- Renal Trajectories in the French RaDiCo Alport Syndrome Cohort
10:00 AM - 12:00 PM
Renal Trajectories in the French RaDiCo Alport Syndrome Cohort
November 06, 2025 | 10:00 AM - 12:00 PM
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- Deep Intronic Single-Nucleotide Variant in COL4A5 Causes X-Linked Alport Syndrome by Aberrant Splicing into a Pseudoexon Containing Intron 6
10:00 AM - 12:00 PM
Deep Intronic Single-Nucleotide Variant in COL4A5 Causes X-Linked Alport Syndrome by Aberrant Splicing into a Pseudoexon Containing Intron 6
November 06, 2025 | 10:00 AM - 12:00 PM
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- Urinary Proteomics in Alport Syndrome to Identify Rapid Progressors
10:00 AM - 12:00 PM
Urinary Proteomics in Alport Syndrome to Identify Rapid Progressors
November 06, 2025 | 10:00 AM - 12:00 PM
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- Understanding Severe Kidney Disease in Pediatric Autosomal Dominant Alport Syndrome
10:00 AM - 12:00 PM
Understanding Severe Kidney Disease in Pediatric Autosomal Dominant Alport Syndrome
November 06, 2025 | 10:00 AM - 12:00 PM
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- Challenges in the Histopathologic Diagnosis of Autosomal Dominant Alport Syndrome: A Comparative Genotype-Based Study
10:00 AM - 12:00 PM
Challenges in the Histopathologic Diagnosis of Autosomal Dominant Alport Syndrome: A Comparative Genotype-Based Study
November 06, 2025 | 10:00 AM - 12:00 PM
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- Novel Intronic Collagen4A5 Mutation Causing Familial Alport Syndrome
10:00 AM - 12:00 PM
Novel Intronic Collagen4A5 Mutation Causing Familial Alport Syndrome
November 06, 2025 | 10:00 AM - 12:00 PM
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- Digenic Inheritance in Alport Syndrome: Clinical and Genetic Insights
10:00 AM - 12:00 PM
Digenic Inheritance in Alport Syndrome: Clinical and Genetic Insights
November 06, 2025 | 10:00 AM - 12:00 PM
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- ADAMTS13 Protects Kidney Function in Alport Syndrome
10:00 AM - 12:00 PM
ADAMTS13 Protects Kidney Function in Alport Syndrome
November 06, 2025 | 10:00 AM - 12:00 PM
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- Integrated Spatial Lipidomic and Proteomic Analysis by Matrix-Assisted Laser Desorption/Ionization Mass Spectrometry Imaging in Thin Basement Membrane Disease and Alport Syndrome: A Pilot Investigation
10:00 AM - 12:00 PM
Integrated Spatial Lipidomic and Proteomic Analysis by Matrix-Assisted Laser Desorption/Ionization Mass Spectrometry Imaging in Thin Basement Membrane Disease and Alport Syndrome: A Pilot Investigation
November 06, 2025 | 10:00 AM - 12:00 PM
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- Deep Learning-Based Screening of Alport Syndrome Using Retinal Optical Coherence Tomography Images
10:00 AM - 12:00 PM
Deep Learning-Based Screening of Alport Syndrome Using Retinal Optical Coherence Tomography Images
November 06, 2025 | 10:00 AM - 12:00 PM
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- Temporal Retinal Thinning as a Preclinical Marker of Alport Syndrome in Cases of Genetic Uncertainty
10:00 AM - 12:00 PM
Temporal Retinal Thinning as a Preclinical Marker of Alport Syndrome in Cases of Genetic Uncertainty
November 06, 2025 | 10:00 AM - 12:00 PM
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- Distinguishing Severe Alport Syndrome from Primary FSGS Using Retinal Optical Coherence Tomography (OCT): Diagnostic Role for Temporal Thinning
10:00 AM - 12:00 PM
Distinguishing Severe Alport Syndrome from Primary FSGS Using Retinal Optical Coherence Tomography (OCT): Diagnostic Role for Temporal Thinning
