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Publications by Ji-Bin Peng

Polycystin-2 Is a Novel Cation Channel Implicated in Defective Intracellular Ca2+ Homeostasis in Polycystic Kidney Disease

Biochemical and Biophysical Research Communications

Molecular Biology

English

Related publications

Polycystin-2, the Protein Mutated in Autosomal Dominant Polycystic Kidney Disease (ADPKD), Is a Ca2+-Permeable Nonselective Cation Channel

Proceedings of the National Academy of Sciences of the United States of America

Multidisciplinary

English

Ciliary Exclusion of Polycystin-2 Promotes Kidney Cystogenesis in an Autosomal Dominant Polycystic Kidney Disease Model

Nature Communications

Molecular Biology

English

Polycystin-2—An Intracellular or Plasma Membrane Channel?

Naunyn-Schmiedeberg's Archives of Pharmacology

English

Functional Polycystin-1 Dosage Governs Autosomal Dominant Polycystic Kidney Disease Severity

Journal of Clinical Investigation

English

Glis3 Is Associated With Primary Cilia and Wwtr1/Taz and Implicated in Polycystic Kidney Disease

Molecular and Cellular Biology

Molecular Biology

English

Autosomal Dominant Polycystic Kidney Disease (ADPKD, MIM 173900, PKD1 and PKD2 Genes, Protein Products Known as Polycystin-1 and Polycystin-2)

European Journal of Human Genetics

English

The Structure of a PKD Domain From Polycystin-1: Implications for Polycystic Kidney Disease

Molecular Biology

English

Thiol/Disulphide Homeostasis in Autosomal Dominant Polycystic Kidney Disease: A Single Center, Cross-Sectional Study

Turkish Nephrology, Dialysis and Transplantation Journal

English

Polycystic Kidney Disease

Nature Reviews Disease Primers

English