Sara Caldrer
University of Verona
Internal medicinePathologyPatch clampMolecular biologyAlleleImmunologyIn vivoTransmembrane proteinEx vivoNeuroblastomaInflammationCystic fibrosisCystic fibrosis transmembrane conductance regulatorSweat testIntestinal organoidsOrganoidCancer researchFlow cytometryDrug developmentMedicineBiology
18Publications
4H-index
109Citations
Publications 18
Newest
#1G. Bellisola (INFN: Istituto Nazionale di Fisica Nucleare)H-Index: 16
#2Sara CaldrerH-Index: 4
Last. Gianfelice CinqueH-Index: 30
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The mid-infrared (IR) spectra of human cystic fibrosis (CF) cells acquired by Fourier transform infrared microspectroscopy were compared with those of non-CF cells. Within the 1700 to 1480 cm(-1) spectral domain of amides, unsupervised explorative principal component analysis identified a few variables reflecting quantitative and qualitative vibrations arising from protein secondary structures and amino acid side chains. Their pattern reflected alpha-helix to beta-sheet transitions in bronchial ...
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#1Sara Caldrer (University of Verona)H-Index: 4
#2Gabriella Bergamini (University of Verona)H-Index: 9
Last. Paola MelottiH-Index: 20
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Cystic fibrosis transmembrane conductance regulator functional evaluations in a G542X+/- IVS8Tn:T7/9 patient with acute recurrent pancreatitis
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#1Paola LeccaH-Index: 8
#1Paola LeccaH-Index: 7
Last. Claudio SorioH-Index: 27
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#1Claudio SorioH-Index: 27
#2Sara CaldrerH-Index: 4
Last. Paola MelottiH-Index: 20
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and pulmonary disease management (ECFS; Sermet-Gaudelus et al. 2010). Results: There are currently 9 children diagnosed with CF following NBS enrolled at the paediatric CF specialized centre (14.8% of all patients), with a mean age of 11 months (range, 3–25). The mean age for confirmatory sweat test was 27 days (range, 11–48). There was a 97.1% compliance rate to ECFS guidelines (33 out of 34 recommendations), especially in the areas of nutritional and pulmonary disease management, with 100% com...
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#1Malvina PrapaH-Index: 6
Last. Massimo DominiciH-Index: 51
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Rationale: Cystic fibrosis (CF) is a common genetic disease caused by mutations of the cystic fibrosis transmembrane conductance regulator (CFTR) gene. Persistent lung inflammation, characterized by increasing polymorphonuclear leukocyte recruitment, is a major cause of the decline in respiratory function in patients with CF and is a leading cause of morbidity and mortality. CFTR is expressed in various cell types, including leukocytes, but its involvement in the regulation of leukocyte recruitm...
36 CitationsSource
#1Malvina PrapaH-Index: 6
#2Sara Caldrer (University of Verona)H-Index: 4
Last. Massimo Dominici (University of Modena and Reggio Emilia)H-Index: 51
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// Malvina Prapa 1 , Sara Caldrer 2 , Carlotta Spano 1 , Marco Bestagno 3 , Giulia Golinelli 1 , Giulia Grisendi 1 , Tiziana Petrachi 1 , Pierfranco Conte 4 , Edwin M. Horwitz 5 , Dario Campana 6 , Paolo Paolucci 1, * , Massimo Dominici 1, * 1 Department of Medical and Surgical Sciences for Children & Adults, Division of Oncology, University-Hospital of Modena and Reggio Emilia, Modena, Italy 2 Department of Pathology and Diagnostics, University of Verona, Verona, Italy 3 International Centre fo...
34 CitationsSource
#1Claudio SorioH-Index: 27
#2Sara CaldrerH-Index: 4
Last. Paola MelottiH-Index: 20
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