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Christopher O'Callaghan

Showing results (91-100 of 99) with videos related to

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Thorax|September 1, 2018
Risk factors for situs defects and congenital heart disease in primary ciliary dyskinesiaSunayna Best, Amelia Shoemark, Bruna Rubbo, et al.
Nature Genetics|May 15, 2012
CCDC103 mutations cause primary ciliary dyskinesia by disrupting assembly of ciliary dynein armsJennifer R Panizzi, Anita Becker-Heck, Victoria H Castleman, et al.
Nature Medicine|January 21, 2025
Author Correction: Single-cell guided prenatal derivation of primary fetal epithelial organoids from human amniotic and tracheal fluidsMattia Francesco Maria Gerli, Giuseppe Calà, Max Arran Beesley, et al.
Nature Medicine|March 4, 2024
Single-cell guided prenatal derivation of primary fetal epithelial organoids from human amniotic and tracheal fluidsMattia Francesco Maria Gerli, Giuseppe Calà, Max Arran Beesley, et al.
Iscience|November 17, 2022
Cell-intrinsic differences between human airway epithelial cells from children and adultsElizabeth F Maughan, Robert E Hynds, Adam Pennycuick, et al.
Human Mutation|December 21, 2012
Mutations in CCDC39 and CCDC40 are the major cause of primary ciliary dyskinesia with axonemal disorganization and absent inner dynein armsDinu Antony, Anita Becker-Heck, Maimoona A Zariwala, et al.
American Journal of Human Genetics|September 6, 2014
CCDC151 mutations cause primary ciliary dyskinesia by disruption of the outer dynein arm docking complex formationRim Hjeij, Alexandros Onoufriadis, Christopher M Watson, et al.
Thorax|August 10, 2017
High prevalence of <i>CCDC103</i> p.His154Pro mutation causing primary ciliary dyskinesia disrupts protein oligomerisation and is associated with normal diagnostic investigationsAmelia Shoemark, Eduardo Moya, Robert A Hirst, et al.
Nature|December 22, 2021
Local and systemic responses to SARS-CoV-2 infection in children and adultsMasahiro Yoshida, Kaylee B Worlock, Ni Huang, et al.
Pageof 10

Showing results (91-100 of 99) with videos related to

Sort By:
Pageof 10
You have reached the last page of results.This site can display upto 99 results.
Thorax|September 1, 2018
Risk factors for situs defects and congenital heart disease in primary ciliary dyskinesiaSunayna Best, Amelia Shoemark, Bruna Rubbo, et al.
Nature Genetics|May 15, 2012
CCDC103 mutations cause primary ciliary dyskinesia by disrupting assembly of ciliary dynein armsJennifer R Panizzi, Anita Becker-Heck, Victoria H Castleman, et al.
Nature Medicine|January 21, 2025
Author Correction: Single-cell guided prenatal derivation of primary fetal epithelial organoids from human amniotic and tracheal fluidsMattia Francesco Maria Gerli, Giuseppe Calà, Max Arran Beesley, et al.
Nature Medicine|March 4, 2024
Single-cell guided prenatal derivation of primary fetal epithelial organoids from human amniotic and tracheal fluidsMattia Francesco Maria Gerli, Giuseppe Calà, Max Arran Beesley, et al.
Iscience|November 17, 2022
Cell-intrinsic differences between human airway epithelial cells from children and adultsElizabeth F Maughan, Robert E Hynds, Adam Pennycuick, et al.
Human Mutation|December 21, 2012
Mutations in CCDC39 and CCDC40 are the major cause of primary ciliary dyskinesia with axonemal disorganization and absent inner dynein armsDinu Antony, Anita Becker-Heck, Maimoona A Zariwala, et al.
American Journal of Human Genetics|September 6, 2014
CCDC151 mutations cause primary ciliary dyskinesia by disruption of the outer dynein arm docking complex formationRim Hjeij, Alexandros Onoufriadis, Christopher M Watson, et al.
Thorax|August 10, 2017
High prevalence of <i>CCDC103</i> p.His154Pro mutation causing primary ciliary dyskinesia disrupts protein oligomerisation and is associated with normal diagnostic investigationsAmelia Shoemark, Eduardo Moya, Robert A Hirst, et al.
Nature|December 22, 2021
Local and systemic responses to SARS-CoV-2 infection in children and adultsMasahiro Yoshida, Kaylee B Worlock, Ni Huang, et al.
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