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Tamae Ohye

Showing results (41-50 of 53) with videos related to

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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.
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.
The Journal of Biological Chemistry|March 19, 2021
Tyrosine hydroxylase conditional KO mice reveal peripheral tissue-dependent differences in dopamine biosynthetic pathwaysKatsuya Miyajima, Chiaki Kawamoto, Satoshi Hara, et al.
Surgery Today|January 23, 2014
Pheochromocytoma as the first manifestation of MEN2A with RET mutation S891A: report of a caseYatsuka Hibi, Tamae Ohye, Kimio Ogawa, et al.
Scientific Reports|September 5, 2013
Definition and refinement of the 7q36.3 duplication region associated with schizophreniaBranko Aleksic, Itaru Kushima, Tamae Ohye, et al.
Human Genome Variation|April 16, 2016
Identification of novel FATP4 mutations in a Japanese patient with ichthyosis prematurity syndromeIkuya Tsuge, Masashi Morishita, Takema Kato, et al.
Scientific Reports|April 3, 2014
Dual roles for the telomeric repeats in chromosomally integrated human herpesvirus-6Tamae Ohye, Hidehito Inagaki, Masaru Ihira, et al.
European Journal of Human Genetics : EJHG|February 25, 2010
Paternal origin of the de novo constitutional t(11;22)(q23;q11)Tamae Ohye, Hidehito Inagaki, Hiroshi Kogo, et al.
Transplant Infectious Disease : an Official Journal of the Transplantation Society|May 20, 2020
Inherited chromosomally integrated human herpesvirus-6 in a patient with XIAP deficiencyKento Inoue, Hiroki Miura, Akihiro Hoshino, et al.
Pageof 6

Showing results (41-50 of 53) with videos related to

Sort By:
Pageof 6
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.
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.
The Journal of Biological Chemistry|March 19, 2021
Tyrosine hydroxylase conditional KO mice reveal peripheral tissue-dependent differences in dopamine biosynthetic pathwaysKatsuya Miyajima, Chiaki Kawamoto, Satoshi Hara, et al.
Surgery Today|January 23, 2014
Pheochromocytoma as the first manifestation of MEN2A with RET mutation S891A: report of a caseYatsuka Hibi, Tamae Ohye, Kimio Ogawa, et al.
Scientific Reports|September 5, 2013
Definition and refinement of the 7q36.3 duplication region associated with schizophreniaBranko Aleksic, Itaru Kushima, Tamae Ohye, et al.
Human Genome Variation|April 16, 2016
Identification of novel FATP4 mutations in a Japanese patient with ichthyosis prematurity syndromeIkuya Tsuge, Masashi Morishita, Takema Kato, et al.
Scientific Reports|April 3, 2014
Dual roles for the telomeric repeats in chromosomally integrated human herpesvirus-6Tamae Ohye, Hidehito Inagaki, Masaru Ihira, et al.
European Journal of Human Genetics : EJHG|February 25, 2010
Paternal origin of the de novo constitutional t(11;22)(q23;q11)Tamae Ohye, Hidehito Inagaki, Hiroshi Kogo, et al.
Transplant Infectious Disease : an Official Journal of the Transplantation Society|May 20, 2020
Inherited chromosomally integrated human herpesvirus-6 in a patient with XIAP deficiencyKento Inoue, Hiroki Miura, Akihiro Hoshino, et al.
Pageof 6