Richard A Steet (Richard Steet)

ORCID

Publication Activity (10 Years)

Years Active: 2019-2023
Publications (10 Years): 10

Top Venues

JIMD reports

Human molecular genetics

Molecular genetics & genomic medicine

eLife

University of Georgia

University of Colorado Boulder (PHD)

This page only lists publications with an associated author ORCID identifier.

Affiliation History

University of Georgia Aug 1o 2006

United States

Associate Professor :: Complex Carbohydrate Researcher Center

Education History

University of Colorado Boulder

United States

PHD :: Chemistry and Biochemistry

Publications

Michelle Dookwah, Shannon K Wagner, Mayumi Ishihara, Seok-Ho Yu, Heidi Ulrichs, Michael J Kulik, Nadja Zeltner, Stephen Dalton, Kevin A Strauss, Kazuhiro Aoki, Richard A Steet, Michael Tiemeyer
Neural-specific alterations in glycosphingolipid biosynthesis and cell signaling associated with two human ganglioside GM3 synthase deficiency variants. Human molecular genetics (2023)
Maxwell B Colonna, Tonya Moss, Sneha Mokashi, Sujata Srikanth, Julie R Jones, Jackson R Foley, Cindy Skinner, Angie Lichty, Anthony Kocur, Tim Wood, Tracy Murray Stewart, Robert A Casero, Heather Flanagan-Steet, Arthur S Edison, Michael J Lyons, Richard A Steet
Functional Assessment of Homozygous ALDH18A1 Variants Reveals Alterations in Amino Acid and Antioxidant Metabolism. Human molecular genetics (2022)
Ryan C Vignogna, Mariateresa Allocca, Maria Monticelli, Joy W Norris, Richard A Steet, Ethan O Perlstein, Giuseppina Andreotti, Gregory I Lang
Evolutionary rescue of phosphomannomutase deficiency in yeast models of human disease. eLife 11 (2022)
Natasha Rudy, Kazuhiro Aoki, Amitha Ananth, Lynda Holloway, Cindy Skinner, Anna Hurst, Michael Tiemeyer, Richard A Steet
Compound heterozygous variants within two conserved sialyltransferase motifs of ST3GAL5 cause GM3 synthase deficiency. JIMD reports 64 (2) (2022)
Natasha Rudy, Kazuhiro Aoki, Amitha Ananth, Lynda Holloway, Cindy Skinner, Anna Hurst, Michael Tiemeyer, Richard A Steet
Compound heterozygous variants within two conserved sialyltransferase motifs of ST3GAL5 cause GM3 synthase deficiency. JIMD reports 64 (2) (2022)
Brianna M Naumchik, Ashish Gupta, Heather Flanagan-Steet, Richard A Steet, Sara S Cathey, Paul J Orchard, Troy C Lund
The Role of Hematopoietic Cell Transplant in the Glycoprotein Diseases. Cells 9 (6) (2020)
Jarrod W Barnes, Megan Aarnio-Peterson, Joy Norris, Mark Haskins, Heather Flanagan-Steet, Richard A Steet
Upregulation of Sortilin, a Lysosomal Sorting Receptor, Corresponds with Reduced Bioavailability of Latent TGFβ in Mucolipidosis II Cells. Biomolecules 10 (5) (2020)
Addison Neighbors, Tonya Moss, Lynda Holloway, Seok-Ho Yu, Fran Annese, Steve Skinner, Russell Saneto, Richard A Steet
Functional analysis of a novel mutation in the TIMM8A gene that causes deafness-dystonia-optic neuronopathy syndrome. Molecular genetics & genomic medicine 8 (3) (2020)
Seok-Ho Yu, Laura Pollard, Tim Wood, Heather Flanagan-Steet, Richard A Steet
A Biochemical Platform to Define the Relative Specific Activity of IDUA Variants Identified by Newborn Screening. International journal of neonatal screening 6 (4) (2020)
Elsenoor Klaver, Peng Zhao, Melanie May, Heather Flanagan-Steet, Hudson H Freeze, Reid Gilmore, Lance Wells, Joseph Contessa, Richard A Steet
Selective inhibition of N-linked glycosylation impairs receptor tyrosine kinase processing. Disease models & mechanisms 12 (6) (2019)

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Publication Activity (10 Years)

Top Topics

Top Venues

Richard A Steet (Richard Steet)