Zobrazeno 1 - 10
of 33
pro vyhledávání: '"Viganò, Cristina"'
Autor:
Di Deo, Priscilla, Vantaggiato, Chiara, Di Modugno, Adriana, Licari, Debora, Savina, Pier Francesco, Zagliani, Arianna, Viganò, Cristina, Grimaldi, Gabriella, Frassanito, Antonio, Lettera, Tommaso, De Corato, Paola, Ammirabile, Massimiliano, Ferraris Fusarini, Chiara, De Liso, Federica, Maregnani, Alessio, Silvani, Iris, Taverriti, Tito Paolo Simone, Ceriotti, Ferruccio, Vidali, Matteo
Publikováno v:
Clinical Chemistry & Laboratory Medicine; Jan2024, Vol. 62 Issue 2, pe44-e47, 4p
Akademický článek
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Autor:
Piralla, Antonio, Lunghi, Giovanna, Percivalle, Elena, Viganò, Cristina, Nasta, Teresa, Pugni, Lorenza, Mosca, Fabio, Stronati, Mauro, Torresani, Erminio, Baldanti, Fausto
Publikováno v:
In Diagnostic Microbiology & Infectious Disease June 2014 79(2):183-186
Autor:
Maggi, Sonia, Viganò, Cristina, Colombo, Pierluigi, Menon, Alessandra, Compagnoni, Riccardo, Cortinovis, Francesca, Morandi, Francesco, Crosio, Alessandro, Randelli, Pietro Simone
Publikováno v:
Archives of Medicine and Surgery of the University of Milan; V. 1 N. 1 (2020); 17-21
Archives of Medicine & Surgery University of Milan; Vol 1 No 1 (2020); 17-21
Archives of Medicine & Surgery University of Milan; Vol 1 No 1 (2020); 17-21
Purpose: Hexadactyly is a congenital physical anomaly, potentially affecting the hand or the food. Aim of this study is to report two case reports of hexadactyly involving the four limbs, with a literature review focused on this pathology. Methods: T
Akademický článek
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Autor:
Fesquet, Didier, Llères, David, Viganò, Cristina, Méchali, Francisca, Boulon, Séverine, Feil, Robert, Coux, Olivier, Bonne-Andrea, Catherine, Baldin, Véronique
Publikováno v:
BioRxiv
BioRxiv, 2019, ⟨10.1101/716332⟩
BioRxiv, 2019, ⟨10.1101/716332⟩
International audience; The nuclear PA28γ is known to activate the 20S proteasome, but its precise cellular functions remains unclear. Here, we identify PA28γ as a key factor that structures heterochromatin. We find that in human cells, a fraction
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::c44ac999c694d3bea37477a8c3a84084
https://hal.archives-ouvertes.fr/hal-02349077
https://hal.archives-ouvertes.fr/hal-02349077
Autor:
Bettinelli, Alberto, Viganò, Cristina, Provero, Maria, Barretta, Francesco, Albisetti, Alessandra, Tedeschi, Silvana, Scicchitano, Barbara, Bianchetti, Mario
Background: Bartter patients may be hypercalciuric. Additional abnormalities in the metabolism of calcium, phosphate, and calciotropic hormones have occasionally been reported. Methods: The metabolism of calcium, phosphate, and calciotropic hormones
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od_______805::0a23ecf4a891b094aabc30b7ab721b4b
http://doc.rero.ch/record/325216/files/467_2014_Article_2846.pdf
http://doc.rero.ch/record/325216/files/467_2014_Article_2846.pdf
Autor:
Bettinelli, Alberto1, Viganò, Cristina2, Provero, Maria, Barretta, Francesco, Albisetti, Alessandra3, Tedeschi, Silvana4, Scicchitano, Barbara1, Bianchetti, Mario mario.bianchetti@pediatrician.ch
Publikováno v:
Pediatric Nephrology. Nov2014, Vol. 29 Issue 11, p2133-2138. 6p.
Autor:
Viganò, Cristina, Amoruso, Chiara, Barretta, Francesco, Minnici, Giuseppe, Albisetti, Walter, Syrèn, Marie-Louise, Bianchetti, Mario, Bettinelli, Alberto
Background: Patients with Gitelman syndrome, a hereditary salt-wasting tubulopathy, have loss-of-function mutations in the SLC12A3 gene coding for the thiazide-sensitive sodium chloride co-transporter in the distal convoluted tubule. Since the bulk o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od_______805::f6ab520f93e415ecd9de45371b21c1d7
http://doc.rero.ch/record/319608/files/467_2012_Article_2297.pdf
http://doc.rero.ch/record/319608/files/467_2012_Article_2297.pdf
Autor:
Viganò, Cristina
Aneuploidy is a state in which cells harbor a chromosome number that is not a whole multiple of the haploid chromosome set. This condition is poorly tolerated during embryogenesis and it the cause of developmental disorders such as Down syndrome (tri
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8005f8e65c18eb2ee0ee1ecb03a6d83e