Publications
Dickson LB et al.
Diverse laboratory colonies of Aedes aegypti harbor the same adult midgut bacterial microbiome
Parasites & Vectors 2018 11(1)
doi: 10.1186/s13071-018-2780-1
Krin E et al.
Expansion of the SOS regulon of Vibrio cholerae through extensive transcriptome analysis and experimental validation
BMC Genomics 2018 19(1)
doi: 10.1186/s12864-018-4716-8
Randrianjatovo-Gbalou I et al.
Enzymatic synthesis of random sequences of RNA and RNA analogues by DNA polymerase theta mutants for the generation of aptamer libraries
Nucleic Acids Research 2018 46(12)
doi: 10.1093/nar/gky413
Varet H et al.
Enteric bacteria boost defences against oxidative stress in Entamoeba histolytica
Scientific Reports 2018 8(1)
doi: 10.1038/s41598-018-27086-w
Garneau JR et al.
High Prevalence and Genetic Diversity of Large phiCD211 (phiCDIF1296T)-Like Prophages in Clostridioides difficile
Applied and Environmental Microbiology 2017 84(3)
doi: 10.1128/AEM.02164-17
Janezic S et al.
Comparative Genomics of Clostridium difficile
Springer International Publishing 2018
doi: 10.1007/978-3-319-72799-8_5
Maikova A et al.
Discovery of new type I toxinantitoxin systems adjacent to CRISPR arrays in Clostridium difficile
Nucleic Acids Research 2018 46(9)
doi: 10.1093/nar/gky124
Poquet i et al.
Clostridium difficile Biofilm: Remodeling Metabolism and Cell Surface to Build a Sparse and Heterogeneously Aggregated Architecture
Frontiers in Microbiology 2018 9
doi: 10.3389/fmicb.2018.02084
Varet H et al.
checkMyIndex: a web-based R/Shiny interface for choosing compatible sequencing indexes
Bioinformatics 2018 35(5)
doi: 10.1093/bioinformatics/bty706
Henriques A et al.
Sphingolipid Metabolism Is Dysregulated at Transcriptomic and Metabolic Levels in the Spinal Cord of an Animal Model of Amyotrophic Lateral Sclerosis
Frontiers in Molecular Neuroscience 2018 10
doi: 10.3389/fnmol.2017.00433
Chatterjee S et al.
Reinstating plasticity and memory in a tauopathy mouse model with an acetyltransferase activator
EMBO Molecular Medicine 2018 10(11)
doi: 10.15252/emmm.201708587
Chézeau L et al.
Short- and long-term gene expression profiles induced by inhaled TiO2 nanostructured aerosol in rat lung
Toxicology and Applied Pharmacology 2018 356
doi: 10.1016/j.taap.2018.07.013
Dembélé D et al.
Analysis of high-throughput biological data using their rank values
Statistical Methods in Medical Research 2018
doi: 10.1177/0962280218764187
El Nagar S et al.
A new genetically engineered mouse model of choroid plexus carcinoma
Biochemical and Biophysical Research Communications 2018 496(2)
doi: 10.1016/j.bbrc.2017.11.192
El-Saafin F et al.
Homozygous TAF8 mutation in a patient with intellectual disability results in undetectable TAF8 protein, but preserved RNA polymerase II transcription
Human Molecular Genetics 2018 27(12)
doi: 10.1093/hmg/ddy126
Grüning B et al.
Bioconda: sustainable and comprehensive software distribution for the life sciences
Nature Methods 2018 15(7)
doi: 10.1038/s41592-018-0046-7
Quartier A et al.
Genes and Pathways Regulated by Androgens in Human Neural Cells, Potential Candidates for the Male Excess in Autism Spectrum Disorder
Biological Psychiatry 2018 84(4)
doi: 10.1016/j.biopsych.2018.01.002
Rabineau M et al.
Chromatin de-condensation by switching substrate elasticity
Scientific Reports 2018 8(1)
doi: 10.1038/s41598-018-31023-2
Soustre-Gacougnolle I et al.
Responses to climatic and pathogen threats differ in biodynamic and conventional vines
Scientific Reports 2018 8(1)
doi: 10.1038/s41598-018-35305-7
Brucato N et al.
The Comoros Show the Earliest Austronesian Gene Flow into the Swahili Corridor
The American Journal of Human Genetics 2018 102(1)
doi: 10.1016/j.ajhg.2017.11.011
Yauy K et al.
B3GAT3-related disorder with craniosynostosis and bone fragility due to a unique mutation
Genetics in Medicine 2017 20(2)
doi: 10.1038/gim.2017.109
Weber A et al.
Epigenome-wide DNA methylation profiling in Progressive Supranuclear Palsy reveals major changes at DLX1
Nature Communications 2018 9(1)
doi: 10.1038/s41467-018-05325-y
Wang-Renault SF et al.
Deregulation of microRNA expression in purified T and B lymphocytes from patients with primary Sjögren’s syndrome
Annals of the Rheumatic Diseases 2017 77(1)
doi: 10.1136/annrheumdis-2017-211417
Vulin A et al.
Severe PATCHED1 Deficiency in Cancer-Prone Gorlin Patient Cells Results in Intrinsic Radiosensitivity
International Journal of Radiation Oncology*Biology*Physics 2018 102(2)
doi: 10.1016/j.ijrobp.2018.05.057
Vuillaume ML et al.
Whole genome sequencing identifies a de novo 2.1?Mb balanced paracentric inversion disrupting FOXP1 and leading to severe intellectual disability
Clinica Chimica Acta 2018 485
doi: 10.1016/j.cca.2018.06.048
Velasco G et al.
Comparative methylome analysis of ICF patients identifies heterochromatin loci that require ZBTB24, CDCA7 and HELLS for their methylated state
Human Molecular Genetics 2018 27(14)
doi: 10.1093/hmg/ddy130
Ulff-Møller CJ et al.
Twin DNA Methylation Profiling Reveals Flare-Dependent Interferon Signature and B Cell Promoter Hypermethylation in Systemic Lupus Erythematosus
Arthritis & Rheumatology 2018 70(6)
doi: 10.1002/art.40422
Tost J et al.
A translational perspective on epigenetics in allergic diseases
Journal of Allergy and Clinical Immunology 2018 142(3)
doi: 10.1016/j.jaci.2018.07.009
Tost J et al.
Epigenetic plasticity of eosinophils and other immune cell subsets in childhood asthma
The Lancet Respiratory Medicine 2018 6(5)
doi: 10.1016/s2213-2600(18)30051-1
Stoeklé HC et al.
La propriété des données génétiques
Médecine/Sciences 2018 34(12)
doi: 10.1051/medsci/2018291