Lectures related to Prader-Villy Syndrome: Genetic Mechanisms and Clinical Implications

Small Molecule Drugs: Genetic Diseases

Delves into the molecular basis of genetic diseases, discussing specific examples like Phenylketonuria and Haemophilia A, and the development of small molecule drugs for genetic disorders.

Genomic Alterations in Cancer

Explores genetic and epigenetic changes in cancer, including mutations, chromosomal alterations, and high-throughput measurement methods.

Patterns of Inheritance in Biology

Explores major themes in biology, patterns of inheritance, Mendel's laws, genetic defects, and the impact of the environment on phenotype.

Angelman Syndrome: Genetic Mechanisms

Explores DNA methylation analysis and gene mutations in Angelman Syndrome.

Mutations and Genetic Variability

Explores mutations, phenotype effects, environmental influences, meiosis, genetic shuffling, and chromosomal abnormalities.

Genetic Variability & Diversity: Mutations and Polymorphisms

Explores mutations and polymorphisms, highlighting their impact on genetic diversity.

Mutations and Cancer: The Role of P53 and HPV

Covers mutations, the role of P53 in cancer, and HPV's impact on tumorigenesis.

Genetic Mutations: Causes and Effects

Explores genetic mutations, chromosomal abnormalities, DNA repair, and disease implications.

Neurogenetics: Building blocks of a gene

Explores 21st-century neurogenetics and the building blocks of genes, emphasizing the impact of environment and genetics on neurodevelopment.

DNA Replication and Cancer

Explores the link between DNA replication, DNA repair mechanisms, and cancer development.

Genetic Variability and Diversity: Mutations

Explores genetic variability, mutations, SNPs, and their impact on the genetic code.

Molecules of Life: Understanding Translation and Protein Synthesis

Provides an overview of translation and protein synthesis, covering the genetic code, tRNA, and the steps involved in protein formation.

Molecular Evolution: Mutations and Genetic Diversity

Explores mutations, genetic diversity, and horizontal gene transfer, emphasizing the impact of errors during replication and exposure to mutagens.

Chromosomal Dosage and Genetic Disorders

Explores chromosomal dosage, genetic disorders, inheritance patterns, and X chromosome inactivation.

Retinoblastoma: Genetic Mechanisms and Clinical Implications

Explores the genetic mechanisms of retinoblastoma and their clinical implications, shedding light on tumor suppression, DNA repair, and genetic recombination.

Chromosome Anomalies: Trisomy and Uniparental Disomy

Covers DNA replication, PCR technology, microsatellites, placental trisomy, and genetic anomalies in prenatal testing.

Regulation of Metabolism: Molecular Mechanisms

Explores the molecular mechanisms regulating enzyme activity and gene expression in metabolism.

Genetic Diversity: Evolution and Mechanisms

Covers genetic diversity's role in evolution, including natural selection, mutation, and speciation.

Chromosome 7: Trisomy Correction Mechanisms

Explores trisomy correction mechanisms, mosaicism, and genetic disorder diagnosis challenges.

Personalized Medicine: Genetic Variability and Drug Response

Explores personalized medicine, genetic variability, and drug response, emphasizing tailoring treatments based on individual genetic and metabolic profiles.