ROVERSI, GAIA

ROVERSI, GAIA  

DIPARTIMENTO DI MEDICINA E CHIRURGIA (SCHOOL OF MEDICINE AND SURGERY)  

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Titolo Tipologia Data di pubblicazione Autori File
RNA hyperediting and alternative splicing of hematopoietic cell phosphatase (PTPN6) gene in acute myeloid leukemia 01 - Articolo su rivista 2000 ROVERSI, GAIA +
Germline mutation in the juxtamembrane domain of the kit gene in a family with gastrointestinal stromal tumors and urticaria pigmentosa 01 - Articolo su rivista 2001 ROVERSI, GAIA +
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 01 - Articolo su rivista 2003 ROVERSI, GAIA +
RNA processing defects of the helicase gene RECQL4 in a compound heterozygous Rothmund-Thomson patient 01 - Articolo su rivista 2003 ROVERSI, GAIA +
Identification of two novel RECQL4 exonic SNPs and genomic characterization of the IVS12 minisatellite 01 - Articolo su rivista 2003 ROVERSI, GAIA +
Identification of oligodendroglioma specific chromosomal copy number changes in the glioblastoma MI-4 cell line by array-CGH and FISH analyses 01 - Articolo su rivista 2005 ROVERSI, GAIA +
Identification of novel genomic markers related to progression to glioblastoma through genomic profiling of 25 primary glioma cell lines 01 - Articolo su rivista 2006 ROVERSI, GAIA +
Rothmund-Thomson syndrome and RECQL4 defect: splitting and lumping 01 - Articolo su rivista 2006 ROVERSI, GAIA +
Piebald trait: implication of kit mutation on in vitro melanocyte survival and on the clinical application of cultured epidermal autografts 01 - Articolo su rivista 2007 ROVERSI, GAIA +
Search for genomic imbalances in a cohort of 24 Cornelia de Lange patients negative for mutations in the NIPBL and SMC1L1 genes 01 - Articolo su rivista 2008 ROVERSI, GAIA +
Atypical Rothmund-Thomson syndrome in a patient with compound Heterozygous Mutations in RECQL4 Gene and phenotypic features in RECQL4 syndromes 01 - Articolo su rivista 2008 ROVERSI, GAIA +
Multiple localization of endogenous MARK4L protein in human glioma 01 - Articolo su rivista 2009 ROVERSI, GAIA +
Rothmund-Thomson syndrome 01 - Articolo su rivista 2010 ROVERSI, GAIA +
Differential cytogenomics and miRNA signature of the Acute Myeloid Leukaemia Kasumi-1 cell line CD34+38- compartment 01 - Articolo su rivista 2010 ROVERSI, GAIA +
Clericuzio-type poikiloderma with neutropenia syndrome in three sibs with mutations in the C16orf57 gene: delineation of the phenotype 01 - Articolo su rivista 2010 ROVERSI, GAIA +
Targeted next-generation sequencing appoints c16orf57 as clericuzio-type poikiloderma with neutropenia gene 01 - Articolo su rivista 2010 ROVERSI, GAIA +
Genetic variation at 9p22.2 and ovarian cancer risk for BRCA1 and BRCA2 mutation carriers 01 - Articolo su rivista 2011 ROVERSI, GAIA +
The CASP8 rs3834129 polymorphism and breast cancer risk in BRCA1 mutation carriers 01 - Articolo su rivista 2011 ROVERSI, GAIA +
Exploring the link between MORF4L1 and risk of breast cancer 01 - Articolo su rivista 2011 ROVERSI, GAIA +
Evidence for a link between TNFRSF11A and risk of breast cancer 01 - Articolo su rivista 2011 ROVERSI, GAIA +