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Avanti Gokhale, Ph.D. - Publications

Affiliations: 
Cell Biology Emory University, Atlanta, GA 
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28 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
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  0.794
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  0.785
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  0.793
2022 Lane A, Gokhale A, Werner E, Roberts A, Freeman A, Roberts B, Faundez V. Sulfur- and phosphorus-standardized metal quantification of biological specimens using inductively coupled plasma mass spectrometry. Star Protocols. 3: 101334. PMID 35496782 DOI: 10.1016/j.xpro.2022.101334  0.736
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  0.774
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  0.802
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  0.815
2020 Valdez-Sinon AN, Gokhale A, Faundez V, Bassell GJ. Protocol for Immuno-Enrichment of FLAG-Tagged Protein Complexes. Star Protocols. 1: 100083. PMID 33111116 DOI: 10.1016/j.xpro.2020.100083  0.567
2020 Valdez-Sinon AN, Lai A, Shi L, Lancaster CL, Gokhale A, Faundez V, Bassell GJ. Cdh1-APC Regulates Protein Synthesis and Stress Granules in Neurons through an FMRP-Dependent Mechanism. Iscience. 23: 101132. PMID 32434143 DOI: 10.1016/J.Isci.2020.101132  0.619
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  0.817
2018 Hunter EL, Lechtreck K, Fu G, Hwang J, Lin H, Gokhale A, Alford LM, Lewis B, Yamamoto R, Kamiya R, Yang F, Nicastro D, Dutcher SK, Wirschell M, Sale WS. The IDA3 adapter, required for IFT transport of I1 dynein, is regulated by ciliary length. Molecular Biology of the Cell. PMID 29467251 DOI: 10.1091/Mbc.E17-12-0729  0.318
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  0.809
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  0.79
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  0.761
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  0.832
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  0.762
2015 Delevoye C, Heiligenstein X, Ripoll L, Gilles-Marsens F, Dennis MK, Linares RA, Derman L, Gokhale A, Morel E, Faundez V, Marks MS, Raposo G. BLOC-1 Brings Together the Actin and Microtubule Cytoskeletons to Generate Recycling Endosomes. Current Biology : Cb. PMID 26725201 DOI: 10.1016/J.Cub.2015.11.020  0.667
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  0.787
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  0.779
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  0.777
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  0.769
2013 Mullin AP, Gokhale A, Moreno-De-Luca A, Sanyal S, Waddington JL, Faundez V. Neurodevelopmental disorders: mechanisms and boundary definitions from genomes, interactomes and proteomes. Translational Psychiatry. 3: e329. PMID 24301647 DOI: 10.1038/Tp.2013.108  0.786
2013 Ryder PV, Vistein R, Gokhale A, Seaman MN, Puthenveedu MA, Faundez V. The WASH complex, an endosomal Arp2/3 activator, interacts with the Hermansky-Pudlak syndrome complex BLOC-1 and its cargo phosphatidylinositol-4-kinase type IIα. Molecular Biology of the Cell. 24: 2269-84. PMID 23676666 DOI: 10.1091/Mbc.E13-02-0088  0.797
2012 Gokhale A, Perez-Cornejo P, Duran C, Hartzell HC, Faundez V. A comprehensive strategy to identify stoichiometric membrane protein interactomes. Cellular Logistics. 2: 189-196. PMID 23676845 DOI: 10.4161/Cl.22717  0.615
2012 Perez-Cornejo P, Gokhale A, Duran C, Cui Y, Xiao Q, Hartzell HC, Faundez V. Anoctamin 1 (Tmem16A) Ca2+-activated chloride channel stoichiometrically interacts with an ezrin-radixin-moesin network. Proceedings of the National Academy of Sciences of the United States of America. 109: 10376-81. PMID 22685202 DOI: 10.1073/Pnas.1200174109  0.615
2012 Gokhale A, Larimore J, Werner E, So L, Moreno-De-Luca A, Lese-Martin C, Lupashin VV, Smith Y, Faundez V. Quantitative proteomic and genetic analyses of the schizophrenia susceptibility factor dysbindin identify novel roles of the biogenesis of lysosome-related organelles complex 1. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 32: 3697-711. PMID 22423091 DOI: 10.1523/Jneurosci.5640-11.2012  0.798
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  0.742
2011 Mullin AP, Gokhale A, Larimore J, Faundez V. Cell biology of the BLOC-1 complex subunit dysbindin, a schizophrenia susceptibility gene. Molecular Neurobiology. 44: 53-64. PMID 21520000 DOI: 10.1007/S12035-011-8183-3  0.795
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