ROVERSI, GAIA

ROVERSI, GAIA  

DIPARTIMENTO DI MEDICINA, CHIRURGIA E ODONTOIATRIA (attivo dal 01/01/1999 al 26/04/2012)  

Mostra records
Risultati 1 - 15 di 15 (tempo di esecuzione: 0.004 secondi).
Titolo Data di pubblicazione Autori Tipo File Abstract
Instability of short arm of acrocentric chromosomes : Lesson from non-acrocentric satellited chromosomes. Report of 24 unrelated cases 2020 Redaelli, SerenaCatusi, IlariaGarzo, MariaMartinoli, EmanuelaPatrizi, AntonellaRecalcati, Maria PaolaRiva, PaolaRoversi, GaiaBentivegna, Angela + Article (author) -
Novel physiological RECQL4 alternative transcript disclosed by molecular characterisation of Rothmund-Thomson Syndrome sibs with mild phenotype 2014 E.A. ColomboL. FontanaG. RoversiG. NegriL. Larizza + Article (author) -
SINDROME DI ROTHMUND-THOMSON: CARATTERIZZAZIONE CLINICO-MOLECOLARE DI TRE NUOVI PAZIENTI 2012 E.A. ColomboL. FontanaG. RoversiG. NegriL. Larizza + Book Part (author) -
Clericuzio-Type Poikiloderma With Neutropenia Syndrome in Three Sibs With Mutations in the C16orf57 Gene : Delineation of the Phenotype 2010 G. RoversiE.A. ColomboL. VolpiL. Larizza + Article (author) -
Differential cytogenomics and miRNA signature of the Acute Myeloid Leukaemia Kasumi-1 cell line CD34(+)38(-) compartment 2010 PEDRANZINI, LAURAF. MottadelliF. RossellaI. MagnaniG. RoversiP. ColapietroP.G. PelicciL. Larizza + Article (author) -
Atypical Rothmund-Thomson syndrome in a patient with compound heterozygous mutations in RECQL4 gene and phenotypic features in RECQL4 syndromes 2008 G. RoversiL. Larizza + Article (author) -
Search for genomic imbalances in a cohort of 24 Cornelia de Lange patients negative for mutations in the NIPBL and SMC1L1 genes 2008 C. GervasiniP. CastronovoG. RoversiM. MasciadriL. Larizza + Article (author) -
Piebald trait: implication of kit mutation on in vitro melanocyte survival and on the clinical application of cultured epidermal autografts 2007 M. BelliniG. RoversiL. Larizza + Article (author) -
Chromosome 13q14.2-q14.3 and 15q26.2-qter deletions detected by array-CGH in two patients with Cornelia de Lange syndrome 2007 G. RoversiC. GervasiniP. CastronovoL. Larizza + Article (author) -
Rothmund-Thomson syndrome and RECQL4 defect : splitting and lumping 2006 L. LarizzaI. MagnaniG. Roversi Article (author) -
Identification of novel genomic markers related to progression to glioblastoma through genomic profiling of 25 primary glioma cell lines 2006 G. RoversiI. MagnaniL. Larizza + Article (author) -
RNA processing defects of the helicase gene RECQL4 in a compound heterozygous Rothmund-Thomson patient 2003 A. BeghiniG. RoversiL. Larizza + Article (author) -
Identification of two novel RECQL4exonic SNPs and genomic characterization of the IVS12 minisatellite 2003 G. RoversiA. BeghiniL. Larizza + Article (author) -
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. BeghiniI. MagnaniG. RoversiA.M. Fuhrman ContiL. Larizza + Article (author) -
RNA hyperediting and alternative splicing of hematopoietic cell phosphatase (PTPN6) gene in acute myeloid leukemia 2000 A. BeghiniG. RoversiL. Larizza + Article (author) -