Genetic testing plays an important role in cystic fibrosis screening and diagnosis. It can help determine if a person has cystic fibrosis or carries gene mutations that cause it. Other tests can also ...

Cystic fibrosis (CF) is an inherited disease caused by a genetic mutation in the cystic fibrosis transmembrane conductance regulator (CFTR) gene, which encodes for an ion channel. This channel sits in ...

Cystic fibrosis is caused by an inherited mutation in the cystic fibrosis transmembrane conductance regulator (CFTR) gene. Due to this mutation, the CFTR protein doesn't embed in cell membranes to ...

Engineers at the University of Pennsylvania and Rice University have refined a technology for editing individual genetic ...

Using an updated version of a recently developed technology called MaMTH-HTS (Mammalian Membrane Two-Hybrid High-Throughput Screening) that allows the detection of membrane-associating factors ...

If you and your partner both are carriers for CF, it doesn’t necessarily mean your child will have CF. But it will likely still affect your pregnancy. Genetic disorders range widely from long-term yet ...

Please provide your email address to receive an email when new articles are posted on . The Cystic Fibrosis Foundation is providing funds to Prime Medicine to advance research on its gene editing ...

Add Yahoo as a preferred source to see more of our stories on Google. The genetic disorder cystic fibrosis is unique because it can cause both breathing and digestive problems. Some 40,000 people in ...

From its first description in 1935 until now, clinical outcomes for patients with cystic fibrosis have undergone a dramatic transformation. While the rare genetic disease was once an early death ...

There are many new drugs to treat cystic fibrosis, but non-white patients are far less likely to receive the latest precision medicines, accord to a new study. These drugs were approved by the U.S.