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Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|June 13, 2014
Meconium ileus in cystic fibrosis is not linked to central repetitive region length variation in MUC1, MUC2, and MUC5ACXueLiang Guo, Rhonda G Pace, Jaclyn R Stonebraker, et al.Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|July 11, 2021
Immunoglobulin GM and KM allotypes are associated with antibody responses to Pseudomonas aeruginosa antigens in chronically infected cystic fibrosis patientsJanardan P Pandey, Aryan M Namboodiri, Paul J Nietert, et al.Clinical Gastroenterology and Hepatology : the Official Clinical Practice Journal of the American Gastroenterological Association|April 12, 2016
Features of Severe Liver Disease With Portal Hypertension in Patients With Cystic FibrosisJaclyn R Stonebraker, Chee Y Ooi, Rhonda G Pace, et al.Genetics in Medicine : Official Journal of the American College of Medical Genetics|October 24, 2002
The I148T CFTR allele occurs on multiple haplotypes: a complex allele is associated with cystic fibrosisElizabeth M Rohlfs, Zhaoqing Zhou, Elaine A Sugarman, et al.Plos One|October 12, 2018
Analysis of a large cohort of cystic fibrosis patients with severe liver disease indicates lung function decline does not significantly differ from that of the general cystic fibrosis populationDeepika Polineni, Annalisa V Piccorelli, William B Hannah, et al.Plos One|November 30, 2020
Mining GWAS and eQTL data for CF lung disease modifiers by gene expression imputationHong Dang, Deepika Polineni, Rhonda G Pace, et al.Plos One|January 27, 2009
Histo-blood group gene polymorphisms as potential genetic modifiers of infection and cystic fibrosis lung disease severityJennifer L Taylor-Cousar, Maimoona A Zariwala, Lauranell H Burch, et al.Plos Genetics|March 23, 2012
Variation in MSRA modifies risk of neonatal intestinal obstruction in cystic fibrosisLindsay B Henderson, Vishal K Doshi, Scott M Blackman, et al.Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|March 6, 2021
SLC26A9 SNP rs7512462 is not associated with lung disease severity or lung function response to ivacaftor in cystic fibrosis patients with G551D-CFTRAlice C Eastman, Rhonda G Pace, Hong Dang, et al.Human Genome Variation|December 6, 2016
Deep resequencing of <i>CFTR</i> in 762 F508del homozygotes reveals clusters of non-coding variants associated with cystic fibrosis disease traitsBriana Vecchio-Pagán, Scott M Blackman, Melissa Lee, et al.Pageof 4