Incontinentia pigmenti inherited from a father with a low level atypical IKBKG deletion mosaicism: a case report

por Kawai, Miki, Sugimoto, Atsuya, Ishihara, Yasunori, Kato, Takema, Kurahashi, Hiroki
Publicado 2022

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 2007

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 2016

Molecular analysis of low‐level mosaicism of the IKBKG mutation using the X Chromosome Inactivation pattern in Incontinentia Pigmenti

por Kawai, Miki, Kato, Takema, Tsutsumi, Makiko, Shinkai, Yasuko, Inagaki, Hidehito, Kurahashi, Hiroki
Publicado 2020

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 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 2011

PCS/MVA syndrome caused by an Alu insertion in the BUB1B gene

por Kato, Maki, Kato, Takema, Hosoba, Eriko, Ohashi, Masanao, Fujisaki, Midori, Ozaki, Mamoru, Yamaguchi, Masatoshi, Sameshima, Hiroshi, Kurahashi, Hiroki
Publicado 2017

Genotype-phenotype correlation of renal lesions in the tuberous sclerosis complex

por Muto, Yoshinari, Sasaki, Hitomi, Sumitomo, Makoto, Inagaki, Hidehito, Kato, Maki, Kato, Takema, Miyai, Shunsuke, Kurahashi, Hiroki, Shiroki, Ryoichi
Publicado 2022

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 2014

Longitudinal study of the vaginal microbiome in pregnancies involving preterm labor

por Sakabe, Yoshiko, Nishizawa, Haruki, Kato, Asuka, Noda, Yoshiteru, Ohwaki, Akiko, Yoshizawa, Hikari, Kato, Takema, Sekiya, Takao, Fujii, Takuma, Kurahashi, Hiroki
Publicado 2022

Exome-First Approach in Fetal Akinesia Reveals Chromosome 1p36 Deletion Syndrome

por Toshimitsu, Masatake, Nagaoka, Shinichi, Kobori, Shuusaku, Ogawa, Maki, Suzuki, Fumihiko, Kato, Takema, Miyai, Shunsuke, Kawamura, Rie, Inagaki, Hidehito, Kurahashi, Hiroki, Murotsuki, Jun
Publicado 2019

An aggressive systemic mastocytosis preceded by ovarian dysgerminoma

por Tsutsumi, Makiko, Miura, Hiroki, Inagaki, Hidehito, Shinkai, Yasuko, Kato, Asuka, Kato, Takema, Hamada-Tsutsumi, Susumu, Tanaka, Makito, Kudo, Kazuko, Yoshikawa, Tetsushi, Kurahashi, Hiroki
Publicado 2020

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 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 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 2015

Remote intracranial recurrence of IDH mutant gliomas is associated with TP53 mutations and an 8q gain

por Nakae, Shunsuke, Kato, Takema, Murayama, Kazuhiro, Sasaki, Hikaru, Abe, Masato, Kumon, Masanobu, Kumai, Tadashi, Yamashiro, Kei, Inamasu, Joji, Hasegawa, Mitsuhiro, Kurahashi, Hiroki, Hirose, Yuichi
Publicado 2017

Placental Genetic Variants in the Upstream Region of the FLT1 Gene in Pre-eclampsia

por Ohwaki, Akiko, Nishizawa, Haruki, Kato, Asuka, Kato, Takema, Miyazaki, Jun, Yoshizawa, Hikari, Noda, Yoshiteru, Sakabe, Yoshiko, Ichikawa, Ryoko, Sekiya, Takao, Fujii, Takuma, Kurahashi, Hiroki
Publicado 2020

Unexpected Mutations by CRISPR-Cas9 CTG Repeat Excision in Myotonic Dystrophy and Use of CRISPR Interference as an Alternative Approach

por Ikeda, Miki, Taniguchi-Ikeda, Mariko, Kato, Takema, Shinkai, Yasuko, Tanaka, Sonoko, Hagiwara, Hiroki, Sasaki, Naomichi, Masaki, Toshihiro, Matsumura, Kiichiro, Sonoo, Masahiro, Kurahashi, Hiroki, Saito, Fumiaki
Publicado 2020

Potential role for nectin-4 in the pathogenesis of pre-eclampsia: a molecular genetic study

por Ito, Mayuko, Nishizawa, Haruki, Tsutsumi, Makiko, Kato, Asuka, Sakabe, Yoshiko, Noda, Yoshiteru, Ohwaki, Akiko, Miyazaki, Jun, Kato, Takema, Shiogama, Kazuya, Sekiya, Takao, Kurahashi, Hiroki, Fujii, Takuma
Publicado 2018

Impact of DPYD, DPYS, and UPB1 gene variations on severe drug‐related toxicity in patients with cancer

por Yokoi, Katsuyuki, Nakajima, Yoko, Matsuoka, Hiroshi, Shinkai, Yasuko, Ishihara, Takuma, Maeda, Yasuhiro, Kato, Takema, Katsuno, Hidetoshi, Masumori, Koji, Kawada, Kenji, Yoshikawa, Tetsushi, Ito, Tetsuya, Kurahashi, Hiroki
Publicado 2020