Base by Base

Base by Base

Por: Gustavo Barra
Base by Base explores advances in genetics and genomics, with a focus on gene-disease associations, variant interpretation, protein structure, and insights from exome and genome sequencing. Each episode breaks down key studies and their clinical relevance—one base at a time.

Powered by AI, Base by Base offers a new way to learn on the go. Special thanks to authors who publish under CC BY 4.0, making open-access science faster to share and easier to explore.
243 episodios disponibles

Latest episodes of the podcast Base by Base

Mostrando página 11 de 13

️ 43: Personalized Molecular Signatures of Insulin Resistance and Type 2 Diabetes 11/06/2025
️ 42: Amino Acids Catalyse RNA Formation — Unlocking Prebiotic Cross-Catalysis 11/06/2025
️ 41: Public Preferences for Genomic Newborn Screening in Australia — Insights from Discrete Choice Experiments 10/06/2025
️ 40: Lysosomal Proton Leak — Uncovering SLC7A11’s Role as an Unconventional H⁺ Transit Pathway 09/06/2025
️ 39: Whole-Genome Polygenic Score Inference — Fast and Memory-Efficient Algorithms for Scalable PRS 07/06/2025
️ 38: Viral Journeys — Tracing the Ancestral Bat Origins of SARS-CoV and SARS-CoV-2 07/06/2025
️ 37: Proteomic Clues — Prioritizing Functional Missense Variants with Chemoproteomics 06/06/2025
️ 36: Bi-allelic POPDC2 Variants: A Novel Autosomal Recessive Cardiac Syndrome 06/06/2025
️ 35: Tracing the Evolutionary History of CCR5Δ32 — Insights from Ancient and Modern Genomes 06/06/2025
️ 34: Enzyme Replacement Therapy in Homocystinuria — Safety and Efficacy of Pegtibatinase in the Phase 1/2 COMPOSE Trial 06/06/2025
️ 33: Mis-splicing-derived Neoantigens — A New Avenue for Immunotherapy in Leukemia 05/06/2025
️ 32: Idursulfase Beta — A New Therapeutic Option for MPS II with Strong Clinical Evidence 05/06/2025
️ 31: Decoding Hidden Signals — Genome Sequencing Reveals Cryptic Splicing Variants in Marfan Syndrome 05/06/2025
️30: Heart in the Genes — A New Genetic Syndrome Linked to POPDC2 26/05/2025
️ 29: Rethinking Agency for Genetic Testing Intention among Latinos — Determining Predictors of Intention for Carrier Screening and Cancer Predisposition Testing 23/05/2025
️ 28: Cell-Type-Resolved TWAS — scPrediXcan Integrates Deep Learning and Single-Cell Data for Transcriptome-Wide Association Studies 22/05/2025
️ 27: Nucleocytosolic Vehicles — A CRISPR RNP Delivery Breakthrough 21/05/2025
️ 26: Reannotation in Focus — Uncovering Functional Non-Coding Mutations in Melanoma 20/05/2025
️ 25: Uncovering Mitochondrial DNA Diseases — The Solve-RD Experience with Genotype and Phenotype Integration 19/05/2025
️ 24: The Role of the X Chromosome in Complex Trait Genetics — Unraveling Dosage-Compensation Mechanisms 18/05/2025
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