Characterization of gene regulation and protein interaction networks for Matrin 3 encoding mutations linked to amyotrophic lateral sclerosis and myopathy by Iradi, M. Carolina Gallego, Triplett, Judy C., Thomas, James D., Davila, Rachel, Crown, Anthony M., Brown, Hilda, Lewis, Jada, Swanson, Maurice S., Xu, Guilian, Rodriguez-Lebron, Edgardo, Borchelt, David R.

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N-terminal sequences in matrin 3 mediate phase separation into droplet-like structures that recruit TDP43 variants lacking RNA binding elements by Gallego-Iradi, M. Carolina, Strunk, Haley, Crown, Anthony M., Davila, Rachel, Brown, Hilda, Rodriguez-Lebron, Edgardo, Borchelt, David R.

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Heterogeneity of Matrin 3 in the developing and aging murine central nervous system by Rayaprolu, Sruti, D'Alton, Simon, Crosby, Keith, Moloney, Christina, Howard, John, Duffy, Colin, Cabrera, Mariela, Siemienski, Zoe, Hernandez, Abigail R., Gallego-Iradi, Carolina, Borchelt, David R., Lewis, Jada

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Subcellular Localization of Matrin 3 Containing Mutations Associated with ALS and Distal Myopathy by Gallego-Iradi, M Carolina, Clare, Alexis M, Brown, Hilda H, Janus, Christopher, Lewis, Jada, Borchelt, David R

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KCNC3R420H , a K+ channel mutation causative in spinocerebellar ataxia 13 displays aberrant intracellular trafficking by Gallego-Iradi, Carolina, Bickford, Justin S, Khare, Swati, Hall, Alexis, Nick, Jerelyn A, Salmasinia, Donya, Wawrowsky, Kolja, Bannykh, Serguei, Huynh, Duong P, Rincon-Limas, Diego E, Pulst, Stefan M, Nick, Harry S, Fernandez-Funez, Pedro, Waters, Michael F

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KCNC3(R420H), a K(+) channel mutation causative in spinocerebellar ataxia 13 displays aberrant intracellular trafficking by Gallego-Iradi, Carolina, Bickford, Justin S, Khare, Swati, Hall, Alexis, Nick, Jerelyn A, Salmasinia, Donya, Wawrowsky, Kolja, Bannykh, Serguei, Huynh, Duong P, Rincon-Limas, Diego E, Pulst, Stefan M, Nick, Harry S, Fernandez-Funez, Pedro, Waters, Michael F

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