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Stephanie A. Zlatic, Ph.D. - Publications

Affiliations: 
Cell Biology Emory University, Atlanta, GA 
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32 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2024 Lane AR, Scher NE, Bhattacharjee S, Zlatic SA, Roberts AM, Gokhale A, Singleton KS, Duong DM, McKenna M, Liu WL, Baiju A, Moctezuma FGR, Tran T, Patel AA, Clayton LB, et al. Adaptive protein synthesis in genetic models of copper deficiency and childhood neurodegeneration. Biorxiv : the Preprint Server For Biology. PMID 39314281 DOI: 10.1101/2024.09.09.612106  0.807
2023 Zlatic SA, Werner E, Surapaneni V, Lee CE, Gokhale A, Singleton K, Duong D, Crocker A, Gentile K, Middleton F, Dalloul JM, Liu WL, Patgiri A, Tarquinio D, Carpenter R, et al. Systemic proteome phenotypes reveal defective metabolic flexibility in Mecp2 mutants. Human Molecular Genetics. PMID 37712894 DOI: 10.1093/hmg/ddad154  0.785
2023 Wynne ME, Ogunbona O, Lane AR, Gokhale A, Zlatic SA, Xu C, Wen Z, Duong DM, Rayaprolu S, Ivanova A, Ortlund EA, Dammer EB, Seyfried NT, Roberts BR, Crocker A, et al. APOE expression and secretion are modulated by mitochondrial dysfunction. Elife. 12. PMID 37171075 DOI: 10.7554/eLife.85779  0.797
2023 Zlatic SA, Werner E, Surapaneni V, Lee CE, Gokhale A, Singleton K, Duong D, Crocker A, Gentile K, Middleton F, Patgiri A, Tarquinio D, Carpenter R, Faundez V. Systemic Metabolic and Mitochondrial Defects in Rett Syndrome Models. Biorxiv : the Preprint Server For Biology. PMID 37066332 DOI: 10.1101/2023.04.03.535431  0.782
2022 Zlatic SA, Duong D, Gadalla KKE, Murage B, Ping L, Shah R, Fink JJ, Khwaja O, Swanson LC, Sahin M, Rayaprolu S, Kumar P, Rangaraju S, Bird A, Tarquinio D, et al. Convergent cerebrospinal fluid proteomes and metabolic ontologies in humans and animal models of Rett syndrome. Iscience. 25: 104966. PMID 36060065 DOI: 10.1016/j.isci.2022.104966  0.732
2021 Wynne ME, Lane AR, Singleton KS, Zlatic SA, Gokhale A, Werner E, Duong D, Kwong JQ, Crocker AJ, Faundez V. Heterogeneous Expression of Nuclear Encoded Mitochondrial Genes Distinguishes Inhibitory and Excitatory Neurons. Eneuro. PMID 34312306 DOI: 10.1523/ENEURO.0232-21.2021  0.785
2021 Gokhale A, Lee CE, Zlatic SA, Freeman AAH, Shearing N, Hartwig C, Ogunbona O, Bassell JL, Wynne ME, Werner E, Xu C, Wen Z, Duong D, Seyfried NT, Bearden CE, et al. Mitochondrial Proteostasis Requires Genes Encoded in a Neurodevelopmental Syndrome Locus. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. PMID 34261699 DOI: 10.1523/JNEUROSCI.2197-20.2021  0.792
2021 Bülow P, Zlatic SA, Wenner PA, Bassell GJ, Faundez V. FMRP attenuates activity dependent modifications in the mitochondrial proteome. Molecular Brain. 14: 75. PMID 33931071 DOI: 10.1186/s13041-021-00783-w  0.732
2020 Hartwig C, Méndez GM, Bhattacharjee S, Vrailas-Mortimer AD, Zlatic SA, Freeman AAH, Gokhale A, Concilli M, Werner E, Sapp Savas C, Rudin-Rush S, Palmer L, Shearing N, Margewich L, McArthy J, et al. Golgi-Dependent Copper Homeostasis Sustains Synaptic Development and Mitochondrial Content. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. PMID 33208468 DOI: 10.1523/JNEUROSCI.1284-20.2020  0.812
