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Serum concentrations of insulin-like growth factor-1 as a biomarker of improved circadian rhythm sleep-wake disorder in school-aged children

Journal of clinical sleep medicine, 2020-12, Vol.16 (12), p.2073-2078

2020

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Parathyroid hormone and parathyroid hormone type-1 receptor accelerate myocyte differentiation

Scientific reports, 2014-06, Vol.4 (1), p.5066, Article 5066

2014

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New type of Sendai virus vector provides transgene-free iPS cells derived from chimpanzee blood

PloS one, 2014-12, Vol.9 (12), p.e113052-e113052

2014

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Increase in the Number and Duration of Sleep Episodes During Class After Reopening of Schools Following Closure due to COVID-19

Kobe journal of the medical sciences, 2022, Vol.68 (1), p.E23-E29

2022

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A Pediatric Case of COLQ -Related Congenital Myasthenic Syndrome with Marked Fatigue

Children (Basel), 2023-04, Vol.10 (5), p.769

2023

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Estimation of muscle strength from actigraph data in Duchenne muscular dystrophy

Pediatrics international, 2014-10, Vol.56 (5), p.748-752

2014

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Clonal Isolation of Muscle-Derived Cells Capable of Enhancing Muscle Regeneration and Bone Healing

The Journal of cell biology, 2000-09, Vol.150 (5), p.1085-1099

2000

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Effective Drug Delivery System for Duchenne Muscular Dystrophy Using Hybrid Liposomes Including Gentamicin along with Reduced Toxicity

Biological and Pharmaceutical Bulletin, 2011/05/01, Vol.34(5), pp.712-716

2011

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SARS-CoV-2 Omicron BA.2.75 Variant May Be Much More Infective than Preexisting Variants Based on In Silico Model

Microorganisms (Basel), 2022-10, Vol.10 (10), p.2090

2022

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Disease modeling and lentiviral gene transfer in patient-specific induced pluripotent stem cells from late-onset Pompe disease patient

Molecular therapy. Methods & clinical development, 2015-01, Vol.2, p.15023-15023, Article 15023

2015

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Smooth muscle-specific dystrophin expression improves aberrant vasoregulation in mdx mice

Human molecular genetics, 2006-07, Vol.15 (14), p.2266-2275

2006

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Core body temperature changes in school-age children with circadian rhythm sleep–wake disorder

Sleep medicine, 2021-11, Vol.87, p.97-104

2021

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A Skeletal Muscle Model of Infantile-onset Pompe Disease with Patient-specific iPS Cells

Scientific reports, 2017-10, Vol.7 (1), p.13473-13, Article 13473

2017

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Increase in cathepsin K gene expression in Duchenne muscular dystrophy skeletal muscle

Neuropathology, 2024-07

2024

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Exon-skipping events in candidates for clinical trials of morpholino

Pediatrics international, 2011-08, Vol.53 (4), p.524-529

2011

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A Case Report of Congenital Fiber Type Disproportion with an Increased Level of Anti-ACh Receptor Antibodies

Case reports in pediatrics, 2013-01, Vol.2013 (2013), p.1-3

2013

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A novel approach to identify Duchenne muscular dystrophy patients for aminoglycoside antibiotics therapy

Brain & development (Tokyo. 1979), 2005-09, Vol.27 (6), p.400-405

2005

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A 2-bp deletion in exon 74 of the dystrophin gene does not clearly induce muscle weakness

Brain & development (Tokyo. 1979), 2009-02, Vol.31 (2), p.169-172

2009

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Myoclonic Epilepsy With Ragged-Red Fibers Without Increased Lactate Levels

Pediatric neurology, 2009-07, Vol.41 (1), p.46-48

2009

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A Pediatric Case of ICOLQ/I-Related Congenital Myasthenic Syndrome with Marked Fatigue

Children (Basel), 2023-04, Vol.10 (5)

2023

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Prediction of infectivity of SARS-CoV2: Mathematical model with analysis of docking simulation for spike proteins and angiotensin-converting enzyme 2

Microbial risk analysis, 2022-12, Vol.22, p.100227, Article 100227

2022

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Clinical outcomes after long-term treatment with alglucosidase alfa in infants and children with advanced Pompe disease

Genetics in medicine, 2009-03, Vol.11 (3), p.210-219

2009

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In silico binding affinity of the spike protein with ACE2 and the relative evolutionary distance of S gene may be potential factors rapidly obtained for the initial risk of SARS-CoV-2

Microbial risk analysis, 2023-12, Vol.25, p.100278, Article 100278

2023

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Muscle stem cells differentiate into haematopoietic lineages but retain myogenic potential

Nature cell biology, 2003-07, Vol.5 (7), p.640-646

2003

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Estimation of muscle strength from actigraph data in D uchenne muscular dystrophy

Pediatrics international, 2014-10, Vol.56 (5), p.748-752

2014

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Serum concentrations of insulin-like growth factor-1 as a biomarker of improved circadian rhythm sleep-wake disorder in school-aged children

Parathyroid hormone and parathyroid hormone type-1 receptor accelerate myocyte differentiation

New type of Sendai virus vector provides transgene-free iPS cells derived from chimpanzee blood

Increase in the Number and Duration of Sleep Episodes During Class After Reopening of Schools Following Closure due to COVID-19

A Pediatric Case of COLQ -Related Congenital Myasthenic Syndrome with Marked Fatigue

Estimation of muscle strength from actigraph data in Duchenne muscular dystrophy

Clonal Isolation of Muscle-Derived Cells Capable of Enhancing Muscle Regeneration and Bone Healing

Effective Drug Delivery System for Duchenne Muscular Dystrophy Using Hybrid Liposomes Including Gentamicin along with Reduced Toxicity

SARS-CoV-2 Omicron BA.2.75 Variant May Be Much More Infective than Preexisting Variants Based on In Silico Model

Disease modeling and lentiviral gene transfer in patient-specific induced pluripotent stem cells from late-onset Pompe disease patient

Smooth muscle-specific dystrophin expression improves aberrant vasoregulation in mdx mice

Core body temperature changes in school-age children with circadian rhythm sleep–wake disorder

A Skeletal Muscle Model of Infantile-onset Pompe Disease with Patient-specific iPS Cells

Increase in cathepsin K gene expression in Duchenne muscular dystrophy skeletal muscle

Exon-skipping events in candidates for clinical trials of morpholino

A Case Report of Congenital Fiber Type Disproportion with an Increased Level of Anti-ACh Receptor Antibodies

A novel approach to identify Duchenne muscular dystrophy patients for aminoglycoside antibiotics therapy

A 2-bp deletion in exon 74 of the dystrophin gene does not clearly induce muscle weakness

Myoclonic Epilepsy With Ragged-Red Fibers Without Increased Lactate Levels

A Pediatric Case of ICOLQ/I-Related Congenital Myasthenic Syndrome with Marked Fatigue

Prediction of infectivity of SARS-CoV2: Mathematical model with analysis of docking simulation for spike proteins and angiotensin-converting enzyme 2

Clinical outcomes after long-term treatment with alglucosidase alfa in infants and children with advanced Pompe disease

In silico binding affinity of the spike protein with ACE2 and the relative evolutionary distance of S gene may be potential factors rapidly obtained for the initial risk of SARS-CoV-2

Muscle stem cells differentiate into haematopoietic lineages but retain myogenic potential

Estimation of muscle strength from actigraph data in D uchenne muscular dystrophy

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