Related Experiment Videos
Genetic models: clues for understanding the pathogenesis of idiopathic nephrotic syndrome
1Department of Genetics and Institut National de la Santé et de la Recherche Médicale U423, Tour Lavoisier 6 étage, Hôpital Necker, 149 rue de Sèvres, 75015 Paris, France. antignac@necker.fr
The Journal of Clinical Investigation
|February 21, 2002
Abstract
No abstract available in PubMed .
Related Concept Videos
Articles linked to this work by shared authors, journal, and citation graph.
Podocin oligomers regulate the ordering of nephrin chains, providing the molecular basis of NPHS2 interallelic interactions.
Proceedings of the National Academy of Sciences of the United States of America·2026
Genetic screening in kidney transplant candidates.
Clinical kidney journal·2026
Exome Sequencing in a Large Cohort with Ciliopathy-Related Kidney Disease.
Clinical journal of the American Society of Nephrology : CJASN·2025
Genome sequencing identifies RMND1 as a strong candidate gene for severe prenatal kidney failure mimicking renal tubular dysgenesis associated with hyporeninism.
Pediatric nephrology (Berlin, Germany)·2025
Targeting tryptophan hydroxylase 1 restricts growth and suppresses plasticity in neuroendocrine prostate cancer.
The Journal of clinical investigation·2026
Balancing lipid synthesis and oxidation promotes B cell response to vaccination during immunosuppression.
The Journal of clinical investigation·2026
Gene-specific machine learning model EpiPred identifies likely pathogenic variants in the epilepsy-related gene STXBP1.
The Journal of clinical investigation·2026
Acute activation of Gq-signaling in pancreatic islet macrophages inhibits insulin secretion through AMPK-sphingolipid axis.
The Journal of clinical investigation·2026
A single dorsal vagal complex circuit mediates the aversive and anorectic responses to GLP1R agonists.
The Journal of clinical investigation·2026
Immune dysregulation and stem-like CD8+ T cell enrichment in type 1 diabetes pancreatic lymph nodes.
The Journal of clinical investigation·2026
Functional Characterization of a Novel Variant of the Thyroid Hormone Receptor Alpha in a Child with Developmental Delay and Abnormal Thyroid Function.
Thyroid : official journal of the American Thyroid Association·2026
Prevalence and penetrance of heritable retinoblastoma in two adult population cohorts: implications for genomic newborn screening.
European journal of human genetics : EJHG·2026
Genetic and pharmacological evidence linking CB1R signaling to hippocampal GABAergic dysfunction in ASD mouse model.
Neurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics·2026