Prevalence of meconium ileus marks the severity of mutations of the Cystic Fibrosis Transmembrane Conductance Regulator (CFTR) gene
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Title
Prevalence of meconium ileus marks the severity of mutations of the Cystic Fibrosis Transmembrane Conductance Regulator (CFTR) gene
Authors
Keywords
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Journal
GENETICS IN MEDICINE
Volume 18, Issue 4, Pages 333-340
Publisher
Springer Nature
Online
2015-06-18
DOI
10.1038/gim.2015.79
References
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Note: Only part of the references are listed.- Prediction of acute pancreatitis risk based on PIP score in children with cystic fibrosis
- (2014) V. Terlizzi et al. Journal of Cystic Fibrosis
- Unraveling the complex genetic model for cystic fibrosis: pleiotropic effects of modifier genes on early cystic fibrosis-related morbidities
- (2013) Weili Li et al. HUMAN GENETICS
- Intestinal CFTR expression alleviates meconium ileus in cystic fibrosis pigs
- (2013) David A. Stoltz et al. JOURNAL OF CLINICAL INVESTIGATION
- Effect of ivacaftor on CFTR forms with missense mutations associated with defects in protein processing or function
- (2013) Fredrick Van Goor et al. Journal of Cystic Fibrosis
- Defining the disease liability of variants in the cystic fibrosis transmembrane conductance regulator gene
- (2013) Patrick R Sosnay et al. NATURE GENETICS
- Genetic modifiers of nutritional status in cystic fibrosis
- (2012) Gia M Bradley et al. AMERICAN JOURNAL OF CLINICAL NUTRITION
- A review of pathophysiology and management of fetuses and neonates with meconium ileus for the pediatric surgeon
- (2012) Brent E. Carlyle et al. JOURNAL OF PEDIATRIC SURGERY
- Multiple apical plasma membrane constituents are associated with susceptibility to meconium ileus in individuals with cystic fibrosis
- (2012) Lei Sun et al. NATURE GENETICS
- Risk factors for onset of persistent respiratory symptoms in children with cystic fibrosis
- (2012) Susanna A. McColley et al. PEDIATRIC PULMONOLOGY
- Variation in MSRA Modifies Risk of Neonatal Intestinal Obstruction in Cystic Fibrosis
- (2012) Lindsay B. Henderson et al. PLoS Genetics
- Association between genotype and pulmonary phenotype in cystic fibrosis patients with severe mutations
- (2011) A. Geborek et al. Journal of Cystic Fibrosis
- Lung function decline from adolescence to young adulthood in cystic fibrosis
- (2011) Stacy L. VandenBranden et al. PEDIATRIC PULMONOLOGY
- New Meconium Biomarkers of Prenatal Methamphetamine Exposure Increase Identification of Affected Neonates
- (2010) T. R. Gray et al. CLINICAL CHEMISTRY
- Do commonin silicotools predict the clinical consequences of amino-acid substitutions in the CFTR gene?
- (2010) R Dorfman et al. CLINICAL GENETICS
- Understanding the population structure of North American patients with cystic fibrosis
- (2010) W Li et al. CLINICAL GENETICS
- Type of CFTR Mutation Determines Risk of Pancreatitis in Patients With Cystic Fibrosis
- (2010) Chee Y. Ooi et al. GASTROENTEROLOGY
- Disease phenotype of a ferret CFTR-knockout model of cystic fibrosis
- (2010) Xingshen Sun et al. JOURNAL OF CLINICAL INVESTIGATION
- Meconium Ileus in Patients With Cystic Fibrosis Is Not a Risk Factor for Clinical Deterioration and Survival: The Israeli Multicenter Study
- (2010) Ori Efrati et al. JOURNAL OF PEDIATRIC GASTROENTEROLOGY AND NUTRITION
- Growth Assessment of Paediatric Patients With CF Comparing Different Auxologic Indicators: A Multicentre Italian Study
- (2009) Vincenzina Lucidi et al. JOURNAL OF PEDIATRIC GASTROENTEROLOGY AND NUTRITION
- Direct interaction of a small-molecule modulator with G551D-CFTR, a cystic fibrosis-causing mutation associated with severe disease
- (2008) Stan Pasyk et al. BIOCHEMICAL JOURNAL
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