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Chinese patent medicine Aidi injection for cancer care: An overview of systematic reviews and meta-analyses. |
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Neuroendocrine transformation from EGFR/ALK-wild type or TKI-naïve non-small cell lung cancer: An under-recognized phenomenon. |
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Genotyping of cerebrospinal fluid in lung cancer patients with leptomeningeal metastasis. |
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Retinoblastoma in Adults: Clinical Features, Gene Mutations and Treatment Outcomes: <i>A Study of Six Cases</i>. |
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The survival impact of CKS1B gains or amplification is dependent on the background karyotype and TP53 deletion status in patients with myeloma. |
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Bi-allelic amplification of ATM gene in blastoid variant of mantle cell lymphoma: a novel mechanism of inactivation due to chromoanagenesis? |
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Whole-exome mutational landscape of neuroendocrine carcinomas of the gallbladder. |
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Coexistence of a secondary STRN-ALK, EML4-ALK double-fusion variant in a lung adenocarcinoma patient with EGFR mutation: a case report. |
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Clinical application of whole transcriptome sequencing for the classification of patients with acute lymphoblastic leukemia. |
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Proposal and clinical application of molecular genetic risk scoring system, MRplus, for BCR-ABL1 negative pediatric B-cell acute lymphoblastic leukemia- report from a single centre. |
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T-Cell Acute Lymphoblastic Leukemia: Biomarkers and Their Clinical Usefulness. |
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<i>ALK</i> Rearrangement in Small-Cell Lung Cancer and Durable Response to Alectinib: A Case Report. |
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The double dealing of cyclin D1. |
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Baoyuan decoction ameliorates apoptosis via AT1-CARP signaling pathway in H9C2 cells and heart failure post-acute myocardial infarction rats. |
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Survival and ocular preservation in a long-term cohort of Japanese patients with retinoblastoma. |
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Comprehensive chromosomal aberrations in a case of a patient with TCF3-HLF-positive BCP-ALL. |
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DNA methylation and copy number variation profiling of T-cell lymphoblastic leukemia and lymphoma. |
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Frequency and prognostic impact of PAX5 p.P80R in pediatric acute lymphoblastic leukemia patients treated on an AIEOP-BFM acute lymphoblastic leukemia protocol. |
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MLPA and DNA index improve the molecular diagnosis of childhood B-cell acute lymphoblastic leukemia. |
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Rewiring of B cell receptor signaling by Epstein-Barr virus LMP2A. |
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Dissection of Anti-tumor Activity of Histone Deacetylase Inhibitor SAHA in Nasopharyngeal Carcinoma Cells <i>via</i> Quantitative Phosphoproteomics. |
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Frequency and Correlation of Common Genes Copy Number Alterations in Childhood Acute Lymphoblastic Leukemia with Prognosis. |
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<i>CCND2</i> and <i>CCND3</i> hijack immunoglobulin light-chain enhancers in cyclin D1<sup>-</sup> mantle cell lymphoma. |
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Human papillomavirus and the landscape of secondary genetic alterations in oral cancers. |
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Copy number alterations in B-cell development genes, drug resistance, and clinical outcome in pediatric B-cell precursor acute lymphoblastic leukemia. |
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Genomic subtyping and therapeutic targeting of acute erythroleukemia. |
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BCR-ABL1-like B-Lymphoblastic Leukemia/Lymphoma with FOXP1-ABL1 Rearrangement: Comprehensive Laboratory Identification Allowing Tyrosine Kinase Inhibitor Use. |
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Ginsenoside Rb1 protects cardiomyocytes from oxygen-glucose deprivation injuries by targeting microRNA-21. |
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Chromosomal microarray analysis is superior in identifying cryptic aberrations in patients with acute lymphoblastic leukemia at diagnosis/relapse as a single assay. |
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Microarray testing as an efficient tool to redefine hyperdiploid paediatric B-cell precursor acute lymphoblastic leukaemia patients. |
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Prognostic gene alterations and clonal changes in childhood B-ALL. |
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Genomic characterisation of breast fibroepithelial lesions in an international cohort. |
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Sinonasal Leiomyosarcoma: Clinicopathological Analysis of Nine Cases with Emphasis on Common Association with Other Malignancies and Late Distant Metastasis. |
