CaMKII binds both substrates and activators at the active site von Özden, Can, Sloutsky, Roman, Mitsugi, Tomohiro, Santos, Nicholas, Agnello, Emily, Gaubitz, Christl, Foster, Joshua, Lapinskas, Emily, Esposito, Edward A., Saneyoshi, Takeo, Kelch, Brian A., Garman, Scott C., Hayashi, Yasunori, Stratton, Margaret M.

Volltext

Human acid sphingomyelinase structures provide insight to molecular basis of Niemann–Pick disease von Zhou, Yan-Feng, Metcalf, Matthew C., Garman, Scott C., Edmunds, Tim, Qiu, Huawei, Wei, Ronnie R.

Volltext

The glycan code of the endoplasmic reticulum: asparagine-linked carbohydrates as protein maturation and quality-control tags von Hebert, Daniel N., Garman, Scott C., Molinari, Maurizio

Volltext

Pharmacological chaperones for human α-N-acetylgalactosaminidase von Clark, Nathaniel E, Metcalf, Matthew C, Best, Daniel, Fleet, George W. J, Garman, Scott C

Volltext

Mutant alpha-galactosidase A enzymes identified in Fabry disease patients with residual enzyme activity: biochemical characterization and restoration of normal intracellular proces... von Ishii, Satoshi, Chang, Hui-Hwa, Kawasaki, Kunito, Yasuda, Kayo, Wu, Hui-Li, Garman, Scott C, Fan, Jian-Qiang

Volltext

Adaptor-Dependent Degradation of a Cell-Cycle Regulator Uses a Unique Substrate Architecture von Rood, Keith L., Clark, Nathaniel E., Stoddard, Patrick R., Garman, Scott C., Chien, Peter

Volltext

Pediatric Fabry Disease von Ries, Markus, Gupta, Surya, Moore, David F, Sachdev, Vandana, Quirk, Jane M, Murray, Gary J, Rosing, Douglas R, Robinson, Chevalia, Schaefer, Ellen, Gal, Andreas, Dambrosia, James M, Garman, Scott C, Brady, Roscoe O, Schiffmann, Raphael

Volltext

The Structure of Human GALNS Reveals the Molecular Basis for Mucopolysaccharidosis IV A von Rivera-Colón, Yadilette, Schutsky, Emily K., Kita, Adriana Z., Garman, Scott C.

Volltext

Proteolytic Activation of Human Cathepsin A von Kolli, Nilima, Garman, Scott C.

Volltext

Ca2+/CaM dependent protein kinase II (CaMKII)α and CaMKIIβ hub domains adopt distinct oligomeric states and stabilities von Özden, Can, MacManus, Sara, Adafia, Ruth, Samkutty, Alfred, Torres‐Ocampo, Ana P., Garman, Scott C., Stratton, Margaret M.

Volltext

The Molecular Defect Leading to Fabry Disease: Structure of Human α-Galactosidase von Garman, Scott C., Garboczi, David N.

Volltext

Unlocking a Caged Lysosomal Protein from a Polymeric Nanogel with a pH Trigger von Molla, Mijanur Rahaman, Marcinko, Tyler, Prasad, Priyaa, Deming, Derrick, Garman, Scott C, Thayumanavan, S

Volltext

Characterization of CaMKIIα holoenzyme stability von Torres‐Ocampo, Ana P., Özden, Can, Hommer, Alexandra, Gardella, Anne, Lapinskas, Emily, Samkutty, Alfred, Esposito, Edward, Garman, Scott C, Stratton, Margaret M

Volltext

Structure-function relationships in α-galactosidase A von Garman, Scott C

Volltext

The 1.9 Å Structure of Human α- N-Acetylgalactosaminidase: The Molecular Basis of Schindler and Kanzaki Diseases von Clark, Nathaniel E., Garman, Scott C.

Volltext

Catalytic mechanism of human alpha-galactosidase von Guce, Abigail I, Clark, Nathaniel E, Salgado, Eric N, Ivanen, Dina R, Kulminskaya, Anna A, Brumer, 3rd, Harry, Garman, Scott C

Volltext

The alpha-galactosidase A p.Arg118Cys variant does not cause a Fabry disease phenotype: Data from individual patients and family studies von Ferreira, Susana, Ortiz, Alberto, Germain, Dominique P., Viana-Baptista, Miguel, Caldeira-Gomes, António, Camprecios, Marta, Fenollar-Cortés, Maria, Gallegos-Villalobos, Ángel, Garcia, Diego, García-Robles, José Antonio, Egido, Jesús, Gutiérrez-Rivas, Eduardo, Herrero, José Antonio, Mas, Sebastián, Oancea, Raluca, Péres, Paloma, Salazar-Martín, Luis Manuel, Solera-Garcia, Jesús, Alves, Helena, Garman, Scott C., Oliveira, João Paulo

Volltext

Ligand-promoted protein folding by biased kinetic partitioning von Hingorani, Karan S, Metcalf, Matthew C, Deming, Derrick T, Garman, Scott C, Powers, Evan T, Gierasch, Lila M

Volltext

Phenotypic characteristics of the p.Asn215Ser (p.N215S) GLA mutation in male and female patients with Fabry disease: A multicenter Fabry Registry study von Germain, Dominique P., Brand, Eva, Burlina, Alessandro, Cecchi, Franco, Garman, Scott C., Kempf, Judy, Laney, Dawn A., Linhart, Aleš, Maródi, László, Nicholls, Kathy, Ortiz, Alberto, Pieruzzi, Federico, Shankar, Suma P., Waldek, Stephen, Wanner, Christoph, Jovanovic, Ana

Volltext

Electrostatic origin of in vitro aggregation of human γ-crystallin von Mohr, Benjamin G, Dobson, Cassidy M, Garman, Scott C, Muthukumar, Murugappan

Volltext