198 results on '"Chung, Ming-Yi"'
Search Results
2. Genome-wide analysis identified novel susceptible genes of restless legs syndrome in migraineurs
3. Immunogenicity and safety of homologous and heterologous ChAdOx1-S and mRNA-1273 vaccinations in healthy adults in Taiwan
4. Multicenter evaluation of four immunoassays for the performance of early diagnosis of COVID-19 and assessment of antibody responses of patients with pneumonia in Taiwan
5. Pseudocoloboma-like maculopathy with biallelicRDH12missense mutations
6. The interactions among organophosphate pesticide exposure, oxidative stress, and genetic polymorphisms of dopamine receptor D4 increase the risk of attention deficit/hyperactivity disorder in children
7. The association between the IL-4, ADRβ2 and ADAM 33 gene polymorphisms and asthma in the Taiwanese population
8. Epidemiologic and clinical features of non-polio enteroviral infections in northern Taiwan in 2008
9. P11 expression and PET in bipolar disorders
10. P11 (S100A10) as a potential biomarker of psychiatric patients at risk of suicide
11. Ossifying low grade endometrial stromal sarcoma with PHF1-BRD8 fusion
12. Phenotype Variability in the Patients of Familial Exudative Vitreoretinopathy: the RCBTB1 case
13. Seroprevalence Surveys for Anti-SARS-CoV-2 Antibody in Different Populations in Taiwan With Low Incidence of COVID-19 in 2020 and Severe Outbreaks of SARS in 2003
14. Imaging the serotonin transporter using 123I-ADAM in the human brain
15. Levels of the potential biomarker p11 in peripheral blood cells distinguish patients with PTSD from those with other major psychiatric disorders
16. Heme Oxygenase-1 Gene Promoter Polymorphism is Associated with Risk of Gastric Adenocarcinoma and Lymphovascular Tumor Invasion
17. CYP19 TCT Tri-Nucleotide Del/Del Genotype Is a Susceptibility Marker for Prostate Cancer in a Taiwanese Population
18. Impact of Circulating Free Tumor Cells in the Peripheral Blood of Colorectal Cancer Patients during Laparoscopic Surgery
19. Four point-of-care lateral flow immunoassays for diagnosis of COVID-19 and for assessing dynamics of antibody responses to SARS-CoV-2
20. Dynamics of anti-SARS-Cov-2 IgM and IgG antibodies among COVID-19 patients
21. Length polymorphisms of heme oxygenase-1 determine the effect of far-infrared therapy on the function of arteriovenous fistula in hemodialysis patients: a novel physicogenomic study
22. Mutations in KCND3 cause spinocerebellar ataxia type 22
23. Absence of mutations in human ubiquitin fusion-degradation protein gene in tetralogy of Fallot
24. Multicenter evaluation of two chemiluminescence and three lateral flow immunoassays for the diagnosis of COVID-19 and assessment of antibody dynamic responses to SARS-CoV-2 in Taiwan
25. Growth inhibitory effect of the human NIT2 gene and its allelic imbalance in cancers
26. Association between the IL-4 promoter polymorphisms and asthma or severity of hyperresponsiveness in Taiwanese
27. Frequent microsatellite alterations of chromosome locus 4q13.1 in oral squamous cell carcinomas
28. Functional genotype in matrix metalloproteinases-2 promoter is a risk factor for oral carcinogenesis
29. Correlation between functional genotypes in the matrix metalloproteinases-1 promoter and risk of oral squamous cell carcinomas
30. SCA19 and SCA22: evidence for one locus with a worldwide distribution
31. A novel autosomal dominant spinocerebellar ataxia (SCA22) linked to chromosome 1p21-q23
32. Mosaic or chimera? Revisiting an old hypothesis about the cause of the 46,XX/46,XY hermaphrodite
33. Systematic Mutation Analysis of the Catechol O-Methyltransferase Gene as a Candidate Gene for Schizophrenia
34. Prevalence and Parental Origin in Tetralogy of Fallot Associated With Chromosome 22q11 Microdeletion
35. Dimethylarginine Dimethylaminohydrolase 1 Polymorphisms and Venous Intimal Hyperplasia in Hemodialysis Patients
36. The association of dimethylarginine dimethylaminohydrolase 1 gene polymorphism with type 2 diabetes: a cohort study
37. SARS exposure and emergency department workers
38. Associations between urinary total arsenic levels, fetal development, and neonatal birth outcomes: A cohort study in Taiwan
39. Genome-wide association study identifies novel susceptibility loci for migraine in Han Chinese resided in Taiwan
40. Modulation of formation of the 3’-end of the human argininosuccinate synthetase mRNA by GT-repeat polymorphism
41. Susceptible genes of restless legs syndrome in migraine
42. Sugar-Sweetened Beverage Consumption Is Adversely Associated with Childhood Attention Deficit/Hyperactivity Disorder
43. Association of Genetic Polymorphisms of Renin–Angiotensin–Aldosterone System-Related Genes with Arterio-Venous Fistula Malfunction in Hemodialysis Patients
44. Attention Deficit/Hyperactivity Disorder and Urinary Nonylphenol Levels: A Case-Control Study in Taiwanese Children
45. Haploinsufficiency ofRCBTB1is associated with Coats disease and familial exudative vitreoretinopathy
46. Genotype polymorphisms of genes regulating nitric oxide synthesis determine long-term arteriovenous fistula patency in male hemodialysis patients
47. Asymmetric dimethylarginine and long-term adverse cardiovascular events in patients with type 2 diabetes: relation with the glycemic control
48. Gene Polymorphisms of Interleukin-10 and Tumor Necrosis Factor-α Are Associated with Contrast-Induced Nephropathy
49. Genotype polymorphisms of genes regulating nitric oxide synthesis determine long-term arteriovenous fistula patency in male hemodialysis patients.
50. Asymmetric dimethylarginine predicts clinical outcomes in ischemic chronic heart failure
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