Abnormal fetal movements, micrognathia and pulmonary hypoplasia: a case report. Abnormal fetal movements

por Morokuma, Seiichi, Anami, Ai, Tsukimori, Kiyomi, Fukushima, Kotaro, Wake, Norio
Publicado 2010

The Maternally Expressed Gene Tssc3 Regulates the Expression of MASH2 Transcription Factor in Mouse Trophoblast Stem Cells through the AKT-Sp1 Signaling Pathway

por Takao, Tomoka, Asanoma, Kazuo, Tsunematsu, Ryosuke, Kato, Kiyoko, Wake, Norio
Publicado 2012

Evaluation of Haplotype Inference Using Definitive Haplotype Data Obtained from Complete Hydatidiform Moles, and Its Significance for the Analyses of Positively Selected Regions

por Higasa, Koichiro, Kukita, Yoji, Kato, Kiyoko, Wake, Norio, Tahira, Tomoko, Hayashi, Kenshi
Publicado 2009

Oxidative Stress Produced by Xanthine Oxidase Induces Apoptosis in Human Extravillous Trophoblast Cells

por MURATA, Masaharu, FUKUSHIMA, Kotaro, TAKAO, Tomoka, SEKI, Hiroyuki, TAKEDA, Satoru, WAKE, Norio
Publicado 2012

Association of MDM2 SNP309 and TP53 Arg72Pro polymorphisms with risk of endometrial cancer

por YONEDA, TOMOKO, KUBOYAMA, AYUMI, KATO, KIYOKO, OHGAMI, TATSUHIRO, OKAMOTO, KANAKO, SAITO, TOSHIAKI, WAKE, NORIO
Publicado 2013

A definitive haplotype map of structural variations determined by microarray analysis of duplicated haploid genomes

por Tahira, Tomoko, Yahara, Koji, Kukita, Yoji, Higasa, Koichiro, Kato, Kiyoko, Wake, Norio, Hayashi, Kenshi
Publicado 2014

Successful Management of Pregnancy Complicated by Klippel-Trenaunay Syndrome Using MR Angiography-Based Evaluation

por Tanaka, Reiko, Fujita, Yasuyuki, Ishibashi Hiasa, Kana, Yumoto, Yasuo, Hidaka, Nobuhiro, Fukushima, Kotaro, Wake, Norio
Publicado 2011

Prognosis and long-term neurodevelopmental outcome in conservatively treated twin-to-twin transfusion syndrome

por Li, Xiangqun, Morokuma, Seiichi, Fukushima, Kotaro, Otera, Yuka, Yumoto, Yasuo, Tsukimori, Kiyomi, Ochiai, Masayuki, Hara, Toshiro, Wake, Norio
Publicado 2011

ZAC, LIT1 (KCNQ1OT1) and p57(KIP2) (CDKN1C) are in an imprinted gene network that may play a role in Beckwith–Wiedemann syndrome

por Arima, Takahiro, Kamikihara, Tetsuya, Hayashida, Toshirou, Kato, Kiyoko, Inoue, Toshiaki, Shirayoshi, Yasuaki, Oshimura, Mitsuo, Soejima, Hidenobu, Mukai, Tunehiro, Wake, Norio
Publicado 2005

Long-Term Effects of Polychlorinated Biphenyls and Dioxins on Pregnancy Outcomes in Women Affected by the Yusho Incident

por Tsukimori, Kiyomi, Tokunaga, Shoji, Shibata, Satoko, Uchi, Hiroshi, Nakayama, Daisuke, Ishimaru, Tadayuki, Nakano, Hitoo, Wake, Norio, Yoshimura, Takesumi, Furue, Masutaka
Publicado 2008

Isolation and Characterization of Human Trophoblast Side-Population (SP) Cells in Primary Villous Cytotrophoblasts and HTR-8/SVneo Cell Line

por Takao, Tomoka, Asanoma, Kazuo, Kato, Kiyoko, Fukushima, Kotaro, Tsunematsu, Ryosuke, Hirakawa, Toshio, Matsumura, Sueo, Seki, Hiroyuki, Takeda, Satoru, Wake, Norio
Publicado 2011

SNP55, a new functional polymorphism of MDM2-P2 promoter, contributes to allele-specific expression of MDM2 in endometrial cancers

por Okamoto, Kanako, Tsunematsu, Ryosuke, Tahira, Tomoko, Sonoda, Kenzo, Asanoma, Kazuo, Yagi, Hiroshi, Yoneda, Tomoko, Hayashi, Kenshi, Wake, Norio, Kato, Kiyoko
Publicado 2015

Neurological outcomes in Chiari type II malformations and their correlation to morphological findings and fetal heart rate patterns: a retrospective study

por Otera, Yuka, Morokuma, Seiichi, Fukushima, Kotaro, Anami, Ai, Yumoto, Yasuo, Ito, Yushi, Ochiai, Masayuki, Hashiguchi, Kimiaki, Wake, Norio, Sago, Haruhiko, Kato, Kiyoko
Publicado 2015

Genomic, Epigenomic, and Transcriptomic Profiling towards Identifying Omics Features and Specific Biomarkers That Distinguish Uterine Leiomyosarcoma and Leiomyoma at Molecular Leve...

por Miyata, Tomoko, Sonoda, Kenzo, Tomikawa, Junko, Tayama, Chiharu, Okamura, Kohji, Maehara, Kayoko, Kobayashi, Hiroaki, Wake, Norio, Kato, Kiyoko, Hata, Kenichiro, Nakabayashi, Kazuhiko
Publicado 2015

Placenta-specific epimutation at H19-DMR among common pregnancy complications: its frequency and effect on the expression patterns of H19 and IGF2

por Yamaguchi, Yuko, Tayama, Chiharu, Tomikawa, Junko, Akaishi, Rina, Kamura, Hiromi, Matsuoka, Kentaro, Wake, Norio, Minakami, Hisanori, Kato, Kiyoko, Yamada, Takahiro, Nakabayashi, Kazuhiko, Hata, Kenichiro
Publicado 2019

FBXW7 is involved in the acquisition of the malignant phenotype in epithelial ovarian tumors

por Kitade, Shoko, Onoyama, Ichiro, Kobayashi, Hiroaki, Yagi, Hiroshi, Yoshida, Sachiko, Kato, Masaya, Tsunematsu, Ryosuke, Asanoma, Kazuo, Sonoda, Kenzo, Wake, Norio, Hata, Kenichiro, Nakayama, Keiichi I., Kato, Kiyoko
Publicado 2016

Genome-wide parent-of-origin DNA methylation analysis reveals the intricacies of human imprinting and suggests a germline methylation-independent mechanism of establishment

por Court, Franck, Tayama, Chiharu, Romanelli, Valeria, Martin-Trujillo, Alex, Iglesias-Platas, Isabel, Okamura, Kohji, Sugahara, Naoko, Simón, Carlos, Moore, Harry, Harness, Julie V., Keirstead, Hans, Sanchez-Mut, Jose Vicente, Kaneki, Eisuke, Lapunzina, Pablo, Soejima, Hidenobu, Wake, Norio, Esteller, Manel, Ogata, Tsutomu, Hata, Kenichiro, Nakabayashi, Kazuhiko, Monk, David
Publicado 2014