WNK3-SPAK interaction is required for the modulation of NCC and other members of the SLC12 family

Cellular Physiology and Biochemistry

Volumn 29, Issue 1-2, 2012, Pages 291-302

  Pacheco Alvarez, Diana ^a   Vázquez, Norma ^b   Castañeda Bueno, María ^b   De Los Heros, Paola ^b,d   Cortes González, César ^b   Moreno, Erika ^b,c   Meade, Patricia ^b   Bobadilla, Norma A ^b   Gamba, Gerardo ^b  

^a UNIVERSIDAD PANAMERICANA   (Mexico)

^b INSTITUTO NACIONAL DE CIENCIAS MÉDICAS Y NUTRICIÓN SALVADOR ZUBIRÁN   (Mexico)

^c Universidad Autónoma del Estado de Hidalgo   (United States)

^d UNIVERSITY OF DUNDEE   (United Kingdom)

Author keywords

Distal tubule; Hypertension; Salt transport; Thiazide; WNK

Indexed keywords

BETA ACTIN; CHLORIDE; MUTANT PROTEIN; PHOSPHOTRANSFERASE; POTASSIUM CHLORIDE COTRANSPORTER 4; PROTEIN SLC12; PROTEIN SPAK; PROTEIN WNK3; SODIUM CHLORIDE COTRANSPORTER; SODIUM POTASSIUM CHLORIDE COTRANSPORTER 1; THREONINE; UNCLASSIFIED DRUG;

ANIMAL CELL; ARTICLE; BINDING SITE; CHLORIDE TRANSPORT; CONTROLLED STUDY; ENZYME PHOSPHORYLATION; FEMALE; HUMAN; HUMAN CELL; NONHUMAN; OOCYTE; PRIORITY JOURNAL; PROTEIN FAMILY; PROTEIN PROTEIN INTERACTION; REGULATORY MECHANISM; XENOPUS LAEVIS;

XENOPUS LAEVIS;

EID: 84858205722     PISSN: 10158987     EISSN: 14219778     Source Type: Journal    
DOI: 10.1159/000337610     Document Type: Article

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