Mutations in kelch-like 3 and cullin 3 cause hypertension and electrolyte abnormalities.
about
Nedd4-2 and the regulation of epithelial sodium transportA molecular marker of artemisinin-resistant Plasmodium falciparum malariaKLHL3 mutations cause familial hyperkalemic hypertension by impairing ion transport in the distal nephronMutations in DSTYK and dominant urinary tract malformationsDCDC2 mutations cause a renal-hepatic ciliopathy by disrupting Wnt signalingUbiquitylation-dependent localization of PLK1 in mitosisRecessive mutations in DGKE cause atypical hemolytic-uremic syndromeKelch-like 3 and Cullin 3 regulate electrolyte homeostasis via ubiquitination and degradation of WNK4Rate of de novo mutations and the importance of father's age to disease riskUbiquitylation and control of renal Na+ balance and blood pressureGene mutations that promote adrenal aldosterone production, sodium retention, and hypertensionA molecular update on pseudohypoaldosteronism type IIProtein trafficking defects in inherited kidney diseasesBuilding and remodelling Cullin-RING E3 ubiquitin ligasesGenetically engineered mouse models for functional studies of SKP1-CUL1-F-box-protein (SCF) E3 ubiquitin ligasesStructural Basis for Cul3 Protein Assembly with the BTB-Kelch Family of E3 Ubiquitin LigasesStructural and biochemical characterization of the KLHL3–WNK kinase interaction important in blood pressure regulationKelch proteins: emerging roles in skeletal muscle development and diseases.Plasmodium falciparum: multifaceted resistance to artemisininsMutations in nuclear pore genes NUP93, NUP205 and XPO5 cause steroid-resistant nephrotic syndromeMutations in TRAF3IP1/IFT54 reveal a new role for IFT proteins in microtubule stabilizationThe inextricable role of the kidney in hypertensionIdentifying disease mutations in genomic medicine settings: current challenges and how to accelerate progressDisease-causing mutations in KLHL3 impair its effect on WNK4 degradationMonoallelic Mutations in the Translation Initiation Codon of KLHL24 Cause Skin FragilityPrimary Aldosteronism: Changing Definitions and New Concepts of Physiology and Pathophysiology Both Inside and Outside the Kidney.Emerging Targets of Diuretic Therapy.Diagnostic tools for hypertension and salt sensitivity testing.Common noncoding UMOD gene variants induce salt-sensitive hypertension and kidney damage by increasing uromodulin expressionFGF5 is a crucial regulator of hair length in humansNaCl cotransporter abundance in urinary vesicles is increased by calcineurin inhibitors and predicts thiazide sensitivity.Mechanism and synergism in epithelial fluid and electrolyte secretion.The clinical impact of artemisinin resistance in Southeast Asia and the potential for future spread.Sympathetic stimulation of thiazide-sensitive sodium chloride cotransport in the generation of salt-sensitive hypertension.A novel Ste20-related proline/alanine-rich kinase (SPAK)-independent pathway involving calcium-binding protein 39 (Cab39) and serine threonine kinase with no lysine member 4 (WNK4) in the activation of Na-K-Cl cotransporters.Is There a Role for Genomics in the Management of Hypertension?KCNJ10 determines the expression of the apical Na-Cl cotransporter (NCC) in the early distal convoluted tubule (DCT1).Regulation of with-no-lysine kinase signaling by Kelch-like proteins.Genetics of human cardiovascular diseaseRenal tubular NEDD4-2 deficiency causes NCC-mediated salt-dependent hypertension
P2860
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P2860
Mutations in kelch-like 3 and cullin 3 cause hypertension and electrolyte abnormalities.
description
2012 nî lūn-bûn
@nan
2012年の論文
@ja
2012年論文
@yue
2012年論文
@zh-hant
2012年論文
@zh-hk
2012年論文
@zh-mo
2012年論文
@zh-tw
2012年论文
@wuu
2012年论文
@zh
2012年论文
@zh-cn
name
Mutations in kelch-like 3 and cullin 3 cause hypertension and electrolyte abnormalities.
@ast
Mutations in kelch-like 3 and cullin 3 cause hypertension and electrolyte abnormalities.
@en
type
label
Mutations in kelch-like 3 and cullin 3 cause hypertension and electrolyte abnormalities.
@ast
Mutations in kelch-like 3 and cullin 3 cause hypertension and electrolyte abnormalities.
@en
prefLabel
Mutations in kelch-like 3 and cullin 3 cause hypertension and electrolyte abnormalities.
@ast
Mutations in kelch-like 3 and cullin 3 cause hypertension and electrolyte abnormalities.
@en
P2093
P2860
P356
P1433
P1476
Mutations in kelch-like 3 and cullin 3 cause hypertension and electrolyte abnormalities.
@en
P2093
Alain Poujol
Alberto Bettinelli
Ali G Gharavi
Anita Farhi
Beatrice Goilav
Ben A Semmekrot
Carol J Nelson-Williams
Craig C Porter
Craig W Belsha
Detlef Bockenhauer
P2860
P2888
P304
P356
10.1038/NATURE10814
P407
P577
2012-01-22T00:00:00Z
P5875
P6179
1039812741