France (FR)

PPARβ/δ: A master regulator of mesenchymal stem cell functions (2016) Djouad F, Ipseiz N, Luz-Crawford P, Scholtysek C, Krönke G, Jorgensen C Journal article Inflammation Modifies the Paradoxical Association between Body Mass Index and Mortality in Hemodialysis Patients (2016) Stenvinkel P, Gillespie IA, Tunks J, Addison J, Kronenberg F, Drueke TB, Marcelli D, et al. Journal article Autoantibodies against Modified Histone Peptides in SLE Patients Are Associated with Disease Activity and Lupus Nephritis (2016) Dieker J, Berden JH, Bakker M, Briand JP, Muller S, Voll R, Sjowall C, et al. Journal article The F4/AS01B HIV-1 Vaccine Candidate Is Safe and Immunogenic, But Does Not Show Viral Efficacy in Antiretroviral Therapy-Naive, HIV-1-Infected Adults: A Randomized Controlled Trial (2016) Dinges W, Girard PM, Podzamczer D, Brockmeyer NH, Garcia F, Harrer T, Lelievre JD, et al. Journal article Serum Autotaxin Activity Correlates With Pruritus in Pediatric Cholestatic Disorders (2016) Kremer A, Gonzales E, Schaap FG, Elferink RPJO, Jacquemin E, Beuers U Journal article The tumor microenvironment and Immunoscore are critical determinants of dissemination to distant metastasis (2016) Mlecnik B, Bindea G, Kirilovsky A, Angell HK, Obenauf AC, Tosolini M, Church SE, et al. Journal article Visual and semiautomated evaluation of epileptogenicity in focal cortical dysplasias - An intracranial EEG study (2016) Gollwitzer S, Valente I, Rodionov R, Scott C, Ritter LM, Wehner T, Hamer H, et al. Journal article Retention, dosing, tolerability and patient reported seizure outcome of Zonisamide as only add-on treatment under real-life conditions in adult patients with partial onset seizures: Results of the observational study ZOOM (2016) Hamer H, Baulac M, Mcmurray R, Kockelmann E Journal article Genotype, Clinical Course, and Therapeutic Decision Making in 76 Infants with Severe Generalized Junctional Epidermolysis Bullosa (2016) Hammersen J, Has C, Naumann-Bartsch N, Stachel D, Kiritsi D, Söder S, Tardieu M, et al. Journal article A novel missense mutation in the gene EDARADD associated with an unusual phenotype of hypohidrotic ectodermal dysplasia (2016) Wohlfart S, Söder S, Smahi A, Schneider H Journal article