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Molecular Cytogenetics
|
September 9, 2011
DNA secondary structure is influenced by genetic variation and alters susceptibility to de novo translocation
Takema Kato, Hidehito Inagaki, Maoqing Tong, et al.
Transplant Infectious Disease : an Official Journal of the Transplantation Society
|
November 19, 2016
Transmission of chromosomally integrated human herpesvirus 6 via cord blood transplantation
Yuji Yamada, Tomoo Osumi, Ken-Ichi Imadome, 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 chromosomes
Tasuku 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 humans
Hidehito Inagaki, Tamae Ohye, Hiroshi Kogo, et al.
The Journal of Infectious Diseases
|
September 28, 2020
Inherited Chromosomally Integrated Human Herpesvirus 6 Is a Risk Factor for Spontaneous Abortion
Hiroki Miura, Yoshiki Kawamura, Tamae Ohye, et al.
Plos One
|
May 9, 2014
Age-related decrease of meiotic cohesins in human oocytes
Makiko Tsutsumi, Reiko Fujiwara, Haruki Nishizawa, et al.
JIMD Reports
|
May 13, 2018
Disruption of the Responsible Gene in a Phosphoglucomutase 1 Deficiency Patient by Homozygous Chromosomal Inversion
Katsuyuki Yokoi, Yoko Nakajima, Tamae Ohye, et al.
Science (New York, N.Y.)
|
February 18, 2006
Genetic variation affects de novo translocation frequency
Takema Kato, Hidehito Inagaki, Kouji Yamada, et al.
F1000Research
|
August 2, 2022
Andrographolide, isolated from <i>Andrographis paniculata</i><i>,</i> induces apoptosis in monocytic leukemia and multiple myeloma cells via augmentation of reactive oxygen species production
Hiroki Doi, Taei Matsui, Johannes M Dijkstra, 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 sperm
Maoqing Tong, Takema Kato, Kouji Yamada, et al.
Page
of 6
Search research articles
Search
Showing results (31-40 of 53) with videos related to
Sort By:
Page
of 6
Molecular Cytogenetics
|
September 9, 2011
DNA secondary structure is influenced by genetic variation and alters susceptibility to de novo translocation
Takema Kato, Hidehito Inagaki, Maoqing Tong, et al.
Transplant Infectious Disease : an Official Journal of the Transplantation Society
|
November 19, 2016
Transmission of chromosomally integrated human herpesvirus 6 via cord blood transplantation
Yuji Yamada, Tomoo Osumi, Ken-Ichi Imadome, 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 chromosomes
Tasuku 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 humans
Hidehito Inagaki, Tamae Ohye, Hiroshi Kogo, et al.
The Journal of Infectious Diseases
|
September 28, 2020
Inherited Chromosomally Integrated Human Herpesvirus 6 Is a Risk Factor for Spontaneous Abortion
Hiroki Miura, Yoshiki Kawamura, Tamae Ohye, et al.
Plos One
|
May 9, 2014
Age-related decrease of meiotic cohesins in human oocytes
Makiko Tsutsumi, Reiko Fujiwara, Haruki Nishizawa, et al.
JIMD Reports
|
May 13, 2018
Disruption of the Responsible Gene in a Phosphoglucomutase 1 Deficiency Patient by Homozygous Chromosomal Inversion
Katsuyuki Yokoi, Yoko Nakajima, Tamae Ohye, et al.
Science (New York, N.Y.)
|
February 18, 2006
Genetic variation affects de novo translocation frequency
Takema Kato, Hidehito Inagaki, Kouji Yamada, et al.
F1000Research
|
August 2, 2022
Andrographolide, isolated from <i>Andrographis paniculata</i><i>,</i> induces apoptosis in monocytic leukemia and multiple myeloma cells via augmentation of reactive oxygen species production
Hiroki Doi, Taei Matsui, Johannes M Dijkstra, 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 sperm
Maoqing Tong, Takema Kato, Kouji Yamada, et al.
Page
of 6