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A Comparative Investigation of the Bile Microbiome in Patients with Choledocholithiasis and Cholecystolithiasis through Metagenomic Analysis

International journal of molecular sciences, 2024-03, Vol.25 (6), p.3297

2024

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Molecular approaches for the detection and monitoring of microbial communities in bioaerosols：A review

Journal of environmental sciences (China), 2017, Vol.51 (1), p.234-247

2017

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Paternally Inherited Noonan Syndrome Caused by a PTPN11 Variant May Exhibit Mild Symptoms: A Case Report and Literature Review

Genes, 2024-04, Vol.15 (4), p.445

2024

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What we can see from very small size sample of metagenomic sequences

BMC bioinformatics, 2018-11, Vol.19 (1), p.399-399, Article 399

2018

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Improving the Yield of Genetic Diagnosis through Additional Genetic Panel Testing in Hereditary Ophthalmic Diseases

Current issues in molecular biology, 2024-05, Vol.46 (5), p.5010-5022

2024

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Novel compound heterozygous mutations in SCN4A as a potential genetic cause contributing to myopathic manifestations: A case report and literature review

Heliyon, 2024-04, Vol.10 (7), p.e28684, Article e28684

2024

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Exploring the antibiotic resistome in activated sludge and anaerobic digestion sludge in an urban wastewater treatment plant via metagenomic analysis

The Journal of Microbiology, 2020, 58(2), , pp.123-130

2020

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Classification and Regression Tree Approach for Prediction of Potential Hazards of Urban Airborne Bacteria during Asian Dust Events

Scientific reports, 2018-08, Vol.8 (1), p.11823-11, Article 11823

2018

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The First Korean Case with Cardiac, Facial, and Digital Anomalies with Developmental Delay Caused by De Novo TRAF7 p.Arg655Gln Variant

International journal of molecular sciences, 2024-04, Vol.25 (7), p.3701

2024

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Diversity of Clinical and Molecular Characteristics in Korean Patients with 16p11.2 Microdeletion Syndrome

International journal of molecular sciences, 2023-12, Vol.25 (1), p.253

2023

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Radiofrequency Irradiation Modulates TRPV1-Related Burning Sensation in Rosacea

Molecules (Basel, Switzerland), 2021-03, Vol.26 (5), p.1424

2021

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Miyoshi Muscular Dystrophy Type 1 with Mutated DYSF Gene Misdiagnosed as Becker Muscular Dystrophy: A Case Report and Literature Review

Genes, 2023-01, Vol.14 (1), p.200

2023

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Anaerobic oxidation of methane coupled with extracellular electron transfer to electrodes

Scientific reports, 2017-07, Vol.7 (1), p.5099-9, Article 5099

2017

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Comparison of In Silico Tools for Splice-Altering Variant Prediction Using Established Spliceogenic Variants: An End-User’s Point of View

International journal of genomics, 2022-10, Vol.2022, p.1-6

2022

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Microbial Analysis in Primary and Persistent Endodontic Infections by Using Pyrosequencing

Journal of endodontics, 2013-09, Vol.39 (9), p.1136-1140

2013

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Intergenerational Influence of Gender and the DM1 Phenotype of the Transmitting Parent in Korean Myotonic Dystrophy Type 1

Genes, 2022-08, Vol.13 (8), p.1465

2022

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Clinical and Genetic Characteristics of Early and Advanced Gastric Cancer

Current issues in molecular biology, 2024-02, Vol.46 (2), p.1208-1218

2024

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A Recurrent De Novo Terminal Duplication of 14q32 in Korean Siblings Associated with Developmental Delay and Intellectual Disability, Growth Retardation, Facial Dysmorphism, and Cerebral Infarction: A Case Report and Literature Review

Genes, 2021-09, Vol.12 (9), p.1388

2021

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Variable Phenotypes of Epilepsy, Intellectual Disability, and Schizophrenia Caused by 12p13.33-p13.32 Terminal Microdeletion in a Korean Family: A Case Report and Literature Review

Genes, 2021-06, Vol.12 (7), p.1001

2021

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Clinical Evaluation of BioFire COVID-19 Test, BioFire Respiratory Panel 2.1, and Cepheid Xpert Xpress SARS-CoV-2 Assays for Sample-to-Answer Detection of SARS-CoV-2

Genes, 2023-01, Vol.14 (1), p.233

2023

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Diagnostic approaches for inherited hemolytic anemia in the genetic era

