Mammalian distal tubule: physiology, pathophysiology, and molecular anatomy. - Wikidata - awgldk - TriplyDB

Mammalian distal tubule: physiology, pathophysiology, and molecular anatomy.

Mammalian distal tubule: physiology, pathophysiology, and molecular anatomy.

http://www.wikidata.org/entity/Q33807213

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The thiazide-sensitive Na-Cl cotransporter is regulated by a WNK kinase signaling complex The thiazide-sensitive Na+-Cl- cotransporter: molecular biology, functional properties, and regulation by WNKs An SGK1 site in WNK4 regulates Na+ channel and K+ channel activity and has implications for aldosterone signaling and K+ homeostasis EAST syndrome: Clinical, pathophysiological, and genetic aspects of mutations in KCNJ10 Ubiquitylation and control of renal Na+ balance and blood pressure Intracellular cAMP signaling by soluble adenylyl cyclase.An inward rectifier K(+) channel at the basolateral membrane of the mouse distal convoluted tubule: similarities with Kir4-Kir5.1 heteromeric channels Redistribution of distal tubule Na+-Cl- cotransporter (NCC) in response to a high-salt diet Interaction with grp58 increases activity of the thiazide-sensitive Na-Cl cotransporter WNK kinases regulate thiazide-sensitive Na-Cl cotransport Role of reduced manganese superoxide dismutase in ischemia-reperfusion injury: a possible trigger for autophagy and mitochondrial biogenesis?Interleukin 18 function in atherosclerosis is mediated by the interleukin 18 receptor and the Na-Cl co-transporter The cdx genes and retinoic acid control the positioning and segmentation of the zebrafish pronephros.Hypomagnesemia: a clinical perspective.Enhanced passive Ca2+ reabsorption and reduced Mg2+ channel abundance explains thiazide-induced hypocalciuria and hypomagnesemia.Mitochondrial dysfunction in inherited renal disease and acute kidney injury Distal renal tubules are deficient in aggresome formation and autophagy upon aldosterone administration.Divalent cation transport by the distal nephron: insights from Bartter's and Gitelman's syndromes.Sodium and calcium transport pathways along the mammalian distal nephron: from rabbit to human.Renal tubular NEDD4-2 deficiency causes NCC-mediated salt-dependent hypertension How do thiazide and thiazide-like diuretics lower blood pressure?Connecting tubule glomerular feedback antagonizes tubuloglomerular feedback in vivo.Molecular basis of decreased Kir4.1 function in SeSAME/EAST syndrome.WNK kinases and renal sodium transport in health and disease: an integrated view.A cluster of metabolic defects caused by mutation in a mitochondrial tRNA.The WNKs: atypical protein kinases with pleiotropic actions.The Cap1-claudin-4 regulatory pathway is important for renal chloride reabsorption and blood pressure regulation.Gd-labeled microparticles in MRI: in vivo imaging of microparticles after intraperitoneal injection.Distal convoluted tubule WNK4-mediated regulation of renal ion transport proteins.γ-Adducin stimulates the thiazide-sensitive NaCl cotransporter Phorbol ester stimulation of RasGRP1 regulates the sodium-chloride cotransporter by a PKC-independent pathway.Abnormal regulation of ENaC: syndromes of salt retention and salt wasting by the collecting duct.Role of the Renin-Angiotensin system and aldosterone on cardiometabolic syndrome.Nedd4-2 modulates renal Na+-Cl- cotransporter via the aldosterone-SGK1-Nedd4-2 pathway.Renal tubule angiotensin II type 1 receptor-associated protein promotes natriuresis and inhibits salt-sensitive blood pressure elevation Hypertrophy in the Distal Convoluted Tubule of an 11β-Hydroxysteroid Dehydrogenase Type 2 Knockout Model.Oxidation of CaMKII determines the cardiotoxic effects of aldosterone.Tubuloglomerular and connecting tubuloglomerular feedback during inhibition of various Na transporters in the nephron Identification of the vitamin D receptor in various cells of the mouse kidney.

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P2860

Mammalian distal tubule: physiology, pathophysiology, and molecular anatomy.

http://www.wikidata.org/entity/Q33807213

description

2000 nî lūn-bûn

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2000 թուականի Յունուարին հրատարակուած գիտական յօդուած

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2000 թվականի հունվարին հրատարակված գիտական հոդված

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2000年の論文

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2000年論文

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2000年論文

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2000年論文

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2000年論文

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2000年論文

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2000年论文

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Mammalian distal tubule: physiology, pathophysiology, and molecular anatomy.

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Mammalian distal tubule: physiology, pathophysiology, and molecular anatomy.

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Mammalian distal tubule: physiology, pathophysiology, and molecular anatomy.

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Mammalian distal tubule: physiology, pathophysiology, and molecular anatomy.

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Ellison DH

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P2860

Paracellin-1, a renal tight junction protein required for paracellular Mg2+ resorption

The skeletal muscle chloride channel in dominant and recessive human myotonia

Gitelman's variant of Bartter's syndrome, inherited hypokalaemic alkalosis, is caused by mutations in the thiazide-sensitive Na-Cl cotransporter

Mutations in the mineralocorticoid receptor gene cause autosomal dominant pseudohypoaldosteronism type I

A common molecular basis for three inherited kidney stone diseases

Mutations in the chloride channel gene, CLCNKB, cause Bartter's syndrome type III

Molecular cloning and functional expression of the K-Cl cotransporter from rabbit, rat, and human. A new member of the cation-chloride cotransporter family

Familial distal renal tubular acidosis is associated with mutations in the red cell anion exchanger (Band 3, AE1) gene

Idiopathic low molecular weight proteinuria associated with hypercalciuric nephrocalcinosis in Japanese children is due to mutations of the renal chloride channel (CLCN5)

Mutations in the chloride-bicarbonate exchanger gene AE1 cause autosomal dominant but not autosomal recessive distal renal tubular acidosis

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pathophysiology