Award

GM083144

Funder: National Institute of General Medical Sciences

Funded outputs count: 11

Funder award ID: GM083144

OpenAlex ID: G8428241663

Essential role of the conserved oligomeric Golgi complex in Toxoplasma gondii

2023 · Clem Marsilia, Mrinalini Batra, et al. · mBio · 12

A Rab33b missense mouse model for Smith-McCort dysplasia shows bone resorption defects and altered protein glycosylation

2023 · Milena Dimori, Irina D. Pokrovskaya, et al. · Frontiers in Genetics · 2

Role of GARP Vesicle Tethering Complex in Golgi Physiology

2023 · Amrita Khakurel, Vladimir V. Lupashin · International Journal of Molecular Sciences · 26

Getting Sugar Coating Right! The Role of the Golgi Trafficking Machinery in Glycosylation

2021 · Zinia D’Souza, Farhana Taher Sumya, et al. · Cells · 25

More than just sugars: Conserved oligomeric Golgi complex deficiency causes glycosylation‐independent cellular defects

2018 · Jessica B. Blackburn, Tetyana Kudlyk, et al. · Traffic · 39

The interactome of the copper transporter ATP7A belongs to a network of neurodevelopmental and neurodegeneration factors

2017 · Heather S Comstra, Jacob McArthy, et al. · eLife · 68

COG Complex Complexities: Detailed Characterization of a Complete Set of HEK293T Cells Lacking Individual COG Subunits

2016 · Jessica Bailey Blackburn, Irina Pokrovskaya, et al. · Frontiers in Cell and Developmental Biology · 72

RETRACTED ARTICLE: Sepsis-induced elevation in plasma serotonin facilitates endothelial hyperpermeability

2016 · Yicong Li, Coedy Hadden, et al. · Scientific Reports · 36

The DNA Sensor, Cyclic GMP–AMP Synthase, Is Essential for Induction of IFN-β during Chlamydia trachomatis Infection

2014 · Yugen Zhang, Laxmi Yeruva, et al. · The Journal of Immunology · 153

Quantitative Proteomic and Genetic Analyses of the Schizophrenia Susceptibility Factor Dysbindin Identify Novel Roles of the Biogenesis of Lysosome-Related Organelles Complex 1

2012 · Avanti Gokhale, Jennifer Larimore, et al. · Journal of Neuroscience · 85

Structural basis for a human glycosylation disorder caused by mutation of the COG4 gene

2009 · Brian C. Richardson, Richard D. Smith, et al. · Proceedings of the National Academy of Sciences · 63