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

Atsuko Okazaki

Showing results (11-20 of 17) with videos related to

Pageof 2
Sort By:
You have reached the last page of results.This site can display upto 17 results.
Biomedical Materials (Bristol, England)|May 30, 2024
Microstripe pattern substrate consisting of alternating planar and nanoprotrusive regions improved hiPSC-derived cardiomyocytes' unidirectional alignment and functional propertiesHideo Saotome, Yukiko Yatsuka, Osamu Minowa, et al.
Neurology. Genetics|December 17, 2025
Identification of Intronic Variants in <i>NDUFA3</i> as a Cause of Leigh Syndrome by Whole Genome Sequencing and RNA SequencingKohta Nakamura, Yoshihito Kishita, Ayumu Sugiura, et al.
HGG Advances|June 10, 2026
Nanopore-based haplotype-resolved X-chromosome inactivation analysis for clinical severity assessment in X-linked disorders: an AIFM1 family study with proof-of-concept application to a mosaic PDHA1 carrierKohta Nakamura, Atsuko Okazaki, Daisuke Motooka, et al.
Nephron|May 11, 2021
Cyclosporine A Treatment of Proteinuria in a New Case of MAFB-Associated Glomerulopathy without Extrarenal Involvement: A Case ReportJun-Ya Kaimori, Tatsuhiko Mori, Tomoko Namba-Hamano, et al.
Journal of Atherosclerosis and Thrombosis|February 18, 2026
Simultaneous Assessment of Genetic and Epigenetic Contributions to the Plasma Lipid Levels with Respect to Cardiovascular RiskFumihiko Takeuchi, Masaya Yamamoto, Masahiro Nakatochi, et al.
Molecular Genetics and Metabolism Reports|September 5, 2022
Severe spinal cord hypoplasia due to a novel <i>ATAD3A</i> compound heterozygous deletionTomohiro Ebihara, Taro Nagatomo, Yohei Sugiyama, et al.
JCI Insight|September 29, 2022
A heterozygous LAMA5 variant may contribute to slowly progressive, vinculin-enhanced familial FSGS and pulmonary defectsJun-Ya Kaimori, Yamato Kikkawa, Daisuke Motooka, et al.
Pageof 2

Showing results (11-20 of 17) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 17 results.
Biomedical Materials (Bristol, England)|May 30, 2024
Microstripe pattern substrate consisting of alternating planar and nanoprotrusive regions improved hiPSC-derived cardiomyocytes' unidirectional alignment and functional propertiesHideo Saotome, Yukiko Yatsuka, Osamu Minowa, et al.
Neurology. Genetics|December 17, 2025
Identification of Intronic Variants in <i>NDUFA3</i> as a Cause of Leigh Syndrome by Whole Genome Sequencing and RNA SequencingKohta Nakamura, Yoshihito Kishita, Ayumu Sugiura, et al.
HGG Advances|June 10, 2026
Nanopore-based haplotype-resolved X-chromosome inactivation analysis for clinical severity assessment in X-linked disorders: an AIFM1 family study with proof-of-concept application to a mosaic PDHA1 carrierKohta Nakamura, Atsuko Okazaki, Daisuke Motooka, et al.
Nephron|May 11, 2021
Cyclosporine A Treatment of Proteinuria in a New Case of MAFB-Associated Glomerulopathy without Extrarenal Involvement: A Case ReportJun-Ya Kaimori, Tatsuhiko Mori, Tomoko Namba-Hamano, et al.
Journal of Atherosclerosis and Thrombosis|February 18, 2026
Simultaneous Assessment of Genetic and Epigenetic Contributions to the Plasma Lipid Levels with Respect to Cardiovascular RiskFumihiko Takeuchi, Masaya Yamamoto, Masahiro Nakatochi, et al.
Molecular Genetics and Metabolism Reports|September 5, 2022
Severe spinal cord hypoplasia due to a novel <i>ATAD3A</i> compound heterozygous deletionTomohiro Ebihara, Taro Nagatomo, Yohei Sugiyama, et al.
JCI Insight|September 29, 2022
A heterozygous LAMA5 variant may contribute to slowly progressive, vinculin-enhanced familial FSGS and pulmonary defectsJun-Ya Kaimori, Yamato Kikkawa, Daisuke Motooka, et al.
Pageof 2