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Michael R Knowles

Showing results (51-60 of 196) with videos related to

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Respiration; International Review of Thoracic Diseases|August 10, 2005
A middle-aged woman with recurrent respiratory infectionsKathryn Chmura, Edward D Chan, Peadar G Noone, et al.
Annals of the American Thoracic Society|February 7, 2014
The role of molecular genetic analysis in the diagnosis of primary ciliary dyskinesiaRaymond H Kim, David A Hall, Ernest Cutz, et al.
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.
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.
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.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 17, 2009
Clinical and genetic aspects of primary ciliary dyskinesia/Kartagener syndromeMargaret W Leigh, Jessica E Pittman, Johnny L Carson, et al.
Proteomics|July 23, 2003
Multiplex proteomic analysis by two-dimensional differential in-gel electrophoresisMichael R Knowles, Sandra Cervino, Heather A Skynner, et al.
Pageof 20

Showing results (51-60 of 196) with videos related to

Sort By:
Pageof 20
Respiration; International Review of Thoracic Diseases|August 10, 2005
A middle-aged woman with recurrent respiratory infectionsKathryn Chmura, Edward D Chan, Peadar G Noone, et al.
Annals of the American Thoracic Society|February 7, 2014
The role of molecular genetic analysis in the diagnosis of primary ciliary dyskinesiaRaymond H Kim, David A Hall, Ernest Cutz, et al.
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.
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.
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.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 17, 2009
Clinical and genetic aspects of primary ciliary dyskinesia/Kartagener syndromeMargaret W Leigh, Jessica E Pittman, Johnny L Carson, et al.
Proteomics|July 23, 2003
Multiplex proteomic analysis by two-dimensional differential in-gel electrophoresisMichael R Knowles, Sandra Cervino, Heather A Skynner, et al.
Pageof 20