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Cytogenetic testing by fluorescence in situ hybridization is improved by plasma cell sorting in multiple myeloma.
- Published in:
- Scientific Reports, 2022, v. 12, n. 1, p. 1, doi. 10.1038/s41598-022-11676-w
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- Publication type:
- Article
The Genotype-Phenotype Correlation in Human 5α-Reductase Type 2 Deficiency: Classified and Analyzed from a SRD5A2 Structural Perspective.
- Published in:
- International Journal of Molecular Sciences, 2023, v. 24, n. 4, p. 3297, doi. 10.3390/ijms24043297
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- Publication type:
- Article
Development and validation of sensitive BCR::ABL1 fusion gene quantitation using next-generation sequencing.
- Published in:
- Cancer Cell International, 2023, v. 23, n. 1, p. 1, doi. 10.1186/s12935-023-02938-2
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- Publication type:
- Article
Optical genome mapping identifies clinically relevant genomic rearrangements in prostate cancer biopsy sample.
- Published in:
- Cancer Cell International, 2022, v. 22, n. 1, p. 1, doi. 10.1186/s12935-022-02728-2
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- Publication type:
- Article
Application of CRISPR/Cas9-based mutant enrichment technique to improve the clinical sensitivity of plasma EGFR testing in patients with non-small cell lung cancer.
- Published in:
- Cancer Cell International, 2022, v. 22, n. 1, p. 1, doi. 10.1186/s12935-022-02504-2
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- Publication type:
- Article
Clinical Application of Optical Genome Mapping for Molecular Diagnosis of Facioscapulohumeral Muscular Dystrophy.
- Published in:
- Annals of Laboratory Medicine, 2024, v. 44, n. 5, p. 437, doi. 10.3343/alm.2023.0437
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- Publication type:
- Article
NUP214 Rearrangements in Leukemia Patients: A Case Series From a Single Institution.
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- Annals of Laboratory Medicine, 2024, v. 44, n. 4, p. 335, doi. 10.3343/alm.2023.0301
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- Publication type:
- Article
Comparison of Optical Genome Mapping With Conventional Diagnostic Methods for Structural Variant Detection in Hematologic Malignancies.
- Published in:
- Annals of Laboratory Medicine, 2024, v. 44, n. 4, p. 324, doi. 10.3343/alm.2023.0339
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- Publication type:
- Article
Association Between Aortic Valve Sclerosis and Clonal Hematopoiesis of Indeterminate Potential.
- Published in:
- Annals of Laboratory Medicine, 2024, v. 44, n. 3, p. 279, doi. 10.3343/alm.2023.0268
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- Publication type:
- Article
Clinical Practice Guideline for Blood-based Circulating Tumor DNA Assays.
- Published in:
- Annals of Laboratory Medicine, 2024, v. 44, n. 3, p. 195, doi. 10.3343/alm.2023.0389
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- Publication type:
- Article
Development of a Next-generation Sequencing-based Gene Panel Test to Detect Measurable Residual Disease in Acute Myeloid Leukemia.
- Published in:
- Annals of Laboratory Medicine, 2023, v. 43, n. 4, p. 328, doi. 10.3343/alm.2023.43.4.328
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- Publication type:
- Article
A Case of STIL-TAL1-positive T-lymphoblastic Leukemia With a Minor Philadelphia-positive Clone.
- Published in:
- Annals of Laboratory Medicine, 2023, v. 43, n. 1, p. 100, doi. 10.3343/alm.2023.43.1.100
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- Publication type:
- Article
Rare Gene Rearrangement t(11;22)(q23;q13)/KMT2A-EP300 in Therapy-related Acute Myeloid Leukemia: A Case Report.
- Published in:
- Annals of Laboratory Medicine, 2022, v. 42, n. 6, p. 693, doi. 10.3343/alm.2022.42.6.693
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- Publication type:
- Article
Clinical Practice Guidelines for Pre-Analytical Procedures of Plasma Epidermal Growth Factor Receptor Variant Testing.
- Published in:
- Annals of Laboratory Medicine, 2022, v. 42, n. 2, p. 141, doi. 10.3343/alm.2022.42.2.141
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- Publication type:
- Article
Concomitant Diagnosis of Primary Bone Marrow B-Cell Non-Hodgkin Lymphoma and Essential Thrombocythemia: A Case Report.
- Published in:
- Annals of Laboratory Medicine, 2022, v. 42, n. 2, p. 282, doi. 10.3343/alm.2022.42.2.282
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- Publication type:
- Article
Deletion of 20p13 and Duplication of 20p13p12.3 in a Patient with Delayed Speech and Development.
