Archives Publications
Bal E. et al.
Mutations in ACTRT1 and its enhancer RNA elements lead to aberrant activation of Hedgehog signaling in inherited and sporadic basal cell carcinomas.
Nat Med. (2017) Oct. 23(10):1226-1233.
doi: 10.1038/nm.4368
Cabanel N. et al.
Molecular bases for multidrug resistance in Yersinia pseudotuberculosis.
Int J Med Microbiol. (2017) Oct. 307(7):371-381.
doi: 10.1016/j.ijmm.2017.08.005
Martins RM. et al.
An ApiAP2 member regulates expression of clonally variant genes of the human malaria parasite Plasmodium falciparum.
Sci Rep. (2017) Oct.7(1):14042.
doi: 10.1038/s41598-017-12578-y
Troudet R. et al.
RNA signature and prediction to treatment response in first episode schizophrenia.
European Neuropsychopharm. (2017) Oct. 27: S597-S597.
doi: 10.1016/S0924-977X(17)31139-2
Nelson I. et al.
Novel recessive splice site mutation in POPDC1 (BVES) is associated with first-degree atrioventricular block and muscular dystrophy.
Neuromus. Dis. (2017) Oct. 27: S139-S140.
doi: 10.1016/j.nmd.2017.06.172
Malfatti E. et al.
Recessive myopalladin mutations cause congenital cap myopathy with unusual rods.
Neuromus. Dis. (2017) Oct. 27: S185-S185.
doi: 10.1016/j.nmd.2017.06.331
Charmet R. et al.
Association of impaired renal function with venous thrombosis: A genetic risk score approach.
Thromb Res. (2017) Oct. 158:102-107.
doi: 10.1016/j.thromres.2017.08.015
Kocher A. et al.
Evaluation of shortmitochondrial metabarcodes for the identification of Amazonian mammals.
Methods in Ecology and Evolution (2017) Oct. 8: 1276–1283.
doi: 10.1111/2041-210X.12729
Auffret P. et al.
Draft genome sequence of enterohemorrhagic Escherichia coli O157:H7 strain MC2 isolated from cattlde in France.
Genome Announc. (2017) Oct. 5(40). pii: e01097-17.
doi: 10.1128/genomeA.01097-17
Capela D. et al.
Recruitment of a lineage-specific virulence regulatorypathway promotes intracellular infection by a plant pathogen experimentally evolved into a legume symbiont.
Mol Biol Evol. (2017) Oct. 34(10):2503-2521.
doi: 10.1093/molbev/msx165