2019 Tower-Gilchrist C, Zlatic SA, Yu D, Chang Q, Wu H, Lin X, Faundez V, Chen P. Adaptor protein-3 complex is required for Vangl2 trafficking and planar cell polarity of the inner ear. Molecular Biology of the Cell. mbcE16080592. PMID 31268833 DOI: 10.1091/Mbc.E16-08-0592  0.754
2019 Morgan MT, Bourassa D, Harankhedkar S, McCallum AM, Zlatic SA, Calvo JS, Meloni G, Faundez V, Fahrni CJ. 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. PMID 31160463 DOI: 10.1073/Pnas.1900172116  0.719
2019 Hartwig C, Zlatic SA, Wallin M, Vrailas-Mortimer A, Fahrni CJ, Faundez V. Trafficking mechanisms of P-type ATPase copper transporters. Current Opinion in Cell Biology. 59: 24-33. PMID 30928671 DOI: 10.1016/J.Ceb.2019.02.009  0.764
2019 Gokhale A, Hartwig C, Freeman AAH, Bassell JL, Zlatic SA, Sapp Savas C, Vadlamudi T, Abudulai F, Pham TT, Crocker A, Werner E, Wen Z, Repetto GM, Gogos JA, Claypool SM, et al. 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. PMID 30833507 DOI: 10.1523/Jneurosci.1983-18.2019  0.805
2018 Zlatic SA, Vrailas-Mortimer A, Gokhale A, Carey LJ, Scott E, Burch R, McCall MM, Rudin-Rush S, Davis JB, Hartwig C, Werner E, Li L, Petris M, Faundez V. Rare Disease Mechanisms Identified by Genealogical Proteomics of Copper Homeostasis Mutant Pedigrees. Cell Systems. PMID 29397366 DOI: 10.1016/J.Cels.2018.01.008  0.799
2017 Comstra HS, McArthy J, Rudin-Rush S, Hartwig C, Gokhale A, Zlatic SA, Blackburn JB, Werner E, Petris M, D'Souza P, Panuwet P, Barr DB, Lupashin V, Vrailas-Mortimer A, Faundez V. The interactome of the copper transporter ATP7A belongs to a network of neurodevelopmental and neurodegeneration factors. Elife. 6. PMID 28355134 DOI: 10.7554/Elife.24722  0.806
2017 Larimore J, Zlatic SA, Arnold M, Singleton KS, Cross R, Rudolph H, Bruegge MV, Sweetman A, Garza C, Whisnant E, Faundez V. Dysbindin Deficiency Modifies the Expression of GABA Neuron and Ion Permeation Transcripts in the Developing Hippocampus. Frontiers in Genetics. 8: 28. PMID 28344592 DOI: 10.3389/Fgene.2017.00028  0.803
2017 Comstra HS, McArthy J, Rudin-Rush S, Hartwig C, Gokhale A, Zlatic SA, Blackburn JB, Werner E, Petris M, D’Souza P, Panuwet P, Barr DB, Lupashin V, Vrailas-Mortimer A, Faundez V. Author response: The interactome of the copper transporter ATP7A belongs to a network of neurodevelopmental and neurodegeneration factors Elife. DOI: 10.7554/Elife.24722.021  0.751
2016 Gokhale A, Hartwig C, Freeman AH, Das R, Zlatic SA, Vistein R, Burch A, Carrot G, Lewis AF, Nelms S, Dickman DK, Puthenveedu MA, Cox DN, Faundez V. 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. PMID 27927957 DOI: 10.1523/Jneurosci.1321-16.2016  0.823
2016 Arnold M, Cross R, Singleton KS, Zlatic S, Chapleau C, Mullin AP, Rolle I, Moore CC, Theibert A, Pozzo-Miller L, Faundez V, Larimore J. The Endosome Localized Arf-GAP AGAP1 Modulates Dendritic Spine Morphology Downstream of the Neurodevelopmental Disorder Factor Dysbindin. Frontiers in Cellular Neuroscience. 10: 218. PMID 27713690 DOI: 10.3389/Fncel.2016.00218  0.812
2016 Gokhale A, Ryder PV, Zlatic SA, Faundez V. Identification of the Interactome of a Palmitoylated Membrane Protein, Phosphatidylinositol 4-Kinase Type II Alpha. Methods in Molecular Biology (Clifton, N.J.). 1376: 35-42. PMID 26552673 DOI: 10.1007/978-1-4939-3170-5_4  0.777
