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Investigation of Molecular Features Involved in Clinical Responses and Survival in Advanced Endometrial Carcinoma Treated by Hormone Therapy
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TOP3A amplification and ATRX inactivation are mutually exclusive events in pediatric osteosarcomas using ALT
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739P Efficacy and safety of maintenance olaparib and bevacizumab (bev) in ovarian cancer (OC) patients (pts) aged ≥65 years (y) from the PAOLA-1/ENGOT-ov25 first-line trial
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Targeted molecular characterization shows differences between primary and secondary myelofibrosis
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Common origin of sequential cutaneous CD30+ lymphoproliferations with nodal involvement evidenced by genome-wide clonal evolution
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A Comparison of DNA Mutation and Copy Number Profiles of Primary Breast Cancers and Paired Brain Metastases for Identifying Clinically Relevant Genetic Alterations in Brain Metastases
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High Response to Cetuximab in a Patient With EGFR -Amplified Heavily Pretreated Metastatic Triple-Negative Breast Cancer
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Head and Body/Tail Pancreatic Carcinomas Are Not the Same Tumors
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Inflammatory breast cancer in 210�patients: A retrospective study on epidemiological, anatomo‑clinical features and therapeutic results
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Poly (ADP-Ribose) Polymerase Inhibitors for De Novo BRCA2-Null Small-Cell Prostate Cancer
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Cegal Protocol : Evaluation of the Feasibility of a Chemogenomic Approach to Identify Personalized Therapy for Relapse or Refractory AML Patients
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Identification of p62/SQSTM1 as a component of non-canonical Wnt VANGL2–JNK signalling in breast cancer
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Comparative genomic analysis of primary tumors and metastases in breast cancer
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Epigenetically centered evolution in an example of myeloid malignancy
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Expression of Genes with Copy Number Alterations and Survival of Patients with Pancreatic Adenocarcinoma.
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Targeted NGS, array-CGH, and patient-derived tumor xenografts for precision medicine in advanced breast cancer: a single-center prospective study
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pH-Cleavable Nucleoside Lipids: A New Paradigm for Controlling the Stability of Lipid-Based Delivery Systems
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Brief Reports: A Distinct DNA Methylation Signature Defines Breast Cancer Stem Cells and Predicts Cancer Outcome
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Comprehensive genome characterization of solitary fibrous tumors using high‐resolution array‐based comparative genomic hybridization
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A new case with 10q23 interstitial deletion encompassing both PTEN and BMPR1A narrows the genetic region deleted in juvenile polyposis syndrome
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La pauvreté en sites d’initiation de la réplication rend-elle fragile certaines régions du génome ?
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Loss of AF6/afadin, a marker of poor outcome in breast cancer, induces cell migration, invasiveness and tumor growth
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Down-Regulation of ECRG4, a Candidate Tumor Suppressor Gene, in Human Breast Cancer
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High-Resolution Comparative Genomic Hybridization of Inflammatory Breast Cancer and Identification of Candidate Genes
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Rare mutations in DNMT3A in myeloproliferative neoplasms and myelodysplastic syndromes
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Absence of R140Q mutation of isocitrate dehydrogenase 2 in gliomas and breast cancers
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BARD1 homozygous deletion, a possible alternative to BRCA1 mutation in basal breast cancer
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Genome profiling of ERBB2-amplified breast cancers
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ASXL1 mutation is associated with poor prognosis and acute transformation in chronic myelomonocytic leukaemia
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Genome profiling of acute myelomonocytic leukemia: alteration of the MYB locus in MYST3-linked cases
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How different are luminal A and basal breast cancers?
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Sixteen–Kinase Gene Expression Identifies Luminal Breast Cancers with Poor Prognosis
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Absence of ESR1 amplification in a series of breast cancers
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Genome profiling of chronic myelomonocytic leukemia: frequent alterations of RAS and RUNX1genes
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Combined translocation with ZNF198-FGFR1 gene fusion and deletion of potential tumor suppressors in a myeloproliferative disorder
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Multicolour-banding fluorescence in situ hybridisation (mbanding-FISH) to identify recurrent chromosomal alterations in breast tumour cell lines
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A Recurrent Chromosome Breakpoint in Breast Cancer at the NRG1 / Neuregulin 1 / Heregulin Gene
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Variant MYST4-CBP gene fusion in a t(10;16) acute myeloid leukaemia
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Comparative multi-methodological measurement of ERBB2 status in breast cancer
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Endogenous retroviral sequence is fused to FGFR1 kinase in the 8p12 stem-cell myeloproliferative disorder with t(8;19)(p12;q13.3)
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A recurrent chromosome translocation breakpoint in breast and pancreatic cancer cell lines targets the neuregulin/ NRG1 gene
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Loss of FHIT protein expression is a marker of adverse evolution in good prognosis localized breast cancer
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Chromosome arm 8p and cancer: a fragile hypothesis
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Reciprocal translocations in breast tumor cell lines: Cloning of a t(3;20) that targets the FHIT gene
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γ-heregulin is the product of a chromosomal translocation fusing the DOC4 and HGL/NRG1 genes in the MDA-MB-175 breast cancer cell line
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A case of inv(8)(p11q24) associated with acute myeloid leukemia involves theMOZ andCBP genes in a masked t(8;16)
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Fibroblast growth factor receptor 1 is fused to FIM in stem-cell myeloproliferative disorder with t(8;13)
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Chromosome region 8p11-p21: Refined mapping and molecular alterations in breast cancer
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Identification of a YAC spanning the translocation breakpoint t(8;22) associated with acute monocytic leukemia
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Characterization of the Region of the Short Arm of Chromosome-8 Amplified in Breast-Carcinoma
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Regional Assignment of Seven Loci to 12p13.2-pter by PCR Analysis of Somatic Cell Hybrids Containing the der(12) or the der(X) Chromosome from a Mesothelioma Showing t(X;12)(q22;p13)
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Assignment of the Gene for the Human Proliferating Cell Nucleolar Protein P120 (NOL1) to Chromosome 12p13 by Fluorescence in Situ Hybridization and Polymerase Chain Reaction with Somatic Cell Hybrids
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