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

Takema Kato

Showing results (31-40 of 75) with videos related to

Pageof 8
Sort By:
Brain & Development|November 3, 2018
A case of dihydropyrimidinase deficiency incidentally detected by urine metabolome analysisHiroki Tsuchiya, Tomoyuki Akiyama, Tomiko Kuhara, et al.
The Tohoku Journal of Experimental Medicine|January 27, 2022
Identification of a Novel Mutation in Carboxyl Ester Lipase Gene in a Patient with MODY-like DiabetesTomomi Kondoh, Yoko Nakajima, Katsuyuki Yokoi, et al.
Fujita Medical Journal|August 11, 2022
Longitudinal study of the vaginal microbiome in pregnancies involving preterm laborYoshiko Sakabe, Haruki Nishizawa, Asuka Kato, et al.
Journal of Human Genetics|February 24, 2019
Obstetric complication-associated ANXA5 promoter polymorphisms may affect gene expression via DNA secondary structuresHidehito Inagaki, Sayuri Ota, Haruki Nishizawa, et al.
Plos One|May 9, 2014
Age-related decrease of meiotic cohesins in human oocytesMakiko Tsutsumi, Reiko Fujiwara, Haruki Nishizawa, et al.
Congenital Anomalies|June 25, 2022
A case of 46,XY disorders of sex development with congenital heart disease caused by a GATA4 variantYui Shichiri, Yoshimi Kato, Hidehito Inagaki, et al.
Journal of Human Genetics|January 14, 2022
Target enrichment long-read sequencing with adaptive sampling can determine the structure of the small supernumerary marker chromosomesTasuku Mariya, Takema Kato, Takeshi Sugimoto, et al.
Genome Research|November 11, 2008
Chromosomal instability mediated by non-B DNA: cruciform conformation and not DNA sequence is responsible for recurrent translocation in humansHidehito Inagaki, Tamae Ohye, Hiroshi Kogo, et al.
Congenital Anomalies|June 22, 2018
Potentially effective method for fetal gender determination by noninvasive prenatal testing for X-linked diseaseYoshiteru Noda, Takema Kato, Asuka Kato, et al.
Human Molecular Genetics|April 16, 2010
Polymorphisms of the 22q11.2 breakpoint region influence the frequency of de novo constitutional t(11;22)s in spermMaoqing Tong, Takema Kato, Kouji Yamada, et al.
Pageof 8

Showing results (31-40 of 75) with videos related to

Sort By:
Pageof 8
Brain & Development|November 3, 2018
A case of dihydropyrimidinase deficiency incidentally detected by urine metabolome analysisHiroki Tsuchiya, Tomoyuki Akiyama, Tomiko Kuhara, et al.
The Tohoku Journal of Experimental Medicine|January 27, 2022
Identification of a Novel Mutation in Carboxyl Ester Lipase Gene in a Patient with MODY-like DiabetesTomomi Kondoh, Yoko Nakajima, Katsuyuki Yokoi, et al.
Fujita Medical Journal|August 11, 2022
Longitudinal study of the vaginal microbiome in pregnancies involving preterm laborYoshiko Sakabe, Haruki Nishizawa, Asuka Kato, et al.
Journal of Human Genetics|February 24, 2019
Obstetric complication-associated ANXA5 promoter polymorphisms may affect gene expression via DNA secondary structuresHidehito Inagaki, Sayuri Ota, Haruki Nishizawa, et al.
Plos One|May 9, 2014
Age-related decrease of meiotic cohesins in human oocytesMakiko Tsutsumi, Reiko Fujiwara, Haruki Nishizawa, et al.
Congenital Anomalies|June 25, 2022
A case of 46,XY disorders of sex development with congenital heart disease caused by a GATA4 variantYui Shichiri, Yoshimi Kato, Hidehito Inagaki, et al.
Journal of Human Genetics|January 14, 2022
Target enrichment long-read sequencing with adaptive sampling can determine the structure of the small supernumerary marker chromosomesTasuku Mariya, Takema Kato, Takeshi Sugimoto, et al.
Genome Research|November 11, 2008
Chromosomal instability mediated by non-B DNA: cruciform conformation and not DNA sequence is responsible for recurrent translocation in humansHidehito Inagaki, Tamae Ohye, Hiroshi Kogo, et al.
Congenital Anomalies|June 22, 2018
Potentially effective method for fetal gender determination by noninvasive prenatal testing for X-linked diseaseYoshiteru Noda, Takema Kato, Asuka Kato, et al.
Human Molecular Genetics|April 16, 2010
Polymorphisms of the 22q11.2 breakpoint region influence the frequency of de novo constitutional t(11;22)s in spermMaoqing Tong, Takema Kato, Kouji Yamada, et al.
Pageof 8