ResearchOpen Access07 Nov 2024Scientific Reports Volume: 14, P: 27036 Cystic fibrosis-related diabetes is associated with reduced islet protein expression of GLP-1 receptor and perturbation of cell-specific transcriptional programs Sina A. Gharib ...
Our end goal would be to change the labeling of Trikafta forpregnant womenand children under 2 years of age. Importantly, this research will also offer women living withcystic fibrosisa sense of normality—a normal pregnancy and all the wonderful experiences that it brings. More information:Danni...
Cystic Fibrosis is a disease that runs in a family. A new drug targeting a specific mutation has been successful so far in helping to treat cystic fibrosis. Women With CF Have Shorter Life Spans Who lives longer and why is the theme of many research studies. Now, a group from England ha...
The article reports on Albany Molecular Research Inc.'s (AMRI) research agreement with Cystic Fibrosis Foundation Therapeutics, a unit of the Cystic Fibrosis Foundation. Under the deal, AMRI will screen its natural products library to find compounds that improve the function of the defective protein...
摘要: In Virginia Morell's Research News article "New light on writing in the Americas" (18 Jan., p. 268), the illustrations on page 268 should have been credited to George Stuart of the National Geographic Society.关键词:Humans Cystic Fibrosis Prenatal Diagnosis Research ...
Recent progress in elucidating disease mechanism and causes of phenotypic variation, as well as in the development of treatments, demonstrates that genetics continues to play an important part in cystic fibrosis research 25 years after the discovery of the disease-causing gene. This is a preview of...
Patient Preference and Adherence Dovepress open access to scientific and medical research Open Access Full Text Article Original Research Treatment satisfaction in cystic fibrosis: early patient experience with tobramycin inhalation powder This article was published in the following Dove Press journal: ...
Cystic fibrosis is a lethal, hereditary, until recently little understood disease, which leads to progressive functional disturbances in various organs, in
Susan A. Joyce, in Pharmacological Research, 2018 6.2 Cystic fibrosis Cystic fibrosis is a heritable autosomal recessive disorder, caused by mutations in the cystic fibrosis transmembrane conductance regulator (CFTR) gene, leading to dysfunction of the CFTR protein, which regulates ion transport at ...
© American College of Medical Genetics and Genomics Original Research Article Improving newborn screening for cystic fibrosis using next-generation sequencing technology: a technical feasibility study Mei W. Baker, MD1,2, Anne E. Atkins, MPH2, Suzanne K. Cordovado, PhD3, Miyo...