Isabelle Janoueix-Lerosey researcher
Janoueix-Lerosey, Isabelle, 19..-....
Janoueix-Lerosey, Isabelle
VIAF ID: 219545095 (Personal)
Permalink: http://viaf.org/viaf/219545095
Preferred Forms
4xx's: Alternate Name Forms (4)
Works
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68Ga-DOTATOC and FDG PET Imaging of Preclinical Neuroblastoma Models |
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Activated Alk triggers prolonged neurogenesis and Ret upregulation providing a therapeutic target in ALK-mutated neuroblastoma |
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Algorithmes d'apprentissage et logiciels pour la statistique, avec applications à la bioinformatique. |
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[ALK, a key gene in the pathogenesis of neuroblastoma]. |
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ALK germline mutations in patients with neuroblastoma: a rare and weakly penetrant syndrome |
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The ALK receptor in sympathetic neuron development and neuroblastoma. |
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BET and CDK Inhibition Reveal Differences in the Proliferation Control of Sympathetic Ganglion Neuroblasts and Adrenal Chromaffin Cells |
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Beta-catenin status in paediatric medulloblastomas: correlation of immunohistochemical expression with mutational status, genetic profiles, and clinical characteristics |
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Caractérisation des amplifications génomiques et des mécanismes de surexpression de la protéine MYCN dans le neuroblastome |
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Characterization of amplicons in neuroblastoma: High-resolution mapping using DNA microarrays, relationship with outcome, and identification of overexpressed genes |
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Characterization of GAPCenA, a GTPase activating protein for Rab6, part of which associates with the centrosome |
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Characterization of novel Rab6-interacting proteins involved in endosome-to-TGN transport |
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Characterization of rearrangements involving the ALK gene reveals a novel truncated form associated with tumor aggressiveness in neuroblastoma |
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Cholinergic switch associated with morphological differentiation in neuroblastoma |
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Clinical characteristics and outcome of patients with neuroblastoma presenting genomic amplification of loci other than MYCN. |
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The constitutive activity of the ALK mutated at positions F1174 or R1275 impairs receptor trafficking |
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Control-free calling of copy number alterations in deep-sequencing data using GC-content normalization |
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Crystal structures of the small G protein Rap2A in complex with its substrate GTP, with GDP and with GTPgammaS. |
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Deep Sequencing Reveals Occurrence of Subclonal ALK Mutations in Neuroblastoma at Diagnosis. |
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ETUDE DE LA PROTEINE HUMAINE RAP2, APPARENTEE AUX PRODUITS DES ONCOGENES |
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[Genetic alterations in neuroblastoma and their usefulness for clinical management] |
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Genomic characterization of pediatric liver tumors and identification of molecular biomarker of therapeutic response.. |
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Germline gain-of-function mutations of ALK disrupt central nervous system development. |
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Germline mutations of the paired-like homeobox 2B |
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Heterogeneity of neuroblastoma cell identity defined by transcriptional circuitries. |
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High-resolution mapping of amplicons of the short arm of chromosome 1 in two neuroblastoma tumors by microarray-based comparative genomic hybridization. |
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HMCan-diff: a method to detect changes in histone modifications in cells with different genetic characteristics |
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Hyperactivation of Alk induces neonatal lethality in knock-in AlkF1178L mice |
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Identification of a specific effector of the small GTP-binding protein Rap2 |
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In-Depth Characterization of Human Retinoblastoma Subtype 2 and Preclinical Models |
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An integrative genomics screen uncovers ncRNA T-UCR functions in neuroblastoma tumours. |
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Interaction of a Golgi-associated kinesin-like protein with Rab6 |
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Learning algorithms and statistical software, with applications to bioinformatics |
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Learning smoothing models of copy number profiles using breakpoint annotations |
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Meta-analysis of neuroblastomas reveals a skewed ALK mutation spectrum in tumors with MYCN amplification |
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Methylation-associated PHOX2B gene silencing is a rare event in human neuroblastoma |
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Molecular analysis of chromosome arm 17q gain in neuroblastoma |
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Molecular pathogenesis of peripheral neuroblastic tumors |
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Neuroblastome, résistance in vivo à l'irinotecan et voie de signalisation ALK |
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The occurrence of intracranial rhabdoid tumours in mice depends on temporal control of Smarcb1 inactivation |
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Overall genomic pattern is a predictor of outcome in neuroblastoma |
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Phosphorylation of Rap1GAP during the Cell Cycle |
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Predicting outcomes for children with neuroblastoma using a multigene-expression signature: a retrospective SIOPEN/COG/GPOH study |
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Preferential occurrence of chromosome breakpoints within early replicating regions in neuroblastoma |
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Prognostic impact of gene expression-based classification for neuroblastoma. |
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QuantumClone: Clonal assessment of functional mutations in cancer based on a genotype-aware method for clonal reconstruction. |
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Radiogenomics of neuroblastomas: Relationships between imaging phenotypes, tumor genomic profile and survival. |
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Recent insights into the biology of neuroblastoma |
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Le récepteur à neurotrophines TrkC, un nouveau récepteur à dépendance impliqué dans la tumorigenèse du neuroblastome. |
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Regulation by miR181 family of the dependence receptor CDON tumor suppressive activity in neuroblastoma |
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Regulation of the GTPase activity of the ras-related rap2 protein |
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Relapsed neuroblastomas show frequent RAS-MAPK pathway mutations |
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Repurposing rotavirus vaccines for intratumoral immunotherapy can overcome resistance to immune checkpoint blockade |
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Revised risk estimation and treatment stratification of low- and intermediate-risk neuroblastoma patients by integrating clinical and molecular prognostic markers |
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Rôle des facteurs de transcription PHOX2B, GATA3 et HAND2 dans l'identité et l'oncogenèse du neuroblastome |
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SegAnnDB: interactive Web-based genomic segmentation |
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Study of chromatin remodeling genes implicates SMARCA4 as a putative player in oncogenesis in neuroblastoma |
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Study of the human rap2 protein, related to the products of the ras proto-oncogenes. |
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SV-Bay: structural variant detection in cancer genomes using a Bayesian approach with correction for GC-content and read mappability |
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SVDetect: a tool to identify genomic structural variations from paired-end and mate-pair sequencing data |
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The sympathetic nervous system: malignancy, disease, and novel functions. |
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Les translocations chromosomiques : des modifications cellulaires à l'oncogenèse |
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Two cases of localized neuroblastoma with multiple segmental chromosomal alterations and metastatic progression |
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Upregulation of MAPK Negative Feedback Regulators and RET in Mutant ALK Neuroblastoma: Implications for Targeted Treatment |
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Use of the Two-Hybrid System to Identify Rab-Interacting Proteins |
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VAMP: visualization and analysis of array-CGH, transcriptome and other molecular profiles |
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Variety and complexity of chromosome 17 translocations in neuroblastoma |
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Whole exome sequencing of cell-free DNA reveals temporo-spatial heterogeneity and identifies treatment-resistant clones in neuroblastoma |
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Wild-type ALK and activating ALK-R1275Q and ALK-F1174L mutations upregulate Myc and initiate tumor formation in murine neural crest progenitor cells |
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