Gender as a Modifying Factor Influencing Myotonic Dystrophy Type 1 Phenotype Severity and Mortality: A Nationwide Multiple Databases Cross-Sectional Observational Study von Dogan, Celine, De Antonio, Marie, Hamroun, Dalil, Varet, Hugo, Fabbro, Marianne, Rougier, Felix, Amarof, Khadija, Arne Bes, Marie-Christine, Bedat-Millet, Anne-Laure, Behin, Anthony, Bellance, Remi, Bouhour, Françoise, Boutte, Celia, Boyer, François, Campana-Salort, Emmanuelle, Chapon, Françoise, Cintas, Pascal, Desnuelle, Claude, Deschamps, Romain, Drouin-Garraud, Valerie, Ferrer, Xavier, Gervais-Bernard, Helene, Ghorab, Karima, Laforet, Pascal, Magot, Armelle, Magy, Laurent, Menard, Dominique, Minot, Marie-Christine, Nadaj-Pakleza, Aleksandra, Pellieux, Sybille, Pereon, Yann, Preudhomme, Marguerite, Pouget, Jean, Sacconi, Sabrina, Sole, Guilhem, Stojkovich, Tanya, Tiffreau, Vincent, Urtizberea, Andoni, Vial, Christophe, Zagnoli, Fabien, Caranhac, Gilbert, Bourlier, Claude, Riviere, Gerard, Geille, Alain, Gherardi, Romain K, Eymard, Bruno, Puymirat, Jack, Katsahian, Sandrine, Bassez, Guillaume

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Therapeutic Potential of Flavonoids in Pain and Inflammation: Mechanisms of Action, Pre-Clinical and Clinical Data, and Pharmaceutical Development von Ferraz, Camila R., Carvalho, Thacyana T., Manchope, Marilia F., Artero, Nayara A., Rasquel-Oliveira, Fernanda S., Fattori, Victor, Casagrande, Rubia, Verri Jr, Waldiceu A.

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Plasmatic extracellular vesicle microRNAs in malignant pleural mesothelioma and asbestos-exposed subjects suggest a 2-miRNA signature as potential biomarker of disease von Cavalleri, Tommaso, Angelici, Laura, Favero, Chiara, Dioni, Laura, Mensi, Carolina, Bareggi, Claudia, Palleschi, Alessandro, Rimessi, Arianna, Consonni, Dario, Bordini, Lorenzo, Todaro, Aldo, Bollati, Valentina, Pesatori, Angela Cecilia

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Gene Expression Profiling in Slow-Type Calf Soleus Muscle of 30 Days Space-Flown Mice von Gambara, Guido, Salanova, Michele, Ciciliot, Stefano, Furlan, Sandra, Gutsmann, Martina, Schiffl, Gudrun, Ungethuem, Ute, Volpe, Pompeo, Gunga, Hanns-Christian, Blottner, Dieter

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Renal Lipotoxicity-Associated Inflammation and Insulin Resistance Affects Actin Cytoskeleton Organization in Podocytes von Martínez-García, Cristina, Izquierdo-Lahuerta, Adriana, Vivas, Yurena, Velasco, Ismael, Yeo, Tet-Kin, Chen, Sheldon, Medina-Gomez, Gema

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Characterisation of CDKL5 Transcript Isoforms in Human and Mouse von Hector, Ralph D, Dando, Owen, Landsberger, Nicoletta, Kilstrup-Nielsen, Charlotte, Kind, Peter C, Bailey, Mark E S, Cobb, Stuart R

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"I Know that You Know that I Know": Neural Substrates Associated with Social Cognition Deficits in DM1 Patients von Serra, Laura, Cercignani, Mara, Bruschini, Michela, Cipolotti, Lisa, Mancini, Matteo, Silvestri, Gabriella, Petrucci, Antonio, Bucci, Elisabetta, Antonini, Giovanni, Licchelli, Loretta, Spanò, Barbara, Giacanelli, Manlio, Caltagirone, Carlo, Meola, Giovanni, Bozzali, Marco

