1. Pfisterer, Ulrich, Petukhov, Viktor, Demharter, Samuel, Kharchenko, Peter V, Khodosevich, Konstantin. 2020. Identification of epilepsy-associated neuronal subtypes and gene expression underlying epileptogenesis. In Nature communications, 11, 5038. doi:10.1038/s41467-020-18752-7. https://pubmed.ncbi.nlm.nih.gov/33028830/
2. Filice, Federica, Blum, Walter, Lauber, Emanuel, Schwaller, Beat. 2019. Inducible and reversible silencing of the Pvalb gene in mice: An in vitro and in vivo study. In The European journal of neuroscience, 50, 2694-2706. doi:10.1111/ejn.14404. https://pubmed.ncbi.nlm.nih.gov/30883994/
3. Riveira-Munoz, Eva, Devuyst, Olivier, Belge, Hendrica, Konrad, Martin, Dahan, Karin. 2008. Evaluating PVALB as a candidate gene for SLC12A3-negative cases of Gitelman's syndrome. In Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association, 23, 3120-5. doi:10.1093/ndt/gfn229. https://pubmed.ncbi.nlm.nih.gov/18469313/
4. Gong, Yiyang, Zhou, Minqin, Zhu, Yanting, Geng, Xitong, Huang, Da. 2024. PVALB Was Identified as an Independent Prognostic Factor for HCC Closely Related to Immunity, and Its Absence Accelerates Tumor Progression by Regulating NK Cell Infiltration. In Journal of hepatocellular carcinoma, 11, 813-838. doi:10.2147/JHC.S450479. https://pubmed.ncbi.nlm.nih.gov/38737383/
5. Cerutti, Janete M, Oler, Gisele, Delcelo, Rosana, Huang, Peng, Riggins, Gregory J. 2010. PVALB, a new Hürthle adenoma diagnostic marker identified through gene expression. In The Journal of clinical endocrinology and metabolism, 96, E151-60. doi:10.1210/jc.2010-1318. https://pubmed.ncbi.nlm.nih.gov/20926528/
智鼠故事 