November 06, 2025 | 10:00 AM - 12:00 PM
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- Crescentic Phase of Alport Syndrome: A Rare Glimpse into Rapid Progression
10:00 AM - 12:00 PM
Crescentic Phase of Alport Syndrome: A Rare Glimpse into Rapid Progression
November 06, 2025 | 10:00 AM - 12:00 PM
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- Intermingled Autoimmune Kidney Disease with Genetic Disorders: A Case of Membranous Glomerulonephritis and Alport Syndrome Coexistence
10:00 AM - 12:00 PM
Intermingled Autoimmune Kidney Disease with Genetic Disorders: A Case of Membranous Glomerulonephritis and Alport Syndrome Coexistence
November 06, 2025 | 10:00 AM - 12:00 PM
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- From Filter to Failure: Serpin-Driven Glomerulotubular Injury in Alport Syndrome
10:00 AM - 12:00 PM
From Filter to Failure: Serpin-Driven Glomerulotubular Injury in Alport Syndrome
November 06, 2025 | 10:00 AM - 12:00 PM
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- Maintenance of Podocyte Slit-Diaphragm Integrity in Alport Syndrome After Restoration of the GBM
10:00 AM - 12:00 PM
Maintenance of Podocyte Slit-Diaphragm Integrity in Alport Syndrome After Restoration of the GBM
November 06, 2025 | 10:00 AM - 12:00 PM
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- Early Variable Gene of Alport Syndrome, Tnfsf15, Is a Protective Factor and Effect Modifier Against Renal Pathology
10:00 AM - 12:00 PM
Early Variable Gene of Alport Syndrome, Tnfsf15, Is a Protective Factor and Effect Modifier Against Renal Pathology
November 06, 2025 | 10:00 AM - 12:00 PM
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- Artificial Intelligence (AI)-Based Quantification of COL4A5 Deposition on Glomerular Basement Membrane in Mice with Alport Syndrome Defines Therapeutic Threshold for Gene Therapy
10:00 AM - 12:00 PM
Artificial Intelligence (AI)-Based Quantification of COL4A5 Deposition on Glomerular Basement Membrane in Mice with Alport Syndrome Defines Therapeutic Threshold for Gene Therapy
November 06, 2025 | 10:00 AM - 12:00 PM
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- Extracellular Vesicles Mitigate Glomerular Endothelial Lipid Dysregulation and Mitochondrial Dysfunction in Alport syndrome
10:00 AM - 12:00 PM
Extracellular Vesicles Mitigate Glomerular Endothelial Lipid Dysregulation and Mitochondrial Dysfunction in Alport syndrome
November 06, 2025 | 10:00 AM - 12:00 PM
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- Effect of Pregnancy on Kidney Disease Progression in Col4a3-/- Alport Mice
10:00 AM - 12:00 PM
Effect of Pregnancy on Kidney Disease Progression in Col4a3-/- Alport Mice
November 06, 2025 | 10:00 AM - 12:00 PM
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- Artificial Intelligence: Driven Gene Therapy for Alport Syndrome
10:00 AM - 12:00 PM
Artificial Intelligence: Driven Gene Therapy for Alport Syndrome
November 06, 2025 | 10:00 AM - 12:00 PM
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- Ultrasound-Mediated Delivery of Nonviral Col4a5 Gene Therapy Vector in X-Linked Alport Syndrome (XLAS) Disease Model Mice and Nonhuman Primates
10:00 AM - 12:00 PM
Ultrasound-Mediated Delivery of Nonviral Col4a5 Gene Therapy Vector in X-Linked Alport Syndrome (XLAS) Disease Model Mice and Nonhuman Primates
November 06, 2025 | 10:00 AM - 12:00 PM
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- Contribution of COL4A3-5 Variants to Idiopathic Nephrotic Syndrome
10:00 AM - 12:00 PM
Contribution of COL4A3-5 Variants to Idiopathic Nephrotic Syndrome
November 06, 2025 | 10:00 AM - 12:00 PM