2015 Gokhale A, Vrailas-Mortimer A, Larimore J, Comstra HS, Zlatic SA, Werner E, Manvich DF, Iuvone PM, Weinshenker D, Faundez V. Neuronal copper homeostasis susceptibility by genetic defects in dysbindin, a schizophrenia susceptibility factor. Human Molecular Genetics. 24: 5512-23. PMID 26199316 DOI: 10.1093/Hmg/Ddv282  0.793
2015 Gokhale A, Mullin AP, Zlatic SA, Easley CA, Merritt ME, Raj N, Larimore J, Gordon DE, Peden AA, Sanyal S, Faundez V. The N-ethylmaleimide-sensitive factor and dysbindin interact to modulate synaptic plasticity. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 35: 7643-53. PMID 25972187 DOI: 10.1523/Jneurosci.4724-14.2015  0.795
2015 Zlatic S, Comstra HS, Gokhale A, Petris MJ, Faundez V. Molecular basis of neurodegeneration and neurodevelopmental defects in Menkes disease. Neurobiology of Disease. PMID 25583185 DOI: 10.1016/J.Nbd.2014.12.024  0.786
2014 Larimore J, Zlatic SA, Gokhale A, Tornieri K, Singleton KS, Mullin AP, Tang J, Talbot K, Faundez V. Mutations in the BLOC-1 subunits dysbindin and muted generate divergent and dosage-dependent phenotypes. The Journal of Biological Chemistry. 289: 14291-300. PMID 24713699 DOI: 10.1074/Jbc.M114.553750  0.789
2013 Tornieri K, Zlatic SA, Mullin AP, Werner E, Harrison R, L'hernault SW, Faundez V. Vps33b pathogenic mutations preferentially affect VIPAS39/SPE-39-positive endosomes. Human Molecular Genetics. 22: 5215-28. PMID 23918659 DOI: 10.1093/Hmg/Ddt378  0.783
2013 Zlatic SA, Grossniklaus EJ, Ryder PV, Salazar G, Mattheyses AL, Peden AA, Faundez V. Chemical-genetic disruption of clathrin function spares adaptor complex 3-dependent endosome vesicle biogenesis. Molecular Biology of the Cell. 24: 2378-88. PMID 23761069 DOI: 10.1091/Mbc.E12-12-0860  0.78
2011 Larimore J, Tornieri K, Ryder PV, Gokhale A, Zlatic SA, Craige B, Lee JD, Talbot K, Pare JF, Smith Y, Faundez V. The schizophrenia susceptibility factor dysbindin and its associated complex sort cargoes from cell bodies to the synapse. Molecular Biology of the Cell. 22: 4854-67. PMID 21998198 DOI: 10.1091/Mbc.E11-07-0592  0.774
2011 Zlatic SA, Tornieri K, L'hernault SW, Faundez V. Metazoan cell biology of the HOPS tethering complex. Cellular Logistics. 1: 111-117. PMID 21922076 DOI: 10.4161/Cl.1.3.17279  0.792
2011 Zlatic SA, Tornieri K, L'Hernault SW, Faundez V. Clathrin-dependent mechanisms modulate the subcellular distribution of class C Vps/HOPS tether subunits in polarized and nonpolarized cells. Molecular Biology of the Cell. 22: 1699-715. PMID 21411634 DOI: 10.1091/Mbc.E10-10-0799  0.786
2010 Zlatic SA, Ryder PV, Salazar G, Faundez V. Isolation of labile multi-protein complexes by in vivo controlled cellular cross-linking and immuno-magnetic affinity chromatography. Journal of Visualized Experiments : Jove. PMID 20216526 DOI: 10.3791/1855  0.777
2009 Zhu GD, Salazar G, Zlatic SA, Fiza B, Doucette MM, Heilman CJ, Levey AI, Faundez V, L'hernault SW. SPE-39 family proteins interact with the HOPS complex and function in lysosomal delivery. Molecular Biology of the Cell. 20: 1223-40. PMID 19109425 DOI: 10.1091/Mbc.E08-07-0728  0.805
2009 Salazar G, Zlatic S, Craige B, Peden AA, Pohl J, Faundez V. Hermansky-Pudlak syndrome protein complexes associate with phosphatidylinositol 4-kinase type II alpha in neuronal and non-neuronal cells. The Journal of Biological Chemistry. 284: 1790-802. PMID 19010779 DOI: 10.1074/Jbc.M805991200  0.817
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