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Cystic fibrosis is a genetic condition that causes persistent lung infections, resulting in progressive damage to the lungs and digestive system. On Tuesday, Jan. 15, Evenings with Genetics, a monthly ...
Cystic fibrosis represents one of the most common inherited genetic disorders affecting people of European descent, touching the lives of approximately 30,000 individuals in the United States ...
Vertex Pharmaceuticals said on Tuesday its next-generation cystic fibrosis treatment has won European Union approval for a ...
Cystic fibrosis (CF) is a genetic condition. Alterations in the CFTR gene, which a person inherits from their parents, affect the function of the CFTR protein, causing thick, sticky mucus.
A scientific team has unlocked a new way to treat serious lung conditions by using specially designed nanoparticles to ...
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.
Cite this: Genetics and Genomics: Providing new Opportunities for the Translation of Basic Research to Clinical Care for Cystic Fibrosis - Medscape - Feb 01, 2008.
Advanced cystic fibrosis makes even simple things like walking or showering arduous and exhausting. She has the most common fatal genetic disease in the U.S., which afflicts 40,000 Americans.
Intellia Therapeutics will work with a private biotechnology company to develop genetic medicines for cystic fibrosis, with an initial focus on people who have limited or no available treatment ...
Cystic fibrosis (CF) is a progressive genetic disease that adversely affects a person's lungs, pancreas and other vital organs, says Dr. Michael Boyle, president and CEO of the Cystic Fibrosis ...
Organically Human on MSN10mon
Cystic fibrosis cure on horizon after scientists fix genetic mutation - MSNA cure for cystic fibrosis is on the horizon after scientists corrected the genetic mutation that causes the condition in ...
Jennifer Guimbellot, M.D., Ph.D., and Gabriela Oates, Ph.D., both assistant professors in the Division of Pediatric Pulmonary and Sleep Medicine, contributed chapters to the new book, “Cystic Fibrosis ...
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