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
A Missing Genomic Dimension: The Small but Central Mitochondrial Genome in Diabetic Kidney Disease Genetics

article Full Text OpenAlex

KDIGO 2025 Clinical Practice Guideline for ADPKD: a commentary on intracranial aneurysms and other vascular manifestations from the ERA Working Group Genes & Kidney

article Full Text OpenAlex

Global Longitudinal Assessment of MASLD Using Magnetic Resonance Elastography ( GOLDMINE ): A Multi‐Center, International Prospective Cohort Study of Imaging Biomarkers in MASLD Clinical Outcomes

article Full Text OpenAlex

Asymmetric Inheritance of the Aged Mother Centriole by Stem Cells Is an Established Causal Fact

article Full Text OpenAlex

The Relapse Prediction

article Full Text OpenAlex

Setmelanotide in Bardet‐Biedl Syndrome: A Case Report

article Full Text OpenAlex

Development of the fluorescent probe CenSpark for labeling centrioles and cilia

article Full Text OpenAlex

The Centriolar Imperative

article Full Text OpenAlex

A stereotyped glial attachment determines the morphology and function of neuronal cilia

article Full Text OpenAlex

Localized active transport shapes the nanoscopic features at the tip of mechanosensory cilia

article Full Text OpenAlex

近5年高被引文献
Primary cilia as dynamic and diverse signalling hubs in development and disease

review Full Text OpenAlex 383 FWCI114.0856

Global trends of cropland phosphorus use and sustainability challenges

article Full Text OpenAlex 382 FWCI39.3326

Hedgehog signaling in tissue homeostasis, cancers and targeted therapies

review Full Text OpenAlex 214 FWCI31.7265

Pathobiology of the Klotho Antiaging Protein and Therapeutic Considerations

review Full Text OpenAlex 196 FWCI25.4738

The global prevalence and ethnic heterogeneity of primary ciliary dyskinesia gene variants: a genetic database analysis

article Full Text OpenAlex 192 FWCI26.4558

Efficacy and safety of setmelanotide, a melanocortin-4 receptor agonist, in patients with Bardet-Biedl syndrome and Alström syndrome: a multicentre, randomised, double-blind, placebo-controlled, phase 3 trial with an open-label period

article Full Text OpenAlex 175 FWCI28.7112

Axonemal structures reveal mechanoregulatory and disease mechanisms

article Full Text OpenAlex 160 FWCI23.765

Urease-powered nanobots for radionuclide bladder cancer therapy

article Full Text OpenAlex 156 FWCI79.4171

A Klotho-derived peptide protects against kidney fibrosis by targeting TGF-β signaling

article Full Text OpenAlex 146 FWCI19.1054

In situ architecture of the ciliary base reveals the stepwise assembly of intraflagellar transport trains

article Full Text OpenAlex 144 FWCI25.9223