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R Knowles

Showing results (731-740 of 950) with videos related to

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American Journal of Respiratory and Critical Care Medicine|December 6, 2003
Primary ciliary dyskinesia: diagnostic and phenotypic featuresPeadar G Noone, Margaret W Leigh, Aruna Sannuti, et al.
American Journal of Respiratory and Critical Care Medicine|July 3, 1999
Effect of aerosolized uridine-5'-triphosphate on airway clearance with cough in patients with primary ciliary dyskinesiaP G Noone, W D Bennett, J A Regnis, 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.
Ultrastructural Pathology|August 21, 2013
A new tool improves diagnostic test performance for transmission em evaluation of axonemal dynein armsW Keith Funkhouser, Marc Niethammer, Johnny L Carson, et al.
Nature Communications|December 5, 2014
Cryo-electron tomography reveals ciliary defects underlying human RSPH1 primary ciliary dyskinesiaJianfeng Lin, Weining Yin, Maria C Smith, et al.
Human Gene Therapy|May 1, 1994
Gene therapy for cystic fibrosis using E1-deleted adenovirus: a phase I trial in the nasal cavity. The University of North Carolina at Chapel HillR C Boucher, M R Knowles, L G Johnson, et al.
Diabetologia|July 9, 2009
A susceptibility gene for type 2 diabetes confers substantial risk for diabetes complicating cystic fibrosisS M Blackman, S Hsu, S E Ritter, et al.
Molecular Genetics & Genomic Medicine|June 16, 2021
Autosomal dominant variants in FOXJ1 causing primary ciliary dyskinesia in two patients with obstructive hydrocephalusAdam J Shapiro, Kimberley Kaspy, M Leigh Ann Daniels, et al.
Molecular Genetics & Genomic Medicine|August 3, 2019
The expanding phenotype of OFD1-related disorders: Hemizygous loss-of-function variants in three patients with primary ciliary dyskinesiaWilliam B Hannah, Suzanne DeBrosse, BreAnna Kinghorn, et al.
Children (Basel, Switzerland)|July 2, 2021
Foundational Movement Skills and Play Behaviors during Recess among Preschool Children: A Compositional AnalysisLawrence Foweather, Matteo Crotti, Jonathan D Foulkes, et al.
Pageof 95

Showing results (731-740 of 950) with videos related to

Sort By:
Pageof 95
American Journal of Respiratory and Critical Care Medicine|December 6, 2003
Primary ciliary dyskinesia: diagnostic and phenotypic featuresPeadar G Noone, Margaret W Leigh, Aruna Sannuti, et al.
American Journal of Respiratory and Critical Care Medicine|July 3, 1999
Effect of aerosolized uridine-5'-triphosphate on airway clearance with cough in patients with primary ciliary dyskinesiaP G Noone, W D Bennett, J A Regnis, 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.
Ultrastructural Pathology|August 21, 2013
A new tool improves diagnostic test performance for transmission em evaluation of axonemal dynein armsW Keith Funkhouser, Marc Niethammer, Johnny L Carson, et al.
Nature Communications|December 5, 2014
Cryo-electron tomography reveals ciliary defects underlying human RSPH1 primary ciliary dyskinesiaJianfeng Lin, Weining Yin, Maria C Smith, et al.
Human Gene Therapy|May 1, 1994
Gene therapy for cystic fibrosis using E1-deleted adenovirus: a phase I trial in the nasal cavity. The University of North Carolina at Chapel HillR C Boucher, M R Knowles, L G Johnson, et al.
Diabetologia|July 9, 2009
A susceptibility gene for type 2 diabetes confers substantial risk for diabetes complicating cystic fibrosisS M Blackman, S Hsu, S E Ritter, et al.
Molecular Genetics & Genomic Medicine|June 16, 2021
Autosomal dominant variants in FOXJ1 causing primary ciliary dyskinesia in two patients with obstructive hydrocephalusAdam J Shapiro, Kimberley Kaspy, M Leigh Ann Daniels, et al.
Molecular Genetics & Genomic Medicine|August 3, 2019
The expanding phenotype of OFD1-related disorders: Hemizygous loss-of-function variants in three patients with primary ciliary dyskinesiaWilliam B Hannah, Suzanne DeBrosse, BreAnna Kinghorn, et al.
Children (Basel, Switzerland)|July 2, 2021
Foundational Movement Skills and Play Behaviors during Recess among Preschool Children: A Compositional AnalysisLawrence Foweather, Matteo Crotti, Jonathan D Foulkes, et al.
Pageof 95