- Increased Phosphorylation of ACTN4 Leads to Podocyte Dysfunction and Focal Segmental Glomerulosclerosis Mimicking Disease-Causing Mutations
10:00 AM - 12:00 PM
Increased Phosphorylation of ACTN4 Leads to Podocyte Dysfunction and Focal Segmental Glomerulosclerosis Mimicking Disease-Causing Mutations
October 22, 2020 | 10:00 AM - 12:00 PM
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- Toward a Molecular Mechanism for Low-Molecular-Weight Proteinuria in Dent Disease
10:00 AM - 12:00 PM
Toward a Molecular Mechanism for Low-Molecular-Weight Proteinuria in Dent Disease
October 22, 2020 | 10:00 AM - 12:00 PM
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- Super-Resolution Imaging of the Filtration Barrier Suggests a Role for Podocin R229Q in Genetic Predisposition to Glomerular Disease
10:00 AM - 12:00 PM
Super-Resolution Imaging of the Filtration Barrier Suggests a Role for Podocin R229Q in Genetic Predisposition to Glomerular Disease
October 22, 2020 | 10:00 AM - 12:00 PM
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- Reduced Glomerular and Nephron Injury due to Albumin Knockout in the Heavily Nephrotic, Polymerization-Defective GBM Laminin B2-Del44 Mutant Mice
10:00 AM - 12:00 PM
Reduced Glomerular and Nephron Injury due to Albumin Knockout in the Heavily Nephrotic, Polymerization-Defective GBM Laminin B2-Del44 Mutant Mice
October 22, 2020 | 10:00 AM - 12:00 PM
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- Klotho Improves Renal Function in Autosomal Dominant Tubulointerstitial Kidney Disease (ADTKD-UMOD)
10:00 AM - 12:00 PM
Klotho Improves Renal Function in Autosomal Dominant Tubulointerstitial Kidney Disease (ADTKD-UMOD)
October 22, 2020 | 10:00 AM - 12:00 PM
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- Spectrum of Mutations in 106 Chinese Patients with Gitelman Syndrome
10:00 AM - 12:00 PM
Spectrum of Mutations in 106 Chinese Patients with Gitelman Syndrome
October 22, 2020 | 10:00 AM - 12:00 PM
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- Glucosylceramide Synthase Inhibition with Venglustat in Classic Fabry Disease Patients Leads to Progressive Reduction of Endothelial Cell Globotriaosylceramide Inclusion Volume
10:00 AM - 12:00 PM
Glucosylceramide Synthase Inhibition with Venglustat in Classic Fabry Disease Patients Leads to Progressive Reduction of Endothelial Cell Globotriaosylceramide Inclusion Volume
October 22, 2020 | 10:00 AM - 12:00 PM
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- The Role of Claudin Variants in the Formation of Kidney Stones
10:00 AM - 12:00 PM
The Role of Claudin Variants in the Formation of Kidney Stones
October 22, 2020 | 10:00 AM - 12:00 PM
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- Elucidation of Molecular Pathogenesis of Lowe Syndrome and Dent Disease Type 2
10:00 AM - 12:00 PM
Elucidation of Molecular Pathogenesis of Lowe Syndrome and Dent Disease Type 2
October 22, 2020 | 10:00 AM - 12:00 PM
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- Atypical Histological Abnormalities in Patients with Nephronophthisis Diagnosed with NPHP1 Deletion
10:00 AM - 12:00 PM
Atypical Histological Abnormalities in Patients with Nephronophthisis Diagnosed with NPHP1 Deletion
October 22, 2020 | 10:00 AM - 12:00 PM
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- Biobank of Urinary Cells and Human Kidney Organoids Reveals Nephropathic Cystinosis Phenotypes and Gene Therapy Strategy
10:00 AM - 12:00 PM
Biobank of Urinary Cells and Human Kidney Organoids Reveals Nephropathic Cystinosis Phenotypes and Gene Therapy Strategy
October 22, 2020 | 10:00 AM - 12:00 PM
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- Clinical and Genetic Features of Autosomal Dominant Alport Syndrome
10:00 AM - 12:00 PM
Clinical and Genetic Features of Autosomal Dominant Alport Syndrome
October 22, 2020 | 10:00 AM - 12:00 PM
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- Beneficial Effect of Oxalobacter formigenes Treatment on Nephrocalcinosis in a Rat Model of Primary Hyperoxaluria
10:00 AM - 12:00 PM
Beneficial Effect of Oxalobacter formigenes Treatment on Nephrocalcinosis in a Rat Model of Primary Hyperoxaluria
October 22, 2020 | 10:00 AM - 12:00 PM
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- The Knockdown of RPL36A Downregulates GLA Expression Associated with Fabry Disease In Vitro Model
10:00 AM - 12:00 PM
The Knockdown of RPL36A Downregulates GLA Expression Associated with Fabry Disease In Vitro Model
October 22, 2020 | 10:00 AM - 12:00 PM
