Modèle
Anna Lokchine et al.
SWS1-complex in premature ovarian insufficiency: SWSAP1 as a new POI gene
Human Reproduction 2025
doi: 10.1093/humrep/deaf177
Marianne Victoria Lemée et al.
Disrupted transcriptional networks regulated by CHD1L during neurodevelopment underlie the mirrored neuroanatomical and growth phenotypes of the 1q21.1 copy number variant
Nucleic Acids Research 2025, vol. 53, issue 18
doi: 10.1093/nar/gkaf934
Baptiste Verron et al.
The linker region of a development-specific DNA polymerase X ensures efficient repair of programmed DNA double-strand breaks in Paramecium tetraurelia
Nucleic Acids Research 2025, vol. 53, issue 7
doi: 10.1093/nar/gkaf286
Alexandra Helleux et al.
TFE3 fusions drive oxidative metabolism and ferroptosis resistance in translocation renal cell carcinoma
EMBO Molecular Medicine 2025
doi: 10.1038/s44321-025-00221-7
Salim Megat et al.
CREB3 gain of function variants protect against ALS
Nature Communications 2025, vol. 16, issue 1
doi: 10.1038/s41467-025-58098-6
Natalie J. Wallis et al.
Canine genome-wide association study identifies DENND1B as an obesity gene in dogs and humans
Science 2025, vol. 387, issue 6741
doi: 10.1126/science.ads2145
Ignacio Caballero et al.
Cystic fibrosis alters the structure of the olfactory epithelium and the expression of olfactory receptors affecting odor perception
Science Advances 2025, vol. 11, issue 9
doi: 10.1126/sciadv.ads1568
Michella Khoury Damaa et al.
Cyclin O controls entry into the cell-cycle variant required for multiciliated cell differentiation
Cell Reports 2024, vol. 44, issue 1
doi: 10.1016/j.celrep.2024.115117
Jacques Serizay et al.
Cyclin switch tailors a cell cycle variant to orchestrate multiciliogenesis
Cell Reports 2024, vol. 44, issue 1
doi: 10.1016/j.celrep.2024.115103
Flavia C Hasenauer et al.
Genome-wide mapping of spontaneous DNA replication error-hotspots using mismatch repair proteins in rapidly proliferating Escherichia coli
Nucleic Acids Research 2024
doi: 10.1093/nar/gkae1196