Calcium channels in the development, maturation, and function of spermatozoa

A Darszon, T Nishigaki, C Beltran… - Physiological …, 2011 - journals.physiology.org
A proper dialogue between spermatozoa and the egg is essential for conception of a new
individual in sexually reproducing animals. Ca2+ is crucial in orchestrating this unique event …

Strategies targeting cAMP signaling in the treatment of polycystic kidney disease

VE Torres, PC Harris - Journal of the American Society of …, 2014 - journals.lww.com
Polycystic kidney disease (PKD) is a leading cause of ESRD worldwide. In PKD, excessive
cell proliferation and fluid secretion, pathogenic interactions of mutated epithelial cells with …

The cell biology of polycystic kidney disease

HC Chapin, MJ Caplan - Journal of Cell Biology, 2010 - rupress.org
Polycystic kidney disease is a common genetic disorder in which fluid-filled cysts displace
normal renal tubules. Here we focus on autosomal dominant polycystic kidney disease …

Autosomal dominant polycystic kidney disease: from pathophysiology of cystogenesis to advances in the treatment

J Reiterová, V Tesař - International Journal of Molecular Sciences, 2022 - mdpi.com
Autosomal dominant polycystic kidney disease (ADPKD) is the most common genetic renal
disease, with an estimated prevalence between 1: 1000 and 1: 2500. It is mostly caused by …

Vasopressin and disruption of calcium signalling in polycystic kidney disease

FT Chebib, CR Sussman, X Wang, PC Harris… - Nature reviews …, 2015 - nature.com
Autosomal dominant polycystic kidney disease (ADPKD) is the most common monogenic
kidney disease and is responsible for 5–10% of cases of end-stage renal disease …

Polycystin-2 activation by inositol 1, 4, 5-trisphosphate-induced Ca2+ release requires its direct association with the inositol 1, 4, 5-trisphosphate receptor in a …

E Sammels, B Devogelaere, D Mekahli… - Journal of Biological …, 2010 - ASBMB
Autosomal dominant polycystic kidney disease is characterized by the loss-of-function of a
signaling complex involving polycystin-1 and polycystin-2 (TRPP2, an ion channel of the …

Structure and function of polycystins: insights into polycystic kidney disease

D Douguet, A Patel, E Honoré - Nature Reviews Nephrology, 2019 - nature.com
Mutations in the polycystins PC1 or PC2 cause autosomal dominant polycystic kidney
disease (ADPKD), which is characterized by the formation of fluid-filled renal cysts that …

[图书][B] Animal lectins: form, function and clinical applications

GS Gupta - 2012 - books.google.com
Animal Lectins: Form, Function and Clinical Applications presents up-to-date knowledge of
animal lectins. Detailed descriptions on biological activities, tissue and/or subcellular …

Modulation of polycystic kidney disease by G-protein coupled receptors and cyclic AMP signaling

CR Sussman, X Wang, FT Chebib, VE Torres - Cellular signalling, 2020 - Elsevier
Abstract Autosomal Dominant Polycystic Kidney Disease (ADPKD) is a systemic disorder
associated with polycystic liver disease (PLD) and other extrarenal manifestations, the most …

Polycystin and calcium signaling in cell death and survival

FO Lemos, BE Ehrlich - Cell calcium, 2018 - Elsevier
Abstract Mutations in polycystin-1 (PC1) and polycystin-2 (PC2) result in a commonly
occurring genetic disorder, called Autosomal Dominant Polycystic Kidney Disease (ADPKD) …