Pages that link to "Q57079861"
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The following pages link to Maria Chiara Scaini (Q57079861):
Displaying 16 items.
- Altered tumor formation and evolutionary selection of genetic variants in the human MDM4 oncogene. (Q37238851) (← links)
- Performance of in silico tools for the evaluation of p16INK4a (CDKN2A) variants in CAGI. (Q38691170) (← links)
- CDKN2A unclassified variants in familial malignant melanoma: combining functional and computational approaches for their assessment. (Q39012719) (← links)
- Dried blood spot sampling for detection of monoclonal immunoglobulin gene rearrangement (Q39107171) (← links)
- Establishment and characterization of xenografts and cancer cell cultures derived from BRCA1 -/- epithelial ovarian cancers (Q40270449) (← links)
- The CHEK2 c.1100delC mutation plays an irrelevant role in breast cancer predisposition in Italy. (Q44955073) (← links)
- Association between MDM2-SNP309 and age at colorectal cancer diagnosis according to p53 mutation status. (Q46944917) (← links)
- Liquid biopsy for monitoring anaplastic lymphoma kinase inhibitors in non-small cell lung cancer: two cases compared. (Q47134673) (← links)
- DNA copy number profile discriminates between esophageal adenocarcinoma and squamous cell carcinoma and represents an independent prognostic parameter in esophageal adenocarcinoma. (Q54574348) (← links)
- Functional impairment of p16(INK4A) due to CDKN2A p.Gly23Asp missense mutation. (Q54724096) (← links)
- Genomic rearrangements of the CDKN2A locus are infrequent in Italian malignant melanoma families without evidence of CDKN2A/CDK4 point mutations. (Q54788111) (← links)
- Contribution of susceptibility gene variants to melanoma risk in families from the Veneto region of Italy (Q58486119) (← links)
- Clinical genetic testing for familial melanoma in Italy: A cooperative study (Q61314849) (← links)
- Survivin expression impacts prognostically on NSCLC but not SCLC (Q61884165) (← links)
- No Evidence for Linkage with Melanoma in Italian Melanoma-Prone Families (Q61917486) (← links)
- BRCA1p.Val1688del Is a Deleterious Mutation That Recurs in Breast and Ovarian Cancer Families From Northeast Italy (Q61970272) (← links)