[HTML][HTML] Ciliopathies and the kidney: a review

DJ McConnachie, JL Stow, AJ Mallett - American Journal of Kidney …, 2021 - Elsevier
Primary cilia are specialized sensory organelles that protrude from the apical surface of most
cell types. Over the past two decades, they have been found to play important roles in tissue …

Molecular mechanisms of mechanotransduction in mammalian sensory neurons

P Delmas, J Hao, L Rodat-Despoix - Nature Reviews Neuroscience, 2011 - nature.com
The somatosensory system mediates fundamental physiological functions, including the
senses of touch, pain and proprioception. This variety of functions is matched by a diverse …

The polycystin complex mediates Wnt/Ca2+ signalling

S Kim, H Nie, V Nesin, U Tran, P Outeda, CX Bai… - Nature cell …, 2016 - nature.com
WNT ligands induce Ca2+ signalling on target cells. PKD1 (polycystin 1) is considered an
orphan, atypical G-protein-coupled receptor complexed with TRPP2 (polycystin 2 or PKD2) …

[图书][B] Mammalian transient receptor potential (TRP) cation channels

B Nilius, V Flockerzi - 2014 - Springer
When we edited in 2007 the first issue on transient receptor potential channel in the
Handbook of Experimental Pharmacology, we were all very excited by the progress in this …

[PDF][PDF] Intraciliary calcium oscillations initiate vertebrate left-right asymmetry

S Yuan, L Zhao, M Brueckner, Z Sun - Current biology, 2015 - cell.com
Background Bilateral symmetry during vertebrate development is broken at the left-right
organizer (LRO) by ciliary motility and the resultant directional flow of extracellular fluid …

Molecular insights into lipid-assisted Ca2+ regulation of the TRP channel Polycystin-2

M Wilkes, MG Madej, L Kreuter, D Rhinow… - Nature structural & …, 2017 - nature.com
Abstract Polycystin-2 (PC2), a calcium-activated cation TRP channel, is involved in diverse
Ca2+ signaling pathways. Malfunctioning Ca2+ regulation in PC2 causes autosomal …

Altered trafficking and stability of polycystins underlie polycystic kidney disease

Y Cai, SV Fedeles, K Dong… - The Journal of …, 2014 - Am Soc Clin Investig
The most severe form of autosomal dominant polycystic kidney disease occurs in patients
with mutations in the gene (PKD1) encoding polycystin-1 (PC1). PC1 is a complex polytopic …

Polycystin-1 maturation requires polycystin-2 in a dose-dependent manner

VG Gainullin, K Hopp, CJ Ward… - The Journal of …, 2015 - Am Soc Clin Investig
Autosomal dominant polycystic kidney disease (ADPKD) is a common inherited
nephropathy responsible for 4%–10% of end-stage renal disease cases. Mutations in the …

[HTML][HTML] A polycystin-centric view of cyst formation and disease: the polycystins revisited

ACM Ong, PC Harris - Kidney international, 2015 - Elsevier
It is 20 years since the identification of PKD1, the major gene mutated in autosomal
dominant polycystic kidney disease (ADPKD), followed closely by the cloning of PKD2 …

[PDF][PDF] Kv1. 1 channels act as mechanical brake in the senses of touch and pain

J Hao, F Padilla, M Dandonneau, C Lavebratt… - Neuron, 2013 - cell.com
Molecular determinants of threshold sensitivity of mammalian mechanoreceptors are
unknown. Here, we identify a mechanosensitive (MS) K+ current (I Kmech) that governs …