Part 5 of Science Live is dedicated to ‘Genetics – Blueprint of Duchenne Muscular Dystrophy’ and covers a range of essential topics over four concise episodes.
In this section we explore the blueprints of Duchenne muscular dystrophy by exploring the dystrophin gene and how genetic mutations occur. Using simple and straightforward language to tackle complex topics such the exons of genes, reading frames, and splice variants, to help you understand the genetic underpinning of Duchenne muscular dystrophy. Join us as we grow our knowledge of Duchenne muscular dystrophy together.
The Dystrophin Gene
Join us as we discuss the dystrophin gene – the largest known gene in the human genome.
Read moreWhat are Exons?
Learn what exons are and their crucial role in gene expression and subsequent protein synthesis.
Read moreGenetic Mutations in Duchenne Muscular Dystrophy
Here we discuss how mutations can occur, and how the genetic mutations in the dystrophin gene leads to Duchenne muscular dystrophy symptoms.
Read moreReading Frames
Explore the fundamental genetic concept of reading frames in our latest video. Dive into how these frames dictate the translation of DNA into proteins, and how changes in the reading frames can alter these proteins.
Read moreWhat is a Splice Site Variant?
Here you will learn how these mutations disrupt gene expression and lead to a range of genetic disorders such as Duchenne muscular dystrophy.
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