| human | Q5 |
| P496 | ORCID iD | 0000-0003-0758-9500 |
| P4012 | Semantic Scholar author ID | 5407970 |
| P69 | educated at | Emory University | Q621043 |
| P108 | employer | Emory University | Q621043 |
| P735 | given name | Stephanie | Q1291472 |
| Stephanie | Q1291472 | ||
| P106 | occupation | researcher | Q1650915 |
| Q30541946 | Chemical-genetic disruption of clathrin function spares adaptor complex 3-dependent endosome vesicle biogenesis. |
| Q37692058 | Dysbindin Deficiency Modifies the Expression of GABA Neuron and Ion Permeation Transcripts in the Developing Hippocampus. |
| Q112312530 | FMRP attenuates activity dependent modifications in the mitochondrial proteome |
| Q102151712 | Golgi-Dependent Copper Homeostasis Sustains Synaptic Development and Mitochondrial Content |
| Q42280237 | Hermansky-Pudlak syndrome protein complexes associate with phosphatidylinositol 4-kinase type II alpha in neuronal and non-neuronal cells. |
| Q47131018 | Identification of the Interactome of a Palmitoylated Membrane Protein, Phosphatidylinositol 4-Kinase Type II Alpha. |
| Q34079255 | Isolation of labile multi-protein complexes by in vivo controlled cellular cross-linking and immuno-magnetic affinity chromatography |
| Q35214573 | Metazoan cell biology of the HOPS tethering complex |
| Q112291577 | Mitochondrial Proteostasis Requires Genes Encoded in a Neurodevelopmental Syndrome Locus |
| Q28088624 | Molecular basis of neurodegeneration and neurodevelopmental defects in Menkes disease |
| Q33619538 | Mutations in the BLOC-1 subunits dysbindin and muted generate divergent and dosage-dependent phenotypes. |
| Q36065482 | Neuronal copper homeostasis susceptibility by genetic defects in dysbindin, a schizophrenia susceptibility factor. |
| Q48514121 | Rare Disease Mechanisms Identified by Genealogical Proteomics of Copper Homeostasis Mutant Pedigrees |
| Q92501236 | Ratiometric two-photon microscopy reveals attomolar copper buffering in normal and Menkes mutant cells |
| Q24310765 | SPE-39 family proteins interact with the HOPS complex and function in lysosomal delivery |
| Q92127596 | Systems Analysis of the 22q11.2 Microdeletion Syndrome Converges on a Mitochondrial Interactome Necessary for Synapse Function and Behavior |
| Q41145637 | The Endosome Localized Arf-GAP AGAP1 Modulates Dendritic Spine Morphology Downstream of the Neurodevelopmental Disorder Factor Dysbindin |
| Q35598755 | The N-ethylmaleimide-sensitive factor and dysbindin interact to modulate synaptic plasticity. |
| Q37490360 | 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 |
| Q33591202 | The interactome of the copper transporter ATP7A belongs to a network of neurodevelopmental and neurodegeneration factors. |
| Q92718919 | Trafficking mechanisms of P-type ATPase copper transporters |
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