About: Marie de Tayrac

Facets (new session)
Description
Metadata
Settings
- owl:sameAs
- Inference Rule:

About: Marie de Tayrac Goto Sponge NotDistinct Permalink

An Entity of Type : foaf:Person, within Data Space : data.idref.fr associated with source document(s)

Attributes	Values
type	Person
sameAs	Tayrac, Marie de (1981-....) Tayrac, Marie de (1981-....)
alternative label	Tayrac, Marie Ève Monique de De Tayrac, Marie
Life Event	http://www.idref.fr/088441121/birth
preferred label	Tayrac, Marie de (1981-....)
name	Marie de Tayrac
dbpedia-owl:citizenship	http://sws.geonames.org/3017382/
Language	http://lexvo.org/id/iso639-3/fra
isni:identifierValid	0000000139124498
Given name	Marie de
familyName	Tayrac
has biographical i...tion (Deprecated)	PU-PH, head of medical bioinformatics unit, CHU Rennes en 2023
gender	female
is sameAs of	Tayrac, Marie de (1981-....)
is Thesis advisor of	http://www.sudoc.fr/272589179/id http://www.sudoc.fr/254777287/id Développement d'un pipeline d'analyse bioinformatique de l'hétérogénéité clonale de tumeurs afin de prédire les réponses aux traitements des patients atteints de cancer http://www.sudoc.fr/25739933X/id http://www.sudoc.fr/272659223/id
is Author of	http://www.sudoc.fr/089031342/id http://www.sudoc.fr/139805257/id Prognostic Significance of EDN/RB, HJURP, p60/CAF-1 and PDLI4, Four New Markers in High-Grade Gliomas. Gene expression profile in hereditary transthyretin amyloidosis: differences in targeted and source organs Mutational Landscape of DDR2 Gene in Lung Squamous Cell Carcinoma Using Next-generation Sequencing Not all polyriboinosinic-polyribocytidylic acids (Poly I:C) are equivalent for inducing maturation of dendritic cells: implication for alpha-type-1 polarized DCs. A Four-Gene Signature Associated with Clinical Outcome in High-Grade Gliomas. Five distinct biological processes and 14 differentially expressed genes characterize TEL/AML1-positive leukemia Implementation of a molecular tumor board at a regional level to improve access to targeted therapy Prognostic signature of ALL blasts at diagnosis: what can we really find? Deciphering the Genetic Etiology of Pediatric Cancers Through an Integrative Gene Network Approach Caractérisation du profil multimodal de la zone péritumorale des glioblastomes CD9 expression can be used to predict childhood TEL/AML1-positive acute lymphoblastic leukemia: proposal for an accelerated diagnostic flowchart. Proteomic analysis of glioblastomas: what is the best brain control sample? Analyse génomique et transcriptomique des glioblastomes multiformes IGHV segment utilization in immunoglobulin gene rearrangement differentiates patients with anti-myelin-associated glycoprotein neuropathy from others immunoglobulin M-gammopathies How silence shapes the brain: synonymous variants alter codon usage and translation of Sonic Hedgehog in holoprosencephaly Rare and low frequency variant stratification in the UK population: Description and impact on association tests Simultaneous analysis of distinct Omics data sets with integration of biological knowledge: Multiple Factor Analysis approach. Homozygous STIL Mutation Causes Holoprosencephaly and Microcephaly in Two Siblings. Genetics of neural tube defects: new candidate genes and complex mode of inheritance Gene Expression Meta-Analysis Identifies Grading and Survival Markers in Anaplastic Glioma. MITF reprograms the extracellular matrix and focal adhesion in melanoma Synonymous variants in holoprosencephaly alter codon usage and impact the Sonic Hedgehog protein http://www.sudoc.fr/259575240/id Combining evidence, biomedical literature and statistical dependence: new insights for functional annotation of gene sets. DGKI Methylation Status Modulates the Prognostic Value of MGMT in Glioblastoma Patients Treated with Combined