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Colin A Johnson

Showing results (11-20 of 132) with videos related to

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Frontiers in Cell and Developmental Biology|January 4, 2021
Primary Cilia, Ciliogenesis and the Actin Cytoskeleton: A Little Less Resorption, A Little More Actin PleaseClaire E L Smith, Alice V R Lake, Colin A Johnson
Frontiers in Pediatrics|December 7, 2017
Meckel-Gruber Syndrome: An Update on Diagnosis, Clinical Management, and Research AdvancesVerity Hartill, Katarzyna Szymanska, Saghira Malik Sharif, et al.
Developmental Biology|March 5, 2013
Aberrant Wnt signalling and cellular over-proliferation in a novel mouse model of Meckel-Gruber syndromeGabrielle Wheway, Zakia Abdelhamed, Subaashini Natarajan, et al.
Kidney International|July 18, 2008
Jouberin localizes to collecting ducts and interacts with nephrocystin-1Lorraine Eley, Christos Gabrielides, Matthew Adams, et al.
Nature Communications|February 25, 2026
Regional nonsense constraint offers biological and clinical insights into genetic diseaseAlexander J M Blakes, Nicola Whiffin, Colin A Johnson, et al.
Materials Today. Bio|December 2, 2022
From mesenchymal niches to engineered <i>in vitro</i> model systems: Exploring and exploiting biomechanical regulation of vertebrate hedgehog signallingFatmah I Ghuloum, Colin A Johnson, Natalia A Riobo-Del Galdo, et al.
The Journal of Biological Chemistry|January 5, 2002
Human class I histone deacetylase complexes show enhanced catalytic activity in the presence of ATP and co-immunoprecipitate with the ATP-dependent chaperone protein Hsp70Colin A Johnson, Darren A White, Jayne S Lavender, et al.
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|March 15, 2022
Unlocking the potential of the UK 100,000 Genomes Project-lessons learned from analysis of the "Congenital Malformations caused by Ciliopathies" cohortSunayna Best, Chris F Inglehearn, Christopher M Watson, et al.
Human Molecular Genetics|December 29, 2021
Interpreting ciliopathy-associated missense variants of uncertain significance (VUS) in Caenorhabditis elegansKaren I Lange, Sunayna Best, Sofia Tsiropoulou, et al.
Human Molecular Genetics|January 4, 2013
Variable expressivity of ciliopathy neurological phenotypes that encompass Meckel-Gruber syndrome and Joubert syndrome is caused by complex de-regulated ciliogenesis, Shh and Wnt signalling defectsZakia A Abdelhamed, Gabrielle Wheway, Katarzyna Szymanska, et al.
Pageof 14

Showing results (11-20 of 132) with videos related to

Sort By:
Pageof 14
Frontiers in Cell and Developmental Biology|January 4, 2021
Primary Cilia, Ciliogenesis and the Actin Cytoskeleton: A Little Less Resorption, A Little More Actin PleaseClaire E L Smith, Alice V R Lake, Colin A Johnson
Frontiers in Pediatrics|December 7, 2017
Meckel-Gruber Syndrome: An Update on Diagnosis, Clinical Management, and Research AdvancesVerity Hartill, Katarzyna Szymanska, Saghira Malik Sharif, et al.
Developmental Biology|March 5, 2013
Aberrant Wnt signalling and cellular over-proliferation in a novel mouse model of Meckel-Gruber syndromeGabrielle Wheway, Zakia Abdelhamed, Subaashini Natarajan, et al.
Kidney International|July 18, 2008
Jouberin localizes to collecting ducts and interacts with nephrocystin-1Lorraine Eley, Christos Gabrielides, Matthew Adams, et al.
Nature Communications|February 25, 2026
Regional nonsense constraint offers biological and clinical insights into genetic diseaseAlexander J M Blakes, Nicola Whiffin, Colin A Johnson, et al.
Materials Today. Bio|December 2, 2022
From mesenchymal niches to engineered <i>in vitro</i> model systems: Exploring and exploiting biomechanical regulation of vertebrate hedgehog signallingFatmah I Ghuloum, Colin A Johnson, Natalia A Riobo-Del Galdo, et al.
The Journal of Biological Chemistry|January 5, 2002
Human class I histone deacetylase complexes show enhanced catalytic activity in the presence of ATP and co-immunoprecipitate with the ATP-dependent chaperone protein Hsp70Colin A Johnson, Darren A White, Jayne S Lavender, et al.
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|March 15, 2022
Unlocking the potential of the UK 100,000 Genomes Project-lessons learned from analysis of the "Congenital Malformations caused by Ciliopathies" cohortSunayna Best, Chris F Inglehearn, Christopher M Watson, et al.
Human Molecular Genetics|December 29, 2021
Interpreting ciliopathy-associated missense variants of uncertain significance (VUS) in Caenorhabditis elegansKaren I Lange, Sunayna Best, Sofia Tsiropoulou, et al.
Human Molecular Genetics|January 4, 2013
Variable expressivity of ciliopathy neurological phenotypes that encompass Meckel-Gruber syndrome and Joubert syndrome is caused by complex de-regulated ciliogenesis, Shh and Wnt signalling defectsZakia A Abdelhamed, Gabrielle Wheway, Katarzyna Szymanska, et al.
Pageof 14