Hui-Pin Hsiao

发表

The effects of acarbose on chemokine and cytokine production in human monocytic THP-1 cells

C. Hung, Chang-Hung Kuo, Yi-Ting Chen, 2019, Hormones.

1,2,3,4,6 penta-O-galloyl-β-D-glucose ameliorates high-fat diet-induced nonalcoholic fatty liver disease and maintains the expression of genes involved in lipid homeostasis in mice.

Hien M. Nguyen, R. Kant, C. Yen, 2020, Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie.

A genome-wide scan identifies mutations in the gene encoding phosphodiesterase 11A4 (PDE11A) in individuals with adrenocortical hyperplasia

I. Bossis, J. Bertherat, X. Bertagna, 2006, Nature Genetics.

Effects of Cushing disease on bone mineral density in a pediatric population.

C. Stratakis, M. Lodish, J. Reynolds, 2010, The Journal of pediatrics.

Association study of LIN28B in girls with precocious puberty

Bai-Hsiun Chen, M. Chao, Hung-Hsun Lin, 2017, Journal of pediatric endocrinology & metabolism : JPEM.

Quantitative DNA Methylation Analysis and Epigenotype-Phenotype Correlations in Taiwanese Patients with Beckwith-Wiedemann Syndrome

Yen-Yin Chou, Hsiang-Yu Lin, Shuan-Pei Lin, 2021, Journal of personalized medicine.

8-Cl-adenosine inhibits proliferation and causes apoptosis in B-lymphocytes via protein kinase A-dependent and independent effects: implications for treatment of Carney complex-associated tumors.

I. Bossis, C. Stratakis, M. Nesterova, 2009, The Journal of clinical endocrinology and metabolism.

Altered Pattern of Macrophage Polarization as a Biomarker for Severity of Childhood Asthma

M. Chao, C. Hung, Chang-Hung Kuo, 2021, Journal of inflammation research.

Clinical and genetic heterogeneity, overlap with other tumor syndromes, and atypical glucocorticoid hormone secretion in adrenocorticotropin-independent macronodular adrenal hyperplasia compared with other adrenocortical tumors.

C. Stratakis, A. Lacroix, M. Nesterova, 2009, The Journal of clinical endocrinology and metabolism.

The AGG interruption pattern within the CGG repeat of the FMR1 gene among Taiwanese population

H. Hsiao, H. Chiu, Hui-Pin Hsiao, 2008, Journal of Genetics.

Role of thyrotropin‐releasing hormone test in re‐evaluation of congenital hypothyroidism

Bai-Hsiun Chen, M. Chao, Yen-Chun Chen, 2014, The Kaohsiung journal of medical sciences.

Case of Chronic Lymphocytic Leukemia with Unusual Chromosome Aberrations

H. Hsiao, M. Chao, Sheng-fung Lin, 2004, International journal of hematology.

Novel SOX9 gene mutation in campomelic dysplasia with autosomal sex reversal.

M. Chao, L. Tsai, Hui-Pin Hsiao, 2006, Journal of the Formosan Medical Association = Taiwan yi zhi.

A study of PVRL1 mutations for non-syndromic cleft lip and/or palate among Taiwanese patients.

H. Hsiao, Hui-Pin Hsiao, H. Hsiao, 2006, International journal of oral and maxillofacial surgery.

Impaired glucose homeostasis and a novel HLCS pathogenic variant in holocarboxylase synthetase deficiency: a report of two cases and brief review

M. Chao, Hui-Pin Hsiao, Hsin-Ru Wu, 2020, Journal of pediatric endocrinology & metabolism : JPEM.

Respiratory adenoviral infections in children: a study of hospitalized cases in southern Taiwan in 2001--2002.

Y. Jong, Yung-Cheng Lin, S. Chiou, 2004, Journal of tropical pediatrics.