22 results on '"Van Roy, N"'
Search Results
2. MicroRNA-193b-3p acts as a tumor suppressor by targeting the MYB oncogene in T-cell acute lymphoblastic leukemia.
3. Identification of a novel recurrent 1q42.2-1qter deletion in high risk MYCN single copy 11q deleted neuroblastomas.
4. Signaling of ERBB receptor tyrosine kinases promotes neuroblastoma growth in vitro and in vivo.
5. MYCN/c-MYC-induced microRNAs repress coding gene networks associated with poor outcome in MYCN/c-MYC-activated tumors.
6. Genome wide measurement of DNA copy number changes in neuroblastoma: dissecting amplicons and mapping losses, gains and breakpoints.
7. A new recurrent inversion, inv(7)(p15q34), leads to transcriptional activation of HOXA10 and HOXA11 in a subset of T-cell acute lymphoblastic leukemias.
8. Comparative genomic hybridization (CGH) analysis of stage 4 neuroblastoma reveals high frequency of 11q deletion in tumors lacking MYCN amplification.
9. Molecular cytogenetic definition of 17q translocation breakpoints in neuroblastoma.
10. Mutation analysis of P73 and TP53 in Merkel cell carcinoma.
11. Refined physical mapping and genomic structure of the EXTL1 gene.
12. Refined physical mapping and genomic structure of the EXTL1 gene.
13. Molecular analysis of 1p36 breakpoints in two Merkel cell carcinomas.
14. Expression of the MDR1 gene product P-glycoprotein in childhood neuroblastoma.
15. Molecular cytogenetic characterization of marker chromosomes found at prenatal diagnosis.
16. Localization by fluorescence in situ hybridization of the human functional β-glucuronidase gene (GUSB) to 7q11.21→q11.22 and two pseudogenes to 5p13 and 5q13.
17. Assignment of the human β-catenin gene (CTNNB1) to 3p22→p21.3 by fluorescence in situ hybridization.
18. Assignment<FOOTREF>[sup 1] </FOOTREF> of SHOX2 (alias OG12X and SHOT) to human chromosome bands 3q25→q26.1 by in situ hybridization.
19. Assignment<FOOTREF>[sup 1] </FOOTREF> of the cellular retinol-binding protein 1 gene (RBP1) and of the coatomer beta> subunit gene (COPB2) to human chromosome band 3q23 by in situ hybridization.
20. Reassignment of MYCL1 to human chromosome 1p34.3 by fluorescence in situ hybridization.
21. EVI1 activation in blast crisis CML due to juxtaposition to the rare 17q22 partner region as part of a 4-way variant translocation t(9;22).
22. Full triploidy in a liveborn preterm infant.
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