Publications

  • Sort By

  • By Page

  • Reset
  • Year(s)

  • Major Publication(s)

  • Technologie(s)

  • Plateform(s) and Project(s)

  • Project(s)

2310 results
Page 55 of 77

Gwenneg Kerdivel et al.
Opposite T3 Response of ACTG1–FOS Subnetwork Differentiate Tailfin Fate in Xenopus Tadpole and Post-hatching Axolotl
Frontiers in Endocrinology 2019, vol. 10
doi: 10.3389/fendo.2019.00194

Willem De Ridder et al.
Muscular dystrophy with arrhythmia caused by loss-of-function mutations in BVES
Neurology Genetics 2019, vol. 5, issue 2
doi: 10.1212/nxg.0000000000000321

Jill K. Olofsson et al.
Phylogenomics using low‐depth whole genome sequencing: A case study with the olive tribe
Molecular Ecology Resources 2019, vol. 19, issue 4
doi: 10.1111/1755-0998.13016

Kang Du et al.
The genome of the arapaima (Arapaima gigas) provides insights into gigantism, fast growth and chromosomal sex determination system
Scientific Reports 2019, vol. 9, issue 1
doi: 10.1038/s41598-019-41457-x

Dorian Chabbert et al.
Postnatal Tshz3 Deletion Drives Altered Corticostriatal Function and Autism Spectrum Disorder–like Behavior
Biological Psychiatry 2019, vol. 86, issue 4
doi: 10.1016/j.biopsych.2019.03.974

Petar Pujic et al.
Omics of the early molecular dialogue between Frankia alni and Alnus glutinosa and the cellulase synton
Environmental Microbiology 2019, vol. 21, issue 9
doi: 10.1111/1462-2920.14606

Alberto Cenci et al.
Effect of paleopolyploidy and allopolyploidy on gene expression in banana
BMC Genomics 2019, vol. 20, issue 1
doi: 10.1186/s12864-019-5618-0

Réjane Troudet et al.
RNA SIGNATURE OF TREATMENT RESPONSE IN FIRST-EPISODE PSYCHOSIS
European Neuropsychopharmacology 2019, vol. 29
doi: 10.1016/j.euroneuro.2017.08.271

Guillaume Beinse et al.
The NRF2 transcriptional target NQO1 has low mRNA levels in TP53-mutated endometrial carcinomas
PLOS ONE 2019, vol. 14, issue 3
doi: 10.1371/journal.pone.0214416

Mathilde Romagnoli et al.
Deciphering the Mammary Stem Cell Niche: A Role for Laminin-Binding Integrins
Stem Cell Reports 2019, vol. 12, issue 4
doi: 10.1016/j.stemcr.2019.02.008

Lou Grangeon et al.
Biallelic MYORG mutation carriers exhibit primary brain calcification with a distinct phenotype
Brain 2019, vol. 142, issue 6
doi: 10.1093/brain/awz095

Nolwenn Lucas et al.
Biology and prognostic impact of clonal plasmacytoid dendritic cells in chronic myelomonocytic leukemia
Leukemia 2019, vol. 33, issue 10
doi: 10.1038/s41375-019-0447-3

Emmanuelle Boscher et al.
Copy Number Variants in miR-138 as a Potential Risk Factor for Early-Onset Alzheimer’s Disease
Journal of Alzheimer’s Disease 2019, vol. 68, issue 3
doi: 10.3233/jad-180940

Wiam Saadi et al.
A critical regulator of Bcl2 revealed by systematic transcript discovery of lncRNAs associated with T-cell differentiation
Scientific Reports 2019, vol. 9, issue 1
doi: 10.1038/s41598-019-41247-5

Niklas Tysklind et al.
Development of nuclear and plastid SNP and INDEL markers for population genetic studies and timber traceability of Carapa species
Conservation Genetics Resources 2019, vol. 11, issue 3
doi: 10.1007/s12686-019-01090-2

Laurent Bouillaut et al.
Role of the global regulator Rex in control of NAD + ‐regeneration in Clostridioides (Clostridium) difficile
Molecular Microbiology 2019, vol. 111, issue 6
doi: 10.1111/mmi.14245

Amna Khamis et al.
Laser capture microdissection of human pancreatic islets reveals novel eQTLs associated with type 2 diabetes
Molecular Metabolism 2019, vol. 24
doi: 10.1016/j.molmet.2019.03.004

Krishna Kishore Gali et al.
Development of a Sequence-Based Reference Physical Map of Pea (Pisum sativum L.)
Frontiers in Plant Science 2019, vol. 10
doi: 10.3389/fpls.2019.00323

Michel Wassef et al.
EZH1/2 function mostly within canonical PRC2 and exhibit proliferation-dependent redundancy that shapes mutational signatures in cancer
Proceedings of the National Academy of Sciences 2019, vol. 116, issue 13
doi: 10.1073/pnas.1814634116

Henri-Corto Stoeklé et al.
Genetic Data, Two-Sided Markets and Dynamic Consent: United States Versus France
Science and Engineering Ethics 2019, vol. 25, issue 5
doi: 10.1007/s11948-019-00085-4

Florence Coussy et al.
A large collection of integrated genomically characterized patient‐derived xenografts highlighting the heterogeneity of triple‐negative breast cancer
International Journal of Cancer 2019
doi: 10.1002/ijc.32266

Lucas Leclère et al.
The genome of the jellyfish Clytia hemisphaerica and the evolution of the cnidarian life-cycle
Nature Ecology & Evolution 2019, vol. 3, issue 5
doi: 10.1038/s41559-019-0833-2

Charlotte Henriet et al.
Water stress combined with sulfur deficiency in pea affects yield components but mitigates the effect of deficiency on seed globulin composition
Journal of Experimental Botany 2019, vol. 70, issue 16
doi: 10.1093/jxb/erz114

Maëva Veyssiere et al.
A novel nonsense variant in SUPT20H gene associated with Rheumatoid Arthritis identified by Whole Exome Sequencing of multiplex families
PLOS ONE 2019, vol. 14, issue 3
doi: 10.1371/journal.pone.0213387

Battle Karimi et al.
Biogeography of Soil Bacterial Networks along a Gradient of Cropping Intensity
Scientific Reports 2019, vol. 9, issue 1
doi: 10.1038/s41598-019-40422-y

M. Ibrahim-Kosta et al.
Minor allele of the factor V K858R variant protects from venous thrombosis only in non-carriers of factor V Leiden mutation
Scientific Reports 2019, vol. 9, issue 1
doi: 10.1038/s41598-019-40172-x

Mélodie Sawicki et al.
On a Cold Night: Transcriptomics of Grapevine Flower Unveils Signal Transduction and Impacted Metabolism
International Journal of Molecular Sciences 2019, vol. 20, issue 5
doi: 10.3390/ijms20051130

Yann Dussert et al.
A High-Quality Grapevine Downy Mildew Genome Assembly Reveals Rapidly Evolving and Lineage-Specific Putative Host Adaptation Genes
Genome Biology and Evolution 2019, vol. 11, issue 3
doi: 10.1093/gbe/evz048

Julie Reveillaud et al.
The Wolbachia mobilome in Culex pipiens includes a putative plasmid
Nature Communications 2019, vol. 10, issue 1
doi: 10.1038/s41467-019-08973-w

Christina Zeitz et al.
Where are the missing gene defects in inherited retinal disorders? Intronic and synonymous variants contribute at least to 4% of CACNA1F ‐mediated inherited retinal disorders
Human Mutation 2019, vol. 40, issue 6
doi: 10.1002/humu.23735

2310 results
Page 55 of 77