1,056 results on '"Chang, Jan-Gowth"'
Search Results
2. #1779 Assessment of inflammation score in immune cells of atypical hemolytic uremic syndrome using single-cell sequencing analysis
3. Polygenic risk score trend and new variants on chromosome 1 are associated with male gout in genome-wide association study
4. Clinical application of liquid biopsy in cancer patients
5. Single-cell RNA sequencing of immune cells in patients with acute gout
6. Identification of 13 Novel Loci in a Genome-Wide Association Study on Taiwanese with Hepatocellular Carcinoma
7. Mutation profile of non-small cell lung cancer revealed by next generation sequencing
8. Fasting glucose-to-HbA1c ratio is a good indicator of G6PD deficiency, but not thalassemia, in patients with type 2 diabetes mellitus
9. Immune responses and safety of COVID-19 vaccination in atypical hemolytic uremic syndrome patients in Taiwan
10. A novel miRNA-based classification model of risks and stages for clear cell renal cell carcinoma patients
11. Comprehensive Analysis and Drug Modulation of Human Endogenous Retrovirus in Hepatocellular Carcinomas
12. Whole genome and RNA sequencing analyses for 254 Taiwanese hepatocellular carcinomas
13. Dysregulation of Immune Cell Subpopulations in Atypical Hemolytic Uremic Syndrome
14. Elucidating the Role of Immune Cell Dysregulation in Atypical Hemolytic Uremic Syndrome: A Comprehensive Single-Cell Sequencing Analysis
15. Identification of Key Prognosis-related microRNAs in Early- and Late- Stage Gynecological Cancers Based on TCGA Data
16. Metabolic Imaging Phenotype Using Radiomics of [18F]FDG PET/CT Associated with Genetic Alterations of Colorectal Cancer
17. Detection of Molecular Alterations in Taiwanese Patients with Medullary Thyroid Cancer Using Whole-Exome Sequencing
18. Correlation of genomic alterations between tumor tissue and circulating tumor DNA by next-generation sequencing
19. G6PD as a predictive marker for glioma risk, prognosis and chemosensitivity
20. Whole exome sequencing in Dandy-Walker variant with intellectual disability reveals an activating CIP2A mutation as novel genetic cause
21. Identification of most influential co-occurring gene suites for gastrointestinal cancer using biomedical literature mining and graph-based influence maximization
22. Highly Mimetic Ex Vivo Lung‐Cancer Spheroid‐Based Physiological Model for Clinical Precision Therapeutics
23. Supplementary Table 1 from Amiloride Modulates Alternative Splicing in Leukemic Cells and Resensitizes Bcr-AblT315I Mutant Cells to Imatinib
24. Data from Amiloride Modulates Alternative Splicing in Leukemic Cells and Resensitizes Bcr-AblT315I Mutant Cells to Imatinib
25. Supplementary Figure 1 from Amiloride Modulates Alternative Splicing in Leukemic Cells and Resensitizes Bcr-AblT315I Mutant Cells to Imatinib
26. Treatment of Spinal Muscular Atrophy by Sodium Butyrate
27. Whole exome sequencing identifies MAP3K1, MSH2, and MLH1 as potential cancer‐predisposing genes in familial early‐onset colorectal cancer.
28. Whole-Exome Sequencing Identifies Genetic Variants for Severe Adolescent Idiopathic Scoliosis in a Taiwanese Population
29. Integrated genomic analyses of hepatocellular carcinoma
30. Genetic alterations in endometrial cancer by targeted next-generation sequencing
31. Whole exome sequencing identifies MAP3K1, MSH2, and MLH1as potential cancer‐predisposing genes in familial early‐onset colorectal cancer
32. The expression signature of very long non-coding RNA in myalgic encephalomyelitis/chronic fatigue syndrome
33. Molecular Classification of Hepatocellular Carcinoma Using Wnt–Hippo Signaling Pathway-Related Genes
34. Exploring RNA modifications, editing, and splicing changes in hyperuricemia and gout
35. Comprehensive characterization of pharmacogenes in a Taiwanese Han population
36. Genome-wide association study of hyperthyroidism based on electronic medical record from Taiwan
37. Cancer carrier screening in the general population using whole‐genome sequencing
38. Genetic contributions to female gout and hyperuricemia using genome-wide association study and polygenic risk score analyses
39. A nine-gene signature identification and prognostic risk prediction for patients with lung adenocarcinoma using novel machine learning approach
40. Divergent Characteristics of T-Cell Receptor Repertoire Between Essential Hypertension and Aldosterone-Producing Adenoma
41. Analysis of Novel Variants Associated with Three Human Ovarian Cancer Cell Lines
42. Combined mutational analysis of RAS, BRAF, PIK3CA, and TP53 genes in Taiwanese patients with oral squamous cell carcinoma
43. lncRNAMap: A map of putative regulatory functions in the long non-coding transcriptome
44. CSNK1E/CTNNB1 Are Synthetic Lethal To TP53 in Colorectal Cancer and Are Markers for Prognosis
45. High-resolution melting analyses for genetic variants in ARID5B and IKZF1 with childhood acute lymphoblastic leukemia susceptibility loci in Taiwan
46. Rapid Screening for Deleted Form of β‐thalassemia by Real‐Time Quantitative PCR
47. Genetic contributions to female gout and hyperuricaemia using genome-wide association study and polygenic risk score analyses.
48. Next-generation sequencing profiling of mitochondrial genomes in gout
49. Mutation Analysis of Second Primary Tumors in Oral Cancer in Taiwanese Patients through Next-Generation Sequencing
50. Application of Whole Exome Sequencing and Functional Annotations to Identify Genetic Variants Associated with Marfan Syndrome
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