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Institut de Génétique et de Biologie Moléculaire et Cellulaire
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Elizabeth Ramos Morales. Biochemical, biophysical and structural study of proteins associated to human diseases : tcDAC2 and ADAT complex. Human health and pathology. Université de Strasbourg, 2021. English. ⟨NNT : 2021STRAJ028⟩. ⟨tel-03706964⟩
Péter Ecsédi, Gergő Gógl, László Nyitray. Studying the Structures of Relaxed and Fuzzy Interactions: The Diverse World of S100 Complexes. Frontiers in Molecular Biosciences, Frontiers Media, 2021, 8, pp.749052. ⟨10.3389/fmolb.2021.749052⟩. ⟨hal-03706776⟩
Pierre-Alexis Billa, yannick Faulconnier, Tao Ye, Mathilde Chervet, Fabienne Le Provost, et al.. Deep RNA-Seq reveals miRNome differences in mammary tissue of lactating Holstein and Montbeliarde cows. BMC Genomics, BioMed Central, 2019, 20, pp.621. ⟨10.1186/s12864-019-5987-4⟩. ⟨hal-03704470⟩
Chengjin Zhu. Structural and biochemical studies on RNA polymerase elongation complexes bound to highly conserved transcription factors NusG and NusA. Human health and pathology. Université de Strasbourg, 2021. English. ⟨NNT : 2021STRAJ107⟩. ⟨tel-03704003⟩
Laia Ortiz López. Study of Hippo effectors, Yap1 et Wwrt1, during proepicardium formation. Human health and pathology. Université de Strasbourg, 2021. English. ⟨NNT : 2021STRAJ101⟩. ⟨tel-03703701⟩
Sirine Souali-Crespo. Rôle de NR5A1 dans le destin des cellules de Sertoli fœtales chez la souris. Médecine humaine et pathologie. Université de Strasbourg, 2021. Français. ⟨NNT : 2021STRAJ105⟩. ⟨tel-03703683⟩
Ayesha Dinshaw Eduljee. Structural and functional studies on transcriptional proofreading by GreA. Human health and pathology. Université de Strasbourg, 2021. English. ⟨NNT : 2021STRAJ011⟩. ⟨tel-03701542⟩
Márton A. Simon, Péter Ecsédi, Gabor M. Kovacs, Adam L. Póti, Attila Reményi, et al.. High‐throughput competitive fluorescence polarization assay reveals functional redundancy in the S100 protein family. FEBS Journal, Wiley, 2020, 287 (13), pp.2834 - 2846. ⟨10.1111/febs.15175⟩. ⟨hal-03700709⟩
Nezih Karasu. Chromatin looping dynamics during the transition from hematopoietic stem cells to T-cells. Human health and pathology. Université de Strasbourg, 2021. English. ⟨NNT : 2021STRAJ012⟩. ⟨tel-03699705⟩
Angeliki Platania. Assessing the links between enhancer-promoter proximity, local chromatin dynamics and gene activity. Human health and pathology. Université de Strasbourg, 2021. English. ⟨NNT : 2021STRAJ102⟩. ⟨tel-03699502⟩
Eric Westhof, Marat M. yusupov, Gulnara yusupova. The multiple flavors of GoU pairs in RNA. Journal of Molecular Recognition, Wiley, 2019, pp.e2782. ⟨10.1002/jmr.2782⟩. ⟨hal-02361230⟩
Megana K. Prasad, Véronique Geoffroy, Serge Vicaire, Bernard Jost, Michael Dumas, et al.. A targeted next-generation sequencing assay for the molecular diagnosis of genetic disorders with orodental involvement. Journal of Medical Genetics, BMJ Publishing Group, 2016, 53 (2), pp.98--110. ⟨10.1136/jmedgenet-2015-103302⟩. ⟨hal-01272929⟩
Mathilde Boussac, Christophe Arbus, Helene Klinger, Alexandre Eusebio, Elodie Hainque, et al.. Personality Related to Quality-of-Life Improvement After Deep Brain Stimulation in Parkinson’s Disease (PSYCHO-STIM II). Journal of Parkinson's disease, Amsterdam : b : IOS Press, 2022, 12 (2), pp.699-711. ⟨10.3233/JPD-212883⟩. ⟨hal-03513907⟩
Floriane Gallais, Pierre Gantner, Delphine Planas, Morgane Solis, Timothée Bruel, et al.. Case Report: Evolution of Humoral and Cellular Immunity in Two COVID-19 Breakthrough Infections After BNT162b2 Vaccine. Frontiers in Immunology, Frontiers, 2022, 13, pp.790212. ⟨10.3389/fimmu.2022.790212⟩. ⟨pasteur-03696752⟩
Adriana Rebelo, Ilse Eidhof, Vivian Cintra, Léna Guillot-Noel, Claudia Pereira, et al.. Biallelic loss-of-function variations in PRDX3 cause cerebellar ataxia. Brain - A Journal of Neurology , Oxford University Press (OUP), 2021, 144 (5), pp.1467-1481. ⟨10.1093/brain/awab071⟩. ⟨hal-03658041⟩
Nathalie Piazzon, Florence Rage, Florence Schlotter, Hervé Moine, Christiane Branlant, et al.. In vitro and in cellulo evidences for association of the survival of motor neuron complex with the fragile X mental retardation protein. Journal of Biological Chemistry, American Society for Biochemistry and Molecular Biology, 2008, 283 (9), pp.5598-5610. ⟨10.1074/jbc.M707304200⟩. ⟨hal-03364368⟩
Bujamin Vokshi. Role of SWI/SNF chromatin-remodeling complexes in tumorigenesis : insights in dedifferentiated melanoma and renal medullary carcinoma. Agricultural sciences. Université de Strasbourg, 2020. English. ⟨NNT : 2020STRAJ116⟩. ⟨tel-03689309⟩
Benjamin Rothé, Régis Back, Marc Quinternet, Jonathan Bizarro, Marie-Cécile Robert, et al.. Characterization of the interaction between protein Snu13p/15.5K and the Rsa1p/NUFIP factor and demonstration of its functional importance for snoRNP assembly. Nucleic Acids Research, Oxford University Press, 2014, 42 (3), pp.2015-2036. ⟨10.1093/nar/gkt1091⟩. ⟨hal-01452718⟩
Supawich Morkmued, Virginie Laugel-Haushalter, Eric Mathieu, Brigitte Schuhbaur, Joseph Hemmerlé, et al.. Retinoic Acid Excess Impairs Amelogenesis Inducing Enamel Defects.. Frontiers in Physiology, Frontiers, 2016, 7, pp.673. ⟨10.3389/fphys.2016.00673⟩. ⟨hal-03686891⟩
G. Iacono, A. Dubos, H. Meziane, M. Benevento, E. Habibi, et al.. Increased H3K9 methylation and impaired expression of Protocadherins are associated with the cognitive dysfunctions of the Kleefstra syndrome. Nucleic Acids Research, Oxford University Press, 2018, 46 (10), pp.4950-4965. ⟨10.1093/nar/gky196⟩. ⟨hal-02187058⟩
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