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Polycystic kidney disease: inheritance, pathophysiology, prognosis, and treatment.

Polycystic kidney disease: inheritance, pathophysiology, prognosis, and treatment.

http://www.wikidata.org/entity/Q34194508

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Effects of TORC1 Inhibition during the Early and Established Phases of Polycystic Kidney Disease Pyrrolidine dithiocarbamate reduces the progression of total kidney volume and cyst enlargement in experimental polycystic kidney disease.Effects of pyrrolidine dithiocarbamate on proliferation and nuclear factor-κB activity in autosomal dominant polycystic kidney disease cells.The polycystins are modulated by cellular oxygen-sensing pathways and regulate mitochondrial function.Anesthetic management in a patient of autosomal dominant polycystic kidney disease with end stage renal disease undergoing endovascular coiling for multiple intracranial aneurysms.Is the light at the end of the tunnel nigh? A review of ADPKD focusing on the burden of disease and tolvaptan as a new treatment.Cystic Kidney Diseases From the Adult Nephrologist's Point of View.

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Polycystic kidney disease: inheritance, pathophysiology, prognosis, and treatment.

http://www.wikidata.org/entity/Q34194508

description

2010 nî lūn-bûn

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2010 թուականի Յունիսին հրատարակուած գիտական յօդուած

@hyw

2010 թվականի հունիսին հրատարակված գիտական հոդված

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2010年の論文

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2010年論文

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2010年論文

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2010年論文

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2010年論文

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2010年論文

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2010年论文

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name

Polycystic kidney disease: inheritance, pathophysiology, prognosis, and treatment.

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Polycystic kidney disease: inheritance, pathophysiology, prognosis, and treatment.

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Polycystic kidney disease: inheritance, pathophysiology, prognosis, and treatment.

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Polycystic kidney disease: inheritance, pathophysiology, prognosis, and treatment.

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Polycystic kidney disease: inheritance, pathophysiology, prognosis, and treatment.

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Polycystic kidney disease: inheritance, pathophysiology, prognosis, and treatment.

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Polycystic kidney disease: inheritance, pathophysiology, prognosis, and treatment.

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Polycystic kidney disease: inheritance, pathophysiology, prognosis, and treatment.

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Polycystic kidney disease: inheritance, pathophysiology, prognosis, and treatment.

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International Journal of Nephrology and Renovascular Disease

P1476

Polycystic kidney disease: inheritance, pathophysiology, prognosis, and treatment.

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P2093

Christian R Halvorson

http://www.w3.org/2001/XMLSchema#string

Matthew S Bremmer

http://www.w3.org/2001/XMLSchema#string

Stephen C Jacobs

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P2860

PKHD1 protein encoded by the gene for autosomal recessive polycystic kidney disease associates with basal bodies and primary cilia in renal epithelial cells

Cardiovascular abnormalities in autosomal-dominant polycystic kidney disease

Potential pharmacological interventions in polycystic kidney disease

Approaches to testing new treatments in autosomal dominant polycystic kidney disease: insights from the CRISP and HALT-PKD studies

Bilineal disease and trans-heterozygotes in autosomal dominant polycystic kidney disease.

Polycystins 1 and 2 mediate mechanosensation in the primary cilium of kidney cells

Cholangiocyte primary cilia are chemosensory organelles that detect biliary nucleotides via P2Y12 purinergic receptors

Deletion of IFT20 in the mouse kidney causes misorientation of the mitotic spindle and cystic kidney disease

Endothelial cilia are fluid shear sensors that regulate calcium signaling and nitric oxide production through polycystin-1

Co-assembly of polycystin-1 and -2 produces unique cation-permeable currents

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2010-06-24T00:00:00Z

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21694932

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pathophysiology

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3108786

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