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American Journal of Human Genetics
|
October 7, 2022
Pleiotropic modifiers of age-related diabetes and neonatal intestinal obstruction in cystic fibrosis
Melis A Aksit, Hua Ling, Rhonda G Pace, et al.
American Journal of Human Genetics
|
October 5, 2022
MagicalRsq: Machine-learning-based genotype imputation quality calibration
Quan Sun, Yingxi Yang, Jonathan D Rosen, et al.
American Journal of Respiratory and Critical Care Medicine
|
March 20, 2019
Correlating Cystic Fibrosis Transmembrane Conductance Regulator Function with Clinical Features to Inform Precision Treatment of Cystic Fibrosis
Allison F McCague, Karen S Raraigh, Matthew J Pellicore, et al.
Human Mutation
|
April 12, 2017
Lessons from the CAGI-4 Hopkins clinical panel challenge
John-Marc Chandonia, Aashish Adhikari, Marco Carraro, et al.
Plos Genetics
|
November 17, 2018
Capitalizing on the heterogeneous effects of CFTR nonsense and frameshift variants to inform therapeutic strategy for cystic fibrosis
Neeraj Sharma, Taylor A Evans, Matthew J Pellicore, et al.
American Journal of Human Genetics
|
February 3, 2015
Gene expression in transformed lymphocytes reveals variation in endomembrane and HLA pathways modifying cystic fibrosis pulmonary phenotypes
Wanda K O'Neal, Paul Gallins, Rhonda G Pace, et al.
Pediatric Pulmonology
|
April 5, 2011
A novel lung disease phenotype adjusted for mortality attrition for cystic fibrosis genetic modifier studies
Chelsea Taylor, Clayton W Commander, Joseph M Collaco, et al.
Molecular Biology of the Cell
|
January 30, 2016
From CFTR biology toward combinatorial pharmacotherapy: expanded classification of cystic fibrosis mutations
Gudio Veit, Radu G Avramescu, Annette N Chiang, et al.
Hepatology (Baltimore, Md.)
|
March 27, 2024
Genetic variation in severe cystic fibrosis liver disease is associated with novel mechanisms for disease pathogenesis
Jaclyn R Stonebraker, Rhonda G Pace, Paul J Gallins, et al.
Human Mutation
|
November 30, 2020
Verifying nomenclature of DNA variants in submitted manuscripts: Guidance for journals
Jan Higgins, Raymond Dalgleish, Johan T den Dunnen, et al.
Page
of 16
Search research articles
Search
Showing results (131-140 of 158) with videos related to
Sort By:
Page
of 16
American Journal of Human Genetics
|
October 7, 2022
Pleiotropic modifiers of age-related diabetes and neonatal intestinal obstruction in cystic fibrosis
Melis A Aksit, Hua Ling, Rhonda G Pace, et al.
American Journal of Human Genetics
|
October 5, 2022
MagicalRsq: Machine-learning-based genotype imputation quality calibration
Quan Sun, Yingxi Yang, Jonathan D Rosen, et al.
American Journal of Respiratory and Critical Care Medicine
|
March 20, 2019
Correlating Cystic Fibrosis Transmembrane Conductance Regulator Function with Clinical Features to Inform Precision Treatment of Cystic Fibrosis
Allison F McCague, Karen S Raraigh, Matthew J Pellicore, et al.
Human Mutation
|
April 12, 2017
Lessons from the CAGI-4 Hopkins clinical panel challenge
John-Marc Chandonia, Aashish Adhikari, Marco Carraro, et al.
Plos Genetics
|
November 17, 2018
Capitalizing on the heterogeneous effects of CFTR nonsense and frameshift variants to inform therapeutic strategy for cystic fibrosis
Neeraj Sharma, Taylor A Evans, Matthew J Pellicore, et al.
American Journal of Human Genetics
|
February 3, 2015
Gene expression in transformed lymphocytes reveals variation in endomembrane and HLA pathways modifying cystic fibrosis pulmonary phenotypes
Wanda K O'Neal, Paul Gallins, Rhonda G Pace, et al.
Pediatric Pulmonology
|
April 5, 2011
A novel lung disease phenotype adjusted for mortality attrition for cystic fibrosis genetic modifier studies
Chelsea Taylor, Clayton W Commander, Joseph M Collaco, et al.
Molecular Biology of the Cell
|
January 30, 2016
From CFTR biology toward combinatorial pharmacotherapy: expanded classification of cystic fibrosis mutations
Gudio Veit, Radu G Avramescu, Annette N Chiang, et al.
Hepatology (Baltimore, Md.)
|
March 27, 2024
Genetic variation in severe cystic fibrosis liver disease is associated with novel mechanisms for disease pathogenesis
Jaclyn R Stonebraker, Rhonda G Pace, Paul J Gallins, et al.
Human Mutation
|
November 30, 2020
Verifying nomenclature of DNA variants in submitted manuscripts: Guidance for journals
Jan Higgins, Raymond Dalgleish, Johan T den Dunnen, et al.
Page
of 16