专题:Genetic and Kidney Cyst Diseases

This cluster of papers focuses on ciliopathies, a group of genetic disorders involving defects in primary cilia structure and function. It covers a range of topics including polycystic kidney disease, intraflagellar transport, hedgehog signaling, Bardet–Biedl syndrome, nephronophthisis, and the role of ciliary proteins. The research aims to understand the genetic mechanisms and signaling pathways underlying these disorders.
最新文献
Centriole Aging Disrupts Two Distinct Functions — Cilia Signaling and MTOC Organisation — Driving Organismal Aging: A Hypothesis

article Full Text OpenAlex

Ovarian Cysts in Polycystic Ovary Syndrome

article Full Text OpenAlex

Genomic analyses implicate hormonal and metabolic dysregulation in polycystic ovary syndrome

article Full Text OpenAlex

Autosomal dominant polycystic kidney disease

article Full Text OpenAlex

KDIGO 2025 Clinical Practice Guideline for the Evaluation, Management, and Treatment of Autosomal Dominant Polycystic Kidney Disease (ADPKD)

article Full Text OpenAlex

Centrioles and Cellular Differentiation

article Full Text OpenAlex

Prevalence of polycystic ovary syndrome: a global and regional systematic review and meta-analysis

review Full Text OpenAlex

A protein complex in the extreme distal tip of vertebrate motile cilia controls their organization, length, and function

article Full Text OpenAlex

Insulin resistance in polycystic ovary syndrome phenotypes and the vicious cycle model in its etiology

article Full Text OpenAlex

Primary cilia function as hubs for signal transduction

article Full Text OpenAlex

近5年高被引文献