Search Results - "Cho, Yong Gon"
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1
A loss function approach to group preference aggregation in the AHP
Published in Computers & operations research (01-03-2008)“…The Analytic Hierarchy Process is a useful method in aggregating group preference. However, judgments are frequently inconsistent, and, in reality, pairwise…”
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2
A novel variant of the POLR3A gene in a patient with hypomyelinating POLR3-related leukodystrophy
Published in Clinica chimica acta (01-08-2022)“…Hypomyelinating POLR3-related leukodystrophy is a group of rare neurological diseases characterized by degeneration of the white matter of the brain with…”
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3
Identification of a novel U2HR mutation in a Korean woman with Marie Unna hereditary hypotrichosis
Published in International journal of dermatology (01-11-2014)“…Marie Unna hereditary hypotrichosis (MUHH) is a rare autosomal dominant genodermatosis characterized by progressive non‐scarring hair loss. Mutation of the…”
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4
Isolation of EpCAM+/CD133− hepatic progenitor cells
Published in Molecules and cells (01-11-2013)“…Progenitor cell-derived hepatocytes are critical for hepatocyte replenishment. Therefore, we established a line of human hepatic progenitor (HNK1) cells and…”
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Diversity of Clinical and Molecular Characteristics in Korean Patients with 16p11.2 Microdeletion Syndrome
Published in International journal of molecular sciences (23-12-2023)“…16p11.2 copy number variations (CNVs) are increasingly recognized as one of the most frequent genomic disorders, and the 16p11.2 microdeletion exhibits broad…”
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6
Clinical and Genetic Characteristics of Early and Advanced Gastric Cancer
Published in Current issues in molecular biology (01-02-2024)“…Gastric cancer (GC) persists as the fourth most prevalent cause of global cancer-related mortality, presenting a challenge due to the scarcity of available…”
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7
SPA0355 prevents ovariectomy-induced bone loss in mice
Published in The Korean journal of physiology & pharmacology (31-01-2019)“…Estrogen withdrawal in post-menopausal women leads to overactivation of osteoclasts, which contributes to the development of osteoporosis. Inflammatory…”
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Accuracy Validation of the Elecsys HBsAg II Quant Assay and Its Utility in Resolving Equivocal Qualitative HBsAg Results
Published in Medicina (Kaunas, Lithuania) (23-02-2023)“…: There are reports of false qualitative HBsAg results, because of various causes, such as samples with low HBsAg concentrations that may produce false…”
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Copy number variation analysis using next-generation sequencing identifies the CFHR3/CFHR1 deletion in atypical hemolytic uremic syndrome: a case report
Published in Hematology (Luxembourg) (01-12-2022)“…OBJECTIVESAtypical hemolytic uremic syndrome (aHUS) is characterized by a triad of thrombocytopenia, microangiopathic hemolytic anemia, and acute renal failure…”
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A NOVEL C.800G>C VARIANT OF THE ITM2B GENE IN FAMILIAL KOREAN DEMENTIA
Published in IBRO neuroscience reports (01-10-2023)Get full text
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Clinical Features and Risk Factors Associated With 30-Day Mortality in Patients With Pneumonia Caused by Hypervirulent Klebsiella pneumoniae (hvKP)
Published in Annals of laboratory medicine (01-11-2020)“…Reports on metastatic or invasive infections by hypervirulent Klebsiella pneumoniae (hvKP) have increased recently. However, the effects of its virulence on…”
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The Korean undiagnosed diseases program phase I: expansion of the nationwide network and the development of long-term infrastructure
Published in Orphanet journal of rare diseases (08-10-2022)“…Phase I of the Korean Undiagnosed Diseases Program (KUDP), performed for 3 years, has been completed. The Phase I program aimed to solve the problem of…”
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13
Case Report: Novel Likely Pathogenic ACTN2 Variant Causing Heterogeneous Phenotype in a Korean Family With Left Ventricular Non-compaction
Published in Frontiers in pediatrics (30-03-2021)“…Left ventricular non-compaction (LVNC) is a very rare primary cardiomyopathy with a genetic etiology, resulting from the failure of myocardial development…”
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Case report: Compound heterozygosity in PKLR gene with a large exon deletion and a novel rare p.Gly536Asp variant as a cause of severe pyruvate kinase deficiency
Published in Frontiers in pediatrics (01-12-2022)“…Red cell pyruvate kinase (PK) deficiency is the most common cause of hereditary nonspherocytic hemolytic anemia and the most frequent enzyme abnormality of the…”
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Dermabacter jinjuensis sp. nov., a novel species of the genus Dermabacter isolated from a clinical specimen
Published in International journal of systematic and evolutionary microbiology (01-07-2016)“…A Gram-stain-positive, catalase-positive, facultatively anaerobic, non-motile, coryneform bacterium, designated strain 32 , was isolated from a closed pus…”
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A case of torsion of a mucinous cystadenoma in triple-X syndrome with pure gonadal dysgenesis
Published in Archives of gynecology and obstetrics (01-06-2006)“…Triple-X female characterized by primary amenorrhea and pure gonadal dysgenesis is extremely rare. We present a patient of triple-X syndrome who has not had…”
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Seroprevalence of Neutralizing Antibodies against Japanese Encephalitis Virus among Adolescents and Adults in Korea: A Prospective Multicenter Study
Published in Vaccines (Basel) (19-06-2020)“…The immunization schedule for the Japanese encephalitis (JE) vaccine in Korea is a two-dose primary series at 12-24 months of age, followed by booster doses 12…”
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18
MYC rearrangement involving a novel non-immunoglobulin chromosomal locus in precursor B-cell acute lymphoblastic leukemia
Published in Annals of laboratory medicine (01-07-2012)“…MYC rearrangement, a characteristic cytogenetic abnormality of Burkitt lymphoma and several subsets of other mature B-cell neoplasms, typically involves an…”
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A double mutation of the ryanodine receptor type 1 gene in a malignant hyperthermia family with multiminicore myopathy
Published in Journal of clinical neurology (Seoul, Korea) (01-09-2008)“…At least 100 Ryanodine receptor type 1 (RYR1) mutations associated with malignant hyperthermia (MH) and central core disease (CCD) have been identified, but 2…”
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20
Saeng-Ji-Hwang has a protective effect on adriamycin-induced cytotoxicity in cardiac muscle cells
Published in Life sciences (1973) (18-03-2005)“…This study examined the effect of Saeng-Ji-Hwang (SJH: Radix Rehmanniae) on cardiac muscle cells. Adriamycin-exposed H9C2 cardiac muscle cells were treated…”
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