- Published in:
- Annals of Laboratory Medicine, 2018, v. 38, n. 1, p. 77, doi. 10.3343/alm.2018.38.1.77
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- Publication type:
- Article
Detection of Immunoglobulin Heavy Chain Gene Clonality by Next-Generation Sequencing for Minimal Residual Disease Monitoring in B-Lymphoblastic Leukemia.
- Published in:
- Annals of Laboratory Medicine, 2017, v. 37, n. 4, p. 331, doi. 10.3343/alm.2017.37.4.331
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- Publication type:
- Article
Concomitant AID Expression and BCL7A Loss Associates With Accelerated Phase Progression and Imatinib Resistance in Chronic Myeloid Leukemia.
- Published in:
- 2017
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- Publication type:
- Case Study
Unraveling trajectories from aplastic anemia to hematologic malignancies: genetic and molecular insights.
- Published in:
- Frontiers in Oncology, 2024, p. 1, doi. 10.3389/fonc.2024.1365614
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- Publication type:
- Article
POU6F2, a novel fusion partner of NUP98 in acute myeloid leukaemia: A case report.
- Published in:
- British Journal of Haematology, 2024, v. 205, n. 4, p. 1632, doi. 10.1111/bjh.19678
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- Publication type:
- Article
Real‐world data on prognostic value of measurable residual disease assessment by fragment analysis or next‐generation sequencing in multiple myeloma.
- Published in:
- British Journal of Haematology, 2022, v. 198, n. 3, p. 503, doi. 10.1111/bjh.18211
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- Publication type:
- Article
Circulating Tumor DNA Reflects Histologic and Clinical Characteristics of Various Lymphoma Subtypes.
- Published in:
- Cancer Research & Treatment, 2024, v. 56, n. 1, p. 314, doi. 10.4143/crt.2023.667
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- Publication type:
- Article
Implication and Influence of Multigene Panel Testing with Genetic Counseling in Korean Patients with BRCA1/2 Mutation-Negative Breast Cancer.
- Published in:
- Cancer Research & Treatment, 2022, v. 54, n. 4, p. 1099, doi. 10.4143/crt.2021.978
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- Publication type:
- Article
SNP-based next-generation sequencing reveals low-level mixed chimerism after allogeneic hematopoietic stem cell transplantation.
- Published in:
- 2018
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- Publication type:
- clinical trial
Emergence of multidrug-resistant <italic>Providencia rettgeri</italic> isolates co-producing NDM-1 carbapenemase and PER-1 extended-spectrum β-lactamase causing a first outbreak in Korea.
- Published in:
- Annals of Clinical Microbiology & Antimicrobials, 2018, v. 17, n. 1, p. N.PAG, doi. 10.1186/s12941-018-0272-y
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- Publication type:
- Article
Next-Generation Sequencing in Korean Children With Autism Spectrum Disorder and Comorbid Epilepsy.
- Published in:
- Frontiers in Pharmacology, 2020, v. 11, p. 1, doi. 10.3389/fphar.2020.00585
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- Publication type:
- Article
Real-World Clinical Utility of Targeted RNA Sequencing in Leukemia Diagnosis and Management.
- Published in:
- Cancers, 2024, v. 16, n. 13, p. 2467, doi. 10.3390/cancers16132467
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- Publication type:
- Article
Circulating Tumor DNA Analysis on Metastatic Prostate Cancer with Disease Progression.
- Published in:
- Cancers, 2023, v. 15, n. 15, p. 3998, doi. 10.3390/cancers15153998
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- Publication type:
- Article
Exploring the Characteristics of Circulating Tumor DNA in Pt1a Clear Cell Renal Cell Carcinoma: A Pilot Study.
- Published in:
- Cancers, 2023, v. 15, n. 13, p. 3306, doi. 10.3390/cancers15133306
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- Publication type:
- Article
Performance Evaluation of New Automated Hepatitis B Viral Markers in the Clinical Laboratory.
- Published in:
- American Journal of Clinical Pathology, 2012, v. 137, n. 5, p. 769, doi. 10.1309/AJCP8QDN7NAUXJFJ
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- Publication type:
- Article
Exosome-based detection of EGFR T790M in plasma and pleural fluid of prospectively enrolled non-small cell lung cancer patients after first-line tyrosine kinase inhibitor therapy.
- Published in:
- Cancer Cell International, 2021, v. 21, n. 1, p. 1, doi. 10.1186/s12935-021-01761-x
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- Publication type:
- Article
Evaluation of an amplicon-based next-generation sequencing panel for detection of BRCA1 and BRCA2 genetic variants.
- Published in:
- Breast Cancer Research & Treatment, 2016, v. 158, n. 3, p. 433, doi. 10.1007/s10549-016-3891-z
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- Publication type:
- Article
A Comparative Study for Detection of EGFR Mutations in Plasma Cell-Free DNA in Korean Clinical Diagnostic Laboratories.
