The Unstable Repeats—Three Evolving Faces of Neurological Disease von Nelson, David L., Orr, Harry T., Warren, Stephen T.

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Expanded GGGGCC repeat RNA associated with amyotrophic lateral sclerosis and frontotemporal dementia causes neurodegeneration von Xu, Zihui, Poidevin, Mickael, Li, Xuekun, Li, Yujing, Shu, Liqi, Nelson, David L., Li, He, Hales, Chadwick M., Gearing, Marla, Wingo, Thomas S., Jin, Peng

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LLPS of FXR1 drives spermiogenesis by activating translation of stored mRNAs von Kang, Jun-Yan, Wen, Ze, Pan, Duo, Zhang, Yuhan, Li, Qing, Zhong, Ai, Yu, Xinghai, Wu, Yi-Chen, Chen, Yu, Zhang, Xiangzheng, Kou, Peng-Cheng, Geng, Junlan, Wang, Ying-Yi, Hua, Min-Min, Zong, Ruiting, Li, Biao, Shi, Hui-Juan, Li, Dangsheng, Fu, Xiang-Dong, Li, Jinsong, Nelson, David L., Guo, Xuejiang, Zhou, Yu, Gou, Lan-Tao, Huang, Ying, Liu, Mo-Fang

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Bmal1 and β-Cell Clock Are Required for Adaptation to Circadian Disruption, and Their Loss of Function Leads to Oxidative Stress-Induced β-Cell Failure in Mice von Lee, Jeongkyung, Moulik, Mousumi, Fang, Zhe, Saha, Pradip, Zou, Fang, Xu, Yong, Nelson, David L., Ma, Ke, Moore, David D., Yechoor, Vijay K.

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Preclinical pharmacological profile of the selective 5-HT1F receptor agonist lasmiditan von Nelson, David L, Phebus, Lee A, Johnson, Kirk W, Wainscott, David B, Cohen, Marlene L, Calligaro, David O, Xu, Yao-Chang

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Ablation of Fmrp in adult neural stem cells disrupts hippocampus-dependent learning von Guo, Weixiang, Allan, Andrea M, Zong, Ruiting, Zhang, Li, Johnson, Eric B, Schaller, Eric G, Murthy, Adeline C, Goggin, Samantha L, Eisch, Amelia J, Oostra, Ben A, Nelson, David L, Jin, Peng, Zhao, Xinyu

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Stereoscopic Height and Wind Retrievals for Aerosol Plumes with the MISR INteractive eXplorer (MINX) von Nelson, D.L., Garay, M.J., Kahn, Ralph A., Dunst, Ben A.

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Altered Hippocampal Synaptic Plasticity in the Fmr1 Gene Family Knockout Mouse Models von Zhang, Jing, Hou, Lingfei, Klann, Eric, Nelson, David L

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Intercepting IRE1 kinase‐FMRP signaling prevents atherosclerosis progression von Yildirim, Zehra, Baboo, Sabyasachi, Hamid, Syed M, Dogan, Asli E, Tufanli, Ozlem, Robichaud, Sabrina, Emerton, Christina, Diedrich, Jolene K, Vatandaslar, Hasan, Nikolos, Fotis, Gu, Yanghong, Iwawaki, Takao, Tarling, Elizabeth, Ouimet, Mireille, Nelson, David L, Yates, John R, Walter, Peter, Erbay, Ebru

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2022 Victor A. McKusick Leadership Award von Nelson, David L.

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Recessive mutations in muscle-specific isoforms of FXR1 cause congenital multi-minicore myopathy von Estañ, María Cristina, Fernández-Núñez, Elisa, Zaki, Maha S., Esteban, María Isabel, Donkervoort, Sandra, Hawkins, Cynthia, Caparros-Martin, José A., Saade, Dimah, Hu, Ying, Bolduc, Véronique, Chao, Katherine Ru-Yui, Nevado, Julián, Lamuedra, Ana, Largo, Raquel, Herrero-Beaumont, Gabriel, Regadera, Javier, Hernandez-Chico, Concepción, Tizzano, Eduardo F., Martinez-Glez, Victor, Carvajal, Jaime J., Zong, Ruiting, Nelson, David L., Otaify, Ghada A., Temtamy, Samia, Aglan, Mona, Issa, Mahmoud, Bönnemann, Carsten G., Lapunzina, Pablo, Yoon, Grace, Ruiz-Perez, Victor L.

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Rescue of behavioral phenotype and neuronal protrusion morphology in Fmr1 KO mice von de Vrij, Femke M.S, Levenga, Josien, van der Linde, Herma C, Koekkoek, Sebastiaan K, De Zeeuw, Chris I, Nelson, David L, Oostra, Ben A, Willemsen, Rob

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Functional consequences of postnatal interventions in a mouse model of Fragile X syndrome von Rais, Maham, Lovelace, Jonathan W., Shuai, Xinghao S., Woodard, Walker, Bishay, Steven, Estrada, Leo, Sharma, Ashwin R., Nguy, Austin, Kulinich, Anna, Pirbhoy, Patricia S., Palacios, Arnold R., Nelson, David L., Razak, Khaleel A., Ethell, Iryna M.

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Stephen T. Warren 1953–2021 von Nelson, David L.

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Homeostatic responses fail to correct defective amygdala inhibitory circuit maturation in fragile X syndrome von Vislay, Rebecca L, Martin, Brandon S, Olmos-Serrano, Jose Luis, Kratovac, Sebila, Nelson, David L, Corbin, Joshua G, Huntsman, Molly M

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Reexamining the role of TACI coding variants in common variable immunodeficiency and selective IgA deficiency von Pan-Hammarström, Qiang, Salzer, Ulrich, Du, Likun, Björkander, Janne, Cunningham-Rundles, Charlotte, Nelson, David L, Bacchelli, Chiara, Gaspar, H Bobby, Offer, Steven, Behrens, Timothy W, Grimbacher, Bodo, Hammarström, Lennart

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FXR1P Limits Long-Term Memory, Long-Lasting Synaptic Potentiation, and De Novo GluA2 Translation von Cook, Denise, Nuro, Erin, Jones, Emma V., Altimimi, Haider F., Farmer, W. Todd, Gandin, Valentina, Hanna, Edith, Zong, Ruiting, Barbon, Alessandro, Nelson, David L., Topisirovic, Ivan, Rochford, Joseph, Stellwagen, David, Béïque, Jean-Claude, Murai, Keith K.

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AFQ056, a new mGluR5 antagonist for treatment of fragile X syndrome von Levenga, Josien, Hayashi, Shigemi, de Vrij, Femke M.S, Koekkoek, Sebastiaan K, van der Linde, Herma C, Nieuwenhuizen, Ingeborg, Song, Cheng, Buijsen, Ronald A.M, Pop, Andreea S, GomezMancilla, Baltazar, Nelson, David L, Willemsen, Rob, Gasparini, Fabrizio, Oostra, Ben A

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Human Serine Racemase: Key Residues/Active Site Motifs and Their Relation to Enzyme Function von Graham, Danielle L, Beio, Matthew L, Nelson, David L, Berkowitz, David B

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Mutations of the Wiskott-Aldrich Syndrome Protein (WASP): hotspots, effect on transcription, and translation and phenotype/genotype correlation von Jin, Yinzhu, Mazza, Cinzia, Christie, Jacinda R., Giliani, Silvia, Fiorini, Maurilia, Mella, Patrizia, Gandellini, Francesca, Stewart, Donn M., Zhu, Qili, Nelson, David L., Notarangelo, Luigi D., Ochs, Hans D.

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