Nov. 14, 2022 —Researchers have developed a simple urine test to measure the severity of the serious disease cystic fibrosis and assess the effect of new ...
Oct. 25, 2022 —Cystic fibrosis is missed more often in newborn screenings for non-white than white babies, creating higher risk for irreversible lung damage and other serious outcomes in Black, Hispanic, Asian, ...
Sep. 29, 2022 —Cystic fibrosis patients who supplement their diet with vitamin C can also derive greater benefit from another antioxidant, vitamin E, resulting in a reduction in damaging inflammation, a study ...
Aug. 1, 2022 —Cystic fibrosis (CF) is caused by a mutation of the CFTR gene. While there are many hundreds of known mutations, not all of them are currently treatable which means a significant number of CF ...
July 27, 2022 —Infants from minoritized racial and ethnic backgrounds who have positive newborn screening tests for cystic fibrosis received their diagnostic follow-up for the disease later than recommended and ...
Oct. 21, 2021 —In the largest study of its kind, researchers found that the lower airways in children with cystic fibrosis (CF) have a higher burden of infection, more inflammation and lower diversity of ...
Oct. 19, 2021 —A dogma-challenging discovery reveals that highly adapted bacterial communities in the sinuses of people with cystic fibrosis become more fragmented and experience mutations that erode their genomes. ...
Aug. 9, 2021 —Researchers corrected mutations that cause cystic fibrosis in cultured human stem cells. They used a technique called prime editing to replace the 'faulty' piece of DNA with a healthy ...
July 19, 2021 —An experimental drug suggests that a 'path is clearly achievable' to treat currently untreatable cases of cystic fibrosis disease caused by nonsense mutations. This includes about 11 ...
June 16, 2021 —A new CF treatment strategy involves small, nucleic acid molecules called oligonucleotides that can correct some of the gene defects that underlie CF but are not addressed by existing modulator ...
May 14, 2021 —New nanotechnology could change the lives of thousands of people living with cystic fibrosis (CF) as groundbreaking research shows it can improve the effectiveness of the CF antibiotic Tobramycin, ...
May 6, 2021 —A team of researchers has developed a molecular catalog of cells in healthy lungs and the lungs of people with cystic ...
Apr. 29, 2021 —Scientists have been able to track how a multi-drug resistant organism is able to evolve and spread widely among cystic fibrosis patients - showing that it can evolve rapidly within an individual ...
Feb. 27, 2021 —Researchers and their partners have discovered a slimy strategy used by bacteria to defeat antibiotics and other drugs used to combat infections afflicting people with cystic ...
Jan. 13, 2021 —Excess mucus in the lungs can be fatal for asthma patients, but scientists have broken up those secretions at the molecular level and reversed their often deadly ...
Dec. 17, 2020 —A drug widely used to treat fungal infections improved key biomarkers in lung tissue cultures as well as in the noses of patients with cystic fibrosis, a clinical study ...
Nov. 19, 2020 —年轻人与囊性纤维化、肺感染ion with Staphylococcus aureus, MRSA, is common and is treated with antibiotics in the hope that this will prevent a decline in lung function. ...
Nov. 4, 2020 —基因的突变导致囊性纤维化may accelerate heart function decline in those with Duchenne muscular dystrophy (DMD), a new study suggests. The findings could help doctors develop ...
Oct. 28, 2020 —New research examines the properties of the mucus of cystic fibrosis (CF) patients and the role it plays in a pathogens' ability to survive. The new information could have important implications ...
