Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Colin A Johnson

Showing results (21-30 of 132) with videos related to

Pageof 14
Sort By:
Histopathology|January 8, 2025
Threonine and tyrosine kinase (TTK) mRNA and protein expression in breast cancer; prognostic significance in the neoadjuvant settingAbrar Ashi, Aeshah A Awaji, Jacquelyn Bond, et al.
Human Mutation|October 21, 2009
Shadow autozygosity mapping by linkage exclusion (SAMPLE): a simple strategy to identify the genetic basis of lethal autosomal recessive disordersIan M Carr, Katarzyna Szymanska, Eamonn Sheridan, et al.
Journal of Medical Genetics|June 24, 2020
Novel loss-of-function mutation in <i>HERC2</i> is associated with severe developmental delay and paediatric lethalityMarilena Elpidorou, Sunayna Best, James A Poulter, et al.
Human Mutation|September 10, 2011
DominantMapper: rule-based analysis of SNP data for rapid mapping of dominant diseases in related nuclear familiesIan M Carr, Colin A Johnson, Alex F Markham, et al.
Development (Cambridge, England)|November 15, 2005
Zebrafish vps33b, an ortholog of the gene responsible for human arthrogryposis-renal dysfunction-cholestasis syndrome, regulates biliary development downstream of the onecut transcription factor hnf6Randolph P Matthews, Nicolas Plumb-Rudewiez, Kristin Lorent, et al.
Biomaterials Advances|October 14, 2023
Towards modular engineering of cell signalling: Topographically-textured microparticles induce osteogenesis via activation of canonical hedgehog signallingFatmah I Ghuloum, Lee A Stevens, Colin A Johnson, et al.
Experimental Cell Research|October 13, 2012
Human Homolog of Drosophila Ariadne (HHARI) is a marker of cellular proliferation associated with nuclear bodiesFatima Elmehdawi, Gabrielle Wheway, Katarzyna Szymanska, et al.
Disease Models & Mechanisms|June 3, 2015
The Meckel-Gruber syndrome protein TMEM67 controls basal body positioning and epithelial branching morphogenesis in mice via the non-canonical Wnt pathwayZakia A Abdelhamed, Subaashini Natarajan, Gabrielle Wheway, et al.
The Journal of Biological Chemistry|July 15, 2024
Glycogen myophosphorylase loss causes increased dependence on glucose in iPSC-derived retinal pigment epitheliumBasudha Basu, Magdalena Karwatka, Becky China, et al.
Journal of Cell Science|July 15, 2009
Nesprin-2 interacts with meckelin and mediates ciliogenesis via remodelling of the actin cytoskeletonHelen R Dawe, Matthew Adams, Gabrielle Wheway, et al.
Pageof 14

Showing results (21-30 of 132) with videos related to

Sort By:
Pageof 14
Histopathology|January 8, 2025
Threonine and tyrosine kinase (TTK) mRNA and protein expression in breast cancer; prognostic significance in the neoadjuvant settingAbrar Ashi, Aeshah A Awaji, Jacquelyn Bond, et al.
Human Mutation|October 21, 2009
Shadow autozygosity mapping by linkage exclusion (SAMPLE): a simple strategy to identify the genetic basis of lethal autosomal recessive disordersIan M Carr, Katarzyna Szymanska, Eamonn Sheridan, et al.
Journal of Medical Genetics|June 24, 2020
Novel loss-of-function mutation in <i>HERC2</i> is associated with severe developmental delay and paediatric lethalityMarilena Elpidorou, Sunayna Best, James A Poulter, et al.
Human Mutation|September 10, 2011
DominantMapper: rule-based analysis of SNP data for rapid mapping of dominant diseases in related nuclear familiesIan M Carr, Colin A Johnson, Alex F Markham, et al.
Development (Cambridge, England)|November 15, 2005
Zebrafish vps33b, an ortholog of the gene responsible for human arthrogryposis-renal dysfunction-cholestasis syndrome, regulates biliary development downstream of the onecut transcription factor hnf6Randolph P Matthews, Nicolas Plumb-Rudewiez, Kristin Lorent, et al.
Biomaterials Advances|October 14, 2023
Towards modular engineering of cell signalling: Topographically-textured microparticles induce osteogenesis via activation of canonical hedgehog signallingFatmah I Ghuloum, Lee A Stevens, Colin A Johnson, et al.
Experimental Cell Research|October 13, 2012
Human Homolog of Drosophila Ariadne (HHARI) is a marker of cellular proliferation associated with nuclear bodiesFatima Elmehdawi, Gabrielle Wheway, Katarzyna Szymanska, et al.
Disease Models & Mechanisms|June 3, 2015
The Meckel-Gruber syndrome protein TMEM67 controls basal body positioning and epithelial branching morphogenesis in mice via the non-canonical Wnt pathwayZakia A Abdelhamed, Subaashini Natarajan, Gabrielle Wheway, et al.
The Journal of Biological Chemistry|July 15, 2024
Glycogen myophosphorylase loss causes increased dependence on glucose in iPSC-derived retinal pigment epitheliumBasudha Basu, Magdalena Karwatka, Becky China, et al.
Journal of Cell Science|July 15, 2009
Nesprin-2 interacts with meckelin and mediates ciliogenesis via remodelling of the actin cytoskeletonHelen R Dawe, Matthew Adams, Gabrielle Wheway, et al.
Pageof 14