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Necroptosis Drives Motor Neuron Death in Models of Both Sporadic and Familial ALS

Neuron (Cambridge, Mass.), 2014-03, Vol.81 (5), p.1001-1008

2014

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Reduced SMN protein impairs maturation of the neuromuscular junctions in mouse models of spinal muscular atrophy

Human molecular genetics, 2008-08, Vol.17 (16), p.2552-2569

2008

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Wafer-Scale Room-Temperature Bonding of Smooth Au/Ti-Based Getter Layer for Vacuum Packaging

Sensors (Basel, Switzerland), 2022-10, Vol.22 (21), p.8144

2022

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Spectrum of Neuropathophysiology in Spinal Muscular Atrophy Type I

Journal of neuropathology and experimental neurology, 2015-01, Vol.74 (1), p.15-24

2015

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Simple and low-temperature vacuum packaging process by using Au/Ta/Ti metal multilayer

Japanese Journal of Applied Physics, 2022-05, Vol.61 (5), p.51004

2022

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A Role for SMN Exon 7 Splicing in the Selective Vulnerability of Motor Neurons in Spinal Muscular Atrophy

Molecular and Cellular Biology, 2012-01, Vol.32 (1), p.126-138

2012

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Postsymptomatic restoration of SMN rescues the disease phenotype in a mouse model of severe spinal muscular atrophy

The Journal of clinical investigation, 2011-08, Vol.121 (8), p.3029-3041

2011

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Bonding formation and gas absorption using Au/Pt/Ti layers for vacuum packaging

Microsystems & nanoengineering, 2022-01, Vol.8 (1), p.2-2, Article 2

2022

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Limitations and Challenges in Modeling Diseases Involving Spinal Motor Neuron Degeneration in Vitro

Frontiers in cellular neuroscience, 2018-03, Vol.12, p.61-61

2018

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Mutant superoxide dismutase 1 (SOD1), a cause of amyotrophic lateral sclerosis, disrupts the recruitment of SMN, the spinal muscular atrophy protein to nuclear Cajal bodies

Human molecular genetics, 2012-08, Vol.21 (15), p.3421-3434

2012

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Longitudinal transcriptomic analysis of mouse sciatic nerve reveals pathways associated with age‐related muscle pathology

Journal of cachexia, sarcopenia and muscle, 2023-06, Vol.14 (3), p.1322-1336

2023

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Spinal Muscular Atrophy: New and Emerging Insights from Model Mice

Current neurology and neuroscience reports, 2010-03, Vol.10 (2), p.108-117

2010

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DNA single-strand break repair is impaired in aprataxin-related ataxia

Annals of neurology, 2007-02, Vol.61 (2), p.162-174

2007

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Humanin detected in skeletal muscles of MELAS patients: a possible new therapeutic agent

Acta neuropathologica, 2005-04, Vol.109 (4), p.367-372

2005

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Humanin inhibits cell death of serum-deprived PC12h cells

Neuroreport, 2002-05, Vol.13 (6), p.903-907

2002

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Requirement of enhanced Survival Motoneuron protein imposed during neuromuscular junction maturation

The Journal of clinical investigation, 2014-02, Vol.124 (2), p.785-800

2014

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Humanin improves impaired metabolic activity and prolongs survival of serum-deprived human lymphocytes

Molecular and cellular biochemistry, 2003-12, Vol.254 (1-2), p.83-89

2003

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A 44-Year-Old Alcohol-Dependent Man Who Recovered from Central Pontine Myelinolysis with Supportive Physical Therapy

The American journal of case reports, 2022-09, Vol.23, p.e937389-e937389

2022

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Effect of humanin on decreased ATP levels of human lymphocytes harboring A3243G mutant mitochondrial DNA

Neuropeptides (Edinburgh), 2005-04, Vol.39 (2), p.97-101

2005

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Physical Exercise Counteracts Aging-Associated White Matter Demyelination Causing Cognitive Decline

Aging and disease, 2024-02

2024

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Loss of function mechanism in aprataxin-related early-onset ataxia

Biochemical and biophysical research communications, 2004-09, Vol.322 (2), p.380-386

2004

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Cardiomyopathy and altered integrin-actin signaling in Fhl1 mutant female mice

Human molecular genetics, 2019-01, Vol.28 (2), p.209-219

2019

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The neuroprotective factor Wld(s) fails to mitigate distal axonal and neuromuscular junction (NMJ) defects in mouse models of spinal muscular atrophy

Neuroscience letters, 2009-01, Vol.449 (3), p.246-251

2009

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Fhl1 W122S causes loss of protein function and late-onset mild myopathy

Human molecular genetics, 2015-02, Vol.24 (3), p.714-726

2015

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Requirement of enhanced survival motoneuron protein imposed during neuromuscular junction maturation

The Journal of clinical investigation, 2014-02, Vol.124 (2), p.785

2014

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Necroptosis Drives Motor Neuron Death in Models of Both Sporadic and Familial ALS

Reduced SMN protein impairs maturation of the neuromuscular junctions in mouse models of spinal muscular atrophy

Wafer-Scale Room-Temperature Bonding of Smooth Au/Ti-Based Getter Layer for Vacuum Packaging

Spectrum of Neuropathophysiology in Spinal Muscular Atrophy Type I

Simple and low-temperature vacuum packaging process by using Au/Ta/Ti metal multilayer

A Role for SMN Exon 7 Splicing in the Selective Vulnerability of Motor Neurons in Spinal Muscular Atrophy

Postsymptomatic restoration of SMN rescues the disease phenotype in a mouse model of severe spinal muscular atrophy

Bonding formation and gas absorption using Au/Pt/Ti layers for vacuum packaging

Limitations and Challenges in Modeling Diseases Involving Spinal Motor Neuron Degeneration in Vitro

Mutant superoxide dismutase 1 (SOD1), a cause of amyotrophic lateral sclerosis, disrupts the recruitment of SMN, the spinal muscular atrophy protein to nuclear Cajal bodies

Longitudinal transcriptomic analysis of mouse sciatic nerve reveals pathways associated with age‐related muscle pathology

Spinal Muscular Atrophy: New and Emerging Insights from Model Mice

DNA single-strand break repair is impaired in aprataxin-related ataxia

Humanin detected in skeletal muscles of MELAS patients: a possible new therapeutic agent

Humanin inhibits cell death of serum-deprived PC12h cells

Requirement of enhanced Survival Motoneuron protein imposed during neuromuscular junction maturation

Humanin improves impaired metabolic activity and prolongs survival of serum-deprived human lymphocytes

A 44-Year-Old Alcohol-Dependent Man Who Recovered from Central Pontine Myelinolysis with Supportive Physical Therapy

Effect of humanin on decreased ATP levels of human lymphocytes harboring A3243G mutant mitochondrial DNA

Physical Exercise Counteracts Aging-Associated White Matter Demyelination Causing Cognitive Decline

Loss of function mechanism in aprataxin-related early-onset ataxia

Cardiomyopathy and altered integrin-actin signaling in Fhl1 mutant female mice

The neuroprotective factor Wld(s) fails to mitigate distal axonal and neuromuscular junction (NMJ) defects in mouse models of spinal muscular atrophy

Fhl1 W122S causes loss of protein function and late-onset mild myopathy

Requirement of enhanced survival motoneuron protein imposed during neuromuscular junction maturation

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