233 results on '"Dorsman, Josephine"'
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2. Genome-wide siRNA screens identify RBBP9 function as a potential target in Fanconi anaemia-deficient head-and-neck squamous cell carcinoma
3. Publisher Correction: BIRC2–BIRC3 amplification: a potentially druggable feature of a subset of head and neck cancers in patients with Fanconi anemia
4. BIRC2–BIRC3 amplification: a potentially druggable feature of a subset of head and neck cancers in patients with Fanconi anemia
5. High-Level MYCN-Amplified RB1-Proficient Retinoblastoma Tumors Retain Distinct Molecular Signatures
6. ELOF1 is a transcription-coupled DNA repair factor that directs RNA polymerase II ubiquitylation
7. CRISPR screens in sister chromatid cohesion defective cells reveal PAXIP1-PAGR1 as regulator of chromatin association of cohesin
8. MRI Features for Identifying MYCN-amplified RB1 Wild-type Retinoblastoma
9. Fanconi anemia‐isogenic head and neck cancer cell line pairs ‐ a basic and translational science resource
10. Effective CRISPR/Cas9-mediated correction of a Fanconi anemia defect by error-prone end joining or templated repair
11. Bone Marrow Mesenchymal Stem Cells Carrying FANCD2 Mutation Differ from the Other Fanconi Anemia Complementation Groups in Terms of TGF-β1 Production
12. CRISPR screens in sister chromatid cohesion defective cells reveal PAXIP1-PAGR1 as regulator of chromatin association of cohesin
13. A reason for intermittent fasting to suppress the awakening of dormant breast tumors
14. Fanconi anemia-isogenic head and neck cancer cell line pairs - a basic and translational science resource
15. Detection and localization of early- and late-stage cancers using platelet RNA
16. Characterisation of retinoblastomas without RB1 mutations: genomic, gene expression, and clinical studies
17. Coregulation of FANCA and BRCA1 in human cells
18. Detection of cytogenetic changes and chromosomal aneuploidy with fluorescent in situ hybridization in cytological specimens of oral cancers in Fanconi anemia—Proof of concept
19. Somatic genomic alterations in retinoblastoma beyond RB1 are rare and limited to copy number changes
20. Loss-of-Function FANCL Mutations Associate with Severe Fanconi Anemia Overlapping the VACTERL Association
21. Proper genomic profiling of (BRCA1-mutated) basal-like breast carcinomas requires prior removal of tumor infiltrating lymphocytes
22. Heterozygote FANCD2 mutations associated with childhood T Cell ALL and testicular seminoma
23. RB1 mutation spectrum in a comprehensive nationwide cohort of retinoblastoma patients
24. BRCA1 and p53 protein expression in cultured ovarian surface epithelial cells derived from women with and without a BRCA1 germline mutation
25. Genome-wide-array-based comparative genomic hybridization reveals genetic homogeneity and frequent copy number increases encompassing CCNE1 in Fallopian tube carcinoma
26. Detection of cytogenetic changes and chromosomal aneuploidy with fluorescent in situ hybridization in cytological specimens of oral cancers in Fanconi anemia—Proof of concept.
27. Small N-terminal mutant huntingtin fragments, but not wild type, are mainly present in monomeric form: Implications for pathogenesis
28. HSF2BP negatively regulates homologous recombination in DNA interstrand crosslink repair
29. Lack of large genomic deletions in BRIP1, PALB2, and FANCD2 genes in BRCA1/2 negative familial breast cancer
30. Array comparative genomic hybridization analysis indicates that serous carcinomas of the ovary, fallopian tube and endometrium are distinct entities
31. Cisplatin and doxorubicin repress Vascular Endothelial Growth Factor expression and differentially down-regulate Hypoxia-inducible Factor I activity in human ovarian cancer cells
32. Neuronal Intranuclear and Neuropil Inclusions for Pathological Assessment of Huntingtonʼs Disease
33. Mutant huntingtin represses CBP, but not p300, by binding and protein degradation
34. Cultures of ovarian surface epithelium from women with and without a hereditary predisposition to develop female adnexal carcinoma
35. Strong aggregation and increased toxicity of polyleucine over polyglutamine stretches in mammalian cells
36. Distribution of Inclusions in Neuronal Nuclei and Dystrophic Neurites in Huntington Disease Brain
37. Bone Marrow Mesenchymal Stem Cells Carrying Fancd2 Mutation Differ From The Other Fanconi Anemia Complementation Groups In Terms Of Tgf-Beta 1 Production
38. HSF2BP Negatively Regulates Homologous Recombination in DNA Interstrand Crosslink Repair in Human Cells by Direct Interaction With BRCA2
39. Loss of p53 suppresses replication-stress-induced DNA breakage in G1/S checkpoint deficient cells
40. Author response: Loss of p53 suppresses replication-stress-induced DNA breakage in G1/S checkpoint deficient cells
41. Genomic landscape of retinoblastoma in Rb−/−p130−/− mice resembles human retinoblastoma
42. Acquired cross linker resistance associated with a novel spliced BRCA2 protein variant for molecular phenotyping of BRCA2 disruption
43. MR Imaging Features of Retinoblastoma: Association with Gene Expression Profiles
44. Non-invasive tumor genotyping using radiogenomic biomarkers, a systematic review and oncology-wide pathway analysis
45. A novel Fanconi anaemia subtype associated with a dominant-negative mutation in RAD51
46. Genomic landscape of retinoblastoma in Rb−/−p130−/− mice resembles human retinoblastoma
47. High resolution SNP array profiling identifies variability in retinoblastoma genome stability
48. A Meta-Analysis of Retinoblastoma Copy Numbers Refines the List of Possible Driver Genes Involved in Tumor Progression
49. The iron-sulfur cluster assembly network component NARFL is a key element in the cellular defense against oxidative stress
50. RNA-Seq of Tumor-Educated Platelets Enables Blood-Based Pan-Cancer, Multiclass, and Molecular Pathway Cancer Diagnostics
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