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Presentation
(Last updated : 2024-09-20 11:38:30)
Yutaka Osawa
Department
Kawasaki Medical School Kawasaki Medical School, Department of Neurology,
Position
Associate Professor with Special Assignment
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Journal
1.
2023/05/01
Becker Muscular Dystrophy Accompanied by Anti-HMGCR Antibody-positive Immune-mediated Necrotizing Myopathy.
2.
2023/05
Circulating α-Klotho Counteracts Transforming Growth Factor-β-Induced Sarcopenia.
3.
2023/04
Alterations of ATG4A and LC3B in neurons derived from Alzheimer's disease patients.
4.
2022/11
Caveolin 3 suppresses phosphorylation-dependent activation of sarcolemmal nNOS.
5.
2022/10
Maximal Multistage Shuttle Run Test-induced Myalgia in a Patient with Muscle Phosphorylase B Kinase Deficiency.
6.
2022/04/15
Maximal Multistage Shuttle Run Test-induced Myalgia in a Patient with Muscle Phosphorylase B Kinase Deficiency
7.
2019/05
Taurine supplementation for prevention of stroke-like episodes in MELAS: a multicentre, open-label, 52-week phase III trial.
8.
2018/01
Proteinuria in neuronal intranuclear inclusion disease
9.
2017/12
A simplified and sensitive method to identify Alzheimer's disease biomarker candidates using patient-derived induced pluripotent stem cells (iPSCs)
10.
2017/10
Clinical and pathological findings in familial amyloid polyneuropathy caused by a transthyretin E61K mutation.
11.
2017/07
Slow-Myofiber Commitment by Semaphorin 3A Secreted from Myogenic Stem Cells.
12.
2016/10
Calcium dysregulation contributes to neurodegeneration in FTLD patient iPSC-derived neurons.
13.
2015/02
Identification of the minimum Peptide from mouse myostatin prodomain for human myostatin inhibition.
14.
2015/01
A Second Pedigree with Amyloid-less Familial Alzheimer's Disease Harboring an Identical Mutation in the Amyloid Precursor Protein Gene (E693delta).
15.
2013/05
Local Applications of Myostatin-siRNA with Atelocollagen Increse Skeletal Muscle Mass and Recovery of Muscle Function
16.
2012/12
Taurine Ameliorates Impaired the Mitochondrial Function and Prevents Stroke-like Episodes in Patients with MELAS
17.
2012/10
Muscle-specific overexpression of caveolin 3 causes muscle atrophy, but not muscular dystrophy
18.
2012/08
An inhibitor of transforming growth factor beta type I receptor ameliorates muscle atrophy in a mouse model of caveolin 3-deficient muscular dystrophy
19.
2011/05
Endoplasmic reticulum stress response in P104L mutant caveolin-3 transgenic mice
20.
2011/03
Follistatin-derived peptide expression in muscle decreases adipose tissue mass and prevents hepatic steatosis
21.
2011/01
Atelocollagen-mediated systemic administration of myostatin-targeting siRNA improves muscular atrophy in caveolin-3-deficient mice
22.
2010/12
Rapid Screening for Japanese Dysferlinopathy by Fluorescent Primer Extension
23.
2010/08
The transthyretin gene is expressed in Schwann cells of peripheral nerves
24.
2010/04
Hereditary sensory ataxic neuropathy associated with proximal muscle weakness in the lower extremities
25.
2008/11
Caveolin-3 regulates myostatin signaling. Mini-review
26.
2008/08
Atelocollagen-mediated local and systemic applications of myostatin-targeting siRNA increase skeletal muscle mass.
27.
2008/05
The transthyretin gene is expressed in human and rodent dorsal root ganglia.
28.
2006/11
Muscular atrophy of caveolin-3-deficient mice is rescued by myostatin inhibition.
29.
2006/08
Bone marrow transplantation improves outcom in a mouse model of congenital muscular dystrophy.
30.
2006/08
Peripheral myelin protein 22 is expressed in human central nervous system.
31.
2005/08
Reduced amplitude of the sural nerve sensory action potential in PARK2 patients.
32.
2005
Is low SNAP amplitude in the sural nerve a useful diagnostic marker of PARK2 patient?
33.
