Searchable abstracts of presentations at key conferences in endocrinology

ea0021p154 | Diabetes and metabolism | SFEBES2009

Infidelity of ectopic transcription using a pseudo splice site: lessons from HNF-1β mutation causing familial juvenile hyperuricaemic nephropathy

Piret Sian , Reed Anita , Reilly Jennifer , Turner Neil , Thakker Rajesh

Ectopic (or ‘illegitimate’) transcripts, which have been widely used to study disease-causing mutations when samples from the appropriate tissue cannot be obtained, are generally faithful representations of the normal tissue-specific counterparts. Here, we report the occurrence of ectopic transcripts of the hepatocyte nuclear factor-1 beta (HNF-1β) gene, mutations of which may result in maturity onset diabetes of the young type 5 (MODY5), the renal cysts ...

ea0015p156 | Diabetes, metabolism and cardiovascular | SFEBES2008

Familial juvenile hyperuricaemic nephropathy is due to mutations in Tamm-Horsfall protein and hepatocyte nuclear factor 1β: further evidence for genetic heterogeneity

Williams Sian , Reed Anita , Reilly Jennifer , Karet Fiona , Lhotta Karl , Strehlau Juergen , Turner Neil , Thakker Rajesh

Familial Juvenile Hyperuricaemic Nephropathy (FJHN) is an autosomal dominant disorder that is associated with gout and progressive renal failure. FJHN in 43 families has been reported to be caused by mutations in the UMOD gene, which encodes Uromodulin, also known as the Tamm-Horsfall Glycoprotein, and two families have been reported to have mutations in the transcription factor Hepatocyte Nuclear Factor 1β (HNF-1β), mutations of which usually cause maturity-o...