Chromosomal translocations and palindromic AT-rich repeats

Por Kato, Takema, Kurahashi, Hiroki, Emanuel1, Beverly S.
Publicado em 2012

Cruciform extrusion propensity of human translocation-mediating palindromic AT-rich repeats

Por Kogo, Hiroshi, Inagaki, Hidehito, Ohye, Tamae, Kato, Takema, Emanuel, Beverly S., Kurahashi, Hiroki
Publicado em 2007

Palindrome-mediated chromosomal translocations in humans

Por Kurahashi, Hiroki, Inagaki, Hidehito, Ohye, Tamae, Kogo, Hiroshi, Kato, Takema, Emanuel, Beverly S.
Publicado em 2006

Palindrome-Mediated Translocations in Humans: A New Mechanistic Model for Gross Chromosomal Rearrangements

Por Inagaki, Hidehito, Kato, Takema, Tsutsumi, Makiko, Ouchi, Yuya, Ohye, Tamae, Kurahashi, Hiroki
Publicado no Front Genet (2016)

Molecular cloning of a translocation breakpoint hotspot in 22q11

Por Kurahashi, Hiroki, Inagaki, Hidehito, Hosoba, Eriko, Kato, Takema, Ohye, Tamae, Kogo, Hiroshi, Emanuel, Beverly S.
Publicado em 2007

Age has no effect on de novo constitutional t(11;22) translocation frequency in sperm

Por Kato, Takema, Yamada, Kouji, Inagaki, Hidehito, Kogo, Hiroshi, Ohye, Tamae, Emanuel, Beverly S., Kurahashi, Hiroki
Publicado em 2007

Comparative gene expression profiling of placentas from patients with severe pre-eclampsia and unexplained fetal growth restriction

Por Nishizawa, Haruki, Ota, Sayuri, Suzuki, Machiko, Kato, Takema, Sekiya, Takao, Kurahashi, Hiroki, Udagawa, Yasuhiro
Publicado em 2011

DNA secondary structure is influenced by genetic variation and alters susceptibility to de novo translocation

Por Kato, Takema, Inagaki, Hidehito, Tong, Maoqing, Kogo, Hiroshi, Ohye, Tamae, Yamada, Kouji, Tsutsumi, Makiko, Emanuel, Beverly S, Kurahashi, Hiroki
Publicado em 2011

Chromosomal instability mediated by non-B DNA: Cruciform conformation and not DNA sequence is responsible for recurrent translocation in humans

Por Inagaki, Hidehito, Ohye, Tamae, Kogo, Hiroshi, Kato, Takema, Bolor, Hasbaira, Taniguchi, Mariko, Shaikh, Tamim H., Emanuel, Beverly S., Kurahashi, Hiroki
Publicado em 2009

Impaired DNA replication prompts deletions within palindromic sequences, but does not induce translocations in human cells

Por Kurahashi, Hiroki, Inagaki, Hidehito, Kato, Takema, Hosoba, Eriko, Kogo, Hiroshi, Ohye, Tamae, Tsutsumi, Makiko, Bolor, Hasbaira, Tong, Maoqing, Emanuel, Beverly S.
Publicado em 2009

Genetic Variation Affects de Novo Translocation Frequency

Por Kato, Takema, Inagaki, Hidehito, Yamada, Kouji, Kogo, Hiroshi, Ohye, Tamae, Kowa, Hiroe, Nagaoka, Kayuri, Taniguchi, Mariko, Emanuel, Beverly S., Kurahashi, Hiroki
Publicado em 2006

Polymorphisms of the 22q11.2 breakpoint region influence the frequency of de novo constitutional t(11;22)s in sperm(†)

Por Tong, Maoqing, Kato, Takema, Yamada, Kouji, Inagaki, Hidehito, Kogo, Hiroshi, Ohye, Tamae, Tsutsumi, Makiko, Wang, Jieru, Emanuel, Beverly S., Kurahashi, Hiroki
Publicado em 2010

