–angiotensin system (RAS) is involved in systemic and local changes that may induce fibrosis. Our aim was to use gene expression and immunohistochemical analysis to investigate the RAS and several fac
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::32e1c95d01a38e290d8db6f5ff5a8b82
http://hdl.handle.net/11577/3241627
http://hdl.handle.net/11577/3241627
Autor:
Francesco Marchini, Marialuisa Valente, Nicola Baldan, R. Graziotto, Lucrezia Furian, Dorella Del Prete, Franca Anglani, Augusto Antonello, Angela D'Angelo, Paolo Rigotti, Giovanni Gambaro
Background The Perforin-Granzyme B and Fas/Fas Ligand apoptotic mechanisms are involved in the development of acute renal rejection (AR). We describe our experience of analyzing the expression of cytotoxic T-lymphotoxins (CTL) in biopsies and periphe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::98cbad8aee6d0881084d60b9139b68f4
http://hdl.handle.net/11562/229995
http://hdl.handle.net/11562/229995
Publikováno v:
Giornale italiano di nefrologia : organo ufficiale della Societa italiana di nefrologia. 20(6)
Dent's disease, a X-linked hypercalciuric nephrolithiasis, is caused by mutations of the CLCN5 gene. The disease is characterised by low molecular weight proteinuria with variable presence of hypercalciuria, hyperphosphaturia, nephrocalcinosis, and k
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::aa325ef21196be5c722441cc95eb3229
https://pubmed.ncbi.nlm.nih.gov/14732909
https://pubmed.ncbi.nlm.nih.gov/14732909
Autor:
Angela D'Angelo, Franca Anglani, Enrica Tosetto, Giovanni Gambaro, R. Graziotto, Dorella Del Prete, Monica Ceol
To the Editor: In mRNA quantitative studies, choosing a reliable internal control is mandatory for monitoring intersample variations and comparing target RNA levels if assays are performed in different experimental sessions and come from different ce
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::be6931b3eac9bcba35e971628c95a605
http://hdl.handle.net/11577/2439737
http://hdl.handle.net/11577/2439737
Publikováno v:
Journal of human genetics. 49(1)
Mutations in the CLCN5 gene have been detected in Dent's disease and its phenotypic variants (X-linked recessive nephrolithiasis, X-linked recessive hypophosphatemic rickets, and idiopathic low-molecular-weight proteinuria of Japanese children). Dent
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::428b018d5ae9c48f8efe3a22f5afdb36
https://pubmed.ncbi.nlm.nih.gov/14673707
https://pubmed.ncbi.nlm.nih.gov/14673707
Autor:
Patrizia Bernich, B. Brezzi, Riccardo Magistroni, Antonio Lupo, Francesca Modena, Alberto Albertazzi, L. Furci, Giuseppe Maschio, Dorella Del Prete, Angela D'Angelo, Giovanni Gambaro, R. Graziotto, Franca Anglani
Publikováno v:
Università degli studi di Modena e Reggio Emilia-IRIS
Precocious activation of genes of the renin-angiotensin system and the fibrogenic cascade in IgA glomerulonephritis. Background The renin-angiotensin system (RAS) seems to play a pivotal role in progression of immunoglobulin A (IgA) nephropathy (IgAN
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::44e704355318124c410a6be6b0d566f1
https://pubmed.ncbi.nlm.nih.gov/12787405
https://pubmed.ncbi.nlm.nih.gov/12787405
Autor:
M, Onisto, L M, Slongo, R, Graziotto, L, Zotti, A, Negro, M, Merico, E, Moro, C, Foresta, O, Maurizio, S M, Liliana, G, Romina, Z, Lorenza, N, Alessandro, M, Maurizio, M, Enrico, F, Carlo
Publikováno v:
Biochemical and Biophysical Research Communications. 285:570
Here we report the cloning and characterization of a novel cDNA named spata 2. SPATA2 is the ortholog of PD1, a human testicular protein which has been suggested to play a role in spermatogenesis. The spata 2 sequence reveals an open reading frame en
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5910e670eafb0ebb8c94eebbfb077936
https://doi.org/10.1006/bbrc.2001.5204
https://doi.org/10.1006/bbrc.2001.5204
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