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1. The FANCM:p.Arg658* truncating variant is associated with risk of triple-negative breast cancer

2. The BRCA2 c.68‐7T > A variant is not pathogenic: A model for clinical calibration of spliceogenicity

3. LKB1 Down-Modulation by miR-17 Identifies Patients With NSCLC Having Worse Prognosis Eligible for Energy-Stress–Based Treatments

4. Atypical cancer risk profile in carriers of Italian founder BRCA1 variant p.His1673del: Implications for classification and clinical management.

7. Abstract 1539: LKB1 down-modulation by miR-17 biologically and clinically mirrors LKB1-mutated NSCLC

8. FANCM c.5791C>T nonsense mutation (rs144567652) induces exon skipping, affects DNA repair activity and is a familial breast cancer risk factor

9. The rs12975333 variant in the miR-125a and breast cancer risk in Germany, Italy, Australia and Spain

10. The FANCM :p.Arg658* truncating variant is associated with risk of triple-negative breast cancer

12. Circulating mir‐320a promotes immunosuppressive macrophages M2 phenotype associated with lung cancer risk

13. Two Missense Variants Detected in Breast Cancer Probands Preventing BRCA2-PALB2 Protein Interaction

14. FANCM c.5791C > T nonsense mutation (rs144567652) induces exon skipping, affects DNA repair activity and is a familial breast cancer risk factor

15. The <italic>BRCA2</italic> c.68‐7T > A variant is not pathogenic: A model for clinical calibration of spliceogenicity.

16. Characterization of an Italian Founder Mutation in the RING-Finger Domain of BRCA1

17. Comparative In Vitro and In Silico Analyses of Variants in Splicing Regions of BRCA1 and BRCA2 Genes and Characterization of Novel Pathogenic Mutations

19. Characterization of an Italian Founder Mutation in the RING-Finger Domain of BRCA1.

20. Characterization of an Italian Founder Mutation in the RING-Finger Domain of BRCA1.

21. Comparative In Vitro and In Silico Analyses of Variants in Splicing Regions of BRCA1 and BRCA2 Genes and Characterization of Novel Pathogenic Mutations.

22. The BRCA2 c.68-7T > A variant is not pathogenic: A model for clinical calibration of spliceogenicity

23. The FANCM:p.Arg658* truncating variant is associated with risk of triple-negative breast cancer

24. The FANCM:p.Arg658* truncating variant is associated with risk of triple-negative breast cancer

25. The FANCM:p.Arg658* truncating variant is associated with risk of triple-negative breast cancer

26. The FANCM :p.Arg658* truncating variant is associated with risk of triple-negative breast cancer.

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