421 results on '"Tsai, Shih-Feng"'
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2. Outbreak investigation in a COVID-19 designated hospital: The combination of phylogenetic analysis and field epidemiology study suggesting airborne transmission
3. Lymphocyte disturbance and functional assessment of the [Asp521Asn] ZAP70 mutation
4. Genetic Factors Contribute to the Phenotypic Variability in GJB2-Related Hearing Impairment
5. Digital health literacy and its determinants among community dwelling elderly people in Taiwan.
6. The signaling role of feedback in the repeated public goods game: Experimental evidence from the laboratory
7. Increased mcr-1 in pathogenic Escherichia coli from diseased swine, Taiwan
8. Epigenetic Enhancement of the Post-replicative DNA Mismatch Repair of Mammalian Genomes by a Hemi-mCpG-Np95-Dnmt1 Axis
9. Clinical and functional characterization of a novel STUB1 frameshift mutation in autosomal dominant spinocerebellar ataxia type 48 (SCA48)
10. Integration of genome-wide association study and expression quantitative trait locus mapping for identification of endometriosis-associated genes
11. Capsule deletion via a λ-Red knockout system perturbs biofilm formation and fimbriae expression in Klebsiella pneumoniae MGH 78578
12. HBV DNA Integration into Telomerase or MLL4 Genes and TERT Promoter Point Mutation as Three Independent Signatures in Subgrouping HBV-Related HCC with Distinct Features.
13. Multiple-omic data analysis of Klebsiella pneumoniae MGH 78578 reveals its transcriptional architecture and regulatory features
14. Fosmid library end sequencing reveals a rarely known genome structure of marine shrimp Penaeus monodon
15. Characterization of Severe Acute Respiratory Syndrome Coronavirus Genomes in Taiwan: Molecular Epidemiology and Genome Evolution
16. Construction and Analysis of a Human-Chimpanzee Comparative Clone Map
17. Wild-type p53 upregulates an early onset breast cancer-associated gene GAS7 to suppress metastasis via GAS7–CYFIP1-mediated signaling pathway
18. Gypsy Retrotransposon as a Tool for the in vivo Analysis of the Regulatory Region of the Optomotor-Blind Gene in Drosophila
19. Genomic profiling with whole‐exome sequencing revealed distinct mutations and novel pathways in Asian melanoma
20. Emergence and Persistent Dominance of Omicron BA.2.3.7 Variant in Community Outbreaks in Taiwan
21. Disclosing an In-Frame Deletion of the Titin Gene as the Possible Predisposing Factor of Anthracycline-Induced Cardiomyopathy: A Case Report
22. SitA contributes to the virulence of Klebsiella pneumoniae in a mouse infection model
23. Clinical Relevance of Plasma DNA Methylation in Colorectal Cancer Patients Identified by Using a Genome-Wide High-Resolution Array
24. High-Throughput Sequencing of Complementarity Determining Region 3 in the Heavy Chain of B-Cell Receptor in Renal Transplant Recipients: A Preliminary Report
25. EGFR Mutation-Harboring Lung Cancer Cells Produce CLEC11A with Endothelial Trophic and Tumor-Promoting Activities
26. A Clinical and Integrated Genetic Study of Isolated and Combined Dystonia in Taiwan
27. Artificial-Intelligence-Assisted Discovery of Genetic Factors for Precision Medicine of Antiplatelet Therapy in Diabetic Peripheral Artery Disease
28. Protein O-fucosyltransferase-1 mutation in familial Dowling-Degos Disease concomitant with atopic dermatitis
29. Diversity of Immunoglobulin Heavy Chain Repertoire in Patients With Rheumatoid Arthritis
30. Ectopic and high CXCL13 chemokine expression in myasthenia gravis with thymic lymphoid hyperplasia
31. Complex Movement Disorders in a Boy with PURA Syndrome
32. The Major Human Erythroid DNA-Binding Protein (GF-1): Primary Sequence and Localization of the Gene to the X Chromosome
33. Human Uroporphyrinogen III Synthase: Molecular Cloning, Nucleotide Sequence, and Expression of a Full-Length cDNA
34. Additional file 1 of Clinical and functional characterization of a novel STUB1 frameshift mutation in autosomal dominant spinocerebellar ataxia type 48 (SCA48)
35. Comparative Genomics of Vibrio vulnificus: Biology and Applications
36. Lymphocyte Disturbance in The [Asp521Asn] ZAP70 Mutation and An Overview of All Phenotype/Genotype
37. A cell-based high-throughput screen for epidermal growth factor receptor pathway inhibitors
38. Dysregulation of GIMAP genes in non-small cell lung cancer
39. Increased epidermal growth factor receptor ( EGFR) gene copy number is strongly associated with EGFR mutations and adenocarcinoma in non-small cell lung cancers: A chromogenic in situ hybridization study of 182 patients
40. Genetic Variants Associated With Phenytoin-Related Severe Cutaneous Adverse Reactions
41. Genetic diversity of capsular polysaccharide biosynthesis in Klebsiella pneumoniae clinical isolates
42. Genome sequencing and comparative analysis of Klebsiella pneumoniae NTUH-K2044, a strain causing liver abscess and meningitis
43. Association of the MSX2 gene polymorphisms with ankylosing spondylitis in Japanese
44. A common virulence plasmid in biotype 2 Vibrio vulnificus and its dissemination aided by a conjugal plasmid
45. Characterization of integrative and conjugative element ICEKp1-associated genomic heterogeneity in a Klebsiella pneumoniae strain isolated from a primary liver abscess
46. Tracing the Genetic Origins of Osteonecrosis of the Femoral Head
47. Diagnosis of Arboleda-Tham syndrome by whole genome sequencing in an Asian boy with severe developmental delay
48. Novel mutations involving the NF1 gene coding sequence in neurofibromatosis type 1 patients from Taiwan
49. Autosomal dominant avascular necrosis of femoral head in two Taiwanese pedigrees and linkage to chromosome 12q13
50. ALPK1 genetic regulation and risk in relation to gout
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