Category
Human genetics
Related lectures (110)
Genetic Traits Analysis
Explores genetic traits inheritance, family tree analysis, and various modes of genetic trait transmission in humans, including specific genetic disorders.
Chromosome 7: Trisomy Correction Mechanisms
Explores trisomy correction mechanisms, mosaicism, and genetic disorder diagnosis challenges.
Chemical Biology: High-Throughput and High-Content Screening
Covers Chemical Biology, high-throughput screening, RNA interference, CRISPR-Cas9, and organoid differentiation for drug discovery.
Genetic Disorders: Interpretation and Analysis
Explores the interpretation and analysis of genetic disorders using real cases of Angelman syndrome.
Prader-Villy Syndrome: Genetic Mechanisms and Clinical Implications
Explores the genetic basis of Prader-Villy syndrome and its comparison with Angelman syndrome, emphasizing DNA methylation patterns and chromosomal abnormalities.
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.
Ethical Issues of Human Biological Research
Explores ethical issues in human biological research, focusing on HeLa cells and informed consent.
Genetics: Mendel's Laws and Inheritance Patterns
Explores Mendel's laws, inheritance patterns, and genetic disorders like sickle-cell disease.
Parkinson's Disease: Genetic Factors
Explores genetic factors in Parkinson's disease, focusing on a-synuclein, Parkin, and PINK1, and their impact on mitochondrial quality control.
Blood Types and Genetic Mutations
Explores blood type inheritance and intriguing human genetic mutations.