2018
Meng A et al.
Analysis of the genomic basis of functional diversity in dinoflagellates using a transcriptome-based sequence similarity network
Molecular Ecology 2018 27(10)
doi: 10.1111/mec.14579
Maurin aT et al.
HITS-CLIP in various brain areas reveals new targets and new modalities of RNA binding by fragile X mental retardation protein
Nucleic Acids Research 2018 46(12)
doi: 10.1093/nar/gky267
Costa A et al.
Fibroblast Heterogeneity and Immunosuppressive Environment in Human Breast Cancer
Cancer Cell 2018 33(3)
doi: 10.1016/j.ccell.2018.01.011
Pace L et al.
The epigenetic control of stemness in CD8$mathplus$ T cell fate commitment
Science 2018 359(6372)
doi: 10.1126/science.aah6499
Baudrin LG et al.
Improved Microsatellite Instability Detection and Identification by Nuclease-Assisted Microsatellite Instability Enrichment Using HSP110 T17
Clinical Chemistry 2018 64(8)
doi: 10.1373/clinchem.2018.287490
de Haan HG et al.
Genome-Wide Association Study Identifies a Novel Genetic Risk Factor for Recurrent Venous Thrombosis
Circulation: Genomic and Precision Medicine 2018 11(2
doi: 10.1161/circgen.117.001827
Lornage X et al.
Novel SPEG Mutations in Congenital Myopathy without Centralized Nuclei
Journal of Neuromuscular Diseases 2018 5(2)
doi: 10.3233/JND-170265
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
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
Dehecq M et al.
Nonsense-mediated mRNA decay involves two distinct Upf1-bound complexes
The EMBO Journal 2018 37(21)
doi: 10.15252/embj.201899278