Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs893595382
rs893595382
0.020 GeneticVariation BEFREE In addition to classic markers of tauopathy, significant neuroinflammation and extensive gliosis were detected in AAV1-Tau(P301L) mice. 26276810

2015

dbSNP: rs893595382
rs893595382
0.020 GeneticVariation BEFREE The Stress c-Jun N-terminal Kinase Signaling Pathway Activation Correlates with Synaptic Pathology and Presents A Sex Bias in P301L Mouse Model of Tauopathy. 30315879

2018

dbSNP: rs886039227
rs886039227
0.010 GeneticVariation BEFREE In conjunction with long disease duration and aging, our findings suggest that the F52L DCTN1 mutation may evoke severe tauopathy and moderate α-synucleinopathy. 29499916

2018

dbSNP: rs866604606
rs866604606
0.010 GeneticVariation BEFREE These findings indicate that the major sites of tau phosphorylation, and the expression of kinases involved in tau phosphorylation are active in P310L mutation as in AD and other tauopathies. 14757934

2003

dbSNP: rs780325052
rs780325052
0.010 GeneticVariation BEFREE Inhibition of Calpain Protects Against Tauopathy in Transgenic P301S Tau Mice. 31156179

2019

dbSNP: rs779612015
rs779612015
0.010 GeneticVariation BEFREE Here, to address the role of p25/Cdk5 in tauopathy, we generated double-transgenic mice by crossing mice overexpressing mutant human tau (P301S) with Δ<i>p35KI</i> mice. 28912154

2017

dbSNP: rs776045205
rs776045205
0.010 GeneticVariation BEFREE Inhibition of Calpain Protects Against Tauopathy in Transgenic P301S Tau Mice. 31156179

2019

dbSNP: rs775645890
rs775645890
0.010 GeneticVariation BEFREE Here, to address the role of p25/Cdk5 in tauopathy, we generated double-transgenic mice by crossing mice overexpressing mutant human tau (P301S) with Δ<i>p35KI</i> mice. 28912154

2017

dbSNP: rs769483065
rs769483065
0.010 GeneticVariation BEFREE These observations in vitro and cell lines are recapitulated in primary neurons and in vivo, as genetic reduction in RanBP9 not only ameliorates tauopathy in Tau-P301S mice but also rescues the deficits in synaptic integrity and plasticity. 29016855

2017

dbSNP: rs768194029
rs768194029
0.010 GeneticVariation BEFREE S-nitrosylation of E3 ubiquitin-protein ligase RNF213 alters non-canonical Wnt/Ca+2 signaling in the P301S mouse model of tauopathy. 30696811

2019

dbSNP: rs763872192
rs763872192
0.010 GeneticVariation BEFREE Neuroprotective effects of low fat-protein diet in the P301L mouse model of tauopathy. 28456717

2017

dbSNP: rs760073870
rs760073870
0.010 GeneticVariation BEFREE P301L tauopathy: confocal immunofluorescence study of perinuclear aggregation of the mutated protein. 12127682

2002

dbSNP: rs755135182
rs755135182
0.020 GeneticVariation BEFREE In this study, we examined whether BFT confers neuroprotection against tau phosphorylation and the generation of neurofibrillary tangles (NFTs) in the P301S mouse model of tauopathy. 29860433

2018

dbSNP: rs755135182
rs755135182
0.020 GeneticVariation BEFREE The present study examined the effects of MB in the P301S mouse model of tauopathy. 24556215

2014

dbSNP: rs752410089
rs752410089
0.010 GeneticVariation BEFREE Inhibition of Calpain Protects Against Tauopathy in Transgenic P301S Tau Mice. 31156179

2019

dbSNP: rs63751438
rs63751438
0.100 GeneticVariation BEFREE α-Lipoic acid improves abnormal behavior by mitigation of oxidative stress, inflammation, ferroptosis, and tauopathy in P301S Tau transgenic mice. 29126071

2018

dbSNP: rs63751438
rs63751438
0.100 GeneticVariation BEFREE To explore this interaction in vivo, we crossed a well-characterized human P301S-tau transgenic mouse model of tauopathy with human G2019S-LRRK2 transgenic mice or LRRK2 knockout (KO) mice. 29088368

2018

dbSNP: rs63751438
rs63751438
0.100 GeneticVariation BEFREE S-nitrosylation of E3 ubiquitin-protein ligase RNF213 alters non-canonical Wnt/Ca+2 signaling in the P301S mouse model of tauopathy. 30696811

2019

dbSNP: rs63751438
rs63751438
0.100 GeneticVariation BEFREE We further demonstrate that peripheral administration of the same antibodies in the more rapidly progressive P301S tauopathy model not only reduces Tau pathology quantitated by biochemical assays and immunohistochemistry, but also significantly delays the onset of motor function decline and weight loss. 21841002

2011

dbSNP: rs63751438
rs63751438
0.100 GeneticVariation BEFREE Inhibition of Calpain Protects Against Tauopathy in Transgenic P301S Tau Mice. 31156179

2019

dbSNP: rs63751438
rs63751438
0.100 GeneticVariation BEFREE P301S mutant human tau transgenic mice manifest early symptoms of human tauopathies with dementia and altered sensorimotor gating. 21698260

2011

dbSNP: rs63751438
rs63751438
0.100 GeneticVariation BEFREE Thus, transgenic mice expressing mutant (for example, P301S) human tau in nerve cells show the essential features of tauopathies, including neurodegeneration and abundant filaments made of hyperphosphorylated tau protein. 19503072

2009

dbSNP: rs63751438
rs63751438
0.100 GeneticVariation BEFREE Tau silencing by siRNA in the P301S mouse model of tauopathy. 25687501

2014

dbSNP: rs63751438
rs63751438
0.100 GeneticVariation BEFREE The present study examined the effects of MB in the P301S mouse model of tauopathy. 24556215

2014

dbSNP: rs63751438
rs63751438
0.100 GeneticVariation BEFREE Mice transgenic for human P301S tau protein exhibit many characteristics of human tauopathies, including neurodegeneration, the formation of neuronal tau inclusions in the brain and the development of a pronounced motor phenotype by 5 months of age. 20004218

2010