Detalhe da pesquisa
1.
Quantitative DNA Methylation Analysis and Epigenotype-Phenotype Correlations in Taiwanese Patients with Silver-Russell Syndrome.
Int J Med Sci
; 21(1): 8-18, 2024.
Artigo
em Inglês
| MEDLINE | ID: mdl-38164354
2.
Congenital generalized lipodystrophy in Taiwan.
J Formos Med Assoc
; 118(1 Pt 1): 142-147, 2019 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-29478747
3.
Suppressive effects of metformin on T-helper 1-related chemokines expression in the human monocytic leukemia cell line THP-1.
Endocr Res
; 43(4): 228-234, 2018 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-29630425
4.
A genome-wide scan identifies mutations in the gene encoding phosphodiesterase 11A4 (PDE11A) in individuals with adrenocortical hyperplasia.
Nat Genet
; 38(7): 794-800, 2006 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-16767104
5.
Syndromic ciliopathy: a taiwanese single-center study.
BMC Med Genomics
; 17(1): 106, 2024 Apr 26.
Artigo
em Inglês
| MEDLINE | ID: mdl-38671463
6.
Spectrum of PHEX Mutations and FGF23 Profiles in a Taiwanese Cohort With X-Linked Hypophosphatemia Including 102 Patients.
In Vivo
; 38(1): 341-350, 2024.
Artigo
em Inglês
| MEDLINE | ID: mdl-38148081
7.
Altered Pattern of Macrophage Polarization as a Biomarker for Severity of Childhood Asthma.
J Inflamm Res
; 14: 6011-6023, 2021.
Artigo
em Inglês
| MEDLINE | ID: mdl-34819741
8.
Quantitative DNA Methylation Analysis and Epigenotype-Phenotype Correlations in Taiwanese Patients with Beckwith-Wiedemann Syndrome.
J Pers Med
; 11(11)2021 Oct 22.
Artigo
em Inglês
| MEDLINE | ID: mdl-34834418
9.
Epigenotype, Genotype, and Phenotype Analysis of Taiwanese Patients with Silver-Russell Syndrome.
J Pers Med
; 11(11)2021 Nov 13.
Artigo
em Inglês
| MEDLINE | ID: mdl-34834549
10.
Effects of Cushing disease on bone mineral density in a pediatric population.
J Pediatr
; 156(6): 1001-1005, 2010 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-20223476
11.
Impaired glucose homeostasis and a novel HLCS pathogenic variant in holocarboxylase synthetase deficiency: a report of two cases and brief review.
J Pediatr Endocrinol Metab
; 33(11): 1481-1486, 2020 Nov 26.
Artigo
em Inglês
| MEDLINE | ID: mdl-32841162
12.
1,2,3,4,6 penta-O-galloyl-ß-D-glucose ameliorates high-fat diet-induced nonalcoholic fatty liver disease and maintains the expression of genes involved in lipid homeostasis in mice.
Biomed Pharmacother
; 129: 110348, 2020 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-32554245
13.
The effects of acarbose on chemokine and cytokine production in human monocytic THP-1 cells.
Hormones (Athens)
; 18(2): 179-187, 2019 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-30827017
14.
Epigenetic regulation of COX2 expression by DNA hypomethylation via NFκB activation in ketamineinduced ulcerative cystitis.
Int J Mol Med
; 44(3): 797-812, 2019 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-31257475
15.
Protein kinase A-independent inhibition of proliferation and induction of apoptosis in human thyroid cancer cells by 8-Cl-adenosine.
J Clin Endocrinol Metab
; 93(3): 1020-9, 2008 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-18073299
16.
Association study of LIN28B in girls with precocious puberty.
J Pediatr Endocrinol Metab
; 30(6): 663-667, 2017 May 24.
Artigo
em Inglês
| MEDLINE | ID: mdl-28525351
17.
Novel SOX9 gene mutation in campomelic dysplasia with autosomal sex reversal.
J Formos Med Assoc
; 105(12): 1013-6, 2006 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-17185244
18.
Feminizing adrenocortical adenoma presenting as heterosexual precocious puberty: report of one case.
Acta Paediatr Taiwan
; 46(2): 97-100, 2005.
Artigo
em Inglês
| MEDLINE | ID: mdl-16302588
19.
Case of chronic lymphocytic leukemia with unusual chromosome aberrations.
Int J Hematol
; 80(4): 351-3, 2004 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-15615260
20.
Role of thyrotropin-releasing hormone test in re-evaluation of congenital hypothyroidism.
Kaohsiung J Med Sci
; 30(8): 383-9, 2014 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-25002375