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

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

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

4. Haplotype analyses of the c.1027C>T and c.2167_2168delAT recurrent truncating mutations in the breast cancer-predisposing gene PALB2

5. Individuals with &ITFANCM&IT biallelic mutations do not develop Fanconi anemia, but show risk for breast cancer, chemotherapy toxicity and may display chromosome fragility

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

7. PALB2, CHEK2 and ATM rare variants and cancer risk: Data from COGS

8. PALB2 sequencing in Italian familial breast cancer cases reveals a high-risk mutation recurrent in the province of Bergamo

9. PALB2, CHEK2 and ATM rare variants and cancer risk:data from COGS

10. PALB2, CHEK2 and ATM rare variants and cancer risk: data from COGS

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

13. Whole Exome Sequencing Suggests Much of Non-BRCA1/BRCA2 Familial Breast Cancer Is Due to Moderate and Low Penetrance Susceptibility Alleles

14. The CASP8 rs3834129 polymorphism and breast cancer risk in BRCA1 mutation carriers

15. SNPs in ultraconserved elements and familial breast cancer risk

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

17. Contribution of MUTYH variants to male breast cancer risk: results from a multicenter study in Italy

18. Haplotype analyses of the c.1027CT and c.2167_2168delAT recurrent truncating mutations in the breast cancer-predisposing gene PALB2

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

20. PALB2 sequencing in Italian familial breast cancer cases reveals a high-risk mutation recurrent in the province of Bergamo

21. The CASP8 rs3834129 polymorphism and breast cancer risk in BRCA1 mutation carriers

22. Detecting Variants in the NBN Gene While Testing for Hereditary Breast Cancer: What to Do Next?

23. Analysis of Italian BRCA1/2 Pathogenic Variants Identifies a Private Spectrum in the Population from the Bergamo Province in Northern Italy.

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

25. Contribution of MUTYH Variants to Male Breast Cancer Risk: Results From a Multicenter Study in Italy.

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

27. Individuals with FANCM biallelic mutations do not develop Fanconi anemia, but show risk for breast cancer, chemotherapy toxicity and may display chromosome fragility.

28. PALB2, CHEK2 and ATM rare variants and cancer risk: data from COGS.

30. Haplotype analyses of the c.1027C>T and c.2167_2168delAT recurrent truncating mutations in the breast cancer-predisposing gene PALB2.

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

32. PALB2 sequencing in Italian familial breast cancer cases reveals a high-risk mutation recurrent in the province of Bergamo.

33. Whole exome sequencing suggests much of non-BRCA1/BRCA2 familial breast cancer is due to moderate and low penetrance susceptibility alleles.

34. Germline mutations in BRIP1 and PALB2 in Jewish high cancer risk families.

36. Sequencing analysis of SLX4/FANCP gene in Italian familial breast cancer cases.

38. The CASP8 rs3834129 polymorphism and breast cancer risk in BRCA1 mutation carriers.

39. Evaluation of SNPs in miR-146a, miR196a2 and miR-499 as low-penetrance alleles in German and Italian familial breast cancer cases.

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