标题
Intestinal Smooth Muscle Dysfunction Develops Postnatally in Cystic Fibrosis Mice
作者
关键词
-
出版物
JOURNAL OF PEDIATRIC GASTROENTEROLOGY AND NUTRITION
Volume 55, Issue 6, Pages 689-694
出版商
Ovid Technologies (Wolters Kluwer Health)
发表日期
2012-11-17
DOI
10.1097/mpg.0b013e3182638bf4
参考文献
相关参考文献
注意:仅列出部分参考文献,下载原文获取全部文献信息。- Cystic fibrosis growth retardation is not correlated with loss of Cftr in the intestinal epithelium
- (2011) Craig A. Hodges et al. AMERICAN JOURNAL OF PHYSIOLOGY-GASTROINTESTINAL AND LIVER PHYSIOLOGY
- Lack of Cystic Fibrosis Transmembrane Conductance Regulator in CD3+Lymphocytes Leads to Aberrant Cytokine Secretion and Hyperinflammatory Adaptive Immune Responses
- (2010) Christian Mueller et al. AMERICAN JOURNAL OF RESPIRATORY CELL AND MOLECULAR BIOLOGY
- Critical role of cytosolic phospholipase A2 in bronchial mucus hypersecretion in CFTR-deficient mice
- (2010) F. Dif et al. EUROPEAN RESPIRATORY JOURNAL
- Fatty acid metabolism in cystic fibrosis
- (2010) Birgitta Strandvik PROSTAGLANDINS LEUKOTRIENES AND ESSENTIAL FATTY ACIDS
- Cyclooxygenase Allosterism, Fatty Acid-mediated Cross-talk between Monomers of Cyclooxygenase Homodimers
- (2009) Chong Yuan et al. JOURNAL OF BIOLOGICAL CHEMISTRY
- Normal mouse intestinal mucus release requires cystic fibrosis transmembrane regulator–dependent bicarbonate secretion
- (2009) Mary Abigail S. Garcia et al. JOURNAL OF CLINICAL INVESTIGATION
- Expression and Distribution of Cystic Fibrosis Transmembrane Conductance Regulator in Neurons of the Human Brain
- (2009) Yong Guo et al. JOURNAL OF HISTOCHEMISTRY & CYTOCHEMISTRY
- Enteric circular muscle dysfunction in the cystic fibrosis mouse small intestine
- (2009) r. c. de lisle et al. NEUROGASTROENTEROLOGY AND MOTILITY
- Role of the Cystic Fibrosis Transmembrane Conductance Channel in Human Airway Smooth Muscle
- (2008) Marie-Claire Michoud et al. AMERICAN JOURNAL OF RESPIRATORY CELL AND MOLECULAR BIOLOGY
- Knockout mouse models for intestinal electrolyte transporters and regulatory PDZ adaptors: new insights into cystic fibrosis, secretory diarrhoea and fructose-induced hypertension
- (2008) Ursula Seidler et al. EXPERIMENTAL PHYSIOLOGY
- Generation of a conditional null allele forCftrin mice
- (2008) Craig A. Hodges et al. GENESIS
- Cell culture models demonstrate that CFTR dysfunction leads to defective fatty acid composition and metabolism
- (2008) Charlotte Andersson et al. JOURNAL OF LIPID RESEARCH
- Altered Eicosanoid Metabolism in the Cystic Fibrosis Mouse Small Intestine
- (2008) Robert C De Lisle et al. JOURNAL OF PEDIATRIC GASTROENTEROLOGY AND NUTRITION
- Cystic fibrosis: impaired bicarbonate secretion and mucoviscidosis
- (2008) Paul M Quinton LANCET
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