- Published in:
- BioMed Research International, 2018, v. 2018, p. 1, doi. 10.1155/2018/7392419
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- Publication type:
- Article
Genetic diagnosis of inborn errors of immunity using clinical exome sequencing.
- Published in:
- Frontiers in Immunology, 2023, p. 1, doi. 10.3389/fimmu.2023.1178582
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- Publication type:
- Article
Genetic diagnosis of inborn errors of immunity using clinical exome sequencing.
- Published in:
- Frontiers in Immunology, 2023, p. 1, doi. 10.3389/fimmu.2023.1178582
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- Publication type:
- Article
Correction: A novel association between relaxin receptor polymorphism and hematopoietic stem cell yield after mobilization.
- Published in:
- 2019
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- Publication type:
- Correction Notice
Common genes and recurrent causative variants in 957 Asian patients with pediatric epilepsy.
- Published in:
- Epilepsia (Series 4), 2024, v. 65, n. 3, p. 766, doi. 10.1111/epi.17857
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- Publication type:
- Article
Copy number variations and multiallelic variants in Korean patients with Leber congenital amaurosis.
- Published in:
- Molecular Vision, 2020, v. 26, p. 26
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- Publication type:
- Article
Analytical and Clinical Validation of Cell-Free Circulating Tumor DNA Assay for the Estimation of Tumor Mutational Burden.
- Published in:
- Clinical Chemistry, 2022, v. 68, n. 12, p. 1519, doi. 10.1093/clinchem/hvac146
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- Publication type:
- Article
Chimerism Assay Using Single Nucleotide Polymorphisms Adjacent and in Linkage- Disequilibrium Enables Sensitive Disease Relapse Monitoring after Hematopoietic Stem-Cell Transplantation.
- Published in:
- Clinical Chemistry, 2021, v. 67, n. 5, p. 781, doi. 10.1093/clinchem/hvab010
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- Publication type:
- Article
Genetic spectrum and characteristics of autosomal optic neuropathy in Korean: Use of next-generation sequencing in suspected hereditary optic atrophy.
- Published in:
- Frontiers in Neurology, 2022, v. 13, p. 1, doi. 10.3389/fneur.2022.978532
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- Publication type:
- Article
Copy‐number analysis by base‐level normalization: An intuitive visualization tool for evaluating copy number variations.
- Published in:
- Clinical Genetics, 2023, v. 103, n. 1, p. 35, doi. 10.1111/cge.14236
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- Publication type:
- Article
Diagnostic yield of targeted next-generation sequencing for pediatric hereditary hemolytic anemia.
- Published in:
- BMC Medical Genomics, 2023, v. 16, n. 1, p. 1, doi. 10.1186/s12920-023-01648-y
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- Publication type:
- Article
Diagnostic yield of targeted next-generation sequencing for pediatric hereditary hemolytic anemia.
- Published in:
- BMC Medical Genomics, 2023, v. 16, n. 1, p. 1, doi. 10.1186/s12920-023-01648-y
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- Publication type:
- Article
Clinical accuracy and utility of plasma microbial cell free DNA whole genome sequencing in the diagnosis of invasive aspergillosis in patients with hematologic malignancies or coronavirus disease.
- Published in:
- Infection & Chemotherapy, 2022, v. 54, p. 281
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- Publication type:
- Article
Genetic Analysis and Clinical Characteristics of Hereditary Pheochromocytoma and Paraganglioma Syndrome in Korean Population.
- Published in:
- Endocrinology & Metabolism, 2020, v. 35, n. 4, p. 858, doi. 10.3803/EnM.2020.683
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- Publication type:
- Article
Enhancing mutation detection in multiple myeloma with an error-corrected ultra-sensitive NGS assay without plasma cell enrichment.
- Published in:
- Cancer Cell International, 2024, v. 24, n. 1, p. 1, doi. 10.1186/s12935-024-03470-7
- By:
- Publication type:
- Article
Monitoring measurable residual disease in paediatric acute lymphoblastic leukaemia using immunoglobulin gene clonality based on next-generation sequencing.
- Published in:
- Cancer Cell International, 2024, v. 24, n. 1, p. 1, doi. 10.1186/s12935-024-03404-3
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- Publication type:
- Article
Comprehensive insights into AML relapse: genetic mutations, clonal evolution, and clinical outcomes.
- Published in:
- Cancer Cell International, 2024, v. 24, n. 1, p. 1, doi. 10.1186/s12935-024-03368-4
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- Publication type:
- Article
Altered Gut Microbiota and Shift in Bacteroidetes between Young Obese and Normal-Weight Korean Children: A Cross-Sectional Observational Study.
- Published in:
- BioMed Research International, 2020, p. 1, doi. 10.1155/2020/6587136
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- Publication type:
- Article