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au.\*:("DIANZANI, Irma")

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Missense mutations associated with Diamond-Blackfan anemia affect the assembly of ribosomal protein S19 into the ribosomeANGELINI, Mara; CANNATA, Stefano; MERCALDO, Valentina et al.Human molecular genetics (Print). 2007, Vol 16, Num 14, pp 1720-1727, issn 0964-6906, 8 p.Article

Genetic susceptibility to malignant pleural mesothelioma and other asbestos-associated diseasesNERI, Monica; UGOLINI, Donatella; DIANZANI, Irma et al.Mutation research. Reviews in mutation research. 2008, Vol 659, Num 1-2, pp 126-136, issn 1383-5742, 11 p.Article

The 423q Polymorphism of the X-Linked Inhibitor of Apoptosis Gene Influences Monocyte Function and Is Associated With Periodic FeverFERRETTI, Massimo; GATTORNO, Marco; BIAVA, Alessandra et al.Arthritis and rheumatism. 2009, Vol 60, Num 11, pp 3476-3484, issn 0004-3591, 9 p.Article

High levels of osteopontin associated with polymorphisms in its gene are a risk factor for development of autoimmunity/lymphoproliferationCHIOCCHETTI, Annalisa; INDELICATO, Manuela; GIACOPELLI, Francesca et al.Blood. 2004, Vol 103, Num 4, pp 1376-1382, issn 0006-4971, 7 p.Article

High frequency of ribosomal protein gene deletions in Italian Diamond-Blackfan anemia patients detected by multiplex ligation-dependent probe amplification assayQUARELLO, Paola; GARELLI, Emanuela; BRUSCO, Alfredo et al.Haematologica (Roma). 2012, Vol 97, Num 12, pp 1813-1817, issn 0390-6078, 5 p.Article

Genetic susceptibility to malignant mesothelioma and exposure to asbestos : The influence of the familial factorUGOLINI, Donatella; NERI, Monica; PUNTONI, Riccardo et al.Mutation research. Reviews in mutation research. 2008, Vol 658, Num 3, pp 162-171, issn 1383-5742, 10 p.Conference Paper

Inherited perforin and Fas mutations in a patient with autoimmune lymphoproliferative syndrome and lymphomaCLEMENTI, Rita; DAGNA, Lorenzo; CICERI, Fabio et al.The New England journal of medicine. 2004, Vol 351, Num 14, pp 1419-1424, issn 0028-4793, 6 p.Article

Diamond-Blackfan anemia: genotype-phenotype correlations in Italian patients with RPL5 and RPL11 mutationsQUARELLO, Paola; GARELLI, Emanuela; BIONDINI, Laura et al.Haematologica (Roma). 2010, Vol 95, Num 2, pp 206-213, issn 0390-6078, 8 p.Article

Interactions between RPS19, mutated in diamond-blackfan anemia, and the PIM-1 oncoproteinCHIOCCHETTI, Annalisa; GIBELLO, Luisa; DIANZANI, Umberto et al.Haematologica (Roma). 2005, Vol 90, Num 11, pp 1453-1462, issn 0390-6078, 10 p.Article

Familial PAX8 small deletion (c.989―992delACCC) associated with extreme phenotype variabilityDE SANCTIS, Luisa; CORRIAS, Andrea; ROMAGNOLO, Damiano et al.The Journal of clinical endocrinology and metabolism. 2004, Vol 89, Num 11, pp 5669-5674, issn 0021-972X, 6 p.Article

Molecular analysis of the GNAS1 gene for the correct diagnosis of Albright hereditary osteodystrophy and pseudohypoparathyroidismDE SANCTIS, Luisa; ROMAGNOLO, Damiano; CAPPA, Marco et al.Pediatric research. 2003, Vol 53, Num 5, pp 749-755, issn 0031-3998, 7 p.Article

A genome-wide association study for malignant mesothelioma riskCADBY, Gemma; MUKHERJEE, Sutapa; BEILBY, John et al.Lung cancer. 2013, Vol 82, Num 1, pp 1-8, issn 0169-5002, 8 p.Article

Pooled analysis of NAT2 genotypes as risk factors for asbestos-related malignant mesotheliomaBETTI, Marta; NERI, Monica; BOTTA, Mario et al.International journal of hygiene and environmental health. 2009, Vol 212, Num 3, pp 322-329, issn 1438-4639, 8 p.Article

Variations of the perforin gene in patients with autoimmunty/lymphoproliferation and defective fas functionCLEMENTI, Rita; CHIOCCHETTI, Annalisa; BOZZI, Valeria et al.Blood. 2006, Vol 108, Num 9, pp 3079-3084, issn 0006-4971, 6 p.Article

Molecular basis of Diamond-Blackfan anemia: new findings from the Italian registry and a review of the literatureCAMPAGNOLI, Maria Francesca; GARELLI, Emanuela; RAMENGHI, Ugo et al.Haematologica (Roma). 2004, Vol 89, Num 4, pp 480-489, issn 0390-6078, 10 p.Article

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