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Brain & Development
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November 6, 2018
A case of early onset life-threatening epilepsy associated with a novel ATP1A3 gene variant
Naoko Ishihara, Hidehito Inagaki, Misa Miyake, et al.
International Journal of Molecular Sciences
|
April 3, 2021
An Analysis of Differentially Expressed Coding and Long Non-Coding RNAs in Multiple Models of Skeletal Muscle Atrophy
Keisuke Hitachi, Masashi Nakatani, Yuri Kiyofuji, et al.
DNA Repair
|
July 11, 2006
Palindrome-mediated chromosomal translocations in humans
Hiroki Kurahashi, Hidehito Inagaki, Tamae Ohye, et al.
Nucleic Acids Research
|
February 1, 2007
Cruciform extrusion propensity of human translocation-mediating palindromic AT-rich repeats
Hiroshi Kogo, Hidehito Inagaki, Tamae Ohye, et al.
Biology of Reproduction
|
April 1, 2011
Characterization of a novel mouse gene encoding an SYCP3-like protein that relocalizes from the XY body to the nucleolus during prophase of male meiosis I
Makiko Tsutsumi, Hiroshi Kogo, Hiroe Kowa-Sugiyama, et al.
Cell Cycle (Georgetown, Tex.)
|
June 9, 2006
Chromosomal translocations mediated by palindromic DNA
Hiroki Kurahashi, Hidehito Inagaki, Tamae Ohye, et al.
Journal of Human Genetics
|
April 18, 2009
Recent advance in our understanding of the molecular nature of chromosomal abnormalities
Hiroki Kurahashi, Hasbaira Bolor, Takema Kato, et al.
Journal of Virological Methods
|
November 10, 2015
A simple cytogenetic method to detect chromosomally integrated human herpesvirus-6
Tamae Ohye, Yoshiki Kawamura, Hidehito Inagaki, et al.
Biochemical and Biophysical Research Communications
|
November 14, 2013
Identification of an enhancer region for immune activation in the human GTP cyclohydrolase I gene
Yu Liang, Hidehito Inagaki, Qinyu Hao, et al.
European Journal of Medical Genetics
|
November 11, 2018
FOXA2 gene mutation in a patient with congenital complex pituitary hormone deficiency
Hiroko Boda, Masafumi Miyata, Hidehito Inagaki, et al.
Page
of 10
Search research articles
Search
Showing results (21-30 of 98) with videos related to
Sort By:
Page
of 10
Brain & Development
|
November 6, 2018
A case of early onset life-threatening epilepsy associated with a novel ATP1A3 gene variant
Naoko Ishihara, Hidehito Inagaki, Misa Miyake, et al.
International Journal of Molecular Sciences
|
April 3, 2021
An Analysis of Differentially Expressed Coding and Long Non-Coding RNAs in Multiple Models of Skeletal Muscle Atrophy
Keisuke Hitachi, Masashi Nakatani, Yuri Kiyofuji, et al.
DNA Repair
|
July 11, 2006
Palindrome-mediated chromosomal translocations in humans
Hiroki Kurahashi, Hidehito Inagaki, Tamae Ohye, et al.
Nucleic Acids Research
|
February 1, 2007
Cruciform extrusion propensity of human translocation-mediating palindromic AT-rich repeats
Hiroshi Kogo, Hidehito Inagaki, Tamae Ohye, et al.
Biology of Reproduction
|
April 1, 2011
Characterization of a novel mouse gene encoding an SYCP3-like protein that relocalizes from the XY body to the nucleolus during prophase of male meiosis I
Makiko Tsutsumi, Hiroshi Kogo, Hiroe Kowa-Sugiyama, et al.
Cell Cycle (Georgetown, Tex.)
|
June 9, 2006
Chromosomal translocations mediated by palindromic DNA
Hiroki Kurahashi, Hidehito Inagaki, Tamae Ohye, et al.
Journal of Human Genetics
|
April 18, 2009
Recent advance in our understanding of the molecular nature of chromosomal abnormalities
Hiroki Kurahashi, Hasbaira Bolor, Takema Kato, et al.
Journal of Virological Methods
|
November 10, 2015
A simple cytogenetic method to detect chromosomally integrated human herpesvirus-6
Tamae Ohye, Yoshiki Kawamura, Hidehito Inagaki, et al.
Biochemical and Biophysical Research Communications
|
November 14, 2013
Identification of an enhancer region for immune activation in the human GTP cyclohydrolase I gene
Yu Liang, Hidehito Inagaki, Qinyu Hao, et al.
European Journal of Medical Genetics
|
November 11, 2018
FOXA2 gene mutation in a patient with congenital complex pituitary hormone deficiency
Hiroko Boda, Masafumi Miyata, Hidehito Inagaki, et al.
Page
of 10