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Publications by Hui-Ping Lin

Mutation Analysis of 73 Southern Chinese Wilson's Disease Patients: Identification of 10 Novel Mutations and Its Clinical Correlation

Journal of Human Genetics

English

Caffeic Acid Phenethyl Ester Causes P21Cip1 Induction, Akt Signaling Reduction, and Growth Inhibition in PC-3 Human Prostate Cancer Cells

Multidisciplinary

English

Related publications

Clinical Features and Outcome of Wilson's Disease With Generalized Epilepsy in Chinese Patients

CNS Neuroscience and Therapeutics

English

The Genetic Creutzfeldt-Jakob Disease With E200K Mutation: Analysis of Clinical, Genetic and Laboratory Features of 30 Chinese Patients

Scientific Reports

Multidisciplinary

English

Molecular Analysis of Wilson Disease in Taiwan: Identification of One Novel Mutation and Evidence of Haplotype-Mutation Association

Journal of Human Genetics

English

Identification of Novel MLC1 Mutations in Chinese Patients With Megalencephalic Leukoencephalopathy With Subcortical Cysts (MLC)

Journal of Human Genetics

English

Proteomic Analysis of Sera of Asymptomatic, Early-Stage Patients With Wilson's Disease

Proteomics - Clinical Applications

Clinical Biochemistry

English

Correlation Between CYP2D6*10 Gene Mutation, and Structure and Function of Its Encoding Prot

Tropical Journal of Pharmaceutical Research

Pharmaceutical Science

English

Dent Disease in Chinese Children and Findings From Heterozygous Mothers: Phenotypic Heterogeneity, Fetal Growth, and 10 Novel Mutations

Journal of Pediatrics

English

Mutational Analysis for Wilson's Disease

English

Two Novel Mutations of the GTP Cyclohydrolase 1 Gene and Genotype–phenotype Correlation in Chinese Dopa-Responsive Dystonia Patients

European Journal of Human Genetics

English