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

Eva Lana-Elola

Showing results (1-10 of 21) with videos related to

Pageof 3
Sort By:
Developmental Biology|October 13, 2007
Cell fate specification during calvarial bone and suture developmentEva Lana-Elola, Ritva Rice, Agamemnon E Grigoriadis, et al.
Disease Models & Mechanisms|September 1, 2011
Down syndrome: searching for the genetic culpritsEva Lana-Elola, Sheona D Watson-Scales, Elizabeth M C Fisher, et al.
Disease Models & Mechanisms|September 4, 2009
New approaches for modelling sporadic genetic disease in the mouseElizabeth M C Fisher, Eva Lana-Elola, Sheona D Watson, et al.
Developmental Biology|February 16, 2010
The essential requirement for Runx1 in the development of the sternumAnna Liakhovitskaia, Eva Lana-Elola, Evangelos Stamateris, et al.
Cardiovascular Research|June 19, 2010
Down's syndrome-like cardiac developmental defects in embryos of the transchromosomic Tc1 mouseLouisa Dunlevy, Mike Bennett, Amy Slender, et al.
Developmental Dynamics : an Official Publication of the American Association of Anatomists|September 6, 2008
Evidence that Fgf10 contributes to the skeletal and visceral defects of an Apert syndrome mouse modelMohammad K Hajihosseini, Raquel Duarte, Jean Pegrum, et al.
Frontiers in Behavioral Neuroscience|July 25, 2024
Dissecting the contribution of human chromosome 21 syntenic regions to recognition memory processes in adult and aged mouse models of Down syndromeTara Canonica, Emma J Kidd, Dorota Gibbins, et al.
Molecular and Cellular Neurosciences|March 11, 2008
Localization and fate of Fgf10-expressing cells in the adult mouse brain implicate Fgf10 in control of neurogenesisMohammad K Hajihosseini, Stijn De Langhe, Eva Lana-Elola, et al.
Human Molecular Genetics|June 24, 2010
Gli3Xt-J/Xt-J mice exhibit lambdoid suture craniosynostosis which results from altered osteoprogenitor proliferation and differentiationDavid P C Rice, Elaine C Connor, Jacqueline M Veltmaat, et al.
Elife|January 15, 2016
Genetic dissection of Down syndrome-associated congenital heart defects using a new mouse mapping panelEva Lana-Elola, Sheona Watson-Scales, Amy Slender, et al.
Pageof 3

Showing results (1-10 of 21) with videos related to

Sort By:
Pageof 3
Developmental Biology|October 13, 2007
Cell fate specification during calvarial bone and suture developmentEva Lana-Elola, Ritva Rice, Agamemnon E Grigoriadis, et al.
Disease Models & Mechanisms|September 1, 2011
Down syndrome: searching for the genetic culpritsEva Lana-Elola, Sheona D Watson-Scales, Elizabeth M C Fisher, et al.
Disease Models & Mechanisms|September 4, 2009
New approaches for modelling sporadic genetic disease in the mouseElizabeth M C Fisher, Eva Lana-Elola, Sheona D Watson, et al.
Developmental Biology|February 16, 2010
The essential requirement for Runx1 in the development of the sternumAnna Liakhovitskaia, Eva Lana-Elola, Evangelos Stamateris, et al.
Cardiovascular Research|June 19, 2010
Down's syndrome-like cardiac developmental defects in embryos of the transchromosomic Tc1 mouseLouisa Dunlevy, Mike Bennett, Amy Slender, et al.
Developmental Dynamics : an Official Publication of the American Association of Anatomists|September 6, 2008
Evidence that Fgf10 contributes to the skeletal and visceral defects of an Apert syndrome mouse modelMohammad K Hajihosseini, Raquel Duarte, Jean Pegrum, et al.
Frontiers in Behavioral Neuroscience|July 25, 2024
Dissecting the contribution of human chromosome 21 syntenic regions to recognition memory processes in adult and aged mouse models of Down syndromeTara Canonica, Emma J Kidd, Dorota Gibbins, et al.
Molecular and Cellular Neurosciences|March 11, 2008
Localization and fate of Fgf10-expressing cells in the adult mouse brain implicate Fgf10 in control of neurogenesisMohammad K Hajihosseini, Stijn De Langhe, Eva Lana-Elola, et al.
Human Molecular Genetics|June 24, 2010
Gli3Xt-J/Xt-J mice exhibit lambdoid suture craniosynostosis which results from altered osteoprogenitor proliferation and differentiationDavid P C Rice, Elaine C Connor, Jacqueline M Veltmaat, et al.
Elife|January 15, 2016
Genetic dissection of Down syndrome-associated congenital heart defects using a new mouse mapping panelEva Lana-Elola, Sheona Watson-Scales, Amy Slender, et al.
Pageof 3