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- Focal Segmental Glomerulosclerosis with Glomerular Basement Membrane Abnormalities Caused by Compound Heterozygous Myosin 1E Gene Mutations
10:00 AM - 12:00 PM
Focal Segmental Glomerulosclerosis with Glomerular Basement Membrane Abnormalities Caused by Compound Heterozygous Myosin 1E Gene Mutations
October 22, 2020 | 10:00 AM - 12:00 PM
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- Metabolic State Modeling of Kidney Single Nuclei Data Reveals Cell-Specific Signatures at Baseline and in Disease
10:00 AM - 12:00 PM
Metabolic State Modeling of Kidney Single Nuclei Data Reveals Cell-Specific Signatures at Baseline and in Disease
October 22, 2020 | 10:00 AM - 12:00 PM
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- Metabolic Dysfunction of Glomerular Endothelial Cells in Alport Syndrome
10:00 AM - 12:00 PM
Metabolic Dysfunction of Glomerular Endothelial Cells in Alport Syndrome
October 22, 2020 | 10:00 AM - 12:00 PM
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- NPHS1 Variants Can Cause Persistent Asymptomatic Proteinuria: Genetic and Clinical Characteristics of Patients with NPHS1 Variants in Japan
10:00 AM - 12:00 PM
NPHS1 Variants Can Cause Persistent Asymptomatic Proteinuria: Genetic and Clinical Characteristics of Patients with NPHS1 Variants in Japan
October 22, 2020 | 10:00 AM - 12:00 PM
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- Ckd.Qld fabRy Epidemiology (aCQuiRE) Study: Fabry Disease Prevalence Among Patients with CKD
10:00 AM - 12:00 PM
Ckd.Qld fabRy Epidemiology (aCQuiRE) Study: Fabry Disease Prevalence Among Patients with CKD
October 22, 2020 | 10:00 AM - 12:00 PM
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- Systems Analyses of Renal Fabry Transcriptome and Response to Enzyme Replacement Therapy (ERT) Identifies a Cross-Validated and Druggable ERT-Resistant Module
10:00 AM - 12:00 PM
Systems Analyses of Renal Fabry Transcriptome and Response to Enzyme Replacement Therapy (ERT) Identifies a Cross-Validated and Druggable ERT-Resistant Module
October 22, 2020 | 10:00 AM - 12:00 PM
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- Circular RNA-Based Biomarker Profile of Patients with Fabry Disease
10:00 AM - 12:00 PM
Circular RNA-Based Biomarker Profile of Patients with Fabry Disease
October 22, 2020 | 10:00 AM - 12:00 PM
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- Outcome of Primary Hyperoxaluria Type 3: Clinics, Diagnostics, and Follow-Up
10:00 AM - 12:00 PM
Outcome of Primary Hyperoxaluria Type 3: Clinics, Diagnostics, and Follow-Up
October 22, 2020 | 10:00 AM - 12:00 PM
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- Patient Journey in Alport Syndrome
10:00 AM - 12:00 PM
Patient Journey in Alport Syndrome
October 22, 2020 | 10:00 AM - 12:00 PM
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- Multidisciplinary Renal Genetics Clinics: Family Perspectives and Preferences
10:00 AM - 12:00 PM
Multidisciplinary Renal Genetics Clinics: Family Perspectives and Preferences
October 22, 2020 | 10:00 AM - 12:00 PM
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- Autosomal Recessive Renal Tubular Dysgenesis Caused by a Founder Mutation of Angiotensinogen (AGT)
10:00 AM - 12:00 PM
Autosomal Recessive Renal Tubular Dysgenesis Caused by a Founder Mutation of Angiotensinogen (AGT)
October 22, 2020 | 10:00 AM - 12:00 PM
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- KIDNEYCODE: A Genetic Testing Program for Patients with CKD
10:00 AM - 12:00 PM
KIDNEYCODE: A Genetic Testing Program for Patients with CKD
October 22, 2020 | 10:00 AM - 12:00 PM
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- Very Rare Mutation Identified in Female Patient with Multisystemic Fabry Disease in the United States
10:00 AM - 12:00 PM
Very Rare Mutation Identified in Female Patient with Multisystemic Fabry Disease in the United States
October 22, 2020 | 10:00 AM - 12:00 PM
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- A Unique Case of COL4A3/4 and ACTN4 Mutations Combined
10:00 AM - 12:00 PM
A Unique Case of COL4A3/4 and ACTN4 Mutations Combined
October 22, 2020 | 10:00 AM - 12:00 PM
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- Kidney Tubuloids Model Cystinosis and Allow Drug Screening
10:00 AM - 12:00 PM
Kidney Tubuloids Model Cystinosis and Allow Drug Screening
October 22, 2020 | 10:00 AM - 12:00 PM
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- Case Report: Familial FSGS Associated with a Novel Variant of WT1