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- Patient-Reported Concerns and Worrying About Kidney Conditions and APOL1 High-Risk Genotypes: A Midwestern US Cohort Study of Black Americans
10:00 AM - 12:00 PM
Patient-Reported Concerns and Worrying About Kidney Conditions and APOL1 High-Risk Genotypes: A Midwestern US Cohort Study of Black Americans
November 06, 2025 | 10:00 AM - 12:00 PM
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- APOL1 Genetic Testing, Family History of Hypertension and Kidney Disease, and Renal Risk Variant Distributions in a Midwestern US Cohort
10:00 AM - 12:00 PM
APOL1 Genetic Testing, Family History of Hypertension and Kidney Disease, and Renal Risk Variant Distributions in a Midwestern US Cohort
November 06, 2025 | 10:00 AM - 12:00 PM
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- Small Molecule Inhibitors of APOL1 Reverse Dysfunctional Signaling Mediated by APOL1 Risk Variants in Immortalized Human Podocytes
10:00 AM - 12:00 PM
Small Molecule Inhibitors of APOL1 Reverse Dysfunctional Signaling Mediated by APOL1 Risk Variants in Immortalized Human Podocytes
November 06, 2025 | 10:00 AM - 12:00 PM
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- Inaxaplin for a Broad Population with APOL1-Mediated Kidney Disease and Comorbid Conditions: Phase 2 Proof-of-Concept Study
10:00 AM - 12:00 PM
Inaxaplin for a Broad Population with APOL1-Mediated Kidney Disease and Comorbid Conditions: Phase 2 Proof-of-Concept Study
November 06, 2025 | 10:00 AM - 12:00 PM
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- Identification of a Monogenic Cause in Steroid-Resistant Nephrotic Syndrome and Related Kidney Diseases
10:00 AM - 12:00 PM
Identification of a Monogenic Cause in Steroid-Resistant Nephrotic Syndrome and Related Kidney Diseases
November 06, 2025 | 10:00 AM - 12:00 PM
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- CureGN Network's Return of Results Study: Participants' Experiences
10:00 AM - 12:00 PM
CureGN Network's Return of Results Study: Participants' Experiences
November 06, 2025 | 10:00 AM - 12:00 PM
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- Transcriptome-First Approach to Diagnose Monogenic Nephrotic Syndrome
10:00 AM - 12:00 PM
Transcriptome-First Approach to Diagnose Monogenic Nephrotic Syndrome
November 06, 2025 | 10:00 AM - 12:00 PM
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- From Mild Proteinuria to Congenital Nephrotic Syndrome: Clinical Heterogeneity of NPHS1 Biallelic Variants in a Japanese Cohort
10:00 AM - 12:00 PM
From Mild Proteinuria to Congenital Nephrotic Syndrome: Clinical Heterogeneity of NPHS1 Biallelic Variants in a Japanese Cohort
November 06, 2025 | 10:00 AM - 12:00 PM
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- Adult-Onset NPHS1 Nephrotic Syndrome: Two Cases Highlighting Diagnostic and Therapeutic Gaps
10:00 AM - 12:00 PM
Adult-Onset NPHS1 Nephrotic Syndrome: Two Cases Highlighting Diagnostic and Therapeutic Gaps
November 06, 2025 | 10:00 AM - 12:00 PM
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- Pathogenic NPHS2 Variants Predominantly Cause Adult-Onset FSGS in the United States While Childhood-Onset Disease Predominates in Europe and East Asia
10:00 AM - 12:00 PM
Pathogenic NPHS2 Variants Predominantly Cause Adult-Onset FSGS in the United States While Childhood-Onset Disease Predominates in Europe and East Asia
November 06, 2025 | 10:00 AM - 12:00 PM
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- Phenotypic and Biopsy Characteristics of Adult-Onset NPHS2-Associated FSGS
10:00 AM - 12:00 PM
Phenotypic and Biopsy Characteristics of Adult-Onset NPHS2-Associated FSGS
