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Publications by E. Zotta

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

Related publications

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

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

Computed Tomography in Autosomal Dominant Polycystic Kidney Disease (Adpkd)

Journal of Evolution of Medical and Dental Sciences

English

Cellular Abnormalities in Autosomal Dominant Polycystic Kidney Disease (ADPKD) Fibroblasts

English

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

Nature Communications

Molecular Biology

English

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

Journal of Clinical Investigation

English

Ectopic Autosomal Dominant Polycystic Kidney Disease (ADPKD)—An Extremely Rare Radiological Finding

Open Journal of Radiology

English

Longitudinal Assessment of Left Ventricular Mass in Autosomal Dominant Polycystic Kidney Disease (ADPKD)

Kidney International Reports

English

Ectopic (Pelvic) Autosomal Dominant Polycystic Kidney Disease

Internal Medicine

Internal Medicine

English