frameshift mutation

Several diseases have frameshift mutations as at least part of the cause.

There are several biological processes that help to prevent frameshift mutations.

Why and how frameshift mutations occur are continually being sought after.

Mutations do occur and frameshift mutation is not the only type.

The detection of frameshift mutations can occur via several different methods.

Based on experimental results longer microsatellites have a higher rate of frameshift mutations.

Finding a cure for the diseases caused by frameshift mutations are rare.

Often, these are frameshift mutations that prevent the cell from producing more than the first part of the necessary protein.

Frameshift mutations can occur randomly or be caused by an external stimuli.

A frameshift mutation drastically changes the coding capacity of the message(genetic information).

As stated previously, frameshift mutations are more likely to occur in a region of repeat sequence.

Most of these individuals showed either a deletion or an insertion resulting in a frameshift mutation.

The frameshift mutations lead to an early stop codon which is known to play a role in the disease in infants.

Patients with Frameshift mutation- or Nonsense mutations suffer poor prognosis.

Frameshift mutations may result in severe genetic diseases such as Tay-Sachs disease.

These include both nonsense and frameshift mutations.

It is possible that the frameshift mutations seen in deafness-dystonia interfere with the interface between Tim8p and Tim13p.

This mutation produced a frameshift mutation, which led to a stop codon at position 131.

Frameshift mutations are found to be more common in repeat regions of DNA.

However not all indels are frameshift mutations.

There was no apparent linkage between the central frameshift mutation and the 3' polymorphism, as the two regions varied independent of one another.

A frameshift mutation within the coding region of the gene can be a factor in Crohn's Disease.

Frameshift mutations will alter all the amino acids encoded by the gene following the mutation.

The flanking DNA can also contribute to frameshift mutations.

They used frameshift mutations and a process called reversions, to add and delete various numbers of nucleotides.