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Stanislav S. Zakharenko

Affiliations: 
St. Jude Children's Research Hospital, San Francisco, CA, United States 
Area:
Synaptic plasticity
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"Stanislav Zakharenko"
Mean distance: 14.13 (cluster 6)
 		SNBCP
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Parents

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Steven A. Siegelbaum post-doc 2000-2005 Columbia

Children

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Yanbo Jiang post-doc
Prakash Devaraju post-doc 2011-

Collaborators

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Eric R. Kandel collaborator 2000-2005 Columbia
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Publications

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Heckmann BL, Teubner BJW, Tummers B, et al. (2020) LC3-Associated Endocytosis Facilitates β-Amyloid Clearance and Mitigates Neurodegeneration in Murine Alzheimer's Disease. Cell. 183: 1733-1734
Heckmann BL, Teubner BJW, Boada-Romero E, et al. (2020) Noncanonical function of an autophagy protein prevents spontaneous Alzheimer's disease. Science Advances. 6: eabb9036
Eom TY, Han SB, Kim J, et al. (2020) Schizophrenia-related microdeletion causes defective ciliary motility and brain ventricle enlargement via microRNA-dependent mechanisms in mice. Nature Communications. 11: 912
Heckmann BL, Teubner BJW, Tummers B, et al. (2019) LC3-Associated Endocytosis Facilitates β-Amyloid Clearance and Mitigates Neurodegeneration in Murine Alzheimer's Disease. Cell
Blundon JA, Roy NC, Teubner BJW, et al. (2017) Restoring auditory cortex plasticity in adult mice by restricting thalamic adenosine signaling. Science (New York, N.Y.). 356: 1352-1356
Eom TY, Bayazitov IT, Anderson K, et al. (2017) Schizophrenia-Related Microdeletion Impairs Emotional Memory through MicroRNA-Dependent Disruption of Thalamic Inputs to the Amygdala. Cell Reports. 19: 1532-1544
Devaraju P, Zakharenko SS. (2017) Mitochondria in complex psychiatric disorders: Lessons from mouse models of 22q11.2 deletion syndrome: Hemizygous deletion of several mitochondrial genes in the 22q11.2 genomic region can lead to symptoms associated with neuropsychiatric disease. Bioessays : News and Reviews in Molecular, Cellular and Developmental Biology
Chun S, Du F, Westmoreland JJ, et al. (2016) Thalamic miR-338-3p mediates auditory thalamocortical disruption and its late onset in models of 22q11.2 microdeletion. Nature Medicine
Diouf B, Devaraju P, Janke LJ, et al. (2016) Msh2 deficiency leads to dysmyelination of the corpus callosum, impaired locomotion, and altered sensory function in mice. Scientific Reports. 6: 30757
Devaraju P, Yu J, Eddins D, et al. (2016) Haploinsufficiency of the 22q11.2 microdeletion gene Mrpl40 disrupts short-term synaptic plasticity and working memory through dysregulation of mitochondrial calcium. Molecular Psychiatry
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