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35 results on '"Liccardo, R."'

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1. Longitudinal profiling identifies co-occurring BRCA1/2 reversions, TP53BP1, RIF1 and PAXIP1 mutations in PARP inhibitor-resistant advanced breast cancer

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

4. Analysis of fatal adverse drug events recorded in several Italian emergency departments (the MEREAFaPS study)

5. Identification and molecular characterization of a novel mutation in MSH2 gene in a lynch syndrome family

9. Identification of seven novel mutations in HNPCC Patients

10. Involvement of large rearrangements in MSH6 and PMS2 genes in southern Italian patients with lynch syndrome

11. Sporadic pediatric severe familial adenomatous polyposis: A case report

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

13. Italian Emergency Department Visits and Hospitalizations for Outpatients’ Adverse Drug Events: 12-Year Active Pharmacovigilance Surveillance (The MEREAFaPS Study)

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

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

16. Germline Variants in MLH1 and ATM Genes in a Young Patient with MSI-H in a Precancerous Colonic Lesion.

17. Hereditary Colorectal Cancer: State of the Art in Lynch Syndrome.

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

19. Sporadic pediatric severe familial adenomatous polyposis: A case report.

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

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

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

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

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

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

26. Incomplete Segregation of MSH6 Frameshift Variants with Phenotype of Lynch Syndrome.

27. Novel Implications in Molecular Diagnosis of Lynch Syndrome.

28. Two novel sequence variants in MSH2 gene in a patient who underwent cancer genetic counseling for a very early-onset epithelial ovarian cancer.

29. Coexistence of MLH3 germline variants in colon cancer patients belonging to families with Lynch syndrome-associated brain tumors.

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

31. Lithium chloride induces mesenchymal‑to‑epithelial reverting transition in primary colon cancer cell cultures.

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

33. Contribution of large genomic rearrangements in Italian Lynch syndrome patients: characterization of a novel alu-mediated deletion.

35. Association of low-risk MSH3 and MSH2 variant alleles with Lynch syndrome: probability of synergistic effects.

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