Blood Research, 2017, 52(2), , pp.84-94

2017

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Phenotypic Diversity of 15q11.2 BP1-BP2 Deletion in Three Korean Families with Development Delay and/or Intellectual Disability: A Case Series and Literature Review

Diagnostics (Basel), 2021-04, Vol.11 (4), p.722

2021

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Circulating Respiratory Syncytial Virus Genotypes and Genetic Variability of the G Gene during 2017 and 2018/2019 Seasonal Epidemics Isolated from Children with Lower Respiratory Tract Infections in Daejeon, Korea

Journal of Korean Medical Science, 2020, 35(49), , pp.1-13

2020

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Seizure duration may increase thyroid-stimulating hormone levels in children experiencing a seizure

Journal of international medical research, 2020-05, Vol.48 (5), p.300060519888401-300060519888401

2020

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Rare Occurrence of Microsatellite Instability in Gastrointestinal Stromal Tumors

Medicina (Kaunas, Lithuania), 2021-02, Vol.57 (2), p.174

2021

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A Comparative Investigation of the Bile Microbiome in Patients with Choledocholithiasis and Cholecystolithiasis through Metagenomic Analysis

Molecular approaches for the detection and monitoring of microbial communities in bioaerosols：A review

Paternally Inherited Noonan Syndrome Caused by a PTPN11 Variant May Exhibit Mild Symptoms: A Case Report and Literature Review

What we can see from very small size sample of metagenomic sequences

Improving the Yield of Genetic Diagnosis through Additional Genetic Panel Testing in Hereditary Ophthalmic Diseases

Novel compound heterozygous mutations in SCN4A as a potential genetic cause contributing to myopathic manifestations: A case report and literature review

Exploring the antibiotic resistome in activated sludge and anaerobic digestion sludge in an urban wastewater treatment plant via metagenomic analysis

Classification and Regression Tree Approach for Prediction of Potential Hazards of Urban Airborne Bacteria during Asian Dust Events

The First Korean Case with Cardiac, Facial, and Digital Anomalies with Developmental Delay Caused by De Novo TRAF7 p.Arg655Gln Variant

Diversity of Clinical and Molecular Characteristics in Korean Patients with 16p11.2 Microdeletion Syndrome

Radiofrequency Irradiation Modulates TRPV1-Related Burning Sensation in Rosacea

Miyoshi Muscular Dystrophy Type 1 with Mutated DYSF Gene Misdiagnosed as Becker Muscular Dystrophy: A Case Report and Literature Review

Anaerobic oxidation of methane coupled with extracellular electron transfer to electrodes

Comparison of In Silico Tools for Splice-Altering Variant Prediction Using Established Spliceogenic Variants: An End-User’s Point of View

Microbial Analysis in Primary and Persistent Endodontic Infections by Using Pyrosequencing

Intergenerational Influence of Gender and the DM1 Phenotype of the Transmitting Parent in Korean Myotonic Dystrophy Type 1

Clinical and Genetic Characteristics of Early and Advanced Gastric Cancer

A Recurrent De Novo Terminal Duplication of 14q32 in Korean Siblings Associated with Developmental Delay and Intellectual Disability, Growth Retardation, Facial Dysmorphism, and Cerebral Infarction: A Case Report and Literature Review

Variable Phenotypes of Epilepsy, Intellectual Disability, and Schizophrenia Caused by 12p13.33-p13.32 Terminal Microdeletion in a Korean Family: A Case Report and Literature Review

Clinical Evaluation of BioFire COVID-19 Test, BioFire Respiratory Panel 2.1, and Cepheid Xpert Xpress SARS-CoV-2 Assays for Sample-to-Answer Detection of SARS-CoV-2

Diagnostic approaches for inherited hemolytic anemia in the genetic era

Phenotypic Diversity of 15q11.2 BP1-BP2 Deletion in Three Korean Families with Development Delay and/or Intellectual Disability: A Case Series and Literature Review

Circulating Respiratory Syncytial Virus Genotypes and Genetic Variability of the G Gene during 2017 and 2018/2019 Seasonal Epidemics Isolated from Children with Lower Respiratory Tract Infections in Daejeon, Korea

Seizure duration may increase thyroid-stimulating hormone levels in children experiencing a seizure

Rare Occurrence of Microsatellite Instability in Gastrointestinal Stromal Tumors

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