Search Results - "Millot, Gael A"
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Cell-type-specific replication initiation programs set fragility of the FRA3B fragile site
Published in Nature (London) (03-02-2011)“…The origins of fragility Some chromosomal locations, known as common fragile sites, are predisposed to breakage. These sites have pathological relevance…”
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High-affinity autoreactive plasma cells disseminate through multiple organs in patients with immune thrombocytopenic purpura
Published in The Journal of clinical investigation (15-06-2022)“…The major therapeutic goal for immune thrombocytopenic purpura (ITP) is to restore normal platelet counts using drugs to promote platelet production or by…”
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The anti-IgE mAb omalizumab induces adverse reactions by engaging Fcγ receptors
Published in The Journal of clinical investigation (02-03-2020)“…Omalizumab is an anti-IgE monoclonal antibody (mAb) approved for the treatment of severe asthma and chronic spontaneous urticaria. Use of omalizumab is…”
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LGP2 binds to PACT to regulate RIG-I- and MDA5-mediated antiviral responses
Published in Science signaling (01-10-2019)“…The retinoic acid-inducible gene I (RIG-I)-like receptors (RLRs) RIG-I, MDA5, and LGP2 stimulate inflammatory and antiviral responses by sensing nonself RNA…”
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Genome-wide mapping of individual replication fork velocities using nanopore sequencing
Published in Nature communications (08-06-2022)“…Little is known about replication fork velocity variations along eukaryotic genomes, since reference techniques to determine fork speed either provide no…”
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Belt and braces: Two escape ways to maintain the cassette reservoir of large chromosomal integrons
Published in PLoS genetics (05-04-2024)“…Integrons are adaptive devices that capture, stockpile, shuffle and express gene cassettes thereby sampling combinatorial phenotypic diversity. Some integrons…”
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A guide for functional analysis of BRCA1 variants of uncertain significance
Published in Human mutation (01-11-2012)“…Germline mutations in the tumor suppressor gene BRCA1 confer an estimated lifetime risk of 56–80% for breast cancer and 15–60% for ovarian cancer. Since the…”
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The Loss of Expression of a Single Type 3 Effector (CT622) Strongly Reduces Chlamydia trachomatis Infectivity and Growth
Published in Frontiers in cellular and infection microbiology (15-05-2018)“…Invasion of epithelial cells by the obligate intracellular bacterium results in its enclosure inside a membrane-bound compartment termed an inclusion. The…”
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Transcription-dependent regulation of replication dynamics modulates genome stability
Published in Nature structural & molecular biology (01-01-2019)“…Common fragile sites (CFSs) are loci that are hypersensitive to replication stress and hotspots for chromosomal rearrangements in cancers. CFSs replicate late…”
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MetaHiC phage-bacteria infection network reveals active cycling phages of the healthy human gut
Published in eLife (26-02-2021)“…Bacteriophages play important roles in regulating the intestinal human microbiota composition, dynamics, and homeostasis, and characterizing their bacterial…”
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Signaling from Mus81-Eme2-Dependent DNA Damage Elicited by Chk1 Deficiency Modulates Replication Fork Speed and Origin Usage
Published in Cell reports (Cambridge) (09-02-2016)“…Mammalian cells deficient in ATR or Chk1 display moderate replication fork slowing and increased initiation density, but the underlying mechanisms have…”
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Serpentine: a flexible 2D binning method for differential Hi-C analysis
Published in Bioinformatics (01-06-2020)“…Abstract Motivation Hi-C contact maps reflect the relative contact frequencies between pairs of genomic loci, quantified through deep sequencing. Differential…”
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Chlamydia trachomatis development requires both host glycolysis and oxidative phosphorylation but has only minor effects on these pathways
Published in The Journal of biological chemistry (01-09-2022)“…The obligate intracellular bacteria Chlamydia trachomatis obtain all nutrients from the cytoplasm of their epithelial host cells and stimulate glucose uptake…”
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A Parent-of-Origin Effect Impacts the Phenotype in Low Penetrance Retinoblastoma Families Segregating the c.1981C>T/p.Arg661Trp Mutation of RB1
Published in PLoS genetics (01-02-2016)“…Retinoblastoma (Rb), the most common pediatric intraocular neoplasm, results from inactivation of both alleles of the RB1 tumor suppressor gene. The second…”
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Contribution of germline deleterious variants in the RAD51 paralogs to breast and ovarian cancers
Published in European journal of human genetics : EJHG (01-12-2017)“…RAD51 paralogs (RAD51B, RAD51C, RAD51D, XRCC2, and XRCC3) have recently been involved in breast and ovarian cancer predisposition: RAD51B, RAD51C, and RAD51D…”
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Heritability of the melatonin synthesis variability in autism spectrum disorders
Published in Scientific reports (18-12-2017)“…Autism Spectrum Disorders (ASD) are heterogeneous neurodevelopmental disorders with a complex genetic architecture. They are characterized by impaired social…”
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Functional Assessment of Genetic Variants with Outcomes Adapted to Clinical Decision-Making
Published in PLoS genetics (06-06-2016)“…Understanding the medical effect of an ever-growing number of human variants detected is a long term challenge in genetic counseling. Functional assays, based…”
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Single-molecule, antibody-free fluorescent visualisation of replication tracts along barcoded DNA molecules
Published in The International journal of developmental biology (2016)“…DNA combing is a standard technique to map DNA replication at the single molecule level. Typically, replicating DNA is metabolically labelled with nucleoside…”
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Integron cassettes integrate into bacterial genomes via widespread non-classical attG sites
Published in Nature microbiology (01-01-2024)“…Integrons are genetic elements involved in bacterial adaptation which capture, shuffle and express genes encoding adaptive functions embedded in cassettes…”
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Mosaicism and prenatal diagnosis options: insights from retinoblastoma
Published in European journal of human genetics : EJHG (01-02-2017)“…In sporadic cases, a post-zygotic mutational event signifies a somatic mosaicism in the affected child only, which implies that these mutations affect only a…”
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