Molecular physiology and genetics of Na+-independent SLC4 anion exchangers von Alper, Seth L

Volltext

Glymphatic System Impairment in Alzheimer’s Disease and Idiopathic Normal Pressure Hydrocephalus von Reeves, Benjamin C., Karimy, Jason K., Kundishora, Adam J., Mestre, Humberto, Cerci, H. Mert, Matouk, Charles, Alper, Seth L., Lundgaard, Iben, Nedergaard, Maiken, Kahle, Kristopher T.

Volltext

Innate immunity pathways regulate the nephropathy gene Apolipoprotein L1 von Nichols, Brendan, Jog, Prachi, Lee, Jessica H., Blackler, Daniel, Wilmot, Michael, D'Agati, Vivette, Markowitz, Glen, Kopp, Jeffrey B., Alper, Seth L., Pollak, Martin R., Friedman, David J.

Volltext

Autosomal dominant tubulointerstitial kidney disease: diagnosis, classification, and management—A KDIGO consensus report von Eckardt, Kai-Uwe, Alper, Seth L., Antignac, Corinne, Bleyer, Anthony J., Chauveau, Dominique, Dahan, Karin, Deltas, Constantinos, Hosking, Andrew, Kmoch, Stanislav, Rampoldi, Luca, Wiesener, Michael, Wolf, Matthias T., Devuyst, Olivier

Volltext

Molecular physiology of SLC4 anion exchangers von Alper, Seth L.

Volltext

Disruption of Cav1.2-mediated signaling is a pathway for ketamine-induced pathology von Chen, Huan, Vandorpe, David H., Xie, Xiang, Alper, Seth L., Zeidel, Mark L., Yu, Weiqun

Volltext

Recruitment of APOL1 kidney disease risk variants to lipid droplets attenuates cell toxicity von Chun, Justin, Zhang, Jia-Yue, Wilkins, Maris S., Subramanian, Balajikarthick, Riella, Cristian, Magraner, Jose M., Alper, Seth L., Friedman, David J., Pollak, Martin R.

Volltext

APOL1 kidney disease risk variants cause cytotoxicity by depleting cellular potassium and inducing stress-activated protein kinases von Olabisi, Opeyemi A., Zhang, Jia-Yue, VerPlank, Lynn, Zahler, Nathan, DiBartolo, Salvatore, Heneghan, John F., Schlöndorff, Johannes S., Suh, Jung Hee, Yan, Paul, Alper, Seth L., Friedman, David J., Pollak, Martin R.

Volltext

Evolution of the primate trypanolytic factor APOL1 von Thomson, Russell, Genovese, Giulio, Canon, Chelsea, Kovacsics, Daniella, Higgins, Matthew K, Carrington, Mark, Winkler, Cheryl A, Kopp, Jeffrey, Rotimi, Charles, Adeyemo, Adebowale, Doumatey, Ayo, Ayodo, George, Alper, Seth L, Pollak, Martin R, Friedman, David J, Raper, Jayne

Volltext

DGAT2 Inhibition Potentiates Lipid Droplet Formation To Reduce Cytotoxicity in APOL1 Kidney Risk Variants von Chun, Justin, Riella, Cristian V, Chung, Hyunjae, Shah, Shrijal S, Wang, Minxian, Magraner, Jose M, Ribas, Guilherme T, Ribas, Hennrique T, Zhang, Jia-Yue, Alper, Seth L, Friedman, David J, Pollak, Martin R

Volltext

K-Cl cotransporters, cell volume homeostasis, and neurological disease von Kahle, Kristopher T, Khanna, Arjun R, Alper, Seth L, Adragna, Norma C, Lauf, Peter K, Sun, Dandan, Delpire, Eric

