Examination of the Antimicrobial Peptide Myticalin A6 Active Site
Okimura, Keiko, Matsubara, Keiko, Suzuki, Rie, Ito, Hanako, Sato, Ayumi, Sugimoto, Kaori
Published in Biological & pharmaceutical bulletin (01.04.2021)
Published in Biological & pharmaceutical bulletin (01.04.2021)
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Journal Article
A nationwide survey of Schaaf-Yang syndrome in Japan
Negishi, Yutaka, Kurosawa, Kenji, Takano, Kyoko, Matsubara, Keiko, Nishiyama, Takeshi, Saitoh, Shinji
Published in Journal of human genetics (01.12.2022)
Published in Journal of human genetics (01.12.2022)
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Journal Article
Role of Imprinting Disorders in Short Children Born SGA and Silver-Russell Syndrome Spectrum
Fuke, Tomoko, Nakamura, Akie, Inoue, Takanobu, Kawashima, Sayaka, Hara, Kaori Isono, Matsubara, Keiko, Sano, Shinichiro, Yamazawa, Kazuki, Fukami, Maki, Ogata, Tsutomu, Kagami, Masayo
Published in The journal of clinical endocrinology and metabolism (08.03.2021)
Published in The journal of clinical endocrinology and metabolism (08.03.2021)
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Journal Article
A patient with Silver-Russell syndrome with multilocus imprinting disturbance, and Schimke immuno-osseous dysplasia unmasked by uniparental isodisomy of chromosome 2
Hara-Isono, Kaori, Matsubara, Keiko, Hamada, Riku, Shimada, Shun, Yamaguchi, Tomomi, Wakui, Keiko, Miyazaki, Osamu, Muroya, Koji, Kurosawa, Kenji, Fukami, Maki, Ogata, Tsutomu, Kosho, Tomoki, Kagami, Masayo
Published in Journal of human genetics (01.11.2021)
Published in Journal of human genetics (01.11.2021)
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Journal Article
Collection of 2429 constrained headshots of 277 volunteers for deep learning
Aoto, Saki, Hangai, Mayumi, Ueno-Yokohata, Hitomi, Ueda, Aki, Igarashi, Maki, Ito, Yoshikazu, Tsukamoto, Motoko, Jinno, Tomoko, Sakamoto, Mika, Okazaki, Yuka, Hasegawa, Fuyuki, Ogata-Kawata, Hiroko, Namura, Saki, Kojima, Kazuaki, Kikuya, Masao, Matsubara, Keiko, Taniguchi, Kosuke, Okamura, Kohji
Published in Scientific reports (08.03.2022)
Published in Scientific reports (08.03.2022)
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Journal Article
De Novo Small Supernumerary Marker Chromosomes Arising From Partial Trisomy Rescue
Matsubara, Keiko, Yanagida, Kaede, Nagai, Toshiro, Kagami, Masayo, Fukami, Maki
Published in Frontiers in genetics (27.02.2020)
Published in Frontiers in genetics (27.02.2020)
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Journal Article
Maternal Uniparental Disomy for Chromosome 20: Physical and Endocrinological Characteristics of Five Patients
Kawashima, Sayaka, Nakamura, Akie, Inoue, Takanobu, Matsubara, Keiko, Horikawa, Reiko, Wakui, Keiko, Takano, Kyoko, Fukushima, Yoshimitsu, Tatematsu, Toshi, Mizuno, Seiji, Tsubaki, Junko, Kure, Shigeo, Matsubara, Yoichi, Ogata, Tsutomu, Fukami, Maki, Kagami, Masayo
Published in The journal of clinical endocrinology and metabolism (01.06.2018)
Published in The journal of clinical endocrinology and metabolism (01.06.2018)
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Journal Article
Genome-wide multilocus imprinting disturbance analysis in Temple syndrome and Kagami-Ogata syndrome
Kagami, Masayo, Matsubara, Keiko, Nakabayashi, Kazuhiko, Nakamura, Akie, Sano, Shinichiro, Okamura, Kohji, Hata, Kenichiro, Fukami, Maki, Ogata, Tsutomu
Published in Genetics in medicine (01.04.2017)
Published in Genetics in medicine (01.04.2017)
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Journal Article
Identification of epigenetic memory candidates associated with gestational age at birth through analysis of methylome and transcriptional data
