Hui‐Pin Hsiao

发表

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

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

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.

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.

Association study of LIN28B in girls with precocious puberty

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

Integrated genomic analysis of nodular tissue in macronodular adrenocortical hyperplasia: progression of tumorigenesis in a disorder associated with multiple benign lesions.

C. Cheadle, C. Stratakis, A. Horvath, 2011, The Journal of clinical endocrinology and metabolism.

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.

Mutations in Pseudohypoparathyroidism 1a and Pseudopseudohypoparathyroidism in Ethnic Chinese

H. Chen, F. Lo, W. Tsai, 2014, PloS one.

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.

Epigenetic regulation of COX-2 expression by DNA hypomethylation via NF-κB activation in ketamine-induced ulcerative cystitis

Wen-Jeng Wu, S. Chuang, Yung-Chin Lee, 2019, International journal of molecular medicine.

Protein kinase A-independent inhibition of proliferation and induction of apoptosis in human thyroid cancer cells by 8-Cl-adenosine.

C. Stratakis, N. Krett, M. Nesterova, 2008, The Journal of clinical endocrinology and metabolism.

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.

Feminizing adrenocortical adenoma presenting as heterosexual precocious puberty: report of one case.

Bai-Hsiun Chen, M. Chao, S. Chiou, 2005, Acta paediatrica Taiwanica = Taiwan er ke yi xue hui za zhi.

Case of Chronic Lymphocytic Leukemia with Unusual Chromosome Aberrations

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

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.

Growth Hormone Deficiency in a Case of Crouzon Syndrome with Hydrocephalus

F. Tsai, M. Chao, M. Wen, 2010, International journal of pediatric endocrinology.

Epigenotype, Genotype, and Phenotype Analysis of Taiwanese Patients with Silver–Russell Syndrome

Yen-Yin Chou, P. Su, Hsiang-Yu Lin, 2021, Journal of Personalized Medicine.

Suppressive effects of metformin on T-helper 1-related chemokines expression in the human monocytic leukemia cell line THP-1

C. Hung, Chang-Hung Kuo, Yi-Ting Chen, 2018, Endocrine research.

RBM15‐MKL1 (OTT‐MAL) fusion transcript in an adult acute myeloid leukemia patient

Ming-Yu Yang, H. Hsiao, M. Chao, 2005, American 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.

Maternal diabetes or hypertension and lifestyle factors may be associated with metabolic syndrome: A population‐based study in Taiwan

H. Chuang, Y. Chiu, Nai-Hua Shih, 2014, The Kaohsiung journal of medical sciences.

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.

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.

Differences in cortisol levels and body mass index between East Asians and Caucasians with Cushing's syndrome: an ‘East Asian’ phenotype for Cushing syndrome

C. Stratakis, S. Boikos, A. Robinson-White, 2007, Clinical endocrinology.

A Taiwanese Boy With Congenital Generalized Lipodystrophy Caused by Homozygous Ile262fs Mutation in the BSCL2 Gene

M. Chao, Tai-Heng Chen, Chia‐Tsuan Huang, 2010, The Kaohsiung journal of medical sciences.

Congenital generalized lipodystrophy in Taiwan.

Y. Chien, W. Hwu, F. Tsai, 2019, 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.

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.

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

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

Spectrum of PHEX Mutations and FGF23 Profiles in a Taiwanese Cohort With X-Linked Hypophosphatemia Including 102 Patients

D. Bau, P. Su, C. Chiu, 2023, In Vivo.