Lists of HumanMethylation450 BeadChip probes with nucleotide-variant information obtained from the Phase 3 data of the 1000 Genomes Project

por Okamura, Kohji, Kawai, Tomoko, Hata, Kenichiro, Nakabayashi, Kazuhiko
Publicado 2015

Human resource development contributes to the creation of outstanding regenerative medicine products

por Nishigaki, Fusako, Ezoe, Sachikon, Kitajima, Hideki, Hata, Kenichiro
Publicado 2017

Whole-exome sequencing of fibroblast and its iPS cell lines derived from a patient diagnosed with xeroderma pigmentosum

por Okamura, Kohji, Toyoda, Masashi, Hata, Kenichiro, Nakabayashi, Kazuhiko, Umezawa, Akihiro
Publicado 2015

Genome-wide single nucleotide polymorphism array analysis unveils the origin of heterozygous androgenetic complete moles

por Usui, Hirokazu, Nakabayashi, Kazuhiko, Maehara, Kayoko, Hata, Kenichiro, Shozu, Makio
Publicado 2019

A novel TP63 variant in a patient with ankyloblepharon-ectodermal defect–cleft lip/palate syndrome and Rapp–Hodgkin syndrome-like ectodermal dysplasia

por Hori, Asuka, Migita, Ohsuke, Isogawa, Nobutaka, Takada, Fumio, Hata, Kenichiro
Publicado 2022

A capture methyl-seq protocol with improved efficiency and cost-effectiveness using pre-pooling and enzymatic conversion

por Hasegawa, Keita, Nakabayashi, Kazuhiko, Ishiwata, Keisuke, Kasuga, Yoshifumi, Hata, Kenichiro, Tanaka, Mamoru
Publicado 2023

Gestational arsenic exposure induces site-specific DNA hypomethylation in active retrotransposon subfamilies in offspring sperm in mice

por Nohara, Keiko, Nakabayashi, Kazuhiko, Okamura, Kazuyuki, Suzuki, Takehiro, Suzuki, Shigekatsu, Hata, Kenichiro
Publicado 2020

DNA Methyltransferase Inhibitor Zebularine Inhibits Human Hepatic Carcinoma Cells Proliferation and Induces Apoptosis

por Nakamura, Kazuaki, Aizawa, Kazuko, Nakabayashi, Kazuhiko, Kato, Natsuko, Yamauchi, Junji, Hata, Kenichiro, Tanoue, Akito
Publicado 2013

An Insulator Element Located at the Cyclin B1 Interacting Protein 1 Gene Locus Is Highly Conserved among Mammalian Species

por Yoshida, Wataru, Tomikawa, Junko, Inaki, Makoto, Kimura, Hiroshi, Onodera, Masafumi, Hata, Kenichiro, Nakabayashi, Kazuhiko
Publicado 2015

Exploration of hydroxymethylation in Kagami-Ogata syndrome caused by hypermethylation of imprinting control regions

por Matsubara, Keiko, Kagami, Masayo, Nakabayashi, Kazuhiko, Hata, Kenichiro, Fukami, Maki, Ogata, Tsutomu, Yamazawa, Kazuki
Publicado 2015

DNA methylation changes involved in the tumor increase in F2 males born to gestationally arsenite‐exposed F1 male mice

por Okamura, Kazuyuki, Nakabayashi, Kazuhiko, Kawai, Tomoko, Suzuki, Takehiro, Sano, Tomoharu, Hata, Kenichiro, Nohara, Keiko
Publicado 2019

A novel TAB2 mutation detected in a putative case of frontometaphyseal dysplasia

por Hori, Asuka, Migita, Ohsuke, Kawaguchi-Kawata, Rika, Narumi-Kishimoto, Yoko, Takada, Fumio, Hata, Kenichiro
Publicado 2021

Variable maternal methylation overlapping the nc886/vtRNA2-1 locus is locked between hypermethylated repeats and is frequently altered in cancer

por Romanelli, Valeria, Nakabayashi, Kazuhiko, Vizoso, Miguel, Moran, Sebastián, Iglesias-Platas, Isabel, Sugahara, Naoko, Sugahara, Naoko, Simón, Carlos, Simón, Carlos, Hata, Kenichiro, Hata, Kenichiro, Esteller, Manel, Esteller, Manel, Court, Franck, Court, Franck, Monk, David, Monk, David
Publicado 2014

Genome-wide association study of preterm birth and gestational age in a Japanese population

por Hasegawa, Keita, Kumasaka, Natsuhiko, Nakabayashi, Kazuhiko, Kamura, Hiromi, Maehara, Kayoko, Kasuga, Yoshifumi, Hata, Kenichiro, Tanaka, Mamoru
Publicado 2023

Gene expression signatures associated with chronic endometritis revealed by RNA sequencing

por Oshina, Kyoko, Kuroda, Keiji, Nakabayashi, Kazuhiko, Tomikawa, Junko, Kitade, Mari, Sugiyama, Rikikazu, Hata, Kenichiro, Itakura, Atsuo
Publicado 2023

The role of maternal-specific H3K9me3 modification in establishing imprinted X-chromosome inactivation and embryogenesis in mice

por Fukuda, Atsushi, Tomikawa, Junko, Miura, Takumi, Hata, Kenichiro, Nakabayashi, Kazuhiko, Eggan, Kevin, Akutsu, Hidenori, Umezawa, Akihiro
Publicado 2014

Genitopatellar syndrome: the first reported case in Japan

por Okano, Satomi, Miyamoto, Akie, Fukuda, Ikue, Tanaka, Hajime, Hata, Kenichiro, Kaname, Tadashi, Matsubara, Yoichi, Makita, Yoshio
Publicado 2018

Epitranscriptomic profiling in human placenta: N6‐methyladenosine modification at the 5′‐untranslated region is related to fetal growth and preeclampsia

por Taniguchi, Kosuke, Kawai, Tomoko, Kitawaki, Jo, Tomikawa, Junko, Nakabayashi, Kazuhiko, Okamura, Kohji, Sago, Haruhiko, Hata, Kenichiro
Publicado 2019

Confined placental mosaicism of trisomy 6 detected through genome‐wide NIPT was associated with placental abruption

por Nishiyama, Miyuki, Wada, Seiji, Hasegawa, Fuyuki, Uehara, Yohji, Ozaki, Mamoru, Hata, Kenichiro, Ito, Yushi, Sago, Haruhiko
Publicado 2021

A novel FLNA variant in a fetus with skeletal dysplasia

por Oshina, Kyoko, Kamei, Yoshimasa, Hori, Asuka, Hasegawa, Fuyuki, Taniguchi, Kosuke, Migita, Ohsuke, Itakura, Atsuo, Hata, Kenichiro
Publicado 2022