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 Curry

Showing results (621-630 of 644) with videos related to

Pageof 65
Sort By:
American Journal of Medical Genetics. Part A|June 18, 2022
Exome sequencing identifies genetic variants in anophthalmia and microphthalmiaJingjing Li, Wei Yang, Yuejun Jessie Wang, et al.
Nature Communications|October 6, 2023
Injectable and biodegradable piezoelectric hydrogel for osteoarthritis treatmentTra Vinikoor, Godwin K Dzidotor, Thinh T Le, et al.
Brain : a Journal of Neurology|April 21, 2021
ATP1A2- and ATP1A3-associated early profound epileptic encephalopathy and polymicrogyriaAnnalisa Vetro, Hang N Nielsen, Rikke Holm, et al.
Nature|May 1, 2024
Probing single electrons across 300-mm spin qubit wafersSamuel Neyens, Otto K Zietz, Thomas F Watson, et al.
Molecular Therapy. Methods & Clinical Development|June 17, 2025
Common AAV gene therapy vectors show nonselective transduction of <i>ex vivo</i> human brain tissueJ P McGinnis, Joshua Ortiz-Guzman, Maria Camila Guevara, et al.
Science (New York, N.Y.)|January 5, 2008
Mutations in the pericentrin (PCNT) gene cause primordial dwarfismAnita Rauch, Christian T Thiel, Detlev Schindler, et al.
Nature Communications|November 11, 2022
Dominant ARF3 variants disrupt Golgi integrity and cause a neurodevelopmental disorder recapitulated in zebrafishGiulia Fasano, Valentina Muto, Francesca Clementina Radio, et al.
American Journal of Medical Genetics. Part A|February 8, 2024
Personal journeys to and in human genetics and dysmorphologyCharles E Schwartz, Arthur S Aylsworth, Judith Allanson, et al.
American Journal of Human Genetics|August 13, 2019
De Novo Missense Variants in FBXW11 Cause Diverse Developmental Phenotypes Including Brain, Eye, and Digit AnomaliesRichard J Holt, Rodrigo M Young, Berta Crespo, et al.
Emerging Infectious Diseases|September 25, 2024
Virulence of Burkholderia pseudomallei ATS2021 Unintentionally Imported to United States in Aromatherapy SprayChristopher K Cote, Kevin D Mlynek, Christopher P Klimko, et al.
Pageof 65

Showing results (621-630 of 644) with videos related to

Sort By:
Pageof 65
American Journal of Medical Genetics. Part A|June 18, 2022
Exome sequencing identifies genetic variants in anophthalmia and microphthalmiaJingjing Li, Wei Yang, Yuejun Jessie Wang, et al.
Nature Communications|October 6, 2023
Injectable and biodegradable piezoelectric hydrogel for osteoarthritis treatmentTra Vinikoor, Godwin K Dzidotor, Thinh T Le, et al.
Brain : a Journal of Neurology|April 21, 2021
ATP1A2- and ATP1A3-associated early profound epileptic encephalopathy and polymicrogyriaAnnalisa Vetro, Hang N Nielsen, Rikke Holm, et al.
Nature|May 1, 2024
Probing single electrons across 300-mm spin qubit wafersSamuel Neyens, Otto K Zietz, Thomas F Watson, et al.
Molecular Therapy. Methods & Clinical Development|June 17, 2025
Common AAV gene therapy vectors show nonselective transduction of <i>ex vivo</i> human brain tissueJ P McGinnis, Joshua Ortiz-Guzman, Maria Camila Guevara, et al.
Science (New York, N.Y.)|January 5, 2008
Mutations in the pericentrin (PCNT) gene cause primordial dwarfismAnita Rauch, Christian T Thiel, Detlev Schindler, et al.
Nature Communications|November 11, 2022
Dominant ARF3 variants disrupt Golgi integrity and cause a neurodevelopmental disorder recapitulated in zebrafishGiulia Fasano, Valentina Muto, Francesca Clementina Radio, et al.
American Journal of Medical Genetics. Part A|February 8, 2024
Personal journeys to and in human genetics and dysmorphologyCharles E Schwartz, Arthur S Aylsworth, Judith Allanson, et al.
American Journal of Human Genetics|August 13, 2019
De Novo Missense Variants in FBXW11 Cause Diverse Developmental Phenotypes Including Brain, Eye, and Digit AnomaliesRichard J Holt, Rodrigo M Young, Berta Crespo, et al.
Emerging Infectious Diseases|September 25, 2024
Virulence of Burkholderia pseudomallei ATS2021 Unintentionally Imported to United States in Aromatherapy SprayChristopher K Cote, Kevin D Mlynek, Christopher P Klimko, et al.
Pageof 65