Radio-Chemotherapy with Temozolomide Catégorisation des glioblastomes : typologie et profilage du génome. [Classification of glioblastoma and genome profiling]. MiR-31-3p do not predict anti-EGFR efficacy in first-line therapy of RAS wild-type metastatic right-sided colon cancer A 4-gene signature associated with clinical outcome in high-grade gliomas. DNA methylation in glioblastoma: impact on gene expression and clinical outcome. Recent advances in understanding inheritance of Holoprosencephaly Contribution of 1p, 19q, 9p and 10q Automated Analysis by FISH to the Diagnosis and Prognosis of Oligodendroglial Tumors According to WHO 2016 Guidelines Integrated clinical and omics approach to rare diseases novel genes and oligogenic inheritance in holoprosencephaly Disrupted hypothalamo-pituitary axis in association with reduced SHH underlies the pathogenesis of NOTCH-deficiency GNPAT variant associated with severe iron overload in HFE hemochromatosis ImmunoFISH is a reliable technique for the assessment of 1p and 19q status in oligodendrogliomas Mouse genetic background impacts both on iron and non-iron metals parameters and on their relationships Automated Analysis of 1p/19q Status by FISH in Oligodendroglial Tumors: Rationale and Proposal of an Algorithm From the core to beyong the margin : Les faces cachées de la zone péritumorale Integrative genome-wide analysis reveals a robust genomic glioblastoma signature associated with copy number driving changes in gene expression. A framework for validating AI in precision medicine: considerations from the European ITFoC consortium Incidental diagnosis of mucopolysaccharidosis type I in an infant with chronic intestinal pseudoobstruction by exome sequencing Quantitative proteomics analysis of glioblastoma multiforme with triplex Isotope-Coded Protein Labeling Analyse protéomique des glioblastones: Quel est le meilleur contrôle? Mutational Spectrum in Holoprosencephaly Shows That FGF is a New Major Signaling Pathway Integration of Genomic Alterations and Expression Profiling in Glioblastoma Multiforme. Depicting the genetic architecture of pediatric cancers through an integrative gene network approach Distinct effects of human glioblastoma immunoregulatory molecules programmed cell death ligand-1 (PDL-1) and indoleamine 2,3-dioxygenase (IDO) on tumour-specific T cell functions. Biomarkers for the prognosis and high-grade glioma clinical outcome Characterizing the peritumoral brain zone in glioblastoma: a multidisciplinary analysis. Genome-wide association study identifies TF as a significant modifier gene of iron metabolism in HFE hemochromatosis From the core to beyond the margin: a genomic picture of glioblastoma intratumor heterogeneity Du cyclope à la réalité Un nouveau regard sur la génétique de l’holoprosencéphalie [From cyclops to reality: a fresh look at the genetics of holoprosencephaly] Integration of transcriptome and proteome profiles in glioblastoma looking for the missing link
is primary topic of	http://www.idref.fr/088441121
is Opponent of	http://www.sudoc.fr/269698078/id http://www.sudoc.fr/270814027/id http://www.sudoc.fr/280069553/id
is Thesis referee of	http://www.sudoc.fr/258804246/id http://www.sudoc.fr/27860370X/id http://www.sudoc.fr/279471211/id http://www.sudoc.fr/262301075/id http://www.sudoc.fr/275435695/id http://www.sudoc.fr/256976570/id http://www.sudoc.fr/260861030/id http://www.sudoc.fr/277256305/id

Faceted Search & Find service v1.13.91 as of Aug 16 2018

Alternative Linked Data Documents: ODE Content Formats:

RDF

ODATA

Microdata

About

OpenLink Virtuoso version 07.20.3229 as of May 14 2019, on Linux (x86_64-pc-linux-gnu), Single-Server Edition (70 GB total memory)
Data on this page belongs to its respective rights holders.
Virtuoso Faceted Browser Copyright © 2009-2025 OpenLink Software