- NBL1 Correlates with Kidney Disease in a Mouse Model for Alport Syndrome, but Is Not Causal
10:00 AM - 12:00 PM
NBL1 Correlates with Kidney Disease in a Mouse Model for Alport Syndrome, but Is Not Causal
October 26, 2024 | 10:00 AM - 12:00 PM
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- Systematic Metabolomics Study in the Serum and Urine of a Mouse Model of Alport Syndrome
10:00 AM - 12:00 PM
Systematic Metabolomics Study in the Serum and Urine of a Mouse Model of Alport Syndrome
October 26, 2024 | 10:00 AM - 12:00 PM
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- Dysregulated Glomerular Proteins in 1-Day-Old Col4a3 Knockout Mice
10:00 AM - 12:00 PM
Dysregulated Glomerular Proteins in 1-Day-Old Col4a3 Knockout Mice
October 26, 2024 | 10:00 AM - 12:00 PM
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- Development and Assessment of Col4a5 Missense Mouse Model of Alport Syndrome
10:00 AM - 12:00 PM
Development and Assessment of Col4a5 Missense Mouse Model of Alport Syndrome
October 26, 2024 | 10:00 AM - 12:00 PM
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- Nephrotic Syndrome-Associated Variants Dysregulate TRIM8 Functions in Biomolecular Condensates, Cell Adhesion, and Glomerular Injury
10:00 AM - 12:00 PM
Nephrotic Syndrome-Associated Variants Dysregulate TRIM8 Functions in Biomolecular Condensates, Cell Adhesion, and Glomerular Injury
October 26, 2024 | 10:00 AM - 12:00 PM
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- Pathogenic Variants in NFATC1 and NFATC3 Can Cause Nephrotic Syndrome
10:00 AM - 12:00 PM
Pathogenic Variants in NFATC1 and NFATC3 Can Cause Nephrotic Syndrome
October 26, 2024 | 10:00 AM - 12:00 PM
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- Transgenic Human Nephrin in Drosophila Nephrocytes Facilitates Variant Analysis
10:00 AM - 12:00 PM
Transgenic Human Nephrin in Drosophila Nephrocytes Facilitates Variant Analysis
October 26, 2024 | 10:00 AM - 12:00 PM
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- Mutation in NUP155 Causes Activation of Autophagy in Podocytes through Retraining the YAP in the Cytoplasm to Induce Podocyte Loss and Subsequent Nephrotic Syndrome
10:00 AM - 12:00 PM
Mutation in NUP155 Causes Activation of Autophagy in Podocytes through Retraining the YAP in the Cytoplasm to Induce Podocyte Loss and Subsequent Nephrotic Syndrome
October 26, 2024 | 10:00 AM - 12:00 PM
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- In Vivo Mechanisms of LAMB2 Variants in Isolated Nephropathy: Insights from Knock-In Mouse Models
10:00 AM - 12:00 PM
In Vivo Mechanisms of LAMB2 Variants in Isolated Nephropathy: Insights from Knock-In Mouse Models
October 26, 2024 | 10:00 AM - 12:00 PM
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- Deletion of Gapvd1 Sensitizes Murine Podocytes to Adriamycin-Induced Injury
10:00 AM - 12:00 PM
Deletion of Gapvd1 Sensitizes Murine Podocytes to Adriamycin-Induced Injury
October 26, 2024 | 10:00 AM - 12:00 PM
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- Characterization of Steroid-Resistant Nephrotic Syndrome-Associated Motor Domain Mutations in MYO1E
10:00 AM - 12:00 PM
Characterization of Steroid-Resistant Nephrotic Syndrome-Associated Motor Domain Mutations in MYO1E
October 26, 2024 | 10:00 AM - 12:00 PM
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- Potentiated JAK-STAT Signaling Differentiates Stem Cell-Derived Podocytes of Patients with APOL1-Associated FSGS from Those of Healthy Carriers with a High-Risk APOL1 Genotype
10:00 AM - 12:00 PM
Potentiated JAK-STAT Signaling Differentiates Stem Cell-Derived Podocytes of Patients with APOL1-Associated FSGS from Those of Healthy Carriers with a High-Risk APOL1 Genotype
