46 results on '"van Drunen, Ellen"'
Search Results
2. The response of mammalian cells to UV-light reveals Rad54-dependent and independent pathways of homologous recombination
3. A Functional Role for Tumor Cell Heterogeneity in a Mouse Model of Small Cell Lung Cancer
4. High EVI1 levels predict adverse outcome in acute myeloid leukemia: prevalence of EVI1 overexpression and chromosome 3q26 abnormalities underestimated
5. Mutation of the mouse Rad17 gene leads to embryonic lethality and reveals a role in DNA damage‐dependent recombination
6. Increased genomic instability is not a prerequisite for shortened lifespan in DNA repair deficient mice
7. JKT-1 is not a human seminoma cell line
8. Positional mapping of loci in the DiGeorge critical region at chromosome 22q11 using a new marker (D22S183)
9. Cytogenetic, Molecular Genetic and Pathological Analyses in 126 Meningiomas
10. TEL/AML1 gene fusion is related to in vitro drug sensitivity forl-asparaginase in childhood acute lymphoblastic leukemia
11. High incidence of t(7;12)(q36;p13) in infant AML but not in infant ALL, with a dismal outcome and ectopic expression of HLXB9.
12. NBS1 cooperates with homologous recombination to counteract chromosome breakage during replication
13. T1768 Generation of a Tightly Regulated Doxycycline-Inducible Model for Studying Mouse Intestinal Biology
14. Generation of a tightly regulated doxycycline‐inducible model for studying mouse intestinal biology
15. ERCC1-XPF Endonuclease Facilitates DNA Double-Strand Break Repair
16. Selective Inhibition of BRCA2-Deficient Mammary Tumor Cell Growth by AZD2281 and Cisplatin
17. Further characterization of the first seminoma cell line TCam-2
18. The structure-specific endonuclease Mus81 contributes to replication restart by generating double-strand DNA breaks
19. Gene expression profiling and gene copy-number changes in malignant mesothelioma cell lines
20. Identification of NUP98 abnormalities in acute leukemia: JARID1A (12p13) as a new partner gene
21. High incidence of t(7;12)(q36;p13) in infant AML but not in infant ALL, with a dismal outcome and ectopic expression ofHLXB9
22. Genomic and Expression Profiling of Human Spermatocytic Seminomas: Primary Spermatocyte as Tumorigenic Precursor and DMRT1 as Candidate Chromosome 9 Gene
23. High Incidence of t(7;12)(q36;p13) with Involvement of HLXB9 in Infant AML.
24. Dynamics of Relative Chromosome Position during the Cell Cycle
25. Novel murine B-cell lymphoma/leukemia model to study BCL2-driven oncogenesis
26. The Structure-Specific Endonuclease Ercc1-Xpf Is Required To Resolve DNA Interstrand Cross-Link-Induced Double-Strand Breaks
27. Molecular cytogenetic and clinical findings inETV6/ABL1-positive leukemia
28. Molecular cytogenetic and clinical findings in ETV6ABL1‐positive leukemia
29. Characterization of complex chromosomal abnormalities in uveal melanoma by fluorescence in situ hybridization, spectral karyotyping, and comparative genomic hybridization
30. Deletions at chromosome regions 7q11.23 and 7q36 in a patient with Williams syndrome
31. Mutation analysis of thePTEN gene in uveal melanoma cell lines
32. Specific Cytogenetic Aberrations in Two Novel Human Prostatic Cell Lines Immortalized by Human Papillomavirus Type 18 DNA
33. Cytogenetic analysis of Barrett's mucosa and adenocarcinoma of the distal esophagus and cardia
34. Establishment and characterization of primary and metastatic uveal melanoma cell lines
35. Constitutional DNA-level aberrations in chromosome 22 in a patient with multiple meningiomas
36. High EVI1levels predict adverse outcome in acute myeloid leukemia: prevalence of EVI1overexpression and chromosome 3q26 abnormalities underestimated
37. Mutation analysis of the PTEN gene in uveal melanoma cell lines.
38. Human Myeloid α3-Fucosyltransferase Is Involved in the Expression of the Sialyl-Lewisx Determinant, a Ligand for E- and P-Selectin
39. High Incidence of t(7;12)(q36;p13) with Involvement of HLXB9in Infant AML.
40. Cytogenetic, Molecular Genetic and Pathological Analyses in 126 Meningiomas
41. NF2 gene mutations in meningiomas and vestibular schwannomas
42. Cloning of a putative meningioma tumor suppressor gene
43. Localization of the meningioma tumor suppressor gene using a translocation
44. Integrated genome-wide genotyping and gene expression profiling reveals BCL11B as a putative oncogene in acute myeloid leukemia with 14q32 aberrations.
45. Generation of a tightly regulated doxycycline-inducible model for studying mouse intestinal biology.
46. Detection of genetic prognostic markers in uveal melanoma biopsies using fluorescence in situ hybridization.
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