Isolation of Labile Multi-protein Complexes by in vivo Controlled Cellular Cross-Linking and Immuno-magnetic Affinity Chromatography

Por Zlatic, Stephanie A., Ryder, Pearl V., Salazar, Gloria, Faundez, Victor
Publicado em 2010

Identification of the interactome of a palmitoylated membrane protein, phosphatidylinositol 4-kinase type II alpha

Por Gokhale, Avanti, Ryder, Pearl V., Zlatic, Stephanie A., Faundez, Victor
Publicado no Methods Mol Biol (2016)

Clathrin-dependent mechanisms modulate the subcellular distribution of class C Vps/HOPS tether subunits in polarized and nonpolarized cells

Por Zlatic, Stephanie A., Tornieri, Karine, L’Hernault, Steven W., Faundez, Victor
Publicado em 2011

Metazoan cell biology of the HOPS tethering complex

Por Zlatic, Stephanie A, Tornieri, Karine, L'Hernault, Steven W, Faundez, Victor
Publicado em 2011

Vps33b pathogenic mutations preferentially affect VIPAS39/SPE-39-positive endosomes

Por Tornieri, Karine, Zlatic, Stephanie A., Mullin, Ariana P., Werner, Erica, Harrison, Robert, L'Hernault, Steven W., Faundez, Victor
Publicado em 2013

Chemical-genetic disruption of clathrin function spares adaptor complex 3–dependent endosome vesicle biogenesis

Por Zlatic, Stephanie A., Grossniklaus, Emily J., Ryder, Pearl V., Salazar, Gloria, Mattheyses, Alexa L., Peden, Andrew A., Faundez, Victor
Publicado em 2013

Mutations in the BLOC-1 Subunits Dysbindin and Muted Generate Divergent and Dosage-dependent Phenotypes

Por Larimore, Jennifer, Zlatic, Stephanie A., Gokhale, Avanti, Tornieri, Karine, Singleton, Kaela S., Mullin, Ariana P., Tang, Junxia, Talbot, Konrad, Faundez, Victor
Publicado em 2014

Neuronal copper homeostasis susceptibility by genetic defects in dysbindin, a schizophrenia susceptibility factor

Por Gokhale, Avanti, Vrailas-Mortimer, Alysia, Larimore, Jennifer, Comstra, Heather S., Zlatic, Stephanie A., Werner, Erica, Manvich, Daniel F., Iuvone, P. Michael, Weinshenker, David, Faundez, Victor
Publicado no Hum Mol Genet (2015)

Dysbindin Deficiency Modifies the Expression of GABA Neuron and Ion Permeation Transcripts in the Developing Hippocampus

Por Larimore, Jennifer, Zlatic, Stephanie A., Arnold, Miranda, Singleton, Kaela S., Cross, Rebecca, Rudolph, Hannah, Bruegge, Martha V., Sweetman, Andrea, Garza, Cecilia, Whisnant, Eli, Faundez, Victor
Publicado no Front Genet (2017)

SPE-39 Family Proteins Interact with the HOPS Complex and Function in Lysosomal Delivery

Por Zhu, Guang-dan, Salazar, Gloria, Zlatic, Stephanie A., Fiza, Babar, Doucette, Michele M., Heilman, Craig J., Levey, Allan I., Faundez, Victor, L'Hernault, Steven W.
Publicado em 2009

The schizophrenia susceptibility factor dysbindin and its associated complex sort cargoes from cell bodies to the synapse

Por Larimore, Jennifer, Tornieri, Karine, Ryder, Pearl V., Gokhale, Avanti, Zlatic, Stephanie A., Craige, Branch, Lee, Joshua D., Talbot, Konrad, Pare, Jean-Francois, Smith, Yoland, Faundez, Victor
Publicado em 2011

The N-Ethylmaleimide-Sensitive Factor and Dysbindin Interact To Modulate Synaptic Plasticity

Por Gokhale, Avanti, Mullin, Ariana P., Zlatic, Stephanie A., Easley, Charles A., Merritt, Megan E., Raj, Nisha, Larimore, Jennifer, Gordon, David E., Peden, Andrew A., Sanyal, Subhabrata, Faundez, Victor
Publicado no J Neurosci (2015)

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

Por Gokhale, Avanti, Hartwig, Cortnie, Freeman, Amanda H., Das, Ravi, Zlatic, Stephanie A., Vistein, Rachel, Burch, Amelia, Carrot, Guillemette, Lewis, Arielle F., Nelms, Sheldon, Dickman, Dion K., Puthenveedu, Manojkumar A., Cox, Daniel N., Faundez, Victor
Publicado no J Neurosci (2016)

Rare Disease Mechanisms Identified by Genealogical Proteomics of Copper Homeostasis Mutant Pedigrees

Por Zlatic, Stephanie A., Vrailas-Mortimer, Alysia, Gokhale, Avanti, Carey, Lucas J., Scott, Elizabeth, Burch, Reid, McCall, Morgan M., Rudin-Rush, Samantha, Davis, John Bowen, Hartwig, Cortnie, Werner, Erica, Li, Lian, Petris, Michael, Faundez, Victor
Publicado no Cell Syst (2018)

The interactome of the copper transporter ATP7A belongs to a network of neurodevelopmental and neurodegeneration factors

Por Comstra, Heather S, McArthy, Jacob, Rudin-Rush, Samantha, Hartwig, Cortnie, Gokhale, Avanti, Zlatic, Stephanie A, Blackburn, Jessica B, Werner, Erica, Petris, Michael, D’Souza, Priya, Panuwet, Parinya, Barr, Dana Boyd, Lupashin, Vladimir, Vrailas-Mortimer, Alysia, Faundez, Victor
Publicado no eLife (2017)