Investigating the role of ciliary localisation of the TRPP Channel, Polycystin2 (PKD2), on development and progression of polycystic kidney disease
<p>Autosomal Dominant Polycystic Kidney Disease (ADPKD) is a common inherited disease, affecting 1:400-1000 people worldwide and leads to end-stage renal failure in most patients before their 6<sup>th</sup> decade. ADPKD is characterised by abnormal persistent cellular proliferatio...
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| フォーマット: | 学位論文 |
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2016
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