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 H Smith

Showing results (371-380 of 588) with videos related to

Pageof 59
Sort By:
Nature Biotechnology|March 11, 2003
Engineering the mouse genome with bacterial artificial chromosomes to create multipurpose allelesGiuseppe Testa, Youming Zhang, Kristina Vintersten, et al.
Plos One|February 15, 2017
Seeing shapes in seemingly random spatial patterns: Fractal analysis of Rorschach inkblotsR P Taylor, T P Martin, R D Montgomery, et al.
European Journal of Biochemistry|July 22, 2004
Distribution of the lipolysis stimulated receptor in adult and embryonic murine tissues and lethality of LSR-/- embryos at 12.5 to 14.5 days of gestationSamir Mesli, Sandrine Javorschi, Annie M Bérard, et al.
Toxicological Sciences : an Official Journal of the Society of Toxicology|June 28, 2000
Effects of di-isononyl phthalate, di-2-ethylhexyl phthalate, and clofibrate in cynomolgus monkeysG Pugh, J S Isenberg, L M Kamendulis, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|October 4, 2022
De novo variants are a common cause of genetic hearing lossMiles J Klimara, Carla Nishimura, Donghong Wang, et al.
Plos Genetics|October 12, 2012
A mutation in the Srrm4 gene causes alternative splicing defects and deafness in the Bronx waltzer mouseYoko Nakano, Israt Jahan, Gregory Bonde, et al.
Anaesthesia|February 18, 2024
Peri-operative cardiac arrest in children as reported to the 7th National Audit Project of the Royal College of AnaesthetistsF C Oglesby, B R Scholefield, T M Cook, et al.
JMIR Bioinformatics and Biotechnology|April 14, 2026
The AudioGene Translational Dashboard for Diagnosing Autosomal Dominant Nonsyndromic Hearing Loss: Phenotypic Data Visualization and Analysis StudyBenjamin DeSollar, Nathan Schaefer, Daniel Walls, et al.
Journal of Medical Genetics|January 20, 2004
A novel locus for autosomal dominant non-syndromic hearing loss, DFNA31, maps to chromosome 6p21.3R L Snoeckx, H Kremer, R J H Ensink, et al.
Blood|August 22, 2009
Chromosome looping at the human alpha-globin locus is mediated via the major upstream regulatory element (HS -40)Douglas Vernimmen, Fatima Marques-Kranc, Jacqueline A Sharpe, et al.
Pageof 59

Showing results (371-380 of 588) with videos related to

Sort By:
Pageof 59
Nature Biotechnology|March 11, 2003
Engineering the mouse genome with bacterial artificial chromosomes to create multipurpose allelesGiuseppe Testa, Youming Zhang, Kristina Vintersten, et al.
Plos One|February 15, 2017
Seeing shapes in seemingly random spatial patterns: Fractal analysis of Rorschach inkblotsR P Taylor, T P Martin, R D Montgomery, et al.
European Journal of Biochemistry|July 22, 2004
Distribution of the lipolysis stimulated receptor in adult and embryonic murine tissues and lethality of LSR-/- embryos at 12.5 to 14.5 days of gestationSamir Mesli, Sandrine Javorschi, Annie M Bérard, et al.
Toxicological Sciences : an Official Journal of the Society of Toxicology|June 28, 2000
Effects of di-isononyl phthalate, di-2-ethylhexyl phthalate, and clofibrate in cynomolgus monkeysG Pugh, J S Isenberg, L M Kamendulis, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|October 4, 2022
De novo variants are a common cause of genetic hearing lossMiles J Klimara, Carla Nishimura, Donghong Wang, et al.
Plos Genetics|October 12, 2012
A mutation in the Srrm4 gene causes alternative splicing defects and deafness in the Bronx waltzer mouseYoko Nakano, Israt Jahan, Gregory Bonde, et al.
Anaesthesia|February 18, 2024
Peri-operative cardiac arrest in children as reported to the 7th National Audit Project of the Royal College of AnaesthetistsF C Oglesby, B R Scholefield, T M Cook, et al.
JMIR Bioinformatics and Biotechnology|April 14, 2026
The AudioGene Translational Dashboard for Diagnosing Autosomal Dominant Nonsyndromic Hearing Loss: Phenotypic Data Visualization and Analysis StudyBenjamin DeSollar, Nathan Schaefer, Daniel Walls, et al.
Journal of Medical Genetics|January 20, 2004
A novel locus for autosomal dominant non-syndromic hearing loss, DFNA31, maps to chromosome 6p21.3R L Snoeckx, H Kremer, R J H Ensink, et al.
Blood|August 22, 2009
Chromosome looping at the human alpha-globin locus is mediated via the major upstream regulatory element (HS -40)Douglas Vernimmen, Fatima Marques-Kranc, Jacqueline A Sharpe, et al.
Pageof 59