Disease: Polycystic kidney disease- type 1
- <em>PKD1</em> Nonsense Variant in a Lagotto Romagnolo Family with Polycystic Kidney Disease
- <em>Tsc2</em> mutation induces renal tubular cell nonautonomous disease
- A novel ARPKD mouse model with near-complete deletion of the Polycystic Kidney and Hepatic Disease 1 (Pkhd1) genomic locus presents with multiple phenotypes but not renal cysts
- A plasma membrane-localized polycystin-1/polycystin-2 complex in endothelial cells elicits vasodilation
- A single heterozygous nonsense mutation in the TTC21B gene causes adult-onset nephronophthisis 12: A case report and review of literature
- Accuracy and processing time of kidney volume measurement methods in rodents polycystic kidney disease models: superiority of semiautomated kidney segmentation
- Ahnak is required to balance calcium ion homeostasis and smooth muscle development in the urinary system
- Ameliorating liver disease in an autosomal recessive polycystic kidney disease mouse model
- Arrhythmogenic Hearts in PKD2 Mutant Mice Are Characterized by Cardiac Fibrosis, Systolic, and Diastolic Dysfunctions
- Autosomal Dominant Polycystic Kidney Disease: Role of Imaging in Diagnosis and Management
- Combining Metformin and Drug-Loaded Kidney-Targeting Micelles for Polycystic Kidney Disease
- Computational study of biomechanical drivers of renal cystogenesis
- Congenital Hepatic Fibrosis as an Early Sign of Presentation of ADPKD
- Cross talk between lysine methyltransferase Smyd2 and TGF-β-Smad3 signaling promotes renal fibrosis in autosomal dominant polycystic kidney disease
- Cystic Kidney Diseases That Require a Differential Diagnosis from Autosomal Dominant Polycystic Kidney Disease (ADPKD)
- Dehydration Accelerates Cytogenesis and Cyst Growth in Pkd1<sup>-/-</sup> Mice by Regulating Macrophage M2 Polarization
- Detecting tandem repeat variants in coding regions using code-adVNTR
- Diagnosis and risk factors for intracranial aneurysms in autosomal polycystic kidney disease: a cross-sectional study from the Genkyst cohort
- Discovery and characterization of a novel PKD-Fn3 domains containing GH44 endoglucanase from a Tibetan metagenomic library
- Disease consequences of higher adiposity uncoupled from its adverse metabolic effects using Mendelian randomisation
- Effect of Averaging Measurements From Multiple MRI Pulse Sequences on Kidney Volume Reproducibility in Autosomal Dominant Polycystic Kidney Disease
- Effect of ultra-mini percutaneous nephrolithotomy and ShuoTong ureteroscopy on the stress response, inflammatory indices, and urokinase level in patients with polycystic kidney disease complicated with renal calculus
- Effects of Suramin on Polycystic Kidney Disease in a Mouse Model of Polycystin-1 Deficiency
- Emerging roles of Glucagon like peptide-1 in the management of autoimmune diseases and diabetes-associated comorbidities
- EMPA-KIDNEY: expanding the range of kidney protection by SGLT2 inhibitors
- Endothelium-Specific Deficiency of Polycystin-1 Promotes Hypertension and Cardiovascular Disorders
- Endovascular aneurysm repair for aorto-iliac artery pathologies in patients with autosomal dominant polycystic kidney disease
- Evaluation of novel compound variants of CEP290 in prenatally suspected case of Meckel syndrome through whole exome sequencing
- Functional TFEB activation characterizes multiple models of renal cystic disease and loss of polycystin-1
- Genetic screening is essential in polycystic kidney disease: It is never too late!
- Genetic testing and prenatal diagnosis for a Chinese pedigree affected with Meckel-Gruber syndrome
- Giant Polycystic Papillary Renal Cell Carcinoma: A Case Report and Literature Review
- HNF1B Alters an Evolutionarily Conserved Nephrogenic Program of Target Genes
- Hypoxia controls expression of kidney-pathogenic <em>MUC1</em> variants
- Identification of 17q12 microdeletion syndrome in a Latin American patient with maturity-onset diabetes of the young subtype 5: a case report
- Identification of Pathogenic Variants in RPGRIP1L with Meckel Syndrome and Preimplantation Genetic Testing in a Chinese Family
- Identification of Pax protein inhibitors that suppress target gene expression and cancer cell proliferation
- In vivo Polycystin-1 interactome using a novel Pkd1 knock-in mouse model
- Interdependent Regulation of Polycystin Expression Influences Starvation-Induced Autophagy and Cell Death
- Involvement of ceramide biosynthesis in increased extracellular vesicle release in <em>Pkd1</em> knock out cells
- Kidney Cyst Lining Epithelial Cells Are Resistant to Low-Dose Cisplatin-Induced DNA Damage in a Preclinical Model of Autosomal Dominant Polycystic Kidney Disease
- Kidney stone formation in a novel murine model of polycystic kidney disease
- Large deletion of Wdr19 in developing renal tubules disrupts primary ciliogenesis, leading to polycystic kidney disease in mice
- Large-scale epidemiological study on feline autosomal dominant polycystic kidney disease and identification of novel PKD1 gene variants
- Long-Term Outcomes of Kidney Transplant Recipients With Juvenile Nephronophthisis
- Mechanism of tethered agonist-mediated signaling by polycystin-1
- Meckel Gruber and Joubert Syndrome Diagnosed Prenatally: Allelism between the Two Ciliopathies, Complexities of Mutation Types and Digenic Inheritance
- Metabolic reprogramming in a slowly developing orthologous model of polycystic kidney disease
- Metformin in therapeutic applications in human diseases: its mechanism of action and clinical study
- MicroRNA-124 Alleviates Retinal Vasoregression via Regulating Microglial Polarization
