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Marian Seda

Showing results (1-10 of 12) with videos related to

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Scientific Reports|April 26, 2023
A CRISPR/Cas9-generated mutation in the zebrafish orthologue of PPP2R3B causes idiopathic scoliosisMarian Seda, Berta Crespo, Michelangelo Corcelli, et al.
Methods in Molecular Biology (Clifton, N.J.)|November 9, 2019
Generating Mutant Renal Cell Lines Using CRISPR TechnologiesNuria Perretta-Tejedor, Grace Freke, Marian Seda, et al.
F1000Research|June 25, 2019
Analysis of transgenic zebrafish expressing the Lenz-Majewski syndrome gene <i>PTDSS1</i> in skeletal cell lineagesMarian Seda, Emma Peskett, Charalambos Demetriou, et al.
Biology of Reproduction|August 3, 2007
Functional and molecular characterization of voltage-gated sodium channels in uteri from nonpregnant ratsMarian Seda, Francisco M Pinto, Susan Wray, et al.
European Journal of Pharmacology|June 6, 2006
Molecular diversity of voltage-gated sodium channel alpha and beta subunit mRNAs in human tissuesLuz Candenas, Marian Seda, Pedro Noheda, 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.
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.
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.
Human Molecular Genetics|April 11, 2018
SNX14 mutations affect endoplasmic reticulum-associated neutral lipid metabolism in autosomal recessive spinocerebellar ataxia 20Dale Bryant, Yang Liu, Sanchari Datta, et al.
Pageof 2

Showing results (1-10 of 12) with videos related to

Sort By:
Pageof 2
Scientific Reports|April 26, 2023
A CRISPR/Cas9-generated mutation in the zebrafish orthologue of PPP2R3B causes idiopathic scoliosisMarian Seda, Berta Crespo, Michelangelo Corcelli, et al.
Methods in Molecular Biology (Clifton, N.J.)|November 9, 2019
Generating Mutant Renal Cell Lines Using CRISPR TechnologiesNuria Perretta-Tejedor, Grace Freke, Marian Seda, et al.
F1000Research|June 25, 2019
Analysis of transgenic zebrafish expressing the Lenz-Majewski syndrome gene <i>PTDSS1</i> in skeletal cell lineagesMarian Seda, Emma Peskett, Charalambos Demetriou, et al.
Biology of Reproduction|August 3, 2007
Functional and molecular characterization of voltage-gated sodium channels in uteri from nonpregnant ratsMarian Seda, Francisco M Pinto, Susan Wray, et al.
European Journal of Pharmacology|June 6, 2006
Molecular diversity of voltage-gated sodium channel alpha and beta subunit mRNAs in human tissuesLuz Candenas, Marian Seda, Pedro Noheda, 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.
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.
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.
Human Molecular Genetics|April 11, 2018
SNX14 mutations affect endoplasmic reticulum-associated neutral lipid metabolism in autosomal recessive spinocerebellar ataxia 20Dale Bryant, Yang Liu, Sanchari Datta, et al.
Pageof 2