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

Anne Seawright

Showing results (1-10 of 8) with videos related to

Pageof 1
Sort By:
Mammalian Genome : Official Journal of the International Mammalian Genome Society|March 13, 2002
Characterization of a novel gene adjacent to PAX6, revealing synteny conservation with functional significanceDirk A Kleinjan, Anne Seawright, Greg Elgar, et al.
Developmental Biology|January 21, 2004
Conserved elements in Pax6 intron 7 involved in (auto)regulation and alternative transcriptionDirk A Kleinjan, Anne Seawright, Andrew J Childs, et al.
Developmental Biology|October 4, 2006
Long-range downstream enhancers are essential for Pax6 expressionDirk A Kleinjan, Anne Seawright, Sebastien Mella, et al.
Plos Genetics|February 20, 2008
Subfunctionalization of duplicated zebrafish pax6 genes by cis-regulatory divergenceDirk A Kleinjan, Ruth M Bancewicz, Philippe Gautier, et al.
Molecular Biology of the Cell|February 21, 2014
Kdm3a lysine demethylase is an Hsp90 client required for cytoskeletal rearrangements during spermatogenesisIoannis Kasioulis, Heather M Syred, Peri Tate, et al.
Human Mutation|May 12, 2017
A recurrent de novo mutation in ACTG1 causes isolated ocular colobomaJoe Rainger, Kathleen A Williamson, Dinesh C Soares, et al.
American Journal of Human Genetics|April 26, 2016
A Restricted Repertoire of De Novo Mutations in ITPR1 Cause Gillespie Syndrome with Evidence for Dominant-Negative EffectMeriel McEntagart, Kathleen A Williamson, Jacqueline K Rainger, et al.
American Journal of Human Genetics|June 7, 2014
Monoallelic and biallelic mutations in MAB21L2 cause a spectrum of major eye malformationsJoe Rainger, Davut Pehlivan, Stefan Johansson, et al.
Pageof 1

Showing results (1-10 of 8) with videos related to

Sort By:
Pageof 1
Mammalian Genome : Official Journal of the International Mammalian Genome Society|March 13, 2002
Characterization of a novel gene adjacent to PAX6, revealing synteny conservation with functional significanceDirk A Kleinjan, Anne Seawright, Greg Elgar, et al.
Developmental Biology|January 21, 2004
Conserved elements in Pax6 intron 7 involved in (auto)regulation and alternative transcriptionDirk A Kleinjan, Anne Seawright, Andrew J Childs, et al.
Developmental Biology|October 4, 2006
Long-range downstream enhancers are essential for Pax6 expressionDirk A Kleinjan, Anne Seawright, Sebastien Mella, et al.
Plos Genetics|February 20, 2008
Subfunctionalization of duplicated zebrafish pax6 genes by cis-regulatory divergenceDirk A Kleinjan, Ruth M Bancewicz, Philippe Gautier, et al.
Molecular Biology of the Cell|February 21, 2014
Kdm3a lysine demethylase is an Hsp90 client required for cytoskeletal rearrangements during spermatogenesisIoannis Kasioulis, Heather M Syred, Peri Tate, et al.
Human Mutation|May 12, 2017
A recurrent de novo mutation in ACTG1 causes isolated ocular colobomaJoe Rainger, Kathleen A Williamson, Dinesh C Soares, et al.
American Journal of Human Genetics|April 26, 2016
A Restricted Repertoire of De Novo Mutations in ITPR1 Cause Gillespie Syndrome with Evidence for Dominant-Negative EffectMeriel McEntagart, Kathleen A Williamson, Jacqueline K Rainger, et al.
American Journal of Human Genetics|June 7, 2014
Monoallelic and biallelic mutations in MAB21L2 cause a spectrum of major eye malformationsJoe Rainger, Davut Pehlivan, Stefan Johansson, et al.
Pageof 1