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Parkin as a tumor suppressor gene for hepatocellular carcinoma

Oncogene, 2008-10, Vol.27 (46), p.6002-6011

2008

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Dexamethasone induces heat shock response and slows down disease progression in mouse and fly models of Huntington's disease

Human molecular genetics, 2014-05, Vol.23 (10), p.2737-2751

2014

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Omi HtrA2 is a positive regulator of autophagy that facilitates the degradation of mutant proteins involved in neurodegenerative diseases

Cell death and differentiation, 2010-11, Vol.17 (11), p.1773-1784

2010

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Polyglutamine length-dependent interaction of Hsp40 and Hsp70 family chaperones with truncated N-terminal huntingtin : their role in suppression of aggregation and cellular toxicity

Human molecular genetics, 2000-08, Vol.9 (13), p.2009-2018

2000

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NF-Y inactivation induces differential ER chaperone downregulations and UBIQUITIN/P62 pathologies in the CNS

Journal of the neurological sciences, 2017-10, Vol.381, p.719-719

2017

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Huntington's Disease Intranuclear Inclusions Contain Truncated, Ubiquitinated Huntingtin Protein

Experimental neurology, 1999-03, Vol.156 (1), p.92-99

1999

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The distribution and the origin of unmyelinated fibers in the central nervous system

Journal of the neurological sciences, 2017-10, Vol.381, p.661-661

2017

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Semi-rational engineering of a coral fluorescent protein into an efficient highlighter

EMBO reports, 2005-03, Vol.6 (3), p.233-238

2005

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Chromogranin-mediated secretion of mutant superoxide dismutase proteins linked to amyotrophic lateral sclerosis

Nature neuroscience, 2006-01, Vol.9 (1), p.108-118

2006

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Inhibition of Proteasomal Function by Curcumin Induces Apoptosis through Mitochondrial Pathway

The Journal of biological chemistry, 2004-03, Vol.279 (12), p.11680-11685

2004

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Eukaryotic Proteasomes Cannot Digest Polyglutamine Sequences and Release Them during Degradation of Polyglutamine-Containing Proteins

Molecular cell, 2004-04, Vol.14 (1), p.95-104

2004

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Co-chaperone CHIP Associates with Expanded Polyglutamine Protein and Promotes Their Degradation by Proteasomes

The Journal of biological chemistry, 2005-03, Vol.280 (12), p.11635-11640

2005

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Dysregulation of non-coding RNA expression in Huntington disease model mouse

Journal of the neurological sciences, 2017-10, Vol.381, p.851-851

2017

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The detection of seeds alpha-synuclein using protein misfolding cyclic amplification(PMCA)

Journal of the neurological sciences, 2017-10, Vol.381, p.972-973

2017

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Amyloid polymorphism derived from human and mouse alpha-synuclein

Journal of the neurological sciences, 2017-10, Vol.381, p.966-966

2017

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Trehalose alleviates polyglutamine-mediated pathology in a mouse model of Huntington disease

Nature medicine, 2004-02, Vol.10 (2), p.148-154

2004

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Increased Susceptibility of Cytoplasmic over Nuclear Polyglutamine Aggregates to Autophagic Degradation

Proceedings of the National Academy of Sciences - PNAS, 2005-09, Vol.102 (37), p.13135-13140

2005

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Association of gamma-secretase with lipid rafts in post-Golgi and endosome membranes

The Journal of biological chemistry, 2004-10, Vol.279 (43), p.44945-44954

2004

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APP717 missense mutation affects the ratio of amyloid beta protein species (A beta 1-42/43 and a beta 1-40) in familial Alzheimer's disease brain

The Journal of biological chemistry, 1994-12, Vol.269 (52), p.32721-32724

1994

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beta Subunits of voltage-gated sodium channels are novel substrates of beta-site amyloid precursor protein-cleaving enzyme (BACE1) and gamma-secretase

The Journal of biological chemistry, 2005-06, Vol.280 (24), p.23009-23017

2005

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rAAV-mediated shRNA ameliorated neuropathology in Huntington disease model mouse

Biochemical and biophysical research communications, 2006-04, Vol.343 (1), p.190-197

2006

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Oxidative stress promotes mutant huntingtin aggregation and mutant huntingtin-dependent cell death by mimicking proteasomal malfunction

Biochemical and biophysical research communications, 2006-03, Vol.342 (1), p.184-190

2006

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Dosage-dependent over-expression of genes in the trisomic region of Ts1Cje mouse model for Down syndrome

Human molecular genetics, 2004-07, Vol.13 (13), p.1333-1340

2004

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Gene expression profiling of medium spiny neurons in Huntington’s disease model mouse

Journal of the neurological sciences, 2017-10, Vol.381, p.583-583

2017

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Mutant huntingtin fragment selectively suppresses Brn-2 POU domain transcription factor to mediate hypothalamic cell dysfunction

Human molecular genetics, 2010-06, Vol.19 (11), p.2099-2112

2010

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Parkin as a tumor suppressor gene for hepatocellular carcinoma

Dexamethasone induces heat shock response and slows down disease progression in mouse and fly models of Huntington's disease

Omi HtrA2 is a positive regulator of autophagy that facilitates the degradation of mutant proteins involved in neurodegenerative diseases

Polyglutamine length-dependent interaction of Hsp40 and Hsp70 family chaperones with truncated N-terminal huntingtin : their role in suppression of aggregation and cellular toxicity

NF-Y inactivation induces differential ER chaperone downregulations and UBIQUITIN/P62 pathologies in the CNS

Huntington's Disease Intranuclear Inclusions Contain Truncated, Ubiquitinated Huntingtin Protein

The distribution and the origin of unmyelinated fibers in the central nervous system

Semi-rational engineering of a coral fluorescent protein into an efficient highlighter

Chromogranin-mediated secretion of mutant superoxide dismutase proteins linked to amyotrophic lateral sclerosis

Inhibition of Proteasomal Function by Curcumin Induces Apoptosis through Mitochondrial Pathway

Eukaryotic Proteasomes Cannot Digest Polyglutamine Sequences and Release Them during Degradation of Polyglutamine-Containing Proteins

Co-chaperone CHIP Associates with Expanded Polyglutamine Protein and Promotes Their Degradation by Proteasomes

Dysregulation of non-coding RNA expression in Huntington disease model mouse

The detection of seeds alpha-synuclein using protein misfolding cyclic amplification(PMCA)

Amyloid polymorphism derived from human and mouse alpha-synuclein

Trehalose alleviates polyglutamine-mediated pathology in a mouse model of Huntington disease

Increased Susceptibility of Cytoplasmic over Nuclear Polyglutamine Aggregates to Autophagic Degradation

Association of gamma-secretase with lipid rafts in post-Golgi and endosome membranes

APP717 missense mutation affects the ratio of amyloid beta protein species (A beta 1-42/43 and a beta 1-40) in familial Alzheimer's disease brain

beta Subunits of voltage-gated sodium channels are novel substrates of beta-site amyloid precursor protein-cleaving enzyme (BACE1) and gamma-secretase

rAAV-mediated shRNA ameliorated neuropathology in Huntington disease model mouse

Oxidative stress promotes mutant huntingtin aggregation and mutant huntingtin-dependent cell death by mimicking proteasomal malfunction

Dosage-dependent over-expression of genes in the trisomic region of Ts1Cje mouse model for Down syndrome

Gene expression profiling of medium spiny neurons in Huntington’s disease model mouse

Mutant huntingtin fragment selectively suppresses Brn-2 POU domain transcription factor to mediate hypothalamic cell dysfunction

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