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Hidehito Inagaki

Showing results (61-70 of 98) with videos related to

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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.
JIMD Reports|November 7, 2022
Maple syrup urine disease due to a paracentric inversion of chr 19 that disrupts <i>BCKDHA</i>: A case reportKatsuyuki Yokoi, Yoko Nakajima, Yuta Sudo, et al.
American Journal of Medical Genetics. Part A|April 2, 2024
Truncating variants of the sterol recognition region of SHH cause hypertelorism phenotype rather than hypotelorism-holoprosencephalyMamiko Yamada, Seiji Mizuno, Mie Inaba, et al.
Science (New York, N.Y.)|February 18, 2006
Genetic variation affects de novo translocation frequencyTakema Kato, Hidehito Inagaki, Kouji Yamada, et al.
American Journal of Reproductive Immunology (New York, N.Y. : 1989)|March 3, 2010
Genetic variation in the indoleamine 2,3-dioxygenase gene in pre-eclampsiaHaruki Nishizawa, Takema Kato, Sayuri Ota, et al.
Journal of Human Genetics|March 27, 2010
Screening of genes involved in chromosome segregation during meiosis I: toward the identification of genes responsible for infertility in humansHiroshi Kogo, Hiroe Kowa-Sugiyama, Kouji Yamada, et al.
Human Molecular Genetics|June 13, 2009
Impaired DNA replication prompts deletions within palindromic sequences, but does not induce translocations in human cellsHiroki Kurahashi, Hidehito Inagaki, Takema 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.
Journal of Human Genetics|June 1, 2012
Screening of genes involved in chromosome segregation during meiosis I: in vitro gene transfer to mouse fetal oocytesMakiko Tsutsumi, Hiroe Kowa-Sugiyama, Hasbaira Bolor, et al.
Journal of Ovarian Research|January 22, 2026
Novel LHX8 variants associated with distinctive oocyte morphological abnormalities and maturation arrest in primary infertilityYusuke Sako, Hidehito Inagaki, Akira Yanagihara, et al.
Pageof 10

Showing results (61-70 of 98) with videos related to

Sort By:
Pageof 10
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.
JIMD Reports|November 7, 2022
Maple syrup urine disease due to a paracentric inversion of chr 19 that disrupts <i>BCKDHA</i>: A case reportKatsuyuki Yokoi, Yoko Nakajima, Yuta Sudo, et al.
American Journal of Medical Genetics. Part A|April 2, 2024
Truncating variants of the sterol recognition region of SHH cause hypertelorism phenotype rather than hypotelorism-holoprosencephalyMamiko Yamada, Seiji Mizuno, Mie Inaba, et al.
Science (New York, N.Y.)|February 18, 2006
Genetic variation affects de novo translocation frequencyTakema Kato, Hidehito Inagaki, Kouji Yamada, et al.
American Journal of Reproductive Immunology (New York, N.Y. : 1989)|March 3, 2010
Genetic variation in the indoleamine 2,3-dioxygenase gene in pre-eclampsiaHaruki Nishizawa, Takema Kato, Sayuri Ota, et al.
Journal of Human Genetics|March 27, 2010
Screening of genes involved in chromosome segregation during meiosis I: toward the identification of genes responsible for infertility in humansHiroshi Kogo, Hiroe Kowa-Sugiyama, Kouji Yamada, et al.
Human Molecular Genetics|June 13, 2009
Impaired DNA replication prompts deletions within palindromic sequences, but does not induce translocations in human cellsHiroki Kurahashi, Hidehito Inagaki, Takema 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.
Journal of Human Genetics|June 1, 2012
Screening of genes involved in chromosome segregation during meiosis I: in vitro gene transfer to mouse fetal oocytesMakiko Tsutsumi, Hiroe Kowa-Sugiyama, Hasbaira Bolor, et al.
Journal of Ovarian Research|January 22, 2026
Novel LHX8 variants associated with distinctive oocyte morphological abnormalities and maturation arrest in primary infertilityYusuke Sako, Hidehito Inagaki, Akira Yanagihara, et al.
Pageof 10