ALS-implicated protein TDP-43 sustains levels of STMN2, a mediator of motor neuron growth and repair von Klim, Joseph R., Williams, Luis A., Limone, Francesco, Guerra San Juan, Irune, Davis-Dusenbery, Brandi N., Mordes, Daniel A., Burberry, Aaron, Steinbaugh, Michael J., Gamage, Kanchana K., Kirchner, Rory, Moccia, Rob, Cassel, Seth H., Chen, Kuchuan, Wainger, Brian J., Woolf, Clifford J., Eggan, Kevin

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Evidence for α-synuclein prions causing multiple system atrophy in humans with parkinsonism von Prusiner, Stanley B., Woerman, Amanda L., Mordes, Daniel A., Watts, Joel C., Rampersaud, Ryan, Berry, David B., Patel, Smita, Oehler, Abby, Lowe, Jennifer K., Kravitz, Stephanie N., Geschwind, Daniel H., Glidden, David V., Halliday, Glenda M., Middleton, Lefkos T., Gentleman, Steve M., Grinberg, Lea T., Giles, Kurt

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Running up that pill for amyotrophic lateral sclerosis von Smeyers, Julie, Mordes, Daniel A

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Kinetics of α-synuclein prions preceding neuropathological inclusions in multiple system atrophy von Woerman, Amanda L, Patel, Smita, Kazmi, Sabeen A, Oehler, Abby, Lee, Jisoo, Mordes, Daniel A, Olson, Steven H, Prusiner, Stanley B

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Implications of Using Hemoglobin A1C for Diagnosing Diabetes Mellitus von Malkani, Samir, MD, Mordes, John P., MD

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TopBP1 activates ATR through ATRIP and a PIKK regulatory domain von Mordes, Daniel A, Glick, Gloria G, Zhao, Runxiang, Cortez, David

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Two familial ALS proteins function in prevention/repair of transcription-associated DNA damage von Hill, Sarah J., Mordes, Daniel A., Cameron, Lisa A., Neuberg, Donna S., Landini, Serena, Eggan, Kevin, Livingston, David M.

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Propagation of prions causing synucleinopathies in cultured cells von Woerman, Amanda L., Stöhr, Jan, Aoyagi, Atsushi, Rampersaud, Ryan, Krejciova, Zuzana, Watts, Joel C., Ohyama, Takao, Patel, Smita, Widjaja, Kartika, Oehler, Abby, Sanders, David W., Diamond, Marc I., Seeley, William W., Middleton, Lefkos T., Gentleman, Steve M., Mordes, Daniel A., Südhof, Thomas C., Giles, Kurt, Prusiner, Stanley B.

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Absence of Survival and Motor Deficits in 500 Repeat C9ORF72 BAC Mice von Mordes, Daniel A., Morrison, Brett M., Ament, Xanthe H., Cantrell, Christopher, Mok, Joanie, Eggan, Pierce, Xue, Carolyn, Wang, Jin-Yuan, Eggan, Kevin, Rothstein, Jeffrey D.

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The E46K mutation modulates α-synuclein prion replication in transgenic mice von Holec, Sara A M, Lee, Jisoo, Oehler, Abby, Batia, Lyn, Wiggins-Gamble, Aryanna, Lau, Jeffrey, Ooi, Felicia K, Merz, Gregory E, Wang, Man, Mordes, Daniel A, Olson, Steven H, Woerman, Amanda L

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Multiple system atrophy prions retain strain specificity after serial propagation in two different Tg(SNCAA53T) mouse lines von Woerman, Amanda L., Oehler, Abby, Kazmi, Sabeen A., Lee, Jisoo, Halliday, Glenda M., Middleton, Lefkos T., Gentleman, Steve M., Mordes, Daniel A., Spina, Salvatore, Grinberg, Lea T., Olson, Steven H., Prusiner, Stanley B.

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Phosphorylation of tau at a single residue inhibits binding to the E3 ubiquitin ligase, CHIP von Nadel, Cory M., Pokhrel, Saugat, Wucherer, Kristin, Oehler, Abby, Thwin, Aye C., Basu, Koli, Callahan, Matthew D., Southworth, Daniel R., Mordes, Daniel A., Craik, Charles S., Gestwicki, Jason E.

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Familial Parkinson’s point mutation abolishes multiple system atrophy prion replication von Woerman, Amanda L., Kazmi, Sabeen A., Patel, Smita, Aoyagi, Atsushi, Oehler, Abby, Widjaja, Kartika, Mordes, Daniel A., Olson, Steven H., Prusiner, Stanley B.

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Pluripotent stem cell strategies for rebuilding the human brain von Limone, Francesco, Klim, Joseph R, Mordes, Daniel A

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Monitoring peripheral nerve degeneration in ALS by label-free stimulated Raman scattering imaging von Tian, Feng, Yang, Wenlong, Mordes, Daniel A., Wang, Jin-Yuan, Salameh, Johnny S., Mok, Joanie, Chew, Jeannie, Sharma, Aarti, Leno-Duran, Ester, Suzuki-Uematsu, Satomi, Suzuki, Naoki, Han, Steve S., Lu, Fa-Ke, Ji, Minbiao, Zhang, Rosanna, Liu, Yue, Strominger, Jack, Shneider, Neil A., Petrucelli, Leonard, Xie, X. Sunney, Eggan, Kevin

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The Basic Cleft of RPA70N Binds Multiple Checkpoint Proteins, Including RAD9, To Regulate ATR Signaling von Xu, Xin, Vaithiyalingam, Sivaraja, Glick, Gloria G., Mordes, Daniel A., Chazin, Walter J., Cortez, David

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Dpb11 activates the Mec1-Ddc2 complex von Mordes, Daniel A, Nam, Edward A, Cortez, David

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MSA prions exhibit remarkable stability and resistance to inactivation von Woerman, Amanda L., Kazmi, Sabeen A., Patel, Smita, Freyman, Yevgeniy, Oehler, Abby, Aoyagi, Atsushi, Mordes, Daniel A., Halliday, Glenda M., Middleton, Lefkos T., Gentleman, Steve M., Olson, Steven H., Prusiner, Stanley B.

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The C9orf72-interacting protein Smcr8 is a negative regulator of autoimmunity and lysosomal exocytosis von Zhang, Yingying, Burberry, Aaron, Wang, Jin-Yuan, Sandoe, Jackson, Ghosh, Sulagna, Udeshi, Namrata D, Svinkina, Tanya, Mordes, Daniel A, Mok, Joanie, Charlton, Maura, Li, Quan-Zhen, Carr, Steven A, Eggan, Kevin

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Exome sequencing in amyotrophic lateral sclerosis implicates a novel gene, DNAJC7, encoding a heat-shock protein von Farhan, Sali M. K., Howrigan, Daniel P., Abbott, Liam E., Klim, Joseph R., Topp, Simon D., Byrnes, Andrea E., Churchhouse, Claire, Phatnani, Hemali, Smith, Bradley N., Rampersaud, Evadnie, Wu, Gang, Wuu, Joanne, Shatunov, Aleksey, Iacoangeli, Alfredo, Al Khleifat, Ahmad, Mordes, Daniel A., Ghosh, Sulagna, Eggan, Kevin, Rademakers, Rosa, McCauley, Jacob L., Schüle, Rebecca, Züchner, Stephan, Benatar, Michael, Taylor, J. Paul, Nalls, Michael, Gotkine, Marc, Shaw, Pamela J., Morrison, Karen E., Al-Chalabi, Ammar, Traynor, Bryan, Shaw, Christopher E., Goldstein, David B., Harms, Matthew B., Daly, Mark J., Neale, Benjamin M.

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