about
An integrated analysis of miRNA and gene copy numbers in xenografts of Ewing's sarcomaMAX inactivation in small cell lung cancer disrupts MYC-SWI/SNF programs and is synthetic lethal with BRG1Glucocorticoid hormones decrease proliferation of embryonic neural stem cells through ubiquitin-mediated degradation of cyclin D1Gain of 1q As a Prognostic Biomarker in Wilms Tumors (WTs) Treated With Preoperative Chemotherapy in the International Society of Paediatric Oncology (SIOP) WT 2001 Trial: A SIOP Renal Tumours Biology Consortium Study.Targeted resequencing of 9p in acute lymphoblastic leukemia yields concordant results with array CGH and reveals novel genomic alterations.A molecular diagnostic approach able to detect the recurrent genetic prognostic factors typical of presenting myelomaHigh Expression of Complement Component 5 (C5) at Tumor Site Associates with Superior Survival in Ewing's Sarcoma Family of Tumour Patients.Clinical relevance of copy number profiling in oral and oropharyngeal squamous cell carcinomaThe CXCR4-CXCL12 axis in Ewing sarcoma: promotion of tumor growth rather than metastatic diseaseGene amplification-associated overexpression of the RNA editing enzyme ADAR1 enhances human lung tumorigenesisEtiology of specific molecular alterations in human malignancies.Combined use of expression and CGH arrays pinpoints novel candidate genes in Ewing sarcoma family of tumors.Multiplex ligation-dependent probe amplification (MLPA) in tumor diagnostics and prognostics.Digital Multiplex Ligation-Dependent Probe Amplification for Detection of Key Copy Number Alterations in T- and B-Cell Lymphoblastic Leukemia.Prediction of outcome in newly diagnosed myeloma: a meta-analysis of the molecular profiles of 1905 trial patients.Frequent Coamplification of Receptor Tyrosine Kinase and Downstream Signaling Genes in Japanese Primary Gastric Cancer and Conversion in Matched Lymph Node Metastasis.KAT6B Is a Tumor Suppressor Histone H3 Lysine 23 Acetyltransferase Undergoing Genomic Loss in Small Cell Lung Cancer.PARD3 Inactivation in Lung Squamous Cell Carcinomas Impairs STAT3 and Promotes Malignant Invasion.MLPA is a powerful tool for detecting lymphoblastic transformation in chronic myeloid leukemia and revealing the clonal origin of relapse in pediatric acute lymphoblastic leukemia.RB1 gene in Merkel cell carcinoma: hypermethylation in all tumors and concurrent heterozygous deletions in the polyomavirus-negative subgroup.Genetic imbalances detected by multiplex ligation-dependent probe amplification in a cohort of patients with oral squamous cell carcinoma-the first step towards clinical personalized medicine.An intragenic ERG deletion is a marker of an oncogenic subtype of B-cell precursor acute lymphoblastic leukemia with a favorable outcome despite frequent IKZF1 deletions.Multiplex ligation-dependent probe amplification and fluorescence in situ hybridization are complementary techniques to detect cytogenetic abnormalities in multiple myeloma.Renal cell carcinoma with smooth muscle stroma lacks chromosome 3p and VHL alterations.Methylation-Specific Multiplex Ligation-Dependent Probe Amplification (MS-MLPA)."Atypical" Pleomorphic Lipomatous Tumor: A Clinicopathologic, Immunohistochemical and Molecular Study of 21 Cases, Emphasizing its Relationship to Atypical Spindle Cell Lipomatous Tumor and Suggesting a Morphologic Spectrum (Atypical Spindle Cell/PlOptimal Fixation Conditions and DNA Extraction Methods for MLPA Analysis on FFPE Tissue-Derived DNA.Genomic profiling of chondrosarcoma: chromosomal patterns in central and peripheral tumors.Validation of 34betaE12 immunoexpression in clear cell papillary renal cell carcinoma as a sensitive biomarker.Clinical correlates of 'BRCAness' in triple-negative breast cancer of patients receiving adjuvant chemotherapy.Routine application of a novel MLPA-based first-line screening test uncovers clinically relevant copy number aberrations in haematological malignancies undetectable by conventional cytogenetics.Sub-clonal copy number is associated with prognosis in multiple myelomaRole of columnar cell lesions in breast carcinogenesis: analysis of chromosome 16 copy number changes by multiplex ligation-dependent probe amplificationHomozygous deletions of cadherin genes in chondrosarcoma—an array comparative genomic hybridization studyAtypical spindle cell lipoma: a clinicopathologic, immunohistochemical, and molecular study emphasizing its relationship to classical spindle cell lipomaCDKN2A deletions in acute lymphoblastic leukemia of adolescents and young adults—An array CGH studyHigh-Throughput Copy Number Profiling by Digital Multiplex Ligation-Dependent Probe Amplification in Multiple MyelomaComprehensive profiling of disease-relevant copy number aberrations for advanced clinical diagnostics of pediatric acute lymphoblastic leukemia
P50
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P50
description
hulumtuese
@sq
researcher
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wetenschapper
@nl
հետազոտող
@hy
name
Suvi Savola
@ast
Suvi Savola
@en
Suvi Savola
@es
Suvi Savola
@nl
Suvi Savola
@sl
type
label
Suvi Savola
@ast
Suvi Savola
@en
Suvi Savola
@es
Suvi Savola
@nl
Suvi Savola
@sl
prefLabel
Suvi Savola
@ast
Suvi Savola
@en
Suvi Savola
@es
Suvi Savola
@nl
Suvi Savola
@sl
P106
P21
P31
P496
0000-0002-6221-8617
P569
2000-01-01T00:00:00Z