Search Results
2. Characterization of a novel fusion gene EML4-NTRK3 in a case of recurrent congenital fibrosarcoma
3. Compound heterozygous inheritance of two novel COQ2 variants results in familial coenzyme Q deficiency
4. Cytogenetic abnormalities in reactive lymphoid hyperplasia: byproducts of the germinal centre reaction or indicators of lymphoma?
5. Cytogenetic analysis of 130 renal oncocytomas identify three distinct and mutually exclusive diagnostic classes of chromosome aberrations
6. Epigenetic Inactivation of TRAIL Decoy Receptors at 8p12-21.3 Commonly Deleted Region Confers Sensitivity to Apo2L/TRAIL-Cisplatin Combination Therapy in Cervical Cancer
7. Frequent Promoter Methylation of CDH1, DAPK, RARB, and HIC1 Genes in Carcinoma of Cervix Uteri: Its Relationship to Clinical Outcome
8. Gene Dosage Alterations Revealed by cDNA Microarray Analysis in Cervical Cancer: Identification of Candidate Amplified and Overexpressed Genes
9. Genetic analysis identifies putative tumor suppressor sites at 2q35–q36.1 and 2q36.3–q37.1 involved in cervical cancer progression
10. Genetic and phenotypic analysis of B-cell post-transplant lymphoproliferative disorders provides insights into disease biology
- « Previous
- Next »
- 1
- 2
- 3