frameshift

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

This results in a frameshift and translation of an almost entirely different protein.

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

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

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

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

In a 2006 study in which 110 patients were tested, 28 suffered from this frameshift mutation.

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

An Absence of Empathy is a 2005 album by Frameshift.

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

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

The first was an interstitial deletion, while the second and third were a nonsense and frameshift.

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

The inserted nucleotides cause a frameshift and result in a translated protein that differs from its gene.

In rare cases, a translating ribosome may shift from one frame to another, a translational frameshift.

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

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.

However, in human, the N-terminus of the predicted protein contains a frameshift and premature stop codon.

Path - tool that compares two frameshift proteins (back-translation principle)

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

However not all indels are frameshift mutations.

Thus, they concluded that the genetic code is a triplet code because it did not cause a frameshift in the reading frame.

Deletion also causes frameshift.

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