Structure–function relationships in α-galactosidase A

بواسطة GARMAN, SCOTT C.
منشور في 2007

Proteolytic Activation of Human Cathepsin A

بواسطة Kolli, Nilima, Garman, Scott C.
منشور في 2014

The 1.9 Å structure of human α-N-acetylgalactosaminidase: The molecular basis of Schindler and Kanzaki diseases

بواسطة Clark, Nathaniel E., Garman, Scott C.
منشور في 2009

Electrostatic origin of in vitro aggregation of human γ-crystallin

بواسطة Mohr, Benjamin G., Dobson, Cassidy M., Garman, Scott C., Muthukumar, Murugappan
منشور في 2013

The molecular basis of pharmacological chaperoning in human α-galactosidase

بواسطة Guce, Abigail I., Clark, Nathaniel E., Rogich, Jerome J., Garman, Scott C.
منشور في 2011

The structure of human GALNS reveals the molecular basis for mucopolysaccharidosis IV A

بواسطة Rivera-Colón, Yadilette, Schutsky, Emily K., Kita, Adriana Z., Garman, Scott C.
منشور في 2012

Unlocking a Caged Lysosomal Protein from a Polymeric Nanogel with a pH Trigger

بواسطة Molla, Mijanur Rahaman, Marcinko, Tyler, Prasad, Priyaa, Deming, Derrick, Garman, Scott C., Thayumanavan, S.
الحاوية / القاعدة Biomacromolecules (2014)

Adaptor-Dependent Degradation of a Cell-Cycle Regulator Uses a Unique Substrate Architecture

بواسطة Rood, Keith L., Clark, Nathaniel E., Stoddard, Patrick R., Garman, Scott C., Chien, Peter
منشور في 2012

Interconversion of the Specificities of Human Lysosomal Enzymes Associated with Fabry and Schindler Diseases

بواسطة Tomasic, Ivan B., Metcalf, Matthew C., Guce, Abigail I., Clark, Nathaniel E., Garman, Scott C.
منشور في 2010

Pharmacological chaperones for human α-N-acetylgalactosaminidase

بواسطة Clark, Nathaniel E., Metcalf, Matthew C., Best, Daniel, Fleet, George W. J., Garman, Scott C.
منشور في 2012

Ligand-Promoted Protein Folding by Biased Kinetic Partitioning

بواسطة Hingorani, Karan S., Metcalf, Matthew C., Deming, Derrick T., Garman, Scott C., Powers, Evan T., Gierasch, Lila M.
الحاوية / القاعدة Nat Chem Biol (2017)

The 1.51-Å structure of the poxvirus L1 protein, a target of potent neutralizing antibodies

بواسطة Su, Hua-Poo, Garman, Scott C., Allison, Timothy J., Fogg, Christiana, Moss, Bernard, Garboczi, David N.
منشور في 2005

Human acid sphingomyelinase structures provide insight to molecular basis of Niemann–Pick disease

بواسطة Zhou, Yan-Feng, Metcalf, Matthew C., Garman, Scott C., Edmunds, Tim, Qiu, Huawei, Wei, Ronnie R.
الحاوية / القاعدة Nat Commun (2016)

Mutant α-galactosidase A enzymes identified in Fabry disease patients with residual enzyme activity: biochemical characterization and restoration of normal intracellular processing...

بواسطة Ishii, Satoshi, Chang, Hui-Hwa, Kawasaki, Kunito, Yasuda, Kayo, Wu, Hui-Li, Garman, Scott C., Fan, Jian-Qiang
منشور في 2007

Catalytic Mechanism of Human α-Galactosidase

بواسطة Guce, Abigail I., Clark, Nathaniel E., Salgado, Eric N., Ivanen, Dina R., Kulminskaya, Anna A., Brumer, Harry, Garman, Scott C.
منشور في 2010

Nickel Superoxide Dismutase: Structural and Functional Roles of His1 and its H-bonding Network

بواسطة Ryan, Kelly C., Guce, Abigail I., Johnson, Olivia E., Brunold, Thomas C., Cabelli, Diane E., Garman, Scott C., Maroney, Michael J.
الحاوية / القاعدة Biochemistry (2015)

Characterization of CaMKIIα holoenzyme stability

بواسطة Torres‐Ocampo, Ana P., Özden, Can, Hommer, Alexandra, Gardella, Anne, Lapinskas, Emily, Samkutty, Alfred, Esposito, Edward, Garman, Scott C, Stratton, Margaret M
الحاوية / القاعدة Protein Sci (2020)

The Role of Conserved Tyrosine Residues in NiSOD Catalysis: A Case of Convergent Evolution

بواسطة Herbst, Robert W., Guce, Abigail, Bryngelson, Peter A., Higgins, Khadine A., Ryan, Kelly C., Cabelli, Diane E., Garman, Scott C., Maroney, Michael J.
منشور في 2009

Poor immunogenicity of a self/tumor antigen derives from peptide–MHC-I instability and is independent of tolerance

بواسطة Yu, Zhiya, Theoret, Marc R., Touloukian, Christopher E., Surman, Deborah R., Garman, Scott C., Feigenbaum, Lionel, Baxter, Tiffany K., Baker, Brian M., Restifo, Nicholas P.
منشور في 2004

Phenotypic characteristics of the p.Asn215Ser (p.N215S) GLA mutation in male and female patients with Fabry disease: A multicenter Fabry Registry study

بواسطة 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
الحاوية / القاعدة Mol Genet Genomic Med (2018)