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Muscle mitochondrial uncoupling dismantles neuromuscular junction and triggers distal degeneration of motor neurons

PloS one, 2009-04, Vol.4 (4), p.e5390-e5390

2009

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Cytoplasmic dynein in neurodegeneration

Pharmacology & therapeutics (Oxford), 2011-06, Vol.130 (3), p.348-363

2011

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Dynein mutations associated with hereditary motor neuropathies impair mitochondrial morphology and function with age

Neurobiology of disease, 2013-10, Vol.58, p.220-230

2013

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A point mutation in the dynein heavy chain gene leads to striatal atrophy and compromises neurite outgrowth of striatal neurons

Human molecular genetics, 2010-11, Vol.19 (22), p.4385-4398

2010

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A mutation in the dynein heavy chain gene compensates for energy deficit of mutant SOD1 mice and increases potentially neuroprotective IGF-1

Molecular neurodegeneration, 2011-04, Vol.6 (1), p.26-26, Article 26

2011

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Energy Metabolism in Residents in the Low- and Moderate Altitude Regions of Central Asia with MAFLD and Type 2 Diabetes Mellitus

Hormone and metabolic research, 2024-04, Vol.56 (4), p.294

2024

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Cover Image, Volume 85, Issue 1

Drug development research, 2024-02, Vol.85 (1)

2024

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[alpha]-Synuclein in Parkinson's Disease: Pathogenic Function and Translation into Animal Models

Neuro-degenerative diseases, 2014-06, Vol.14 (1), p.1-17

2014

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Mutual exacerbation of peroxisome proliferator-activated receptor γ coactivator 1α deregulation and α-synuclein oligomerization

Annals of neurology, 2015-01, Vol.77 (1), p.15-32

2015

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α-Synuclein in Parkinson's Disease: Pathogenic Function and Translation into Animal Models

Neuro-degenerative diseases, 2014, Vol.14 (1), p.1-17

2014

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PGC-1 is a male-specific disease modifier of human and experimental amyotrophic lateral sclerosis

Human molecular genetics, 2013-09, Vol.22 (17), p.3477-3484

2013

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Drug upgrade: A complete methodology from old drug to new chemical entities using Nematic Protein Organization Technique

Drug development research, 2024-02, Vol.85 (1), p.e22151-n/a

2024

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PGC-1α is a male-specific disease modifier of human and experimental amyotrophic lateral sclerosis

Human molecular genetics, 2013-09, Vol.22 (17), p.3477-3484

2013

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“OpenLAB”: A 2‐hour PCR‐based practical for high school students

Biochemistry and molecular biology education, 2010-09, Vol.38 (5), p.296-302

2010

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The Golgi-localized, gamma ear-containing, ARF-binding (GGA) protein family alters alpha synuclein (α-syn) oligomerization and secretion

Aging (Albany, NY.), 2017-07, Vol.9 (7), p.1677-1697

2017

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Mice with a mutation in the dynein heavy chain 1 gene display sensory neuropathy but lack motor neuron disease

Experimental neurology, 2009, Vol.215 (1), p.146-152

2009

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Full-length PGC-1[alpha] salvages the phenotype of a mouse model of human neuropathy through mitochondrial proliferation

Human molecular genetics, 2013-12, Vol.22 (25), p.5096-5106

2013

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Mutual exacerbation of peroxisome proliferator-activated receptor [gamma] coactivator 1[alpha] deregulation and [alpha]-synuclein oligomerization

Annals of neurology, 2015-01, Vol.77 (1), p.15

2015

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Mutual exacerbation of PGC-1α deregulation and α-synuclein oligomerization

Annals of neurology, 2014-12, Vol.77 (1), p.15-32

2014

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Full-length PGC-1α salvages the phenotype of a mouse model of human neuropathy through mitochondrial proliferation

Human molecular genetics, 2013-12, Vol.22 (25), p.5096-5106

2013

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Mutations in cytoplasmic dynein lead to a Huntington's disease-like defect in energy metabolism of brown and white adipose tissues

