Grand Projet
Arandel L. et al.
Immortalized human myotonic dystrophy muscle cell lines to assess therapeutic compounds.
Disease Models Mechanisms (2017) Feb. 10: 487-497.
doi: 10.1242/dmm.027367
Mercier S. et al.
Expanding the spectrum of congenital myopathy linked to recessive mutations in SCN4A.
Neurology (2017) Jan. 88(4):414-416.
doi: 10.1212/WNL.0000000000003535
Neto OA. et al.
Nonlethal CHRNA1-related congenital Myasthenic Syndrome with a homozygous null mutation.
Canadian Journal of Neurological Sciences (2017) Jan. 44 (1):125-127
doi: 10.1017/cjn.2016.322
Monat C. et al.
De novo assemblies of three Oryza glaberrima accessions provide first insights about pan-genome of african rices.
Genome Biol Evol. (2017) Jan 1. 9(1):1-6.
doi: 10.1093/gbe/evw253
Duyen T Bui et al.
Mismatch Repair Incompatibilities in Diverse Yeast Populations
Genetics 2017, vol. 205, issue 4
doi: 10.1534/genetics.116.199513
Stéphanie Bauché et al.
Impaired Presynaptic High-Affinity Choline Transporter Causes a Congenital Myasthenic Syndrome with Episodic Apnea
The American Journal of Human Genetics 2016, vol. 99, issue 3
doi: 10.1016/j.ajhg.2016.06.033
Kilan Le Guennec et al.
ABCA7 rare variants and Alzheimer disease risk
Neurology 2016, vol. 86, issue 23
doi: 10.1212/wnl.0000000000002627
S Terrat et al.
Improving soil bacterial taxa–area relationships assessment using DNA meta-barcoding
Heredity 2014, vol. 114, issue 5
doi: 10.1038/hdy.2014.91
Sebastien Terrat et al.
Meta-barcoded evaluation of the ISO standard 11063 DNA extraction procedure to characterize soil bacterial and fungal community diversity and composition
Microbial Biotechnology 2014, vol. 8, issue 1
doi: 10.1111/1751-7915.12162
M. Legendre et al.
Thirty-thousand-year-old distant relative of giant icosahedral DNA viruses with a pandoravirus morphology
Proceedings of the National Academy of Sciences 2014, vol. 111, issue 11
doi: 10.1073/pnas.1320670111