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1. Frequent promoter hypermethylation of the APC and RASSF1A tumour suppressors in parathyroid tumours.

2. Molecular signatures associated with tumor-specific immune response in melanoma patients treated with dendritic cell-based immunotherapy

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3. HRPT2, encoding parafibromin, is mutated in hyperparathyroidism-jaw tumor syndrome

4. Mutation analysis of MEN1, HRPT2, CASR, CDKN1B, and AIP genes in primary hyperparathyroidism patients with features of genetic predisposition

5. Suspension bead array branch migration displacement assay for rapid STR analysis

6. Dental findings in a family with hyperparathyroidism–jaw tumor syndrome and a novel HRPT2 gene mutation

7. Multiple endocrine neoplasia type 1 (MEN1): genetic and clinical analysis in the Southern Chinese

8. Involvement of the MEN1 gene locus in familial isolated hyperparathyroidism

9. Genetic Screening for MEN1 Mutations in Families Presenting with Familial Primary Hyperparathyroidism

10. Genetic and clinical characterization of sporadic cystic parathyroid tumours

11. Founder effect in multiple endocrine neoplasia type 1 (MEN 1) in Finland

12. Detection of serological biomarkers by proximity extension assay for detection of colorectal neoplasias in symptomatic individuals

13. A synthetic peptide homologous to il-10 functional domain induces monocyte differentiation to tgf-beta plus tolerogenic dendritic cells

14. Parafibromin and APC as screening markers for malignant potential in atypical parathyroid adenomas

15. Frequent promoter hypermethylation of the APC and RASSF1A tumour suppressors in parathyroid tumours

16. Loss of expression for the Wnt pathway components adenomatous polyposis coli and glycogen synthase kinase 3-beta in parathyroid carcinomas

17. Branch migration displacement assay with automated heuristic analysis for discrete DNA length measurement using DNA microarrays

18. Loss of parafibromin expression in a subset of parathyroid adenomas

19. Loss of chromosome 13q is a frequently acquired event in genetic progression of soft tissue sarcomas in the abdominal cavity

20. Homozygous inactivation of the MEN1 gene as a specific somatic event in a case of secondary hyperparathyroidism

21. Molecular Genetics of Familial Hyperparathyroidism

22. Multiplexed homogeneous proximity ligation assays for high-throughput protein biomarker research in serological material

23. Loss of expression for the Wnt pathway components adenomatous polyposis coli and glycogen synthase kinase 3-β in parathyroid carcinomas

24. PathogenMip Assay: A Multiplex Pathogen Detection Assay

25. Germline and de novo mutations in the HRPT2 tumour suppressor gene in familial isolated hyperparathyroidism (FIHP)