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KLHL3 gene

Known as: KLHL3, KIAA1129, KELCH-LIKE 3 
National Institutes of Health

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2019
2019
The Role of Genetic Mutations in Genes WNK1, WNK4, CUL3, KLHL3 in Gordon's Syndrome
2017
2017
WNK4 is indispensable for the pathogenesis of pseudohypoaldosteronism type II caused by mutant KLHL3.
2017
2017
Three cases of Gordon syndrome with dominant KLHL3 mutations
Abstract Background: Gordon syndrome (GS) is a rare form of monogenic hypertension characterized by low renin hypertension… 
2016
2016
A patient with pseudohypoaldosteronism type II complicated by congenital hypopituitarism carrying a KLHL3 mutation
Abstract. Pseudohypoaldosteronism type II (PHA II) is a renal tubular disease that causes hyperkalemia, hypertension, and… 
2016
2016
[OP.LB01.10] THE SKIPPING OF EXON 9 IN CULLIN-3 CAUSES A SEVERE FORM OF FAMILIAL HYPERKALEMIC HYPERTENSION IN MICE
Objective: Familial Hyperkalemic Hypertension (FHHt) is caused by mutations in WNK1, WNK4, KLHL3 or CUL3 (cullin-3). Patients… 
2015
2015
Familial Hyperkalemic Hypertension (FHHt) KLHL3 Mutations Disrupt Binding of ROMK Endocytic Regulatory Protein ARH
Fammilial Hyperkalemic Hypertension (FHHt) is caused by mutations in CUL3 and KLHL3, components of an E3 ligase complex, and is… 
2015
2015
Hypercalciuria in Familial Hyperkalemia and Hypertension with KLHL3 Mutations
Background: Familial hyperkalemia and hypertension (FHHt) is a rare genetic disorder manifested by hyperkalemia and early… 
2013
2013
KLHL2 interacts with and ubiquitinates WNK kinases.
2000
2000
Molecular characterization of KLHL3, a human homologue of the Drosophila kelch gene.
The Drosophila kelch protein is a structural component of ring canals and is required for oocyte maturation. Here, we report the… 
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