October 26, 2024 | 10:00 AM - 12:00 PM
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- Differential Pathway Activation by APOL1 G1 and G2 Variants in Induced Pluripotent Stem Cell (iPSC)-Derived Endothelial Cells: Insights from Proteomic Analysis
10:00 AM - 12:00 PM
Differential Pathway Activation by APOL1 G1 and G2 Variants in Induced Pluripotent Stem Cell (iPSC)-Derived Endothelial Cells: Insights from Proteomic Analysis
October 26, 2024 | 10:00 AM - 12:00 PM
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- APOL1 Induction Increases Cytosolic Calcium in 293 Cells but Not HeLa or Isogenic Induced Pluripotent Stem Cell (iPSC)-Derived Podocytes
10:00 AM - 12:00 PM
APOL1 Induction Increases Cytosolic Calcium in 293 Cells but Not HeLa or Isogenic Induced Pluripotent Stem Cell (iPSC)-Derived Podocytes
October 26, 2024 | 10:00 AM - 12:00 PM
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- The Novel MYH9 Variant, c.1270C>G, p.Arg424Gly, Causes Epstein-Fechtner Syndrome by the Modification of Nonmuscular Myosin IIA Contraction
10:00 AM - 12:00 PM
The Novel MYH9 Variant, c.1270C>G, p.Arg424Gly, Causes Epstein-Fechtner Syndrome by the Modification of Nonmuscular Myosin IIA Contraction
October 26, 2024 | 10:00 AM - 12:00 PM
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- Biallelic Variant in ENPP6 Alters Choline Metabolism in Humans and Conveys Loss of Enzymatic Function In Vitro
10:00 AM - 12:00 PM
Biallelic Variant in ENPP6 Alters Choline Metabolism in Humans and Conveys Loss of Enzymatic Function In Vitro
October 26, 2024 | 10:00 AM - 12:00 PM
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- A Novel CLC-Kb Pore Mutation Disrupts Glycosylation and Associates with Distal Tubular Remodeling
10:00 AM - 12:00 PM
A Novel CLC-Kb Pore Mutation Disrupts Glycosylation and Associates with Distal Tubular Remodeling
October 26, 2024 | 10:00 AM - 12:00 PM
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- Characterization of a Novel Mutation Associated with Renal Tubular Acidosis
10:00 AM - 12:00 PM
Characterization of a Novel Mutation Associated with Renal Tubular Acidosis
October 26, 2024 | 10:00 AM - 12:00 PM
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- Identification of Pathogenetic Pathways in Autosomal Dominant Tubulointerstitial Kidney Disease Due to Mutations in REN
10:00 AM - 12:00 PM
Identification of Pathogenetic Pathways in Autosomal Dominant Tubulointerstitial Kidney Disease Due to Mutations in REN
October 26, 2024 | 10:00 AM - 12:00 PM
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- Mesencephalic Astrocyte-Derived Neurotrophic Factor (MANF) Is Indispensable for Maintaining Mitochondrial Homeostasis in Uromodulin-Associated CKD
10:00 AM - 12:00 PM
Mesencephalic Astrocyte-Derived Neurotrophic Factor (MANF) Is Indispensable for Maintaining Mitochondrial Homeostasis in Uromodulin-Associated CKD
October 26, 2024 | 10:00 AM - 12:00 PM
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- Unraveling the Role of Mitochondrial Dysfunction in the Pathogenesis of Clc-k2-Deficient Bartter Syndrome Mice
10:00 AM - 12:00 PM
Unraveling the Role of Mitochondrial Dysfunction in the Pathogenesis of Clc-k2-Deficient Bartter Syndrome Mice
October 26, 2024 | 10:00 AM - 12:00 PM
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- Novel Models to Study Fanconi Syndrome and CKD Due to Heterozygous GATMP341L Mutations
10:00 AM - 12:00 PM
Novel Models to Study Fanconi Syndrome and CKD Due to Heterozygous GATMP341L Mutations
October 26, 2024 | 10:00 AM - 12:00 PM
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- Establishment of a Quantitative Evaluation System for Interferon Pathways in Patients with Lupus Nephritis
