Searchable abstracts of presentations at key conferences in endocrinology
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A novel GATA3 mutation, Tyr345Cys, in hypoparathyroidism, deafness and renal dysplasia (HDR) syndrome results in abolished DNA binding
Irina Grigorieva; Katie Gaynor; Treena Cranston; Catherine McWilliam; Faisal Ahmed; M Andrew Nesbit; Rajesh Thakker
http://www.endocrine-abstracts.org/ea/0021/ea0021p16.htm
Published: 2010-03-31

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Mice deleted for the transcription factor Gata3 have fewer parathyroid cells expressing Gcm2, develop hypocalcaemia and have an earlier onset of mortality when challenged with a low calcium-vitamin D diet
Irina Grigorieva; Samantha Mirczuk; Katie Gaynor; M Andrew Nesbit; Elena Grigorieva; Qiaozhi Wei; der Wees Jacqueline van; Willi
http://www.endocrine-abstracts.org/ea/0021/ea0021oc4.3.htm
Published: 2010-03-31

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A 5′-untranslated region mutation of the growth and differentiation factor 5 (Gdf5) gene increases expression and is associated with decreased urinary excretion of the cartilage degradation product, CTX-II: relevance to osteoarthritis
M Andrew Nesbit; Chris Esapa; Rosie Head; Katie Gaynor; Roger Cox; Steve Brown; Rajesh Thakker
http://www.endocrine-abstracts.org/ea/0025/ea0025p17.htm
Published: 2011-04-01

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Increased frequency and earlier onset of pituitary tumours in mice deleted for a multiple endocrine neoplasia type 1 allele and null for prolyl hydroxylase domain protein 1 (Men1+/−/Phd1−/−)
Mark Stevenson; Sian Piret; Mahsa Javid; Tammie Bishop; Anita Reed; Gerard Walls; Katie Gaynor; Paul Newey; Paul Christie; Lynn
http://www.endocrine-abstracts.org/ea/0034/ea0034oc5.1.htm
Published: 2014-03-01

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