Expression of renal cystic genes in patients with HNF1B mutations

Nephron - Clinical Practice

Volumn 120, Issue 2, 2012, Pages

  Faguer, Stanislas ^a,b   Decramer, Stéphane ^b,c   Devuyst, Olivier ^d   Lengelé, Jean Philippe ^d   Fournié, Gilbert J ^b   Chauveau, Dominique ^a,b  

^a CHU RANGUEIL   (France)

^b INSERM   (France)

^c HÔPITAL DES ENFANTS   (France)

^d UNIVERSITY OF ZURICH   (Switzerland)

Author keywords

HNF1B; Hypomagnesemia; Inherited renal disease; Tubulopathy; Urinary mRNA

Indexed keywords

ADENOSINE TRIPHOSPHATASE (POTASSIUM SODIUM); FIBROCYSTIN; HEPATOCYTE NUCLEAR FACTOR 1BETA; MAGNESIUM ION; MESSENGER RNA; POLYCYSTIN 1; POLYCYSTIN 2;

ADOLESCENT; ADULT; ARTICLE; ATP1A1 GENE; CHILD; CLDN16 GENE; CLINICAL ARTICLE; CONTROLLED STUDY; ENZYME SUBUNIT; FEMALE; FXYD2 GENE; GENE; GENE EXPRESSION; GENE MUTATION; HOMEOSTASIS; HUMAN; HUMAN CELL; HUMAN TISSUE; HYPOMAGNESEMIA; IFT88 GENE; KIDNEY POLYCYSTIC DISEASE; MALE; PATHOPHYSIOLOGY; PRESCHOOL CHILD; PRIORITY JOURNAL; TMEM27 GENE; UMOD GENE; URINE SEDIMENT;

ADOLESCENT; ADULT; CHILD; CHILD, PRESCHOOL; FEMALE; FRANCE; GENE EXPRESSION; HEPATOCYTE NUCLEAR FACTOR 1-BETA; HUMANS; KIDNEY DISEASES, CYSTIC; MALE; MIDDLE AGED; MUTATION; SODIUM-POTASSIUM-EXCHANGING ATPASE; YOUNG ADULT;

EID: 84861586068     PISSN: None     EISSN: 16602110     Source Type: Journal    
DOI: 10.1159/000334954     Document Type: Article

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