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

J David Brook

Showing results (21-30 of 45) with videos related to

Pageof 5
Sort By:
Journal of Anatomy|February 29, 2024
Effect of deletion of the protein kinase PRKD1 on development of the mouse embryonic heartQazi Waheed-Ullah, Anna Wilsdon, Aseel Abbad, et al.
Molecular and Cellular Biology|February 11, 2009
Physical interaction between TBX5 and MEF2C is required for early heart developmentTushar K Ghosh, Fei Fei Song, Elizabeth A Packham, et al.
Congenital Heart Disease|October 21, 2011
Combined mutation screening of NKX2-5, GATA4, and TBX5 in congenital heart disease: multiple heterozygosity and novel mutationsJavier T Granados-Riveron, Mark Pope, Frances A Bu'lock, et al.
Human Molecular Genetics|July 27, 2010
Alpha-cardiac myosin heavy chain (MYH6) mutations affecting myofibril formation are associated with congenital heart defectsJavier T Granados-Riveron, Tushar K Ghosh, Mark Pope, et al.
Journal of Molecular and Cellular Cardiology|April 1, 2017
Tropomyosin 1: Multiple roles in the developing heart and in the formation of congenital heart defectsJennifer England, Javier Granados-Riveron, Luis Polo-Parada, et al.
BMC Genetics|June 21, 2013
Low-frequency intermediate penetrance variants in the ROCK1 gene predispose to Tetralogy of FallotJulian Palomino Doza, Ana Topf, Jamie Bentham, et al.
Human Molecular Genetics|November 2, 2013
High-content screening identifies small molecules that remove nuclear foci, affect MBNL distribution and CELF1 protein levels via a PKC-independent pathway in myotonic dystrophy cell linesAmi Ketley, Catherine Z Chen, Xin Li, et al.
Genome Medicine|August 30, 2020
Systems genetics analysis identifies calcium-signaling defects as novel cause of congenital heart diseaseJose M G Izarzugaza, Sabrina G Ellesøe, Canan Doganli, et al.
Nature Genetics|March 1, 2005
Mutation in myosin heavy chain 6 causes atrial septal defectYung-Hao Ching, Tushar K Ghosh, Steve J Cross, et al.
Plos One|March 25, 2009
Genetic variation in VEGF does not contribute significantly to the risk of congenital cardiovascular malformationHelen R Griffin, Darroch H Hall, Ana Topf, et al.
Pageof 5

Showing results (21-30 of 45) with videos related to

Sort By:
Pageof 5
Journal of Anatomy|February 29, 2024
Effect of deletion of the protein kinase PRKD1 on development of the mouse embryonic heartQazi Waheed-Ullah, Anna Wilsdon, Aseel Abbad, et al.
Molecular and Cellular Biology|February 11, 2009
Physical interaction between TBX5 and MEF2C is required for early heart developmentTushar K Ghosh, Fei Fei Song, Elizabeth A Packham, et al.
Congenital Heart Disease|October 21, 2011
Combined mutation screening of NKX2-5, GATA4, and TBX5 in congenital heart disease: multiple heterozygosity and novel mutationsJavier T Granados-Riveron, Mark Pope, Frances A Bu'lock, et al.
Human Molecular Genetics|July 27, 2010
Alpha-cardiac myosin heavy chain (MYH6) mutations affecting myofibril formation are associated with congenital heart defectsJavier T Granados-Riveron, Tushar K Ghosh, Mark Pope, et al.
Journal of Molecular and Cellular Cardiology|April 1, 2017
Tropomyosin 1: Multiple roles in the developing heart and in the formation of congenital heart defectsJennifer England, Javier Granados-Riveron, Luis Polo-Parada, et al.
BMC Genetics|June 21, 2013
Low-frequency intermediate penetrance variants in the ROCK1 gene predispose to Tetralogy of FallotJulian Palomino Doza, Ana Topf, Jamie Bentham, et al.
Human Molecular Genetics|November 2, 2013
High-content screening identifies small molecules that remove nuclear foci, affect MBNL distribution and CELF1 protein levels via a PKC-independent pathway in myotonic dystrophy cell linesAmi Ketley, Catherine Z Chen, Xin Li, et al.
Genome Medicine|August 30, 2020
Systems genetics analysis identifies calcium-signaling defects as novel cause of congenital heart diseaseJose M G Izarzugaza, Sabrina G Ellesøe, Canan Doganli, et al.
Nature Genetics|March 1, 2005
Mutation in myosin heavy chain 6 causes atrial septal defectYung-Hao Ching, Tushar K Ghosh, Steve J Cross, et al.
Plos One|March 25, 2009
Genetic variation in VEGF does not contribute significantly to the risk of congenital cardiovascular malformationHelen R Griffin, Darroch H Hall, Ana Topf, et al.
Pageof 5