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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NDNF variants are rare in patients with congenital hypogonadotropic hypogonadism
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Published in Human genome variation (02.02.2021)
Published in Human genome variation (02.02.2021)
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Intrauterine Hyponutrition Reduces Fetal Testosterone Production and Postnatal Sperm Count in the Mouse
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Published in Journal of the Endocrine Society (01.04.2022)
Published in Journal of the Endocrine Society (01.04.2022)
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A case of combined 21‐hydroxylase deficiency and CHARGE syndrome featuring micropenis and cryptorchidism
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Published in Molecular genetics & genomic medicine (01.06.2019)
Published in Molecular genetics & genomic medicine (01.06.2019)
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A novel C-terminal truncating NR5A1 mutation in dizygotic twins
Hattori, Atsushi, Zukeran, Hiroaki, Igarashi, Maki, Toguchi, Suzuka, Toubaru, Yuji, Inoue, Takanobu, Katoh-Fukui, Yuko, Fukami, Maki
Published in Human genome variation (16.03.2017)
Published in Human genome variation (16.03.2017)
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Testicular dysgenesis/regression without campomelic dysplasia in patients carrying missense mutations and upstream deletion of SOX9
Katoh‐Fukui, Yuko, Igarashi, Maki, Nagasaki, Keisuke, Horikawa, Reiko, Nagai, Toshiro, Tsuchiya, Takayoshi, Suzuki, Erina, Miyado, Mami, Hata, Kenichiro, Nakabayashi, Kazuhiko, Hayashi, Keiko, Matsubara, Yoichi, Baba, Takashi, Morohashi, Ken‐ichirou, Igarashi, Arisa, Ogata, Tsutomu, Takada, Shuji, Fukami, Maki
Published in Molecular genetics & genomic medicine (01.11.2015)
Published in Molecular genetics & genomic medicine (01.11.2015)
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Germ cells are essential for sexual dimorphism in the medaka gonad
Kurokawa, Hiromi, Saito, Daisuke, Nakamura, Shuhei, Katoh-Fukui, Yuko, Ohta, Kohei, Baba, Takashi, Morohashi, Ken-ichiro, Tanaka, Minoru
Published in Proceedings of the National Academy of Sciences - PNAS (23.10.2007)
Published in Proceedings of the National Academy of Sciences - PNAS (23.10.2007)
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Quantification of Maternal Microchimeric Cells in the Liver of Children With Biliary Atresia
Tamaoka, Satoshi, Fukuda, Akinari, Katoh‐Fukui, Yuko, Hattori, Atsushi, Uchida, Hajime, Shimizu, Seiichi, Yanagi, Yusuke, Kanaan, Sami B., Sakamoto, Seisuke, Kasahara, Mureo, Yoshioka, Takako, Fukami, Maki
Published in Journal of pediatric gastroenterology and nutrition (01.04.2022)
Published in Journal of pediatric gastroenterology and nutrition (01.04.2022)
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Importance of forkhead transcription factor Fkhl18 for development of testicular vasculature
Sato, Yuko, Baba, Takashi, Zubair, Mohamad, Miyabayashi, Kanako, Toyama, Yoshiro, Maekawa, Mamiko, Owaki, Akiko, Mizusaki, Hirofumi, Sawamura, Tatsuya, Toshimori, Kiyotaka, Morohashi, Ken-Ichirou, Katoh-Fukui, Yuko
Published in Molecular reproduction and development (01.09.2008)
Published in Molecular reproduction and development (01.09.2008)
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Expression levels and DNA methylation profiles of the growth gene SHOX in cartilage tissues and chondrocytes
Hattori, Atsushi, Seki, Atsuhito, Inaba, Naoto, Nakabayashi, Kazuhiko, Takeda, Kazue, Tatsusmi, Kuniko, Naiki, Yasuhiro, Nakamura, Akie, Ishiwata, Keisuke, Matsumoto, Kenji, Nasu, Michiyo, Okamura, Kohji, Michigami, Toshimi, Katoh-Fukui, Yuko, Umezawa, Akihiro, Ogata, Tsutomu, Kagami, Masayo, Fukami, Maki
Published in Scientific reports (05.04.2024)
Published in Scientific reports (05.04.2024)
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Cbx2, a Polycomb Group Gene, Is Required for Sry Gene Expression in Mice
Katoh-Fukui, Yuko, Miyabayashi, Kanako, Komatsu, Tomoko, Owaki, Akiko, Baba, Takashi, Shima, Yuichi, Kidokoro, Tomohide, Kanai, Yoshiakira, Schedl, Andreas, Wilhelm, Dagmar, Koopman, Peter, Okuno, Yasushi, Morohashi, Ken-ichirou
Published in Endocrinology (Philadelphia) (01.02.2012)
