A fluorescent reporter for rapid assessment of autophagic flux reveals unique autophagy signatures during C. elegans post-embryonic development and identifies compounds that modula... von Dawson, Zachary D, Sundaramoorthi, Hemalatha, Regmi, Suk, Zhang, Bo, Morrison, Stephanie, Fielder, Sara M, Zhang, Jessie R, Hoang, Hieu, Perlmutter, David H, Luke, Cliff J, Silverman, Gary A, Pak, Stephen C

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A motor independent requirement for dynein light chain in Caenorhabditis elegans meiotic synapsis von Fielder, Sara M, Kent, Tori, Ling, Huiping, Gleason, Elizabeth J, Kelly, William G

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Functional analysis of a novel de novo variant in PPP5C associated with microcephaly, seizures, and developmental delay von Fielder, Sara M., Rosenfeld, Jill A., Burrage, Lindsay C., Emrick, Lisa, Lalani, Seema, Attali, Ruben, Bembenek, Joshua N., Hoang, Hieu, Baldridge, Dustin, Silverman, Gary A., Schedl, Tim, Pak, Stephen C.

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Supplemental Materials for Fielder et al., 2021 von Fielder, Sara M., Kent, Tori, Ling, Huiping, Gleason, Elizabeth J., Kelly, William G.

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Horizon scanning: Tools to identify emerging threats to plant health in a changing world von Antoniou, A., Abergel, M., Akrivou, A., Beale, T., Day, R., Fielder, H., Larenaudie, M., MacLeod, A., Rosace, M. C., Sarakatsani, E., Stinziano, J. R., Szyniszewska, A. M., Suffert, M., Tramontini, S.

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Genomic analysis across 53 canine cancer types reveals novel mutations and high clinical actionability potential von Sakthikumar, Sharadha, Warrier, Manisha, Whitley, Derick, Facista, Salvatore, Adkins, Jonathan, Aman, Sara, Tsinajinnie, Darwin, Duran, Natalie, Siravegna, Giulia, Ahmed, Zeeshan, Day, Kenneth, Jenkins, Brooklyn, Patel, Nidhi, Ryden, Kirk, Nadai, Joe, Banovich, Kathryn, Powers, Barbara, Edwards, Jeffrey, Steinberg, Jennifer, Fielder, Susan, Wong, Shukmei, Byron, Sara A., Izatt, Tyler, Zismann, Victoria, Boateng, Martin, Zhu, Zhanyang, Chuang, Han‐Yu, Trent, Jeffrey M., Haworth, David, Chon, Esther, Hendricks, William, Wang, Guannan

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Mutations in the transmembrane domain of FGFR3 cause the most common genetic form of dwarfism, achondroplasia von Shiang, Rita, Thompson, Leslie M., Zhu, Ya-Zhen, Church, Deanna M., Fielder, Thomas J., Bocian, Maureen, Winokur, Sara T., Wasmuth, John J.

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