10:00 AM - 12:00 PM
Establishment of a Quantitative Evaluation System for Interferon Pathways in Patients with Lupus Nephritis
October 26, 2024 | 10:00 AM - 12:00 PM
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- Chromatin Conformation and Histone Modification Profiling across Human Kidney Anatomic Regions
10:00 AM - 12:00 PM
Chromatin Conformation and Histone Modification Profiling across Human Kidney Anatomic Regions
October 26, 2024 | 10:00 AM - 12:00 PM
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- Targeted Delivery of Small Interfering RNA (siRNA) to Proximal Tubule Cells in the Kidneys
10:00 AM - 12:00 PM
Targeted Delivery of Small Interfering RNA (siRNA) to Proximal Tubule Cells in the Kidneys
October 26, 2024 | 10:00 AM - 12:00 PM
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- Towards a Translatable Model for Studying Therapeutic Efficacy in Alport Syndrome
10:00 AM - 12:00 PM
Towards a Translatable Model for Studying Therapeutic Efficacy in Alport Syndrome
October 26, 2024 | 10:00 AM - 12:00 PM
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- Oral L-lysine Treatment Ameliorates Proximal Tubular Damage in Mice with Alport Syndrome
10:00 AM - 12:00 PM
Oral L-lysine Treatment Ameliorates Proximal Tubular Damage in Mice with Alport Syndrome
October 26, 2024 | 10:00 AM - 12:00 PM
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- Kidney Protection by a Novel Keap1-Nrf2 Protein-Protein Interaction Inhibitor for a Mouse Model of Alport Syndrome
10:00 AM - 12:00 PM
Kidney Protection by a Novel Keap1-Nrf2 Protein-Protein Interaction Inhibitor for a Mouse Model of Alport Syndrome
October 26, 2024 | 10:00 AM - 12:00 PM
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- Protective Effect of Ambrisentan on Proteinuria in Patients with Alport Syndrome
10:00 AM - 12:00 PM
Protective Effect of Ambrisentan on Proteinuria in Patients with Alport Syndrome
October 26, 2024 | 10:00 AM - 12:00 PM
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- Adeno-Associated Virus (AAV)-Mediated Gene Therapy in Nphs1 Knockout Mice: A Strategy for Treating Congenital Nephrotic Syndrome
10:00 AM - 12:00 PM
Adeno-Associated Virus (AAV)-Mediated Gene Therapy in Nphs1 Knockout Mice: A Strategy for Treating Congenital Nephrotic Syndrome
October 26, 2024 | 10:00 AM - 12:00 PM
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- Treatment of Autosomal Dominant Tubulointerstitial Kidney Disease Uromodulin (ADTKD-UMOD) with Antisense Oligonucleotides
10:00 AM - 12:00 PM
Treatment of Autosomal Dominant Tubulointerstitial Kidney Disease Uromodulin (ADTKD-UMOD) with Antisense Oligonucleotides
October 26, 2024 | 10:00 AM - 12:00 PM
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- Ccr2 Targeting Does Not Ameliorate Disease Phenotype in a Model of UMOD-Related Autosomal Dominant Tubulointerstitial Kidney Disease
10:00 AM - 12:00 PM
Ccr2 Targeting Does Not Ameliorate Disease Phenotype in a Model of UMOD-Related Autosomal Dominant Tubulointerstitial Kidney Disease
October 26, 2024 | 10:00 AM - 12:00 PM
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- Developing New Therapies for Autosomal Dominant Tubulointerstitial Kidney Disease Caused by Uromodulin Mutations by Screening a Small Molecule Library
10:00 AM - 12:00 PM
Developing New Therapies for Autosomal Dominant Tubulointerstitial Kidney Disease Caused by Uromodulin Mutations by Screening a Small Molecule Library
October 26, 2024 | 10:00 AM - 12:00 PM
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- Characterization and Regulation of the Disease-Causing Mucin 1 Frameshift Protein in Patient-Derived Cells Affected by Autosomal Dominant Tubulointerstitial Kidney Disease (ADTKD)-MUC1
