Lista de obras - Yuji Kajiwara - Dominio Público Uruguay

A critical role for human caspase-4 in endotoxin sensitivity

artículo científico publicado en 2014

Analysis of a purported SHANK3 mutation in a boy with autism: clinical impact of rare variant research in neurodevelopmental disabilities

artículo científico publicado en 2010

Autism-like Deficits in Shank3-Deficient Mice Are Rescued by Targeting Actin Regulators

artículo científico publicado en 2015

Behavioral Phenotyping of an Improved Mouse Model of Phelan-McDermid Syndrome with a Complete Deletion of the Gene

article

Calsenilin interacts with transcriptional co-repressor C-terminal binding protein(s).

artículo científico publicado en 2006

Canonical Inflammasomes Drive IFN-γ to Prime Caspase-11 in Defense against a Cytosol-Invasive Bacterium

artículo científico publicado en 2015

Characterization of SLITRK1 variation in obsessive-compulsive disorder

scientific journal article

Compound heterozygous PNPLA6 mutations cause Boucher-Neuhäuser syndrome with late-onset ataxia

artículo científico publicado en 2014

Extensive proteomic screening identifies the obesity-related NYGGF4 protein as a novel LRP1-interactor, showing reduced expression in early Alzheimer's disease

scientific journal article

FE65 binds Teashirt, inhibiting expression of the primate-specific caspase-4

artículo científico publicado en 2009

GJA1 (connexin43) is a key regulator of Alzheimer's disease pathogenesis

artículo científico publicado en 2018

Haploinsufficiency of the autism-associated Shank3 gene leads to deficits in synaptic function, social interaction, and social communication

artículo científico publicado en 2010

Identification of small exonic CNV from whole-exome sequence data and application to autism spectrum disorder

artículo científico publicado en 2013

Integrative network analysis of nineteen brain regions identifies molecular signatures and networks underlying selective regional vulnerability to Alzheimer's disease

artículo científico publicado en 2016

Intestinal dysmotility in a zebrafish () mutant model of autism

artículo científico publicado en 2019

Phenotypic and functional analysis of SHANK3 stop mutations identified in individuals with ASD and/or ID.

artículo científico publicado en 2015

Presenilin 1 is necessary for neuronal, but not glial, EGFR expression and neuroprotection via γ-secretase-independent transcriptional mechanisms.

artículo científico publicado en 2015

Presenilin1/γ-secretase protects neurons from glucose deprivation-induced death by regulating miR-212 and PEA15.

artículo científico

SLITRK1 binds 14-3-3 and regulates neurite outgrowth in a phosphorylation-dependent manner

scientific journal article

The bZIP-like motif of hnRNP C directs the nuclear accumulation of pre-mRNA and lethality in yeast.

artículo científico publicado en 2001

The human-specific CASP4 gene product contributes to Alzheimer-related synaptic and behavioural deficits

artículo científico publicado en 2016

cGAS drives noncanonical-inflammasome activation in age-related macular degeneration.

artículo científico publicado en 2017

Lista de obras de Yuji Kajiwara

A critical role for human caspase-4 in endotoxin sensitivity

Analysis of a purported SHANK3 mutation in a boy with autism: clinical impact of rare variant research in neurodevelopmental disabilities

Autism-like Deficits in Shank3-Deficient Mice Are Rescued by Targeting Actin Regulators

Behavioral Phenotyping of an Improved Mouse Model of Phelan-McDermid Syndrome with a Complete Deletion of the Gene

Calsenilin interacts with transcriptional co-repressor C-terminal binding protein(s).

Canonical Inflammasomes Drive IFN-γ to Prime Caspase-11 in Defense against a Cytosol-Invasive Bacterium

Characterization of SLITRK1 variation in obsessive-compulsive disorder

Compound heterozygous PNPLA6 mutations cause Boucher-Neuhäuser syndrome with late-onset ataxia

Extensive proteomic screening identifies the obesity-related NYGGF4 protein as a novel LRP1-interactor, showing reduced expression in early Alzheimer's disease

FE65 binds Teashirt, inhibiting expression of the primate-specific caspase-4

GJA1 (connexin43) is a key regulator of Alzheimer's disease pathogenesis

Haploinsufficiency of the autism-associated Shank3 gene leads to deficits in synaptic function, social interaction, and social communication

Identification of small exonic CNV from whole-exome sequence data and application to autism spectrum disorder

Integrative network analysis of nineteen brain regions identifies molecular signatures and networks underlying selective regional vulnerability to Alzheimer's disease

Intestinal dysmotility in a zebrafish () mutant model of autism

Phenotypic and functional analysis of SHANK3 stop mutations identified in individuals with ASD and/or ID.

Presenilin 1 is necessary for neuronal, but not glial, EGFR expression and neuroprotection via γ-secretase-independent transcriptional mechanisms.

Presenilin1/γ-secretase protects neurons from glucose deprivation-induced death by regulating miR-212 and PEA15.

SLITRK1 binds 14-3-3 and regulates neurite outgrowth in a phosphorylation-dependent manner

The bZIP-like motif of hnRNP C directs the nuclear accumulation of pre-mRNA and lethality in yeast.

The human-specific CASP4 gene product contributes to Alzheimer-related synaptic and behavioural deficits

cGAS drives noncanonical-inflammasome activation in age-related macular degeneration.