Zobrazeno 1 - 10
of 160
pro vyhledávání: '"CFTR, cystic fibrosis transmembrane conductance regulator"'
Publikováno v:
Frontiers in Pharmacology, Vol 15 (2024)
Externí odkaz:
https://doaj.org/article/7d9167ebf42f4eb493a4889e34ee602c
Autor:
Mohini A. Gunnett, Elizabeth Baker, Cathy Mims, Staci T. Self, Hector H. Gutierrez, Jennifer S. Guimbellot
Publikováno v:
Frontiers in Pediatrics, Vol 11 (2023)
BackgroundSome infants undergoing newborn screening (NBS) tests have inconclusive sweat chloride test (SCT) results that lead to the designation of Cystic Fibrosis Screen Positive, Inconclusive Diagnosis/CFTR-related metabolic syndrome (CFSPID/CRMS).
Externí odkaz:
https://doaj.org/article/8035a43de04d4eb3973b919031e6fc56
Autor:
David C. Whitcomb
Publikováno v:
Frontiers in Pediatrics, Vol 10 (2022)
Traditional approaches to understanding the origins of chronic pancreatitis (CP) and find treatments led to abysmal failure. Thus, no drugs now exists to meet this need. Outdated concepts of the etiopathogenesis of CP have been replaced with new insi
Externí odkaz:
https://doaj.org/article/81d324cffa974e37ad61cc7d32e4bde0
Autor:
Zhuo-Er Qiu, Jian-Bang Xu, Lei Chen, Ze-Xin Huang, Tian-Lun Lei, Zi-Yang Huang, Xiao-Chun Hou, Hai-Long Yang, Qin-Hua Lin, Yun-Xin Zhu, Lei Zhao, Wen-Liang Zhou, Yi-Lin Zhang
Publikováno v:
Frontiers in Pharmacology, Vol 13 (2022)
Airway epithelium plays critical roles in regulating airway surface liquid (ASL), the alteration of which causes mucus stasis symptoms. Allicin is a compound released from garlic and harbors the capacity of lung-protection. However, the potential reg
Externí odkaz:
https://doaj.org/article/f0ad04e4d82244cbbd3c1030ce836bdc
Publikováno v:
Frontiers in Pediatrics, Vol 10 (2022)
Background and AimCystic fibrosis (CF) is a genetic disease that is difficult to treat and caused by dysfunction of the cystic fibrosis transmembrane conductance regulator (CFTR) protein. Small molecules have been used to treat the symptom caused by
Externí odkaz:
https://doaj.org/article/479b9ffa5c4e4e27a494259f96bf00b0
Publikováno v:
Frontiers in Physiology, Vol 12 (2022)
Externí odkaz:
https://doaj.org/article/b8ca86ef49cd4deb9191b158c911ea35
Autor:
Szymczak Angelika, Ksiazek Piotr, Mojsym-Korybska Sylwia, Skorupa Wojciech, Zbikowska-Machul Albertyna
Publikováno v:
Current Issues in Pharmacy and Medical Sciences, Vol 31, Iss 4, Pp 200-203 (2018)
Cystic fibrosis is one of the most common genetic diseases among Caucasians due to its prevalence. Modern methods of molecular diagnostics and treatment of the disease allow to prolong the life of patients. In order to apply the appropriate treatment
Externí odkaz:
https://doaj.org/article/44b7b7dec984467dae0c085ea62c5457
Publikováno v:
Cellular and Molecular Gastroenterology and Hepatology, Vol 13, Iss 3, Pp 695-716 (2022)
Cellular and Molecular Gastroenterology and Hepatology
Cellular and Molecular Gastroenterology and Hepatology
Background & Aims Diarrhea is one of the most common illnesses and is often caused by bacterial infection. Recently, we have shown that human Na+/H+ exchanger NHE3 (hNHE3), but not non-human NHE3s, interacts with the E3 ubiquitin ligase Nedd4-2. We h
Publikováno v:
Frontiers in Pharmacology, Vol 9 (2018)
Cystic fibrosis (CF) is caused by mutations in the cystic fibrosis transmembrane conductance regulator (CFTR) gene and remains the most common life-shortening diseases affecting the exocrine organs. The absence of this channel results in an imbalance
Externí odkaz:
https://doaj.org/article/6a233c8e33a149c79ae8619d09fd836e
Autor:
George M. Solomon, Julianna Bailey, James Lawlor, Peter Scalia, Gregory S. Sawicki, Christopher Dowd, Kathryn A. Sabadosa, Aricca Van Citters
Publikováno v:
Journal of Cystic Fibrosis
Background During the COVID-19 pandemic, CF centers shifted to a telehealth delivery model. Our study aimed to determine how people with CF (PwCF) and their families experienced telehealth and assessed its quality and acceptability for future CF care