M. De Rosa

发表

Familial adenomatous polyposis coli: Five novel mutations in exon 15 of the adenomatous polyposis coli (APC) gene in Italian patients

N. Carlomagno, G. Riegler, P. Izzo, 1999 .

Genetics, diagnosis and treatment of Lynch syndrome: Old lessons and current challenges

P. Izzo, M. De Rosa, Francesca Duraturo, 2019, Oncology letters.

Real-time PCR quantification of human DKC1 expression in colorectal cancer

M. Furia, P. Izzo, M. De Rosa, 2008, Acta oncologica.

Differential expression of PTEN gene correlates with phenotypic heterogeneity in three cases of patients showing clinical manifestations of PTEN hamartoma tumour syndrome

P. Delrio, L. Paparo, P. Izzo, 2013, Hereditary cancer in clinical practice.

Dyskerin Downregulation Can Induce ER Stress and Promote Autophagy via AKT-mTOR Signaling Deregulation

R. Vicidomini, M. Furia, M. De Rosa, 2022, Biomedicines.

Synergistic effect of interleukin-10-receptor variants in a case of early-onset ulcerative colitis.

P. Delrio, A. Staiano, E. Miele, 2013, World journal of gastroenterology.

A dramatic case of early‐onset familial adenomatous polyposis

G. Boccia, A. Staiano, E. Miele, 2004, Clinical genetics.

Autophagy genes variants and paediatric Crohn's disease phenotype: a single-centre experience.

A. Staiano, E. Miele, R. Troncone, 2014, Digestive and Liver Disease.

Implications of Splicing Alterations in the Onset and Phenotypic Variability of a Family with Subclinical Manifestation of Peutz–Jeghers Syndrome: Bioinformatic and Molecular Evidence

A. Staiano, E. Miele, P. Izzo, 2020, International journal of molecular sciences.

Abstract. The molecular characterization of patients with Lynch syndrome (LS) involves germline testing to detect a deleterious mutation in one of the genes of the mismatch repair

P. Izzo, M. De Rosa, M. Lambiase, 2022 .

A homozygous PMS2 founder mutation with an attenuated constitutional mismatch repair deficiency phenotype

Michael J. McGuffin, S. Gruber, W. Foulkes, 2015, Journal of Medical Genetics.

Novel variants of unknown significance in the PMS2 gene identified in patients with hereditary colon cancer

P. Izzo, M. De Rosa, N. Mitilini, 2019, Cancer management and research.

Novel MSH2 splice-site mutation in a young patient with Lynch syndrome

P. Izzo, M. De Rosa, Francesca Duraturo, 2018, Molecular medicine reports.

Hereditary Colorectal Cancer: State of the Art in Lynch Syndrome

P. Izzo, M. De Rosa, Francesca Duraturo, 2022, Cancers.

Novel Implications in Molecular Diagnosis of Lynch Syndrome

P. Izzo, M. De Rosa, Francesca Duraturo, 2017, Gastroenterology research and practice.

Genetics, diagnosis and management of colorectal cancer (Review)

P. Delrio, P. Izzo, M. De Rosa, 2015, Oncology reports.

Lithium chloride induces mesenchymal-to-epithelial reverting transition in primary colon cancer cell cultures

P. Delrio, R. Genesio, L. Nitsch, 2015, International journal of oncology.

Characterisation of mesenchymal colon tumour-derived cells in tumourspheres as a model for colorectal cancer progression

P. Delrio, C. Dodaro, P. Izzo, 2018, International journal of oncology.

The biological complexity of colorectal cancer: insights into biomarkers for early detection and personalized care

P. Delrio, P. Izzo, M. De Rosa, 2016, Therapeutic advances in gastroenterology.

Promising Colorectal Cancer Biomarkers for Precision Prevention and Therapy

P. Delrio, P. Izzo, M. De Rosa, 2019, Cancers.

Beta catenin and cytokine pathway dysregulation in patients with manifestations of the "PTEN hamartoma tumor syndrome"

L. Paparo, M. Galatola, P. Izzo, 2012, BMC Medical Genetics.

The Italian external quality control program for familial adenomatous polyposis of the colon: five years of experience.

