Global ETD Search
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Showing 1 to 2 of 2 for “"DZIP1L"”.
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Identifikation und Charakterisierung von Interaktionspartnern des Zystennierenproteins DZIP1L
… in the formation of cystic kidneys genes is DZIP1L. DZIP1L has previously been identified in our group as a new gene for polycystic kidney disease by homozygosity mapping of a family with autosomal recessive polycystic kidney disease. It encodes a homolog of the iguana protein in zebrafish, …
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An in vivo study of novel genetic modifiers in autosomal recessive polycystic kidney disease (ARPKD)
… 50% of affected neonates. Mutations in PKHD1 and DZIP1L have been identified as causative genes for ARPKD, with the protein products of both genes localising to the primary cilium. Ciliary signalling pathways, such as Wnt signalling, have been investigated to dissect potential molecular mechanisms …