k RNA repeats in myotonic dystrophy, molecular model Molecular model of the extended messenger RNA ribonucleic acid molecule produced in type 2 myotonic dystrophy DM2. DM2 is a genetic disease that causes muscle loss and weakness that gets worse over time. The muscles are also often unable to relax after use. It is caused by a segment of DNA being repeated an abnormal number of times. When the DNA is transcribed to mRNA it produces an unusually long mRNA molecule that forms clumps in the cell. The clumps interfere with the production of proteins and prevent the normal functioning of the cell, leading to the symptoms of DM2. Stock Photo - Afloimages
Sign up
Login
All images
RNA repeats in myotonic dystrophy, molecular model Molecular model of the extended messenger RNA  ribonucleic acid  molecule produced in type 2 myotonic dystrophy  DM2 . DM2 is a genetic disease that causes muscle loss and weakness that gets worse over time. The muscles are also often unable to relax after use. It is caused by a segment of DNA being repeated an abnormal number of times. When the DNA is transcribed to mRNA it produces an unusually long mRNA molecule that forms clumps in the cell. The clumps interfere with the production of proteins and prevent the normal functioning of the cell, leading to the symptoms of DM2.
RM

RNA repeats in myotonic dystrophy, molecular model

Molecular model of the extended messenger RNA (ribonucleic acid) molecule produced in type 2 myotonic dystrophy (DM2). DM2 is a genetic disease that causes muscle loss and weakness that gets worse over time. The muscles are also often unable to relax after use. It is caused by a segment of DNA being repeated an abnormal number of times. When the DNA is transcribed to mRNA it produces an unusually long mRNA molecule that forms clumps in the cell. The clumps interfere with the production of proteins and prevent the normal functioning of the cell, leading to the symptoms of DM2.

Details

ID
145499155

Collection

License type
Rights Managed

Photographer



Sign in
Member access
Login not found.