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Volumn 13, Issue 6, 2002, Pages 1442-1448
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Functional expression of mutations in the human NaCl cotransporter: Evidence for impaired routing mechanisms in Gitelman's syndrome
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Author keywords
[No Author keywords available]
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Indexed keywords
CARRIER PROTEIN;
GLYCOPROTEIN;
GLYCOSIDASE;
METOLAZONE;
SODIUM 22;
SODIUM CHLORIDE;
CALCIUM;
COTRANSPORTER;
DRUG RECEPTOR;
MAGNESIUM;
SLC12A3 PROTEIN, HUMAN;
SODIUM;
SODIUM CHLORIDE COTRANSPORTER;
THIAZIDE RECEPTOR;
ANIMAL CELL;
ARTICLE;
AUTOSOMAL RECESSIVE DISORDER;
CELL MEMBRANE;
CELLULAR DISTRIBUTION;
CONTROLLED STUDY;
ENDOPLASMIC RETICULUM;
GENE EXPRESSION;
GENE MUTATION;
GITELMAN SYNDROME;
GOLGI COMPLEX;
IMMUNOBLOTTING;
IMMUNOCYTOCHEMISTRY;
ION TRANSPORT;
KIDNEY TUBULE DISORDER;
NONHUMAN;
PRIORITY JOURNAL;
PROTEIN GLYCOSYLATION;
PROTEIN LOCALIZATION;
PROTEIN PROCESSING;
SODIUM TRANSPORT;
WESTERN BLOTTING;
XENOPUS LAEVIS;
ALKALOSIS;
ANIMAL;
BLOOD;
FEMALE;
GENETICS;
GLYCOSYLATION;
HUMAN;
HYPOKALEMIA;
IMMUNOHISTOCHEMISTRY;
METABOLISM;
MOLECULAR WEIGHT;
MUTATION;
OOCYTE;
SYNDROME;
URINE;
ALKALOSIS;
ANIMALS;
CALCIUM;
CARRIER PROTEINS;
FEMALE;
GLYCOSYLATION;
HUMANS;
HYPOKALEMIA;
IMMUNOHISTOCHEMISTRY;
MAGNESIUM;
METOLAZONE;
MOLECULAR WEIGHT;
MUTATION;
OOCYTES;
RECEPTORS, DRUG;
SODIUM;
SODIUM CHLORIDE SYMPORTERS;
SYMPORTERS;
SYNDROME;
XENOPUS LAEVIS;
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EID: 0036014925
PISSN: 10466673
EISSN: None
Source Type: Journal
DOI: 10.1097/01.ASN.0000017904.77985.03 Document Type: Article |
Times cited : (134)
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References (29)
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