脂质控制囊性纤维化中的黏液产生。 - Suppr

Suppr

超能文献

Lipids control mucus production in cystic fibrosis.

作者信息

Gulbins Erich

机构信息

Department of Molecular Biology, University of Duisburg-Essen, Essen, Germany.

出版信息

Nat Med. 2010 Mar;16(3):267-8. doi: 10.1038/nm0310-267.

DOI:10.1038/nm0310-267

PMID:20208510

Abstract

摘要

相似文献

Lipids control mucus production in cystic fibrosis.

Nat Med. 2010 Mar;16(3):267-8. doi: 10.1038/nm0310-267.

Pharmacological correction of a defect in PPAR-gamma signaling ameliorates disease severity in Cftr-deficient mice.

Nat Med. 2010 Mar;16(3):313-8. doi: 10.1038/nm.2101. Epub 2010 Feb 14.

Increased airway epithelial Na+ absorption produces cystic fibrosis-like lung disease in mice.

Nat Med. 2004 May;10(5):487-93. doi: 10.1038/nm1028. Epub 2004 Apr 11.

Pass the bicarb: the importance of HCO3- for mucin release.

J Clin Invest. 2009 Sep;119(9):2535-7. doi: 10.1172/JCI40598. Epub 2009 Aug 24.

Critical role of cytosolic phospholipase A2{alpha} in bronchial mucus hypersecretion in CFTR-deficient mice.

Eur Respir J. 2010 Nov;36(5):1120-30. doi: 10.1183/09031936.00183409. Epub 2010 Apr 22.

Finally, mice with CF lung disease.

Nat Med. 2004 May;10(5):452-4. doi: 10.1038/nm0504-452.

[Mucus buildup: the starting point of cystic fibrosis lung disease pathogenesis].

Med Sci (Paris). 2019 Dec;35(12):1217-1220. doi: 10.1051/medsci/2019234. Epub 2020 Jan 6.

CFTR dysfunction induces vascular endothelial growth factor synthesis in airway epithelium.

Eur Respir J. 2013 Dec;42(6):1553-62. doi: 10.1183/09031936.00164212. Epub 2013 Mar 21.

Therapeutic options for hydrating airway mucus in cystic fibrosis.

Pharmacology. 2015;95(3-4):117-32. doi: 10.1159/000377638. Epub 2015 Mar 19.

Decreased peroxisome proliferator activated receptor alpha is associated with bile duct injury in cystic fibrosis transmembrane conductance regulator-/- mice.

J Pediatr Gastroenterol Nutr. 2006 Mar;42(3):275-81. doi: 10.1097/01.mpg.0000189368.37535.42.

引用本文的文献

Lipidomic alterations in human saliva from cystic fibrosis patients.

Sci Rep. 2023 Jan 12;13(1):600. doi: 10.1038/s41598-022-24429-6.

Protein histidine [de]phosphorylation in insulin secretion: abnormalities in models of impaired insulin secretion.

Naunyn Schmiedebergs Arch Pharmacol. 2011 Oct;384(4-5):383-90. doi: 10.1007/s00210-011-0616-z. Epub 2011 Apr 6.

本文引用的文献

Pharmacological correction of a defect in PPAR-gamma signaling ameliorates disease severity in Cftr-deficient mice.

Nat Med. 2010 Mar;16(3):313-8. doi: 10.1038/nm.2101. Epub 2010 Feb 14.

Activation of PPARgamma by rosiglitazone attenuates intestinal Cl- secretion.

Am J Physiol Gastrointest Liver Physiol. 2009 Jul;297(1):G82-9. doi: 10.1152/ajpgi.90640.2008. Epub 2009 May 14.

cAMP-mediated regulation of cholesterol accumulation in cystic fibrosis and Niemann-Pick type C cells.

Am J Physiol Lung Cell Mol Physiol. 2008 Nov;295(5):L809-19. doi: 10.1152/ajplung.90402.2008. Epub 2008 Sep 12.

Peroxisome proliferator-activated receptor-gamma in cystic fibrosis lung epithelium.

Am J Physiol Lung Cell Mol Physiol. 2008 Aug;295(2):L303-13. doi: 10.1152/ajplung.90276.2008. Epub 2008 Jun 13.

Ceramide accumulation mediates inflammation, cell death and infection susceptibility in cystic fibrosis.

Nat Med. 2008 Apr;14(4):382-91. doi: 10.1038/nm1748. Epub 2008 Mar 30.

Decreased expression of peroxisome proliferator activated receptor gamma in cftr-/- mice.

J Cell Physiol. 2004 Aug;200(2):235-44. doi: 10.1002/jcp.20020.

Localization of cystic fibrosis transmembrane conductance regulator to lipid rafts of epithelial cells is required for Pseudomonas aeruginosa-induced cellular activation.

J Immunol. 2004 Jan 1;172(1):418-25. doi: 10.4049/jimmunol.172.1.418.

Abnormal levels of prostaglandins and fatty acids in blood of children with cystic fibrosis.

Lancet. 1978 Jul 29;2(8083):236-8. doi: 10.1016/s0140-6736(78)91746-4.

