Search Results - "Seong Dae Kim"
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Mesenchymal stem cells in suppression or progression of hematologic malignancy: current status and challenges
Published in Leukemia (01-03-2019)“…Mesenchymal stem cells (MSCs) are known for being multi-potent. However, they also possess anticancer properties, which has prompted efforts to adapt MSCs for…”
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Expanding the Therapeutic Window of EGFR-Targeted PE24 Immunotoxin for EGFR-Overexpressing Cancers by Tailoring the EGFR Binding Affinity
Published in International journal of molecular sciences (13-12-2022)“…Immunotoxins (ITs), which are toxin-fused tumor antigen-specific antibody chimeric proteins, have been developed to selectively kill targeted cancer cells. The…”
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3
Simultaneous measurement of the size and methylation of chromosome 4qA-D4Z4 repeats in facioscapulohumeral muscular dystrophy by long-read sequencing
Published in Journal of translational medicine (08-11-2022)“…Facioscapulohumeral muscular dystrophy (FSHD) is an autosomal dominant muscular disorder characterized by asymmetric muscle wasting and weakness. FSHD can be…”
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4
Novel Strategy for the Formulation of High‐Energy‐Density Cathodes via Porous Carbon for Li‐S Batteries
Published in ChemSusChem (19-05-2023)“…Porous carbon is considered an attractive host material for high‐energy sulfur electrodes. This study concerns the design of a porous carbon‐based sulfur…”
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Understanding Hidden Risks from Disasters: Cases of Hurricane Katrina and Fukushima Nuclear Meltdown
Published in Journal of management in engineering (01-09-2017)“…AbstractRisks or uncertainties have been characterized in many ways and are fairly well understood, but hidden risks have been underemphasized. This study…”
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Genetic Variants Associated with Episodic Ataxia in Korea
Published in Scientific reports (23-10-2017)“…Episodic ataxia (EA) is a rare neurological condition characterized by recurrent spells of truncal ataxia and incoordination. Five genes ( KCNA1 , CACNA1A ,…”
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Myasthenia gravis seronegative for acetylcholine receptor antibodies in South Korea: Autoantibody profiles and clinical features
Published in PloS one (08-03-2018)“…Acquired myasthenia gravis (MG) is a prototype autoimmune disease of the neuromuscular junction, caused in most patients by autoantibodies to the muscle…”
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Characterization of congenital myopathies at a Korean neuromuscular center
Published in Muscle & nerve (01-08-2018)“…ABSTRACT Introduction: Congenital myopathies are muscle diseases characterized by specific histopathologic features, generalized hypotonia from birth, and…”
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9
Comparison of Diagnostic Performances Between Cerebrospinal Fluid Biomarkers and Amyloid PET in a Clinical Setting
Published in Journal of Alzheimer's disease (01-01-2020)“…The diagnostic performances of cerebrospinal fluid (CSF) biomarkers and amyloid positron emission tomography (PET) were compared by examining the association…”
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Body Distribution of Inhaled Fluorescent Magnetic Nanoparticles in the Mice
Published in Journal of Occupational Health (2008)“…Body Distribution of Inhaled Fluorescent Magnetic Nanoparticles in the Mice:Jung-Taek KWON, et al. Laboratory of Toxicology, College of Veterinary Medicine,…”
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Atypical clinical manifestations of Miller Fisher syndrome
Published in Neurological sciences (2019)“…Miller Fisher syndrome (MFS) is characterized by a clinical triad of ophthalmoplegia, ataxia, and areflexia, and is closely associated with serum anti-GQ1b…”
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Myofibrillar myopathy caused by a novel FHL1 mutation presenting a mild myopathy with ankle contracture
Published in Clinical neurology and neurosurgery (01-05-2019)“…•We report a case with FHL1 myopathy with mild weakness with ankle contracture.•This case is at an extreme end of phenotypic spectrum of FHL1 myopathy.•The…”
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Long‐term therapy with clevudine for chronic hepatitis B can be associated with myopathy characterized by depletion of mitochondrial DNA
Published in Hepatology (Baltimore, Md.) (01-06-2009)“…Clevudine (Revovir), a pyrimidine nucleoside analogue, is a recently introduced antiviral drug. Clinical trials have demonstrated potent, sustained antiviral…”
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NEB‐related core‐rod myopathy with distinct clinical and pathological features
Published in Muscle & nerve (01-03-2016)“…ABSTRACT Introduction: Mutations in the gene encoding nebulin (NEB) are known to cause several types of congenital myopathy including recessive nemaline…”
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Functional recovery of a novel knockin mouse model of dysferlinopathy by readthrough of nonsense mutation
Published in Molecular therapy. Methods & clinical development (11-06-2021)“…Biallelic mutations in the dysferlin gene cause limb-girdle muscular dystrophy 2B or Miyoshi distal myopathy. We found that nonsense mutations are the most…”
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Targeted population screening of late onset pompe disease in unspecified myopathy patients for korean population
Published in Neuromuscular disorders : NMD (01-06-2017)“…Highlights • We performed first targeted population screening of LOPD for Asian population. • We found 2 LOPD patients and 14 false positive patients with…”
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Meralgia paresthetica caused by a pancreatic pseudocyst
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18
Clinical practice with steroid therapy for Duchenne muscular dystrophy: An expert survey in Asia and Oceania
Published in Brain & development (Tokyo. 1979) (01-03-2020)“…Several studies on clinical practice for Duchenne muscular dystrophy (DMD) have been conducted in Western countries. However, there have been only a few…”
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Nogo-A Is Critical for Pro-Inflammatory Gene Regulation in Myocytes and Macrophages
Published in Cells (Basel, Switzerland) (31-01-2021)“…Nogo-A (Rtn 4A), a member of the reticulon 4 (Rtn4) protein family, is a neurite outgrowth inhibitor protein that is primarily expressed in the central nervous…”
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Schisandrae fructus enhances myogenic differentiation and inhibits atrophy through protein synthesis in human myotubes
Published in International journal of nanomedicine (01-01-2016)“…Schisandrae fructus (SF) has recently been reported to increase skeletal muscle mass and inhibit atrophy in mice. We investigated the effect of SF extract on…”
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