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Biorxiv : the Preprint Server for Biology|February 6, 2026
Distinct signaling mechanisms and proteome phenotypes are elicited by compartment-specific genetic defects of copper homeostasisAlicia R Lane, Nadia Gonzalez, Avanti Gokhale, et al.
Molecular Biology of the Cell|May 13, 2026
Distinct signaling mechanisms and proteome phenotypes are elicited by compartment-specific genetic defects of copper homeostasisAlicia R Lane, Nadia Gonzalez, Avanti Gokhale, et al.
Cell Systems|February 5, 2018
Rare Disease Mechanisms Identified by Genealogical Proteomics of Copper Homeostasis Mutant PedigreesStephanie A Zlatic, Alysia Vrailas-Mortimer, Avanti Gokhale, et al.
Biorxiv : the Preprint Server for Biology|January 16, 2026
Suppressive Genetic Interactions Between Haploinsufficient Mitochondrial Genes Encoded in the 22q11.2 Microdeletion Locus Define Brain and Cardiac PhenotypesMeghan Wynne, Stephanie A Zlatic, Austin S Park, et al.
Elife|March 30, 2017
The interactome of the copper transporter ATP7A belongs to a network of neurodevelopmental and neurodegeneration factorsHeather S Comstra, Jacob McArthy, Samantha Rudin-Rush, et al.
Biorxiv : the Preprint Server for Biology|April 17, 2023
Systemic Proteome Phenotypes Reveal Defective Metabolic Flexibility in Mecp2 MutantsStephanie A Zlatic, Erica Werner, Veda Surapaneni, et al.
Human Molecular Genetics|September 15, 2023
Systemic proteome phenotypes reveal defective metabolic flexibility in Mecp2 mutantsStephanie A Zlatic, Erica Werner, Veda Surapaneni, et al.
Molecular & Cellular Proteomics : MCP|June 27, 2024
Proximity Labeling Proteomics Reveals Kv1.3 Potassium Channel Immune Interactors in MicrogliaChristine A Bowen, Hai M Nguyen, Young Lin, et al.
Biorxiv : the Preprint Server for Biology|March 3, 2025
Mitochondrially Transcribed dsRNA Mediates Manganese-induced NeuroinflammationAvanti Gokhale, Hadassah Mendez-Vazquez, Maureen M Sampson, et al.
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