ASN's Mission

To create a world without kidney diseases, the ASN Alliance for Kidney Health elevates care by educating and informing, driving breakthroughs and innovation, and advocating for policies that create transformative changes in kidney medicine throughout the world.

learn more

Contact ASN

The Latest on X

Kidney Week

ASN / Education & Meetings / Kidney Week /

Posters

ADPKD and Cystic Kidney Disease - 1

October 22, 2026 | 10:00 AM - 12:00 PM

Location: Exhibit Hall A, Convention Center

Session Description

Poster Session

Posters

Small-Molecule Correction of Trafficking-Defective PKD1 Variants Restores Ciliary Polycystin-1 Localization in ADPKD

Decreased Branched-Chain Amino Acids (BCAAs) Catabolism Is Important for mTORC1 Activation and Cystogenesis in ADPKD

Reduced Cholesterol as a Potential Mechanism of Phenotypic Convergence for PKD1 and PKD2 Variants

Real-World Outcomes of GLP-1 Receptor Agonist Therapy in Nondiabetic ADPKD: Effects on Mortality and Progression to ESRD in a TriNetX Cohort

In Vivo Clustered Regularly Interspaced Short Palindromic Repeats (CRISPR) Screening Identifies Epigenetic Regulation of Intrinsic Immunogenicity in ADPKD

Loss of Polycystin-1 Increases DCLK1 Expression in Intestinal Epithelia and Is Regulated by the GPR109A Receptor

Collecting Duct-Targeted Dual-siRNA Micelles Attenuate ADPKD

The CKD Hierarchical Composite End Point (HCE) in ADPKD

Evaluation of TMEM67 Haploinsufficiency as a Cause or Modifier of ADPKD

Interplay Between Primary Cilia and Integrin β1 Signaling in Kidney Maintenance

Genotype-Phenotype Correlations in an ADPKD Population in the All of Us Cohort

Exon-Level Distribution and Clustering of Variants of Uncertain Significance in ADPKD

Genomic Landscape of ADPKD: Towards Precision Diagnostics

Kidney-Targeted Lipid Nanoparticle-Delivered Clustered Regularly Interspaced Short Palindromic Repeats (LNP-CRISPR) Gene Editing as a Mutation-Agnostic, Single-Intervention Therapeutic Strategy for ADPKD

Resolvin D1 Inhibits cAMP/PKA Signaling Through Formyl Peptide Receptor 2 Activation and Slows PKD Progression

Periostin-Integrin Signaling Orchestrates Inflammation and Fibrosis in ADPKD

Chemical Chaperones Improve PC1 Ciliary Trafficking and Rescue the Cystic Phenotype in ADPKD Mouse Three-Dimensional (3D) Spheroids

Asparagine Synthetase (ASNS) Is the Primary Regulator of Glutamine Use Supporting Reductive Carboxylation in PKD

Targeting Runx1 Slows Cyst Growth in ADPKD

Gene-Based Rare Variant Associations Identify Known and Candidate Loci in Polycystic Kidney Disease Across Population-Scale Cohorts

Factors Associated with Kidney Failure in a Large Population of Patients with ADPKD and PKD1 Truncating Variants: A Multicenter Study

ADPKD-Associated Risk of Incident and Recurrent Urinary Tract Infection

Concepts of Importance to Patients with ADPKD and Psychometric Validity of Corresponding Clinical Outcome Assessments (COAs): A Targeted Literature Review (TLR)

Clinical Characteristics of ADPKD in Thailand

Real-World Experience with Panel Genetic Testing in Clinical Nephrology

Spatially Resolved Microenvironmental Changes in Tubules at Early Cystogenesis in an mTOR-Overactivated Polycystic Kidney Disease Mouse Model

Comprehensive Plasma Proteomic Profiling Reveals Immune, Inflammatory, and Extracellular Matrix Dysregulation in ADPKD

Plasma Metabolomic Profiling Identifies Distinct Lipid and Energy-Metabolism Signatures in ADPKD

