ROVERSI, GAIA
ROVERSI, GAIA
DIPARTIMENTO DI MEDICINA, CHIRURGIA E ODONTOIATRIA (attivo dal 01/01/1999 al 26/04/2012)
Instability of short arm of acrocentric chromosomes : Lesson from non-acrocentric satellited chromosomes. Report of 24 unrelated cases
2020 S. Redaelli, D. Conconi, N. Villa, E. Sala, F. Crosti, C. Corti, I. Catusi, M. Garzo, L. Romitti, E. Martinoli, A. Patrizi, R. Malgara, M.P. Recalcati, L. Dalprà, M. Lavitrano, P. Riva, G. Roversi, A. Bentivegna
Novel physiological RECQL4 alternative transcript disclosed by molecular characterisation of Rothmund-Thomson Syndrome sibs with mild phenotype
2014 E.A. Colombo, L. Fontana, G. Roversi, G. Negri, D. Castiglia, M. Paradisi, G. Zambruno, L. Larizza
SINDROME DI ROTHMUND-THOMSON: CARATTERIZZAZIONE CLINICO-MOLECOLARE DI TRE NUOVI PAZIENTI
2012 E.A. Colombo, L. Fontana, G. Roversi, G. Negri, M. Paradisi, D. Castiglia, A. Locatelli, G. Zambruno, L. Larizza
Differential cytogenomics and miRNA signature of the Acute Myeloid Leukaemia Kasumi-1 cell line CD34(+)38(-) compartment
2010 L. Pedranzini, F. Mottadelli, S. Ronzoni, F. Rossella, M. Ferracin, I. Magnani, G. Roversi, P. Colapietro, M. Negrini, P.G. Pelicci, L. Larizza
Clericuzio-Type Poikiloderma With Neutropenia Syndrome in Three Sibs With Mutations in the C16orf57 Gene : Delineation of the Phenotype
2010 D. Concolino, G. Roversi, G.L. Muzzi, S. Sestito, E.A. Colombo, L. Volpi, L. Larizza, P. Strisciuglio
Atypical Rothmund-Thomson syndrome in a patient with compound heterozygous mutations in RECQL4 gene and phenotypic features in RECQL4 syndromes
2008 Y. Sznajer, H.A. Siitonen, G. Roversi, C. Dangoisse, M. Scaillon, F. Ziereisen, S. Tenoutasse, M. Kestilä, L. Larizza
Search for genomic imbalances in a cohort of 24 Cornelia de Lange patients negative for mutations in the NIPBL and SMC1L1 genes
2008 C. Gervasini, R. Pfundt, P. Castronovo, S. Russo, G. Roversi, M. Masciadri, D. Milani, G. Zampino, A. Selicorni, E. Schoenmakers, L. Larizza
Chromosome 13q14.2-q14.3 and 15q26.2-qter deletions detected by array-CGH in two patients with Cornelia de Lange syndrome
2007 G. Roversi, C. Gervasini, P. Castronovo, R. Pfundt, S. Russo, D. Milani, A. Selicorni, A. Musio, E.F. Schoenmakers, L. Larizza
Piebald trait: implication of kit mutation on in vitro melanocyte survival and on the clinical application of cultured epidermal autografts
2007 S. Bondanza, M. Bellini, G. Roversi, D. Raskovic, R. Maurelli, E. Paionni, P. Paterna, E. Dellambra, L. Larizza, L. Guerra
Rothmund-Thomson syndrome and RECQL4 defect : splitting and lumping
2006 L. Larizza, I. Magnani, G. Roversi
Identification of novel genomic markers related to progression to glioblastoma through genomic profiling of 25 primary glioma cell lines
2006 G. Roversi, R. Pfundt, R.F. Moroni, I. Magnani, S. van Reijmersdal, B. Pollo, H. Straatman, L. Larizza, E. Schoenmakers
RNA processing defects of the helicase gene RECQL4 in a compound heterozygous Rothmund-Thomson patient
2003 A. Beghini, P. Castorina, G. Roversi, P. Modiano, L. Larizza
Identification of two novel RECQL4exonic SNPs and genomic characterization of the IVS12 minisatellite
2003 G. Roversi, A. Beghini, G. Zambruno, M. Paradisi, L. Larizza
The neural progenitor-restricted isoform of the MARK4 gene in 19q13.2 is upregulated in human gliomas and overexpressed in a subset of glioblastoma cell lines
2003 A. Beghini, I. Magnani, G. Roversi, T. Piepoli, S. Di Terlizzi, R.F. Moroni, B. Pollo, A.M. Fuhrman Conti, J.K. Cowell, G. Finocchiaro, L. Larizza
RNA hyperediting and alternative splicing of hematopoietic cell phosphatase (PTPN6) gene in acute myeloid leukemia
2000 A. Beghini, C. B. Ripamonti, P. Peterlongo, G. Roversi, R. Cairoli, E. Morra, L. Larizza