Published in Endocrinology (Philadelphia) (01.02.2012)
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Aristaless related homeobox gene, Arx, is implicated in mouse fetal Leydig cell differentiation possibly through expressing in the progenitor cells
Miyabayashi, Kanako, Katoh-Fukui, Yuko, Ogawa, Hidesato, Baba, Takashi, Shima, Yuichi, Sugiyama, Noriyuki, Kitamura, Kunio, Morohashi, Ken-ichirou
Published in PloS one (28.06.2013)
Published in PloS one (28.06.2013)
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MYRF haploinsufficiency causes 46,XY and 46,XX disorders of sex development: bioinformatics consideration
Hamanaka, Kohei, Takata, Atsushi, Uchiyama, Yuri, Miyatake, Satoko, Miyake, Noriko, Mitsuhashi, Satomi, Iwama, Kazuhiro, Fujita, Atsushi, Imagawa, Eri, Alkanaq, Ahmed N, Koshimizu, Eriko, Azuma, Yoshiki, Nakashima, Mitsuko, Mizuguchi, Takeshi, Saitsu, Hirotomo, Wada, Yuka, Minami, Sawako, Katoh-Fukui, Yuko, Masunaga, Yohei, Fukami, Maki, Hasegawa, Tomonobu, Ogata, Tsutomu, Matsumoto, Naomichi
Published in Human molecular genetics (15.07.2019)
Published in Human molecular genetics (15.07.2019)
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Compound heterozygous KCTD19 variants in a man with isolated nonobstructive azoospermia
Muranishi, Yuki, Katoh-Fukui, Yuko, Hattori, Atsushi, Kobori, Yoshitomo, Osaka, Akiyoshi, Okada, Hiroshi, Iwahata, Toshiyuki, Kon, Masafumi, Shinohara, Nobuo, Fukami, Maki
Published in Reproductive medicine and biology (01.01.2024)
Published in Reproductive medicine and biology (01.01.2024)
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A critical time window of Sry action in gonadal sex determination in mice
Ryuji Hiramatsu, Shogo Matoba, Masami Kanai-Azuma, Naoki Tsunekawa, Yuko Katoh-Fukui, Masamichi Kurohmaru, Ken-ichirou Morohashi, Dagmar Wilhelm, Peter Koopman, Yoshiakira Kanai
Published in Development (Cambridge) (01.01.2009)
Published in Development (Cambridge) (01.01.2009)
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Homozygous 6-bp deletion of IGFALS in a prepubertal boy with short stature
Doi, Hibiki, Kageyama, Ikuko, Katoh-Fukui, Yuko, Hattori, Atsushi, Fukami, Maki, Shimura, Naoto
Published in Human genome variation (26.07.2024)
Published in Human genome variation (26.07.2024)
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Journal Article
Next generation sequencing-based mutation screening of 86 patients with idiopathic short stature
Atsushi Hattori, Yuko Katoh-Fukui, Akie Nakamura, Keiko Matsubara, Tsutomu Kamimaki, Hiroyuki Tanaka, Sumito Dateki, Masanori Adachi, Koji Muroya, Shinobu Yoshida, Shinobu Ida, Marie Mitani, Keisuke Nagasaki, Tsutomu Ogata, Erina Suzuki, Kenichiro Hata, Kazuhiko Nakabayashi, Yoichi Matsubara, Satoshi Narumi, Toshiaki Tanaka, Maki Fukami, on behalf of the Japanese SHOX study group
Published in ENDOCRINE JOURNAL (01.10.2017)
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Published in ENDOCRINE JOURNAL (01.10.2017)
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Enhanced Self-Renewal of Hematopoietic Stem Cells Mediated by the Polycomb Gene Product Bmi-1
Iwama, Atsushi, Oguro, Hideyuki, Negishi, Masamitsu, Kato, Yuko, Morita, Youhei, Tsukui, Hiroko, Ema, Hideo, Kamijo, Takehiko, Katoh-Fukui, Yuko, Koseki, Haruhiko, van Lohuizen, Maarten, Nakauchi, Hiromitsu
Published in Immunity (Cambridge, Mass.) (01.12.2004)
Published in Immunity (Cambridge, Mass.) (01.12.2004)
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PTPN11 and FLNA variants in a boy with ambiguous genitalia, short stature, and non-specific dysmorphic features
Muranishi, Yuki, Itonaga, Tomoyo, Ihara, Kenji, Katoh-Fukui, Yuko, Tamaoka, Satoshi, Hattori, Atsushi, Kon, Masafumi, Shinohara, Nobuo, Fukami, Maki
Published in Clinical Pediatric Endocrinology (2024)
Published in Clinical Pediatric Endocrinology (2024)
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WDR11 is another causative gene for coloboma, cardiac anomaly and growth retardation in 10q26 deletion syndrome
Sutani, Akito, Shima, Hirohito, Hijikata, Atsushi, Hosokawa, Susumu, Katoh-Fukui, Yuko, Takasawa, Kei, Suzuki, Erina, Doi, Shozaburo, Shirai, Tsuyoshi, Morio, Tomohiro, Fukami, Maki, Kashimada, Kenichi
Published in European journal of medical genetics (01.01.2020)
Published in European journal of medical genetics (01.01.2020)
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