AIRLINK 72.59 Increased By ▲ 3.39 (4.9%)
BOP 4.99 Increased By ▲ 0.09 (1.84%)
CNERGY 4.29 Increased By ▲ 0.03 (0.7%)
DFML 31.71 Increased By ▲ 0.46 (1.47%)
DGKC 80.90 Increased By ▲ 3.65 (4.72%)
FCCL 21.42 Increased By ▲ 1.42 (7.1%)
FFBL 35.19 Increased By ▲ 0.19 (0.54%)
FFL 9.33 Increased By ▲ 0.21 (2.3%)
GGL 9.82 Increased By ▲ 0.02 (0.2%)
HBL 112.40 Decreased By ▼ -0.36 (-0.32%)
HUBC 136.50 Increased By ▲ 3.46 (2.6%)
HUMNL 7.14 Increased By ▲ 0.19 (2.73%)
KEL 4.35 Increased By ▲ 0.12 (2.84%)
KOSM 4.35 Increased By ▲ 0.10 (2.35%)
MLCF 37.67 Increased By ▲ 1.07 (2.92%)
OGDC 137.75 Increased By ▲ 4.88 (3.67%)
PAEL 23.41 Increased By ▲ 0.77 (3.4%)
PIAA 24.55 Increased By ▲ 0.35 (1.45%)
PIBTL 6.63 Increased By ▲ 0.17 (2.63%)
PPL 125.05 Increased By ▲ 8.75 (7.52%)
PRL 26.99 Increased By ▲ 1.09 (4.21%)
PTC 13.32 Increased By ▲ 0.24 (1.83%)
SEARL 52.70 Increased By ▲ 0.70 (1.35%)
SNGP 70.80 Increased By ▲ 3.20 (4.73%)
SSGC 10.54 No Change ▼ 0.00 (0%)
TELE 8.33 Increased By ▲ 0.05 (0.6%)
TPLP 10.95 Increased By ▲ 0.15 (1.39%)
TRG 60.60 Increased By ▲ 1.31 (2.21%)
UNITY 25.10 Decreased By ▼ -0.03 (-0.12%)
WTL 1.28 Increased By ▲ 0.01 (0.79%)
BR100 7,566 Increased By 157.7 (2.13%)
BR30 24,786 Increased By 749.4 (3.12%)
KSE100 71,902 Increased By 1235.2 (1.75%)
KSE30 23,595 Increased By 371 (1.6%)
Editorials

Scientists restore deafness in mice through gene-therapy

The evolving technology of gene therapy has led to many breakthroughs in the field of science. New research has sho
Published February 26, 2019 Updated February 27, 2019

The evolving technology of gene therapy has led to many breakthroughs in the field of science. New research has shown that gene therapy can now also cure inborn deafness.

According to a new research, gene therapy can now be used to cure and restore congenital deafness, as the results were positive in deaf mice that developed the ability to hear almost as well as healthy mice.

The mice suffered from DFNB9 deafness, a hearing disorder which accounts for between 2% and 8% of gene-related cases of human deafness. In this particular type of deafness, a protein named ‘otoferlin’ is unable to perform is task of submitting sound information gather by the fine hairs in the inner ear, explained Futurism.

In a first, scientists attempt to halt blindness through gene therapy

As described in the study published in the journal PNAS, after altering the deaf mice’s genomes with specially-crafted viruses by only a single intracochlear injection, the animals were able to hear almost as clearly as mice born with working otoferlin since their DNA segments were recombined, reported the team.

Even after altering the same specific gene in mice as what causes the DFNB9 deafness in humans, it still too early to claim that gene-editing technology can treat people as good as it did with the animals.

Copyright Business Recorder, 2019

Comments

Comments are closed.