Age-Related Decrease of Meiotic Cohesins in Human Oocytes

Por Tsutsumi, Makiko, Fujiwara, Reiko, Nishizawa, Haruki, Ito, Mayuko, Kogo, Hiroshi, Inagaki, Hidehito, Ohye, Tamae, Kato, Takema, Fujii, Takuma, Kurahashi, Hiroki
Publicado em 2014

Whole Genomic Analysis of an Unusual Human G6P[14] Rotavirus Strain Isolated from a Child with Diarrhea in Thailand: Evidence for Bovine-To-Human Interspecies Transmission and Reas...

Por Tacharoenmuang, Ratana, Komoto, Satoshi, Guntapong, Ratigorn, Ide, Tomihiko, Haga, Kei, Katayama, Kazuhiko, Kato, Takema, Ouchi, Yuya, Kurahashi, Hiroki, Tsuji, Takao, Sangkitporn, Somchai, Taniguchi, Koki
Publicado no PLoS One (2015)

Emergence and Characterization of Unusual DS-1-Like G1P[8] Rotavirus Strains in Children with Diarrhea in Thailand

Por Komoto, Satoshi, Tacharoenmuang, Ratana, Guntapong, Ratigorn, Ide, Tomihiko, Haga, Kei, Katayama, Kazuhiko, Kato, Takema, Ouchi, Yuya, Kurahashi, Hiroki, Tsuji, Takao, Sangkitporn, Somchai, Taniguchi, Koki
Publicado no PLoS One (2015)

Identification of novel FATP4 mutations in a Japanese patient with ichthyosis prematurity syndrome

Por Tsuge, Ikuya, Morishita, Masashi, Kato, Takema, Tsutsumi, Makiko, Inagaki, Hidehito, Mori, Yuji, Yamawaki, Kazuo, Inuo, Chisato, Ieda, Kuniko, Ohye, Tamae, Hayakawa, Akinori, Kurahashi, Hiroki
Publicado no Hum Genome Var (2015)

Paternal origin of the de novo constitutional t(11;22)(q23;q11)

Por Ohye, Tamae, Inagaki, Hidehito, Kogo, Hiroshi, Tsutsumi, Makiko, Kato, Takema, Tong, Maoqing, Macville, Merryn V E, Medne, Livija, Zackai, Elaine H, Emanuel, Beverly S, Kurahashi, Hiroki
Publicado em 2010

Breakpoint analysis of the recurrent constitutional t(8;22)(q24.13;q11.21) translocation

Por Mishra, Divya, Kato, Takema, Inagaki, Hidehito, Kosho, Tomoki, Wakui, Keiko, Kido, Yasuhiro, Sakazume, Satoru, Taniguchi-Ikeda, Mariko, Morisada, Naoya, Iijima, Kazumoto, Fukushima, Yoshimitsu, Emanuel, Beverly S, Kurahashi, Hiroki
Publicado no Mol Cytogenet (2014)

Intragenic duplication in the PHKD1 gene in autosomal recessive polycystic kidney disease

Por Miyazaki, Jun, Ito, Mayuko, Nishizawa, Haruki, Kato, Takema, Minami, Yukito, Inagaki, Hidehito, Ohye, Tamae, Miyata, Masafumi, Boda, Hiroko, Kiriyama, Yuka, Kuroda, Makoto, Sekiya, Takao, Kurahashi, Hiroki, Fujii, Takuma
Publicado no BMC Med Genet (2015)

Analysis of the t(3;8) of Hereditary Renal Cell Carcinoma: A Palindrome-Mediated Translocation

Por Kato, Takema, Franconi, Colleen P., Sheridan, Molly B., Hacker, April M., Inagakai, Hidehito, Glover, Thomas W., Arlt, Martin F., Drabkin, Harry A., Gemmill, Robert M., Kurahashi, Hiroki, Emanuel, Beverly S.
Publicado em 2014