Stephanie A. Zlatic, Ph.D.
Affiliations: | Cell Biology | Emory University, Atlanta, GA |
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"Stephanie Zlatic"Mean distance: 17.88 (cluster 32) | S | N | B | C | P |
Parents
Sign in to add mentor| Victor Faundez | grad student | 2006-2011 | Emory | |
| (Targeting of The Lysosomal Tether, The HOPS Complex, By Clathrin-Dependent Mechanisms.) | ||||
| Victor Faundez | post-doc | 2011- | Emory | |
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Publications
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| Hartwig C, Méndez GM, Bhattacharjee S, et al. (2020) Golgi-Dependent Copper Homeostasis Sustains Synaptic Development and Mitochondrial Content. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience |
| Tower-Gilchrist C, Zlatic SA, Yu D, et al. (2019) Adaptor protein-3 complex is required for Vangl2 trafficking and planar cell polarity of the inner ear. Molecular Biology of the Cell. mbcE16080592 |
| Morgan MT, Bourassa D, Harankhedkar S, et al. (2019) Ratiometric two-photon microscopy reveals attomolar copper buffering in normal and Menkes mutant cells. Proceedings of the National Academy of Sciences of the United States of America |
| Hartwig C, Zlatic SA, Wallin M, et al. (2019) Trafficking mechanisms of P-type ATPase copper transporters. Current Opinion in Cell Biology. 59: 24-33 |
| Gokhale A, Hartwig C, Freeman AAH, et al. (2019) Systems Analysis of the 22q11.2 Microdeletion Syndrome Converges on a Mitochondrial Interactome Necessary for Synapse Function and Behavior. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience |
| Zlatic SA, Vrailas-Mortimer A, Gokhale A, et al. (2018) Rare Disease Mechanisms Identified by Genealogical Proteomics of Copper Homeostasis Mutant Pedigrees. Cell Systems |
| Comstra HS, McArthy J, Rudin-Rush S, et al. (2017) The interactome of the copper transporter ATP7A belongs to a network of neurodevelopmental and neurodegeneration factors. Elife. 6 |
| Larimore J, Zlatic SA, Arnold M, et al. (2017) Dysbindin Deficiency Modifies the Expression of GABA Neuron and Ion Permeation Transcripts in the Developing Hippocampus. Frontiers in Genetics. 8: 28 |
| Gokhale A, Hartwig C, Freeman AH, et al. (2016) The Proteome of BLOC-1 Genetic Defects Identifies the Arp2/3 Actin Polymerization Complex to Function Downstream of the Schizophrenia Susceptibility Factor Dysbindin at the Synapse. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 36: 12393-12411 |
| Arnold M, Cross R, Singleton KS, et al. (2016) The Endosome Localized Arf-GAP AGAP1 Modulates Dendritic Spine Morphology Downstream of the Neurodevelopmental Disorder Factor Dysbindin. Frontiers in Cellular Neuroscience. 10: 218 |