- Molecular diagnostic in fetuses with isolated congenital anomalies of the kidney and urinary tract by whole-exome sequencing
- Multiomic identification of factors associated with progression to cystic kidney disease in mice with nephron Ift88 disruption
- Myofibroblast depletion reduces kidney cyst growth and fibrosis in autosomal dominant polycystic kidney disease
- Native nephrectomy in patients with autosomal dominant polycystic kidney disease in the kidney transplant program - single-center retrospective results of 2000-2020
- Neurofibromatosis 1 in the setting of dual diagnosis: Diagnostic and management conundrums
- NOS3 gene intron 4 a/b polymorphism is associated with ESRD in autosomal dominant polycystic kidney disease patients
- Novel <em>PKD2</em> Missense Mutation p.Ile424Ser in an Individual with Multiple Hepatic Cysts: A Case Report
- Novel 3D capsule device to restrict kidney volume expansion on polycystic kidney progression: feasibility study in a rat model
- Novel insight into ferroptosis in kidney diseases
- Oral-Facial-Digital Syndrome Type 1: A Case Report and Review
- Oral-facial-digital syndrome type 1: the kidney cystic disease that mimics autosomal dominant polycystic kidney disease
- Outcomes of arteriovenous fistula for hemodialysis in pediatric age group
- Pathophysiologic Implications and Therapeutic Approach of Klotho in Chronic Kidney Disease: A Systematic Review
- Pkhd1<sup>cyli/cyli</sup> mice have altered renal Pkhd1 mRNA processing and hormonally sensitive liver disease
- Polycystic kidney disease 2-like 1 channel contributes to the bitter aftertaste perception of quinine
- Polycystic Kidney Disease and Polycystic Liver Disease Associated to Advanced Gastric Cancer: an External Complication of Potter III Disease
- Polycystin-2 (TRPP2) regulates primary cilium length in LLC-PK1 renal epithelial cells
- Potential Roles of Glucagon-Like Peptide 1 Receptor Agonists (GLP-1 RAs) in Nondiabetic Populations
- Predicting the Risk of Progression in Indian ADPKD Cohort using PROPKD Score - A Single-Center Retrospective Study
- Prenatal ultrasound in fetuses with polycystic kidney appearance - expanding the diagnostic algorithm
- Pretransplant Dialysis and Preemptive Transplant in Living Donor Kidney Recipients
- Probenecid slows disease progression in a murine model of autosomal dominant polycystic kidney disease
- Quantitative Proteomic Study Unmasks Fibrinogen Pathway in Polycystic Liver Disease
- Recent advances in understanding ion transport mechanisms in polycystic kidney disease
- Renal Cyst
- Risk Severity Model for Pediatric Autosomal Dominant Polycystic Kidney Disease Using 3D Ultrasound Volumetry
- Role of abnormal energy metabolism in the progression of chronic kidney disease and drug intervention
- Role of the polycystic kidney disease domain in matriptase chaperone activity and localization of hepatocyte growth factor activator inhibitor-1
- SGLT2 inhibitors in non-diabetic kidney disease
- Single-Cell and CellChat Resolution Identifies Collecting Duct Cell Subsets and Their Communications with Adjacent Cells in PKD Kidneys
- Small hairpin inhibitory RNA delivery in the metanephric organ culture identifies long noncoding RNA <em>Pvt1</em> as a modulator of cyst growth
- Stable G-quadruplex DNA structures promote replication-dependent genome instability
- Strategies for Treatment of Multiple Brain Aneurysms Without Intraoperative Adjuncts
- Successful management of multiple obstructing renal calculi in a 30-year-old patient with autosomal dominant polycystic kidney disease using Frequency-Doubled Double-Pulse neodymium: Yttrium - Aluminium garnet laser lithotripsy
- The ciliary transition zone protein TMEM218 synergistically interacts with the NPHP module and its reduced dosage leads to a wide range of syndromic ciliopathies
- The Clinical and Mutational Spectrum of 69 Turkish Children with Autosomal Recessive or Autosomal Dominant Polycystic Kidney Disease: A Multicenter Retrospective Cohort Study
- The Joubert-Meckel-Nephronophthisis Spectrum of Ciliopathies
- The KIDNEYCODE Program: Diagnostic Yield and Clinical Features of Individuals with CKD
- The regulatory and modulatory roles of TRP family channels in malignant tumors and relevant therapeutic strategies
- The Role of Angiotensin II Type 1 Receptor A1166C Polymorphism in Autosomal Dominant Polycystic Kidney Disease
- The tryptophan-metabolizing enzyme indoleamine 2,3-dioxygenase 1 regulates polycystic kidney disease progression
- Three Novel Variants of CEP290 and CC2D2DA and a Link Between ZNF77 and SHH Signaling Pathway Are Found in Two Meckel-Gruber Syndrome Fetuses
- Transcription factor FoxM1 promotes cyst growth in PKD1 mutant ADPKD
- Upregulated Angiotensin Ia Receptors in the Hypothalamic Paraventricular Nucleus Sensitize Neuroendocrine Vasopressin Release and Blood Pressure in a Rodent Model of Polycystic Kidney Disease
- Variable phenotypes and penetrance between and within different zebrafish ciliary transition zone mutants
- Visual inspection reveals a novel pathogenic mutation in <em>PKD1</em> missed by the variant caller in whole‑exome sequencing
- Weight change and risk of obesity-related complications: A retrospective population-based cohort study of a UK primary care database
- Whole-Exome Sequencing Revealed the Mutational Profiles of Primary Central Nervous System Lymphoma
- XBP1 Activation Reduces Severity of Polycystic Kidney Disease due to a Nontruncating Polycystin-1 Mutation in Mice
- β3 adrenergic receptor as potential therapeutic target in ADPKD