Results 191 to 200 of about 3,048,198 (365)
The NIH Science of Behavior Change Program: Transforming the science through a focus on mechanisms of change.
Behaviour Research and Therapy, 2017 L. Nielsen, Melissa Riddle, J. King, W. Aklin, Wen Chen, Dave Clark, Elaine Collier, S. Czajkowski, L. Esposito, R. Ferrer, Paige Green, Christine Hunter, K. Kehl, Rosalind B. King, L. Onken, Janine M. Simmons, L. Stoeckel, C. Stoney, L. Tully, W. Weber +19 moresemanticscholar +1 more sourceRelationship Between Neurologic Symptoms and Signs and FMR1 Genotype in Premutation Carriers
Annals of Clinical and Translational Neurology, EarlyView.ABSTRACT Background and Objectives
Fragile X‐associated Tremor/Ataxia Syndrome (FXTAS) is the most severe late‐onset condition caused by a premutation in the FMR1 gene, characterized by expanded CGG triplet repeats of 55–200. Clinical presentations of FXTAS, including gait ataxia, kinetic tremor, cognitive decline, and rare Parkinsonism, are linked to ...Flora Tassone, Freddy Chafota, Miguel E. Rentería, Randi J. Hagerman, Ellery Santos, Anna Atkinson, Nicholas G. Martin, Elsdon Storey, Danuta Z. Loesch +8 morewiley +1 more sourceThe Library of Integrated Network-Based Cellular Signatures NIH Program: System-Level Cataloging of Human Cells Response to Perturbations.
Cell Systems, 2017 A. Keenan, Sherry L. Jenkins, Kathleen M. Jagodnik, Simon Koplev, Edward He, Denis Torre, Zichen Wang, Anders B. Dohlman, Moshe C. Silverstein, Alexander Lachmann, Maxim V. Kuleshov, Avi Ma’ayan, Vasileios Stathias, Raymond Terryn, Daniel J. Cooper, M. Forlin, Amar Koleti, D. Vidović, Caty Chung, S. Schürer, Jouzas Vasiliauskas, M. Pilarczyk, Behrouz Shamsaei, Mehdi Fazel, Yan Ren, Wen Niu, Nicholas A. Clark, Shana White, N. Mahi, Lixia Zhang, Michal Kouril, J. Reichard, S. Sivaganesan, M. Medvedovic, J. Meller, R. J. Koch, M. Birtwistle, R. Iyengar, E. Sobie, E. Azeloglu, J. Kaye, Jeannette M. Osterloh, K. Haston, Jaslin Kalra, Steve Finkbiener, Jonathan Li, P. Milani, Miriam Adam, Renan Escalante-Chong, K. Sachs, A. LeNail, D. Ramamoorthy, E. Fraenkel, G. Daigle, Uzma Hussain, A. Coye, J. Rothstein, D. Sareen, L. Ornelas, M. Bañuelos, B. Mandefro, Ritchie Ho, C. Svendsen, Ryan G. Lim, Jennifer T. Stocksdale, M. Casale, T. Thompson, Jie Wu, L. Thompson, V. Dardov, Vidya Venkatraman, Andrea D. Matlock, J. V. Van Eyk, Jacob D. Jaffe, Malvina Papanastasiou, A. Subramanian, T. Golub, S. Erickson, M. Fallahi‐Sichani, M. Hafner, N. Gray, Jia-Ren Lin, Caitlin E. Mills, J. Muhlich, M. Niepel, C. Shamu, Elizabeth H. Williams, D. Wrobel, P. Sorger, Laura M. Heiser, J. Gray, J. Korkola, G. Mills, Mark A. LaBarge, H. Feiler, Mark A. Dane, Elmar Bucher, M. Nederlof, D. Sudar, Sean M. Gross, David Kilburn, Rebecca Smith, Kaylyn L. Devlin, R. Margolis, L. Derr, Albert Lee, Ajay Pillai +106 moresemanticscholar +1 more sourceGAD65 Antibody ELISA With Extended Reportable Range: Validation and Guidance for Neurological Practice
Annals of Clinical and Translational Neurology, EarlyView.ABSTRACT Objective
To (1) validate GAD65‐ELISA detection and quantification for type 1 diabetes mellitus and autoimmune neurological diagnoses, (2) correlate ELISA results (reference range < 5 IU/mL) with established radioimmunoprecipitation assay (RIA; ≤ 0.02 nmol/L), and (3) define ELISA clinical utility and pitfalls.Andrew McKeon, Dana Olofson, Diana Anissian, Divyanshu Dubey, Eoin P. Flanagan, Max C. Herman, Sarosh R. Irani, Daniel H. Lachance, Maria A. Willrich, Sean Pittock, John R. Mills, Anastasia Zekeridou +11 morewiley +1 more sourceP655: Improved representation of functional data in ClinVar
Genetics in Medicine OpenMelissa Landrum, Kuljeet Kaur, Shanmuga Chitipiralla, Guangfeng Song, Chunlei Liu, Zenith Maddipatla, Garth Brown, Chao Chen, Jennifer Hart, Douglas Hoffman, Wonhee Jang, Rama Maiti, Joseph Mitchell, Tayebeh Rezaie, George Riley, Jinpeng Yang, Andrew Russette, Brandi Kattman +17 moredoaj +1 more source