D. Taruscio, V. Falbo, M. Salvatore, 2010, Genetic testing and molecular biomarkers.

Inhibition of Interleukin-6-Induced Matrix Metalloproteinase-2 Expression and Invasive Ability of Lemon Peel Polyphenol Extract in Human Primary Colon Cancer Cells

M. Masullo, Rosarita Nasso, V. Pagliara, 2021, Molecules.

Contribution of Large Genomic Rearrangements in Italian Lynch Syndrome Patients: Characterization of a Novel Alu-Mediated Deletion

P. Izzo, M. De Rosa, G. Diana, 2012, BioMed research international.

Three novel germline mutations in the adenomatous polyposis coli gene

N. Carlomagno, P. Izzo, M. Scarano, 1997, Human mutation.

Multiple splenic hamartomas and familial adenomatous polyposis: a case report and review of the literature

A. Calogero, M. Candida, N. Carlomagno, 2015, Journal of Medical Case Reports.

Wnt Pathway, Angiogenetic and Hormonal Markers in Sporadic and Familial Adenomatous Polyposis-associated Juvenile Nasopharyngeal Angiofibromas (JNA)

S. Seidenari, G. Pellacani, P. Izzo, 2008, Applied immunohistochemistry & molecular morphology : AIMM.

Characterization of novel, large duplications in the MSH2 gene of three unrelated Lynch syndrome patients.

P. Izzo, G. Rossi, M. De Rosa, 2018, Cancer genetics.

Incomplete Segregation of MSH6 Frameshift Variants with Phenotype of Lynch Syndrome

N. Carlomagno, P. Izzo, G. Rossi, 2017, International journal of molecular sciences.

Multivariate analysis as a method for evaluating the pathogenicity of novel genetic MLH1 variants in patients with colorectal cancer and microsatellite instability.

P. Izzo, G. Rossi, M. De Rosa, 2015, International journal of molecular medicine.

Implication of Adenomatous Polyposis Coli and MUTYH Mutations in Familial Colorectal Polyposis

M. Galatola, P. Izzo, S. Masone, 2009, Diseases of the colon and rectum.

The role of mutation analysis of the APC gene in the management of FAP patients. A controversial issue.

C. Dodaro, M. Santangelo, P. Izzo, 2016, Annali italiani di chirurgia.

MiR-137 Targets the 3′ Untranslated Region of MSH2: Potential Implications in Lynch Syndrome-Related Colorectal Cancer

M. Grosso, R. Sessa, P. Izzo, 2021, Cancers.

Alternative splicing and nonsense-mediated mRNA decay in the regulation of a new adenomatous polyposis coli transcript.

P. Delrio, P. Izzo, G. Rossi, 2007, Gene.

A Potential Role of IL-6/IL-6R in the Development and Management of Colon Cancer

P. Izzo, M. De Rosa, M. Turano, 2021, Membranes.

Nitrodi thermal water downregulates protein S-nitrosylation in RKO cells

P. Izzo, M. De Rosa, A. de Paulis, 2020, International journal of molecular medicine.

MSH2 Overexpression Due to an Unclassified Variant in 3’-Untranslated Region in a Patient with Colon Cancer

P. Izzo, M. De Rosa, M. Lambiase, 2020, Biomedicines.

Lithium chloride increases sensitivity to photon irradiation treatment in primary mesenchymal colon cancer cells

P. Delrio, G. Pierantoni, P. Muto, 2020, Molecular medicine reports.

Same MSH2 Gene Mutation But Variable Phenotypes in 2 Families With Lynch Syndrome: Two Case Reports and Review of Genotype-Phenotype Correlation

M. De Rosa, Francesca Duraturo, Raffaella Liccardo, 2018, Clinical medicine insights. Case reports.

Specific Alu elements involved in a significant percentage of copy number variations of the STK11 gene in patients with Peutz–Jeghers syndrome

A. Pławski, J. Walkowiak, B. Nedoszytko, 2015, Familial Cancer.

Alu-mediated genomic deletion of the serine/threonine protein kinase 11 (STK11) gene in Peutz-Jeghers syndrome.

A. Staiano, E. Miele, M. Galatola, 2010, Gastroenterology.

Familial adenomatous polyposis coli: five novel mutations in exon 15 of the adenomatous polyposis coli (APC) gene in Italian patients. Mutations in brief no. 225. Online.

N. Carlomagno, G. Riegler, P. Izzo, 1999, Human mutation.

The Role of Colonoscopy in the Management of Individuals with Lynch Syndrome: A Narrative Review

P. Delrio, F. Tatangelo, M. De Bellis, 2023, Cancers.

Significance of rare variants in genes involved in the pathogenesis of Lynch syndrome

P. Izzo, M. De Rosa, M. Lambiase, 2022, International journal of molecular medicine.

Wnt Pathway, Angiogenetic and Hormonal Markers in Sporadic and Familial Adenomatous Polyposis-associated Juvenile Nasopharyngeal Angiofibromas (JNA)

S. Seidenari, G. Pellacani, P. Izzo, 2008, Applied immunohistochemistry & molecular morphology : AIMM.