A Metabolomic Analysis of ADPKD Dietary Intervention Trials

Cyst-Type Epithelial Heterogeneity Shapes Therapeutic Responsiveness in ADPKD

Development of an Artificial Intelligence (AI) Pipeline to Mechanistically Decipher Signaling Crosstalk and Predict Synergistic Combinations in ADPKD

Practice Patterns in Native Nephrectomy for ADPKD: A Cross-Sectional Survey of US Clinicians

Internal Validation of Quantitative Variant Scores for ADPKD Pathogenicity Classification

Epithelial Pregnancy-Associated Plasma Protein A and Circulating Insulin-Like Growth Factor Binding Protein 4 Fragments Indicate Insulin-Like Growth Factor Axis Dysregulation in ADPKD

Downregulation of Bone Morphogenetic Protein (BMP) Signaling Promotes ADPKD Progression

Association of Mayo Classification with Severity of Vascular Dysfunction in ADPKD

Functional Investigation of Notch3 Dysregulation in ADPKD Indicates Vasculature Involvement

CP6 Regulates Autophagy Through Integrin-AKT Signaling in Polycystic Kidney Disease

Predicting ADPKD Progression via Cyst Tracking

Federated Clinical and Genetic Analysis of International ADPKD Cohorts Using the Rare Disease Cures Accelerator-Data and Analytics Platform (RDCA-DAP)

Preclinical Safety and Pharmacokinetic Characterization of Oral 2-Deoxyglucose Supporting First-in-Human Trial Design in ADPKD

A Unique Case of Atypical ADPKD with Multicystic Gene Variants

Removal of FPCIP in Renal Tubules Leads to a Predominantly Fibrotic Phenotype

Apelinergic System Signaling Is Altered in Human ADPKD Cell Lines

Patient Journey and Lived Experiences of People Living with ADPKD

Intracranial Aneurysm Prevalence and Risk Factors in ADPKD: A Single-Center Analysis

Global Proteomics Identifies Early-Stage Alterations in Human Tissue Samples of ADPKD

Peripheral Microvascular Endothelial Dysfunction Is Associated with Kidney Structural Disease Severity in Individuals with Early ADPKD

Genotype-Specific Cardiac Phenotypes in ADPKD

Role of Aurora Kinase A in Polycystic Kidney Disease

Scoping Review of Clinical Trial Outcomes in Patients with ADPKD

Disease Progression in Patients Diagnosed with ADPKD by Variant Subgroups in HALT-PKD and CRISP

Guanine Quadruplex-Based Genome Instability and Polycystin Disruption in ADPKD

RNA Structure and Protein Interactome Mapping of PKD1 Identifies Targetable Post-Transcriptional Regulators in ADPKD

Dual PKD1/ALG5 Variants Presenting as Atypical ADPKD: A Case Report

Intravital Two-Photon Imaging Reveals an Early Proximal-Tubule Endocytic Deficiency in Pkd1 Haploinsufficient Mouse Kidneys

Unexpectedly Mild Adult-Onset ADPKD in Patients with Digenic Hypomorphic PKD1 and Truncating PKD2 Variants

Exploring the Regulation of PKD1-Mediated G-Protein Signaling

Longitudinal Intravital Imaging Reveals Epithelial Proliferation and Impaired Fluid Clearance During Early Cyst Expansion in Pkd1 Kidneys

Multifaceted Comparative PKD1/PKD2 Missense Variant Profiling Improves ADPKD Molecular Diagnosis and Reveals a Common Pathomechanism/Disease Determinant and Variant Complexity

HTD1801 Suppresses Cyst Expansion in PKD1-Mutant Nephron Organoids: Evidence for AMPK-NLRP3 Axis Efficacy in ADPKD

GRK6 Promotes PKD1 Trafficking to Primary Cilia

Largest Reported TSC2/PKD1 Contiguous Gene Deletion Syndrome (CGS) with Additional Deletion of IFT140

Using a Diphtheria Toxin (DT)-Based Genome Engineering Approach ("Xential") for Functional Analysis of PKD1 and PKD2

This site requires javascript, which you do not appear to have enabled. In order for everything to function properly, please enable javascript. .animsition, .animsition-overlay { opacity: 1; } .top-bar-wrapper { display: none; }