185 results on '"Fan, Wen‐Lang"'
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2. Phenotype, genotype, and clinical outcome of Taiwanese with congenital nephrotic syndrome
3. The abundances of LTF and SOD2 in amniotic fluid are potential biomarkers of gestational age and preterm birth
4. Author Correction: The abundances of LTF and SOD2 in amniotic fluid are potential biomarkers of gestational age and preterm birth
5. Contribution of genetic variants associated with primary immunodeficiencies to childhood-onset systemic lupus erythematous
6. Association of ITPKB, IL1R2 and COQ7 with Parkinson's disease in Taiwan
7. Incomplete penetrance of NOD2 C483W mutation underlining Blau syndrome
8. Characteristics and genetic analysis of patients suspected with early-onset systemic lupus erythematosus
9. Whole-exome sequencing identifies biosignatures that predict adverse survival outcomes in surgically treated patients with oral cavity squamous cell carcinoma
10. Autosomal Recessive Renal Tubular Dysgenesis Caused by a Founder Mutation of Angiotensinogen
11. A New Phenotype of TUBB4A Mutation in a Family With Adult-Onset Progressive Spastic Paraplegia and Isolated Hypomyelination Leukodystrophy: A Case Report and Literature Review
12. Clinical features, genetic background, and outcome in infants with urinary tract infection and type IV renal tubular acidosis
13. A combined analysis of maximum standardized uptake value on FDG-PET, genetic markers, and clinicopathological risk factors in the prognostic stratification of patients with resected oral cavity squamous cell carcinoma
14. Lipopolysaccharide stimulation test on cultured PBMCs assists the discrimination of cryopyrin-associated periodic syndrome from systemic juvenile idiopathic arthritis
15. Whole-exome sequencing detects mutations in pediatric patients with atypical hemolytic uremic syndrome in Taiwan
16. A CRYBB2 mutation in a Taiwanese family with autosomal dominant cataract
17. Phenotype, genotype, and clinical outcome of Taiwanese with congenital nephrotic syndrome
18. Genomes: at the edge of chaos with maximum information capacity
19. The Function of HLA-B*13:01 Involved in the Pathomechanism of Dapsone-Induced Severe Cutaneous Adverse Reactions
20. Compositional and functional variations of oral microbiota associated with the mutational changes in oral cancer
21. Impact of Genomic Alterations on the Clinical Outcome of Patients With Hepatitis B-related Hepatocellular Carcinoma Receiving Curative Surgery: A Retrospective Cohort Study
22. Randomized, controlled trial of TNF-[alpha] antagonist in CTL-mediated severe cutaneous adverse reactions
23. Novel Compound Heterozygous Mutations in the SYNE1 Gene in a Taiwanese Family: A Case Report and Literature Review
24. Impact of the HLA-B*58:01 Allele and Renal Impairment on Allopurinol-Induced Cutaneous Adverse Reactions
25. Long-Term Outcome of Neonatal Seizure with PACS2 Mutation: Case Series and Literature Review
26. Genomic and transcriptomic analyses of the medicinal fungus Antrodia cinnamomea for its metabolite biosynthesis and sexual development
27. Randomized, controlled trial of TNF-α antagonist in CTL-mediated severe cutaneous adverse reactions
28. Additional file 1 of Incomplete penetrance of NOD2 C483W mutation underlining Blau syndrome
29. Rare Occurrence of Aristolochic Acid Mutational Signatures in Oro-Gastrointestinal Tract Cancers
30. Association of AXIN1 With Parkinson’s Disease in a Taiwanese Population
31. Transcriptional profiling of adult Drosophila antennae by high-throughput sequencing
32. NOTCH1 mutations as prognostic marker in oral squamous cell carcinoma
33. Association of ITPKB, IL1R2 and COQ7 with Parkinson's disease in Taiwan
34. Pathogenic Variants in CEP85L Cause Sporadic and Familial Posterior Predominant Lissencephaly
35. Prognostic Genetic Biomarkers Based on Oncogenic Signaling Pathways for Outcome Prediction in Patients with Oral Cavity Squamous Cell Carcinoma
36. Effect of Hydrocortisone on Angiotensinogen (AGT) Mutation–Causing Autosomal Recessive Renal Tubular Dysgenesis
37. Leptin Is Associated with Poor Clinical Outcomes and Promotes Clear Cell Renal Cell Carcinoma Progression
38. Complement Factor I Mutation May Contribute to Development of Thrombotic Microangiopathy in Lupus Nephritis
39. Whole-Exome Sequencing Identified Novel CLMP Mutations in a Family With Congenital Short Bowel Syndrome Presenting Differently in Two Probands
40. Integration of metagenomics‐metabolomics reveals specific signatures and functions of airway microbiota in mite‐sensitized childhood asthma
41. A Novel CD3G Mutation in a Taiwanese Patient With Normal T Regulatory Function Presenting With the CVID Phenotype Free of Autoimmunity—Analysis of all Genotypes and Phenotypes
42. Clinical features, genetic background, and outcome in infants with urinary tract infection and type IV renal tubular acidosis
43. A combined analysis of maximum standardized uptake value on FDG-PET, genetic markers, and clinicopathological risk factors in the prognostic stratification of patients with resected oral cavity squamous cell carcinoma
44. Ghrelin Upregulates Oncogenic Aurora A to Promote Renal Cell Carcinoma Invasion
45. HLA Association with Drug-Induced Adverse Reactions
46. Novel discovery of association between the mutation in exon 14 of the ATP2A2 gene and Darier's disease
47. HLA Alleles andCYP 2C9*3as Predictors of Phenytoin Hypersensitivity in East Asians
48. Genome-wide prediction of CRISPR/Cas9 targets in Kluyveromyces marxianus and its application to obtain a stable haploid strain
49. Whole-Genome Sequencing of a Family with Hereditary Pulmonary Alveolar Proteinosis Identifies a Rare Structural Variant Involving CSF2RA/CRLF2/IL3RA Gene Disruption
50. Exome Sequencing of Oral Squamous Cell Carcinoma Reveals Molecular Subgroups and Novel Therapeutic Opportunities
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