Yuji Kajiwara

Affiliations: 
Icahn School of Medicine at Mount Sinai, New York, NY, United States 
Area:
alzheimer
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"Yuji Kajiwara"
Cross-listing: Neurotree

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Joseph D. Buxbaum grad student 2009 Mount Sinai School of Medicine
 (The APP-binding protein FE65 complexes with Teashirt proteins, inhibiting expression of the caspase-4, a primate-specific inflammatory caspase.)
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Publications

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Darvish H, Azcona LJ, Tafakhori A, et al. (2020) Phenotypic and genotypic characterization of families with complex intellectual disability identified pathogenic genetic variations in known and novel disease genes. Scientific Reports. 10: 968
James DM, Kozol RA, Kajiwara Y, et al. (2019) Intestinal dysmotility in a zebrafish () mutant model of autism. Molecular Autism. 10: 3
Drapeau E, Riad M, Kajiwara Y, et al. (2019) BEHAVIOR PHENOTYPING OF A MOUSE MODEL OF PHELAN MCDERMID SYNDROME WITH A FULL DELETION OF SHANK3 GENE European Neuropsychopharmacology. 29: S961
Kajiwara Y, Wang E, Wang M, et al. (2018) GJA1 (connexin43) is a key regulator of Alzheimer's disease pathogenesis. Acta Neuropathologica Communications. 6: 144
Drapeau E, Riad M, Kajiwara Y, et al. (2018) Behavioral Phenotyping of an Improved Mouse Model of Phelan-McDermid Syndrome with a Complete Deletion of the Gene. Eneuro. 5
Kerur N, Fukuda S, Banerjee D, et al. (2017) cGAS drives noncanonical-inflammasome activation in age-related macular degeneration. Nature Medicine
Wang M, Roussos P, McKenzie A, et al. (2016) Integrative network analysis of nineteen brain regions identifies molecular signatures and networks underlying selective regional vulnerability to Alzheimer's disease. Genome Medicine. 8: 104
Kajiwara Y, McKenzie A, Dorr N, et al. (2016) The human-specific CASP4 gene contributes to Alzheimer-related synaptic and behavioral deficits. Human Molecular Genetics
Aachoui Y, Kajiwara Y, Leaf IA, et al. (2015) Canonical Inflammasomes Drive IFN-γ to Prime Caspase-11 in Defense against a Cytosol-Invasive Bacterium. Cell Host & Microbe. 18: 320-32
Cochoy DM, Kolevzon A, Kajiwara Y, et al. (2015) Phenotypic and functional analysis of SHANK3 stop mutations identified in individuals with ASD and/or ID. Molecular Autism. 6: 23
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