Organization and Maintenance of Molecular Domains in Myelinated Axons

von Buttermore, Elizabeth D., Thaxton, Courtney L., Bhat, Manzoor A.
Veröffentlicht 2013

Localization of the paranodal protein Caspr in the mammalian retina

von O’Brien, Brendan J., Hirano, Arlene A., Buttermore, Elizabeth D., Bhat, Manzoor A., Peles, Elior
Veröffentlicht 2010

The Cytoskeletal Adaptor Protein Band 4.1B Is Required for the Maintenance of Paranodal Axoglial Septate Junctions in Myelinated Axons

von Buttermore, Elizabeth D., Dupree, Jeffrey L., Cheng, JrGang, An, Xiuli, Tessarollo, Lino, Bhat, Manzoor A.
Veröffentlicht 2011

Pinceau Organization in the Cerebellum Requires Distinct Functions of Neurofascin in Purkinje and Basket Neurons during Postnatal Development

von Buttermore, Elizabeth D., Piochon, Claire, Wallace, Michael L., Philpot, Benjamin D., Hansel, Christian, Bhat, Manzoor A.
Veröffentlicht 2012

The Septate Junction Protein Caspr Is Required for Structural Support and Retention of KCNQ4 at Calyceal Synapses of Vestibular Hair Cells

von Sousa, Aurea D., Andrade, Leonardo R., Salles, Felipe T., Pillai, Anilkumar M., Buttermore, Elizabeth D., Bhat, Manzoor A., Kachar, Bechara
Veröffentlicht 2009

Biallelic Mutations in TSC2 Lead to Abnormalities Associated with Cortical Tubers in Human iPSC-Derived Neurons

von Winden, Kellen D., Sundberg, Maria, Yang, Cindy, Wafa, Syed M.A., Dwyer, Sean, Chen, Pin-Fang, Buttermore, Elizabeth D., Sahin, Mustafa
Veröffentlicht in J Neurosci (2019)

Generation and characterization of six human induced pluripotent stem cell lines (iPSC) from three families with AP4B1-associated hereditary spastic paraplegia (SPG47)

von Teinert, Julian, Behne, Robert, D’Amore, Angelica, Wimmer, Miriam, Dwyer, Sean, Chen, Teresa, Buttermore, Elizabeth D., Chen, Ivy Pin-Fang, Sahin, Mustafa, Ebrahimi-Fakhari, Darius
Veröffentlicht in Stem Cell Res (2019)

Modeling pain in vitro using nociceptor neurons reprogrammed from fibroblasts

von Wainger, Brian J., Buttermore, Elizabeth D., Oliveira, Julia T., Mellin, Cassidy, Lee, Seungkyu, Saber, Wardiya Afshar, Wang, Amy, Ichida, Justin K., Chiu, Isaac M., Barrett, Lee, Huebner, Eric A., Bilgin, Canan, Tsujimoto, Naomi, Brenneis, Christian, Kapur, Kush, Rubin, Lee L., Eggan, Kevin, Woolf, Clifford J.
Veröffentlicht in Nat Neurosci (2014)

Underrepresentation of Phenotypic Variability of 16p13.11 Microduplication Syndrome Assessed With an Online Self-Phenotyping Tool (Phenotypr): Cohort Study

von Li, Jianqiao, Hojlo, Margaret A, Chennuri, Sampath, Gujral, Nitin, Paterson, Heather L, Shefchek, Kent A, Genetti, Casie A, Cohn, Emily L, Sewalk, Kara C, Garvey, Emily A, Buttermore, Elizabeth D, Anderson, Nickesha C, Beggs, Alan H, Agrawal, Pankaj B, Brownstein, John S, Haendel, Melissa A, Holm, Ingrid A, Gonzalez-Heydrich, Joseph, Brownstein, Catherine A
Veröffentlicht in J Med Internet Res (2021)

Adaptor protein complex 4 deficiency: a paradigm of childhood-onset hereditary spastic paraplegia caused by defective protein trafficking

von Behne, Robert, Teinert, Julian, Wimmer, Miriam, D’Amore, Angelica, Davies, Alexandra K, Scarrott, Joseph M, Eberhardt, Kathrin, Brechmann, Barbara, Chen, Ivy Pin-Fang, Buttermore, Elizabeth D, Barrett, Lee, Dwyer, Sean, Chen, Teresa, Hirst, Jennifer, Wiesener, Antje, Segal, Devorah, Martinuzzi, Andrea, Duarte, Sofia T, Bennett, James T, Bourinaris, Thomas, Houlden, Henry, Roubertie, Agathe, Santorelli, Filippo M, Robinson, Margaret, Azzouz, Mimoun, Lipton, Jonathan O, Borner, Georg H H, Sahin, Mustafa, Ebrahimi-Fakhari, Darius
Veröffentlicht in Hum Mol Genet (2020)