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- Mouse Pus1 Knockout Project (CRISPR/Cas9)
- Overexpression Screens Identify Conserved Dosage Chromosome
- A Uniparental Isodisomy Event Introducing Homozygous
- Mutation Into Adulthood
- A Master Autoantigen-Ome Links Alternative Splicing, Female Predilection, and COVID-19 to Autoimmune Diseases
- A Mark of Disease: How Mrna Modifications Shape Genetic and Acquired Pathologies
- The Emerging Roles of RNA Modifications in Glioblastoma
- The MYCL and MXD1 Transcription Factors Regulate the Fitness of Murine Dendritic Cells
- Mitokondriesykdommer V03
- Epitranscriptomic Code and Its Alterations in Human Disease
- Biomolecules-10-00729-V2.Pdf
- Pseudouridine Synthase 1 Deficient Mice, a Model for Mitochondrial Myopathy with Sideroblastic Anemia, Exhibit Muscle Morphology and Physiology Alterations
- Chemical and Conformational Diversity of Modified Nucleosides Affects Trna Structure and Function
- The 2020 Version of the Gene Table of Neuromuscular Disorders (Nuclear Genome) Louise Benarroch, Gisèle Bonne, Francois Rivier, Dalil Hamroun
- The 2021 Version of the Gene Table of Neuromuscular Disorders (Nuclear Genome) Louise Benarroch, Gisèle Bonne, Francois Rivier, Dalil Hamroun
- Substrate Binding and Catalysis by the Pseudouridine Synthases Rlua and Trub