2004/09
Skeletal muscle hyperplasia in the transgenic mice overexpressing the myostatin prodomain
34.
2004/01
Overexpression of P104L mutant caveolin-3 in mice develops hypertrophic cardiomyopathy with enhanced contractility in association with increased endothelial nitric oxide synthase activity.
35.
2004
Restration of a myopathic phenotype of mutant caveolin-3 transgenic mice by crossing with mutant myostatin transgenic mice
36.
2003/10
Conduction block of varicella zoster virus neuropathy
37.
2001
Caveolin-3 and muscular dystrophy
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Presentation
1.
2024/09/13
Caveolin 3 inhibits phosphorylation-dependent activation of sarcolemmal nNOS (口頭,一般)
2.
2024/05/30
Circulating alpha-Klotho counteracts TGF-beta-induced sarcopeniaAlpha beta (口頭,シンポジウム・ワークショップ パネル(指名))
3.
2023/06/02
Circulating alpha-Klotho combats TGF-beta-induced sarcopenia (口頭,一般)
4.
2022/05/19
nNOS activation in the pathogenesis of caveolin-3-deficient limb-girdle muscular dystrophy 1C. (ポスター掲示,一般)
5.
2022/05/18
A stapled myostatin inhibitory core peptide: its effect on caveolin-3- or dystrophin-deficient mice. (口頭,一般)
6.
2021/05/22
Molecular crosstalk between caveolin 3 and nNOS: implications for Limb-girdle muscular dystrophy 1C (口頭,一般)
7.
2021/05/21
Regulation of nNOS by Caveolin 3: Implications in the Pathogenesis Leading to LGMD1C. (ポスター掲示,一般)
8.
2021/05/21
Therapeutic effects of an optimized myostatin inhibitory peptide. (口頭,一般)
9.
2020/09/02
Caveolin 3 suppresses activation of sarcolemmal nNOS: implications in the pathogenesis of LGMD1C (口頭,一般)
10.
2018/06/04
Taurine supplementation prevents stroke-like episodes in MELAS,the first-ever tRNA modification disorder (ポスター掲示,一般)
11.
2017/11/05
The Effect of Myostatin Inhibition on Bone Loss in Murine Osteoporosis Models (ポスター掲示,一般)
12.
2017/11/05
The effect of myostatin inhibition on bone loss in murine osteoporosis models. (ポスター掲示,一般)
13.
2017/09/20
CAVEOLIN-3 CONTROLS SARCOLEMMAL nNOS ACTIVITY: IMPLICATION IN LIMB-GIRDLE MUSCULAR DYSTROPHY 1C (ポスター掲示,一般)
14.
2017/09/19
The inhibitory core of myostatin prodomain: its suppression of ligand-receptor binding and potential for muscle wasting disorders. (ポスター掲示,一般)
15.
2016/10
MELAS, a first-ever tRNA modification disorder is alleviated by taurine supplimentation therapy (ポスター掲示,一般)
16.
2016/09/10
Hetreditary sensory ataxic neuropathy associated with proximal muscle weakness in the lower extremities: a new clinical entity? (口頭,一般)
17.
2015/10/04
Taurine supplemental therapy in prevention of stroke-like episodes in MELAS
18.
2013/09/22
Taurine ameliorates mitochondrial dysfunction and prevents stroke-like episodes in patients with MELAS (ポスター掲示,一般)
19.
2012/09/07
Regulation of caveolin-3 in myogenesis and muscular atrophy through type I TGF-beta receptor kinase. (ポスター掲示,一般)
20.
2012/08/16
Caveolin-3 controls satellite cells and myoblasts through type I TGF-beta receptor kinase (口頭,一般)
21.
2012/06/07
Roles of the caveolin-3-transforming gowth factor-beta axis in skeletal myogenesis and muscle atrophy. (口頭,一般)
22.
2011/12/02
プロセシング酵素Furinの機能阻害とMyf5陽性筋細胞の動態 (口頭)
23.
2011/11/19
Transthyretin gene expression in Schwann cells of peripheral nerves (口頭,一般)
24.
2011/09/19
Sarcolemmal nNOS prevents muscular wasting in a caveolin-3-deficient limb-girdle muscular dystrophy 1C model (口頭,一般)
25.
