Synaptic dysfunction induced by glycine‐alanine dipeptides in C9orf72‐ALS/FTD is rescued by SV2 replenishment
Jensen, Brigid K, Schuldi, Martin H, McAvoy, Kevin, Russell, Katelyn A, Boehringer, Ashley, Curran, Bridget M, Krishnamurthy, Karthik, Wen, Xinmei, Westergard, Thomas, Ma, Le, Haeusler, Aaron R, Edbauer, Dieter, Pasinelli, Piera, Trotti, Davide
Published in EMBO molecular medicine (08.05.2020)
Published in EMBO molecular medicine (08.05.2020)
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Fragile X protein mitigates TDP-43 toxicity by remodeling RNA granules and restoring translation
Coyne, Alyssa N, Yamada, Shizuka B, Siddegowda, Bhavani Bagevalu, Estes, Patricia S, Zaepfel, Benjamin L, Johannesmeyer, Jeffrey S, Lockwood, Donovan B, Pham, Linh T, Hart, Michael P, Cassel, Joel A, Freibaum, Brian, Boehringer, Ashley V, Taylor, J Paul, Reitz, Allen B, Gitler, Aaron D, Zarnescu, Daniela C
Published in Human molecular genetics (15.12.2015)
Published in Human molecular genetics (15.12.2015)
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Motor neurons and glia exhibit specific individualized responses to TDP-43 expression in a Drosophila model of amyotrophic lateral sclerosis
Estes, Patricia S, Daniel, Scott G, McCallum, Abigail P, Boehringer, Ashley V, Sukhina, Alona S, Zwick, Rebecca A, Zarnescu, Daniela C
Published in Disease models & mechanisms (01.05.2013)
Published in Disease models & mechanisms (01.05.2013)
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Generation of two induced pluripotent stem cell (iPSC) lines from an ALS patient with simultaneous mutations in KIF5A and MATR3 genes
Medina, David X., Boehringer, Ashley, Dominick, Marissa, Lorenzini, Ileana, Saez-Atienzar, Sara, Pioro, Erik P., Sattler, Rita, Traynor, Bryan, Bowser, Robert
Published in Stem cell research (01.01.2021)
Published in Stem cell research (01.01.2021)
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Mutations in the Matrin 3 gene cause familial amyotrophic lateral sclerosis
Johnson, Janel O, Pioro, Erik P, Boehringer, Ashley, Chia, Ruth, Feit, Howard, Renton, Alan E, Pliner, Hannah A, Abramzon, Yevgeniya, Marangi, Giuseppe, Winborn, Brett J, Gibbs, J Raphael, Nalls, Michael A, Morgan, Sarah, Shoai, Maryam, Hardy, John, Pittman, Alan, Orrell, Richard W, Malaspina, Andrea, Sidle, Katie C, Fratta, Pietro, Harms, Matthew B, Baloh, Robert H, Pestronk, Alan, Weihl, Conrad C, Rogaeva, Ekaterina, Zinman, Lorne, Drory, Vivian E, Borghero, Giuseppe, Mora, Gabriele, Calvo, Andrea, Rothstein, Jeffrey D, Drepper, Carsten, Sendtner, Michael, Singleton, Andrew B, Taylor, J Paul, Cookson, Mark R, Restagno, Gabriella, Sabatelli, Mario, Bowser, Robert, Chiò, Adriano, Traynor, Bryan J
Published in Nature neuroscience (01.05.2014)
Published in Nature neuroscience (01.05.2014)
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Journal Article
Synaptic dysfunction induced by glycine‐alanine dipeptides in C9orf72‐ ALS / FTD is rescued by SV 2 replenishment
Jensen, Brigid K, Schuldi, Martin H, McAvoy, Kevin, Russell, Katelyn A, Boehringer, Ashley, Curran, Bridget M, Krishnamurthy, Karthik, Wen, Xinmei, Westergard, Thomas, Ma, Le, Haeusler, Aaron R, Edbauer, Dieter, Pasinelli, Piera, Trotti, Davide
Published in EMBO molecular medicine (08.05.2020)
Published in EMBO molecular medicine (08.05.2020)
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Journal Article
KapBeta2 is a modifier of the C9orf72-linked glycine-arginine dipeptide neurotoxicity
Cicardi, Maria Elena, Kankate, Vaishnavi, Sriramoji, Sindhu, Krishnamurthy, Karthik, Shashirekha Shamamandrimarkandaiah, Verdone-Morris, Brandie, Girdhar, Amandeep, Nelson, Andrew T, Rivas, Linda B, Boehringer, Ashley, Haeusler, Aaron, Pasinelli, Piera, Guo, Lin, Trotti, Davide
Published in bioRxiv (03.10.2022)
Published in bioRxiv (03.10.2022)
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