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The cell biology of polycystic kidney disease

The cell biology of polycystic kidney disease

http://www.wikidata.org/entity/Q34149966

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Role of the Polycystins in Cell Migration, Polarity, and Tissue Morphogenesis The renal channelopathies Purinergic signalling in the kidney in health and disease Autophagy and regulation of cilia function and assembly Polycystin-1 cleavage and the regulation of transcriptional pathways Characterization of the SAM domain of the PKD-related protein ANKS6 and its interaction with ANKS3 Antennas of organ morphogenesis: the roles of cilia in vertebrate kidney development Physiological mechanisms and therapeutic potential of bone mechanosensing.The ciliary protein nephrocystin-4 translocates the canonical Wnt regulator Jade-1 to the nucleus to negatively regulate β-catenin signaling Mini-review: emerging roles of microRNAs in the pathophysiology of renal diseases Pkd1 regulates lymphatic vascular morphogenesis during development Trafficking to the primary cilium membrane.The Nek8 protein kinase, mutated in the human cystic kidney disease nephronophthisis, is both activated and degraded during ciliogenesis.Vertebrate kidney tubules elongate using a planar cell polarity-dependent, rosette-based mechanism of convergent extension Virtual-tissue computer simulations define the roles of cell adhesion and proliferation in the onset of kidney cystic disease Naringenin inhibits the growth of Dictyostelium and MDCK-derived cysts in a TRPP2 (polycystin-2)-dependent manner.The Ca2+-activated Cl- channel ANO1/TMEM16A regulates primary ciliogenesis TGF-β-activated kinase 1 is crucial in podocyte differentiation and glomerular capillary formation.Cure of ADPKD by selection for spontaneous genetic repair events in Pkd1-mutated iPS cells Reduced ciliary polycystin-2 in induced pluripotent stem cells from polycystic kidney disease patients with PKD1 mutations Kidney: polycystic kidney disease.End-stage renal disease in autosomal dominant polycystic kidney disease: a comparison of dialysis-related utilization and costs with other chronic kidney diseases The role of phospholipase D in modulating the MTOR signaling pathway in polycystic kidney disease.Cilium, centrosome and cell cycle regulation in polycystic kidney disease.Radiologic and clinical bronchiectasis associated with autosomal dominant polycystic kidney disease.Fibrosis and progression of autosomal dominant polycystic kidney disease (ADPKD).Identification of novel PKD1 and PKD2 mutations in Korean patients with autosomal dominant polycystic kidney disease Molecular pathways and therapies in autosomal-dominant polycystic kidney disease ROCK1-directed basement membrane positioning coordinates epithelial tissue polarity.Polycystin-1 Is a Cardiomyocyte Mechanosensor That Governs L-Type Ca2+ Channel Protein Stability Exploitation of the Polymeric Immunoglobulin Receptor for Antibody Targeting to Renal Cyst Lumens in Polycystic Kidney Disease Successful disease-specific induced pluripotent stem cell generation from patients with kidney transplantation.Quantitative proteomics identifies vasopressin-responsive nuclear proteins in collecting duct cells.Epigenetic silencing of the MUPCDH gene as a possible prognostic biomarker for cyst growth in ADPKD.Human polycystin-2 transgene dose-dependently rescues ADPKD phenotypes in Pkd2 mutant mice.The regulation of cystogenesis in a tissue engineered kidney disease system by abnormal matrix interactions.Cargo-selective apical exocytosis in epithelial cells is conducted by Myo5B, Slp4a, Vamp7, and Syntaxin 3.VIP17/MAL expression modulates epithelial cyst formation and ciliogenesis Suppressing angiotensinogen synthesis attenuates kidney cyst formation in a Pkd1 mouse model.TGF-β-activated kinase-1: New insights into the mechanism of TGF-β signaling and kidney disease.

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The cell biology of polycystic kidney disease

http://www.wikidata.org/entity/Q34149966

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2010 nî lūn-bûn

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2010 թուականի Նոյեմբերին հրատարակուած գիտական յօդուած

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2010年の論文

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The cell biology of polycystic kidney disease

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The cell biology of polycystic kidney disease

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The cell biology of polycystic kidney disease

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The cell biology of polycystic kidney disease

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Hannah C Chapin

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Michael J Caplan

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P2860

Specific association of the gene product of PKD2 with the TRPC1 channel

Strong homophilic interactions of the Ig-like domains of polycystin-1, the protein product of an autosomal dominant polycystic kidney disease gene, PKD1

The Ciliopathies: An Emerging Class of Human Genetic Disorders

Polycystin-2, the protein mutated in autosomal dominant polycystic kidney disease (ADPKD), is a Ca2+-permeable nonselective cation channel

Polycystin-2 is an intracellular calcium release channel

Expression of PKD1 and PKD2 transcripts and proteins in human embryo and during normal kidney development

Trafficking of TRPP2 by PACS proteins represents a novel mechanism of ion channel regulation

PIGEA-14, a novel coiled-coil protein affecting the intracellular distribution of polycystin-2

Polycystin-1 and polycystin-2 regulate the cell cycle through the helix-loop-helix inhibitor Id2

Carboxy terminal tail of polycystin-1 regulates localization of TSC2 to repress mTOR

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21079243

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autosomal dominant polycystic kidney

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2983067

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