A dominant negative mitofusin causes mitochondrial perinuclear clusters because of aberrant tethering

por Sloat, Stephanie R, Hoppins, Suzanne
Publicado 2022

Defective nucleotide-dependent assembly and membrane fusion in Mfn2 CMT2A variants improved by Bax

por Samanas, Nyssa B, Engelhart, Emily A, Hoppins, Suzanne
Publicado 2020

Identification of a mitofusin specificity region that confers unique activities to Mfn1 and Mfn2

por Sloat, S. R., Whitley, B. N., Engelhart, E. A., Hoppins, S.
Publicado 2019

Mitochondrial outer and inner membrane fusion requires a modified carrier protein

por Hoppins, Suzanne, Horner, Jennifer, Song, Cheng, McCaffery, J. Michael, Nunnari, Jodi
Publicado 2009

Coassembly of Mgm1 isoforms requires cardiolipin and mediates mitochondrial inner membrane fusion

por DeVay, Rachel M., Dominguez-Ramirez, Lenin, Lackner, Laura L., Hoppins, Suzanne, Stahlberg, Henning, Nunnari, Jodi
Publicado 2009

A mitochondrial-focused genetic interaction map reveals a scaffold-like complex required for inner membrane organization in mitochondria

por Hoppins, Suzanne, Collins, Sean R., Cassidy-Stone, Ann, Hummel, Eric, DeVay, Rachel M., Lackner, Laura L., Westermann, Benedikt, Schuldiner, Maya, Weissman, Jonathan S., Nunnari, Jodi
Publicado 2011

8-Oxoguanine Affects DNA Backbone Conformation in the EcoRI Recognition Site and Inhibits Its Cleavage by the Enzyme

por Hoppins, Joanna J., Gruber, David R., Miears, Heather L., Kiryutin, Alexey S., Kasymov, Rustem D., Petrova, Darya V., Endutkin, Anton V., Popov, Alexander V., Yurkovskaya, Alexandra V., Fedechkin, Stanislav O., Brockerman, Jacob A., Zharkov, Dmitry O., Smirnov, Serge L.
Publicado 2016

Uniform nomenclature for the mitochondrial contact site and cristae organizing system

por Pfanner, Nikolaus, van der Laan, Martin, Amati, Paolo, Capaldi, Roderick A., Caudy, Amy A., Chacinska, Agnieszka, Darshi, Manjula, Deckers, Markus, Hoppins, Suzanne, Icho, Tateo, Jakobs, Stefan, Ji, Jianguo, Kozjak-Pavlovic, Vera, Meisinger, Chris, Odgren, Paul R., Park, Sang Ki, Rehling, Peter, Reichert, Andreas S., Sheikh, M. Saeed, Taylor, Susan S., Tsuchida, Nobuo, van der Bliek, Alexander M., van der Klei, Ida J., Weissman, Jonathan S., Westermann, Benedikt, Zha, Jiping, Neupert, Walter, Nunnari, Jodi
Publicado 2014

Full-length Isoform Sequencing for Resolving the Molecular Basis of Charcot-Marie-Tooth 2A

por Stergachis, Andrew B., Blue, Elizabeth E., Gillentine, Madelyn A., Wang, Lee-Kai, Schwarze, Ulrike, Cortés, Adriana Sedeño, Ranchalis, Jane, Allworth, Aimee, Bland, Austin E., Chanprasert, Sirisak, Chen, Jingheng, Doherty, Daniel, Folta, Andrew B., Glass, Ian, Horike-Pyne, Martha, Huang, Alden Y., Khan, Alyna T., Leppig, Kathleen A., Miller, Danny E., Mirzaa, Ghayda, Parhin, Azma, Raskind, Wendy H., Rosenthal, Elisabeth A., Sheppeard, Sam, Strohbehn, Samuel, Sybert, Virginia P., Tran, Thao T., Wener, Mark H., Byers, Peter H. H., Nelson, Stanley F., Bamshad, Michael J., Dipple, Katrina M., Jarvik, Gail P., Hoppins, Suzanne, Hisama, Fuki M.
Publicado 2023

Full-length isoform sequencing for resolving the molecular basis of Charcot-Marie-Tooth 2A

por Stergachis, Andrew B., Blue, Elizabeth E., Gillentine, Madelyn A, Wang, Lee-kai, Schwarze, Ulrike, Cortés, Adriana Sedeño, Ranchalis, Jane, Allworth, Aimee, Bland, Austin E., Chanprasert, Sirisak, Chen, Jingheng, Doherty, Daniel, Folta, Andrew B., Glass, Ian, Horike-Pyne, Martha, Huang, Alden Y., Khan, Alyna T., Leppig, Kathleen A., Miller, Danny E., Mirzaa, Ghayda, Parhin, Azma, Raskind, Wendy, Rosenthal, Elisabeth A., Sheppeard, Sam, Strohbehn, Samuel, Sybert, Virginia P., Tran, Thao T., Wener, Mark, Byers, Peter H., Nelson, Stanley F., Bamshad, Michael J., Dipple, Katrina M., Jarvik, Gail P., Hoppins, Suzanne, Hisama, Fuki M.
Publicado 2023