Biochimica et biophysica acta, 2011, Vol.1812 (1), p.59-69

2011

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Mutations in cytoplasmic dynein lead to a Huntington's disease-like defect in energy metabolism of brown and white adipose tissues

Biochimica et biophysica acta. Molecular basis of disease, 2010-11, Vol.1812 (1)

2010

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Wärmeentwicklung bei der Keimung. Experimente zur Bestimmung der Keimungswärme

Berichte des Institutes für Didaktik der Biologie der Westfälischen Wilhelms-Universität Münster, IDB, 1999 (8), p.53-68

1999

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Original Reports on Focus Area: Health Disparities--Advancing the Science of Health Disparities Research

Ethnicity & disease, 2007-06, Vol.17 (3), p.427-433

Artinian, Nancy T Warnecke, Richard B Kelly, Kimberly M Weiner, Janet Lurie, Nicole Flack, John M Mettei, Josiemer Eschbach, Karl Long, Judith A Furumoto-Dawson, Alice Hankin, Janet R DeGraffinreid, Cecilia

2007

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Designing and Evaluating Opioid Misuse Prevention Training for Rural Communities and Health Care Providers

Health promotion practice, 2023-05, p.15248399231174920-15248399231174920

2023

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Muscle mitochondrial uncoupling dismantles neuromuscular junction and triggers distal degeneration of motor neurons

Cytoplasmic dynein in neurodegeneration

Dynein mutations associated with hereditary motor neuropathies impair mitochondrial morphology and function with age

A point mutation in the dynein heavy chain gene leads to striatal atrophy and compromises neurite outgrowth of striatal neurons

A mutation in the dynein heavy chain gene compensates for energy deficit of mutant SOD1 mice and increases potentially neuroprotective IGF-1

Energy Metabolism in Residents in the Low- and Moderate Altitude Regions of Central Asia with MAFLD and Type 2 Diabetes Mellitus

Cover Image, Volume 85, Issue 1

[alpha]-Synuclein in Parkinson's Disease: Pathogenic Function and Translation into Animal Models

Mutual exacerbation of peroxisome proliferator-activated receptor γ coactivator 1α deregulation and α-synuclein oligomerization

α-Synuclein in Parkinson's Disease: Pathogenic Function and Translation into Animal Models

PGC-1 is a male-specific disease modifier of human and experimental amyotrophic lateral sclerosis

Drug upgrade: A complete methodology from old drug to new chemical entities using Nematic Protein Organization Technique

PGC-1α is a male-specific disease modifier of human and experimental amyotrophic lateral sclerosis

“OpenLAB”: A 2‐hour PCR‐based practical for high school students

The Golgi-localized, gamma ear-containing, ARF-binding (GGA) protein family alters alpha synuclein (α-syn) oligomerization and secretion

Mice with a mutation in the dynein heavy chain 1 gene display sensory neuropathy but lack motor neuron disease

Full-length PGC-1[alpha] salvages the phenotype of a mouse model of human neuropathy through mitochondrial proliferation

Mutual exacerbation of peroxisome proliferator-activated receptor [gamma] coactivator 1[alpha] deregulation and [alpha]-synuclein oligomerization

Mutual exacerbation of PGC-1α deregulation and α-synuclein oligomerization

Full-length PGC-1α salvages the phenotype of a mouse model of human neuropathy through mitochondrial proliferation

Mutations in cytoplasmic dynein lead to a Huntington's disease-like defect in energy metabolism of brown and white adipose tissues

Mutations in cytoplasmic dynein lead to a Huntington's disease-like defect in energy metabolism of brown and white adipose tissues

Wärmeentwicklung bei der Keimung. Experimente zur Bestimmung der Keimungswärme

Original Reports on Focus Area: Health Disparities--Advancing the Science of Health Disparities Research

Designing and Evaluating Opioid Misuse Prevention Training for Rural Communities and Health Care Providers

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