about
Cloning and function of the rat colonic epithelial K+ channel KVLQT1Epilepsy, ataxia, sensorineural deafness, tubulopathy, and KCNJ10 mutationsThe small conductance K+ channel, KCNQ1: expression, function, and subunit composition in murine tracheaDisruption of the K+ channel beta-subunit KCNE3 reveals an important role in intestinal and tracheal Cl- transportMutations in SLC6A19, encoding B0AT1, cause Hartnup disorderKCNE beta subunits determine pH sensitivity of KCNQ1 potassium channelsMineralocorticoid receptor knockout mice: pathophysiology of Na+ metabolismKCNJ10 gene mutations causing EAST syndrome (epilepsy, ataxia, sensorineural deafness, and tubulopathy) disrupt channel functionThe cardiac K+ channel KCNQ1 is essential for gastric acid secretionEffects of I(Ks) channel inhibitors in insulin-secreting INS-1 cellsARF6-dependent interaction of the TWIK1 K+ channel with EFA6, a GDP/GTP exchange factor for ARF6Expression and function of epithelial anoctaminsLMX1B is essential for the maintenance of differentiated podocytes in adult kidneys.Mistargeting of peroxisomal EHHADH and inherited renal Fanconi's syndrome.Expression and function of colonic epithelial KvLQT1 K+ channels.Task2 potassium channels set central respiratory CO2 and O2 sensitivity.The very small-conductance K+ channel KvLQT1 and epithelial function.A novel KCNJ5-insT149 somatic mutation close to, but outside, the selectivity filter causes resistant hypertension by loss of selectivity for potassiumSomatic mutations in ATP1A1 and ATP2B3 lead to aldosterone-producing adenomas and secondary hypertension.Proximal renal tubular acidosis in TASK2 K+ channel-deficient mice reveals a mechanism for stabilizing bicarbonate transportThe multifaceted phenotype of the knockout mouse for the KCNE1 potassium channel gene.Bestrophin and TMEM16-Ca(2+) activated Cl(-) channels with different functions.Potassium channels in epithelial transport.Two-pore domain potassium channels in the adrenal cortex.TWIK1, a unique background channel with variable ion selectivity.Invalidation of TASK1 potassium channels disrupts adrenal gland zonation and mineralocorticoid homeostasisNo potassium, no acid: K+ channels and gastric acid secretion.Altered potassium balance and aldosterone secretion in a mouse model of human congenital long QT syndromePhysiology and pathophysiology of potassium channels in gastrointestinal epithelia.a Novel Y152C KCNJ5 mutation responsible for familial hyperaldosteronism type III.TASK1 and TASK3 potassium channels: determinants of aldosterone secretion and adrenocortical zonation.The salt-wasting phenotype of EAST syndrome, a disease with multifaceted symptoms linked to the KCNJ10 K+ channel.Renal Fanconi syndrome: taking a proximal look at the nephron.Local Control of Aldosterone Production and Primary Aldosteronism.Pathogenesis of Adrenal Aldosterone-Producing Adenomas Carrying Mutations of the Na(+)/K(+)-ATPase.Diastrophic dysplasia sulfate transporter (SLC26A2) is expressed in the adrenal cortex and regulates aldosterone secretion.Pharmacology and pathophysiology of mutated KCNJ5 found in adrenal aldosterone-producing adenomas.Sex-dependent differences in the in vivo respiratory phenotype of the TASK-1 potassium channel knockout mouse.Visinin-like 1 is upregulated in aldosterone-producing adenomas with KCNJ5 mutations and protects from calcium-induced apoptosis.Potassium channel silencing by constitutive endocytosis and intracellular sequestration.
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P50
description
hulumtues
@sq
onderzoeker
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ricercatore
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հետազոտող
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name
Richard Warth
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Richard Warth
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Richard Warth
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Richard Warth
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Richard Warth
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Richard Warth
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type
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Richard Warth
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Richard Warth
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Richard Warth
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Richard Warth
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Richard Warth
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Richard Warth
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prefLabel
Richard Warth
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Richard Warth
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Richard Warth
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Richard Warth
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Richard Warth
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Richard Warth
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P227
P101
P1053
N-7119-2014
P106
P21
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9984147270674735700005
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1111789428
P2798
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P3829
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