Kashima, Kohei, Kawai, Tomoko, Nishimura, Riki, Shiwa, Yuh, Urayama, Kevin Y, Kamura, Hiromi, Takeda, Kazue, Aoto, Saki, Ito, Atsushi, Matsubara, Keiko, Nagamatsu, Takeshi, Fujii, Tomoyuki, Omori, Isaku, Shimizu, Mitsumasa, Hyodo, Hironobu, Kugu, Koji, Matsumoto, Kenji, Shimizu, Atsushi, Oka, Akira, Mizuguchi, Masashi, Nakabayashi, Kazuhiko, Hata, Kenichiro, Takahashi, Naoto
Published in Scientific reports (09.02.2021)
Published in Scientific reports (09.02.2021)
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Journal Article
The IG-DMR and the MEG3-DMR at human chromosome 14q32.2: hierarchical interaction and distinct functional properties as imprinting control centers
Kagami, Masayo, O'Sullivan, Maureen J, Green, Andrew J, Watabe, Yoshiyuki, Arisaka, Osamu, Masawa, Nobuhide, Matsuoka, Kentarou, Fukami, Maki, Matsubara, Keiko, Kato, Fumiko, Ferguson-Smith, Anne C, Ogata, Tsutomu
Published in PLoS genetics (17.06.2010)
Published in PLoS genetics (17.06.2010)
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Journal Article
Uniparental disomy as a cause of pediatric endocrine disorders
Matsubara, Keiko, Kagami, Masayo, Fukami, Maki
Published in Clinical Pediatric Endocrinology (01.01.2018)
Published in Clinical Pediatric Endocrinology (01.01.2018)
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Journal Article
Next generation sequencing-based mutation screening of 86 patients with idiopathic short stature
Hattori, Atsushi, Katoh-Fukui, Yuko, Nakamura, Akie, Matsubara, Keiko, Kamimaki, Tsutomu, Tanaka, Hiroyuki, Dateki, Sumito, Adachi, Masanori, Muroya, Koji, Yoshida, Shinobu, Ida, Shinobu, Mitani, Marie, Nagasaki, Keisuke, Ogata, Tsutomu, Suzuki, Erina, Hata, Kenichiro, Nakabayashi, Kazuhiko, Matsubara, Yoichi, Narumi, Satoshi, Tanaka, Toshiaki, Fukami, Maki
Published in Endocrine Journal (01.01.2017)
Published in Endocrine Journal (01.01.2017)
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Journal Article
Regulation of Matrix Metalloproteinases-2 and -9 Gene Expression in Cultured Human Fetal Membrane Cells by Influenza Virus Infection
Uchide, Noboru, Obatake, Kyoko, Yamada, Rie, Sadanari, Hidetaka, Matsubara, Keiko, Murayama, Tsugiya, Ohyama, Kunio
Published in Biological & pharmaceutical bulletin (01.12.2016)
Published in Biological & pharmaceutical bulletin (01.12.2016)
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Journal Article
Frequency and clinical characteristics of distinct etiologies in patients with Silver-Russell syndrome diagnosed based on the Netchine-Harbison clinical scoring system
Fuke, Tomoko, Nakamura, Akie, Inoue, Takanobu, Kawashima, Sayaka, Hara-Isono, Kaori, Matsubara, Keiko, Sano, Shinichiro, Yamazawa, Kazuki, Fukami, Maki, Ogata, Tsutomu, Kagami, Masayo
Published in Journal of human genetics (01.10.2022)
Published in Journal of human genetics (01.10.2022)
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Journal Article
Perinatal and neonatal characteristics of Prader–Willi syndrome in Japan
Oto, Yuji, Murakami, Nobuyuki, Imatani, Kaishi, Inoue, Takeshi, Itabashi, Hisashi, Shiraishi, Masahisa, Nitta, Akihisa, Matsubara, Keiko, Kobayashi, Sayuki, Ihara, Hiroshi, Nagai, Toshiro, Matsubara, Tomoyo
Published in Pediatrics international (01.01.2023)
Published in Pediatrics international (01.01.2023)
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Journal Article
Exome‐based genome‐wide screening of rare variants associated with the risk of polycystic ovary syndrome
Tamaoka, Satoshi, Saito, Kazuki, Yoshida, Tomoko, Nakabayashi, Kazuhiko, Tatsumi, Kenichi, Kawamura, Toshihiro, Matsuzaki, Toshiya, Matsubara, Keiko, Ogata‐Kawata, Hiroko, Hata, Kenichiro, Kato‐Fukui, Yuko, Fukami, Maki
Published in Reproductive medicine and biology (01.01.2023)
Published in Reproductive medicine and biology (01.01.2023)
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Journal Article