Sélection 2019
Marie Dumont et al.
Human chromosome‐specific aneuploidy is influenced by DNA ‐dependent centromeric features
The EMBO Journal 2019, vol. 39, issue 2
doi: 10.15252/embj.2019102924
Rafael Galupa et al.
A Conserved Noncoding Locus Regulates Random Monoallelic Xist Expression across a Topological Boundary
Molecular Cell 2019, vol. 77, issue 2
doi: 10.1016/j.molcel.2019.10.030
Morgane Baron et al.
Loss-of-function mutations in MRAP2 are pathogenic in hyperphagic obesity with hyperglycemia and hypertension
Nature Medicine 2019, vol. 25, issue 11
doi: 10.1038/s41591-019-0622-0
Rahel T. Florian et al.
Unstable TTTTA/TTTCA expansions in MARCH6 are associated with Familial Adult Myoclonic Epilepsy type 3
Nature Communications 2019, vol. 10, issue 1
doi: 10.1038/s41467-019-12763-9
Fabienne Levi-Acobas et al.
Compatibility of 5-ethynyl-2′F-ANA UTP with in vitro selection for the generation of base-modified, nuclease resistant aptamers
Organic & Biomolecular Chemistry 2019, vol. 17, issue 35
doi: 10.1039/c9ob01515a
Céline Forzani et al.
Mutations of the AtYAK1 Kinase Suppress TOR Deficiency in Arabidopsis
Cell Reports 2019, vol. 27, issue 12
doi: 10.1016/j.celrep.2019.05.074
Thibault Leroy et al.
Oak symbolism in the light of genomics
New Phytologist 2019, vol. 226, issue 4
doi: 10.1111/nph.15987
Joke G. van Bemmel et al.
The bipartite TAD organization of the X-inactivation center ensures opposing developmental regulation of Tsix and Xist
Nature Genetics 2019, vol. 51, issue 6
doi: 10.1038/s41588-019-0412-0
Raphaël Enaud et al.
Intestinal Inflammation in Children with Cystic Fibrosis Is Associated with Crohn’s-Like Microbiota Disturbances
Journal of Clinical Medicine 2019, vol. 8, issue 5
doi: 10.3390/jcm8050645
Nadjet Belbachir et al.
RRAD mutation causes electrical and cytoskeletal defects in cardiomyocytes derived from a familial case of Brugada syndrome
European Heart Journal 2019, vol. 40, issue 37
doi: 10.1093/eurheartj/ehz308