Search Results - "Tayrac, Marie de"
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1
MITF reprograms the extracellular matrix and focal adhesion in melanoma
Published in eLife (13-01-2021)“…The microphthalmia-associated transcription factor (MITF) is a critical regulator of melanocyte development and differentiation. It also plays an important…”
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2
DNA methylation in glioblastoma: impact on gene expression and clinical outcome
Published in BMC genomics (14-12-2010)“…Changes in promoter DNA methylation pattern of genes involved in key biological pathways have been reported in glioblastoma. Genome-wide assessments of DNA…”
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3
Automated Analysis of 1p/19q Status by FISH in Oligodendroglial Tumors: Rationale and Proposal of an Algorithm
Published in PloS one (02-07-2015)“…To propose a new algorithm facilitating automated analysis of 1p and 19q status by FISH technique in oligodendroglial tumors with software packages available…”
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4
Contribution of 1p, 19q, 9p and 10q Automated Analysis by FISH to the Diagnosis and Prognosis of Oligodendroglial Tumors According to WHO 2016 Guidelines
Published in PloS one (28-12-2016)“…To study the feasibility and the diagnostic and prognostic interest of automated analysis of 1p, 19q, 9p and 10q status by FISH technique in oligodendroglial…”
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5
Implementation of a molecular tumor board at a regional level to improve access to targeted therapy
Published in International journal of clinical oncology (01-07-2020)“…Background With the development of precision oncology, Molecular Tumor Boards (MTB) are developing in many institutions. However, the implementation of MTB in…”
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6
ImmunoFISH is a reliable technique for the assessment of 1p and 19q status in oligodendrogliomas
Published in PloS one (20-06-2014)“…To develop a new ImmunoFISH technique for the study of oligodendrogliomas by combining a standard immunohistochemical stain using MIB-1 antibody with a…”
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7
Five distinct biological processes and 14 differentially expressed genes characterize TEL/AML1-positive leukemia
Published in BMC genomics (23-10-2007)“…The t(12;21)(p13;q22) translocation is found in 20 to 25% of cases of childhood B-lineage acute lymphoblastic leukemia (B-ALL). This rearrangement results in…”
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8
GNPAT Variant associated with severe iron overload in HFE hemochromatosis
Published in Hepatology (Baltimore, Md.) (01-12-2015)Get full text
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9
Disrupted Hypothalamo-Pituitary Axis in Association With Reduced SHH Underlies the Pathogenesis of NOTCH-Deficiency
Published in The journal of clinical endocrinology and metabolism (01-09-2020)“…In human, Sonic hedgehog (SHH) haploinsufficiency is the predominant cause of holoprosencephaly, a structural malformation of the forebrain midline…”
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10
Depicting the genetic architecture of pediatric cancers through an integrative gene network approach
Published in Scientific reports (27-01-2020)“…The genetic etiology of childhood cancers still remains largely unknown. It is therefore essential to develop novel strategies to unravel the spectrum of…”
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11
Mutational Spectrum in Holoprosencephaly Shows That FGF is a New Major Signaling Pathway
Published in Human mutation (01-12-2016)“…ABSTRACT Holoprosencephaly (HPE) is the most common congenital cerebral malformation in humans, characterized by impaired forebrain cleavage and midline facial…”
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12
A framework for validating AI in precision medicine: considerations from the European ITFoC consortium
Published in BMC medical informatics and decision making (02-10-2021)“…Background Artificial intelligence (AI) has the potential to transform our healthcare systems significantly. New AI technologies based on machine learning…”
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13
Characterizing the peritumoral brain zone in glioblastoma: a multidisciplinary analysis
Published in Journal of neuro-oncology (01-03-2015)“…Glioblastoma (GB) is the most frequent and aggressive type of primary brain tumor. Recurrences are mostly located at the margin of the resection cavity in the…”
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14
Simultaneous analysis of distinct Omics data sets with integration of biological knowledge: Multiple Factor Analysis approach
Published in BMC genomics (20-01-2009)“…Genomic analysis will greatly benefit from considering in a global way various sources of molecular data with the related biological knowledge. It is thus of…”
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15
Prognostic significance of EDN/RB, HJURP, p60/CAF-1 and PDLI4, four new markers in high-grade gliomas
Published in PloS one (11-09-2013)“…Recent studies have highlighted the heterogeneity of gliomas and demonstrated that molecular and genetic analysis could help in their classification and in the…”
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Impact of 9p deletion and p16, Cyclin D1, and Myc hyperexpression on the outcome of anaplastic oligodendrogliomas
Published in PloS one (28-02-2018)“…To study the presence of 9p deletion and p16, cyclin D1 and Myc expression and their respective diagnostic and prognostic interest in oligodendrogliomas. We…”
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17
Genome-wide association study identifies TF as a significant modifier gene of iron metabolism in HFE hemochromatosis
Published in Journal of hepatology (01-03-2015)“…Background & Aims Hereditary hemochromatosis (HH) is the most common form of genetic iron loading disease. It is mainly related to the homozygous C282Y/C282Y…”
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18
Homozygous STIL mutation causes holoprosencephaly and microcephaly in two siblings
Published in PloS one (06-02-2015)“…Holoprosencephaly (HPE) is a frequent congenital malformation of the brain characterized by impaired forebrain cleavage and midline facial anomalies…”
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19
DGKI methylation status modulates the prognostic value of MGMT in glioblastoma patients treated with combined radio-chemotherapy with temozolomide
Published in PloS one (18-09-2014)“…Consistently reported prognostic factors for glioblastoma (GBM) are age, extent of surgery, performance status, IDH1 mutational status, and MGMT promoter…”
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20
Mouse genetic background impacts both on iron and non-iron metals parameters and on their relationships
Published in Biometals (01-08-2015)“…Iron is reported to interact with other metals. In addition, it has been shown that genetic background may impact iron metabolism. Our objective was to…”
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