Results 231 to 240 of about 352,696 (330)

Nutritional supplements in cystic fibrosis [PDF]

, 2006
Griese, Matthias, Kappler, Matthias
core   +1 more source

Trikafta Rescues F508del‐CFTR by Tightening Specific Phosphorylation‐Dependent Interdomain Interactions

Natural Sciences, EarlyView.
The most common cystic fibrosis mutation, F508del, destabilizes the first of two nucleotide‐binding domains (NBD1 and NBD2) and compromises Mg/ATP‐dependent gating at the interface between two transmembrane domains (TMD1 and TMD2) in the human cystic fibrosis transmembrane conductance regulator (CFTR).
Guangyu Wang
wiley   +1 more source

Exploration of Olfaction and ChiPSO in Pediatric Cystic Fibrosis. [PDF]

J Clin Med
Saak TM, Tervo JP, Moore BM, Wang AS, DiMango E, Sadeghi H, Gudis DA, Overdevest JB.   +7 more
europepmc   +1 more source

Cystic fibrosis or fibrocystic disease: The sweat test for fibrocystic disease

, 1967
Thomas Dreyer
openalex   +2 more sources

The Renin-Angiotensin-Aldosterone System in Patients with Cystic Fibrosis of the Pancreas [PDF]

, 1971
Artemis P. Simopoulos, Allen Lapey, T F Boat, Paul A. di Sant'Agnese, Frederic C. Bartter   +4 more
openalex   +1 more source

Teratoid Hepatoblastoma: Clinicopathologic Features and Outcomes

Pediatric Blood &Cancer, EarlyView.
ABSTRACT Background Teratoid hepatoblastoma (HB) is a rare histologic subtype of the most common pediatric liver cancer. Understanding of the clinicopathologic features and outcomes of patients with this disease is currently limited. Methods Multi‐institution, retrospective chart review was conducted to compare 20 children with teratoid HB to 129 ...
Brian T. Hickner, Andres F. Espinoza, Soo Jin Cho, Stephen Sarabia, Martin Urbicain, Ann Wang, Sanjeev A. Vasudevan, Dolores H. López‐Terrada, Kalyani R. Patel   +8 more
wiley   +1 more source

Cystic fibrosis in Vietnam and Southeast Asia: underdiagnosis and genetic spectrum. [PDF]

J Community Genet
Cao-Pham HG, Tran-Le QK, Nguyen-Ho L.
europepmc   +1 more source

Recent Progress in Treating Airway Mucus Hypersecretion by Targeting the Epidermal Growth Factor Receptor Signaling Pathway

Pediatric Discovery, EarlyView.
ABSTRACT Asthma, chronic pulmonary obstructive disease (COPD), cystic fibrosis, and acute respiratory infections are severe respiratory conditions that significantly contribute to global morbidity and mortality. Airway mucus hypersecretion is an important common pathophysiological and clinical manifestation of these diseases and is closely associated ...
Yuanyuan Zhang, Fuping Yang, Chunyu Yan, Yu Deng, Enmei Liu   +4 more
wiley   +1 more source

Fueling Health: Overcoming Food Barriers in Cystic Fibrosis Care. [PDF]

Pediatr Pulmonol
Wright BA, Godfrey KC, Gryp EE, Harklau NM, Colsch LB.   +4 more
europepmc   +1 more source

Cellular immunity to bacteria: impairment of in vitro lymphocyte responses to Pseudomonas aeruginosa in cystic fibrosis patients [PDF]

, 1977
Ricardo U. Sorensen, Robert C. Stern, Stephen H. Polmar   +2 more
openalex   +1 more source