158 results on '"Cho, Eun Hae"'
Search Results
2. Deep learning model integrating cfDNA methylation and fragment size profiles for lung cancer diagnosis
3. Wearable quantum dots organic light-emitting diodes patch for high-power near infra-red photomedicene with real-time wavelength control
4. Integrative modeling of tumor genomes and epigenomes for enhanced cancer diagnosis by cell-free DNA
5. Impact of COVID-19 infection during the postoperative period in patients who underwent gastrointestinal surgery: a retrospective study
6. Recurrence Patterns and Risk Factors after Curative Resection for Colorectal Cancer: Insights for Postoperative Surveillance Strategies
7. Genetic heterogeneity and prognostic impact of recurrent ANK2 and TP53 mutations in mantle cell lymphoma: a multi-centre cohort study
8. Copy number aberrations in ctDNA enables prognosis prediction and molecular characterization of breast cancer
9. Different parental origins of supernumerary X chromosomes in brothers with Klinefelter syndrome: A case report
10. Genome-wide copy number alteration and VEGFA amplification of circulating cell-free DNA as a biomarker in advanced hepatocellular carcinoma patients treated with Sorafenib
11. Liquid biopsy using cfDNA to predict radiation therapy response in solid tumors
12. Carrier frequency of Wilson’s disease in the Korean population: a DNA-based approach
13. Shallow Whole-Genome Sequencing of Cell-Free DNA (cfDNA) Detects Epithelial Ovarian Cancer and Predicts Patient Prognosis
14. Plasma Circulating Cell-free DNA in Advanced Hepatocellular Carcinoma Patients Treated With Radiation Therapy
15. Development and performance evaluation of an artificial intelligence algorithm using cell-free DNA fragment distance for non-invasive prenatal testing (aiD-NIPT)
16. Copy number aberrations in circulating tumor DNA enables prognosis prediction and molecular characterization of breast cancer.
17. Kallmann syndrome with a Tyr113His PROKR2 mutation
18. Pharmacokinetics and Genetic Factors of Atorvastatin in Healthy Korean Subjects
19. Abstract PD6-07: Whole genome sequencing-based circulating tumor DNA profiling of metastatic breast cancer patients for molecular characterization and therapy response prediction
20. Targeted next generation sequencing of circulating tumor DNA provides prognostic information for management in breast cancer patients
21. Identification of the KCNJ2 Mutation in a Korean Family with Andersen-Tawil Syndrome and Developmental Delay
22. Genomic Instability of Circulating Tumor DNA as a Prognostic Marker for Pancreatic Cancer Survival: A Prospective Cohort Study
23. Aberrant Transcript Usage Is Associated with Homologous Recombination Deficiency and Predicts Therapeutic Response
24. Prenatal diagnosis of combined methylmalonic acidemia and homocystinuria cobalamin C type using clinical exome sequencing and targeted gene analysis
25. Acute promyelocytic leukemia with trisomy 8 showing normal PML-RARA FISH signal patterns: diagnostic application of long-distance polymerase chain reaction in molecularly discrepant leukemia cases
26. Detection of SET-NUP214 rearrangement using multiplex reverse transcriptase-polymerase chain reaction (RT-PCR) in acute leukemias: a case report and literature review on a Korean case series
27. A Population-Based Analysis of BRCA1/2 Genes and Associated Breast and Ovarian Cancer Risk in Korean Patients: A Multicenter Cohort Study
28. Case report of juvenile polyposis/hereditary hemorrhagic telangiectasia syndrome: first report in Korea with a novel mutation in the SMAD4 gene
29. Genomic analysis of a four-way t(4;11;22;10) associated with MLL-AF4 in an adult acute lymphoblastic leukemia
30. Association between acute lymphoblastic leukemia (ALL) and der(8;9)(q10;q10): a novel case of double der(8;9) in Ph+ adult B cell ALL
31. Simultaneous Detection of Gaucherʼs Disease and Renal Involvement of non-Hodgkinʼs Lymphoma: the First Asian Case Report and a Review of Literature
32. A Novel Three-Way Ph Variant t(8;9;22) in Adult Acute Lymphoblastic Leukemia
33. T-cell Acute Lymphoblastic Leukemia Associated with Complex Karyotype and SET-NUP214 Rearrangement: A Case Study and Review of the Literature
34. Exon splicing analysis of intronic variants in multigene cancer panel testing for hereditary breast/ovarian cancer
35. T-Cell Receptor Rearrangements Determined Using Fragment Analysis in Patients With T-Acute Lymphoblastic Leukemia
36. Novel Mutation (c.8725T>C) in Two Siblings With Late-Onset LAMA2-Related Muscular Dystrophy
37. Findings of a 1303 Korean whole-exome sequencing study
38. Different parental origins of supernumerary X chromosomes in brothers with Klinefelter syndrome: A case report.
39. Mutation profiling of 19 candidate genes in acute myeloid leukemia suggests significance of DNMT3A mutations
40. Identification of a HeterozygousSPG11Mutation by Clinical Exome Sequencing in a Patient With Hereditary Spastic Paraplegia: A Case Report
41. A Novel Case of Extreme Thrombocytosis in Acute Myeloid Leukemia Associated With Isochromosome 17q and Copy Neutral Loss of Heterozygosity
42. Identification of a Novel De Novo Variant in the PAX3 Gene in Waardenburg Syndrome by Diagnostic Exome Sequencing: The First Molecular Diagnosis in Korea
43. The First Korean Patient with Potocki-Shaffer Syndrome: A Rare Cause of Multiple Exostoses
44. Long-Term Follow-up Results after Imatinib Discontinuation in Chronic Myeloid Leukemia Patients with Undetectable Minimal Residual Disease
45. Rapid Sequential Gain of ABL1 Kinase Domain Mutations with a Complex Karyotype in the Progression of Chronic Myelogenous Leukemia
46. Atypical teratoid rhabdoid brain tumor in an infant with ring chromosome 22
47. Mowat–Wilson syndrome detected by using high resolution microarray
48. A Rare Case of Transformation of Childhood Myelodysplastic Syndrome to Acute Lymphoblastic Leukemia
49. Identification of Proteins Regulated by Ferulic Acid in a Middle Cerebral Artery Occlusion Animal Model-A Proteomics Approach
50. Letter to the Editor: Detection of EML4-ALK and Other ALK Fusion Genes in Lung Cancer: A Lesson from the Leukemia Fusion Gene Analysis and Future Application
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