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Annals of the American Thoracic Society
|
July 28, 2016
Primary Ciliary Dyskinesia: First Health-related Quality-of-Life Measures for Pediatric Patients
Sharon D Dell, Margaret W Leigh, Jane S Lucas, et al.
Pediatric Pulmonology
|
September 22, 2018
The prevalence of the defining features of primary ciliary dyskinesia within a cri du chat syndrome cohort
Catherine D Sanders, Margaret W Leigh, Kay C Chao, et al.
Plos One
|
January 27, 2009
Histo-blood group gene polymorphisms as potential genetic modifiers of infection and cystic fibrosis lung disease severity
Jennifer L Taylor-Cousar, Maimoona A Zariwala, Lauranell H Burch, et al.
American Journal of Respiratory Cell and Molecular Biology
|
November 15, 2005
SERCA pump inhibitors do not correct biosynthetic arrest of deltaF508 CFTR in cystic fibrosis
Barbara R Grubb, Sherif E Gabriel, April Mengos, et al.
Plos One
|
October 22, 2014
Sperm-associated antigen 6 (SPAG6) deficiency and defects in ciliogenesis and cilia function: polarity, density, and beat
Maria E Teves, Patrick R Sears, Wei Li, et al.
American Journal of Respiratory Cell and Molecular Biology
|
April 23, 2005
Identification and analysis of axonemal dynein light chain 1 in primary ciliary dyskinesia patients
Judit Horváth, Manfred Fliegauf, Heike Olbrich, et al.
Plos Genetics
|
March 23, 2012
Variation in MSRA modifies risk of neonatal intestinal obstruction in cystic fibrosis
Lindsay B Henderson, Vishal K Doshi, Scott M Blackman, et al.
Pediatric Pulmonology
|
January 4, 2011
Age of Pseudomonas aeruginosa acquisition and subsequent severity of cystic fibrosis lung disease
Jessica E Pittman, Elizabeth H Calloway, Michelle Kiser, 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-CFTR
Alice 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 traits
Briana Vecchio-Pagán, Scott M Blackman, Melissa Lee, et al.
Page
of 20
Search research articles
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Showing results (81-90 of 196) with videos related to
Sort By:
Page
of 20
Annals of the American Thoracic Society
|
July 28, 2016
Primary Ciliary Dyskinesia: First Health-related Quality-of-Life Measures for Pediatric Patients
Sharon D Dell, Margaret W Leigh, Jane S Lucas, et al.
Pediatric Pulmonology
|
September 22, 2018
The prevalence of the defining features of primary ciliary dyskinesia within a cri du chat syndrome cohort
Catherine D Sanders, Margaret W Leigh, Kay C Chao, et al.
Plos One
|
January 27, 2009
Histo-blood group gene polymorphisms as potential genetic modifiers of infection and cystic fibrosis lung disease severity
Jennifer L Taylor-Cousar, Maimoona A Zariwala, Lauranell H Burch, et al.
American Journal of Respiratory Cell and Molecular Biology
|
November 15, 2005
SERCA pump inhibitors do not correct biosynthetic arrest of deltaF508 CFTR in cystic fibrosis
Barbara R Grubb, Sherif E Gabriel, April Mengos, et al.
Plos One
|
October 22, 2014
Sperm-associated antigen 6 (SPAG6) deficiency and defects in ciliogenesis and cilia function: polarity, density, and beat
Maria E Teves, Patrick R Sears, Wei Li, et al.
American Journal of Respiratory Cell and Molecular Biology
|
April 23, 2005
Identification and analysis of axonemal dynein light chain 1 in primary ciliary dyskinesia patients
Judit Horváth, Manfred Fliegauf, Heike Olbrich, et al.
Plos Genetics
|
March 23, 2012
Variation in MSRA modifies risk of neonatal intestinal obstruction in cystic fibrosis
Lindsay B Henderson, Vishal K Doshi, Scott M Blackman, et al.
Pediatric Pulmonology
|
January 4, 2011
Age of Pseudomonas aeruginosa acquisition and subsequent severity of cystic fibrosis lung disease
Jessica E Pittman, Elizabeth H Calloway, Michelle Kiser, 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-CFTR
Alice 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 traits
Briana Vecchio-Pagán, Scott M Blackman, Melissa Lee, et al.
Page
of 20