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Laura A Devlin

Showing results (1-10 of 6) with videos related to

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Current Opinion in Genetics & Development|August 17, 2019
Renal ciliopathiesLaura A Devlin, John A Sayer
Current Topics in Developmental Biology|April 20, 2025
Renal ciliopathiesLaura A Devlin, Rebecca M Dewhurst, Praveen D Sudhindar, et al.
Scientific Reports|July 27, 2019
Targeted exon skipping rescues ciliary protein composition defects in Joubert syndrome patient fibroblastsElisa Molinari, Simon A Ramsbottom, Shalabh Srivastava, et al.
Proceedings of the National Academy of Sciences of the United States of America|November 18, 2018
Targeted exon skipping of a <i>CEP290</i> mutation rescues Joubert syndrome phenotypes in vitro and in a murine modelSimon A Ramsbottom, Elisa Molinari, Shalabh Srivastava, et al.
Proceedings of the National Academy of Sciences of the United States of America|December 28, 2019
Mouse genetics reveals Barttin as a genetic modifier of Joubert syndromeSimon A Ramsbottom, Peter E Thelwall, Katrina M Wood, et al.
Clinical Genetics|October 23, 2022
Biallelic variants in CEP164 cause a motile ciliopathy-like syndromeLaura A Devlin, Janice Coles, Claire L Jackson, et al.
Pageof 1

Showing results (1-10 of 6) with videos related to

Sort By:
Pageof 1
Current Opinion in Genetics & Development|August 17, 2019
Renal ciliopathiesLaura A Devlin, John A Sayer
Current Topics in Developmental Biology|April 20, 2025
Renal ciliopathiesLaura A Devlin, Rebecca M Dewhurst, Praveen D Sudhindar, et al.
Scientific Reports|July 27, 2019
Targeted exon skipping rescues ciliary protein composition defects in Joubert syndrome patient fibroblastsElisa Molinari, Simon A Ramsbottom, Shalabh Srivastava, et al.
Proceedings of the National Academy of Sciences of the United States of America|November 18, 2018
Targeted exon skipping of a <i>CEP290</i> mutation rescues Joubert syndrome phenotypes in vitro and in a murine modelSimon A Ramsbottom, Elisa Molinari, Shalabh Srivastava, et al.
Proceedings of the National Academy of Sciences of the United States of America|December 28, 2019
Mouse genetics reveals Barttin as a genetic modifier of Joubert syndromeSimon A Ramsbottom, Peter E Thelwall, Katrina M Wood, et al.
Clinical Genetics|October 23, 2022
Biallelic variants in CEP164 cause a motile ciliopathy-like syndromeLaura A Devlin, Janice Coles, Claire L Jackson, et al.
Pageof 1