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Patients experiencing statin-induced myalgia exhibit a unique program of skeletal muscle gene expression following statin re-challenge von Elam, Marshall B, Majumdar, Gipsy, Mozhui, Khyobeni, Gerling, Ivan C, Vera, Santiago R, Fish-Trotter, Hannah, Williams, Robert W, Childress, Richard D, Raghow, Rajendra

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Mutation analysis of multiple pilomatricomas in a patient with myotonic dystrophy type 1 suggests a DM1-associated hypermutation phenotype von Ruebben, Albert, Wahl, Renate Ursula, Eggermann, Thomas, Dahl, Edgar, Ortiz-Bruechle, Nadina, Cacchi, Claudio

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Differences in splicing defects between the grey and white matter in myotonic dystrophy type 1 patients von Nishi, Masamitsu, Kimura, Takashi, Igeta, Masataka, Furuta, Mitsuru, Suenaga, Koichi, Matsumura, Tsuyoshi, Fujimura, Harutoshi, Jinnai, Kenji, Yoshikawa, Hiroo

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Learning epistatic gene interactions from perturbation screens von Elmes, Kieran, Schmich, Fabian, Szczurek, Ewa, Jenkins, Jeremy, Beerenwinkel, Niko, Gavryushkin, Alex

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Klf15 Is Critical for the Development and Differentiation of Drosophila Nephrocytes von Ivy, Jessica R, Drechsler, Maik, Catterson, James H, Bodmer, Rolf, Ocorr, Karen, Paululat, Achim, Hartley, Paul S

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Sense and Antisense DMPK RNA Foci Accumulate in DM1 Tissues during Development von Michel, Lise, Huguet-Lachon, Aline, Gourdon, Geneviève

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Towards development of a statistical framework to evaluate myotonic dystrophy type 1 mRNA biomarkers in the context of a clinical trial von Kurkiewicz, Adam, Cooper, Anneli, Mcllwaine, Emily, Cumming, Sarah A., Adam, Bent, Krahe, Ralf, Puymirat, Jack, Schoser, Benedikt, Timchenko, Lubov, Ashizawa, Tetsuo, Thornton, Charles A., Rogers, Simon, McClure, John D., Monckton, Darren G.

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GW-Bodies and P-Bodies Constitute Two Separate Pools of Sequestered Non-Translating RNAs von Patel, Prajal H, Barbee, Scott A, Blankenship, J Todd

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Short Review: Investigating ARSACS: models for understanding cerebellar degeneration von Artero Castro, A., Machuca, C., Rodriguez Jimenez, F. J., Jendelova, P., Erceg, S.

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A Circadian Clock Gene, Cry, Affects Heart Morphogenesis and Function in Drosophila as Revealed by Optical Coherence Microscopy von Alex, Aneesh, Li, Airong, Zeng, Xianxu, Tate, Rebecca E, McKee, Mary L, Capen, Diane E, Zhang, Zhan, Tanzi, Rudolph E, Zhou, Chao

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Reconstructing the Rasch-Built Myotonic Dystrophy Type 1 Activity and Participation Scale von Hermans, Mieke C E, Hoeijmakers, Janneke G J, Faber, Catharina G, Merkies, Ingemar S J

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Inheritance patterns of ATCCT repeat interruptions in spinocerebellar ataxia type 10 (SCA10) expansions von Landrian, Ivette, McFarland, Karen N, Liu, Jilin, Mulligan, Connie J, Rasmussen, Astrid, Ashizawa, Tetsuo

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Transcriptome Analysis of Ullrich Congenital Muscular Dystrophy Fibroblasts Reveals a Disease Extracellular Matrix Signature and Key Molecular Regulators von Paco, Sonia, Casserras, Teresa, Rodríguez, Maria Angels, Jou, Cristina, Puigdelloses, Montserrat, Ortez, Carlos I, Diaz-Manera, Jordi, Gallardo, Eduardo, Colomer, Jaume, Nascimento, Andrés, Kalko, Susana G, Jimenez-Mallebrera, Cecilia

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