Mouse models for congenital nephrogenic diabetes insipidus: What can we learn from them?

Nephrology Dialysis Transplantation

Volumn 22, Issue 4, 2007, Pages 1023-1026

  Deen, Peter M T ^a,b  

^a RADBOUD UNIVERSITY MEDICAL CENTER   (Netherlands)

^b NONE   (Netherlands)

Author keywords

Aquaporin mutations; Congenital diseases; Nephrogenic diabetes insipidus; Trafficking

Indexed keywords

AMILORIDE; AQUAPORIN 2; DIURETIC AGENT; HYDROCHLOROTHIAZIDE; PHOSPHODIESTERASE IV INHIBITOR; ROLIPRAM;

APICAL MEMBRANE; ARTICLE; DEHYDRATION; DISEASE SEVERITY; DIURESIS; FLUID THERAPY; GENE EXPRESSION; GENE MUTATION; GROWTH RETARDATION; HUMAN; HYDRONEPHROSIS; KIDNEY COLLECTING TUBULE; KIDNEY CONCENTRATING CAPACITY; KIDNEY FAILURE; NEPHROGENIC DIABETES INSIPIDUS; NONHUMAN; PHENOTYPE; PRIORITY JOURNAL; URINE OSMOLALITY; URINE VOLUME;

AMINO ACID SEQUENCE; ANIMALS; AQUAPORIN 2; DIABETES INSIPIDUS, NEPHROGENIC; DISEASE MODELS, ANIMAL; HUMANS; MICE; MICE, KNOCKOUT; MOLECULAR SEQUENCE DATA; MUTATION; NEPHROLOGY; PHENOTYPE;

EID: 34047171515     PISSN: 09310509     EISSN: 14602385     Source Type: Journal    
DOI: 10.1093/ndt/gfl787     Document Type: Article

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