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Deficiency of monoacylglycerol lipase enhances IgM plasma levels and limits atherogenesis in a CB2-dependent manner Guillamat Prats, Raquel; Rami, Martina; Ring, Larisa; Rinne, Petteri; ... Steffens, Sabine 2019
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Uncovering the heterogeneity and temporal complexity of neurodegenerative diseases with Subtype and Stage Inference Young, Alexandra L; Marinescu, Razvan V; Oxtoby, Neil P; Bocchetta, Martina; ... Alexander, Daniel C 2018
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VTA DA neuron excitatory synapses in Shank3 Δex4-9 mouse line Bariselli, Sebastiano; Bellone, Camilla 2017
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Significant Locus and Metabolic Genetic Correlations Revealed in Genome-Wide Association Study of Anorexia Nervosa Duncan, Laramie; Yilmaz, Zeynep; Gaspar, Helena; Walters, Raymond; ... Bulik, Cynthia M 2017
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Serum Osteopontin Levels Are Decreased in Focal Adenomyosis Streuli, Marie Isabelle; Santulli, Pietro; Chouzenoux, Sandrine; Chapron, Charles; Batteux, Frédéric 2017
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Inborn errors in RNA polymerase III underlie severe varicella zoster virus infections Ogunjimi, Benson; Zhang, Shen-Ying; Sørensen, Katrine B; Fluss, Joel Victor; ... Mogensen, Trine H 2017
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Genetic and phenotypic dissection of 1q43q44 microdeletion syndrome and neurodevelopmental phenotypes associated with mutations in ZBTB18 and HNRNPU Korff, Christian; Bottani, Armand 2017
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GRIN2B encephalopathy: novel findings on phenotype, variant clustering, functional consequences and treatment aspects Ranza, Emmanuelle Nathalie; Korff, Christian 2017
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Clinical spectrum and genotype-phenotype associations of KCNA2-related encephalopathies Masnada, Silvia; Hedrich, Ulrike B S; Gardella, Elena; Korff, Christian; ... Rubboli, Guido 2017
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Cardiovascular risk in patients with rheumatoid arthritis Lauper, Kim; Gabay, Cem 2017
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Impact of CD14 Polymorphisms on Anti-Apolipoprotein A-1 IgG-Related Coronary Artery Disease Prediction in the General Population Antiochos, Panagiotis; Marques-Vidal, Pedro; Virzi, Julien; Pagano, Sabrina; ... Vuilleumier, Nicolas 2017
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Exploring venlafaxine pharmacokinetic variability with a phenotyping approach, a multicentric french-swiss study (MARVEL study) Lloret-Linares, Célia; Daali, Youssef; Chevret, Sylvie; Nieto, Isabelle; ... Bellivier, Frank 2017
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The Elephant in the Room: The Role of Microtubules in Cancer Cirillo, Luca; Gotta, Monica; Meraldi, Patrick 2017
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Genetic variants associated with response to lithium treatment in bipolar disorder: a genome-wide association study Hou, Liping; Heilbronner, Urs; Degenhardt, Franziska; Kelsoe, John R; ... Schulze, Thomas G 2016
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Loss of VPS13C Function in Autosomal-Recessive Parkinsonism Causes Mitochondrial Dysfunction and Increases PINK1/Parkin-Dependent Mitophagy French Parkinson's Disease Genetics Study, International Parkinson's Disease Genomics Consortium 2016
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Gait phenotype from mild cognitive impairment to moderate dementia: results from the GOOD initiative Allali, Gilles; Annweiler, C; Blumen, H M; Callisaya, M L; ... Beauchet, Olivier 2016
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Beta Cell Hubs Dictate Pancreatic Islet Responses to Glucose Johnston, Natalie R; Mitchell, Ryan K; Haythorne, Elizabeth; Pessoa, Maria Paiva; ... Hodson, David J 2016
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Formation of new chromatin domains determines pathogenicity of genomic duplications Franke, Martin; Ibrahim, Daniel M; Andrey, Guillaume; Schwarzer, Wibke; ... Mundlos, Stefan 2016
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Chemoattractant Signals and Adhesion Molecules Promoting Human Regulatory T Cell Recruitment to Porcine Endothelium Ehirchiou, Driss; Muller, Yannick D; Chicheportiche, Rachel; Heyrani Nobari, Ruhollah; ... Seebach, Jorg Dieter 2016
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Comparative Genomics Analysis of Streptococcus tigurinus Strains Identifies Genetic Elements Specifically and Uniquely Present in Highly Virulent Strains Diene, Seydina Mouhamadou; Francois, Patrice; Zbinden, Andrea; Entenza, José Manuel; Resch, Grégory 2016
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