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

Takeshi Mizuguchi

Showing results (11-20 of 185) with videos related to

Pageof 19
Sort By:
Proceedings of the National Academy of Sciences of the United States of America|November 2, 2011
A homolog of male sex-determining factor SRY cooperates with a transposon-derived CENP-B protein to control sex-specific directed recombinationEmiko Matsuda, Rie Sugioka-Sugiyama, Takeshi Mizuguchi, et al.
Frontiers in Neurology|February 26, 2024
Case report: Neuronal intranuclear inclusion disease initially mimicking reversible cerebral vasoconstriction syndrome: serial neuroimaging findings during an 11-year follow-upGha-Hyun Lee, Eugene Jung, Na-Yeon Jung, et al.
Molecular Cell|January 8, 2011
Asf1/HIRA facilitate global histone deacetylation and associate with HP1 to promote nucleosome occupancy at heterochromatic lociKenichi Yamane, Takeshi Mizuguchi, Bowen Cui, et al.
Brain & Development|November 27, 2020
Clinical variations of epileptic syndrome associated with PACS2 variantTomoko Mizuno, Rie Miyata, Akira Hojo, et al.
American Journal of Medical Genetics. Part A|July 13, 2006
Mild craniosynostosis with 1p36.3 trisomy and 1p36.3 deletion syndrome caused by familial translocation t(Y;1)Yoko Hiraki, Hiroko Fujita, Shunji Yamamori, et al.
European Journal of Medical Genetics|September 21, 2025
Late-onset Vitamin B6-dependent epilepsy caused by compound heterozygous pathogenic PLPBP variantsSadao Nakamura, Yasutsugu Chinen, Hirotaka Minema, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 12, 2017
Shelterin components mediate genome reorganization in response to replication stressTakeshi Mizuguchi, Nitika Taneja, Emiko Matsuda, et al.
American Journal of Medical Genetics. Part A|January 19, 2006
Narrowing candidate region for monosomy 9p syndrome to a 4.7-Mb segment at 9p22.2-p23Hiroki Kawara, Toshiyuki Yamamoto, Naoki Harada, et al.
Journal of Human Genetics|May 22, 2019
A novel de novo frameshift variant in SETD1B causes epilepsyKouhei Den, Mitsuhiro Kato, Tokito Yamaguchi, et al.
Brain & Development|March 25, 2023
A case of epilepsy with myoclonic atonic seizures caused by SLC6A1 gene mutation due to balanced chromosomal translocationTatsuo Mori, Masamune Sakamoto, Takahiro Tayama, et al.
Pageof 19

Showing results (11-20 of 185) with videos related to

Sort By:
Pageof 19
Proceedings of the National Academy of Sciences of the United States of America|November 2, 2011
A homolog of male sex-determining factor SRY cooperates with a transposon-derived CENP-B protein to control sex-specific directed recombinationEmiko Matsuda, Rie Sugioka-Sugiyama, Takeshi Mizuguchi, et al.
Frontiers in Neurology|February 26, 2024
Case report: Neuronal intranuclear inclusion disease initially mimicking reversible cerebral vasoconstriction syndrome: serial neuroimaging findings during an 11-year follow-upGha-Hyun Lee, Eugene Jung, Na-Yeon Jung, et al.
Molecular Cell|January 8, 2011
Asf1/HIRA facilitate global histone deacetylation and associate with HP1 to promote nucleosome occupancy at heterochromatic lociKenichi Yamane, Takeshi Mizuguchi, Bowen Cui, et al.
Brain & Development|November 27, 2020
Clinical variations of epileptic syndrome associated with PACS2 variantTomoko Mizuno, Rie Miyata, Akira Hojo, et al.
American Journal of Medical Genetics. Part A|July 13, 2006
Mild craniosynostosis with 1p36.3 trisomy and 1p36.3 deletion syndrome caused by familial translocation t(Y;1)Yoko Hiraki, Hiroko Fujita, Shunji Yamamori, et al.
European Journal of Medical Genetics|September 21, 2025
Late-onset Vitamin B6-dependent epilepsy caused by compound heterozygous pathogenic PLPBP variantsSadao Nakamura, Yasutsugu Chinen, Hirotaka Minema, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 12, 2017
Shelterin components mediate genome reorganization in response to replication stressTakeshi Mizuguchi, Nitika Taneja, Emiko Matsuda, et al.
American Journal of Medical Genetics. Part A|January 19, 2006
Narrowing candidate region for monosomy 9p syndrome to a 4.7-Mb segment at 9p22.2-p23Hiroki Kawara, Toshiyuki Yamamoto, Naoki Harada, et al.
Journal of Human Genetics|May 22, 2019
A novel de novo frameshift variant in SETD1B causes epilepsyKouhei Den, Mitsuhiro Kato, Tokito Yamaguchi, et al.
Brain & Development|March 25, 2023
A case of epilepsy with myoclonic atonic seizures caused by SLC6A1 gene mutation due to balanced chromosomal translocationTatsuo Mori, Masamune Sakamoto, Takahiro Tayama, et al.
Pageof 19