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Publications by Fucheng Li

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

Journal of Pediatrics

English

Long Intergenic Non-Coding RNA 01121 Promotes Breast Cancer Cell Proliferation, Migration, and Invasion via the miR-150-5p/HMGA2 Axis

Cancer Management and Research

English

Related publications

Molecular and Phenotypic Abnormalities in Individuals With Germline Heterozygous PTEN Mutations and Autism

Molecular Psychiatry

Molecular Neuroscience

Molecular Biology

English

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

Journal of Human Genetics

English

Novel PYGL Mutations in Chinese Children Leading to Glycogen Storage Disease Type VI: Two Case Reports

BMC Medical Genetics

English

Functional and Phenotypic Heterogeneity of Th17 Cells in Health and Disease

European Journal of Clinical Investigation

Clinical Biochemistry

English

PTPN11 Mutations in Noonan Syndrome: Molecular Spectrum, Genotype-Phenotype Correlation, and Phenotypic Heterogeneity

American Journal of Human Genetics

English

From Lowe Syndrome to Dent Disease: Correlations Between Mutations of the OCRL1 Gene and Clinical and Biochemical Phenotypes

English

Three Novel Α-L-Iduronidase Mutations in 10 Unrelated Chinese Mucopolysaccharidosis Type I Families

Genetics and Molecular Biology

Molecular Biology

English

Comparison of Clinical Findings Between Lowe Syndrome and Dent Disease With OCRL 1 Mutation

Nihon Shoni Jinzobyo Gakkai Zasshi

English

Novel Heterozygous Mutations in JAG1 and NOTCH2 Genes in a Neonatal Patient With Alagille Syndrome

Case Reports in Pediatrics

English