10:00 AM - 12:00 PM
Characterization and Regulation of the Disease-Causing Mucin 1 Frameshift Protein in Patient-Derived Cells Affected by Autosomal Dominant Tubulointerstitial Kidney Disease (ADTKD)-MUC1
October 26, 2024 | 10:00 AM - 12:00 PM
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- Proximal Tubule-Targeted Adeno-Associated Virus (AAV) Gene Therapy for Cystinuria
10:00 AM - 12:00 PM
Proximal Tubule-Targeted Adeno-Associated Virus (AAV) Gene Therapy for Cystinuria
October 26, 2024 | 10:00 AM - 12:00 PM
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- 2,8-Dihydroxyadenine Impacts Kidney Cell Health and Barrier Integrity in an In Vitro Model of Adenine Phosphoribosyltransferase (APRT) Deficiency
10:00 AM - 12:00 PM
2,8-Dihydroxyadenine Impacts Kidney Cell Health and Barrier Integrity in an In Vitro Model of Adenine Phosphoribosyltransferase (APRT) Deficiency
October 26, 2024 | 10:00 AM - 12:00 PM
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- Clinical Utility of a Novel Ultraperformance Liquid Chromatography-Tandem Mass Spectrometry (UPLC-MS/MS) Plasma 2,8-Dihydroxyadenine Assay in Patients with Adenine Phosphoribosyltransferase (APRT) Deficiency
10:00 AM - 12:00 PM
Clinical Utility of a Novel Ultraperformance Liquid Chromatography-Tandem Mass Spectrometry (UPLC-MS/MS) Plasma 2,8-Dihydroxyadenine Assay in Patients with Adenine Phosphoribosyltransferase (APRT) Deficiency
October 26, 2024 | 10:00 AM - 12:00 PM
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- Effect of Allopurinol and Febuxostat on Plasma and Urine 2,8-Dihydroxyadenine: A Clinical Trial
10:00 AM - 12:00 PM
Effect of Allopurinol and Febuxostat on Plasma and Urine 2,8-Dihydroxyadenine: A Clinical Trial
October 26, 2024 | 10:00 AM - 12:00 PM
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- Burden of Illness of Primary Hyperoxaluria with CKD
10:00 AM - 12:00 PM
Burden of Illness of Primary Hyperoxaluria with CKD
October 26, 2024 | 10:00 AM - 12:00 PM
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- Evaluation of the Impact of SGLT2 Inhibitor Treatment in a Mouse Model of Dent Disease
10:00 AM - 12:00 PM
Evaluation of the Impact of SGLT2 Inhibitor Treatment in a Mouse Model of Dent Disease
October 26, 2024 | 10:00 AM - 12:00 PM
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- Nedosiran in Pediatric Patients with PH1 (PHYOX8)
10:00 AM - 12:00 PM
Nedosiran in Pediatric Patients with PH1 (PHYOX8)
October 26, 2024 | 10:00 AM - 12:00 PM
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- Lucerastat Effect on Kidney Function in Patients with Fabry Disease: Results from the Phase 3 Clinical Program
10:00 AM - 12:00 PM
Lucerastat Effect on Kidney Function in Patients with Fabry Disease: Results from the Phase 3 Clinical Program
October 26, 2024 | 10:00 AM - 12:00 PM
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- A Phase 4 Study to Evaluate the Safety and Tolerability of Higher Infusion Rates of Agalsidase Beta to Shorten Infusion Duration in Fabry Disease: Interim Analysis
10:00 AM - 12:00 PM
A Phase 4 Study to Evaluate the Safety and Tolerability of Higher Infusion Rates of Agalsidase Beta to Shorten Infusion Duration in Fabry Disease: Interim Analysis
October 26, 2024 | 10:00 AM - 12:00 PM
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- Early Intervention with Angiotensin Blockade to Reverse Proteinuria in Glycogen Storage Disease Type Ia (GSD Ia)
10:00 AM - 12:00 PM
Early Intervention with Angiotensin Blockade to Reverse Proteinuria in Glycogen Storage Disease Type Ia (GSD Ia)
October 26, 2024 | 10:00 AM - 12:00 PM
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