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Nature Genetics|November 12, 2005
The gene disrupted in Marinesco-Sjögren syndrome encodes SIL1, an HSPA5 cochaperoneAnna-Kaisa Anttonen, Ibrahim Mahjneh, Riikka H Hämäläinen, et al.
Euro Surveillance : Bulletin Europeen Sur Les Maladies Transmissibles = European Communicable Disease Bulletin|March 27, 2020
Outbreak of pneumococcal pneumonia among shipyard workers in Marseille, France, January to February 2020Nadim Cassir, Laurence Pascal, David Ferrieux, et al.
Frontiers in Microbiology|June 8, 2017
Gut Bacteria Missing in Severe Acute Malnutrition, Can We Identify Potential Probiotics by Culturomics?Maryam Tidjani Alou, Matthieu Million, Sory I Traore, et al.
Journal of Clinical Medicine|December 10, 2021
Factors Associated with 90-Day Mortality in Invasively Ventilated Patients with COVID-19 in Marseille, FranceMaxime Volff, David Tonon, Youri Bommel, et al.
Nature Neuroscience|March 2, 2011
Long pre-mRNA depletion and RNA missplicing contribute to neuronal vulnerability from loss of TDP-43Magdalini Polymenidou, Clotilde Lagier-Tourenne, Kasey R Hutt, et al.
Expert Review of Clinical Immunology|December 28, 2020
Natural history of COVID-19 and therapeutic optionsPhilippe Gautret, Matthieu Million, Pierre-André Jarrot, et al.
International Journal of Antimicrobial Agents|March 25, 2020
RETRACTED: Hydroxychloroquine and azithromycin as a treatment of COVID-19: results of an open-label non-randomized clinical trialPhilippe Gautret, Jean-Christophe Lagier, Philippe Parola, et al.
Scientific Reports|May 18, 2016
Increased Gut Redox and Depletion of Anaerobic and Methanogenic Prokaryotes in Severe Acute MalnutritionMatthieu Million, Maryam Tidjani Alou, Saber Khelaifia, et al.
Biorxiv : the Preprint Server for Biology|March 17, 2025
Recurrent patterns of widespread neuronal genomic damage shared by major neurodegenerative disordersZinan Zhou, Lovelace J Luquette, Guanlan Dong, et al.
Human Molecular Genetics|January 19, 2010
Variant CCG and GGC repeats within the CTG expansion dramatically modify mutational dynamics and likely contribute toward unusual symptoms in some myotonic dystrophy type 1 patientsClaudia Braida, Rhoda K A Stefanatos, Berit Adam, et al.
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