Volltext

Multiple clinical forms of dehydrated hereditary stomatocytosis arise from mutations in PIEZO1 von Andolfo, Immacolata, Alper, Seth L., De Franceschi, Lucia, Auriemma, Carla, Russo, Roberta, De Falco, Luigia, Vallefuoco, Fara, Esposito, Maria Rosaria, Vandorpe, David H., Shmukler, Boris E., Narayan, Rupa, Montanaro, Donatella, D'Armiento, Maria, Vetro, Annalisa, Limongelli, Ivan, Zuffardi, Orsetta, Glader, Bertil E., Schrier, Stanley L., Brugnara, Carlo, Stewart, Gordon W., Delaunay, Jean, Iolascon, Achille

Volltext

Developmentally regulated KCC2 phosphorylation is essential for dynamic GABA-mediated inhibition and survival von Watanabe, Miho, Zhang, Jinwei, Mansuri, M Shahid, Duan, Jingjing, Karimy, Jason K, Delpire, Eric, Alper, Seth L, Lifton, Richard P, Fukuda, Atsuo, Kahle, Kristopher T

Volltext

Modulation of brain cation-Cl− cotransport via the SPAK kinase inhibitor ZT-1a von Zhang, Jinwei, Bhuiyan, Mohammad Iqbal H., Zhang, Ting, Karimy, Jason K., Wu, Zhijuan, Fiesler, Victoria M., Zhang, Jingfang, Huang, Huachen, Hasan, Md Nabiul, Skrzypiec, Anna E., Mucha, Mariusz, Duran, Daniel, Huang, Wei, Pawlak, Robert, Foley, Lesley M., Hitchens, T. Kevin, Minnigh, Margaret B., Poloyac, Samuel M., Alper, Seth L., Molyneaux, Bradley J., Trevelyan, Andrew J., Kahle, Kristopher T., Sun, Dandan, Deng, Xianming

Volltext

Transmembrane insertases and N-glycosylation critically determine synthesis, trafficking, and activity of the nonselective cation channel TRPC6 von Talbot, Brianna E., Vandorpe, David H., Stotter, Brian R., Alper, Seth L., Schlondorff, Johannes S.

Volltext

Hereditary anemia caused by multilocus inheritance of PIEZO1, SLC4A1 and ABCB6 mutations: a diagnostic and therapeutic challenge von Rosato, Barbara Eleni, Alper, Seth L, Tomaiuolo, Giovanna, Russo, Roberta, Iolascon, Achille, Andolfo, Immacolata

Volltext

Inhibition of WNK3 Kinase Signaling Reduces Brain Damage and Accelerates Neurological Recovery After Stroke von Begum, Gulnaz, Yuan, Hui, Kahle, Kristopher T, Li, Liaoliao, Wang, Shaoxia, Shi, Yejie, Shmukler, Boris E, Yang, Sung-Sen, Lin, Shih-Hua, Alper, Seth L, Sun, Dandan

Volltext

Challenges to dialysis treatment during the COVID-19 pandemic: a qualitative study of patients’ and experts’ perspectives von Oviedo Flores, Krystell, Stamm, Tanja, Alper, Seth L., Ritschl, Valentin, Vychytil, Andreas

Volltext

FSGS-Causing INF2 Mutation Impairs Cleaved INF2 N-Fragment Functions in Podocytes von Subramanian, Balajikarthick, Chun, Justin, Perez-Gill, Chandra, Yan, Paul, Stillman, Isaac E., Higgs, Henry N., Alper, Seth L., Schlondorff, Johannes S., Pollak, Martin R.

Volltext

A new molecular link between defective autophagy and erythroid abnormalities in chorea-acanthocytosis von Lupo, Francesca, Tibaldi, Elena, Matte, Alessandro, Sharma, Alok K., Brunati, Anna Maria, Alper, Seth L., Zancanaro, Carlo, Benati, Donatella, Siciliano, Angela, Bertoldi, Mariarita, Zonta, Francesca, Storch, Alexander, Walker, Ruth H., Danek, Adrian, Bader, Benedikt, Hermann, Andreas, De Franceschi, Lucia

Volltext