2011/09/18
Sarcolemmal nNOS prevents muscular wasting in a caveolin-3 deficient limb-girdle muscular dystrophy 1C model. (口頭,一般)
26.
2011/09/18
Sarcolemmal nNOS prevents muscular wasting in a caveolin-3-deficient limb-girdle muscular dystrophy 1C model (ポスター掲示,一般)
27.
2011/09/18
Wnt signalling acts as a switch controlling myoblast cell proliferation and differentiation (ポスター掲示,一般)
28.
2010/10/14
Reprogrammed fibroblasts as a feasible source of cell-based therapy for muscular dystrophy (ポスター掲示,一般)
29.
2010/10/13
A novel homozygous mutation of selenoprotein gene causes rigid spine syndorome with muscular dystrophy (ポスター掲示,一般)
30.
2010/10
Reprogrammed fibroblasts as a feasible source of cell-based therapy for muscular dystrophy. (口頭,一般)
31.
2010/07/21
Wound-healing MRL-MpJ phenotype improves outcome of dystrophin deficient
mdx
mice. (口頭,一般)
32.
2010/07/18
Reprogrammed fibroblats are a source of cell therapy for caveolin-3-deficient and laminin α-2-deficient muscular dystrophies (口頭,一般)
33.
2010/06/28
Transthyretin gene expression in dorsal root ganglia:where in it? (口頭)
34.
2009/09/11
Introduction of wound-healing MRL-MpJ phenotype improves skeletal muscle pathology in mdx mouse. (ポスター掲示,一般)
35.
2009/09
Introduction of wound-healing MRL-MpJ phenotype improves skeletal muscle pathology in mdx mouse. (口頭,一般)
36.
2009/07/04
Muscle mass regulation by myostatin-signaling related molecules (口頭,シンポジウム・ワークショップ パネル(その他))
37.
2009/07/04
Myostatin blockade therapy for muscular dystrophy. (口頭,一般)
38.
2008/10/01
A small-molecule inhibitor targeting transforming growth factor-b type Ⅰ receptor kinase ameliorate muscular atrophy in a mouse model of caveolin-3-deficient muscular dystrophy. (口頭,一般)
39.
2007/10/17
Myostatin inhibition increases atrogin-1 expression and accelerates skeletal muscle atrophy under denervated conditions. (ポスター掲示,一般)
40.
2007/07/14
Myostatin inhibition reverses satellite cell number in caveolin-3-deficient mouse muscle. (ポスター掲示,一般)
41.
2007/07/14
Therapeutic effects of small-molecule inhibitors of type I TGF-b receptors for the treatment of muscular dystrophy. (ポスター掲示,一般)
42.
2007/06/08
Inhibition of myostatin signaling through type I and type II myostatin receptors. (口頭,一般)
43.
2006/10/04
Bone marrow transplantation improves outcome in a mouse model of congenital muscular dystrohy (ポスター掲示,一般)
44.
2006/10/04
Molecular pathogenesis of caveolinopathy in a mouse model of LGMD1C (口頭,一般)
45.
2006/10/04
MRL/MpJ wound-healing phenotype increases the myofiber size in mdx mouse skeletal muscle (ポスター掲示,一般)
46.
2006/07/04
Myostatin inhibition can delay the onset of muscle weakness in a mouse model of amyotrophic lateral sclerosis. (口頭,一般)
47.
2005/06/25
Dramatic reversal of muscular atrophy in caveolinopathy by myostatin blockade (ポスター掲示,一般)
48.
2005/02/02
Is low SNAP amplitude in the sural nerve a useful diagnostic marker of PARK2 patient? (ポスター掲示,一般)
49.
2004/10/04
Expression of Peripheral Myelin Protein 22 in Human Central Nervous System (ポスター掲示,一般)
50.
2004/06/14
Reduced sural sensory nerve action potential (SNAP) amplitude as a possible diagnostic indicator of autosomal recessive juvenile parkinsonism (ポスター掲示,一般)
51.
2003/09/03
Non-transcriptional activation of nitric oxide synthase induces hypertrophic cardiomyopathy with enhanced contractility in the P104L mutant caveolin-3 transgenic mice (ポスター掲示,一般)
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