| Year |
Citation |
Score |
| 2020 |
Lee FY, Larimore J, Faundez V, Dell'Angelica EC, Ghiani CA. Sex-dimorphic effects of biogenesis of lysosome-related organelles complex-1 deficiency on mouse perinatal brain development. Journal of Neuroscience Research. PMID 32436302 DOI: 10.1002/Jnr.24620 |
0.629 |
|
| 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 |
0.79 |
|
| 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 |
0.783 |
|
| 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 |
0.743 |
|
| 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 |
0.759 |
|
| 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 |
0.712 |
|
| 2013 |
Chapleau CA, Lane J, Larimore J, Li W, Pozzo-Miller L, Percy AK. Recent Progress in Rett Syndrome and MeCP2 Dysfunction: Assessment of Potential Treatment Options. Future Neurology. 8. PMID 24348096 DOI: 10.2217/Fnl.12.79 |
0.425 |
|
| 2013 |
Larimore J, Ryder PV, Kim KY, Ambrose LA, Chapleau C, Calfa G, Gross C, Bassell GJ, Pozzo-Miller L, Smith Y, Talbot K, Park IH, Faundez V. MeCP2 regulates the synaptic expression of a Dysbindin-BLOC-1 network component in mouse brain and human induced pluripotent stem cell-derived neurons. Plos One. 8: e65069. PMID 23750231 DOI: 10.1371/Journal.Pone.0065069 |
0.821 |
|
| 2012 |
Li W, Calfa G, Larimore J, Pozzo-Miller L. Activity-dependent BDNF release and TRPC signaling is impaired in hippocampal neurons of Mecp2 mutant mice. Proceedings of the National Academy of Sciences of the United States of America. 109: 17087-92. PMID 23027959 DOI: 10.1073/Pnas.1205271109 |
0.429 |
|
| 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 |
0.772 |
|
| 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 |
0.681 |
|
| 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 |
0.787 |
|
| 2009 |
Chapleau CA, Larimore JL, Theibert A, Pozzo-Miller L. Modulation of dendritic spine development and plasticity by BDNF and vesicular trafficking: fundamental roles in neurodevelopmental disorders associated with mental retardation and autism. Journal of Neurodevelopmental Disorders. 1: 185-96. PMID 19966931 DOI: 10.1007/S11689-009-9027-6 |
0.374 |
|
| 2009 |
Chapleau CA, Calfa GD, Lane MC, Albertson AJ, Larimore JL, Kudo S, Armstrong DL, Percy AK, Pozzo-Miller L. Dendritic spine pathologies in hippocampal pyramidal neurons from Rett syndrome brain and after expression of Rett-associated MECP2 mutations. Neurobiology of Disease. 35: 219-33. PMID 19442733 DOI: 10.1016/J.Nbd.2009.05.001 |
0.377 |
|
| 2009 |
Larimore JL, Chapleau CA, Kudo S, Theibert A, Percy AK, Pozzo-Miller L. Bdnf overexpression in hippocampal neurons prevents dendritic atrophy caused by Rett-associated MECP2 mutations. Neurobiology of Disease. 34: 199-211. PMID 19217433 DOI: 10.1016/J.Nbd.2008.12.011 |
0.342 |
|
| 2007 |
Moore CD, Thacker EE, Larimore J, Gaston D, Underwood A, Kearns B, Patterson SI, Jackson T, Chapleau C, Pozzo-Miller L, Theibert A. The neuronal Arf GAP centaurin alpha1 modulates dendritic differentiation. Journal of Cell Science. 120: 2683-93. PMID 17635995 DOI: 10.1242/Jcs.006346 |
0.396 |
|
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