Extensive analytical evaluation of the performances of the new DiaSys PCT assay and comparison with Elecsys B·R·A·H·M·S PCT test on Roche Cobas and B·R·A·H·M·S PCT-sensitive Kryptor.

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

An unusual presentation of isolated polydactyly: four limbs hexadactyly

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

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

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5e5c4740f0e352d1fb9f5f7ccac3a632
https://riviste.unimi.it/index.php/AMSUM/article/view/13402

The 20S proteasome activator PA28γ controls the compaction of HP1β-linked heterochromatin

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⟩

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

Renal phosphate handling in Gitelman syndrome—the results of a case-control study

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

Quantitative proteomic and phospho-proteomic analysis of human DLD1 cells differing in ploidy and chromosome stability

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