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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1973 1
1974 1
1975 1
1976 1
1979 1
1980 1
1981 3
1982 1
1983 2
1984 1
1988 1
1989 1
1990 3
1991 1
1992 2
1993 5
1994 2
1995 6
1996 6
1997 3
1998 8
1999 10
2000 9
2001 16
2002 18
2003 18
2004 23
2005 14
2006 26
2007 15
2008 19
2009 24
2010 22
2011 14
2012 10
2013 19
2014 16
2015 13
2016 13
2017 17
2018 16
2019 12
2020 16
2021 16
2022 9
2023 8
2024 11

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408 results

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Page 1
Glutathione metabolism and its implications for health.
Wu G, Fang YZ, Yang S, Lupton JR, Turner ND. Wu G, et al. J Nutr. 2004 Mar;134(3):489-92. doi: 10.1093/jn/134.3.489. J Nutr. 2004. PMID: 14988435 Free article. Review.
Glutathione (gamma-glutamyl-cysteinyl-glycine; GSH) is the most abundant low-molecular-weight thiol, and GSH/glutathione disulfide is the major redox couple in animal cells. ...Glutathione deficiency contributes to oxidative stress, which plays a key role in …
Glutathione (gamma-glutamyl-cysteinyl-glycine; GSH) is the most abundant low-molecular-weight thiol, and GSH/glutathione disul …
Improving nutrition in cystic fibrosis: A systematic literature review.
Mielus M, Sands D, Woynarowski M. Mielus M, et al. Nutrition. 2022 Oct;102:111725. doi: 10.1016/j.nut.2022.111725. Epub 2022 May 6. Nutrition. 2022. PMID: 35816813 Free article. Review.
With increasing life expectancy of patients with cystic fibrosis (CF), gastrointestinal manifestations of the disease have been increasingly brought into focus. ...In contrast, the supplementation of probiotics, lipids, docosahexaenoic, glutathione, or antiox …
With increasing life expectancy of patients with cystic fibrosis (CF), gastrointestinal manifestations of the disease have bee …
CFTR Protein: Not Just a Chloride Channel?
Hanssens LS, Duchateau J, Casimir GJ. Hanssens LS, et al. Cells. 2021 Oct 22;10(11):2844. doi: 10.3390/cells10112844. Cells. 2021. PMID: 34831067 Free PMC article. Review.
Cystic fibrosis (CF) is a recessive genetic disease caused by mutations in a gene encoding a protein called Cystic Fibrosis Transmembrane Conductance Regulator (CFTR). ...Yet, the CFTR protein also regulates numerous other pathways, such as the transpo …
Cystic fibrosis (CF) is a recessive genetic disease caused by mutations in a gene encoding a protein called Cystic F …
Multifaceted Roles of Ferroptosis in Lung Diseases.
Li Y, Yang Y, Yang Y. Li Y, et al. Front Mol Biosci. 2022 Jun 24;9:919187. doi: 10.3389/fmolb.2022.919187. eCollection 2022. Front Mol Biosci. 2022. PMID: 35813823 Free PMC article. Review.
Ferroptosis is a distinct type of programmed cell death (PCD) that depends on iron and is characterized by the accumulation of intracellular iron, exhaustion of glutathione, deactivation of glutathione peroxidase, and promotion of lipid peroxidation. ...In this revi …
Ferroptosis is a distinct type of programmed cell death (PCD) that depends on iron and is characterized by the accumulation of intracellular …
Oral Glutathione and Growth in Cystic Fibrosis: A Multicenter, Randomized, Placebo-controlled, Double-blind Trial.
Bozic M, Goss CH, Tirouvanziam RM, Baines A, Kloster M, Antoine L, Borowitz D, Schwarzenberg SJ; GROW study group. Bozic M, et al. J Pediatr Gastroenterol Nutr. 2020 Dec;71(6):771-777. doi: 10.1097/MPG.0000000000002948. J Pediatr Gastroenterol Nutr. 2020. PMID: 32960827 Free PMC article. Clinical Trial.
OBJECTIVES: The nutritional status of children with cystic fibrosis (CF) is associated with mortality and morbidity. Intestinal inflammation may contribute to impaired digestion, absorption, and nutrient utilization in patients with CF and oral glutathione ma …
OBJECTIVES: The nutritional status of children with cystic fibrosis (CF) is associated with mortality and morbidity. Intestina …
Novel Therapy of Bicarbonate, Glutathione, and Ascorbic Acid Improves Cystic Fibrosis Mucus Transport.
Adewale AT, Falk Libby E, Fu L, Lenzie A, Boitet ER, Birket SE, Petty CF, Johns JD, Mazur M, Tearney GJ, Copeland D, Durham C, Rowe SM. Adewale AT, et al. Am J Respir Cell Mol Biol. 2020 Sep;63(3):362-373. doi: 10.1165/rcmb.2019-0287OC. Am J Respir Cell Mol Biol. 2020. PMID: 32374624 Free PMC article.
Defective airway mucus clearance is a defining characteristic of cystic fibrosis lung disease, and improvements to current mucolytic strategies are needed. ...This response was absent in CFBE41o(-) F508del cells treated with VX-809 and primary human bronchial epithe …
Defective airway mucus clearance is a defining characteristic of cystic fibrosis lung disease, and improvements to current muc …
New insights into the pathogenesis of cystic fibrosis: pivotal role of glutathione system dysfunction and implications for therapy.
Hudson VM. Hudson VM. Treat Respir Med. 2004;3(6):353-63. doi: 10.2165/00151829-200403060-00003. Treat Respir Med. 2004. PMID: 15658882 Review.
The cystic fibrosis transmembrane regulator (CFTR) should no longer be viewed primarily as a 'chloride channel' but recognized as a channel that also controls the efflux of other physiologically important anions, such as glutathione (GSH) and bicarbonate. ... …
The cystic fibrosis transmembrane regulator (CFTR) should no longer be viewed primarily as a 'chloride channel' but recognized …
Pancreatitis Overview.
Shelton C, LaRusch J, Whitcomb DC. Shelton C, et al. 2014 Mar 13 [updated 2020 Jul 2]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2024. 2014 Mar 13 [updated 2020 Jul 2]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2024. PMID: 24624459 Free Books & Documents. Review.
Glutathione and bicarbonate nanoparticles improve mucociliary transport in cystic fibrosis epithelia.
Cho DY, Rivers NJ, Lim DJ, Zhang S, Skinner D, Yang L, Menon AJ, Kelly OJ, Jones MP, Bicknell BT, Grayson JW, Harris E, Rowe SM, Woodworth BA. Cho DY, et al. Int Forum Allergy Rhinol. 2024 Jun;14(6):1026-1035. doi: 10.1002/alr.23301. Epub 2023 Nov 17. Int Forum Allergy Rhinol. 2024. PMID: 37975554
INTRODUCTION: Cystic fibrosis (CF) airway disease is characterized by thick mucus and impaired mucociliary transport (MCT). Loss of functional cystic fibrosis transmembrane receptor (CFTR) leads to acidification and oxidation of airway surface mucus. . …
INTRODUCTION: Cystic fibrosis (CF) airway disease is characterized by thick mucus and impaired mucociliary transport (MCT). Lo …
408 results