10:00 AM - 12:00 PM
Case Report: Familial FSGS Associated with a Novel Variant of WT1
October 22, 2020 | 10:00 AM - 12:00 PM
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- Positive Identification of Genetic Causes of FSGS Increases with Proper Patient Selection
10:00 AM - 12:00 PM
Positive Identification of Genetic Causes of FSGS Increases with Proper Patient Selection
October 22, 2020 | 10:00 AM - 12:00 PM
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- A Rare Case of Nephrotic Syndrome Associated with Dent Disease
10:00 AM - 12:00 PM
A Rare Case of Nephrotic Syndrome Associated with Dent Disease
October 22, 2020 | 10:00 AM - 12:00 PM
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- Mitochondriopathy Manifesting as Inherited Tubulointerstitial Nephropathy Without Symptomatic Other Organ Involvement
10:00 AM - 12:00 PM
Mitochondriopathy Manifesting as Inherited Tubulointerstitial Nephropathy Without Symptomatic Other Organ Involvement
October 22, 2020 | 10:00 AM - 12:00 PM
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- Discovery of CHK-336: A First-in-Class, Liver-Targeted, Small Molecule Inhibitor of Lactate Dehydrogenase for the Treatment of Primary Hyperoxaluria
10:00 AM - 12:00 PM
Discovery of CHK-336: A First-in-Class, Liver-Targeted, Small Molecule Inhibitor of Lactate Dehydrogenase for the Treatment of Primary Hyperoxaluria
October 22, 2020 | 10:00 AM - 12:00 PM
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- Disease Manifestations, Treatment, and Healthcare Resource Use (HRU) in Primary Hyperoxaluria Type 1 (PH1): An International Online Chart Review Study
10:00 AM - 12:00 PM
Disease Manifestations, Treatment, and Healthcare Resource Use (HRU) in Primary Hyperoxaluria Type 1 (PH1): An International Online Chart Review Study
October 22, 2020 | 10:00 AM - 12:00 PM
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- Recurrent SLC12A3 Mutations in Taiwanese Families with Gitelman Syndrome: A Rapid Detection for the Higher Prevalence
10:00 AM - 12:00 PM
Recurrent SLC12A3 Mutations in Taiwanese Families with Gitelman Syndrome: A Rapid Detection for the Higher Prevalence
October 22, 2020 | 10:00 AM - 12:00 PM
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- AVR-RD-01, an Investigational Lentiviral Gene Therapy for Fabry Disease, Reduces Gb3 Substrate in Endothelial Cells of Renal Peritubular Capillaries
10:00 AM - 12:00 PM
AVR-RD-01, an Investigational Lentiviral Gene Therapy for Fabry Disease, Reduces Gb3 Substrate in Endothelial Cells of Renal Peritubular Capillaries
October 22, 2020 | 10:00 AM - 12:00 PM
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- ILLUMINATE-B, a Phase 3 Open-Label Study to Evaluate Lumasiran, an RNAi Therapeutic, in Young Children with Primary Hyperoxaluria Type 1 (PH1)
10:00 AM - 12:00 PM
ILLUMINATE-B, a Phase 3 Open-Label Study to Evaluate Lumasiran, an RNAi Therapeutic, in Young Children with Primary Hyperoxaluria Type 1 (PH1)
October 22, 2020 | 10:00 AM - 12:00 PM
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- PHYOX3: A Long-Term, Open-Label Extension Trial of Nedosiran in Patients with Primary Hyperoxaluria Type 1, 2, or 3
10:00 AM - 12:00 PM
PHYOX3: A Long-Term, Open-Label Extension Trial of Nedosiran in Patients with Primary Hyperoxaluria Type 1, 2, or 3
October 22, 2020 | 10:00 AM - 12:00 PM
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- A Case of De Novo X-Linked Alport Syndrome Treated by Kidney Transplantation from the Patient’s Healthy Mother
10:00 AM - 12:00 PM
A Case of De Novo X-Linked Alport Syndrome Treated by Kidney Transplantation from the Patient’s Healthy Mother
October 22, 2020 | 10:00 AM - 12:00 PM
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- Clinical and Economic Impact of Primary Hyperoxaluria: A Retrospective Claims Analysis
10:00 AM - 12:00 PM
Clinical and Economic Impact of Primary Hyperoxaluria: A Retrospective Claims Analysis
October 22, 2020 | 10:00 AM - 12:00 PM
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- Identification of Genetic Drivers of Age-Related Renal Histopathology
10:00 AM - 12:00 PM
Identification of Genetic Drivers of Age-Related Renal Histopathology
October 22, 2020 | 10:00 AM - 12:00 PM
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- Epigenome-wide Association Study of Kidney Function
10:00 AM - 12:00 PM
Epigenome-wide Association Study of Kidney Function
October 22, 2020 | 10:00 AM - 12:00 PM
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