CareLit Fachartikel

A high-throughput drug-screen for new therapies in cystic kidney disease using a zebrafish model system

M Schmidts, D Osborn, P Beales · Klinische Pädiatrie · 2011 · Heft 03

Dokument
1016386
CareLit-ID
Jahr
2011
Publikation
PDF
nein
Metadaten
DOI
ja
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Bibliografische Angaben

Zeitschrift
Klinische Pädiatrie
Autor:innen
M Schmidts, D Osborn, P Beales
Ausgabe
Heft 03 / 2011
Seiten
–
Erschienen: 2011-03-23 00:00:00
ISSN
0300-8630

Zusammenfassung

Aims: Cystic kidney disease is a common cause of chronic renal failure in children and adults with autosomal-dominant polycystic kidney disease (ADPKD) being a lot more common than autosomal-recessive polycystic kidney disease (ARPKD). Several syndromic diseases such as Meckel-Gruber-Syndrome and Bardet-Biedl-Syndrome are associated with cystic kidneys as well as Nephronophthisis/ Joubert-syndrome. Together, these diseases represent a significant health and economic burden and so far, depsite several promising approaches in mice using m-Tor inhibitors, CFTR-inhibitors, Vasopressin-inhbitors or TNF-alpha blockers…

Schlagworte

Drug screen Kidney cyst Zebrafish model Bardet-Biedl Syndrome Klinische Pädiatrie