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Search results 101 to 125 out of 125 for Klhl3

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0.019s
Type Details Score
Publication        
First Author: The Gene Ontology Consortium
Year: 2010
Title: Automated transfer of experimentally-verified manual GO annotation data to mouse-human orthologs
Publication
First Author: Diez-Roux G
Year: 2011
Journal: PLoS Biol
Title: A high-resolution anatomical atlas of the transcriptome in the mouse embryo.
Volume: 9
Issue: 1
Pages: e1000582
Publication      
First Author: Mouse Genome Informatics Scientific Curators
Year: 2010
Journal: Database Download
Title: Mouse Microarray Data Integration in Mouse Genome Informatics, the Affymetrix GeneChip Mouse Genome U74 Array Platform (A, B, C v2).
Publication        
First Author: Mouse Genome Informatics Scientific Curators
Year: 2002
Title: Mouse Genome Informatics Computational Sequence to Gene Associations
Publication        
First Author: Marc Feuermann, Huaiyu Mi, Pascale Gaudet, Dustin Ebert, Anushya Muruganujan, Paul Thomas
Year: 2010
Title: Annotation inferences using phylogenetic trees
Publication      
First Author: Mouse Genome Informatics Group
Year: 2003
Journal: Database Procedure
Title: Automatic Encodes (AutoE) Reference
Publication      
First Author: Mouse Genome Informatics Scientific Curators
Year: 2009
Journal: Database Download
Title: Mouse Microarray Data Integration in Mouse Genome Informatics, the Affymetrix GeneChip Mouse Gene 1.0 ST Array Platform
Publication      
First Author: Bairoch A
Year: 1999
Journal: Database Release
Title: SWISS-PROT Annotated protein sequence database
Publication        
First Author: Mouse Genome Informatics Scientific Curators
Year: 2005
Title: Obtaining and loading genome assembly coordinates from NCBI annotations
Publication      
First Author: Mouse Genome Database and National Center for Biotechnology Information
Year: 2000
Journal: Database Release
Title: Entrez Gene Load
Publication      
First Author: Mouse Genome Informatics (MGI) and The National Center for Biotechnology Information (NCBI)
Year: 2010
Journal: Database Download
Title: Consensus CDS project
Publication      
First Author: Mouse Genome Informatics
Year: 2010
Journal: Database Release
Title: Protein Ontology Association Load.
Publication      
First Author: Allen Institute for Brain Science
Year: 2004
Journal: Allen Institute
Title: Allen Brain Atlas: mouse riboprobes
Publication        
First Author: Mouse Genome Informatics Scientific Curators
Year: 2005
Title: Obtaining and Loading Genome Assembly Coordinates from Ensembl Annotations
Publication
First Author: Wu G
Year: 2013
Journal: FEBS Lett
Title: Disease-causing mutations in KLHL3 impair its effect on WNK4 degradation.
Volume: 587
Issue: 12
Pages: 1717-22
Publication
First Author: Louis-Dit-Picard H
Year: 2012
Journal: Nat Genet
Title: KLHL3 mutations cause familial hyperkalemic hypertension by impairing ion transport in the distal nephron.
Volume: 44
Issue: 4
Pages: 456-60, S1-3
Publication
First Author: Cornelius RJ
Year: 2018
Journal: J Am Soc Nephrol
Title: Renal COP9 Signalosome Deficiency Alters CUL3-KLHL3-WNK Signaling Pathway.
Volume: 29
Issue: 11
Pages: 2627-2640
Publication
First Author: López-Cayuqueo KI
Year: 2018
Journal: Kidney Int
Title: A mouse model of pseudohypoaldosteronism type II reveals a novel mechanism of renal tubular acidosis.
Volume: 94
Issue: 3
Pages: 514-523
Publication
First Author: Kasagi Y
Year: 2017
Journal: Biochem Biophys Res Commun
Title: Impaired degradation of medullary WNK4 in the kidneys of KLHL2 knockout mice.
Volume: 487
Issue: 2
Pages: 368-374
Publication
First Author: Anderegg MA
Year: 2021
Journal: Kidney Int
Title: The sodium/proton exchanger NHA2 regulates blood pressure through a WNK4-NCC dependent pathway in the kidney.
Volume: 99
Issue: 2
Pages: 350-363
Publication
First Author: Araki Y
Year: 2015
Journal: Biol Open
Title: Generation and analysis of knock-in mice carrying pseudohypoaldosteronism type II-causing mutations in the cullin 3 gene.
Volume: 4
Issue: 11
Pages: 1509-17
Publication
First Author: Schumacher FR
Year: 2015
Journal: EMBO Mol Med
Title: Characterisation of the Cullin-3 mutation that causes a severe form of familial hypertension and hyperkalaemia.
Volume: 7
Issue: 10
Pages: 1285-306
Publication
First Author: Pathare G
Year: 2013
Journal: Am J Physiol Renal Physiol
Title: A molecular update on pseudohypoaldosteronism type II.
Volume: 305
Issue: 11
Pages: F1513-20
Publication
First Author: Ishizawa K
Year: 2019
Journal: Proc Natl Acad Sci U S A
Title: Calcineurin dephosphorylates Kelch-like 3, reversing phosphorylation by angiotensin II and regulating renal electrolyte handling.
Volume: 116
Issue: 8
Pages: 3155-3160
Publication
First Author: Bazúa-Valenti S
Year: 2018
Journal: J Am Soc Nephrol
Title: The Calcium-Sensing Receptor Increases Activity of the Renal NCC through the WNK4-SPAK Pathway.
Volume: 29
Issue: 7
Pages: 1838-1848