about
SDHA loss-of-function mutations in KIT-PDGFRA wild-type gastrointestinal stromal tumors identified by massively parallel sequencing.MemPype: a pipeline for the annotation of eukaryotic membrane proteins.Integrated genomic study of quadruple-WT GIST (KIT/PDGFRA/SDH/RAS pathway wild-type GIST).SDHC methylation in gastrointestinal stromal tumors (GIST): a case report.Whole exome sequencing (WES) on formalin-fixed, paraffin-embedded (FFPE) tumor tissue in gastrointestinal stromal tumors (GIST).Molecular characterization of metastatic exon 11 mutant gastrointestinal stromal tumors (GIST) beyond KIT/PDGFRα genotype evaluated by next generation sequencing (NGS)Whole transcriptome sequencing identifies BCOR internal tandem duplication as a common feature of clear cell sarcoma of the kidney.Analysis of all subunits, SDHA, SDHB, SDHC, SDHD, of the succinate dehydrogenase complex in KIT/PDGFRA wild-type GIST.Hh/Gli antagonist in acute myeloid leukemia with CBFA2T3-GLIS2 fusion gene.Copy number gain of chromosome 3q is a recurrent event in patients with intraductal papillary mucinous neoplasm (IPMN) associated with disease progression.Characterization of pancreatic ductal adenocarcinoma using whole transcriptome sequencing and copy number analysis by single-nucleotide polymorphism array.DHH-RHEBL1 fusion transcript: a novel recurrent feature in the new landscape of pediatric CBFA2T3-GLIS2-positive acute myeloid leukemia.Adaptive Immunity in Fibrosarcomatous Dermatofibrosarcoma Protuberans and Response to Imatinib Treatment.Expression of IGF-1 receptor in KIT/PDGF receptor-α wild-type gastrointestinal stromal tumors with succinate dehydrogenase complex dysfunction.Dystrophin deregulation is associated with tumor progression in KIT/PDGFRA mutant gastrointestinal stromal tumorsGenomic complexity and dynamics of clonal evolution in childhood acute myeloid leukemia studied with whole-exome sequencing.Identification of the NUP98-PHF23 fusion gene in pediatric cytogenetically normal acute myeloid leukemia by whole-transcriptome sequencing.CBFA2T3-GLIS2 fusion transcript is a novel common feature in pediatric, cytogenetically normal AML, not restricted to FAB M7 subtype.The prediction of organelle-targeting peptides in eukaryotic proteins with Grammatical-Restrained Hidden Conditional Random Fields.Integrating miRNA and gene expression profiling analysis revealed regulatory networks in gastrointestinal stromal tumors.Integrated Molecular Characterization of Gastrointestinal Stromal Tumors (GIST) Harboring the Rare D842V Mutation in PDGFRA Gene.Genome-Wide Analysis Identifies MEN1 and MAX Mutations and a Neuroendocrine-Like Molecular Heterogeneity in Quadruple WT GIST.Efficacy and Biological Activity of Imatinib in Metastatic Dermatofibrosarcoma Protuberans (DFSP).Good survival outcome of metastatic SDH-deficient gastrointestinal stromal tumors harboring SDHA mutations.Identification of an Actionable Mutation of KIT in a Case of Extraskeletal Myxoid ChondrosarcomaWhole transcriptome sequencing of a paediatric case of de novo acute myeloid leukaemia with del(5q) reveals RUNX1-USP42 and PRDM16-SKI fusion transcriptsActivity of sunitinib in extraskeletal myxoid chondrosarcomaComparative Assessment of Antitumor Effects and Autophagy Induction as a Resistance Mechanism by Cytotoxics and EZH2 Inhibition in INI1-Negative Epithelioid Sarcoma Patient-Derived XenograftInfluence of Atopic Dermatitis on Cow's Milk Allergy in ChildrenThe Emerging Role of the FGF/FGFR Pathway in Gastrointestinal Stromal TumorSkeletal Muscle Gene Expression in Long-Term Endurance and Resistance Trained Elderly
P50
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P50
description
hulumtuese
@sq
researcher
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wetenschapper
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հետազոտող
@hy
name
Valentina Indio
@ast
Valentina Indio
@en
Valentina Indio
@es
Valentina Indio
@nl
Valentina Indio
@sl
type
label
Valentina Indio
@ast
Valentina Indio
@en
Valentina Indio
@es
Valentina Indio
@nl
Valentina Indio
@sl
prefLabel
Valentina Indio
@ast
Valentina Indio
@en
Valentina Indio
@es
Valentina Indio
@nl
Valentina Indio
@sl
P1053
G-1869-2011
P106
P1153
41861844600
P21
P31
P3829
P496
0000-0002-8854-3821