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High frequency of intermediate and poor risk copy number abnormalities in pediatric cohort of B-ALL correlate with high MRD post induction. |
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IKZF1<sup>plus</sup> Defines a New Minimal Residual Disease-Dependent Very-Poor Prognostic Profile in Pediatric B-Cell Precursor Acute Lymphoblastic Leukemia. |
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Simultaneous detection of ABL1 mutation and IKZF1 deletion in Philadelphia chromosome-positive acute lymphoblastic leukemia using a customized target enrichment system panel. |
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Ginsenoside Rb1 inhibit apoptosis in rat model of Alzheimer's disease induced by Aβ<sub>1-40</sub>. |
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<i>ALK</i>-rearrangement neuroendocrine carcinoma of the lung: a comprehensive study of a rare case series and review of literature. |
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Improved cytogenetic characterization and risk stratification of pediatric acute lymphoblastic leukemia using single nucleotide polymorphism array analysis: A single center experience of 296 cases. |
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Loss of the candidate tumor suppressor ZEB1 (TCF8, ZFHX1A) in Sézary syndrome. |
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Gene copy number alteration profile and its clinical correlation in B-cell acute lymphoblastic leukemia. |
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Rb silencing mediated by the down-regulation of MeCP2 is involved in cell transformation induced by long-term exposure to hydroquinone. |
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Tumor suppressors BTG1 and IKZF1 cooperate during mouse leukemia development and increase relapse risk in B-cell precursor acute lymphoblastic leukemia patients. |
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Prognostic Implications of Monosomies in Patients With Multiple Myeloma. |
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Correlates of Prenatal and Early-Life Tobacco Smoke Exposure and Frequency of Common Gene Deletions in Childhood Acute Lymphoblastic Leukemia. |
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Additional-structural-chromosomal aberrations are associated with inferior clinical outcome in patients with hyperdiploid multiple myeloma: a single-institution experience. |
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Dual occurrence of ALK G1202R solvent front mutation and small cell lung cancer transformation as resistance mechanisms to second generation ALK inhibitors without prior exposure to crizotinib. Pitfall of solely relying on liquid re-biopsy? |
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Molecular profiling of gene copy number abnormalities in key regulatory genes in high-risk B-lineage acute lymphoblastic leukemia: frequency and their association with clinicopathological findings in Indian patients. |
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Preclinical development of G1T38: A novel, potent and selective inhibitor of cyclin dependent kinases 4/6 for use as an oral antineoplastic in patients with CDK4/6 sensitive tumors. |
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An integrated genomic profile that includes copy number alterations is highly predictive of minimal residual disease status in childhood precursor B-lineage acute lymphoblastic leukemia. |
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Retinoblastoma and Neuroblastoma Predisposition and Surveillance. |
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The correlation between Pax5 deletion and patients survival in Iranian children with precursor B-cell acute lymphocytic leukemia. |
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B-cell Acute Lymphoblastic Leukemia With t(9;22)(q34;q11) Translocation and Clonal Divergence Through ider(22) Chromosome and t(13;17)(q14;q25) Translocation. |
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Monoallelic and biallelic deletions of 13q14 in a group of CLL/SLL patients investigated by CGH Haematological Cancer and SNP array (8x60K). |
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[Detection of copy number variations in pediatric ETV6/RUNX1-positive acute lymphoblastic leukemia with multiplex ligation-dependent probe amplification]. |
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miR-590 promotes cell proliferation and invasion in T-cell acute lymphoblastic leukaemia by inhibiting RB1. |
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Comprehensive genomic analysis reveals FLT3 activation and a therapeutic strategy for a patient with relapsed adult B-lymphoblastic leukemia. |
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The combination effects of Shen-Ling-Bai-Zhu on promoting apoptosis of transplanted H22 hepatocellular carcinoma in mice receiving chemotherapy. |
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miR-494-3p Induces Cellular Senescence and Enhances Radiosensitivity in Human Oral Squamous Carcinoma Cells. |
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Histopathological transformation to small-cell lung carcinoma in non-small cell lung carcinoma tumors. |
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OTX015 (MK-8628), a novel BET inhibitor, exhibits antitumor activity in non-small cell and small cell lung cancer models harboring different oncogenic mutations. |
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An RB-EZH2 Complex Mediates Silencing of Repetitive DNA Sequences. |
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The role of CDKN2A/B deletions in pediatric acute lymphoblastic leukemia. |
