Practically Useful: What the Rosetta Protein Modeling Suite Can Do for You

por Kaufmann, Kristian W., Lemmon, Gordon H., DeLuca, Samuel L., Sheehan, Jonathan H., Meiler, Jens
Publicado 2010

Second-site suppressors of HIV-1 capsid mutations: restoration of intracellular activities without correction of intrinsic capsid stability defects

por Yang, Ruifeng, Shi, Jiong, Byeon, In-Ja L, Ahn, Jinwoo, Sheehan, Jonathan H, Meiler, Jens, Gronenborn, Angela M, Aiken, Christopher
Publicado 2012

Phenotypic Profiling in Subjects Heterozygous for 1 of 2 Rare Variants in the Hypophosphatasia Gene (ALPL)

por Tilden, Daniel R, Sheehan, Jonathan H, Newman, John H, Meiler, Jens, Capra, John A, Ramirez, Andrea, Simmons, Jill, Dahir, Kathryn
Publicado 2020

Three-dimensional spatial analysis of missense variants in RTEL1 identifies pathogenic variants in patients with Familial Interstitial Pneumonia

por Sivley, R. Michael, Sheehan, Jonathan H., Kropski, Jonathan A., Cogan, Joy, Blackwell, Timothy S., Phillips, John A., Bush, William S., Meiler, Jens, Capra, John A.
Publicado 2018

A novel, likely pathogenic variant in UBTF‐related neurodegeneration with brain atrophy is associated with a severe divergent neurodevelopmental phenotype

por Tinker, Rory J., Guess, Tiffany, Rinker, David C., Sheehan, Jonathan H., Lubarsky, Daniel, Porath, Binu, Mosera, Mackenzie, Mayo, Ping, Solem, Emily, Lee, Laura A., Sharam, Asha, Brault, Jennifer
Publicado 2022

Protocols for Molecular Modeling with Rosetta3 and RosettaScripts

por Bender, Brian J., Cisneros, Alberto, Duran, Amanda M., Finn, Jessica A., Fu, Darwin, Lokits, Alyssa D., Mueller, Benjamin K., Sangha, Amandeep K., Sauer, Marion F., Sevy, Alexander M., Sliwoski, Gregory, Sheehan, Jonathan H., DiMaio, Frank, Meiler, Jens, Moretti, Rocco
Publicado 2016

Personalized structural biology reveals the molecular mechanisms underlying heterogeneous epileptic phenotypes caused by de novo KCNC2 variants

por Mukherjee, Souhrid, Cassini, Thomas A., Hu, Ningning, Yang, Tao, Li, Bian, Shen, Wangzhen, Moth, Christopher W., Rinker, David C., Sheehan, Jonathan H., Cogan, Joy D., Newman, John H., Hamid, Rizwan, Macdonald, Robert L., Roden, Dan M., Meiler, Jens, Kuenze, Georg, Phillips, John A., Capra, John A.
Publicado 2022

IgG4‐related disease: Association with a rare gene variant expressed in cytotoxic T cells

por Newman, John H., Shaver, Aaron, Sheehan, Jonathan H., Mallal, Simon, Stone, John H., Pillai, Shiv, Bastarache, Lisa, Riebau, Derek, Allard‐Chamard, Hugues, Stone, William M., Perugino, Cory, Pilkinton, Mark, Smith, Scott A., McDonnell, Wyatt J., Capra, John A., Meiler, Jens, Cogan, Joy, Xing, Kelly, Mahajan, Vinay S., Mattoo, Hamid, Hamid, Rizwan, Phillips, John A.
Publicado 2019

Modeling Immunity with Rosetta: Methods for Antibody and Antigen Design

por Schoeder, Clara T., Schmitz, Samuel, Adolf-Bryfogle, Jared, Sevy, Alexander M., Finn, Jessica A., Sauer, Marion F., Bozhanova, Nina G., Mueller, Benjamin K., Sangha, Amandeep K., Bonet, Jaume, Sheehan, Jonathan H., Kuenze, Georg, Marlow, Brennica, Smith, Shannon T., Woods, Hope, Bender, Brian J., Martina, Cristina E., del Alamo, Diego, Kodali, Pranav, Gulsevin, Alican, Schief, William R., Correia, Bruno E., Crowe, James E., Meiler, Jens, Moretti, Rocco
Publicado 2021