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Dagan Jenkins

Showing results (11-20 of 34) with videos related to

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Elife|April 17, 2018
Crystal structure of intraflagellar transport protein 80 reveals a homo-dimer required for ciliogenesisMichael Taschner, Anna Lorentzen, André Mourão, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|September 12, 2009
Analysis of TSHZ2 and TSHZ3 genes in congenital pelvi-ureteric junction obstructionDagan Jenkins, Xavier Caubit, Aleksandar Dimovski, et al.
Methods in Molecular Biology (Clifton, N.J.)|October 19, 2023
Affinity Purification of Intraflagellar Transport (IFT) Proteins in Mice Using Endogenous Streptavidin/FLAG TagsTina Beyer, Tiago Martins, Jeshmi Jeyabalan Srikaran, et al.
The EMBO Journal|March 7, 2024
Structure and tethering mechanism of dynein-2 intermediate chains in intraflagellar transportAakash G Mukhopadhyay, Katerina Toropova, Lydia Daly, et al.
Human Mutation|March 18, 2011
Carpenter syndrome: extended RAB23 mutation spectrum and analysis of nonsense-mediated mRNA decayDagan Jenkins, Gareth Baynam, Luc De Catte, et al.
Molecular Syndromology|April 13, 2019
An FDA-Approved Drug Screen for Compounds Influencing Craniofacial Skeletal Development and CraniosynostosisMarian Seda, Maartje Geerlings, Peggy Lim, et al.
Development (Cambridge, England)|September 9, 2008
Teashirt 3 is necessary for ureteral smooth muscle differentiation downstream of SHH and BMP4Xavier Caubit, Claire M Lye, Elise Martin, et al.
Molecular & Cellular Proteomics : MCP|January 29, 2025
Ciliopathy-Associated Missense Mutations in IFT140 are Tolerated by the Inherent Resilience of the IFT MachineryTina Beyer, Gaurav D Diwan, Tobias Leonhard, et al.
Plos Genetics|March 17, 2017
COLEC10 is mutated in 3MC patients and regulates early craniofacial developmentMustafa M Munye, Anna Diaz-Font, Louise Ocaka, et al.
European Journal of Human Genetics : EJHG|February 18, 2011
Metopic and sagittal synostosis in Greig cephalopolysyndactyly syndrome: five cases with intragenic mutations or complete deletions of GLI3Jane A Hurst, Dagan Jenkins, Pradeep C Vasudevan, et al.
Pageof 4

Showing results (11-20 of 34) with videos related to

Sort By:
Pageof 4
Elife|April 17, 2018
Crystal structure of intraflagellar transport protein 80 reveals a homo-dimer required for ciliogenesisMichael Taschner, Anna Lorentzen, André Mourão, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|September 12, 2009
Analysis of TSHZ2 and TSHZ3 genes in congenital pelvi-ureteric junction obstructionDagan Jenkins, Xavier Caubit, Aleksandar Dimovski, et al.
Methods in Molecular Biology (Clifton, N.J.)|October 19, 2023
Affinity Purification of Intraflagellar Transport (IFT) Proteins in Mice Using Endogenous Streptavidin/FLAG TagsTina Beyer, Tiago Martins, Jeshmi Jeyabalan Srikaran, et al.
The EMBO Journal|March 7, 2024
Structure and tethering mechanism of dynein-2 intermediate chains in intraflagellar transportAakash G Mukhopadhyay, Katerina Toropova, Lydia Daly, et al.
Human Mutation|March 18, 2011
Carpenter syndrome: extended RAB23 mutation spectrum and analysis of nonsense-mediated mRNA decayDagan Jenkins, Gareth Baynam, Luc De Catte, et al.
Molecular Syndromology|April 13, 2019
An FDA-Approved Drug Screen for Compounds Influencing Craniofacial Skeletal Development and CraniosynostosisMarian Seda, Maartje Geerlings, Peggy Lim, et al.
Development (Cambridge, England)|September 9, 2008
Teashirt 3 is necessary for ureteral smooth muscle differentiation downstream of SHH and BMP4Xavier Caubit, Claire M Lye, Elise Martin, et al.
Molecular & Cellular Proteomics : MCP|January 29, 2025
Ciliopathy-Associated Missense Mutations in IFT140 are Tolerated by the Inherent Resilience of the IFT MachineryTina Beyer, Gaurav D Diwan, Tobias Leonhard, et al.
Plos Genetics|March 17, 2017
COLEC10 is mutated in 3MC patients and regulates early craniofacial developmentMustafa M Munye, Anna Diaz-Font, Louise Ocaka, et al.
European Journal of Human Genetics : EJHG|February 18, 2011
Metopic and sagittal synostosis in Greig cephalopolysyndactyly syndrome: five cases with intragenic mutations or complete deletions of GLI3Jane A Hurst, Dagan Jenkins, Pradeep C Vasudevan, et al.
Pageof 4