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Determining Factors Affecting the Acceptance of Medical Education eLearning Platforms during the COVID-19 Pandemic in the Philippines: UTAUT2 Approach

Healthcare (Basel), 2021-06, Vol.9 (7), p.780

2021

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Human Huntington's disease pluripotent stem cell-derived microglia develop normally but are abnormally hyper-reactive and release elevated levels of reactive oxygen species

Journal of neuroinflammation, 2021-04, Vol.18 (1), p.94-17, Article 94

2021

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A novel pathogenic pathway of immune activation detectable before clinical onset in Huntington's disease

The Journal of experimental medicine, 2008-08, Vol.205 (8), p.1869-1877

2008

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Mislocalization of Nucleocytoplasmic Transport Proteins in Human Huntington's Disease PSC-Derived Striatal Neurons

Frontiers in cellular neuroscience, 2021-09, Vol.15, p.742763-742763

2021

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Misfolded PrP impairs the UPS by interaction with the 20S proteasome and inhibition of substrate entry

The EMBO journal, 2011-08, Vol.30 (15), p.3065-3077

2011

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Determining the Factors Affecting a Career Shifter’s Use of Software Testing Tools amidst the COVID-19 Crisis in the Philippines: TTF-TAM Approach

Sustainability, 2022-09, Vol.14 (17), p.11084

2022

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Characterisation of immune cell function in fragment and full-length Huntington's disease mouse models

Neurobiology of disease, 2015-01, Vol.73, p.388-398

2015

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Mutant Huntingtin Does Not Affect the Intrinsic Phenotype of Human Huntington's Disease T Lymphocytes

PloS one, 2015-11, Vol.10 (11), p.e0141793-e0141793

2015

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Misfolded PrP and a novel mechanism of proteasome inhibition

Prion, 2012-01, Vol.6 (1), p.32-36

2012

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Regulation of expression of the novel IL‐1 receptor family members in the mouse brain

Journal of neurochemistry, 2005-10, Vol.95 (2), p.324-330

2005

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FAN1 modifies Huntington's disease progression by stabilizing the expanded HTT CAG repeat

Human molecular genetics, 2019-02, Vol.28 (4), p.650-661

2019

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Disruption of immune cell function by mutant huntingtin in Huntington's disease pathogenesis

Current opinion in pharmacology, 2016-02, Vol.26, p.33-38

2016

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Simple Machines Made Simple

St. Andre, Ralph E

1993

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HTT-lowering reverses Huntington's disease immune dysfunction caused by NFκB pathway dysregulation

Brain (London, England : 1878), 2014-03, Vol.137 (Pt 3), p.819-833

2014

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An exploratory double‐blind, randomized clinical trial with selisistat, a SirT1 inhibitor, in patients with Huntington's disease

British journal of clinical pharmacology, 2015-03, Vol.79 (3), p.465-476

2015

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A30 The role of huntingtin in human myeloid cells

Journal of neurology, neurosurgery and psychiatry, 2018-09, Vol.89 (Suppl 1), p.A11

2018

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Mutant huntingtin impairs immune cell migration in Huntington disease

The Journal of clinical investigation, 2012-12, Vol.122 (12), p.4737-4747

2012

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Prion-mediated neurodegeneration is associated with early impairment of the ubiquitin–proteasome system

Acta neuropathologica, 2016-03, Vol.131 (3), p.411-425

2016

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Wild-type huntingtin regulates human macrophage function

Scientific reports, 2020-10, Vol.10 (1), p.17269-17269, Article 17269

2020

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Mutant huntingtin fragmentation in immune cells tracks Huntington's disease progression

The Journal of clinical investigation, 2012-10, Vol.122 (10), p.3731-3736

2012

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In vivo neutralization of the protagonist role of macrophages during the chronic inflammatory stage of Huntington’s disease

Scientific reports, 2018-07, Vol.8 (1), p.11447-14, Article 11447

2018

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IL-1Rrp2 expression and IL-1F9 (IL-1H1) actions in brain cells

Journal of neuroimmunology, 2003-06, Vol.139 (1), p.36-43

2003

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Inhibition of tumour necrosis factor alpha in the R6/2 mouse model of Huntington’s disease by etanercept treatment

Scientific reports, 2019-05, Vol.9 (1), p.7202, Article 7202

2019

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Expression of mutant exon 1 huntingtin fragments in human neural stem cells and neurons causes inclusion formation and mitochondrial dysfunction

The FASEB journal, 2020-06, Vol.34 (6), p.8139-8154

2020

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RNA-Seq of Huntington's disease patient myeloid cells reveals innate transcriptional dysregulation associated with proinflammatory pathway activation

Human molecular genetics, 2016-07, Vol.25 (14), p.2893-2904

2016

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Determining Factors Affecting the Acceptance of Medical Education eLearning Platforms during the COVID-19 Pandemic in the Philippines: UTAUT2 Approach

Human Huntington's disease pluripotent stem cell-derived microglia develop normally but are abnormally hyper-reactive and release elevated levels of reactive oxygen species

A novel pathogenic pathway of immune activation detectable before clinical onset in Huntington's disease

Mislocalization of Nucleocytoplasmic Transport Proteins in Human Huntington's Disease PSC-Derived Striatal Neurons

Misfolded PrP impairs the UPS by interaction with the 20S proteasome and inhibition of substrate entry

Determining the Factors Affecting a Career Shifter’s Use of Software Testing Tools amidst the COVID-19 Crisis in the Philippines: TTF-TAM Approach

Characterisation of immune cell function in fragment and full-length Huntington's disease mouse models

Mutant Huntingtin Does Not Affect the Intrinsic Phenotype of Human Huntington's Disease T Lymphocytes

Misfolded PrP and a novel mechanism of proteasome inhibition

Regulation of expression of the novel IL‐1 receptor family members in the mouse brain

FAN1 modifies Huntington's disease progression by stabilizing the expanded HTT CAG repeat

Disruption of immune cell function by mutant huntingtin in Huntington's disease pathogenesis

Simple Machines Made Simple

HTT-lowering reverses Huntington's disease immune dysfunction caused by NFκB pathway dysregulation

An exploratory double‐blind, randomized clinical trial with selisistat, a SirT1 inhibitor, in patients with Huntington's disease

A30 The role of huntingtin in human myeloid cells

Mutant huntingtin impairs immune cell migration in Huntington disease

Prion-mediated neurodegeneration is associated with early impairment of the ubiquitin–proteasome system

Wild-type huntingtin regulates human macrophage function

Mutant huntingtin fragmentation in immune cells tracks Huntington's disease progression

In vivo neutralization of the protagonist role of macrophages during the chronic inflammatory stage of Huntington’s disease

IL-1Rrp2 expression and IL-1F9 (IL-1H1) actions in brain cells

Inhibition of tumour necrosis factor alpha in the R6/2 mouse model of Huntington’s disease by etanercept treatment

Expression of mutant exon 1 huntingtin fragments in human neural stem cells and neurons causes inclusion formation and mitochondrial dysfunction

RNA-Seq of Huntington's disease patient myeloid cells reveals innate transcriptional dysregulation associated with proinflammatory pathway activation

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