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Novel gene targets detected by genomic profiling in a consecutive series of 126 adults with acute lymphoblastic leukemia. |
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The p16(INK4A)/pRb pathway and telomerase activity define a subgroup of Ph+ adult Acute Lymphoblastic Leukemia associated with inferior outcome. |
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Early B-cell-specific inactivation of ATM synergizes with ectopic CyclinD1 expression to promote pre-germinal center B-cell lymphomas in mice. |
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A population-based single nucleotide polymorphism array analysis of genomic aberrations in younger adult acute lymphoblastic leukemia patients. |
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High-dose cytarabine does not overcome the adverse prognostic value of CDKN2A and TP53 deletions in mantle cell lymphoma. |
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Genomic and Clinicopathologic Features of Primary Myelofibrosis With Isolated 13q Deletion. |
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Distinctive genotypes in infants with T-cell acute lymphoblastic leukaemia. |
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Frequency of copy number abnormalities in common genes associated with B-cell precursor acute lymphoblastic leukemia cytogenetic subtypes in Brazilian children. |
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Characterization and pharmacologic targeting of EZH2, a fetal retinal protein and epigenetic regulator, in human retinoblastoma. |
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Mutations in the BCR-ABL1 Kinase Domain and Elsewhere in Chronic Myeloid Leukemia. |
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The mutational landscape of cutaneous T cell lymphoma and Sézary syndrome. |
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An international study of intrachromosomal amplification of chromosome 21 (iAMP21): cytogenetic characterization and outcome. |
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Whole-genome sequencing of an aggressive BRAF wild-type papillary thyroid cancer identified EML4-ALK translocation as a therapeutic target. |
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Blastic plasmacytoid dendritic cell neoplasm: a clinicopathologic review. |
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The genomic landscape of mantle cell lymphoma is related to the epigenetically determined chromatin state of normal B cells. |
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Small-cell lung cancers in patients who never smoked cigarettes. |
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Frequent disruption of the RB pathway in indolent follicular lymphoma suggests a new combination therapy. |
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Establishment and characterization of a singaporean chinese lung adenocarcinoma cell line with four copies of the epidermal growth factor receptor gene. |
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Epstein-Barr virus infection is inversely correlated with the expression of retinoblastoma protein in Reed-Sternberg cells in classic Hodgkin lymphoma. |
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Development and characterization of a novel human Waldenström macroglobulinemia cell line: RPCI-WM1, Roswell Park Cancer Institute - Waldenström Macroglobulinemia 1. |
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The genomic landscape of hypodiploid acute lymphoblastic leukemia. |
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A rare case of transformation of childhood myelodysplastic syndrome to acute lymphoblastic leukemia. |
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Genes commonly deleted in childhood B-cell precursor acute lymphoblastic leukemia: association with cytogenetics and clinical features. |
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Induction of prolonged early G1 arrest by CDK4/CDK6 inhibition reprograms lymphoma cells for durable PI3Kδ inhibition through PIK3IP1. |
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Allelic loss of selected tumor suppressor genes in acute lymphoblastic leukemia in children. |
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RNAi mediated Tiam1 gene knockdown inhibits invasion of retinoblastoma. |
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Promoter methylation patterns in Richter syndrome affect stem-cell maintenance and cell cycle regulation and differ from de novo diffuse large B-cell lymphoma. |
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Radiation therapy: retinal tumors. |
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Protein arginine methyltransferase 5 (PRMT5) inhibition induces lymphoma cell death through reactivation of the retinoblastoma tumor suppressor pathway and polycomb repressor complex 2 (PRC2) silencing. |
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Clinical and molecular characterization of diffuse large B-cell lymphomas with 13q14.3 deletion. |
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High frequency of BTG1 deletions in acute lymphoblastic leukemia in children with down syndrome. |
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Genetics of primary intraocular tumors. |
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IGH@ translocations, CRLF2 deregulation, and microdeletions in adolescents and adults with acute lymphoblastic leukemia. |
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