November 06, 2025 | 10:00 AM - 12:00 PM
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- Clinical Spectrum and Genotype-Phenotype Associations in Coenzyme Q10 Deficiency Nephropathy in a Chinese Cohort
10:00 AM - 12:00 PM
Clinical Spectrum and Genotype-Phenotype Associations in Coenzyme Q10 Deficiency Nephropathy in a Chinese Cohort
November 06, 2025 | 10:00 AM - 12:00 PM
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- Potentially Treatable Steroid-Resistant Nephrotic Syndrome (SRNS) Diagnosed via Comprehensive Renal Genetic Testing
10:00 AM - 12:00 PM
Potentially Treatable Steroid-Resistant Nephrotic Syndrome (SRNS) Diagnosed via Comprehensive Renal Genetic Testing
November 06, 2025 | 10:00 AM - 12:00 PM
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- ADCK4-Related Steroid-Resistant Nephrotic Syndrome with Intrafamilial Variability: A Case of Three Siblings
10:00 AM - 12:00 PM
ADCK4-Related Steroid-Resistant Nephrotic Syndrome with Intrafamilial Variability: A Case of Three Siblings
November 06, 2025 | 10:00 AM - 12:00 PM
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- Novel Gene Disease Association Between MEFV and Nephrotic Syndrome
10:00 AM - 12:00 PM
Novel Gene Disease Association Between MEFV and Nephrotic Syndrome
November 06, 2025 | 10:00 AM - 12:00 PM
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- Cell-Specific Evaluation of AAV9-Mediated SGPL1 Gene Delivery in a Sgpl1-/- Mouse Model with Nephrotic Syndrome
10:00 AM - 12:00 PM
Cell-Specific Evaluation of AAV9-Mediated SGPL1 Gene Delivery in a Sgpl1-/- Mouse Model with Nephrotic Syndrome
November 06, 2025 | 10:00 AM - 12:00 PM
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- Molecular Characterization of Podocytes in Podocyte-Specific Nup160 Knockout Mice
10:00 AM - 12:00 PM
Molecular Characterization of Podocytes in Podocyte-Specific Nup160 Knockout Mice
November 06, 2025 | 10:00 AM - 12:00 PM
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- FSGS-Associated Myosin1e Mutations Disrupt Its Motor Activity and Intracellular Localization
10:00 AM - 12:00 PM
FSGS-Associated Myosin1e Mutations Disrupt Its Motor Activity and Intracellular Localization
November 06, 2025 | 10:00 AM - 12:00 PM
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- Proteomic Analysis of Podocytopathy Protein NOS1AP Reveals Novel PTPN14 Interaction Disrupted in Disease
10:00 AM - 12:00 PM
Proteomic Analysis of Podocytopathy Protein NOS1AP Reveals Novel PTPN14 Interaction Disrupted in Disease
November 06, 2025 | 10:00 AM - 12:00 PM
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- Single-Dose Adeno-Associated Virus Gene Therapy for C3 Glomerulopathy in an Avatar Mouse Model of Human Complement-Mediated Kidney Disease
10:00 AM - 12:00 PM
Single-Dose Adeno-Associated Virus Gene Therapy for C3 Glomerulopathy in an Avatar Mouse Model of Human Complement-Mediated Kidney Disease
November 06, 2025 | 10:00 AM - 12:00 PM
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- B Cell-Targeted Transgenic Expression of the Human Lupus Gene BANK1 in Mice Leads to Immune Phenotypes and Lupus Nephritis
10:00 AM - 12:00 PM
B Cell-Targeted Transgenic Expression of the Human Lupus Gene BANK1 in Mice Leads to Immune Phenotypes and Lupus Nephritis
November 06, 2025 | 10:00 AM - 12:00 PM
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- Uncovering the Truth: Genetic Testing Reshapes Pediatric Diagnosis and Treatment
10:00 AM - 12:00 PM
Uncovering the Truth: Genetic Testing Reshapes Pediatric Diagnosis and Treatment
November 06, 2025 | 10:00 AM - 12:00 PM
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