文献AI研究员

20分钟写一篇综述，助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型，支持多种主流文档格式。

立即体验

Lipids control mucus production in cystic fibrosis.

作者信息

Gulbins Erich

机构信息

Department of Molecular Biology, University of Duisburg-Essen, Essen, Germany.

出版信息

Nat Med. 2010 Mar;16(3):267-8. doi: 10.1038/nm0310-267.

DOI:10.1038/nm0310-267

PMID:20208510

Abstract

摘要

相似文献

Lipids control mucus production in cystic fibrosis.

Nat Med. 2010 Mar;16(3):267-8. doi: 10.1038/nm0310-267.

Pharmacological correction of a defect in PPAR-gamma signaling ameliorates disease severity in Cftr-deficient mice.

Nat Med. 2010 Mar;16(3):313-8. doi: 10.1038/nm.2101. Epub 2010 Feb 14.

Increased airway epithelial Na+ absorption produces cystic fibrosis-like lung disease in mice.

Nat Med. 2004 May;10(5):487-93. doi: 10.1038/nm1028. Epub 2004 Apr 11.

Pass the bicarb: the importance of HCO3- for mucin release.

J Clin Invest. 2009 Sep;119(9):2535-7. doi: 10.1172/JCI40598. Epub 2009 Aug 24.

Critical role of cytosolic phospholipase A2{alpha} in bronchial mucus hypersecretion in CFTR-deficient mice.

Eur Respir J. 2010 Nov;36(5):1120-30. doi: 10.1183/09031936.00183409. Epub 2010 Apr 22.

Finally, mice with CF lung disease.

Nat Med. 2004 May;10(5):452-4. doi: 10.1038/nm0504-452.

[Mucus buildup: the starting point of cystic fibrosis lung disease pathogenesis].

Med Sci (Paris). 2019 Dec;35(12):1217-1220. doi: 10.1051/medsci/2019234. Epub 2020 Jan 6.

CFTR dysfunction induces vascular endothelial growth factor synthesis in airway epithelium.

Eur Respir J. 2013 Dec;42(6):1553-62. doi: 10.1183/09031936.00164212. Epub 2013 Mar 21.

Therapeutic options for hydrating airway mucus in cystic fibrosis.

Pharmacology. 2015;95(3-4):117-32. doi: 10.1159/000377638. Epub 2015 Mar 19.

Decreased peroxisome proliferator activated receptor alpha is associated with bile duct injury in cystic fibrosis transmembrane conductance regulator-/- mice.

J Pediatr Gastroenterol Nutr. 2006 Mar;42(3):275-81. doi: 10.1097/01.mpg.0000189368.37535.42.

引用本文的文献

Lipidomic alterations in human saliva from cystic fibrosis patients.

Sci Rep. 2023 Jan 12;13(1):600. doi: 10.1038/s41598-022-24429-6.

Protein histidine [de]phosphorylation in insulin secretion: abnormalities in models of impaired insulin secretion.

Naunyn Schmiedebergs Arch Pharmacol. 2011 Oct;384(4-5):383-90. doi: 10.1007/s00210-011-0616-z. Epub 2011 Apr 6.

本文引用的文献

Pharmacological correction of a defect in PPAR-gamma signaling ameliorates disease severity in Cftr-deficient mice.

Nat Med. 2010 Mar;16(3):313-8. doi: 10.1038/nm.2101. Epub 2010 Feb 14.

Activation of PPARgamma by rosiglitazone attenuates intestinal Cl- secretion.

Am J Physiol Gastrointest Liver Physiol. 2009 Jul;297(1):G82-9. doi: 10.1152/ajpgi.90640.2008. Epub 2009 May 14.

cAMP-mediated regulation of cholesterol accumulation in cystic fibrosis and Niemann-Pick type C cells.

Am J Physiol Lung Cell Mol Physiol. 2008 Nov;295(5):L809-19. doi: 10.1152/ajplung.90402.2008. Epub 2008 Sep 12.

Peroxisome proliferator-activated receptor-gamma in cystic fibrosis lung epithelium.

Am J Physiol Lung Cell Mol Physiol. 2008 Aug;295(2):L303-13. doi: 10.1152/ajplung.90276.2008. Epub 2008 Jun 13.

Ceramide accumulation mediates inflammation, cell death and infection susceptibility in cystic fibrosis.

Nat Med. 2008 Apr;14(4):382-91. doi: 10.1038/nm1748. Epub 2008 Mar 30.

Decreased expression of peroxisome proliferator activated receptor gamma in cftr-/- mice.

J Cell Physiol. 2004 Aug;200(2):235-44. doi: 10.1002/jcp.20020.

Localization of cystic fibrosis transmembrane conductance regulator to lipid rafts of epithelial cells is required for Pseudomonas aeruginosa-induced cellular activation.

J Immunol. 2004 Jan 1;172(1):418-25. doi: 10.4049/jimmunol.172.1.418.

Abnormal levels of prostaglandins and fatty acids in blood of children with cystic fibrosis.

Lancet. 1978 Jul 29;2(8083):236-8. doi: 10.1016/s0140-6736(78)91746-4.